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                <rdf:li rdf:resource="https://crispr.tyerslab.com/wiki/results/exp514?rev=1767843420&amp;do=diff"/>
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                <rdf:li rdf:resource="https://crispr.tyerslab.com/wiki/results/exp528?rev=1767843420&amp;do=diff"/>
                <rdf:li rdf:resource="https://crispr.tyerslab.com/wiki/results/exp529?rev=1767843420&amp;do=diff"/>
                <rdf:li rdf:resource="https://crispr.tyerslab.com/wiki/results/exp530?rev=1767843420&amp;do=diff"/>
                <rdf:li rdf:resource="https://crispr.tyerslab.com/wiki/results/exp531?rev=1767843420&amp;do=diff"/>
                <rdf:li rdf:resource="https://crispr.tyerslab.com/wiki/results/exp532?rev=1767843420&amp;do=diff"/>
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    </channel>
    <image rdf:about="https://crispr.tyerslab.com/_media/wiki/dokuwiki.svg">
        <title>The Human Chemical-Genetic Interaction Map Project</title>
        <link>https://crispr.tyerslab.com/</link>
        <url>https://crispr.tyerslab.com/_media/wiki/dokuwiki.svg</url>
    </image>
    <item rdf:about="https://crispr.tyerslab.com/wiki/results/exp1?rev=1767843420&amp;do=diff">
        <dc:format>text/html</dc:format>
        <dc:date>2026-01-08T03:37:00+00:00</dc:date>
        <dc:creator>Anonymous (anonymous@undisclosed.example.com)</dc:creator>
        <title>5-Fluorouracil 2μM R00 exp1</title>
        <link>https://crispr.tyerslab.com/wiki/results/exp1?rev=1767843420&amp;do=diff</link>
        <description>5-Fluorouracil 2μM R00 exp1

Mechanism of Action

Thymidylate synthase inhibitor, blocks DNA replication

	*  Class / Subclass 1: Metabolism / Antimetabolite
	*  Class / Subclass 2: DNA Damage, Repair and Replication / Replication Inhibitor

Technical Notes</description>
    </item>
    <item rdf:about="https://crispr.tyerslab.com/wiki/results/exp2?rev=1767843420&amp;do=diff">
        <dc:format>text/html</dc:format>
        <dc:date>2026-01-08T03:37:00+00:00</dc:date>
        <dc:creator>Anonymous (anonymous@undisclosed.example.com)</dc:creator>
        <title>5-Fluorouracil 20μM R00 exp2</title>
        <link>https://crispr.tyerslab.com/wiki/results/exp2?rev=1767843420&amp;do=diff</link>
        <description>5-Fluorouracil 20μM R00 exp2

Mechanism of Action

Thymidylate synthase inhibitor, blocks DNA replication

	*  Class / Subclass 1: Metabolism / Antimetabolite
	*  Class / Subclass 2: DNA Damage, Repair and Replication / Replication Inhibitor

Technical Notes</description>
    </item>
    <item rdf:about="https://crispr.tyerslab.com/wiki/results/exp3?rev=1767843420&amp;do=diff">
        <dc:format>text/html</dc:format>
        <dc:date>2026-01-08T03:37:00+00:00</dc:date>
        <dc:creator>Anonymous (anonymous@undisclosed.example.com)</dc:creator>
        <title>Actinomycin-D 0.001μM R00 exp3</title>
        <link>https://crispr.tyerslab.com/wiki/results/exp3?rev=1767843420&amp;do=diff</link>
        <description>Actinomycin-D 0.001μM R00 exp3

Mechanism of Action

Inhibits RNA polymerases, intercalates DNA, prevents chain elongation

	*  Class / Subclass 1: Gene Regulation / Transcription Inhibitor

Technical Notes

	*  PubChem Name: Dactinomycin
		*  Synonyms:</description>
    </item>
    <item rdf:about="https://crispr.tyerslab.com/wiki/results/exp4?rev=1767843420&amp;do=diff">
        <dc:format>text/html</dc:format>
        <dc:date>2026-01-08T03:37:00+00:00</dc:date>
        <dc:creator>Anonymous (anonymous@undisclosed.example.com)</dc:creator>
        <title>Actinomycin-D 0.01μM R00 exp4</title>
        <link>https://crispr.tyerslab.com/wiki/results/exp4?rev=1767843420&amp;do=diff</link>
        <description>Actinomycin-D 0.01μM R00 exp4

Mechanism of Action

Inhibits RNA polymerases, intercalates DNA, prevents chain elongation

	*  Class / Subclass 1: Gene Regulation / Transcription Inhibitor

Technical Notes

	*  PubChem Name: Dactinomycin
		*  Synonyms:</description>
    </item>
    <item rdf:about="https://crispr.tyerslab.com/wiki/results/exp5?rev=1767843420&amp;do=diff">
        <dc:format>text/html</dc:format>
        <dc:date>2026-01-08T03:37:00+00:00</dc:date>
        <dc:creator>Anonymous (anonymous@undisclosed.example.com)</dc:creator>
        <title>Alpha-Amanitin 0.5μM R00 exp5</title>
        <link>https://crispr.tyerslab.com/wiki/results/exp5?rev=1767843420&amp;do=diff</link>
        <description>Alpha-Amanitin 0.5μM R00 exp5

Mechanism of Action

Inhibits RNA polymerase II and III, interferes with translocation

	*  Class / Subclass 1: Gene Regulation / Transcription Inhibitor
	*  Class / Subclass 2: Environmental Stresses / Toxin

Technical Notes</description>
    </item>
    <item rdf:about="https://crispr.tyerslab.com/wiki/results/exp6?rev=1767843420&amp;do=diff">
        <dc:format>text/html</dc:format>
        <dc:date>2026-01-08T03:37:00+00:00</dc:date>
        <dc:creator>Anonymous (anonymous@undisclosed.example.com)</dc:creator>
        <title>Bortezomib 0.005μM R00 exp6</title>
        <link>https://crispr.tyerslab.com/wiki/results/exp6?rev=1767843420&amp;do=diff</link>
        <description>Bortezomib 0.005μM R00 exp6

Mechanism of Action

Inhibits 26S proteasome, binds reversibly to chymotrypsin-like catalytic sites

	*  Class / Subclass 1: Proteostasis / Proteasome Inhibitor

Technical Notes

	*  PubChem Name: Bortezomib
		*  Synonyms:</description>
    </item>
    <item rdf:about="https://crispr.tyerslab.com/wiki/results/exp7?rev=1767843420&amp;do=diff">
        <dc:format>text/html</dc:format>
        <dc:date>2026-01-08T03:37:00+00:00</dc:date>
        <dc:creator>Anonymous (anonymous@undisclosed.example.com)</dc:creator>
        <title>Bortezomib 0.05μM R00 exp7</title>
        <link>https://crispr.tyerslab.com/wiki/results/exp7?rev=1767843420&amp;do=diff</link>
        <description>Bortezomib 0.05μM R00 exp7

Mechanism of Action

Inhibits 26S proteasome, binds reversibly to chymotrypsin-like catalytic sites

	*  Class / Subclass 1: Proteostasis / Proteasome Inhibitor

Technical Notes

	*  PubChem Name: Bortezomib
		*  Synonyms:</description>
    </item>
    <item rdf:about="https://crispr.tyerslab.com/wiki/results/exp8?rev=1767843420&amp;do=diff">
        <dc:format>text/html</dc:format>
        <dc:date>2026-01-08T03:37:00+00:00</dc:date>
        <dc:creator>Anonymous (anonymous@undisclosed.example.com)</dc:creator>
        <title>Brefeldin A 0.02μM R00 exp8</title>
        <link>https://crispr.tyerslab.com/wiki/results/exp8?rev=1767843420&amp;do=diff</link>
        <description>Brefeldin A 0.02μM R00 exp8

Mechanism of Action

Inhibits Golgi to ER transport, forms uncompetitive complex with GBF1 and GDP-bound Arf1

	*  Class / Subclass 1: Organelle Function / Vesicule Trafficking Inhibitor

Technical Notes

	*  PubChem Name:</description>
    </item>
    <item rdf:about="https://crispr.tyerslab.com/wiki/results/exp10?rev=1767843420&amp;do=diff">
        <dc:format>text/html</dc:format>
        <dc:date>2026-01-08T03:37:00+00:00</dc:date>
        <dc:creator>Anonymous (anonymous@undisclosed.example.com)</dc:creator>
        <title>CCCP 0.1μM R00 exp10</title>
        <link>https://crispr.tyerslab.com/wiki/results/exp10?rev=1767843420&amp;do=diff</link>
        <description>CCCP 0.1μM R00 exp10

Mechanism of Action

Mitochondrial proton gradient uncoupler, disrupts ATP synthesis

	*  Class / Subclass 1: Organelle Function / Mitochondrial Inhibitor

Technical Notes

	*  PubChem Name: (3-Chlorophenyl)hydrazonomalononitrile</description>
    </item>
    <item rdf:about="https://crispr.tyerslab.com/wiki/results/exp11?rev=1767843420&amp;do=diff">
        <dc:format>text/html</dc:format>
        <dc:date>2026-01-08T03:37:00+00:00</dc:date>
        <dc:creator>Anonymous (anonymous@undisclosed.example.com)</dc:creator>
        <title>CCCP 1μM R00 exp11</title>
        <link>https://crispr.tyerslab.com/wiki/results/exp11?rev=1767843420&amp;do=diff</link>
        <description>CCCP 1μM R00 exp11

Mechanism of Action

Mitochondrial proton gradient uncoupler, disrupts ATP synthesis

	*  Class / Subclass 1: Organelle Function / Mitochondrial Inhibitor

Technical Notes

	*  PubChem Name: (3-Chlorophenyl)hydrazonomalononitrile</description>
    </item>
    <item rdf:about="https://crispr.tyerslab.com/wiki/results/exp12?rev=1767843420&amp;do=diff">
        <dc:format>text/html</dc:format>
        <dc:date>2026-01-08T03:37:00+00:00</dc:date>
        <dc:creator>Anonymous (anonymous@undisclosed.example.com)</dc:creator>
        <title>Chloramphenicol 2μM R00 exp12</title>
        <link>https://crispr.tyerslab.com/wiki/results/exp12?rev=1767843420&amp;do=diff</link>
        <description>Chloramphenicol 2μM R00 exp12

Mechanism of Action

Binds 23S rRNA of 50S ribosomal subunit, inhibits protein synthesis

	*  Class / Subclass 1: Infectious Disease / Antibiotic
	*  Class / Subclass 2: Organelle Function / Mitochondrial Inhibitor

Technical Notes</description>
    </item>
    <item rdf:about="https://crispr.tyerslab.com/wiki/results/exp13?rev=1767843420&amp;do=diff">
        <dc:format>text/html</dc:format>
        <dc:date>2026-01-08T03:37:00+00:00</dc:date>
        <dc:creator>Anonymous (anonymous@undisclosed.example.com)</dc:creator>
        <title>Chloramphenicol 20μM R00 exp13</title>
        <link>https://crispr.tyerslab.com/wiki/results/exp13?rev=1767843420&amp;do=diff</link>
        <description>Chloramphenicol 20μM R00 exp13

Mechanism of Action

Binds 23S rRNA of 50S ribosomal subunit, inhibits protein synthesis

	*  Class / Subclass 1: Infectious Disease / Antibiotic
	*  Class / Subclass 2: Organelle Function / Mitochondrial Inhibitor

Technical Notes</description>
    </item>
    <item rdf:about="https://crispr.tyerslab.com/wiki/results/exp14?rev=1767843420&amp;do=diff">
        <dc:format>text/html</dc:format>
        <dc:date>2026-01-08T03:37:00+00:00</dc:date>
        <dc:creator>Anonymous (anonymous@undisclosed.example.com)</dc:creator>
        <title>Cycloheximide 0.02μM R00 exp14</title>
        <link>https://crispr.tyerslab.com/wiki/results/exp14?rev=1767843420&amp;do=diff</link>
        <description>Cycloheximide 0.02μM R00 exp14

Mechanism of Action

Translation elongation inhibitor, binds 60S ribosomal subunit

	*  Class / Subclass 1: Proteostasis / Translation Inhibitor
	*  Class / Subclass 2: Environmental Stresses / Toxin

Technical Notes</description>
    </item>
    <item rdf:about="https://crispr.tyerslab.com/wiki/results/exp15?rev=1767843420&amp;do=diff">
        <dc:format>text/html</dc:format>
        <dc:date>2026-01-08T03:37:00+00:00</dc:date>
        <dc:creator>Anonymous (anonymous@undisclosed.example.com)</dc:creator>
        <title>Cycloheximide 0.2μM R00 exp15</title>
        <link>https://crispr.tyerslab.com/wiki/results/exp15?rev=1767843420&amp;do=diff</link>
        <description>Cycloheximide 0.2μM R00 exp15

Mechanism of Action

Translation elongation inhibitor, binds 60S ribosomal subunit

	*  Class / Subclass 1: Proteostasis / Translation Inhibitor
	*  Class / Subclass 2: Environmental Stresses / Toxin

Technical Notes</description>
    </item>
    <item rdf:about="https://crispr.tyerslab.com/wiki/results/exp16?rev=1767843420&amp;do=diff">
        <dc:format>text/html</dc:format>
        <dc:date>2026-01-08T03:37:00+00:00</dc:date>
        <dc:creator>Anonymous (anonymous@undisclosed.example.com)</dc:creator>
        <title>DABN 2μM R00 exp16</title>
        <link>https://crispr.tyerslab.com/wiki/results/exp16?rev=1767843420&amp;do=diff</link>
        <description>DABN 2μM R00 exp16

Mechanism of Action

Unknown

	*  Class / Subclass 1: Uncharacterized Mechanism / Chemical Screen Hit

Technical Notes

	*  PubChem Name: [1,1&#039;-Binaphthalene]-2,2&#039;-diamine
		*  Synonyms: N/A
		*  CAS #: 4488-22-6
		*  PubChem CID:</description>
    </item>
    <item rdf:about="https://crispr.tyerslab.com/wiki/results/exp17?rev=1767843420&amp;do=diff">
        <dc:format>text/html</dc:format>
        <dc:date>2026-01-08T03:37:00+00:00</dc:date>
        <dc:creator>Anonymous (anonymous@undisclosed.example.com)</dc:creator>
        <title>DABN 20μM R00 exp17</title>
        <link>https://crispr.tyerslab.com/wiki/results/exp17?rev=1767843420&amp;do=diff</link>
        <description>DABN 20μM R00 exp17

Mechanism of Action

Unknown

	*  Class / Subclass 1: Uncharacterized Mechanism / Chemical Screen Hit

Technical Notes

	*  PubChem Name: [1,1&#039;-Binaphthalene]-2,2&#039;-diamine
		*  Synonyms: N/A
		*  CAS #: 4488-22-6
		*  PubChem CID:</description>
    </item>
    <item rdf:about="https://crispr.tyerslab.com/wiki/results/exp18?rev=1767843420&amp;do=diff">
        <dc:format>text/html</dc:format>
        <dc:date>2026-01-08T03:37:00+00:00</dc:date>
        <dc:creator>Anonymous (anonymous@undisclosed.example.com)</dc:creator>
        <title>Doxycycline 10μM R00 exp18</title>
        <link>https://crispr.tyerslab.com/wiki/results/exp18?rev=1767843420&amp;do=diff</link>
        <description>Doxycycline 10μM R00 exp18

Mechanism of Action

Inhibits bacterial 30S ribosome, also used in tet-on/tet-off gene expression control

	*  Class / Subclass 1: Infectious Disease / Antibiotic
	*  Class / Subclass 2: Organelle Function / Mitochondrial Inhibitor</description>
    </item>
    <item rdf:about="https://crispr.tyerslab.com/wiki/results/exp19?rev=1767843420&amp;do=diff">
        <dc:format>text/html</dc:format>
        <dc:date>2026-01-08T03:37:00+00:00</dc:date>
        <dc:creator>Anonymous (anonymous@undisclosed.example.com)</dc:creator>
        <title>Etoposide 1μM R00 exp19</title>
        <link>https://crispr.tyerslab.com/wiki/results/exp19?rev=1767843420&amp;do=diff</link>
        <description>Etoposide 1μM R00 exp19

Mechanism of Action

Binds DNA-TopII complex, blocks re-ligation, induces strand breaks, semi-synthetic derivative of podophyllotoxin

	*  Class / Subclass 1: DNA Damage, Repair and Replication / Topoisomerase II Inhibitor

Technical Notes</description>
    </item>
    <item rdf:about="https://crispr.tyerslab.com/wiki/results/exp20?rev=1767843420&amp;do=diff">
        <dc:format>text/html</dc:format>
        <dc:date>2026-01-08T03:37:00+00:00</dc:date>
        <dc:creator>Anonymous (anonymous@undisclosed.example.com)</dc:creator>
        <title>Etoposide 10μM R00 exp20</title>
        <link>https://crispr.tyerslab.com/wiki/results/exp20?rev=1767843420&amp;do=diff</link>
        <description>Etoposide 10μM R00 exp20

Mechanism of Action

Binds DNA-TopII complex, blocks re-ligation, induces strand breaks, semi-synthetic derivative of podophyllotoxin

	*  Class / Subclass 1: DNA Damage, Repair and Replication / Topoisomerase II Inhibitor</description>
    </item>
    <item rdf:about="https://crispr.tyerslab.com/wiki/results/exp21?rev=1767843420&amp;do=diff">
        <dc:format>text/html</dc:format>
        <dc:date>2026-01-08T03:37:00+00:00</dc:date>
        <dc:creator>Anonymous (anonymous@undisclosed.example.com)</dc:creator>
        <title>MLN-4924 0.2μM R00 exp21</title>
        <link>https://crispr.tyerslab.com/wiki/results/exp21?rev=1767843420&amp;do=diff</link>
        <description>MLN-4924 0.2μM R00 exp21

Mechanism of Action

Inhibits NEDD8-activating enzyme (NAE), prevents activity of cullin-RING ligase (CRL) E3 enzymes

	*  Class / Subclass 1: Proteostasis / NEDDylation Inhibitor

Technical Notes

	*  PubChem Name: Pevonedistat</description>
    </item>
    <item rdf:about="https://crispr.tyerslab.com/wiki/results/exp22?rev=1767843420&amp;do=diff">
        <dc:format>text/html</dc:format>
        <dc:date>2026-01-08T03:37:00+00:00</dc:date>
        <dc:creator>Anonymous (anonymous@undisclosed.example.com)</dc:creator>
        <title>MLN-4924 2μM R00 exp22</title>
        <link>https://crispr.tyerslab.com/wiki/results/exp22?rev=1767843420&amp;do=diff</link>
        <description>MLN-4924 2μM R00 exp22

Mechanism of Action

Inhibits NEDD8-activating enzyme (NAE), prevents activity of cullin-RING ligase (CRL) E3 enzymes

	*  Class / Subclass 1: Proteostasis / NEDDylation Inhibitor

Technical Notes

	*  PubChem Name: Pevonedistat</description>
    </item>
    <item rdf:about="https://crispr.tyerslab.com/wiki/results/exp23?rev=1767843420&amp;do=diff">
        <dc:format>text/html</dc:format>
        <dc:date>2026-01-08T03:37:00+00:00</dc:date>
        <dc:creator>Anonymous (anonymous@undisclosed.example.com)</dc:creator>
        <title>Nocodazole 0.02μM R00 exp23</title>
        <link>https://crispr.tyerslab.com/wiki/results/exp23?rev=1767843420&amp;do=diff</link>
        <description>Nocodazole 0.02μM R00 exp23

Mechanism of Action

Inhibits microtubule polymerization and mitotic spindle formation, induces spindle assembly checkpoint (SAC)

	*  Class / Subclass 1: Cell Cycle / Microtubule Poison
	*  Class / Subclass 2: Organelle Function / Cytoskeletal Inhibitor</description>
    </item>
    <item rdf:about="https://crispr.tyerslab.com/wiki/results/exp24?rev=1767843420&amp;do=diff">
        <dc:format>text/html</dc:format>
        <dc:date>2026-01-08T03:37:00+00:00</dc:date>
        <dc:creator>Anonymous (anonymous@undisclosed.example.com)</dc:creator>
        <title>Nocodazole 0.2μM R00 exp24</title>
        <link>https://crispr.tyerslab.com/wiki/results/exp24?rev=1767843420&amp;do=diff</link>
        <description>Nocodazole 0.2μM R00 exp24

Mechanism of Action

Inhibits microtubule polymerization and mitotic spindle formation, induces spindle assembly checkpoint (SAC)

	*  Class / Subclass 1: Cell Cycle / Microtubule Poison
	*  Class / Subclass 2: Organelle Function / Cytoskeletal Inhibitor</description>
    </item>
    <item rdf:about="https://crispr.tyerslab.com/wiki/results/exp25?rev=1767843420&amp;do=diff">
        <dc:format>text/html</dc:format>
        <dc:date>2026-01-08T03:37:00+00:00</dc:date>
        <dc:creator>Anonymous (anonymous@undisclosed.example.com)</dc:creator>
        <title>Oligomycin-A 2μM R00 exp25</title>
        <link>https://crispr.tyerslab.com/wiki/results/exp25?rev=1767843420&amp;do=diff</link>
        <description>Oligomycin-A 2μM R00 exp25

Mechanism of Action

Inhibits F0 proton channel of mitochondrial ATP synthase, blocks electron flow through ETC

	*  Class / Subclass 1: Organelle Function / Mitochondrial Inhibitor

Technical Notes

	*  PubChem Name: Oligomycin A</description>
    </item>
    <item rdf:about="https://crispr.tyerslab.com/wiki/results/exp26?rev=1767843420&amp;do=diff">
        <dc:format>text/html</dc:format>
        <dc:date>2026-01-08T03:37:00+00:00</dc:date>
        <dc:creator>Anonymous (anonymous@undisclosed.example.com)</dc:creator>
        <title>Oligomycin-A 20μM R00 exp26</title>
        <link>https://crispr.tyerslab.com/wiki/results/exp26?rev=1767843420&amp;do=diff</link>
        <description>Oligomycin-A 20μM R00 exp26

Mechanism of Action

Inhibits F0 proton channel of mitochondrial ATP synthase, blocks electron flow through ETC

	*  Class / Subclass 1: Organelle Function / Mitochondrial Inhibitor

Technical Notes

	*  PubChem Name: Oligomycin A</description>
    </item>
    <item rdf:about="https://crispr.tyerslab.com/wiki/results/exp27?rev=1767843420&amp;do=diff">
        <dc:format>text/html</dc:format>
        <dc:date>2026-01-08T03:37:00+00:00</dc:date>
        <dc:creator>Anonymous (anonymous@undisclosed.example.com)</dc:creator>
        <title>Pimelic-diphenylamide-106 0.5μM R00 exp27</title>
        <link>https://crispr.tyerslab.com/wiki/results/exp27?rev=1767843420&amp;do=diff</link>
        <description>Pimelic-diphenylamide-106 0.5μM R00 exp27

Mechanism of Action

Inhibits HDAC3 selectively, benzamide derivative

	*  Class / Subclass 1: Gene Regulation / Epigenetic Inhibitor

Technical Notes

	*  PubChem Name: Pimelic Diphenylamide 106
		*  Synonyms:</description>
    </item>
    <item rdf:about="https://crispr.tyerslab.com/wiki/results/exp28?rev=1767843420&amp;do=diff">
        <dc:format>text/html</dc:format>
        <dc:date>2026-01-08T03:37:00+00:00</dc:date>
        <dc:creator>Anonymous (anonymous@undisclosed.example.com)</dc:creator>
        <title>Pimelic-diphenylamide-106 5μM R00 exp28</title>
        <link>https://crispr.tyerslab.com/wiki/results/exp28?rev=1767843420&amp;do=diff</link>
        <description>Pimelic-diphenylamide-106 5μM R00 exp28

Mechanism of Action

Inhibits HDAC3 selectively, benzamide derivative

	*  Class / Subclass 1: Gene Regulation / Epigenetic Inhibitor

Technical Notes

	*  PubChem Name: Pimelic Diphenylamide 106
		*  Synonyms:</description>
    </item>
    <item rdf:about="https://crispr.tyerslab.com/wiki/results/exp29?rev=1767843420&amp;do=diff">
        <dc:format>text/html</dc:format>
        <dc:date>2026-01-08T03:37:00+00:00</dc:date>
        <dc:creator>Anonymous (anonymous@undisclosed.example.com)</dc:creator>
        <title>Rapamycin 1μM R00 exp29</title>
        <link>https://crispr.tyerslab.com/wiki/results/exp29?rev=1767843420&amp;do=diff</link>
        <description>Rapamycin 1μM R00 exp29

Mechanism of Action

Allosteric mTORC1 inhibitor, forms ternary complex with FKBP12 and mTOR, attenuates protein synthesis and metabolism

	*  Class / Subclass 1: Signal Transduction / Kinase Inhibitor
	*  Class / Subclass 2:</description>
    </item>
    <item rdf:about="https://crispr.tyerslab.com/wiki/results/exp30?rev=1767843420&amp;do=diff">
        <dc:format>text/html</dc:format>
        <dc:date>2026-01-08T03:37:00+00:00</dc:date>
        <dc:creator>Anonymous (anonymous@undisclosed.example.com)</dc:creator>
        <title>Rapamycin 10μM R00 exp30</title>
        <link>https://crispr.tyerslab.com/wiki/results/exp30?rev=1767843420&amp;do=diff</link>
        <description>Rapamycin 10μM R00 exp30

Mechanism of Action

Allosteric mTORC1 inhibitor, forms ternary complex with FKBP12 and mTOR, attenuates protein synthesis and metabolism

	*  Class / Subclass 1: Signal Transduction / Kinase Inhibitor
	*  Class / Subclass 2:</description>
    </item>
    <item rdf:about="https://crispr.tyerslab.com/wiki/results/exp31?rev=1767843420&amp;do=diff">
        <dc:format>text/html</dc:format>
        <dc:date>2026-01-08T03:37:00+00:00</dc:date>
        <dc:creator>Anonymous (anonymous@undisclosed.example.com)</dc:creator>
        <title>Rifampicin 1μM R00 exp31</title>
        <link>https://crispr.tyerslab.com/wiki/results/exp31?rev=1767843420&amp;do=diff</link>
        <description>Rifampicin 1μM R00 exp31

Mechanism of Action

Inhibits bacterial RNA polymerase, induces hepatic cytochrome P450 enzymes

	*  Class / Subclass 1: Infectious Disease / Antibiotic

Technical Notes

	*  PubChem Name: Rifampicin
		*  Synonyms: Rifampin; Rifamycin AMP</description>
    </item>
    <item rdf:about="https://crispr.tyerslab.com/wiki/results/exp32?rev=1767843420&amp;do=diff">
        <dc:format>text/html</dc:format>
        <dc:date>2026-01-08T03:37:00+00:00</dc:date>
        <dc:creator>Anonymous (anonymous@undisclosed.example.com)</dc:creator>
        <title>Rifampicin 10μM R00 exp32</title>
        <link>https://crispr.tyerslab.com/wiki/results/exp32?rev=1767843420&amp;do=diff</link>
        <description>Rifampicin 10μM R00 exp32

Mechanism of Action

Inhibits bacterial RNA polymerase, induces hepatic cytochrome P450 enzymes

	*  Class / Subclass 1: Infectious Disease / Antibiotic

Technical Notes

	*  PubChem Name: Rifampicin
		*  Synonyms: Rifampin; Rifamycin AMP</description>
    </item>
    <item rdf:about="https://crispr.tyerslab.com/wiki/results/exp33?rev=1767843420&amp;do=diff">
        <dc:format>text/html</dc:format>
        <dc:date>2026-01-08T03:37:00+00:00</dc:date>
        <dc:creator>Anonymous (anonymous@undisclosed.example.com)</dc:creator>
        <title>Rotenone 2μM R00 exp33</title>
        <link>https://crispr.tyerslab.com/wiki/results/exp33?rev=1767843420&amp;do=diff</link>
        <description>Rotenone 2μM R00 exp33

Mechanism of Action

Inhibits complex I, blocks electron transfer from iron-sulfur centers to ubiquinone, generates ROS, also inhibits microtubule assembly

	*  Class / Subclass 1: Organelle Function / Mitochondrial Inhibitor</description>
    </item>
    <item rdf:about="https://crispr.tyerslab.com/wiki/results/exp34?rev=1767843420&amp;do=diff">
        <dc:format>text/html</dc:format>
        <dc:date>2026-01-08T03:37:00+00:00</dc:date>
        <dc:creator>Anonymous (anonymous@undisclosed.example.com)</dc:creator>
        <title>Rotenone 20μM R00 exp34</title>
        <link>https://crispr.tyerslab.com/wiki/results/exp34?rev=1767843420&amp;do=diff</link>
        <description>Rotenone 20μM R00 exp34

Mechanism of Action

Inhibits complex I, blocks electron transfer from iron-sulfur centers to ubiquinone, generates ROS, also inhibits microtubule assembly

	*  Class / Subclass 1: Organelle Function / Mitochondrial Inhibitor</description>
    </item>
    <item rdf:about="https://crispr.tyerslab.com/wiki/results/exp35?rev=1767843420&amp;do=diff">
        <dc:format>text/html</dc:format>
        <dc:date>2026-01-08T03:37:00+00:00</dc:date>
        <dc:creator>Anonymous (anonymous@undisclosed.example.com)</dc:creator>
        <title>TRAIL 5ng/ml R00 exp35</title>
        <link>https://crispr.tyerslab.com/wiki/results/exp35?rev=1767843420&amp;do=diff</link>
        <description>TRAIL 5ng/ml R00 exp35

Mechanism of Action

TNF-related apoptosis-inducing ligand, TNF superfamily member, induces extrinsic apoptosis

	*  Class / Subclass 1: Signal Transduction / Other Receptor Agonist

Technical Notes

	*  PubChem Name: N/A
		*</description>
    </item>
    <item rdf:about="https://crispr.tyerslab.com/wiki/results/exp36?rev=1767843420&amp;do=diff">
        <dc:format>text/html</dc:format>
        <dc:date>2026-01-08T03:37:00+00:00</dc:date>
        <dc:creator>Anonymous (anonymous@undisclosed.example.com)</dc:creator>
        <title>TRAIL 50ng/ml R00 exp36</title>
        <link>https://crispr.tyerslab.com/wiki/results/exp36?rev=1767843420&amp;do=diff</link>
        <description>TRAIL 50ng/ml R00 exp36

Mechanism of Action

TNF-related apoptosis-inducing ligand, TNF superfamily member, induces extrinsic apoptosis

	*  Class / Subclass 1: Signal Transduction / Other Receptor Agonist

Technical Notes

	*  PubChem Name: N/A
		*</description>
    </item>
    <item rdf:about="https://crispr.tyerslab.com/wiki/results/exp37?rev=1767843420&amp;do=diff">
        <dc:format>text/html</dc:format>
        <dc:date>2026-01-08T03:37:00+00:00</dc:date>
        <dc:creator>Anonymous (anonymous@undisclosed.example.com)</dc:creator>
        <title>Wortmannin 0.5μM R00 exp37</title>
        <link>https://crispr.tyerslab.com/wiki/results/exp37?rev=1767843420&amp;do=diff</link>
        <description>Wortmannin 0.5μM R00 exp37

Mechanism of Action

Inhibits PI3K and PI3K-related enzymes, non-specific covalent inhibitor

	*  Class / Subclass 1: Signal Transduction / Kinase Inhibitor
	*  Class / Subclass 2: Proteostasis / Autophagy Inhibitor

Technical Notes</description>
    </item>
    <item rdf:about="https://crispr.tyerslab.com/wiki/results/exp38?rev=1767843420&amp;do=diff">
        <dc:format>text/html</dc:format>
        <dc:date>2026-01-08T03:37:00+00:00</dc:date>
        <dc:creator>Anonymous (anonymous@undisclosed.example.com)</dc:creator>
        <title>Wortmannin 5μM R00 exp38</title>
        <link>https://crispr.tyerslab.com/wiki/results/exp38?rev=1767843420&amp;do=diff</link>
        <description>Wortmannin 5μM R00 exp38

Mechanism of Action

Inhibits PI3K and PI3K-related enzymes, non-specific covalent inhibitor

	*  Class / Subclass 1: Signal Transduction / Kinase Inhibitor
	*  Class / Subclass 2: Proteostasis / Autophagy Inhibitor

Technical Notes</description>
    </item>
    <item rdf:about="https://crispr.tyerslab.com/wiki/results/exp40?rev=1767843420&amp;do=diff">
        <dc:format>text/html</dc:format>
        <dc:date>2026-01-08T03:37:00+00:00</dc:date>
        <dc:creator>Anonymous (anonymous@undisclosed.example.com)</dc:creator>
        <title>2-Methoxyestradiol 0.2μM R01 exp40</title>
        <link>https://crispr.tyerslab.com/wiki/results/exp40?rev=1767843420&amp;do=diff</link>
        <description>2-Methoxyestradiol 0.2μM R01 exp40

Mechanism of Action

Endogenous estradiol metabolite, weak agonist for estrogen receptor, agonist of GPER1, microtubule destabilizer

	*  Class / Subclass 1: Metabolism / Metabolite
	*  Class / Subclass 2: Signal Transduction / GPCR Agonist</description>
    </item>
    <item rdf:about="https://crispr.tyerslab.com/wiki/results/exp41?rev=1767843420&amp;do=diff">
        <dc:format>text/html</dc:format>
        <dc:date>2026-01-08T03:37:00+00:00</dc:date>
        <dc:creator>Anonymous (anonymous@undisclosed.example.com)</dc:creator>
        <title>BI-2536 0.001μM R01 exp41</title>
        <link>https://crispr.tyerslab.com/wiki/results/exp41?rev=1767843420&amp;do=diff</link>
        <description>BI-2536 0.001μM R01 exp41

Mechanism of Action

Inhibits PLK1 kinase, causes G2/M arrest

	*  Class / Subclass 1: Cell Cycle / Mitotic Inhibitor
	*  Class / Subclass 2: Signal Transduction / Kinase Inhibitor

Technical Notes

	*  PubChem Name: BI-2536</description>
    </item>
    <item rdf:about="https://crispr.tyerslab.com/wiki/results/exp42?rev=1767843420&amp;do=diff">
        <dc:format>text/html</dc:format>
        <dc:date>2026-01-08T03:37:00+00:00</dc:date>
        <dc:creator>Anonymous (anonymous@undisclosed.example.com)</dc:creator>
        <title>BI-6727 0.001μM R01 exp42</title>
        <link>https://crispr.tyerslab.com/wiki/results/exp42?rev=1767843420&amp;do=diff</link>
        <description>BI-6727 0.001μM R01 exp42

Mechanism of Action

Inhibits PLK1 kinase, causes G2/M arrest, improved version of BI-2536

	*  Class / Subclass 1: Cell Cycle / Mitotic Inhibitor
	*  Class / Subclass 2: Signal Transduction / Kinase Inhibitor

Technical Notes</description>
    </item>
    <item rdf:about="https://crispr.tyerslab.com/wiki/results/exp45?rev=1767843420&amp;do=diff">
        <dc:format>text/html</dc:format>
        <dc:date>2026-01-08T03:37:00+00:00</dc:date>
        <dc:creator>Anonymous (anonymous@undisclosed.example.com)</dc:creator>
        <title>Docetaxel 0.002μM R01 exp45</title>
        <link>https://crispr.tyerslab.com/wiki/results/exp45?rev=1767843420&amp;do=diff</link>
        <description>Docetaxel 0.002μM R01 exp45

Mechanism of Action

Inihibts microtubule depolymerization, semi-synthetic analog of the paclitaxel

	*  Class / Subclass 1: Cell Cycle / Microtubule Poison
	*  Class / Subclass 2: Organelle Function / Cytoskeletal Inhibitor</description>
    </item>
    <item rdf:about="https://crispr.tyerslab.com/wiki/results/exp46?rev=1767843420&amp;do=diff">
        <dc:format>text/html</dc:format>
        <dc:date>2026-01-08T03:37:00+00:00</dc:date>
        <dc:creator>Anonymous (anonymous@undisclosed.example.com)</dc:creator>
        <title>HMS-I1 1μM R01 exp46</title>
        <link>https://crispr.tyerslab.com/wiki/results/exp46?rev=1767843420&amp;do=diff</link>
        <description>HMS-I1 1μM R01 exp46

Mechanism of Action

Inhibits HDAC

	*  Class / Subclass 1: Uncharacterized Mechanism / Chemical Screen Hit

Technical Notes

	*  PubChem Name: 2-(2,3-Dihydro-1,4-benzodioxin-6-yl)-6-methylimidazo[1,2-a]pyridine
		*  Synonyms: N/A</description>
    </item>
    <item rdf:about="https://crispr.tyerslab.com/wiki/results/exp47?rev=1767843420&amp;do=diff">
        <dc:format>text/html</dc:format>
        <dc:date>2026-01-08T03:37:00+00:00</dc:date>
        <dc:creator>Anonymous (anonymous@undisclosed.example.com)</dc:creator>
        <title>Lapatinib 5μM R01 exp47</title>
        <link>https://crispr.tyerslab.com/wiki/results/exp47?rev=1767843420&amp;do=diff</link>
        <description>Lapatinib 5μM R01 exp47

Mechanism of Action

Inhibits EGFR and ErbB2 receptor tyrosine kinases

	*  Class / Subclass 1: Signal Transduction / Kinase Inhibitor

Technical Notes

	*  PubChem Name: Lapatinib Ditosylate
		*  Synonyms: GW-572016 ditosylate</description>
    </item>
    <item rdf:about="https://crispr.tyerslab.com/wiki/results/exp48?rev=1767843420&amp;do=diff">
        <dc:format>text/html</dc:format>
        <dc:date>2026-01-08T03:37:00+00:00</dc:date>
        <dc:creator>Anonymous (anonymous@undisclosed.example.com)</dc:creator>
        <title>Mubritinib 0.2μM R01 exp48</title>
        <link>https://crispr.tyerslab.com/wiki/results/exp48?rev=1767843420&amp;do=diff</link>
        <description>Mubritinib 0.2μM R01 exp48

Mechanism of Action

Inhibits HER2 (Erb2) EGFR receptor tyrosine kinase

	*  Class / Subclass 1: Signal Transduction / Kinase Inhibitor

Technical Notes

	*  PubChem Name: Mubritinib
		*  Synonyms: TAK-165
		*  CAS #: 366017-09-6</description>
    </item>
    <item rdf:about="https://crispr.tyerslab.com/wiki/results/exp49?rev=1767843420&amp;do=diff">
        <dc:format>text/html</dc:format>
        <dc:date>2026-01-08T03:37:00+00:00</dc:date>
        <dc:creator>Anonymous (anonymous@undisclosed.example.com)</dc:creator>
        <title>NFN1 0.1μM R01 exp49</title>
        <link>https://crispr.tyerslab.com/wiki/results/exp49?rev=1767843420&amp;do=diff</link>
        <description>NFN1 0.1μM R01 exp49

Mechanism of Action

Nitrofuran derivative, candidate ALDH2 inhibitor

	*  Class / Subclass 1: Infectious Disease / Antibiotic

Technical Notes

	*  PubChem Name: Ethyl 5-ethyl-2-[(5-nitrofuran-2-carbonyl)amino]thiophene-3-carboxylate</description>
    </item>
    <item rdf:about="https://crispr.tyerslab.com/wiki/results/exp50?rev=1767843420&amp;do=diff">
        <dc:format>text/html</dc:format>
        <dc:date>2026-01-08T03:37:00+00:00</dc:date>
        <dc:creator>Anonymous (anonymous@undisclosed.example.com)</dc:creator>
        <title>Nicotinamide 2000μM R01 exp50</title>
        <link>https://crispr.tyerslab.com/wiki/results/exp50?rev=1767843420&amp;do=diff</link>
        <description>Nicotinamide 2000μM R01 exp50

Mechanism of Action

NAD biosynthetic precursor, activates SIRT1

	*  Class / Subclass 1: Metabolism / Metabolite

Technical Notes

	*  PubChem Name: Nicotinamide
		*  Synonyms: Niacinamide; Nicotinic acid amide; Vitamin B3</description>
    </item>
    <item rdf:about="https://crispr.tyerslab.com/wiki/results/exp51?rev=1767843420&amp;do=diff">
        <dc:format>text/html</dc:format>
        <dc:date>2026-01-08T03:37:00+00:00</dc:date>
        <dc:creator>Anonymous (anonymous@undisclosed.example.com)</dc:creator>
        <title>Nifuroxazide 1μM R01 exp51</title>
        <link>https://crispr.tyerslab.com/wiki/results/exp51?rev=1767843420&amp;do=diff</link>
        <description>Nifuroxazide 1μM R01 exp51

Mechanism of Action

Nitrofuran antibiotic

	*  Class / Subclass 1: Infectious Disease / Antibiotic

Technical Notes

	*  PubChem Name: Nifuroxazide
		*  Synonyms: N/A
		*  CAS #: 965-52-6
		*  PubChem CID: 5337997
		*  IUPAC: 4-hydroxy-N-[(E)-(5-nitrofuran-2-yl)methylideneamino]benzamide</description>
    </item>
    <item rdf:about="https://crispr.tyerslab.com/wiki/results/exp52?rev=1767843420&amp;do=diff">
        <dc:format>text/html</dc:format>
        <dc:date>2026-01-08T03:37:00+00:00</dc:date>
        <dc:creator>Anonymous (anonymous@undisclosed.example.com)</dc:creator>
        <title>Ribavirin 10μM R01 exp52</title>
        <link>https://crispr.tyerslab.com/wiki/results/exp52?rev=1767843420&amp;do=diff</link>
        <description>Ribavirin 10μM R01 exp52

Mechanism of Action

Prodrug metabolized to purine RNA nucleotide mimetic, also inhibits EIF4E

	*  Class / Subclass 1: Infectious Disease / Antiviral
	*  Class / Subclass 2: Metabolism / Antimetabolite
	*  Class / Subclass 3:</description>
    </item>
    <item rdf:about="https://crispr.tyerslab.com/wiki/results/exp53?rev=1767843420&amp;do=diff">
        <dc:format>text/html</dc:format>
        <dc:date>2026-01-08T03:37:00+00:00</dc:date>
        <dc:creator>Anonymous (anonymous@undisclosed.example.com)</dc:creator>
        <title>Suberoylanilide-Hydroxamic-Acid 0.02μM R01 exp53</title>
        <link>https://crispr.tyerslab.com/wiki/results/exp53?rev=1767843420&amp;do=diff</link>
        <description>Suberoylanilide-Hydroxamic-Acid 0.02μM R01 exp53

Mechanism of Action

Inhibits class I, II, IV HDACs, chelates active site zinc ion

	*  Class / Subclass 1: Gene Regulation / Epigenetic Inhibitor

Technical Notes

	*  PubChem Name: Vorinostat
		*</description>
    </item>
    <item rdf:about="https://crispr.tyerslab.com/wiki/results/exp54?rev=1767843420&amp;do=diff">
        <dc:format>text/html</dc:format>
        <dc:date>2026-01-08T03:37:00+00:00</dc:date>
        <dc:creator>Anonymous (anonymous@undisclosed.example.com)</dc:creator>
        <title>Taxol 0.002μM R01 exp54</title>
        <link>https://crispr.tyerslab.com/wiki/results/exp54?rev=1767843420&amp;do=diff</link>
        <description>Taxol 0.002μM R01 exp54

Mechanism of Action

Inhibits microtubule depolymerisation, blocks metaphase to anaphase transition

	*  Class / Subclass 1: Cell Cycle / Microtubule Poison
	*  Class / Subclass 2: Organelle Function / Cytoskeletal Inhibitor</description>
    </item>
    <item rdf:about="https://crispr.tyerslab.com/wiki/results/exp58?rev=1767843420&amp;do=diff">
        <dc:format>text/html</dc:format>
        <dc:date>2026-01-08T03:37:00+00:00</dc:date>
        <dc:creator>Anonymous (anonymous@undisclosed.example.com)</dc:creator>
        <title>UM131593 0.1μM R01 exp58</title>
        <link>https://crispr.tyerslab.com/wiki/results/exp58?rev=1767843420&amp;do=diff</link>
        <description>UM131593 0.1μM R01 exp58

Mechanism of Action

Unknown

	*  Class / Subclass 1: Uncharacterized Mechanism / Chemical Screen Hit

Technical Notes

	*  PubChem Name: N/A
		*  Synonyms: N/A
		*  CAS #: N/A
		*  PubChem CID: N/A
		*  IUPAC: N/A
		*  INCHI Name:</description>
    </item>
    <item rdf:about="https://crispr.tyerslab.com/wiki/results/exp59?rev=1767843420&amp;do=diff">
        <dc:format>text/html</dc:format>
        <dc:date>2026-01-08T03:37:00+00:00</dc:date>
        <dc:creator>Anonymous (anonymous@undisclosed.example.com)</dc:creator>
        <title>UMK57 1μM R01 exp59</title>
        <link>https://crispr.tyerslab.com/wiki/results/exp59?rev=1767843420&amp;do=diff</link>
        <description>UMK57 1μM R01 exp59

Mechanism of Action

Potentiates kinesin-13 (MCAK), destabilizes kinetochore-MT attachment, suppresses chromosome mis-segregation

	*  Class / Subclass 1: Cell Cycle / Mitotic Inhibitor
	*  Class / Subclass 2: Organelle Function / Cytoskeletal Inhibitor</description>
    </item>
    <item rdf:about="https://crispr.tyerslab.com/wiki/results/exp60?rev=1767843420&amp;do=diff">
        <dc:format>text/html</dc:format>
        <dc:date>2026-01-08T03:37:00+00:00</dc:date>
        <dc:creator>Anonymous (anonymous@undisclosed.example.com)</dc:creator>
        <title>Vinblastine 0.002μM R01 exp60</title>
        <link>https://crispr.tyerslab.com/wiki/results/exp60?rev=1767843420&amp;do=diff</link>
        <description>Vinblastine 0.002μM R01 exp60

Mechanism of Action

Inhibits microtubule polymerization and mitotic spindle formation, induces spindle assembly checkpoint (SAC)

	*  Class / Subclass 1: Cell Cycle / Microtubule Poison
	*  Class / Subclass 2: Organelle Function / Cytoskeletal Inhibitor</description>
    </item>
    <item rdf:about="https://crispr.tyerslab.com/wiki/results/exp61?rev=1767843420&amp;do=diff">
        <dc:format>text/html</dc:format>
        <dc:date>2026-01-08T03:37:00+00:00</dc:date>
        <dc:creator>Anonymous (anonymous@undisclosed.example.com)</dc:creator>
        <title>YM155 0.0002μM R01 exp61</title>
        <link>https://crispr.tyerslab.com/wiki/results/exp61?rev=1767843420&amp;do=diff</link>
        <description>YM155 0.0002μM R01 exp61

Mechanism of Action

Inhibits expression of survivin, amongst other ascribed mechanisms

	*  Class / Subclass 1: Gene Regulation / Transcription Inhibitor
	*  Class / Subclass 2: Signal Transduction / Apoptosis Activator

Technical Notes</description>
    </item>
    <item rdf:about="https://crispr.tyerslab.com/wiki/results/exp64?rev=1767843420&amp;do=diff">
        <dc:format>text/html</dc:format>
        <dc:date>2026-01-08T03:37:00+00:00</dc:date>
        <dc:creator>Anonymous (anonymous@undisclosed.example.com)</dc:creator>
        <title>Nocodazole 0.2μM R02 exp64</title>
        <link>https://crispr.tyerslab.com/wiki/results/exp64?rev=1767843420&amp;do=diff</link>
        <description>Nocodazole 0.2μM R02 exp64

Mechanism of Action

Inhibits microtubule polymerization and mitotic spindle formation, induces spindle assembly checkpoint (SAC)

	*  Class / Subclass 1: Cell Cycle / Microtubule Poison
	*  Class / Subclass 2: Organelle Function / Cytoskeletal Inhibitor</description>
    </item>
    <item rdf:about="https://crispr.tyerslab.com/wiki/results/exp65?rev=1767843420&amp;do=diff">
        <dc:format>text/html</dc:format>
        <dc:date>2026-01-08T03:37:00+00:00</dc:date>
        <dc:creator>Anonymous (anonymous@undisclosed.example.com)</dc:creator>
        <title>Mubritinib 0.2μM R02 exp65</title>
        <link>https://crispr.tyerslab.com/wiki/results/exp65?rev=1767843420&amp;do=diff</link>
        <description>Mubritinib 0.2μM R02 exp65

Mechanism of Action

Inhibits HER2 (Erb2) EGFR receptor tyrosine kinase

	*  Class / Subclass 1: Signal Transduction / Kinase Inhibitor

Technical Notes

	*  PubChem Name: Mubritinib
		*  Synonyms: TAK-165
		*  CAS #: 366017-09-6</description>
    </item>
    <item rdf:about="https://crispr.tyerslab.com/wiki/results/exp66?rev=1767843420&amp;do=diff">
        <dc:format>text/html</dc:format>
        <dc:date>2026-01-08T03:37:00+00:00</dc:date>
        <dc:creator>Anonymous (anonymous@undisclosed.example.com)</dc:creator>
        <title>BI-D1870 3.15μM R02 exp66</title>
        <link>https://crispr.tyerslab.com/wiki/results/exp66?rev=1767843420&amp;do=diff</link>
        <description>BI-D1870 3.15μM R02 exp66

Mechanism of Action

Inhibits ribosomal p90 S6 Kinase, active against RSK1/2/3/4 isoforms

	*  Class / Subclass 1: Signal Transduction / Kinase Inhibitor

Technical Notes

	*  PubChem Name: 2-((3,5-Difluoro-4-hydroxyphenyl)amino)-8-isopentyl-5,7-dimethyl-7,8-dihydropteridin-6(5H)-one</description>
    </item>
    <item rdf:about="https://crispr.tyerslab.com/wiki/results/exp67?rev=1767843420&amp;do=diff">
        <dc:format>text/html</dc:format>
        <dc:date>2026-01-08T03:37:00+00:00</dc:date>
        <dc:creator>Anonymous (anonymous@undisclosed.example.com)</dc:creator>
        <title>BVD-523 15μM R02 exp67</title>
        <link>https://crispr.tyerslab.com/wiki/results/exp67?rev=1767843420&amp;do=diff</link>
        <description>BVD-523 15μM R02 exp67

Mechanism of Action

Inhibits ERK1/2, ATP-competitive

	*  Class / Subclass 1: Signal Transduction / Kinase Inhibitor

Technical Notes

	*  PubChem Name: Ulixertinib
		*  Synonyms: BVD-523; VRT752271
		*  CAS #: 869886-67-9
		*</description>
    </item>
    <item rdf:about="https://crispr.tyerslab.com/wiki/results/exp68?rev=1767843420&amp;do=diff">
        <dc:format>text/html</dc:format>
        <dc:date>2026-01-08T03:37:00+00:00</dc:date>
        <dc:creator>Anonymous (anonymous@undisclosed.example.com)</dc:creator>
        <title>Clomiphene 4.4μM R02 exp68</title>
        <link>https://crispr.tyerslab.com/wiki/results/exp68?rev=1767843420&amp;do=diff</link>
        <description>Clomiphene 4.4μM R02 exp68

Mechanism of Action

Nonsteroidal&amp;nbsp;selective estrogen receptor modulator (SERM), mixed agonist and antagonist of ER

	*  Class / Subclass 1: Metabolism / Hormone Antagonist
	*  Class / Subclass 2: Gene Regulation / Nuclear Receptor Ligand</description>
    </item>
    <item rdf:about="https://crispr.tyerslab.com/wiki/results/exp69?rev=1767843420&amp;do=diff">
        <dc:format>text/html</dc:format>
        <dc:date>2026-01-08T03:37:00+00:00</dc:date>
        <dc:creator>Anonymous (anonymous@undisclosed.example.com)</dc:creator>
        <title>Deguelin 0.05μM R02 exp69</title>
        <link>https://crispr.tyerslab.com/wiki/results/exp69?rev=1767843420&amp;do=diff</link>
        <description>Deguelin 0.05μM R02 exp69

Mechanism of Action

Derivative of rotenone, putative AKT inhibitor, complex I inhibitor

	*  Class / Subclass 1: Signal Transduction / Kinase Inhibitor
	*  Class / Subclass 2: Organelle Function / Mitochondrial Inhibitor</description>
    </item>
    <item rdf:about="https://crispr.tyerslab.com/wiki/results/exp70?rev=1767843420&amp;do=diff">
        <dc:format>text/html</dc:format>
        <dc:date>2026-01-08T03:37:00+00:00</dc:date>
        <dc:creator>Anonymous (anonymous@undisclosed.example.com)</dc:creator>
        <title>INK128 0.2μM R02 exp70</title>
        <link>https://crispr.tyerslab.com/wiki/results/exp70?rev=1767843420&amp;do=diff</link>
        <description>INK128 0.2μM R02 exp70

Mechanism of Action

Inhibits mTORC1 and mTORC2, ATP-competitive

	*  Class / Subclass 1: Signal Transduction / Kinase Inhibitor
	*  Class / Subclass 2: Proteostasis / mTOR inhibitor

Technical Notes

	*  PubChem Name: Sapanisertib</description>
    </item>
    <item rdf:about="https://crispr.tyerslab.com/wiki/results/exp71?rev=1767843420&amp;do=diff">
        <dc:format>text/html</dc:format>
        <dc:date>2026-01-08T03:37:00+00:00</dc:date>
        <dc:creator>Anonymous (anonymous@undisclosed.example.com)</dc:creator>
        <title>KU-0063794 3.8μM R02 exp71</title>
        <link>https://crispr.tyerslab.com/wiki/results/exp71?rev=1767843420&amp;do=diff</link>
        <description>KU-0063794 3.8μM R02 exp71

Mechanism of Action

ATP-competitive mTORC1 and mTORC2 inhibitor

	*  Class / Subclass 1: Proteostasis / mTOR inhibitor
	*  Class / Subclass 2: Signal Transduction / Kinase Inhibitor

Technical Notes

	*  PubChem Name: Ku-0063794</description>
    </item>
    <item rdf:about="https://crispr.tyerslab.com/wiki/results/exp72?rev=1767843420&amp;do=diff">
        <dc:format>text/html</dc:format>
        <dc:date>2026-01-08T03:37:00+00:00</dc:date>
        <dc:creator>Anonymous (anonymous@undisclosed.example.com)</dc:creator>
        <title>LB-100 4.1μM R02 exp72</title>
        <link>https://crispr.tyerslab.com/wiki/results/exp72?rev=1767843420&amp;do=diff</link>
        <description>LB-100 4.1μM R02 exp72

Mechanism of Action

Inhibits protein phosphatase 2A

	*  Class / Subclass 1: Signal Transduction / Phosphatase Inhibitor

Technical Notes

	*  PubChem Name: LB-100
		*  Synonyms: N/A
		*  CAS #: 1026680-07-8
		*  PubChem CID:</description>
    </item>
    <item rdf:about="https://crispr.tyerslab.com/wiki/results/exp73?rev=1767843420&amp;do=diff">
        <dc:format>text/html</dc:format>
        <dc:date>2026-01-08T03:37:00+00:00</dc:date>
        <dc:creator>Anonymous (anonymous@undisclosed.example.com)</dc:creator>
        <title>LJH685 5μM R02 exp73</title>
        <link>https://crispr.tyerslab.com/wiki/results/exp73?rev=1767843420&amp;do=diff</link>
        <description>LJH685 5μM R02 exp73

Mechanism of Action

Inhibits p90 ribosomal S6 kinase (RSK)

	*  Class / Subclass 1: Signal Transduction / Kinase Inhibitor

Technical Notes

	*  PubChem Name: 2,6-Difluoro-4-{4-[4-(4-Methylpiperazin-1-Yl)phenyl]pyridin-3-Yl}phenol</description>
    </item>
    <item rdf:about="https://crispr.tyerslab.com/wiki/results/exp75?rev=1767843420&amp;do=diff">
        <dc:format>text/html</dc:format>
        <dc:date>2026-01-08T03:37:00+00:00</dc:date>
        <dc:creator>Anonymous (anonymous@undisclosed.example.com)</dc:creator>
        <title>MK-1775 0.32μM R02 exp75</title>
        <link>https://crispr.tyerslab.com/wiki/results/exp75?rev=1767843420&amp;do=diff</link>
        <description>MK-1775 0.32μM R02 exp75

Mechanism of Action

Inhibits Wee1, alleviates CDK inhibition

	*  Class / Subclass 1: Cell Cycle / Kinase Inhibitor
	*  Class / Subclass 2: Signal Transduction / Kinase Inhibitor
	*  Class / Subclass 3: DNA Damage, Repair and Replication / Checkpoint Signaling Inhibitor</description>
    </item>
    <item rdf:about="https://crispr.tyerslab.com/wiki/results/exp77?rev=1767843420&amp;do=diff">
        <dc:format>text/html</dc:format>
        <dc:date>2026-01-08T03:37:00+00:00</dc:date>
        <dc:creator>Anonymous (anonymous@undisclosed.example.com)</dc:creator>
        <title>Prochlorperazine 5.2μM R02 exp77</title>
        <link>https://crispr.tyerslab.com/wiki/results/exp77?rev=1767843420&amp;do=diff</link>
        <description>Prochlorperazine 5.2μM R02 exp77

Mechanism of Action

Antagonist of DRD2 receptors, used to treat nausea, schizophrenia, migraines, anxiety

	*  Class / Subclass 1: Signal Transduction / GPCR Antagonist

Technical Notes

	*  PubChem Name: Prochlorperazine maleate</description>
    </item>
    <item rdf:about="https://crispr.tyerslab.com/wiki/results/exp78?rev=1767843420&amp;do=diff">
        <dc:format>text/html</dc:format>
        <dc:date>2026-01-08T03:37:00+00:00</dc:date>
        <dc:creator>Anonymous (anonymous@undisclosed.example.com)</dc:creator>
        <title>Pterostilbene 16μM R02 exp78</title>
        <link>https://crispr.tyerslab.com/wiki/results/exp78?rev=1767843420&amp;do=diff</link>
        <description>Pterostilbene 16μM R02 exp78

Mechanism of Action

Putative sirtuin activator, anti-oxidant, anti-inflammatory, anti-carcinogenic, anti-diabetic, anti-obesity, analog of resveratrol

	*  Class / Subclass 1: Gene Regulation / Epigenetic Activator

Technical Notes</description>
    </item>
    <item rdf:about="https://crispr.tyerslab.com/wiki/results/exp79?rev=1767843420&amp;do=diff">
        <dc:format>text/html</dc:format>
        <dc:date>2026-01-08T03:37:00+00:00</dc:date>
        <dc:creator>Anonymous (anonymous@undisclosed.example.com)</dc:creator>
        <title>Q15 2.7μM R02 exp79</title>
        <link>https://crispr.tyerslab.com/wiki/results/exp79?rev=1767843420&amp;do=diff</link>
        <description>Q15 2.7μM R02 exp79

Mechanism of Action

Putative condensin inhibitor

	*  Class / Subclass 1: Cell Cycle / Chromosome Dynamics Inhibitor

Technical Notes

	*  PubChem Name: N/A
		*  Synonyms: N/A
		*  CAS #: 1071780-64-7
		*  PubChem CID: N/A
		*</description>
    </item>
    <item rdf:about="https://crispr.tyerslab.com/wiki/results/exp80?rev=1767843420&amp;do=diff">
        <dc:format>text/html</dc:format>
        <dc:date>2026-01-08T03:37:00+00:00</dc:date>
        <dc:creator>Anonymous (anonymous@undisclosed.example.com)</dc:creator>
        <title>RO-3307 4.7μM R02 exp80</title>
        <link>https://crispr.tyerslab.com/wiki/results/exp80?rev=1767843420&amp;do=diff</link>
        <description>RO-3307 4.7μM R02 exp80

Mechanism of Action

Inhibits CDK1, ATP-competitive, causes G2/M arrest

	*  Class / Subclass 1: Cell Cycle / Kinase Inhibitor

Technical Notes

	*  PubChem Name: (5Z)-5-(Quinolin-6-ylmethylidene)-2-[(thiophen-2-ylmethyl)amino]-1,3-thiazol-4(5H)-one</description>
    </item>
    <item rdf:about="https://crispr.tyerslab.com/wiki/results/exp81?rev=1767843420&amp;do=diff">
        <dc:format>text/html</dc:format>
        <dc:date>2026-01-08T03:37:00+00:00</dc:date>
        <dc:creator>Anonymous (anonymous@undisclosed.example.com)</dc:creator>
        <title>Selumetinib 20μM R02 exp81</title>
        <link>https://crispr.tyerslab.com/wiki/results/exp81?rev=1767843420&amp;do=diff</link>
        <description>Selumetinib 20μM R02 exp81

Mechanism of Action

Inhibits MEK1 and MEK2

	*  Class / Subclass 1: Signal Transduction / Kinase Inhibitor

Technical Notes

	*  PubChem Name: Selumetinib
		*  Synonyms: AZD6244; ARRY-142886
		*  CAS #: 606143-52-6
		*</description>
    </item>
    <item rdf:about="https://crispr.tyerslab.com/wiki/results/exp82?rev=1767843420&amp;do=diff">
        <dc:format>text/html</dc:format>
        <dc:date>2026-01-08T03:37:00+00:00</dc:date>
        <dc:creator>Anonymous (anonymous@undisclosed.example.com)</dc:creator>
        <title>Torin1 0.08μM R02 exp82</title>
        <link>https://crispr.tyerslab.com/wiki/results/exp82?rev=1767843420&amp;do=diff</link>
        <description>Torin1 0.08μM R02 exp82

Mechanism of Action

Inhibits mTORC1 and mTORC2, ATP competitive

	*  Class / Subclass 1: Proteostasis / mTOR inhibitor
	*  Class / Subclass 2: Signal Transduction / Kinase Inhibitor

Technical Notes

	*  PubChem Name: Torin 1</description>
    </item>
    <item rdf:about="https://crispr.tyerslab.com/wiki/results/exp83?rev=1767843420&amp;do=diff">
        <dc:format>text/html</dc:format>
        <dc:date>2026-01-08T03:37:00+00:00</dc:date>
        <dc:creator>Anonymous (anonymous@undisclosed.example.com)</dc:creator>
        <title>Trametinib 10μM R02 exp83</title>
        <link>https://crispr.tyerslab.com/wiki/results/exp83?rev=1767843420&amp;do=diff</link>
        <description>Trametinib 10μM R02 exp83

Mechanism of Action

Inhibits MEK1 and MEK2, reversible allosteric mechanism, used in combination with BRAF V600E inhibitors

	*  Class / Subclass 1: Signal Transduction / Kinase Inhibitor

Technical Notes

	*  PubChem Name:</description>
    </item>
    <item rdf:about="https://crispr.tyerslab.com/wiki/results/exp84?rev=1767843420&amp;do=diff">
        <dc:format>text/html</dc:format>
        <dc:date>2026-01-08T03:37:00+00:00</dc:date>
        <dc:creator>Anonymous (anonymous@undisclosed.example.com)</dc:creator>
        <title>UM0125461 0.74μM R02 exp84</title>
        <link>https://crispr.tyerslab.com/wiki/results/exp84?rev=1767843420&amp;do=diff</link>
        <description>UM0125461 0.74μM R02 exp84

Mechanism of Action

Unknown

	*  Class / Subclass 1: Uncharacterized Mechanism / Chemical Screen Hit

Technical Notes

	*  PubChem Name: N/A
		*  Synonyms: N/A
		*  CAS #: N/A
		*  PubChem CID: N/A
		*  IUPAC: N/A
		*  INCHI Name:</description>
    </item>
    <item rdf:about="https://crispr.tyerslab.com/wiki/results/exp85?rev=1767843420&amp;do=diff">
        <dc:format>text/html</dc:format>
        <dc:date>2026-01-08T03:37:00+00:00</dc:date>
        <dc:creator>Anonymous (anonymous@undisclosed.example.com)</dc:creator>
        <title>UM0129480 7μM R02 exp85</title>
        <link>https://crispr.tyerslab.com/wiki/results/exp85?rev=1767843420&amp;do=diff</link>
        <description>UM0129480 7μM R02 exp85

Mechanism of Action

Unknown

	*  Class / Subclass 1: Uncharacterized Mechanism / Chemical Screen Hit

Technical Notes

	*  PubChem Name: N/A
		*  Synonyms: N/A
		*  CAS #: N/A
		*  PubChem CID: N/A
		*  IUPAC: N/A
		*  INCHI Name:</description>
    </item>
    <item rdf:about="https://crispr.tyerslab.com/wiki/results/exp89?rev=1767843420&amp;do=diff">
        <dc:format>text/html</dc:format>
        <dc:date>2026-01-08T03:37:00+00:00</dc:date>
        <dc:creator>Anonymous (anonymous@undisclosed.example.com)</dc:creator>
        <title>Vemurafenib 6.6μM R02 exp89</title>
        <link>https://crispr.tyerslab.com/wiki/results/exp89?rev=1767843420&amp;do=diff</link>
        <description>Vemurafenib 6.6μM R02 exp89

Mechanism of Action

Inhibits BRAF-V300E, paradoxical RAF activation by stabilization of CRAF/BRAF heterodimer

	*  Class / Subclass 1: Signal Transduction / Kinase Inhibitor

Technical Notes

	*  PubChem Name: Vemurafenib</description>
    </item>
    <item rdf:about="https://crispr.tyerslab.com/wiki/results/exp90?rev=1767843420&amp;do=diff">
        <dc:format>text/html</dc:format>
        <dc:date>2026-01-08T03:37:00+00:00</dc:date>
        <dc:creator>Anonymous (anonymous@undisclosed.example.com)</dc:creator>
        <title>WYE-354 6μM R02 exp90</title>
        <link>https://crispr.tyerslab.com/wiki/results/exp90?rev=1767843420&amp;do=diff</link>
        <description>WYE-354 6μM R02 exp90

Mechanism of Action

Inhibits mTORC1 and mTORC2, ATP-competitive inhibitor

	*  Class / Subclass 1: Signal Transduction / Kinase Inhibitor
	*  Class / Subclass 2: Proteostasis / mTOR inhibitor

Technical Notes

	*  PubChem Name:</description>
    </item>
    <item rdf:about="https://crispr.tyerslab.com/wiki/results/exp93?rev=1767843420&amp;do=diff">
        <dc:format>text/html</dc:format>
        <dc:date>2026-01-08T03:37:00+00:00</dc:date>
        <dc:creator>Anonymous (anonymous@undisclosed.example.com)</dc:creator>
        <title>DABN racemic mixture R03 exp93</title>
        <link>https://crispr.tyerslab.com/wiki/results/exp93?rev=1767843420&amp;do=diff</link>
        <description>DABN racemic mixture R03 exp93

Mechanism of Action

Unknown, (R) atropisomer of 1,1&#039;-Binaphthyl-2,2&#039;-diamine

	*  Class / Subclass 1: Uncharacterized Mechanism / Chemical Screen Hit

Technical Notes

(R)-DABN



	*  PubChem Name: [1,1&#039;-Binaphthalene]-2,2&#039;-diamine</description>
    </item>
    <item rdf:about="https://crispr.tyerslab.com/wiki/results/exp94?rev=1767843420&amp;do=diff">
        <dc:format>text/html</dc:format>
        <dc:date>2026-01-08T03:37:00+00:00</dc:date>
        <dc:creator>Anonymous (anonymous@undisclosed.example.com)</dc:creator>
        <title>Nocodazole 0.1μM R03 exp94</title>
        <link>https://crispr.tyerslab.com/wiki/results/exp94?rev=1767843420&amp;do=diff</link>
        <description>Nocodazole 0.1μM R03 exp94

Mechanism of Action

Inhibits microtubule polymerization and mitotic spindle formation, induces spindle assembly checkpoint (SAC)

	*  Class / Subclass 1: Cell Cycle / Microtubule Poison
	*  Class / Subclass 2: Organelle Function / Cytoskeletal Inhibitor</description>
    </item>
    <item rdf:about="https://crispr.tyerslab.com/wiki/results/exp95?rev=1767843420&amp;do=diff">
        <dc:format>text/html</dc:format>
        <dc:date>2026-01-08T03:37:00+00:00</dc:date>
        <dc:creator>Anonymous (anonymous@undisclosed.example.com)</dc:creator>
        <title>BI-2536 0.0042μM R03 exp95</title>
        <link>https://crispr.tyerslab.com/wiki/results/exp95?rev=1767843420&amp;do=diff</link>
        <description>BI-2536 0.0042μM R03 exp95

Mechanism of Action

Inhibits PLK1 kinase, causes G2/M arrest

	*  Class / Subclass 1: Cell Cycle / Mitotic Inhibitor
	*  Class / Subclass 2: Signal Transduction / Kinase Inhibitor

Technical Notes

	*  PubChem Name: BI-2536</description>
    </item>
    <item rdf:about="https://crispr.tyerslab.com/wiki/results/exp96?rev=1767843420&amp;do=diff">
        <dc:format>text/html</dc:format>
        <dc:date>2026-01-08T03:37:00+00:00</dc:date>
        <dc:creator>Anonymous (anonymous@undisclosed.example.com)</dc:creator>
        <title>BI-2536 0.02μM R03 exp96</title>
        <link>https://crispr.tyerslab.com/wiki/results/exp96?rev=1767843420&amp;do=diff</link>
        <description>BI-2536 0.02μM R03 exp96

Mechanism of Action

Inhibits PLK1 kinase, causes G2/M arrest

	*  Class / Subclass 1: Cell Cycle / Mitotic Inhibitor
	*  Class / Subclass 2: Signal Transduction / Kinase Inhibitor

Technical Notes

	*  PubChem Name: BI-2536</description>
    </item>
    <item rdf:about="https://crispr.tyerslab.com/wiki/results/exp97?rev=1767843420&amp;do=diff">
        <dc:format>text/html</dc:format>
        <dc:date>2026-01-08T03:37:00+00:00</dc:date>
        <dc:creator>Anonymous (anonymous@undisclosed.example.com)</dc:creator>
        <title>BI-6727 0.0125μM R03 exp97</title>
        <link>https://crispr.tyerslab.com/wiki/results/exp97?rev=1767843420&amp;do=diff</link>
        <description>BI-6727 0.0125μM R03 exp97

Mechanism of Action

Inhibits PLK1 kinase, causes G2/M arrest, improved version of BI-2536

	*  Class / Subclass 1: Cell Cycle / Mitotic Inhibitor
	*  Class / Subclass 2: Signal Transduction / Kinase Inhibitor

Technical Notes</description>
    </item>
    <item rdf:about="https://crispr.tyerslab.com/wiki/results/exp98?rev=1767843420&amp;do=diff">
        <dc:format>text/html</dc:format>
        <dc:date>2026-01-08T03:37:00+00:00</dc:date>
        <dc:creator>Anonymous (anonymous@undisclosed.example.com)</dc:creator>
        <title>BI-6727 0.04μM R03 exp98</title>
        <link>https://crispr.tyerslab.com/wiki/results/exp98?rev=1767843420&amp;do=diff</link>
        <description>BI-6727 0.04μM R03 exp98

Mechanism of Action

Inhibits PLK1 kinase, causes G2/M arrest, improved version of BI-2536

	*  Class / Subclass 1: Cell Cycle / Mitotic Inhibitor
	*  Class / Subclass 2: Signal Transduction / Kinase Inhibitor

Technical Notes</description>
    </item>
    <item rdf:about="https://crispr.tyerslab.com/wiki/results/exp99?rev=1767843420&amp;do=diff">
        <dc:format>text/html</dc:format>
        <dc:date>2026-01-08T03:37:00+00:00</dc:date>
        <dc:creator>Anonymous (anonymous@undisclosed.example.com)</dc:creator>
        <title>NFN1 0.4μM R03 exp99</title>
        <link>https://crispr.tyerslab.com/wiki/results/exp99?rev=1767843420&amp;do=diff</link>
        <description>NFN1 0.4μM R03 exp99

Mechanism of Action

Nitrofuran derivative, candidate ALDH2 inhibitor

	*  Class / Subclass 1: Infectious Disease / Antibiotic

Technical Notes

	*  PubChem Name: Ethyl 5-ethyl-2-[(5-nitrofuran-2-carbonyl)amino]thiophene-3-carboxylate</description>
    </item>
    <item rdf:about="https://crispr.tyerslab.com/wiki/results/exp100?rev=1767843420&amp;do=diff">
        <dc:format>text/html</dc:format>
        <dc:date>2026-01-08T03:37:00+00:00</dc:date>
        <dc:creator>Anonymous (anonymous@undisclosed.example.com)</dc:creator>
        <title>NFN1 1μM R03 exp100</title>
        <link>https://crispr.tyerslab.com/wiki/results/exp100?rev=1767843420&amp;do=diff</link>
        <description>NFN1 1μM R03 exp100

Mechanism of Action

Nitrofuran derivative, candidate ALDH2 inhibitor

	*  Class / Subclass 1: Infectious Disease / Antibiotic

Technical Notes

	*  PubChem Name: Ethyl 5-ethyl-2-[(5-nitrofuran-2-carbonyl)amino]thiophene-3-carboxylate</description>
    </item>
    <item rdf:about="https://crispr.tyerslab.com/wiki/results/exp101?rev=1767843420&amp;do=diff">
        <dc:format>text/html</dc:format>
        <dc:date>2026-01-08T03:37:00+00:00</dc:date>
        <dc:creator>Anonymous (anonymous@undisclosed.example.com)</dc:creator>
        <title>Nicotinamide 1000μM R03 exp101</title>
        <link>https://crispr.tyerslab.com/wiki/results/exp101?rev=1767843420&amp;do=diff</link>
        <description>Nicotinamide 1000μM R03 exp101

Mechanism of Action

NAD biosynthetic precursor, activates SIRT1

	*  Class / Subclass 1: Metabolism / Metabolite

Technical Notes

	*  PubChem Name: Nicotinamide
		*  Synonyms: Niacinamide; Nicotinic acid amide; Vitamin B3</description>
    </item>
    <item rdf:about="https://crispr.tyerslab.com/wiki/results/exp102?rev=1767843420&amp;do=diff">
        <dc:format>text/html</dc:format>
        <dc:date>2026-01-08T03:37:00+00:00</dc:date>
        <dc:creator>Anonymous (anonymous@undisclosed.example.com)</dc:creator>
        <title>Nifuroxazide 5μM R03 exp102</title>
        <link>https://crispr.tyerslab.com/wiki/results/exp102?rev=1767843420&amp;do=diff</link>
        <description>Nifuroxazide 5μM R03 exp102

Mechanism of Action

Nitrofuran antibiotic

	*  Class / Subclass 1: Infectious Disease / Antibiotic

Technical Notes

	*  PubChem Name: Nifuroxazide
		*  Synonyms: N/A
		*  CAS #: 965-52-6
		*  PubChem CID: 5337997
		*  IUPAC:</description>
    </item>
    <item rdf:about="https://crispr.tyerslab.com/wiki/results/exp103?rev=1767843420&amp;do=diff">
        <dc:format>text/html</dc:format>
        <dc:date>2026-01-08T03:37:00+00:00</dc:date>
        <dc:creator>Anonymous (anonymous@undisclosed.example.com)</dc:creator>
        <title>Taxol 0.004μM R03 exp103</title>
        <link>https://crispr.tyerslab.com/wiki/results/exp103?rev=1767843420&amp;do=diff</link>
        <description>Taxol 0.004μM R03 exp103

Mechanism of Action

Inhibits microtubule depolymerisation, blocks metaphase to anaphase transition

	*  Class / Subclass 1: Cell Cycle / Microtubule Poison
	*  Class / Subclass 2: Organelle Function / Cytoskeletal Inhibitor</description>
    </item>
    <item rdf:about="https://crispr.tyerslab.com/wiki/results/exp106?rev=1767843420&amp;do=diff">
        <dc:format>text/html</dc:format>
        <dc:date>2026-01-08T03:37:00+00:00</dc:date>
        <dc:creator>Anonymous (anonymous@undisclosed.example.com)</dc:creator>
        <title>UM131593 0.2μM R03 exp106</title>
        <link>https://crispr.tyerslab.com/wiki/results/exp106?rev=1767843420&amp;do=diff</link>
        <description>UM131593 0.2μM R03 exp106

Mechanism of Action

Unknown

	*  Class / Subclass 1: Uncharacterized Mechanism / Chemical Screen Hit

Technical Notes

	*  PubChem Name: N/A
		*  Synonyms: N/A
		*  CAS #: N/A
		*  PubChem CID: N/A
		*  IUPAC: N/A
		*  INCHI Name:</description>
    </item>
    <item rdf:about="https://crispr.tyerslab.com/wiki/results/exp107?rev=1767843420&amp;do=diff">
        <dc:format>text/html</dc:format>
        <dc:date>2026-01-08T03:37:00+00:00</dc:date>
        <dc:creator>Anonymous (anonymous@undisclosed.example.com)</dc:creator>
        <title>UMK57 0.6μM R03 exp107</title>
        <link>https://crispr.tyerslab.com/wiki/results/exp107?rev=1767843420&amp;do=diff</link>
        <description>UMK57 0.6μM R03 exp107

Mechanism of Action

Potentiates kinesin-13 (MCAK), destabilizes kinetochore-MT attachment, suppresses chromosome mis-segregation

	*  Class / Subclass 1: Cell Cycle / Mitotic Inhibitor
	*  Class / Subclass 2: Organelle Function / Cytoskeletal Inhibitor</description>
    </item>
    <item rdf:about="https://crispr.tyerslab.com/wiki/results/exp108?rev=1767843420&amp;do=diff">
        <dc:format>text/html</dc:format>
        <dc:date>2026-01-08T03:37:00+00:00</dc:date>
        <dc:creator>Anonymous (anonymous@undisclosed.example.com)</dc:creator>
        <title>Vinblastine 0.2μM R03 exp108</title>
        <link>https://crispr.tyerslab.com/wiki/results/exp108?rev=1767843420&amp;do=diff</link>
        <description>Vinblastine 0.2μM R03 exp108

Mechanism of Action

Inhibits microtubule polymerization and mitotic spindle formation, induces spindle assembly checkpoint (SAC)

	*  Class / Subclass 1: Cell Cycle / Microtubule Poison
	*  Class / Subclass 2: Organelle Function / Cytoskeletal Inhibitor</description>
    </item>
    <item rdf:about="https://crispr.tyerslab.com/wiki/results/exp111?rev=1767843420&amp;do=diff">
        <dc:format>text/html</dc:format>
        <dc:date>2026-01-08T03:37:00+00:00</dc:date>
        <dc:creator>Anonymous (anonymous@undisclosed.example.com)</dc:creator>
        <title>R-DABN 8μM R03 exp111</title>
        <link>https://crispr.tyerslab.com/wiki/results/exp111?rev=1767843420&amp;do=diff</link>
        <description>R-DABN 8μM R03 exp111

Mechanism of Action

Unknown, (R) atropisomer of 1,1&#039;-Binaphthyl-2,2&#039;-diamine

	*  Class / Subclass 1: Uncharacterized Mechanism / Chemical Screen Hit

Technical Notes

	*  PubChem Name: [1,1&#039;-Binaphthalene]-2,2&#039;-diamine
		*</description>
    </item>
    <item rdf:about="https://crispr.tyerslab.com/wiki/results/exp112?rev=1767843420&amp;do=diff">
        <dc:format>text/html</dc:format>
        <dc:date>2026-01-08T03:37:00+00:00</dc:date>
        <dc:creator>Anonymous (anonymous@undisclosed.example.com)</dc:creator>
        <title>S-DABN 8μM R03 exp112</title>
        <link>https://crispr.tyerslab.com/wiki/results/exp112?rev=1767843420&amp;do=diff</link>
        <description>S-DABN 8μM R03 exp112

Mechanism of Action

Unknown, (S) atropisomer of 1,1&#039;-Binaphthyl-2,2&#039;-diamine

	*  Class / Subclass 1: Uncharacterized Mechanism / Chemical Screen Hit

Technical Notes

	*  PubChem Name: [1,1&#039;-Binaphthalene]-2,2&#039;-diamine
		*</description>
    </item>
    <item rdf:about="https://crispr.tyerslab.com/wiki/results/exp113?rev=1767843420&amp;do=diff">
        <dc:format>text/html</dc:format>
        <dc:date>2026-01-08T03:37:00+00:00</dc:date>
        <dc:creator>Anonymous (anonymous@undisclosed.example.com)</dc:creator>
        <title>1-Methyl-nicotinamide-chloride 1000μM R03 exp113</title>
        <link>https://crispr.tyerslab.com/wiki/results/exp113?rev=1767843420&amp;do=diff</link>
        <description>1-Methyl-nicotinamide-chloride 1000μM R03 exp113

Mechanism of Action

Nicotinamde metabolite, generated by nicotinamide N-methyltransferase (NNMT)

	*  Class / Subclass 1: Metabolism / Metabolite

Technical Notes

	*  PubChem Name: 3-Carbamyl-1-methylpyridinium chloride</description>
    </item>
    <item rdf:about="https://crispr.tyerslab.com/wiki/results/exp114?rev=1767843420&amp;do=diff">
        <dc:format>text/html</dc:format>
        <dc:date>2026-01-08T03:37:00+00:00</dc:date>
        <dc:creator>Anonymous (anonymous@undisclosed.example.com)</dc:creator>
        <title>A-196 10μM R03 exp114</title>
        <link>https://crispr.tyerslab.com/wiki/results/exp114?rev=1767843420&amp;do=diff</link>
        <description>A-196 10μM R03 exp114

Mechanism of Action

Inhibits SUV420H1 and SUV420H2 inhibitor, blocks di/trimethylation of H4K20me

	*  Class / Subclass 1: Gene Regulation / Epigenetic Inhibitor

Technical Notes

	*  PubChem Name: 6,7-Dichloro-N-cyclopentyl-4-(pyridin-4-yl)phthalazin-1-amine</description>
    </item>
    <item rdf:about="https://crispr.tyerslab.com/wiki/results/exp115?rev=1767843420&amp;do=diff">
        <dc:format>text/html</dc:format>
        <dc:date>2026-01-08T03:37:00+00:00</dc:date>
        <dc:creator>Anonymous (anonymous@undisclosed.example.com)</dc:creator>
        <title>A-366 10μM R03 exp115</title>
        <link>https://crispr.tyerslab.com/wiki/results/exp115?rev=1767843420&amp;do=diff</link>
        <description>A-366 10μM R03 exp115

Mechanism of Action

Inhibits G9a/EHMT1, blocks methylation of H3K9

	*  Class / Subclass 1: Gene Regulation / Epigenetic Inhibitor

Technical Notes

	*  PubChem Name: CID 76285486
		*  Synonyms: N/A
		*  CAS #: 1527503-11-2
		*</description>
    </item>
    <item rdf:about="https://crispr.tyerslab.com/wiki/results/exp116?rev=1767843420&amp;do=diff">
        <dc:format>text/html</dc:format>
        <dc:date>2026-01-08T03:37:00+00:00</dc:date>
        <dc:creator>Anonymous (anonymous@undisclosed.example.com)</dc:creator>
        <title>AICAR 240μM R03 exp116</title>
        <link>https://crispr.tyerslab.com/wiki/results/exp116?rev=1767843420&amp;do=diff</link>
        <description>AICAR 240μM R03 exp116

Mechanism of Action

Metabolic intermediate in purine biosynthesis, activates AMPK, has other putative targets

	*  Class / Subclass 1: Metabolism / Metabolite
	*  Class / Subclass 2: Signal Transduction / Kinase Activator

Technical Notes</description>
    </item>
    <item rdf:about="https://crispr.tyerslab.com/wiki/results/exp120?rev=1767843420&amp;do=diff">
        <dc:format>text/html</dc:format>
        <dc:date>2026-01-08T03:37:00+00:00</dc:date>
        <dc:creator>Anonymous (anonymous@undisclosed.example.com)</dc:creator>
        <title>Dimethyl-Sulfoxide 1pc R03 exp120</title>
        <link>https://crispr.tyerslab.com/wiki/results/exp120?rev=1767843420&amp;do=diff</link>
        <description>Dimethyl-Sulfoxide 1pc R03 exp120

Mechanism of Action

N/A

	*  Class / Subclass 1: Chemogenomic Negative Control / Solvent

Technical Notes

	*  PubChem Name: Dimethyl sulfoxide
		*  Synonyms: N/A
		*  CAS #: 67-68-5
		*  PubChem CID: 679
		*  IUPAC:</description>
    </item>
    <item rdf:about="https://crispr.tyerslab.com/wiki/results/exp121?rev=1767843420&amp;do=diff">
        <dc:format>text/html</dc:format>
        <dc:date>2026-01-08T03:37:00+00:00</dc:date>
        <dc:creator>Anonymous (anonymous@undisclosed.example.com)</dc:creator>
        <title>Golgicide-A 2μM R03 exp121</title>
        <link>https://crispr.tyerslab.com/wiki/results/exp121?rev=1767843420&amp;do=diff</link>
        <description>Golgicide-A 2μM R03 exp121

Mechanism of Action

Inhibits cis-Golgi ArfGEF, blocks secretion at ER-Golgi

	*  Class / Subclass 1: Organelle Function / Vesicule Trafficking Inhibitor

Technical Notes

	*  PubChem Name: 6,8-Difluoro-4-pyridin-3-yl-3a,4,5,9b-tetrahydro-3H-cyclopenta[c]quinoline</description>
    </item>
    <item rdf:about="https://crispr.tyerslab.com/wiki/results/exp122?rev=1767843420&amp;do=diff">
        <dc:format>text/html</dc:format>
        <dc:date>2026-01-08T03:37:00+00:00</dc:date>
        <dc:creator>Anonymous (anonymous@undisclosed.example.com)</dc:creator>
        <title>Golgicide-A 4μM R03 exp122</title>
        <link>https://crispr.tyerslab.com/wiki/results/exp122?rev=1767843420&amp;do=diff</link>
        <description>Golgicide-A 4μM R03 exp122

Mechanism of Action

Inhibits cis-Golgi ArfGEF, blocks secretion at ER-Golgi

	*  Class / Subclass 1: Organelle Function / Vesicule Trafficking Inhibitor

Technical Notes

	*  PubChem Name: 6,8-Difluoro-4-pyridin-3-yl-3a,4,5,9b-tetrahydro-3H-cyclopenta[c]quinoline</description>
    </item>
    <item rdf:about="https://crispr.tyerslab.com/wiki/results/exp123?rev=1767843420&amp;do=diff">
        <dc:format>text/html</dc:format>
        <dc:date>2026-01-08T03:37:00+00:00</dc:date>
        <dc:creator>Anonymous (anonymous@undisclosed.example.com)</dc:creator>
        <title>GSK-LSD1 10μM R03 exp123</title>
        <link>https://crispr.tyerslab.com/wiki/results/exp123?rev=1767843420&amp;do=diff</link>
        <description>GSK-LSD1 10μM R03 exp123

Mechanism of Action

Inhibits LSD1 histone demethylase (H3K4me/me2, H3K9me)

	*  Class / Subclass 1: Gene Regulation / Epigenetic Inhibitor

Technical Notes

	*  PubChem Name: GSK-LSD1 Dihydrochloride
		*  Synonyms: N/A
		*</description>
    </item>
    <item rdf:about="https://crispr.tyerslab.com/wiki/results/exp124?rev=1767843420&amp;do=diff">
        <dc:format>text/html</dc:format>
        <dc:date>2026-01-08T03:37:00+00:00</dc:date>
        <dc:creator>Anonymous (anonymous@undisclosed.example.com)</dc:creator>
        <title>GSK343 3μM R03 exp124</title>
        <link>https://crispr.tyerslab.com/wiki/results/exp124?rev=1767843420&amp;do=diff</link>
        <description>GSK343 3μM R03 exp124

Mechanism of Action

Inhibits EZH1 catalytic subunit of PRC2 histone methyltransferase (H3K27me3)

	*  Class / Subclass 1: Gene Regulation / Epigenetic Inhibitor

Technical Notes

	*  PubChem Name: N-[(6-Methyl-2-oxo-4-propyl-1H-pyridin-3-yl)methyl]-6-[2-(4-methylpiperazin-1-yl)pyridin-4-yl]-1-propan-2-ylindazole-4-carboxamide</description>
    </item>
    <item rdf:about="https://crispr.tyerslab.com/wiki/results/exp125?rev=1767843420&amp;do=diff">
        <dc:format>text/html</dc:format>
        <dc:date>2026-01-08T03:37:00+00:00</dc:date>
        <dc:creator>Anonymous (anonymous@undisclosed.example.com)</dc:creator>
        <title>GSK461364A 0.005μM R03 exp125</title>
        <link>https://crispr.tyerslab.com/wiki/results/exp125?rev=1767843420&amp;do=diff</link>
        <description>GSK461364A 0.005μM R03 exp125

Mechanism of Action

Inhibits PLK1

	*  Class / Subclass 1: Signal Transduction / Kinase Inhibitor
	*  Class / Subclass 2: Cell Cycle / Mitotic Inhibitor

Technical Notes

	*  PubChem Name: Gsk-461364
		*  Synonyms: GSK461364A</description>
    </item>
    <item rdf:about="https://crispr.tyerslab.com/wiki/results/exp126?rev=1767843420&amp;do=diff">
        <dc:format>text/html</dc:format>
        <dc:date>2026-01-08T03:37:00+00:00</dc:date>
        <dc:creator>Anonymous (anonymous@undisclosed.example.com)</dc:creator>
        <title>GSK461364A 0.1μM R03 exp126</title>
        <link>https://crispr.tyerslab.com/wiki/results/exp126?rev=1767843420&amp;do=diff</link>
        <description>GSK461364A 0.1μM R03 exp126

Mechanism of Action

Inhibits PLK1

	*  Class / Subclass 1: Signal Transduction / Kinase Inhibitor
	*  Class / Subclass 2: Cell Cycle / Mitotic Inhibitor

Technical Notes

	*  PubChem Name: Gsk-461364
		*  Synonyms: GSK461364A</description>
    </item>
    <item rdf:about="https://crispr.tyerslab.com/wiki/results/exp128?rev=1767843420&amp;do=diff">
        <dc:format>text/html</dc:format>
        <dc:date>2026-01-08T03:37:00+00:00</dc:date>
        <dc:creator>Anonymous (anonymous@undisclosed.example.com)</dc:creator>
        <title>GSK591 2.6μM R03 exp128</title>
        <link>https://crispr.tyerslab.com/wiki/results/exp128?rev=1767843420&amp;do=diff</link>
        <description>GSK591 2.6μM R03 exp128

Mechanism of Action

Inhibits protein arginine methyltransferase PRMT5, inactive control is SGC2096

	*  Class / Subclass 1: Gene Regulation / Epigenetic Inhibitor

Technical Notes

	*  PubChem Name: 2-(Cyclobutylamino)-N-[(2S)-3-(3,4-dihydro-1H-isoquinolin-2-yl)-2-hydroxypropyl]pyridine-4-carboxamide</description>
    </item>
    <item rdf:about="https://crispr.tyerslab.com/wiki/results/exp129?rev=1767843420&amp;do=diff">
        <dc:format>text/html</dc:format>
        <dc:date>2026-01-08T03:37:00+00:00</dc:date>
        <dc:creator>Anonymous (anonymous@undisclosed.example.com)</dc:creator>
        <title>Isonicotinamide 500μM R03 exp129</title>
        <link>https://crispr.tyerslab.com/wiki/results/exp129?rev=1767843420&amp;do=diff</link>
        <description>Isonicotinamide 500μM R03 exp129

Mechanism of Action

nicotinamide antagonist, putative SIRT1 activator

	*  Class / Subclass 1: Metabolism / Metabolite

Technical Notes

	*  PubChem Name: Isonicotinamide
		*  Synonyms: N/A
		*  CAS #: 1453-82-3
		*</description>
    </item>
    <item rdf:about="https://crispr.tyerslab.com/wiki/results/exp130?rev=1767843420&amp;do=diff">
        <dc:format>text/html</dc:format>
        <dc:date>2026-01-08T03:37:00+00:00</dc:date>
        <dc:creator>Anonymous (anonymous@undisclosed.example.com)</dc:creator>
        <title>JQ1 0.01μM R03 exp130</title>
        <link>https://crispr.tyerslab.com/wiki/results/exp130?rev=1767843420&amp;do=diff</link>
        <description>JQ1 0.01μM R03 exp130

Mechanism of Action

Inhibits BET bromodomain proteins BRD2, BRD3, BRD4, BRDT

	*  Class / Subclass 1: Gene Regulation / Epigenetic Inhibitor

Technical Notes

	*  PubChem Name: JQ1 compound
		*  Synonyms: JQ1
		*  CAS #: 1268524-70-4</description>
    </item>
    <item rdf:about="https://crispr.tyerslab.com/wiki/results/exp131?rev=1767843420&amp;do=diff">
        <dc:format>text/html</dc:format>
        <dc:date>2026-01-08T03:37:00+00:00</dc:date>
        <dc:creator>Anonymous (anonymous@undisclosed.example.com)</dc:creator>
        <title>L-74142 5μM R03 exp131</title>
        <link>https://crispr.tyerslab.com/wiki/results/exp131?rev=1767843420&amp;do=diff</link>
        <description>L-74142 5μM R03 exp131

Mechanism of Action

DRD4 receptor antagonist

	*  Class / Subclass 1: Signal Transduction / GPCR antagonist

Technical Notes

	*  PubChem Name: 5-(4-Chlorophenyl)-4-methyl-3-(1-(2-phenylethyl)piperidin-4-YL)isoxazole hydrochloride</description>
    </item>
    <item rdf:about="https://crispr.tyerslab.com/wiki/results/exp132?rev=1767843420&amp;do=diff">
        <dc:format>text/html</dc:format>
        <dc:date>2026-01-08T03:37:00+00:00</dc:date>
        <dc:creator>Anonymous (anonymous@undisclosed.example.com)</dc:creator>
        <title>Metformin 40μM R03 exp132</title>
        <link>https://crispr.tyerslab.com/wiki/results/exp132?rev=1767843420&amp;do=diff</link>
        <description>Metformin 40μM R03 exp132

Mechanism of Action

Inhibits mitochondrial respiratory chain complex I, indirectly activates AMPK

	*  Class / Subclass 1: Organelle Function / Mitochondrial Inhibitor
	*  Class / Subclass 2: Signal Transduction / Kinase Activator</description>
    </item>
    <item rdf:about="https://crispr.tyerslab.com/wiki/results/exp133?rev=1767843420&amp;do=diff">
        <dc:format>text/html</dc:format>
        <dc:date>2026-01-08T03:37:00+00:00</dc:date>
        <dc:creator>Anonymous (anonymous@undisclosed.example.com)</dc:creator>
        <title>MKC9989 10μM R03 exp133</title>
        <link>https://crispr.tyerslab.com/wiki/results/exp133?rev=1767843420&amp;do=diff</link>
        <description>MKC9989 10μM R03 exp133

Mechanism of Action

Inhibits IRE1, prevents ER unfolded protein response

	*  Class / Subclass 1: Proteostasis / Unfolded Protein Response Inhibitor
	*  Class / Subclass 2: Signal Transduction / Kinase Inhibitor

Technical Notes</description>
    </item>
    <item rdf:about="https://crispr.tyerslab.com/wiki/results/exp134?rev=1767843420&amp;do=diff">
        <dc:format>text/html</dc:format>
        <dc:date>2026-01-08T03:37:00+00:00</dc:date>
        <dc:creator>Anonymous (anonymous@undisclosed.example.com)</dc:creator>
        <title>MS023 2μM R03 exp134</title>
        <link>https://crispr.tyerslab.com/wiki/results/exp134?rev=1767843420&amp;do=diff</link>
        <description>MS023 2μM R03 exp134

Mechanism of Action

Inhibits protein arginine N-methyltransferase PRMT1

	*  Class / Subclass 1: Gene Regulation / Epigenetic Inhibitor

Technical Notes

	*  PubChem Name: MS023 (dihydrochloride)
		*  Synonyms: N/A
		*  CAS #:</description>
    </item>
    <item rdf:about="https://crispr.tyerslab.com/wiki/results/exp135?rev=1767843420&amp;do=diff">
        <dc:format>text/html</dc:format>
        <dc:date>2026-01-08T03:37:00+00:00</dc:date>
        <dc:creator>Anonymous (anonymous@undisclosed.example.com)</dc:creator>
        <title>MS023 7μM R03 exp135</title>
        <link>https://crispr.tyerslab.com/wiki/results/exp135?rev=1767843420&amp;do=diff</link>
        <description>MS023 7μM R03 exp135

Mechanism of Action

Inhibits protein arginine N-methyltransferase PRMT1

	*  Class / Subclass 1: Gene Regulation / Epigenetic Inhibitor

Technical Notes

	*  PubChem Name: MS023 (dihydrochloride)
		*  Synonyms: N/A
		*  CAS #:</description>
    </item>
    <item rdf:about="https://crispr.tyerslab.com/wiki/results/exp136?rev=1767843420&amp;do=diff">
        <dc:format>text/html</dc:format>
        <dc:date>2026-01-08T03:37:00+00:00</dc:date>
        <dc:creator>Anonymous (anonymous@undisclosed.example.com)</dc:creator>
        <title>MS094 2μM R03 exp136</title>
        <link>https://crispr.tyerslab.com/wiki/results/exp136?rev=1767843420&amp;do=diff</link>
        <description>MS094 2μM R03 exp136

Mechanism of Action

Inactive control for MS023 PRMT1 inhibitor

	*  Class / Subclass 1: Gene Regulation / Epigenetic Inhibitor

Technical Notes

	*  PubChem Name: N/A
		*  Synonyms: N/A
		*  CAS #: 1831110-55-4
		*  PubChem CID:</description>
    </item>
    <item rdf:about="https://crispr.tyerslab.com/wiki/results/exp139?rev=1767843420&amp;do=diff">
        <dc:format>text/html</dc:format>
        <dc:date>2026-01-08T03:37:00+00:00</dc:date>
        <dc:creator>Anonymous (anonymous@undisclosed.example.com)</dc:creator>
        <title>Nicotinamide Riboside 100μM R03 exp139</title>
        <link>https://crispr.tyerslab.com/wiki/results/exp139?rev=1767843420&amp;do=diff</link>
        <description>Nicotinamide Riboside 100μM R03 exp139

Mechanism of Action

NAD precursor, activates SIRT1

	*  Class / Subclass 1: Metabolism / Metabolite

Technical Notes

	*  PubChem Name: Nicotinamide riboside chloride
		*  Synonyms: N/A
		*  CAS #: 23111-00-4</description>
    </item>
    <item rdf:about="https://crispr.tyerslab.com/wiki/results/exp140?rev=1767843420&amp;do=diff">
        <dc:format>text/html</dc:format>
        <dc:date>2026-01-08T03:37:00+00:00</dc:date>
        <dc:creator>Anonymous (anonymous@undisclosed.example.com)</dc:creator>
        <title>Nicotinate 1000μM R03 exp140</title>
        <link>https://crispr.tyerslab.com/wiki/results/exp140?rev=1767843420&amp;do=diff</link>
        <description>Nicotinate 1000μM R03 exp140

Mechanism of Action

NAD precursor (a.k.a. niacin, vitamin B3)

	*  Class / Subclass 1: Metabolism / Metabolite

Technical Notes

	*  PubChem Name: Nicotinic acid
		*  Synonyms: Nicotinic acid; Vitamin B3
		*  CAS #: 59-67-6</description>
    </item>
    <item rdf:about="https://crispr.tyerslab.com/wiki/results/exp141?rev=1767843420&amp;do=diff">
        <dc:format>text/html</dc:format>
        <dc:date>2026-01-08T03:37:00+00:00</dc:date>
        <dc:creator>Anonymous (anonymous@undisclosed.example.com)</dc:creator>
        <title>Nifurtimox 1μM R03 exp141</title>
        <link>https://crispr.tyerslab.com/wiki/results/exp141?rev=1767843420&amp;do=diff</link>
        <description>Nifurtimox 1μM R03 exp141

Mechanism of Action

Nitrofuran derivative, forms nitro-anion radical metabolite, induces ROS

	*  Class / Subclass 1: Infectious Disease / Antitrypanosomal

Technical Notes

	*  PubChem Name: Nifurtimox
		*  Synonyms: N/A</description>
    </item>
    <item rdf:about="https://crispr.tyerslab.com/wiki/results/exp142?rev=1767843420&amp;do=diff">
        <dc:format>text/html</dc:format>
        <dc:date>2026-01-08T03:37:00+00:00</dc:date>
        <dc:creator>Anonymous (anonymous@undisclosed.example.com)</dc:creator>
        <title>OICR-9429 10μM R03 exp142</title>
        <link>https://crispr.tyerslab.com/wiki/results/exp142?rev=1767843420&amp;do=diff</link>
        <description>OICR-9429 10μM R03 exp142

Mechanism of Action

Inhibits interaction between WDR5 and MLL1 (KMT2A) in MLL H3K4 trimethylase complex

	*  Class / Subclass 1: Gene Regulation / Epigenetic Inhibitor

Technical Notes

	*  PubChem Name: N-[2-(4-Methylpiperazin-1-yl)-5-[3-(morpholin-4-ylmethyl)phenyl]phenyl]-6-oxo-4-(trifluoromethyl)-1H-pyridine-3-carboxamide</description>
    </item>
    <item rdf:about="https://crispr.tyerslab.com/wiki/results/exp143?rev=1767843420&amp;do=diff">
        <dc:format>text/html</dc:format>
        <dc:date>2026-01-08T03:37:00+00:00</dc:date>
        <dc:creator>Anonymous (anonymous@undisclosed.example.com)</dc:creator>
        <title>Phenformin 20μM R03 exp143</title>
        <link>https://crispr.tyerslab.com/wiki/results/exp143?rev=1767843420&amp;do=diff</link>
        <description>Phenformin 20μM R03 exp143

Mechanism of Action

Inhibits mitochondrial respiratory chain complex I, indirectly activates AMPK

	*  Class / Subclass 1: Organelle Function / Mitochondrial Inhibitor
	*  Class / Subclass 2: Metabolism / Metabolic Enzyme Activator</description>
    </item>
    <item rdf:about="https://crispr.tyerslab.com/wiki/results/exp144?rev=1767843420&amp;do=diff">
        <dc:format>text/html</dc:format>
        <dc:date>2026-01-08T03:37:00+00:00</dc:date>
        <dc:creator>Anonymous (anonymous@undisclosed.example.com)</dc:creator>
        <title>PFI-3 10μM R03 exp144</title>
        <link>https://crispr.tyerslab.com/wiki/results/exp144?rev=1767843420&amp;do=diff</link>
        <description>PFI-3 10μM R03 exp144

Mechanism of Action

Inhibits SMARCA2/4 and PB1 bromodomain proteins, components of SNF/SWI chromatin remodelling complex

	*  Class / Subclass 1: Gene Regulation / Epigenetic Inhibitor

Technical Notes

	*  PubChem Name: (E)-1-(2-Hydroxyphenyl)-3-[(1R,4R)-5-pyridin-2-yl-2,5-diazabicyclo[2.2.1]heptan-2-yl]prop-2-en-1-one</description>
    </item>
    <item rdf:about="https://crispr.tyerslab.com/wiki/results/exp145?rev=1767843420&amp;do=diff">
        <dc:format>text/html</dc:format>
        <dc:date>2026-01-08T03:37:00+00:00</dc:date>
        <dc:creator>Anonymous (anonymous@undisclosed.example.com)</dc:creator>
        <title>PNU96415E 10μM R03 exp145</title>
        <link>https://crispr.tyerslab.com/wiki/results/exp145?rev=1767843420&amp;do=diff</link>
        <description>PNU96415E 10μM R03 exp145

Mechanism of Action

Antagonist of DRD4 and 5-HT2A receptors

	*  Class / Subclass 1: Signal Transduction / GPCR Antagonist

Technical Notes

	*  PubChem Name: 1-(4-Fluorophenyl)-4-(2-(isochroman-1-yl)ethyl)piperazine dihydrochloride</description>
    </item>
    <item rdf:about="https://crispr.tyerslab.com/wiki/results/exp146?rev=1767843420&amp;do=diff">
        <dc:format>text/html</dc:format>
        <dc:date>2026-01-08T03:37:00+00:00</dc:date>
        <dc:creator>Anonymous (anonymous@undisclosed.example.com)</dc:creator>
        <title>Quinacrine 2.5μM R03 exp146</title>
        <link>https://crispr.tyerslab.com/wiki/results/exp146?rev=1767843420&amp;do=diff</link>
        <description>Quinacrine 2.5μM R03 exp146

Mechanism of Action

Intercalates into DNA and RNA, interferes with transcription and translation

	*  Class / Subclass 1: Infectious Disease / Antimalarial
	*  Class / Subclass 2: DNA Damage, Repair and Replication / Intercalating Agent</description>
    </item>
    <item rdf:about="https://crispr.tyerslab.com/wiki/results/exp147?rev=1767843420&amp;do=diff">
        <dc:format>text/html</dc:format>
        <dc:date>2026-01-08T03:37:00+00:00</dc:date>
        <dc:creator>Anonymous (anonymous@undisclosed.example.com)</dc:creator>
        <title>Resveratrol 16μM R03 exp147</title>
        <link>https://crispr.tyerslab.com/wiki/results/exp147?rev=1767843420&amp;do=diff</link>
        <description>Resveratrol 16μM R03 exp147

Mechanism of Action

Putative sirtuin activator, many other ascribed activities, analog of pterostilbene

	*  Class / Subclass 1: Gene Regulation / Epigenetic Activator

Technical Notes

	*  PubChem Name: Resveratrol
		*</description>
    </item>
    <item rdf:about="https://crispr.tyerslab.com/wiki/results/exp148?rev=1767843420&amp;do=diff">
        <dc:format>text/html</dc:format>
        <dc:date>2026-01-08T03:37:00+00:00</dc:date>
        <dc:creator>Anonymous (anonymous@undisclosed.example.com)</dc:creator>
        <title>SB202190 10μM R03 exp148</title>
        <link>https://crispr.tyerslab.com/wiki/results/exp148?rev=1767843420&amp;do=diff</link>
        <description>SB202190 10μM R03 exp148

Mechanism of Action

Inhibits p38‘± (MAPK14)and p38‘_ (MAPK11) kinase, ATP competitive

	*  Class / Subclass 1: Signal Transduction / Kinase Inhibitor

Technical Notes

	*  PubChem Name: 4-(4-Fluorophenyl)-2-(4-hydroxyphenyl)-5-(4-pyridyl)imidazole</description>
    </item>
    <item rdf:about="https://crispr.tyerslab.com/wiki/results/exp149?rev=1767843420&amp;do=diff">
        <dc:format>text/html</dc:format>
        <dc:date>2026-01-08T03:37:00+00:00</dc:date>
        <dc:creator>Anonymous (anonymous@undisclosed.example.com)</dc:creator>
        <title>SB203580 25μM R03 exp149</title>
        <link>https://crispr.tyerslab.com/wiki/results/exp149?rev=1767843420&amp;do=diff</link>
        <description>SB203580 25μM R03 exp149

Mechanism of Action

p38 MAP kinase inhibitor

	*  Class / Subclass 1: Signal Transduction / Kinase Inhibitor
	*  Class / Subclass 2: Proteostasis / Autophagy Inhibitor

Technical Notes

	*  PubChem Name: 4-(4-Fluorophenyl)-2-(4-methylsulfinylphenyl)-5-(4-pyridyl)-1H-imidazole</description>
    </item>
    <item rdf:about="https://crispr.tyerslab.com/wiki/results/exp150?rev=1767843420&amp;do=diff">
        <dc:format>text/html</dc:format>
        <dc:date>2026-01-08T03:37:00+00:00</dc:date>
        <dc:creator>Anonymous (anonymous@undisclosed.example.com)</dc:creator>
        <title>SGC0649 7μM R03 exp150</title>
        <link>https://crispr.tyerslab.com/wiki/results/exp150?rev=1767843420&amp;do=diff</link>
        <description>SGC0649 7μM R03 exp150

Mechanism of Action

Inactive control for SGC0649 (DOT1L methyltransferase inhibitor)

	*  Class / Subclass 1: Gene Regulation / Epigenetic Inhibitor

Technical Notes

	*  PubChem Name: N/A
		*  Synonyms: N/A
		*  CAS #: N/A</description>
    </item>
    <item rdf:about="https://crispr.tyerslab.com/wiki/results/exp151?rev=1767843420&amp;do=diff">
        <dc:format>text/html</dc:format>
        <dc:date>2026-01-08T03:37:00+00:00</dc:date>
        <dc:creator>Anonymous (anonymous@undisclosed.example.com)</dc:creator>
        <title>SGC0946 7μM R03 exp151</title>
        <link>https://crispr.tyerslab.com/wiki/results/exp151?rev=1767843420&amp;do=diff</link>
        <description>SGC0946 7μM R03 exp151

Mechanism of Action

DOT1L methyltransferase inhibitor

	*  Class / Subclass 1: Gene Regulation / Epigenetic Inhibitor

Technical Notes

	*  PubChem Name: 1-[3-[[(2R,3S,4R,5R)-5-(4-Amino-5-bromopyrrolo[2,3-d]pyrimidin-7-yl)-3,4-dihydroxyoxolan-2-yl]methyl-propan-2-ylamino]propyl]-3-(4-tert-butylphenyl)urea</description>
    </item>
    <item rdf:about="https://crispr.tyerslab.com/wiki/results/exp152?rev=1767843420&amp;do=diff">
        <dc:format>text/html</dc:format>
        <dc:date>2026-01-08T03:37:00+00:00</dc:date>
        <dc:creator>Anonymous (anonymous@undisclosed.example.com)</dc:creator>
        <title>SGC2043 10μM R03 exp152</title>
        <link>https://crispr.tyerslab.com/wiki/results/exp152?rev=1767843420&amp;do=diff</link>
        <description>SGC2043 10μM R03 exp152

Mechanism of Action

Inactive control for A-196 (SUV420H1/H2 inhibitor)

	*  Class / Subclass 1: Gene Regulation / Epigenetic Inhibitor

Technical Notes

	*  PubChem Name: N/A
		*  Synonyms: N/A
		*  CAS #: N/A
		*  PubChem CID:</description>
    </item>
    <item rdf:about="https://crispr.tyerslab.com/wiki/results/exp153?rev=1767843420&amp;do=diff">
        <dc:format>text/html</dc:format>
        <dc:date>2026-01-08T03:37:00+00:00</dc:date>
        <dc:creator>Anonymous (anonymous@undisclosed.example.com)</dc:creator>
        <title>SGC2096 2.6μM R03 exp153</title>
        <link>https://crispr.tyerslab.com/wiki/results/exp153?rev=1767843420&amp;do=diff</link>
        <description>SGC2096 2.6μM R03 exp153

Mechanism of Action

Inactive control for GSK591 (PRMT5 inhibitor)

	*  Class / Subclass 1: Gene Regulation / Epigenetic Inhibitor

Technical Notes

	*  PubChem Name: N/A
		*  Synonyms: N/A
		*  CAS #: N/A
		*  PubChem CID:</description>
    </item>
    <item rdf:about="https://crispr.tyerslab.com/wiki/results/exp155?rev=1767843420&amp;do=diff">
        <dc:format>text/html</dc:format>
        <dc:date>2026-01-08T03:37:00+00:00</dc:date>
        <dc:creator>Anonymous (anonymous@undisclosed.example.com)</dc:creator>
        <title>UNC1999 2μM R03 exp155</title>
        <link>https://crispr.tyerslab.com/wiki/results/exp155?rev=1767843420&amp;do=diff</link>
        <description>UNC1999 2μM R03 exp155

Mechanism of Action

Inhibits EZH2 catalytic subunit of PRC2 histone methyltransferase (H3K27me3)

	*  Class / Subclass 1: Gene Regulation / Epigenetic Inhibitor

Technical Notes

	*  PubChem Name: N-[(6-Methyl-2-oxo-4-propyl-1H-pyridin-3-yl)methyl]-1-propan-2-yl-6-[6-(4-propan-2-ylpiperazin-1-yl)pyridin-3-yl]indazole-4-carboxamide</description>
    </item>
    <item rdf:about="https://crispr.tyerslab.com/wiki/results/exp156?rev=1767843420&amp;do=diff">
        <dc:format>text/html</dc:format>
        <dc:date>2026-01-08T03:37:00+00:00</dc:date>
        <dc:creator>Anonymous (anonymous@undisclosed.example.com)</dc:creator>
        <title>UNC2400 2μM R03 exp156</title>
        <link>https://crispr.tyerslab.com/wiki/results/exp156?rev=1767843420&amp;do=diff</link>
        <description>UNC2400 2μM R03 exp156

Mechanism of Action

Inactive control for UNC1999 (EZH2 inhibitor)

	*  Class / Subclass 1: Gene Regulation / Epigenetic Inhibitor

Technical Notes

	*  PubChem Name: N-[(1,6-Dimethyl-2-oxo-4-propylpyridin-3-yl)methyl]-N-methyl-1-propan-2-yl-6-[6-(4-propan-2-ylpiperazin-1-yl)pyridin-3-yl]indazole-4-carboxamide</description>
    </item>
    <item rdf:about="https://crispr.tyerslab.com/wiki/results/exp159?rev=1767843420&amp;do=diff">
        <dc:format>text/html</dc:format>
        <dc:date>2026-01-08T03:37:00+00:00</dc:date>
        <dc:creator>Anonymous (anonymous@undisclosed.example.com)</dc:creator>
        <title>Docetaxel 0.001 to 0.002μM on day4 R04 exp159</title>
        <link>https://crispr.tyerslab.com/wiki/results/exp159?rev=1767843420&amp;do=diff</link>
        <description>Docetaxel 0.001 to 0.002μM on day4 R04 exp159

Mechanism of Action

Inihibts microtubule depolymerization, semi-synthetic analog of the paclitaxel

	*  Class / Subclass 1: Cell Cycle / Microtubule Poison
	*  Class / Subclass 2: Organelle Function / Cytoskeletal Inhibitor</description>
    </item>
    <item rdf:about="https://crispr.tyerslab.com/wiki/results/exp160?rev=1767843420&amp;do=diff">
        <dc:format>text/html</dc:format>
        <dc:date>2026-01-08T03:37:00+00:00</dc:date>
        <dc:creator>Anonymous (anonymous@undisclosed.example.com)</dc:creator>
        <title>Ribavirin 10 to 15μM on day4 R04 exp160</title>
        <link>https://crispr.tyerslab.com/wiki/results/exp160?rev=1767843420&amp;do=diff</link>
        <description>Ribavirin 10 to 15μM on day4 R04 exp160

Mechanism of Action

Prodrug metabolized to purine RNA nucleotide mimetic, also inhibits EIF4E

	*  Class / Subclass 1: Infectious Disease / Antiviral
	*  Class / Subclass 2: Metabolism / Antimetabolite
	*  Class / Subclass 3:</description>
    </item>
    <item rdf:about="https://crispr.tyerslab.com/wiki/results/exp162?rev=1767843420&amp;do=diff">
        <dc:format>text/html</dc:format>
        <dc:date>2026-01-08T03:37:00+00:00</dc:date>
        <dc:creator>Anonymous (anonymous@undisclosed.example.com)</dc:creator>
        <title>BI-D1870 2μM R04 exp162</title>
        <link>https://crispr.tyerslab.com/wiki/results/exp162?rev=1767843420&amp;do=diff</link>
        <description>BI-D1870 2μM R04 exp162

Mechanism of Action

Inhibits ribosomal p90 S6 Kinase, active against RSK1/2/3/4 isoforms

	*  Class / Subclass 1: Signal Transduction / Kinase Inhibitor

Technical Notes

	*  PubChem Name: 2-((3,5-Difluoro-4-hydroxyphenyl)amino)-8-isopentyl-5,7-dimethyl-7,8-dihydropteridin-6(5H)-one</description>
    </item>
    <item rdf:about="https://crispr.tyerslab.com/wiki/results/exp164?rev=1767843420&amp;do=diff">
        <dc:format>text/html</dc:format>
        <dc:date>2026-01-08T03:37:00+00:00</dc:date>
        <dc:creator>Anonymous (anonymous@undisclosed.example.com)</dc:creator>
        <title>Q15 1 to 2μM on day4 R04 exp164</title>
        <link>https://crispr.tyerslab.com/wiki/results/exp164?rev=1767843420&amp;do=diff</link>
        <description>Q15 1 to 2μM on day4 R04 exp164

Mechanism of Action

Putative condensin inhibitor

	*  Class / Subclass 1: Cell Cycle / Chromosome Dynamics Inhibitor

Technical Notes

	*  PubChem Name: N/A
		*  Synonyms: N/A
		*  CAS #: 1071780-64-7
		*  PubChem CID:</description>
    </item>
    <item rdf:about="https://crispr.tyerslab.com/wiki/results/exp165?rev=1767843420&amp;do=diff">
        <dc:format>text/html</dc:format>
        <dc:date>2026-01-08T03:37:00+00:00</dc:date>
        <dc:creator>Anonymous (anonymous@undisclosed.example.com)</dc:creator>
        <title>RO-3306 3 to 4μM on day4 R04 exp165</title>
        <link>https://crispr.tyerslab.com/wiki/results/exp165?rev=1767843420&amp;do=diff</link>
        <description>RO-3306 3 to 4μM on day4 R04 exp165

Mechanism of Action

Inhibits CDK1, ATP-competitive, causes G2/M arrest

	*  Class / Subclass 1: Cell Cycle / Kinase Inhibitor

Technical Notes

	*  PubChem Name: (5Z)-5-(Quinolin-6-ylmethylidene)-2-[(thiophen-2-ylmethyl)amino]-1,3-thiazol-4(5H)-one</description>
    </item>
    <item rdf:about="https://crispr.tyerslab.com/wiki/results/exp169?rev=1767843420&amp;do=diff">
        <dc:format>text/html</dc:format>
        <dc:date>2026-01-08T03:37:00+00:00</dc:date>
        <dc:creator>Anonymous (anonymous@undisclosed.example.com)</dc:creator>
        <title>BH1 1μM R04 exp169</title>
        <link>https://crispr.tyerslab.com/wiki/results/exp169?rev=1767843420&amp;do=diff</link>
        <description>BH1 1μM R04 exp169

Mechanism of Action

Unknown

	*  Class / Subclass 1: Uncharacterized Mechanism / Chemical Screen Hit

Technical Notes

	*  PubChem Name: 4-Amino-N-[4-[5-[(4-aminobenzoyl)amino]-4-chloro-1H-benzimidazol-2-yl]-2-chlorophenyl]benzamide</description>
    </item>
    <item rdf:about="https://crispr.tyerslab.com/wiki/results/exp170?rev=1767843420&amp;do=diff">
        <dc:format>text/html</dc:format>
        <dc:date>2026-01-08T03:37:00+00:00</dc:date>
        <dc:creator>Anonymous (anonymous@undisclosed.example.com)</dc:creator>
        <title>Metformin 100 to 150μM on day4 R04 exp170</title>
        <link>https://crispr.tyerslab.com/wiki/results/exp170?rev=1767843420&amp;do=diff</link>
        <description>Metformin 100 to 150μM on day4 R04 exp170

Mechanism of Action

Inhibits mitochondrial respiratory chain complex I, indirectly activates AMPK

	*  Class / Subclass 1: Organelle Function / Mitochondrial Inhibitor
	*  Class / Subclass 2: Signal Transduction / Kinase Activator</description>
    </item>
    <item rdf:about="https://crispr.tyerslab.com/wiki/results/exp175?rev=1767843420&amp;do=diff">
        <dc:format>text/html</dc:format>
        <dc:date>2026-01-08T03:37:00+00:00</dc:date>
        <dc:creator>Anonymous (anonymous@undisclosed.example.com)</dc:creator>
        <title>3-Bromopyruvate 7μM R04 exp175</title>
        <link>https://crispr.tyerslab.com/wiki/results/exp175?rev=1767843420&amp;do=diff</link>
        <description>3-Bromopyruvate 7μM R04 exp175

Mechanism of Action

Inhibits hexokinase II, pyruvate analog, enzyme alkylator, blocks glycolysis

	*  Class / Subclass 1: Metabolism / Metabolic Enzyme Inhibitor

Technical Notes

	*  PubChem Name: Bromopyruvic acid</description>
    </item>
    <item rdf:about="https://crispr.tyerslab.com/wiki/results/exp176?rev=1767843420&amp;do=diff">
        <dc:format>text/html</dc:format>
        <dc:date>2026-01-08T03:37:00+00:00</dc:date>
        <dc:creator>Anonymous (anonymous@undisclosed.example.com)</dc:creator>
        <title>Apcin 50 to 100μM on day4 R04 exp176</title>
        <link>https://crispr.tyerslab.com/wiki/results/exp176?rev=1767843420&amp;do=diff</link>
        <description>Apcin 50 to 100μM on day4 R04 exp176

Mechanism of Action

Inhibits substrate interactions with APC/C-Cdc20

	*  Class / Subclass 1: Proteostasis / E3 ubiquitin ligase inhibitor
	*  Class / Subclass 2: Cell Cycle / Mitotic Inhibitor

Technical Notes</description>
    </item>
    <item rdf:about="https://crispr.tyerslab.com/wiki/results/exp177?rev=1767843420&amp;do=diff">
        <dc:format>text/html</dc:format>
        <dc:date>2026-01-08T03:37:00+00:00</dc:date>
        <dc:creator>Anonymous (anonymous@undisclosed.example.com)</dc:creator>
        <title>Apcin 25μM plus proTAME 2μM R04 exp177</title>
        <link>https://crispr.tyerslab.com/wiki/results/exp177?rev=1767843420&amp;do=diff</link>
        <description>Apcin 25μM plus proTAME 2μM R04 exp177

Mechanism of Action

Inhibits substrate interactions with APC/C-Cdc20

	*  Class / Subclass 1: Proteostasis / E3 ubiquitin ligase inhibitor
	*  Class / Subclass 2: Cell Cycle / Mitotic Inhibitor

Technical Notes</description>
    </item>
    <item rdf:about="https://crispr.tyerslab.com/wiki/results/exp179?rev=1767843420&amp;do=diff">
        <dc:format>text/html</dc:format>
        <dc:date>2026-01-08T03:37:00+00:00</dc:date>
        <dc:creator>Anonymous (anonymous@undisclosed.example.com)</dc:creator>
        <title>Combretastatin A4 0.002 to 0.003μM day4 R04 exp179</title>
        <link>https://crispr.tyerslab.com/wiki/results/exp179?rev=1767843420&amp;do=diff</link>
        <description>Combretastatin A4 0.002 to 0.003μM day4 R04 exp179

Mechanism of Action

Inhibits microtubule polymerization

	*  Class / Subclass 1: Cell Cycle / Microtubule Poison
	*  Class / Subclass 2: Organelle Function / Cytoskeletal Inhibitor

Technical Notes</description>
    </item>
    <item rdf:about="https://crispr.tyerslab.com/wiki/results/exp180?rev=1767843420&amp;do=diff">
        <dc:format>text/html</dc:format>
        <dc:date>2026-01-08T03:37:00+00:00</dc:date>
        <dc:creator>Anonymous (anonymous@undisclosed.example.com)</dc:creator>
        <title>Dynasore 10μM R04 exp180</title>
        <link>https://crispr.tyerslab.com/wiki/results/exp180?rev=1767843420&amp;do=diff</link>
        <description>Dynasore 10μM R04 exp180

Mechanism of Action

Putative dynamin GTPase inhibitor, blocks endocytosis

	*  Class / Subclass 1: Organelle Function / Vesicule Trafficking Inhibitor

Technical Notes

	*  PubChem Name: Dynasore
		*  Synonyms: N/A
		*  CAS #:</description>
    </item>
    <item rdf:about="https://crispr.tyerslab.com/wiki/results/exp182?rev=1767843420&amp;do=diff">
        <dc:format>text/html</dc:format>
        <dc:date>2026-01-08T03:37:00+00:00</dc:date>
        <dc:creator>Anonymous (anonymous@undisclosed.example.com)</dc:creator>
        <title>IU1-47 25μM R04 exp182</title>
        <link>https://crispr.tyerslab.com/wiki/results/exp182?rev=1767843420&amp;do=diff</link>
        <description>IU1-47 25μM R04 exp182

Mechanism of Action

Inhibits USP14, enhances protein degradation by 26S proteasome

	*  Class / Subclass 1: Proteostasis / Deubiquitinase (DUB) Inhibitor

Technical Notes

	*  PubChem Name: 1-[1-(4-Chlorophenyl)-2,5-dimethyl-1H-pyrrol-3-yl]-2-(piperidin-1-yl)ethan-1-one</description>
    </item>
    <item rdf:about="https://crispr.tyerslab.com/wiki/results/exp183?rev=1767843420&amp;do=diff">
        <dc:format>text/html</dc:format>
        <dc:date>2026-01-08T03:37:00+00:00</dc:date>
        <dc:creator>Anonymous (anonymous@undisclosed.example.com)</dc:creator>
        <title>IU1-C 25μM R04 exp183</title>
        <link>https://crispr.tyerslab.com/wiki/results/exp183?rev=1767843420&amp;do=diff</link>
        <description>IU1-C 25μM R04 exp183

Mechanism of Action

Inactive analog of IU1-47

	*  Class / Subclass 1: Proteostasis / Ubiquitin-Proteasome Inhibitor

Technical Notes

	*  PubChem Name: [1-(4-Fluorophenyl)-2,5-dimethylpyrrol-3-yl]-(4-methylpiperidin-1-yl)methanone</description>
    </item>
    <item rdf:about="https://crispr.tyerslab.com/wiki/results/exp184?rev=1767843420&amp;do=diff">
        <dc:format>text/html</dc:format>
        <dc:date>2026-01-08T03:37:00+00:00</dc:date>
        <dc:creator>Anonymous (anonymous@undisclosed.example.com)</dc:creator>
        <title>Ixabepilone 0.004 to 0.005μM on day4 R04 exp184</title>
        <link>https://crispr.tyerslab.com/wiki/results/exp184?rev=1767843420&amp;do=diff</link>
        <description>Ixabepilone 0.004 to 0.005μM on day4 R04 exp184

Mechanism of Action

Inhibits microtubule depolymerization, semi-synthetic analog of epothilone

	*  Class / Subclass 1: Cell Cycle / Microtubule Poison
	*  Class / Subclass 2: Organelle Function / Cytoskeletal Inhibitor</description>
    </item>
    <item rdf:about="https://crispr.tyerslab.com/wiki/results/exp185?rev=1767843420&amp;do=diff">
        <dc:format>text/html</dc:format>
        <dc:date>2026-01-08T03:37:00+00:00</dc:date>
        <dc:creator>Anonymous (anonymous@undisclosed.example.com)</dc:creator>
        <title>L-BMAA 500 to 750μM on day4 R04 exp185</title>
        <link>https://crispr.tyerslab.com/wiki/results/exp185?rev=1767843420&amp;do=diff</link>
        <description>L-BMAA 500 to 750μM on day4 R04 exp185

Mechanism of Action

‘_-Methylamino-l-alanine, cyanobacterial neurotoxin, possible causative agent of ALS

	*  Class / Subclass 1: Environmental Stresses / Toxin

Technical Notes

	*  PubChem Name: (S)-2-Amino-3-(methylamino)propanoic acid hydrochloride</description>
    </item>
    <item rdf:about="https://crispr.tyerslab.com/wiki/results/exp187?rev=1767843420&amp;do=diff">
        <dc:format>text/html</dc:format>
        <dc:date>2026-01-08T03:37:00+00:00</dc:date>
        <dc:creator>Anonymous (anonymous@undisclosed.example.com)</dc:creator>
        <title>proTAME 5μM R04 exp187</title>
        <link>https://crispr.tyerslab.com/wiki/results/exp187?rev=1767843420&amp;do=diff</link>
        <description>proTAME 5μM R04 exp187

Mechanism of Action

Inhibits APC/C interaction with Cdc20/Cdh1 substrate recognition cofactors

	*  Class / Subclass 1: Proteostasis / E3 ubiquitin ligase inhibitor
	*  Class / Subclass 2: Cell Cycle / Mitotic Inhibitor

Technical Notes</description>
    </item>
    <item rdf:about="https://crispr.tyerslab.com/wiki/results/exp189?rev=1767843420&amp;do=diff">
        <dc:format>text/html</dc:format>
        <dc:date>2026-01-08T03:37:00+00:00</dc:date>
        <dc:creator>Anonymous (anonymous@undisclosed.example.com)</dc:creator>
        <title>Temozolomide 200μM R04 exp189</title>
        <link>https://crispr.tyerslab.com/wiki/results/exp189?rev=1767843420&amp;do=diff</link>
        <description>Temozolomide 200μM R04 exp189

Mechanism of Action

Alkylates purine bases, prodrug hydrolyzes to 3-methyl-(triazen-1-yl)imidazole-4-carboxamide (MTIC)

	*  Class / Subclass 1: DNA Damage, Repair and Replication / Base Alkylation

Technical Notes

	*</description>
    </item>
    <item rdf:about="https://crispr.tyerslab.com/wiki/results/exp190?rev=1767843420&amp;do=diff">
        <dc:format>text/html</dc:format>
        <dc:date>2026-01-08T03:37:00+00:00</dc:date>
        <dc:creator>Anonymous (anonymous@undisclosed.example.com)</dc:creator>
        <title>Vincristine 0.0005μM R04 exp190</title>
        <link>https://crispr.tyerslab.com/wiki/results/exp190?rev=1767843420&amp;do=diff</link>
        <description>Vincristine 0.0005μM R04 exp190

Mechanism of Action

Inhibits microtubule polymerization and mitotic spindle formation, induces spindle assembly checkpoint (SAC)

	*  Class / Subclass 1: Cell Cycle / Microtubule Poison
	*  Class / Subclass 2: Organelle Function / Cytoskeletal Inhibitor</description>
    </item>
    <item rdf:about="https://crispr.tyerslab.com/wiki/results/exp191?rev=1767843420&amp;do=diff">
        <dc:format>text/html</dc:format>
        <dc:date>2026-01-08T03:37:00+00:00</dc:date>
        <dc:creator>Anonymous (anonymous@undisclosed.example.com)</dc:creator>
        <title>Hypoxia 5%O2 R04 exp191</title>
        <link>https://crispr.tyerslab.com/wiki/results/exp191?rev=1767843420&amp;do=diff</link>
        <description>Hypoxia 5%O2 R04 exp191

Mechanism of Action

Reduced growth oxygen

	*  Class / Subclass 1: Environmental Stresses / Stress Condition

Screen Summary

	*  Round: 04
		*  Dose: N/A
		*  Days of incubation: 12
		*  Doublings: N/A
		*  Numbers of reads</description>
    </item>
    <item rdf:about="https://crispr.tyerslab.com/wiki/results/exp198?rev=1767843420&amp;do=diff">
        <dc:format>text/html</dc:format>
        <dc:date>2026-01-08T03:37:00+00:00</dc:date>
        <dc:creator>Anonymous (anonymous@undisclosed.example.com)</dc:creator>
        <title>Etoposide 0.1μM R05 exp198</title>
        <link>https://crispr.tyerslab.com/wiki/results/exp198?rev=1767843420&amp;do=diff</link>
        <description>Etoposide 0.1μM R05 exp198

Mechanism of Action

Binds DNA-TopII complex, blocks re-ligation, induces strand breaks, semi-synthetic derivative of podophyllotoxin

	*  Class / Subclass 1: DNA Damage, Repair and Replication / Topoisomerase II Inhibitor</description>
    </item>
    <item rdf:about="https://crispr.tyerslab.com/wiki/results/exp199?rev=1767843420&amp;do=diff">
        <dc:format>text/html</dc:format>
        <dc:date>2026-01-08T03:37:00+00:00</dc:date>
        <dc:creator>Anonymous (anonymous@undisclosed.example.com)</dc:creator>
        <title>Etoposide 0.3μM R05 exp199</title>
        <link>https://crispr.tyerslab.com/wiki/results/exp199?rev=1767843420&amp;do=diff</link>
        <description>Etoposide 0.3μM R05 exp199

Mechanism of Action

Binds DNA-TopII complex, blocks re-ligation, induces strand breaks, semi-synthetic derivative of podophyllotoxin

	*  Class / Subclass 1: DNA Damage, Repair and Replication / Topoisomerase II Inhibitor</description>
    </item>
    <item rdf:about="https://crispr.tyerslab.com/wiki/results/exp208?rev=1767843420&amp;do=diff">
        <dc:format>text/html</dc:format>
        <dc:date>2026-01-08T03:37:00+00:00</dc:date>
        <dc:creator>Anonymous (anonymous@undisclosed.example.com)</dc:creator>
        <title>Vinblastine 0.015μM R05 exp208</title>
        <link>https://crispr.tyerslab.com/wiki/results/exp208?rev=1767843420&amp;do=diff</link>
        <description>Vinblastine 0.015μM R05 exp208

Mechanism of Action

Inhibits microtubule polymerization and mitotic spindle formation, induces spindle assembly checkpoint (SAC)

	*  Class / Subclass 1: Cell Cycle / Microtubule Poison
	*  Class / Subclass 2: Organelle Function / Cytoskeletal Inhibitor</description>
    </item>
    <item rdf:about="https://crispr.tyerslab.com/wiki/results/exp209?rev=1767843420&amp;do=diff">
        <dc:format>text/html</dc:format>
        <dc:date>2026-01-08T03:37:00+00:00</dc:date>
        <dc:creator>Anonymous (anonymous@undisclosed.example.com)</dc:creator>
        <title>Deguelin 0.15μM R05 exp209</title>
        <link>https://crispr.tyerslab.com/wiki/results/exp209?rev=1767843420&amp;do=diff</link>
        <description>Deguelin 0.15μM R05 exp209

Mechanism of Action

Derivative of rotenone, putative AKT inhibitor, complex I inhibitor

	*  Class / Subclass 1: Signal Transduction / Kinase Inhibitor
	*  Class / Subclass 2: Organelle Function / Mitochondrial Inhibitor</description>
    </item>
    <item rdf:about="https://crispr.tyerslab.com/wiki/results/exp210?rev=1767843420&amp;do=diff">
        <dc:format>text/html</dc:format>
        <dc:date>2026-01-08T03:37:00+00:00</dc:date>
        <dc:creator>Anonymous (anonymous@undisclosed.example.com)</dc:creator>
        <title>LB-100 2μM R05 exp210</title>
        <link>https://crispr.tyerslab.com/wiki/results/exp210?rev=1767843420&amp;do=diff</link>
        <description>LB-100 2μM R05 exp210

Mechanism of Action

Inhibits protein phosphatase 2A

	*  Class / Subclass 1: Signal Transduction / Phosphatase Inhibitor

Technical Notes

	*  PubChem Name: LB-100
		*  Synonyms: N/A
		*  CAS #: 1026680-07-8
		*  PubChem CID:</description>
    </item>
    <item rdf:about="https://crispr.tyerslab.com/wiki/results/exp211?rev=1767843420&amp;do=diff">
        <dc:format>text/html</dc:format>
        <dc:date>2026-01-08T03:37:00+00:00</dc:date>
        <dc:creator>Anonymous (anonymous@undisclosed.example.com)</dc:creator>
        <title>AICAR 240μM R05 exp211</title>
        <link>https://crispr.tyerslab.com/wiki/results/exp211?rev=1767843420&amp;do=diff</link>
        <description>AICAR 240μM R05 exp211

Mechanism of Action

Metabolic intermediate in purine biosynthesis, activates AMPK, has other putative targets

	*  Class / Subclass 1: Metabolism / Metabolite
	*  Class / Subclass 2: Signal Transduction / Kinase Activator

Technical Notes</description>
    </item>
    <item rdf:about="https://crispr.tyerslab.com/wiki/results/exp212?rev=1767843420&amp;do=diff">
        <dc:format>text/html</dc:format>
        <dc:date>2026-01-08T03:37:00+00:00</dc:date>
        <dc:creator>Anonymous (anonymous@undisclosed.example.com)</dc:creator>
        <title>Phenformin 20μM R05 exp212</title>
        <link>https://crispr.tyerslab.com/wiki/results/exp212?rev=1767843420&amp;do=diff</link>
        <description>Phenformin 20μM R05 exp212

Mechanism of Action

Inhibits mitochondrial respiratory chain complex I, indirectly activates AMPK

	*  Class / Subclass 1: Organelle Function / Mitochondrial Inhibitor
	*  Class / Subclass 2: Metabolism / Metabolic Enzyme Activator</description>
    </item>
    <item rdf:about="https://crispr.tyerslab.com/wiki/results/exp214?rev=1767843420&amp;do=diff">
        <dc:format>text/html</dc:format>
        <dc:date>2026-01-08T03:37:00+00:00</dc:date>
        <dc:creator>Anonymous (anonymous@undisclosed.example.com)</dc:creator>
        <title>2-Deoxy-D-glucose 800μM R05 exp214</title>
        <link>https://crispr.tyerslab.com/wiki/results/exp214?rev=1767843420&amp;do=diff</link>
        <description>2-Deoxy-D-glucose 800μM R05 exp214

Mechanism of Action

Inhibits phosphoglucoisomerase, competitive, blocks glycolysis

	*  Class / Subclass 1: Metabolism / Metabolic Enzyme Inhibitor

Technical Notes

	*  PubChem Name: Deoxyglucose
		*  Synonyms: 2-Deoxy-D-arabino-hexose; D-Arabino-2-deoxyhexose</description>
    </item>
    <item rdf:about="https://crispr.tyerslab.com/wiki/results/exp215?rev=1767843420&amp;do=diff">
        <dc:format>text/html</dc:format>
        <dc:date>2026-01-08T03:37:00+00:00</dc:date>
        <dc:creator>Anonymous (anonymous@undisclosed.example.com)</dc:creator>
        <title>Colchicine 0.009μM R05 exp215</title>
        <link>https://crispr.tyerslab.com/wiki/results/exp215?rev=1767843420&amp;do=diff</link>
        <description>Colchicine 0.009μM R05 exp215

Mechanism of Action

Inhibits microtubule polymerization

	*  Class / Subclass 1: Cell Cycle / Microtubule Poison
	*  Class / Subclass 2: Organelle Function / Cytoskeletal Inhibitor

Technical Notes

	*  PubChem Name:</description>
    </item>
    <item rdf:about="https://crispr.tyerslab.com/wiki/results/exp216?rev=1767843420&amp;do=diff">
        <dc:format>text/html</dc:format>
        <dc:date>2026-01-08T03:37:00+00:00</dc:date>
        <dc:creator>Anonymous (anonymous@undisclosed.example.com)</dc:creator>
        <title>Erlotinib 10μM R05 exp216</title>
        <link>https://crispr.tyerslab.com/wiki/results/exp216?rev=1767843420&amp;do=diff</link>
        <description>Erlotinib 10μM R05 exp216

Mechanism of Action

Inhibits EGFR, also cyclin G-associated kinase (GAK)

	*  Class / Subclass 1: Signal Transduction / Kinase Inhibitor

Technical Notes

	*  PubChem Name: Erlotinib
		*  Synonyms: CP-358774; NSC 718781; OSI-774</description>
    </item>
    <item rdf:about="https://crispr.tyerslab.com/wiki/results/exp217?rev=1767843420&amp;do=diff">
        <dc:format>text/html</dc:format>
        <dc:date>2026-01-08T03:37:00+00:00</dc:date>
        <dc:creator>Anonymous (anonymous@undisclosed.example.com)</dc:creator>
        <title>Mdivi-1 15μM R05 exp217</title>
        <link>https://crispr.tyerslab.com/wiki/results/exp217?rev=1767843420&amp;do=diff</link>
        <description>Mdivi-1 15μM R05 exp217

Mechanism of Action

Inhibits GTPase dynamin-related protein 1 (Drp1), impairs mitochondrial fission, also inhibits respiratory complex I

	*  Class / Subclass 1: Organelle Function / Mitochondrial Inhibitor

Technical Notes</description>
    </item>
    <item rdf:about="https://crispr.tyerslab.com/wiki/results/exp218?rev=1767843420&amp;do=diff">
        <dc:format>text/html</dc:format>
        <dc:date>2026-01-08T03:37:00+00:00</dc:date>
        <dc:creator>Anonymous (anonymous@undisclosed.example.com)</dc:creator>
        <title>A-395 10μM R05 exp218</title>
        <link>https://crispr.tyerslab.com/wiki/results/exp218?rev=1767843420&amp;do=diff</link>
        <description>A-395 10μM R05 exp218

Mechanism of Action

Inhibits EED subunit of PRC2 complex, blocks H3K27me3

	*  Class / Subclass 1: Gene Regulation / Epigenetic Inhibitor

Technical Notes

	*  PubChem Name: (3R,4S)-1-(7-Fluoro-2,3-dihydro-1H-inden-1-yl)-N,N-dimethyl-4-[4-(4-methylsulfonylpiperazin-1-yl)phenyl]pyrrolidin-3-amine</description>
    </item>
    <item rdf:about="https://crispr.tyerslab.com/wiki/results/exp219?rev=1767843420&amp;do=diff">
        <dc:format>text/html</dc:format>
        <dc:date>2026-01-08T03:37:00+00:00</dc:date>
        <dc:creator>Anonymous (anonymous@undisclosed.example.com)</dc:creator>
        <title>A-395N 10μM R05 exp219</title>
        <link>https://crispr.tyerslab.com/wiki/results/exp219?rev=1767843420&amp;do=diff</link>
        <description>A-395N 10μM R05 exp219

Mechanism of Action

Inactive analog of A-395 EED inhibitor

	*  Class / Subclass 1: Gene Regulation / Epigenetic Inhibitor

Technical Notes

	*  PubChem Name: (3S,4R)-1-Benzyl-N,N-dimethyl-4-(4-(4-(methylsulfonyl)piperazin-1-yl)phenyl)pyrrolidin-3-amine</description>
    </item>
    <item rdf:about="https://crispr.tyerslab.com/wiki/results/exp220?rev=1767843420&amp;do=diff">
        <dc:format>text/html</dc:format>
        <dc:date>2026-01-08T03:37:00+00:00</dc:date>
        <dc:creator>Anonymous (anonymous@undisclosed.example.com)</dc:creator>
        <title>BAY-598 4μM R05 exp220</title>
        <link>https://crispr.tyerslab.com/wiki/results/exp220?rev=1767843420&amp;do=diff</link>
        <description>BAY-598 4μM R05 exp220

Mechanism of Action

Inhibits SMYD2 lysine methyltransferase that acts on H3K4me, H3K36me, p53 and other substrates

	*  Class / Subclass 1: Gene Regulation / Epigenetic Inhibitor

Technical Notes

	*  PubChem Name: N-[(4S)-2-[N-Cyano-N&#039;-[3-(difluoromethoxy)phenyl]carbamimidoyl]-5-(3,4-dichlorophenyl)-3,4-dihydropyrazol-4-yl]-N-ethyl-2-hydroxyacetamide</description>
    </item>
    <item rdf:about="https://crispr.tyerslab.com/wiki/results/exp222?rev=1767843420&amp;do=diff">
        <dc:format>text/html</dc:format>
        <dc:date>2026-01-08T03:37:00+00:00</dc:date>
        <dc:creator>Anonymous (anonymous@undisclosed.example.com)</dc:creator>
        <title>Betulinic acid 10 to 15μM on day4 R05 exp222</title>
        <link>https://crispr.tyerslab.com/wiki/results/exp222?rev=1767843420&amp;do=diff</link>
        <description>Betulinic acid 10 to 15μM on day4 R05 exp222

Mechanism of Action

Pentacyclic triterpenoid, claimed antiretroviral, antimalarial, anti-inflammatory, topoisomerase I/II inhibitor

	*  Class / Subclass 1: Infectious Disease / Antiviral
	*  Class / Subclass 2:</description>
    </item>
    <item rdf:about="https://crispr.tyerslab.com/wiki/results/exp223?rev=1767843420&amp;do=diff">
        <dc:format>text/html</dc:format>
        <dc:date>2026-01-08T03:37:00+00:00</dc:date>
        <dc:creator>Anonymous (anonymous@undisclosed.example.com)</dc:creator>
        <title>Cabazitaxel 0.001μM R05 exp223</title>
        <link>https://crispr.tyerslab.com/wiki/results/exp223?rev=1767843420&amp;do=diff</link>
        <description>Cabazitaxel 0.001μM R05 exp223

Mechanism of Action

Microtubule stabilizer, semi-synthetic taxane

	*  Class / Subclass 1: Cell Cycle / Microtubule Poison
	*  Class / Subclass 2: Organelle Function / Cytoskeletal Inhibitor

Technical Notes

	*  PubChem Name:</description>
    </item>
    <item rdf:about="https://crispr.tyerslab.com/wiki/results/exp224?rev=1767843420&amp;do=diff">
        <dc:format>text/html</dc:format>
        <dc:date>2026-01-08T03:37:00+00:00</dc:date>
        <dc:creator>Anonymous (anonymous@undisclosed.example.com)</dc:creator>
        <title>CB-839 10μM R05 exp224</title>
        <link>https://crispr.tyerslab.com/wiki/results/exp224?rev=1767843420&amp;do=diff</link>
        <description>CB-839 10μM R05 exp224

Mechanism of Action

Inhibits glutaminase (GLS1), reversible

	*  Class / Subclass 1: Metabolism / Metabolic Enzyme Inhibitor

Technical Notes

	*  PubChem Name: CB-839
		*  Synonyms: CB-839
		*  CAS #: 1439399-58-2
		*  PubChem CID:</description>
    </item>
    <item rdf:about="https://crispr.tyerslab.com/wiki/results/exp225?rev=1767843420&amp;do=diff">
        <dc:format>text/html</dc:format>
        <dc:date>2026-01-08T03:37:00+00:00</dc:date>
        <dc:creator>Anonymous (anonymous@undisclosed.example.com)</dc:creator>
        <title>Celastrol 0.12μM R05 exp225</title>
        <link>https://crispr.tyerslab.com/wiki/results/exp225?rev=1767843420&amp;do=diff</link>
        <description>Celastrol 0.12μM R05 exp225

Mechanism of Action

Putative antioxidant, anti-inflammatory, antiobesity anticancer, proteasome inhibitor

	*  Class / Subclass 1: Uncharacterized Mechanism / Natural Product
	*  Class / Subclass 2: Proteostasis / Ubiquitin-Proteasome Inhibitor</description>
    </item>
    <item rdf:about="https://crispr.tyerslab.com/wiki/results/exp226?rev=1767843420&amp;do=diff">
        <dc:format>text/html</dc:format>
        <dc:date>2026-01-08T03:37:00+00:00</dc:date>
        <dc:creator>Anonymous (anonymous@undisclosed.example.com)</dc:creator>
        <title>Cerivastatin 0.15μM R05 exp226</title>
        <link>https://crispr.tyerslab.com/wiki/results/exp226?rev=1767843420&amp;do=diff</link>
        <description>Cerivastatin 0.15μM R05 exp226

Mechanism of Action

Inhibits HMG-CoA reductase, decreases cholesterol biogenesis, upregulates LDL receptors

	*  Class / Subclass 1: Metabolism / Metabolic Enzyme Inhibitor

Technical Notes

	*  PubChem Name: Cerivastatin sodium</description>
    </item>
    <item rdf:about="https://crispr.tyerslab.com/wiki/results/exp227?rev=1767843420&amp;do=diff">
        <dc:format>text/html</dc:format>
        <dc:date>2026-01-08T03:37:00+00:00</dc:date>
        <dc:creator>Anonymous (anonymous@undisclosed.example.com)</dc:creator>
        <title>Cryptotanshinone 12μM R05 exp227</title>
        <link>https://crispr.tyerslab.com/wiki/results/exp227?rev=1767843420&amp;do=diff</link>
        <description>Cryptotanshinone 12μM R05 exp227

Mechanism of Action

Putative acetylcholinesterase and STAT3 inhibitor

	*  Class / Subclass 1: Uncharacterized Mechanism / Natural Product

Technical Notes

	*  PubChem Name: Cryptotanshinone
		*  Synonyms: Cryptotanshinon; Tanshinone c</description>
    </item>
    <item rdf:about="https://crispr.tyerslab.com/wiki/results/exp228?rev=1767843420&amp;do=diff">
        <dc:format>text/html</dc:format>
        <dc:date>2026-01-08T03:37:00+00:00</dc:date>
        <dc:creator>Anonymous (anonymous@undisclosed.example.com)</dc:creator>
        <title>Demecolcine 0.03μM R05 exp228</title>
        <link>https://crispr.tyerslab.com/wiki/results/exp228?rev=1767843420&amp;do=diff</link>
        <description>Demecolcine 0.03μM R05 exp228

Mechanism of Action

Inhibits microtubule polymerization, a.k.a. colcemid

	*  Class / Subclass 1: Cell Cycle / Microtubule Poison
	*  Class / Subclass 2: Organelle Function / Cytoskeletal Inhibitor

Technical Notes

	*</description>
    </item>
    <item rdf:about="https://crispr.tyerslab.com/wiki/results/exp229?rev=1767843420&amp;do=diff">
        <dc:format>text/html</dc:format>
        <dc:date>2026-01-08T03:37:00+00:00</dc:date>
        <dc:creator>Anonymous (anonymous@undisclosed.example.com)</dc:creator>
        <title>Dimethyloxaloylglycine 100μM R05 exp229</title>
        <link>https://crispr.tyerslab.com/wiki/results/exp229?rev=1767843420&amp;do=diff</link>
        <description>Dimethyloxaloylglycine 100μM R05 exp229

Mechanism of Action

Prolylhydroxylase inhibitor, induces HIF-1α accumulation

	*  Class / Subclass 1: Metabolism / Metabolic Enzyme Inhibitor
	*  Class / Subclass 2: Signal Transduction / Other inhibitor

Technical Notes</description>
    </item>
    <item rdf:about="https://crispr.tyerslab.com/wiki/results/exp230?rev=1767843420&amp;do=diff">
        <dc:format>text/html</dc:format>
        <dc:date>2026-01-08T03:37:00+00:00</dc:date>
        <dc:creator>Anonymous (anonymous@undisclosed.example.com)</dc:creator>
        <title>Epigallocatechin gallate 20μM R05 exp230</title>
        <link>https://crispr.tyerslab.com/wiki/results/exp230?rev=1767843420&amp;do=diff</link>
        <description>Epigallocatechin gallate 20μM R05 exp230

Mechanism of Action

Polyphenol antioxidant from green tea, numerous claimed activities

	*  Class / Subclass 1: Metabolism / Nutraceutical
	*  Class / Subclass 2: Environmental Stresses / Food Additive

Technical Notes</description>
    </item>
    <item rdf:about="https://crispr.tyerslab.com/wiki/results/exp231?rev=1767843420&amp;do=diff">
        <dc:format>text/html</dc:format>
        <dc:date>2026-01-08T03:37:00+00:00</dc:date>
        <dc:creator>Anonymous (anonymous@undisclosed.example.com)</dc:creator>
        <title>Epothilone-B 0.0015μM R05 exp231</title>
        <link>https://crispr.tyerslab.com/wiki/results/exp231?rev=1767843420&amp;do=diff</link>
        <description>Epothilone-B 0.0015μM R05 exp231

Mechanism of Action

Inhibits microtubule depolymerization, parent compound of ixabepilone

	*  Class / Subclass 1: Cell Cycle / Microtubule Poison
	*  Class / Subclass 2: Organelle Function / Cytoskeletal Inhibitor</description>
    </item>
    <item rdf:about="https://crispr.tyerslab.com/wiki/results/exp232?rev=1767843420&amp;do=diff">
        <dc:format>text/html</dc:format>
        <dc:date>2026-01-08T03:37:00+00:00</dc:date>
        <dc:creator>Anonymous (anonymous@undisclosed.example.com)</dc:creator>
        <title>Epothilone-D 0.004 to 0.006μM on day4 R05 exp232</title>
        <link>https://crispr.tyerslab.com/wiki/results/exp232?rev=1767843420&amp;do=diff</link>
        <description>Epothilone-D 0.004 to 0.006μM on day4 R05 exp232

Mechanism of Action

Microtubule stabilizer

	*  Class / Subclass 1: Organelle Function / Cytoskeletal Inhibitor
	*  Class / Subclass 2: Cell Cycle / Microtubule Poison

Technical Notes

	*  PubChem Name:</description>
    </item>
    <item rdf:about="https://crispr.tyerslab.com/wiki/results/exp233?rev=1767843420&amp;do=diff">
        <dc:format>text/html</dc:format>
        <dc:date>2026-01-08T03:37:00+00:00</dc:date>
        <dc:creator>Anonymous (anonymous@undisclosed.example.com)</dc:creator>
        <title>EPZ-5676 30μM R05 exp233</title>
        <link>https://crispr.tyerslab.com/wiki/results/exp233?rev=1767843420&amp;do=diff</link>
        <description>EPZ-5676 30μM R05 exp233

Mechanism of Action

Inhibits DOT1L lysine methyltransferase (H3K79me2)

	*  Class / Subclass 1: Gene Regulation / Epigenetic Inhibitor

Technical Notes

	*  PubChem Name: Pinometostat
		*  Synonyms: EPZ-5676
		*  CAS #: 1380288-87-8</description>
    </item>
    <item rdf:about="https://crispr.tyerslab.com/wiki/results/exp234?rev=1767843420&amp;do=diff">
        <dc:format>text/html</dc:format>
        <dc:date>2026-01-08T03:37:00+00:00</dc:date>
        <dc:creator>Anonymous (anonymous@undisclosed.example.com)</dc:creator>
        <title>Ethanol 0.01 R05 exp234</title>
        <link>https://crispr.tyerslab.com/wiki/results/exp234?rev=1767843420&amp;do=diff</link>
        <description>Ethanol 0.01 R05 exp234

Mechanism of Action

Pleiotropic effects on membranes, ion channels, enzymes, receptors

	*  Class / Subclass 1: Environmental Stresses / Solvent

Technical Notes

	*  PubChem Name: Ethanol
		*  Synonyms: N/A
		*  CAS #: 64-17-5</description>
    </item>
    <item rdf:about="https://crispr.tyerslab.com/wiki/results/exp235?rev=1767843420&amp;do=diff">
        <dc:format>text/html</dc:format>
        <dc:date>2026-01-08T03:37:00+00:00</dc:date>
        <dc:creator>Anonymous (anonymous@undisclosed.example.com)</dc:creator>
        <title>Geldanamycin 0.01μM R05 exp235</title>
        <link>https://crispr.tyerslab.com/wiki/results/exp235?rev=1767843420&amp;do=diff</link>
        <description>Geldanamycin 0.01μM R05 exp235

Mechanism of Action

HSP90 inhibitor

	*  Class / Subclass 1: Proteostasis / Chaperone Inhibitor

Technical Notes

	*  PubChem Name: Geldanamycin
		*  Synonyms: N/A
		*  CAS #: 30562-34-6
		*  PubChem CID: 5288382
		*  IUPAC:</description>
    </item>
    <item rdf:about="https://crispr.tyerslab.com/wiki/results/exp236?rev=1767843420&amp;do=diff">
        <dc:format>text/html</dc:format>
        <dc:date>2026-01-08T03:37:00+00:00</dc:date>
        <dc:creator>Anonymous (anonymous@undisclosed.example.com)</dc:creator>
        <title>GSK2606414 1μM R05 exp236</title>
        <link>https://crispr.tyerslab.com/wiki/results/exp236?rev=1767843420&amp;do=diff</link>
        <description>GSK2606414 1μM R05 exp236

Mechanism of Action

Inhibits PERK, also KIT receptor

	*  Class / Subclass 1: Signal Transduction / Kinase Inhibitor

Technical Notes

	*  PubChem Name: CID 53469448
		*  Synonyms: N/A
		*  CAS #: 1337531-36-8
		*  PubChem CID:</description>
    </item>
    <item rdf:about="https://crispr.tyerslab.com/wiki/results/exp237?rev=1767843420&amp;do=diff">
        <dc:format>text/html</dc:format>
        <dc:date>2026-01-08T03:37:00+00:00</dc:date>
        <dc:creator>Anonymous (anonymous@undisclosed.example.com)</dc:creator>
        <title>NN-Diethyl-meta-toluamide 100μM R05 exp237</title>
        <link>https://crispr.tyerslab.com/wiki/results/exp237?rev=1767843420&amp;do=diff</link>
        <description>NN-Diethyl-meta-toluamide 100μM R05 exp237

Mechanism of Action

Insect repellent

	*  Class / Subclass 1: Environmental Stresses / Environmental Contaminant

Technical Notes

	*  PubChem Name: N,N-Diethyl-3-methylbenzamide
		*  Synonyms: DEET; N,N-Diethyl-m-toluamide; DEET;N,N-Diethyl-m-toluamide</description>
    </item>
    <item rdf:about="https://crispr.tyerslab.com/wiki/results/exp238?rev=1767843420&amp;do=diff">
        <dc:format>text/html</dc:format>
        <dc:date>2026-01-08T03:37:00+00:00</dc:date>
        <dc:creator>Anonymous (anonymous@undisclosed.example.com)</dc:creator>
        <title>Parthenolide 2.5μM R05 exp238</title>
        <link>https://crispr.tyerslab.com/wiki/results/exp238?rev=1767843420&amp;do=diff</link>
        <description>Parthenolide 2.5μM R05 exp238

Mechanism of Action

Sesquiterpene lactone with attributed activities in microtubule function, NF-κB activation, HDAC1 inhibition, MDM2 ubiquitination. Parthenolide is a sesquiterpene lactone found in the medicinal herb Feverfew</description>
    </item>
    <item rdf:about="https://crispr.tyerslab.com/wiki/results/exp239?rev=1767843420&amp;do=diff">
        <dc:format>text/html</dc:format>
        <dc:date>2026-01-08T03:37:00+00:00</dc:date>
        <dc:creator>Anonymous (anonymous@undisclosed.example.com)</dc:creator>
        <title>PFI-2 4μM R05 exp239</title>
        <link>https://crispr.tyerslab.com/wiki/results/exp239?rev=1767843420&amp;do=diff</link>
        <description>PFI-2 4μM R05 exp239

Mechanism of Action

Inhibits SETD7 lysine methyltransferase (H3K4me)

	*  Class / Subclass 1: Gene Regulation / Epigenetic Inhibitor

Technical Notes

	*  PubChem Name: 8-Fluoro-N-[(2S)-1-oxo-1-pyrrolidin-1-yl-3-[3-(trifluoromethyl)phenyl]propan-2-yl]-1,2,3,4-tetrahydroisoquinoline-6-sulfonamide;hydrochloride</description>
    </item>
    <item rdf:about="https://crispr.tyerslab.com/wiki/results/exp240?rev=1767843420&amp;do=diff">
        <dc:format>text/html</dc:format>
        <dc:date>2026-01-08T03:37:00+00:00</dc:date>
        <dc:creator>Anonymous (anonymous@undisclosed.example.com)</dc:creator>
        <title>Pyridostatin 4μM R05 exp240</title>
        <link>https://crispr.tyerslab.com/wiki/results/exp240?rev=1767843420&amp;do=diff</link>
        <description>Pyridostatin 4μM R05 exp240

Mechanism of Action

Binds and stabilizes telomeric and interstitial G-quadruplexes

	*  Class / Subclass 1: DNA Damage, Repair and Replication / G-Quadruplex Stabilizer

Technical Notes

	*  PubChem Name: Pyridostatin
		*</description>
    </item>
    <item rdf:about="https://crispr.tyerslab.com/wiki/results/exp241?rev=1767843420&amp;do=diff">
        <dc:format>text/html</dc:format>
        <dc:date>2026-01-08T03:37:00+00:00</dc:date>
        <dc:creator>Anonymous (anonymous@undisclosed.example.com)</dc:creator>
        <title>QNZ 0.01μM R05 exp241</title>
        <link>https://crispr.tyerslab.com/wiki/results/exp241?rev=1767843420&amp;do=diff</link>
        <description>QNZ 0.01μM R05 exp241

Mechanism of Action

Inhibits NF-κB activation, TNF-α production

	*  Class / Subclass 1: Gene Regulation / Transcription Inhibitor
	*  Class / Subclass 2: Signal Transduction / Apoptosis Inhibitor

Technical Notes

	*  PubChem Name:</description>
    </item>
    <item rdf:about="https://crispr.tyerslab.com/wiki/results/exp242?rev=1767843420&amp;do=diff">
        <dc:format>text/html</dc:format>
        <dc:date>2026-01-08T03:37:00+00:00</dc:date>
        <dc:creator>Anonymous (anonymous@undisclosed.example.com)</dc:creator>
        <title>Radicicol 0.16μM R05 exp242</title>
        <link>https://crispr.tyerslab.com/wiki/results/exp242?rev=1767843420&amp;do=diff</link>
        <description>Radicicol 0.16μM R05 exp242

Mechanism of Action

Inhibits HSP90

	*  Class / Subclass 1: Proteostasis / Chaperone Inhibitor
	*  Class / Subclass 2: Infectious Disease / Antifungal

Technical Notes

	*  PubChem Name: Radicicol
		*  Synonyms: N/A
		*</description>
    </item>
    <item rdf:about="https://crispr.tyerslab.com/wiki/results/exp243?rev=1767843420&amp;do=diff">
        <dc:format>text/html</dc:format>
        <dc:date>2026-01-08T03:37:00+00:00</dc:date>
        <dc:creator>Anonymous (anonymous@undisclosed.example.com)</dc:creator>
        <title>S-trityl-L-cysteine 0.5μM R05 exp243</title>
        <link>https://crispr.tyerslab.com/wiki/results/exp243?rev=1767843420&amp;do=diff</link>
        <description>S-trityl-L-cysteine 0.5μM R05 exp243

Mechanism of Action

Inhibits Eg5 kinesin, blocks centrosome separation and bipolar spindle formation, arrests cells with monoastral spindles

	*  Class / Subclass 1: Organelle Function / Cytoskeletal Inhibitor</description>
    </item>
    <item rdf:about="https://crispr.tyerslab.com/wiki/results/exp244?rev=1767843420&amp;do=diff">
        <dc:format>text/html</dc:format>
        <dc:date>2026-01-08T03:37:00+00:00</dc:date>
        <dc:creator>Anonymous (anonymous@undisclosed.example.com)</dc:creator>
        <title>SB743921 0.001μM R05 exp244</title>
        <link>https://crispr.tyerslab.com/wiki/results/exp244?rev=1767843420&amp;do=diff</link>
        <description>SB743921 0.001μM R05 exp244

Mechanism of Action

Inhibits Eg5 kinesin, derivative of S-trityl-L-cysteine

	*  Class / Subclass 1: Cell Cycle / Mitotic Inhibitor

Technical Notes

	*  PubChem Name: N-(3-Aminopropyl)-N-[(1R)-1-(3-benzyl-7-chloro-4-oxochromen-2-yl)-2-methylpropyl]-4-methylbenzamide;hydrochloride</description>
    </item>
    <item rdf:about="https://crispr.tyerslab.com/wiki/results/exp245?rev=1767843420&amp;do=diff">
        <dc:format>text/html</dc:format>
        <dc:date>2026-01-08T03:37:00+00:00</dc:date>
        <dc:creator>Anonymous (anonymous@undisclosed.example.com)</dc:creator>
        <title>UM0011500 5μM R05 exp245</title>
        <link>https://crispr.tyerslab.com/wiki/results/exp245?rev=1767843420&amp;do=diff</link>
        <description>UM0011500 5μM R05 exp245

Mechanism of Action

Unknown

	*  Class / Subclass 1: Uncharacterized Mechanism / Chemical Screen Hit

Technical Notes

	*  PubChem Name: 3-(5,6-Dimethyl-1,3-dihydroisoindol-2-yl)-N-[(Z)-furan-2-ylmethylideneamino]benzamide</description>
    </item>
    <item rdf:about="https://crispr.tyerslab.com/wiki/results/exp246?rev=1767843420&amp;do=diff">
        <dc:format>text/html</dc:format>
        <dc:date>2026-01-08T03:37:00+00:00</dc:date>
        <dc:creator>Anonymous (anonymous@undisclosed.example.com)</dc:creator>
        <title>UM0011500 10μM R05 exp246</title>
        <link>https://crispr.tyerslab.com/wiki/results/exp246?rev=1767843420&amp;do=diff</link>
        <description>UM0011500 10μM R05 exp246

Mechanism of Action

Unknown

	*  Class / Subclass 1: Uncharacterized Mechanism / Chemical Screen Hit

Technical Notes

	*  PubChem Name: 3-(5,6-Dimethyl-1,3-dihydroisoindol-2-yl)-N-[(Z)-furan-2-ylmethylideneamino]benzamide</description>
    </item>
    <item rdf:about="https://crispr.tyerslab.com/wiki/results/exp247?rev=1767843420&amp;do=diff">
        <dc:format>text/html</dc:format>
        <dc:date>2026-01-08T03:37:00+00:00</dc:date>
        <dc:creator>Anonymous (anonymous@undisclosed.example.com)</dc:creator>
        <title>UM0130462 0.025 to 0.035μM day4 R05 exp247</title>
        <link>https://crispr.tyerslab.com/wiki/results/exp247?rev=1767843420&amp;do=diff</link>
        <description>UM0130462 0.025 to 0.035μM day4 R05 exp247

Mechanism of Action

Unknown

	*  Class / Subclass 1: Uncharacterized Mechanism / Chemical Screen Hit

Technical Notes

	*  PubChem Name: 1-Chloro-2-(2-chloroethyl)-3-methylpyrido[1,2-a]benzimidazole-4-carbonitrile</description>
    </item>
    <item rdf:about="https://crispr.tyerslab.com/wiki/results/exp248?rev=1767843420&amp;do=diff">
        <dc:format>text/html</dc:format>
        <dc:date>2026-01-08T03:37:00+00:00</dc:date>
        <dc:creator>Anonymous (anonymous@undisclosed.example.com)</dc:creator>
        <title>UM0131023 0.05μM R05 exp248</title>
        <link>https://crispr.tyerslab.com/wiki/results/exp248?rev=1767843420&amp;do=diff</link>
        <description>UM0131023 0.05μM R05 exp248

Mechanism of Action

Unknown

	*  Class / Subclass 1: Uncharacterized Mechanism / Chemical Screen Hit

Technical Notes

	*  PubChem Name: N/A
		*  Synonyms: N/A
		*  CAS #: N/A
		*  PubChem CID: N/A
		*  IUPAC: N/A
		*</description>
    </item>
    <item rdf:about="https://crispr.tyerslab.com/wiki/results/exp249?rev=1767843420&amp;do=diff">
        <dc:format>text/html</dc:format>
        <dc:date>2026-01-08T03:37:00+00:00</dc:date>
        <dc:creator>Anonymous (anonymous@undisclosed.example.com)</dc:creator>
        <title>Vinorelbine 0.001μM R05 exp249</title>
        <link>https://crispr.tyerslab.com/wiki/results/exp249?rev=1767843420&amp;do=diff</link>
        <description>Vinorelbine 0.001μM R05 exp249

Mechanism of Action

Inhibits microtubule polymerization and mitotic spindle formation, induces spindle assembly checkpoint (SAC)

	*  Class / Subclass 1: Cell Cycle / Microtubule Poison
	*  Class / Subclass 2: Organelle Function / Cytoskeletal Inhibitor</description>
    </item>
    <item rdf:about="https://crispr.tyerslab.com/wiki/results/exp256?rev=1767843420&amp;do=diff">
        <dc:format>text/html</dc:format>
        <dc:date>2026-01-08T03:37:00+00:00</dc:date>
        <dc:creator>Anonymous (anonymous@undisclosed.example.com)</dc:creator>
        <title>HMS-I1 10μM R06 exp256</title>
        <link>https://crispr.tyerslab.com/wiki/results/exp256?rev=1767843420&amp;do=diff</link>
        <description>HMS-I1 10μM R06 exp256

Mechanism of Action

Inhibits HDAC

	*  Class / Subclass 1: Uncharacterized Mechanism / Chemical Screen Hit

Technical Notes

	*  PubChem Name: 2-(2,3-Dihydro-1,4-benzodioxin-6-yl)-6-methylimidazo[1,2-a]pyridine
		*  Synonyms:</description>
    </item>
    <item rdf:about="https://crispr.tyerslab.com/wiki/results/exp259?rev=1767843420&amp;do=diff">
        <dc:format>text/html</dc:format>
        <dc:date>2026-01-08T03:37:00+00:00</dc:date>
        <dc:creator>Anonymous (anonymous@undisclosed.example.com)</dc:creator>
        <title>6-Thio-2-deoxyguanosine 2μM R06 exp259</title>
        <link>https://crispr.tyerslab.com/wiki/results/exp259?rev=1767843420&amp;do=diff</link>
        <description>6-Thio-2-deoxyguanosine 2μM R06 exp259

Mechanism of Action

Nucleoside analog, incorporated into telomeric DNA by telomerase, impairs proliferation of telomerase-positive cells

	*  Class / Subclass 1: Metabolism / Antimetabolite
	*  Class / Subclass 2:</description>
    </item>
    <item rdf:about="https://crispr.tyerslab.com/wiki/results/exp260?rev=1767843420&amp;do=diff">
        <dc:format>text/html</dc:format>
        <dc:date>2026-01-08T03:37:00+00:00</dc:date>
        <dc:creator>Anonymous (anonymous@undisclosed.example.com)</dc:creator>
        <title>ABT-702 0.1μM R06 exp260</title>
        <link>https://crispr.tyerslab.com/wiki/results/exp260?rev=1767843420&amp;do=diff</link>
        <description>ABT-702 0.1μM R06 exp260

Mechanism of Action

Inhibits adenosine kinase (ADK)

	*  Class / Subclass 1: Metabolism / Metabolic Enzyme Inhibitor

Technical Notes

	*  PubChem Name: Adenosine Kinase Inhibitor
		*  Synonyms: N/A
		*  CAS #: 1188890-28-9</description>
    </item>
    <item rdf:about="https://crispr.tyerslab.com/wiki/results/exp261?rev=1767843420&amp;do=diff">
        <dc:format>text/html</dc:format>
        <dc:date>2026-01-08T03:37:00+00:00</dc:date>
        <dc:creator>Anonymous (anonymous@undisclosed.example.com)</dc:creator>
        <title>ABT-702 5μM R06 exp261</title>
        <link>https://crispr.tyerslab.com/wiki/results/exp261?rev=1767843420&amp;do=diff</link>
        <description>ABT-702 5μM R06 exp261

Mechanism of Action

Inhibits adenosine kinase (ADK)

	*  Class / Subclass 1: Metabolism / Metabolic Enzyme Inhibitor

Technical Notes

	*  PubChem Name: Adenosine Kinase Inhibitor
		*  Synonyms: N/A
		*  CAS #: 1188890-28-9</description>
    </item>
    <item rdf:about="https://crispr.tyerslab.com/wiki/results/exp262?rev=1767843420&amp;do=diff">
        <dc:format>text/html</dc:format>
        <dc:date>2026-01-08T03:37:00+00:00</dc:date>
        <dc:creator>Anonymous (anonymous@undisclosed.example.com)</dc:creator>
        <title>Alda-1 10μM R06 exp262</title>
        <link>https://crispr.tyerslab.com/wiki/results/exp262?rev=1767843420&amp;do=diff</link>
        <description>Alda-1 10μM R06 exp262

Mechanism of Action

Activates mitochondrial aldehyde dehydrogenase (ALDH2), may attenuate ethanol addiction

	*  Class / Subclass 1: Metabolism / Metabolic Enzyme Activator

Technical Notes

	*  PubChem Name: N-(1,3-Benzodioxol-5-ylmethyl)-2,6-dichlorobenzamide</description>
    </item>
    <item rdf:about="https://crispr.tyerslab.com/wiki/results/exp263?rev=1767843420&amp;do=diff">
        <dc:format>text/html</dc:format>
        <dc:date>2026-01-08T03:37:00+00:00</dc:date>
        <dc:creator>Anonymous (anonymous@undisclosed.example.com)</dc:creator>
        <title>Aphidicolin 0.04μM R06 exp263</title>
        <link>https://crispr.tyerslab.com/wiki/results/exp263?rev=1767843420&amp;do=diff</link>
        <description>Aphidicolin 0.04μM R06 exp263

Mechanism of Action

Inhibits DNA polymerases Polα, Polδ, Polϵ and Polζ

	*  Class / Subclass 1: DNA Damage, Repair and Replication / Replication Inhibitor
	*  Class / Subclass 2: Cell Cycle / Replication Inhibitor</description>
    </item>
    <item rdf:about="https://crispr.tyerslab.com/wiki/results/exp264?rev=1767843420&amp;do=diff">
        <dc:format>text/html</dc:format>
        <dc:date>2026-01-08T03:37:00+00:00</dc:date>
        <dc:creator>Anonymous (anonymous@undisclosed.example.com)</dc:creator>
        <title>Arsenate 40μM R06 exp264</title>
        <link>https://crispr.tyerslab.com/wiki/results/exp264?rev=1767843420&amp;do=diff</link>
        <description>Arsenate 40μM R06 exp264

Mechanism of Action

Heavy metal toxin, environmental contaminant

	*  Class / Subclass 1: Environmental Stresses / Heavy Metal

Technical Notes

	*  PubChem Name: Sodium arsenate heptahydrate
		*  Synonyms: N/A
		*  CAS #:</description>
    </item>
    <item rdf:about="https://crispr.tyerslab.com/wiki/results/exp269?rev=1767843420&amp;do=diff">
        <dc:format>text/html</dc:format>
        <dc:date>2026-01-08T03:37:00+00:00</dc:date>
        <dc:creator>Anonymous (anonymous@undisclosed.example.com)</dc:creator>
        <title>Bisphenol A 100μM R06 exp269</title>
        <link>https://crispr.tyerslab.com/wiki/results/exp269?rev=1767843420&amp;do=diff</link>
        <description>Bisphenol A 100μM R06 exp269

Mechanism of Action

Widely-used in plastics and epoxy resins, endocrine disrupter

	*  Class / Subclass 1: Environmental Stresses / Industrial Chemical

Technical Notes

	*  PubChem Name: Bisphenol A
		*  Synonyms: N/A</description>
    </item>
    <item rdf:about="https://crispr.tyerslab.com/wiki/results/exp270?rev=1767843420&amp;do=diff">
        <dc:format>text/html</dc:format>
        <dc:date>2026-01-08T03:37:00+00:00</dc:date>
        <dc:creator>Anonymous (anonymous@undisclosed.example.com)</dc:creator>
        <title>Campthothecin 0.001μM R06 exp270</title>
        <link>https://crispr.tyerslab.com/wiki/results/exp270?rev=1767843420&amp;do=diff</link>
        <description>Campthothecin 0.001μM R06 exp270

Mechanism of Action

Inhibits topoisomerase I, stabilizes TopoI-DNA complex, causes DNA strand breaks

	*  Class / Subclass 1: DNA Damage, Repair and Replication / Clastogen

Technical Notes

	*  PubChem Name: Camptothecin</description>
    </item>
    <item rdf:about="https://crispr.tyerslab.com/wiki/results/exp271?rev=1767843420&amp;do=diff">
        <dc:format>text/html</dc:format>
        <dc:date>2026-01-08T03:37:00+00:00</dc:date>
        <dc:creator>Anonymous (anonymous@undisclosed.example.com)</dc:creator>
        <title>CCT251545 0.2μM R06 exp271</title>
        <link>https://crispr.tyerslab.com/wiki/results/exp271?rev=1767843420&amp;do=diff</link>
        <description>CCT251545 0.2μM R06 exp271

Mechanism of Action

Inhibits CDK8 and CDK19 mediator-associated kinases

	*  Class / Subclass 1: Gene Regulation / Transcription Inhibitor
	*  Class / Subclass 2: Signal Transduction / Kinase Inhibitor

Technical Notes</description>
    </item>
    <item rdf:about="https://crispr.tyerslab.com/wiki/results/exp272?rev=1767843420&amp;do=diff">
        <dc:format>text/html</dc:format>
        <dc:date>2026-01-08T03:37:00+00:00</dc:date>
        <dc:creator>Anonymous (anonymous@undisclosed.example.com)</dc:creator>
        <title>CHIR-124 0.04μM R06 exp272</title>
        <link>https://crispr.tyerslab.com/wiki/results/exp272?rev=1767843420&amp;do=diff</link>
        <description>CHIR-124 0.04μM R06 exp272

Mechanism of Action

Inhibits CHK1, blocks checkpoint arrest, potentiates DNA damaging agents

	*  Class / Subclass 1: DNA Damage, Repair and Replication / Checkpoint Signaling Inhibitor
	*  Class / Subclass 2: Signal Transduction / Kinase Inhibitor</description>
    </item>
    <item rdf:about="https://crispr.tyerslab.com/wiki/results/exp273?rev=1767843420&amp;do=diff">
        <dc:format>text/html</dc:format>
        <dc:date>2026-01-08T03:37:00+00:00</dc:date>
        <dc:creator>Anonymous (anonymous@undisclosed.example.com)</dc:creator>
        <title>Cisplatin 0.35μM R06 exp273</title>
        <link>https://crispr.tyerslab.com/wiki/results/exp273?rev=1767843420&amp;do=diff</link>
        <description>Cisplatin 0.35μM R06 exp273

Mechanism of Action

Intrastrand cross-linker

	*  Class / Subclass 1: DNA Damage, Repair and Replication / Inter/Intra-strand Crosslinker

Technical Notes

	*  PubChem Name: Cisplatin
		*  Synonyms: CDDP; cis-Diaminodichloroplatinum</description>
    </item>
    <item rdf:about="https://crispr.tyerslab.com/wiki/results/exp274?rev=1767843420&amp;do=diff">
        <dc:format>text/html</dc:format>
        <dc:date>2026-01-08T03:37:00+00:00</dc:date>
        <dc:creator>Anonymous (anonymous@undisclosed.example.com)</dc:creator>
        <title>Citral 50μM R06 exp274</title>
        <link>https://crispr.tyerslab.com/wiki/results/exp274?rev=1767843420&amp;do=diff</link>
        <description>Citral 50μM R06 exp274

Mechanism of Action

putative ALDH inhibitor, essential oil

	*  Class / Subclass 1: Uncharacterized Mechanism / Natural Product
	*  Class / Subclass 2: Metabolism / Metabolic Enzyme Inhibitor

Technical Notes

	*  PubChem Name:</description>
    </item>
    <item rdf:about="https://crispr.tyerslab.com/wiki/results/exp275?rev=1767843420&amp;do=diff">
        <dc:format>text/html</dc:format>
        <dc:date>2026-01-08T03:37:00+00:00</dc:date>
        <dc:creator>Anonymous (anonymous@undisclosed.example.com)</dc:creator>
        <title>Citral 75μM R06 exp275</title>
        <link>https://crispr.tyerslab.com/wiki/results/exp275?rev=1767843420&amp;do=diff</link>
        <description>Citral 75μM R06 exp275

Mechanism of Action

putative ALDH inhibitor, essential oil

	*  Class / Subclass 1: Uncharacterized Mechanism / Natural Product
	*  Class / Subclass 2: Metabolism / Metabolic Enzyme Inhibitor

Technical Notes

	*  PubChem Name:</description>
    </item>
    <item rdf:about="https://crispr.tyerslab.com/wiki/results/exp277?rev=1767843420&amp;do=diff">
        <dc:format>text/html</dc:format>
        <dc:date>2026-01-08T03:37:00+00:00</dc:date>
        <dc:creator>Anonymous (anonymous@undisclosed.example.com)</dc:creator>
        <title>Curcumin 6.5μM R06 exp277</title>
        <link>https://crispr.tyerslab.com/wiki/results/exp277?rev=1767843420&amp;do=diff</link>
        <description>Curcumin 6.5μM R06 exp277

Mechanism of Action

Component of tumeric spice, many claimed activities but viewed as pan-assay interference compound

	*  Class / Subclass 1: Uncharacterized Mechanism / Natural Product
	*  Class / Subclass 2: Metabolism / Nutraceutical</description>
    </item>
    <item rdf:about="https://crispr.tyerslab.com/wiki/results/exp278?rev=1767843420&amp;do=diff">
        <dc:format>text/html</dc:format>
        <dc:date>2026-01-08T03:37:00+00:00</dc:date>
        <dc:creator>Anonymous (anonymous@undisclosed.example.com)</dc:creator>
        <title>CVT-10216 0.1μM R06 exp278</title>
        <link>https://crispr.tyerslab.com/wiki/results/exp278?rev=1767843420&amp;do=diff</link>
        <description>CVT-10216 0.1μM R06 exp278

Mechanism of Action

Inhibits mitochondrial aldehyde dehydrogenase (ALDH2), main enzyme for oxidative alcohol metabolism

	*  Class / Subclass 1: Metabolism / Metabolic Enzyme Inhibitor

Technical Notes

	*  PubChem Name:</description>
    </item>
    <item rdf:about="https://crispr.tyerslab.com/wiki/results/exp279?rev=1767843420&amp;do=diff">
        <dc:format>text/html</dc:format>
        <dc:date>2026-01-08T03:37:00+00:00</dc:date>
        <dc:creator>Anonymous (anonymous@undisclosed.example.com)</dc:creator>
        <title>D-Fructose 10000μM R06 exp279</title>
        <link>https://crispr.tyerslab.com/wiki/results/exp279?rev=1767843420&amp;do=diff</link>
        <description>D-Fructose 10000μM R06 exp279

Mechanism of Action

Monosaccharide

	*  Class / Subclass 1: Metabolism / Nutrient

Technical Notes

	*  PubChem Name: D-(-)-Fructose
		*  Synonyms: D(-?)?-?Fructose
		*  CAS #: 57-48-7
		*  PubChem CID: 5984
		*  IUPAC: (3S,4R,5R)-1,3,4,5,6-pentahydroxyhexan-2-one</description>
    </item>
    <item rdf:about="https://crispr.tyerslab.com/wiki/results/exp280?rev=1767843420&amp;do=diff">
        <dc:format>text/html</dc:format>
        <dc:date>2026-01-08T03:37:00+00:00</dc:date>
        <dc:creator>Anonymous (anonymous@undisclosed.example.com)</dc:creator>
        <title>Daidzin 10μM R06 exp280</title>
        <link>https://crispr.tyerslab.com/wiki/results/exp280?rev=1767843420&amp;do=diff</link>
        <description>Daidzin 10μM R06 exp280

Mechanism of Action

Isoflavone from soy bean, putative ALDH inhibitor

	*  Class / Subclass 1: Uncharacterized Mechanism / Natural Product
	*  Class / Subclass 2: Metabolism / Metabolic Enzyme Inhibitor

Technical Notes

	*</description>
    </item>
    <item rdf:about="https://crispr.tyerslab.com/wiki/results/exp281?rev=1767843420&amp;do=diff">
        <dc:format>text/html</dc:format>
        <dc:date>2026-01-08T03:37:00+00:00</dc:date>
        <dc:creator>Anonymous (anonymous@undisclosed.example.com)</dc:creator>
        <title>Disulfiram 4.3μM R06 exp281</title>
        <link>https://crispr.tyerslab.com/wiki/results/exp281?rev=1767843420&amp;do=diff</link>
        <description>Disulfiram 4.3μM R06 exp281

Mechanism of Action

ALDH1 inhibitor, putative 26S proteasome inhibitor

	*  Class / Subclass 1: Metabolism / Metabolic Enzyme Inhibitor
	*  Class / Subclass 2: Proteostasis / Ubiquitin-Proteasome Inhibitor

Technical Notes</description>
    </item>
    <item rdf:about="https://crispr.tyerslab.com/wiki/results/exp282?rev=1767843420&amp;do=diff">
        <dc:format>text/html</dc:format>
        <dc:date>2026-01-08T03:37:00+00:00</dc:date>
        <dc:creator>Anonymous (anonymous@undisclosed.example.com)</dc:creator>
        <title>Fluvastatin 2.2μM R06 exp282</title>
        <link>https://crispr.tyerslab.com/wiki/results/exp282?rev=1767843420&amp;do=diff</link>
        <description>Fluvastatin 2.2μM R06 exp282

Mechanism of Action

Inhibits HMG-CoA reductase, decreases cholesterol biogenesis, upregulates LDL-receptors

	*  Class / Subclass 1: Metabolism / Metabolic Enzyme Inhibitor

Technical Notes

	*  PubChem Name: Fluvastatin sodium</description>
    </item>
    <item rdf:about="https://crispr.tyerslab.com/wiki/results/exp283?rev=1767843420&amp;do=diff">
        <dc:format>text/html</dc:format>
        <dc:date>2026-01-08T03:37:00+00:00</dc:date>
        <dc:creator>Anonymous (anonymous@undisclosed.example.com)</dc:creator>
        <title>Glyphosate 1000μM R06 exp283</title>
        <link>https://crispr.tyerslab.com/wiki/results/exp283?rev=1767843420&amp;do=diff</link>
        <description>Glyphosate 1000μM R06 exp283

Mechanism of Action

Inhibits 5-enolpyruvylshikimate-3-phosphate synthase, a.k.a Roundup

	*  Class / Subclass 1: Environmental Stresses / Herbicide

Technical Notes

	*  PubChem Name: Glyphosate
		*  Synonyms: N/A
		*</description>
    </item>
    <item rdf:about="https://crispr.tyerslab.com/wiki/results/exp285?rev=1767843420&amp;do=diff">
        <dc:format>text/html</dc:format>
        <dc:date>2026-01-08T03:37:00+00:00</dc:date>
        <dc:creator>Anonymous (anonymous@undisclosed.example.com)</dc:creator>
        <title>GW501516 25μM R06 exp285</title>
        <link>https://crispr.tyerslab.com/wiki/results/exp285?rev=1767843420&amp;do=diff</link>
        <description>GW501516 25μM R06 exp285

Mechanism of Action

PPARδ receptor agonist, increases metabolism, banned performance enhancer

	*  Class / Subclass 1: Gene Regulation / Nuclear Receptor Ligand
	*  Class / Subclass 2: Metabolism / Hormone Agonist

Technical Notes</description>
    </item>
    <item rdf:about="https://crispr.tyerslab.com/wiki/results/exp286?rev=1767843420&amp;do=diff">
        <dc:format>text/html</dc:format>
        <dc:date>2026-01-08T03:37:00+00:00</dc:date>
        <dc:creator>Anonymous (anonymous@undisclosed.example.com)</dc:creator>
        <title>HMS-I2 1μM R06 exp286</title>
        <link>https://crispr.tyerslab.com/wiki/results/exp286?rev=1767843420&amp;do=diff</link>
        <description>HMS-I2 1μM R06 exp286

Mechanism of Action

putative HDAC inhibitor from cell-based screen

	*  Class / Subclass 1: Uncharacterized Mechanism / Chemical Screen Hit

Technical Notes

	*  PubChem Name: N-(1-Benzothiophen-2-yl)-4-[(2-chloro-6-fluorophenyl)methyl]piperazine-1-carboxamide</description>
    </item>
    <item rdf:about="https://crispr.tyerslab.com/wiki/results/exp287?rev=1767843420&amp;do=diff">
        <dc:format>text/html</dc:format>
        <dc:date>2026-01-08T03:37:00+00:00</dc:date>
        <dc:creator>Anonymous (anonymous@undisclosed.example.com)</dc:creator>
        <title>HMS-I2 5μM R06 exp287</title>
        <link>https://crispr.tyerslab.com/wiki/results/exp287?rev=1767843420&amp;do=diff</link>
        <description>HMS-I2 5μM R06 exp287

Mechanism of Action

putative HDAC inhibitor from cell-based screen

	*  Class / Subclass 1: Uncharacterized Mechanism / Chemical Screen Hit

Technical Notes

	*  PubChem Name: N-(1-Benzothiophen-2-yl)-4-[(2-chloro-6-fluorophenyl)methyl]piperazine-1-carboxamide</description>
    </item>
    <item rdf:about="https://crispr.tyerslab.com/wiki/results/exp288?rev=1767843420&amp;do=diff">
        <dc:format>text/html</dc:format>
        <dc:date>2026-01-08T03:37:00+00:00</dc:date>
        <dc:creator>Anonymous (anonymous@undisclosed.example.com)</dc:creator>
        <title>HMS-I2 10μM R06 exp288</title>
        <link>https://crispr.tyerslab.com/wiki/results/exp288?rev=1767843420&amp;do=diff</link>
        <description>HMS-I2 10μM R06 exp288

Mechanism of Action

putative HDAC inhibitor from cell-based screen

	*  Class / Subclass 1: Uncharacterized Mechanism / Chemical Screen Hit

Technical Notes

	*  PubChem Name: N-(1-Benzothiophen-2-yl)-4-[(2-chloro-6-fluorophenyl)methyl]piperazine-1-carboxamide</description>
    </item>
    <item rdf:about="https://crispr.tyerslab.com/wiki/results/exp289?rev=1767843420&amp;do=diff">
        <dc:format>text/html</dc:format>
        <dc:date>2026-01-08T03:37:00+00:00</dc:date>
        <dc:creator>Anonymous (anonymous@undisclosed.example.com)</dc:creator>
        <title>Hydroxyurea 15μM R06 exp289</title>
        <link>https://crispr.tyerslab.com/wiki/results/exp289?rev=1767843420&amp;do=diff</link>
        <description>Hydroxyurea 15μM R06 exp289

Mechanism of Action

Inhibits ribonucleotide reductase, scavenges tyrosyl radicals

	*  Class / Subclass 1: Metabolism / Metabolic Enzyme Inhibitor
	*  Class / Subclass 2: DNA Damage, Repair and Replication / Replication Inhibitor</description>
    </item>
    <item rdf:about="https://crispr.tyerslab.com/wiki/results/exp290?rev=1767843420&amp;do=diff">
        <dc:format>text/html</dc:format>
        <dc:date>2026-01-08T03:37:00+00:00</dc:date>
        <dc:creator>Anonymous (anonymous@undisclosed.example.com)</dc:creator>
        <title>LLY-283 2.6μM R06 exp290</title>
        <link>https://crispr.tyerslab.com/wiki/results/exp290?rev=1767843420&amp;do=diff</link>
        <description>LLY-283 2.6μM R06 exp290

Mechanism of Action

Inhibits protein arginine methyltransferase PRMT5, inactive control is LLY-284

	*  Class / Subclass 1: Gene Regulation / Epigenetic Inhibitor

Technical Notes

	*  PubChem Name: (2R,3R,4S,5R)-2-(4-Aminopyrrolo[2,3-d]pyrimidin-7-yl)-5-[(R)-hydroxy(phenyl)methyl]oxolane-3,4-diol</description>
    </item>
    <item rdf:about="https://crispr.tyerslab.com/wiki/results/exp291?rev=1767843420&amp;do=diff">
        <dc:format>text/html</dc:format>
        <dc:date>2026-01-08T03:37:00+00:00</dc:date>
        <dc:creator>Anonymous (anonymous@undisclosed.example.com)</dc:creator>
        <title>LLY-284 2.6μM R06 exp291</title>
        <link>https://crispr.tyerslab.com/wiki/results/exp291?rev=1767843420&amp;do=diff</link>
        <description>LLY-284 2.6μM R06 exp291

Mechanism of Action

Inactive control for LLY-283 PRMT5 inhibitor

	*  Class / Subclass 1: Gene Regulation / Epigenetic Inhibitor

Technical Notes

	*  PubChem Name: (2R,3R,4S,5R)-2-(4-Aminopyrrolo[2,3-d]pyrimidin-7-yl)-5-[(S)-hydroxy(phenyl)methyl]oxolane-3,4-diol</description>
    </item>
    <item rdf:about="https://crispr.tyerslab.com/wiki/results/exp292?rev=1767843420&amp;do=diff">
        <dc:format>text/html</dc:format>
        <dc:date>2026-01-08T03:37:00+00:00</dc:date>
        <dc:creator>Anonymous (anonymous@undisclosed.example.com)</dc:creator>
        <title>Menadione 5μM R06 exp292</title>
        <link>https://crispr.tyerslab.com/wiki/results/exp292?rev=1767843420&amp;do=diff</link>
        <description>Menadione 5μM R06 exp292

Mechanism of Action

Synthetic analog of vitamin K, quinone redox cycle generates ROS

	*  Class / Subclass 1: Metabolism / Nutrient
	*  Class / Subclass 2: Environmental Stresses / Food Additive

Technical Notes

	*  PubChem Name:</description>
    </item>
    <item rdf:about="https://crispr.tyerslab.com/wiki/results/exp293?rev=1767843420&amp;do=diff">
        <dc:format>text/html</dc:format>
        <dc:date>2026-01-08T03:37:00+00:00</dc:date>
        <dc:creator>Anonymous (anonymous@undisclosed.example.com)</dc:creator>
        <title>Myriocin 25μM R06 exp293</title>
        <link>https://crispr.tyerslab.com/wiki/results/exp293?rev=1767843420&amp;do=diff</link>
        <description>Myriocin 25μM R06 exp293

Mechanism of Action

Inhibits serine palmitoyltransferase (SPT1), sphingolipid biosynthesis

	*  Class / Subclass 1: Infectious Disease / Antibiotic
	*  Class / Subclass 2: Metabolism / Metabolic Enzyme Inhibitor

Technical Notes</description>
    </item>
    <item rdf:about="https://crispr.tyerslab.com/wiki/results/exp294?rev=1767843420&amp;do=diff">
        <dc:format>text/html</dc:format>
        <dc:date>2026-01-08T03:37:00+00:00</dc:date>
        <dc:creator>Anonymous (anonymous@undisclosed.example.com)</dc:creator>
        <title>Nutlin-3A 1.6μM R06 exp294</title>
        <link>https://crispr.tyerslab.com/wiki/results/exp294?rev=1767843420&amp;do=diff</link>
        <description>Nutlin-3A 1.6μM R06 exp294

Mechanism of Action

Inhibits p53-MDM2 interaction

	*  Class / Subclass 1: Proteostasis / E3 ubiquitin ligase inhibitor
	*  Class / Subclass 2: Signal Transduction / Apoptosis Activator

Technical Notes

	*  PubChem Name:</description>
    </item>
    <item rdf:about="https://crispr.tyerslab.com/wiki/results/exp295?rev=1767843420&amp;do=diff">
        <dc:format>text/html</dc:format>
        <dc:date>2026-01-08T03:37:00+00:00</dc:date>
        <dc:creator>Anonymous (anonymous@undisclosed.example.com)</dc:creator>
        <title>Pyronaridine 1μM R06 exp295</title>
        <link>https://crispr.tyerslab.com/wiki/results/exp295?rev=1767843420&amp;do=diff</link>
        <description>Pyronaridine 1μM R06 exp295

Mechanism of Action

Prevents sequestration of heme into hemozoin, forms toxic complex with heme, enhances hematin-induced red blood cell lysis, also intercalates into DNA

	*  Class / Subclass 1: Infectious Disease / Antimalarial</description>
    </item>
    <item rdf:about="https://crispr.tyerslab.com/wiki/results/exp298?rev=1767843420&amp;do=diff">
        <dc:format>text/html</dc:format>
        <dc:date>2026-01-08T03:37:00+00:00</dc:date>
        <dc:creator>Anonymous (anonymous@undisclosed.example.com)</dc:creator>
        <title>Sucrose 20000μM R06 exp298</title>
        <link>https://crispr.tyerslab.com/wiki/results/exp298?rev=1767843420&amp;do=diff</link>
        <description>Sucrose 20000μM R06 exp298

Mechanism of Action

Disaccharide composed of glucose and fructose

	*  Class / Subclass 1: Metabolism / Nutrient

Technical Notes

	*  PubChem Name: Sucrose
		*  Synonyms: D-(+)-Saccharose
		*  CAS #: 57-50-1
		*  PubChem CID:</description>
    </item>
    <item rdf:about="https://crispr.tyerslab.com/wiki/results/exp299?rev=1767843420&amp;do=diff">
        <dc:format>text/html</dc:format>
        <dc:date>2026-01-08T03:37:00+00:00</dc:date>
        <dc:creator>Anonymous (anonymous@undisclosed.example.com)</dc:creator>
        <title>Talazoparib 0.006μM R06 exp299</title>
        <link>https://crispr.tyerslab.com/wiki/results/exp299?rev=1767843420&amp;do=diff</link>
        <description>Talazoparib 0.006μM R06 exp299

Mechanism of Action

Inhibits PARP1 and PARP2, blocks ssDNA break repair, selectively toxic to BRCA1/2 negative cancers

	*  Class / Subclass 1: DNA Damage, Repair and Replication / PARP Inhibitor

Technical Notes

	*</description>
    </item>
    <item rdf:about="https://crispr.tyerslab.com/wiki/results/exp300?rev=1767843420&amp;do=diff">
        <dc:format>text/html</dc:format>
        <dc:date>2026-01-08T03:37:00+00:00</dc:date>
        <dc:creator>Anonymous (anonymous@undisclosed.example.com)</dc:creator>
        <title>VE-822 0.04μM R06 exp300</title>
        <link>https://crispr.tyerslab.com/wiki/results/exp300?rev=1767843420&amp;do=diff</link>
        <description>VE-822 0.04μM R06 exp300

Mechanism of Action

Inhibits ATR

	*  Class / Subclass 1: DNA Damage, Repair and Replication / Checkpoint Signaling Inhibitor
	*  Class / Subclass 2: Signal Transduction / Kinase Inhibitor

Technical Notes

	*  PubChem Name:</description>
    </item>
    <item rdf:about="https://crispr.tyerslab.com/wiki/results/exp301?rev=1767843420&amp;do=diff">
        <dc:format>text/html</dc:format>
        <dc:date>2026-01-08T03:37:00+00:00</dc:date>
        <dc:creator>Anonymous (anonymous@undisclosed.example.com)</dc:creator>
        <title>VER-155008 3.9μM R06 exp301</title>
        <link>https://crispr.tyerslab.com/wiki/results/exp301?rev=1767843420&amp;do=diff</link>
        <description>VER-155008 3.9μM R06 exp301

Mechanism of Action

Inhibits HSP70

	*  Class / Subclass 1: Proteostasis / Chaperone Inhibitor

Technical Notes

	*  PubChem Name: 5&#039;-O-[(4-Cyanophenyl)methyl]-8-[[(3,4-dichlorophenyl)methyl]amino]-adenosine
		*  Synonyms:</description>
    </item>
    <item rdf:about="https://crispr.tyerslab.com/wiki/results/exp302?rev=1767843420&amp;do=diff">
        <dc:format>text/html</dc:format>
        <dc:date>2026-01-08T03:37:00+00:00</dc:date>
        <dc:creator>Anonymous (anonymous@undisclosed.example.com)</dc:creator>
        <title>35°C R06 exp302</title>
        <link>https://crispr.tyerslab.com/wiki/results/exp302?rev=1767843420&amp;do=diff</link>
        <description>35°C R06 exp302

Mechanism of Action

Reduced growth temperature

	*  Class / Subclass 1: Environmental Stresses / Stress Condition

Screen Summary

	*  Round: 06
		*  Dose: N/A
		*  Days of incubation: 8
		*  Doublings: 6.4
		*  Numbers of reads: 7989918</description>
    </item>
    <item rdf:about="https://crispr.tyerslab.com/wiki/results/exp303?rev=1767843420&amp;do=diff">
        <dc:format>text/html</dc:format>
        <dc:date>2026-01-08T03:37:00+00:00</dc:date>
        <dc:creator>Anonymous (anonymous@undisclosed.example.com)</dc:creator>
        <title>39°C R06 exp303</title>
        <link>https://crispr.tyerslab.com/wiki/results/exp303?rev=1767843420&amp;do=diff</link>
        <description>39°C R06 exp303

Mechanism of Action

Elevated growth temperature

	*  Class / Subclass 1: Environmental Stresses / Stress Condition

Screen Summary

	*  Round: 06
		*  Dose: N/A
		*  Days of incubation: 8
		*  Doublings: 7.8
		*  Numbers of reads: 6641990</description>
    </item>
    <item rdf:about="https://crispr.tyerslab.com/wiki/results/exp306?rev=1767843420&amp;do=diff">
        <dc:format>text/html</dc:format>
        <dc:date>2026-01-08T03:37:00+00:00</dc:date>
        <dc:creator>Anonymous (anonymous@undisclosed.example.com)</dc:creator>
        <title>Rapamycin 2μM R07 exp306</title>
        <link>https://crispr.tyerslab.com/wiki/results/exp306?rev=1767843420&amp;do=diff</link>
        <description>Rapamycin 2μM R07 exp306

Mechanism of Action

Allosteric mTORC1 inhibitor, forms ternary complex with FKBP12 and mTOR, attenuates protein synthesis and metabolism

	*  Class / Subclass 1: Signal Transduction / Kinase Inhibitor
	*  Class / Subclass 2:</description>
    </item>
    <item rdf:about="https://crispr.tyerslab.com/wiki/results/exp307?rev=1767843420&amp;do=diff">
        <dc:format>text/html</dc:format>
        <dc:date>2026-01-08T03:37:00+00:00</dc:date>
        <dc:creator>Anonymous (anonymous@undisclosed.example.com)</dc:creator>
        <title>Rapamycin 2μM plus Cyclosporin-A 3μM R07 exp307</title>
        <link>https://crispr.tyerslab.com/wiki/results/exp307?rev=1767843420&amp;do=diff</link>
        <description>Rapamycin 2μM plus Cyclosporin-A 3μM R07 exp307

Mechanism of Action

Allosteric mTORC1 inhibitor, forms ternary complex with FKBP12 and mTOR, attenuates protein synthesis and metabolism

	*  Class / Subclass 1: Signal Transduction / Kinase Inhibitor</description>
    </item>
    <item rdf:about="https://crispr.tyerslab.com/wiki/results/exp308?rev=1767843420&amp;do=diff">
        <dc:format>text/html</dc:format>
        <dc:date>2026-01-08T03:37:00+00:00</dc:date>
        <dc:creator>Anonymous (anonymous@undisclosed.example.com)</dc:creator>
        <title>Rapamycin 2μM plus FK-506 5μM R07 exp308</title>
        <link>https://crispr.tyerslab.com/wiki/results/exp308?rev=1767843420&amp;do=diff</link>
        <description>Rapamycin 2μM plus FK-506 5μM R07 exp308

Mechanism of Action

Allosteric mTORC1 inhibitor, forms ternary complex with FKBP12 and mTOR, attenuates protein synthesis and metabolism

	*  Class / Subclass 1: Signal Transduction / Kinase Inhibitor
	*</description>
    </item>
    <item rdf:about="https://crispr.tyerslab.com/wiki/results/exp310?rev=1767843420&amp;do=diff">
        <dc:format>text/html</dc:format>
        <dc:date>2026-01-08T03:37:00+00:00</dc:date>
        <dc:creator>Anonymous (anonymous@undisclosed.example.com)</dc:creator>
        <title>2-Methoxyestradiol 0.55μM R07 exp310</title>
        <link>https://crispr.tyerslab.com/wiki/results/exp310?rev=1767843420&amp;do=diff</link>
        <description>2-Methoxyestradiol 0.55μM R07 exp310

Mechanism of Action

Endogenous estradiol metabolite, weak agonist for estrogen receptor, agonist of GPER1, microtubule destabilizer

	*  Class / Subclass 1: Metabolism / Metabolite
	*  Class / Subclass 2: Signal Transduction / GPCR Agonist</description>
    </item>
    <item rdf:about="https://crispr.tyerslab.com/wiki/results/exp311?rev=1767843420&amp;do=diff">
        <dc:format>text/html</dc:format>
        <dc:date>2026-01-08T03:37:00+00:00</dc:date>
        <dc:creator>Anonymous (anonymous@undisclosed.example.com)</dc:creator>
        <title>2-Methoxyestradiol 0.55 to 0.75μM  on day4 R07 exp311</title>
        <link>https://crispr.tyerslab.com/wiki/results/exp311?rev=1767843420&amp;do=diff</link>
        <description>2-Methoxyestradiol 0.55 to 0.75μM  on day4 R07 exp311

Mechanism of Action

Endogenous estradiol metabolite, weak agonist for estrogen receptor, agonist of GPER1, microtubule destabilizer

	*  Class / Subclass 1: Metabolism / Metabolite
	*  Class / Subclass 2:</description>
    </item>
    <item rdf:about="https://crispr.tyerslab.com/wiki/results/exp312?rev=1767843420&amp;do=diff">
        <dc:format>text/html</dc:format>
        <dc:date>2026-01-08T03:37:00+00:00</dc:date>
        <dc:creator>Anonymous (anonymous@undisclosed.example.com)</dc:creator>
        <title>2-Methoxyestradiol 0.55 to 1μM on day4 R07 exp312</title>
        <link>https://crispr.tyerslab.com/wiki/results/exp312?rev=1767843420&amp;do=diff</link>
        <description>2-Methoxyestradiol 0.55 to 1μM on day4 R07 exp312

Mechanism of Action

Endogenous estradiol metabolite, weak agonist for estrogen receptor, agonist of GPER1, microtubule destabilizer

	*  Class / Subclass 1: Metabolism / Metabolite
	*  Class / Subclass 2:</description>
    </item>
    <item rdf:about="https://crispr.tyerslab.com/wiki/results/exp314?rev=1767843420&amp;do=diff">
        <dc:format>text/html</dc:format>
        <dc:date>2026-01-08T03:37:00+00:00</dc:date>
        <dc:creator>Anonymous (anonymous@undisclosed.example.com)</dc:creator>
        <title>Dimethyloxaloylglycine 11μM R07 exp314</title>
        <link>https://crispr.tyerslab.com/wiki/results/exp314?rev=1767843420&amp;do=diff</link>
        <description>Dimethyloxaloylglycine 11μM R07 exp314

Mechanism of Action

Prolylhydroxylase inhibitor, induces HIF-1α accumulation

	*  Class / Subclass 1: Metabolism / Metabolic Enzyme Inhibitor
	*  Class / Subclass 2: Signal Transduction / Other inhibitor

Technical Notes</description>
    </item>
    <item rdf:about="https://crispr.tyerslab.com/wiki/results/exp316?rev=1767843420&amp;do=diff">
        <dc:format>text/html</dc:format>
        <dc:date>2026-01-08T03:37:00+00:00</dc:date>
        <dc:creator>Anonymous (anonymous@undisclosed.example.com)</dc:creator>
        <title>Geldanamycin 0.015 to 0.025μM on day4 R07 exp316</title>
        <link>https://crispr.tyerslab.com/wiki/results/exp316?rev=1767843420&amp;do=diff</link>
        <description>Geldanamycin 0.015 to 0.025μM on day4 R07 exp316

Mechanism of Action

HSP90 inhibitor

	*  Class / Subclass 1: Proteostasis / Chaperone Inhibitor

Technical Notes

	*  PubChem Name: Geldanamycin
		*  Synonyms: N/A
		*  CAS #: 30562-34-6
		*  PubChem CID:</description>
    </item>
    <item rdf:about="https://crispr.tyerslab.com/wiki/results/exp317?rev=1767843420&amp;do=diff">
        <dc:format>text/html</dc:format>
        <dc:date>2026-01-08T03:37:00+00:00</dc:date>
        <dc:creator>Anonymous (anonymous@undisclosed.example.com)</dc:creator>
        <title>Geldanamycin 0.015 to 0.05μM on day4 R07 exp317</title>
        <link>https://crispr.tyerslab.com/wiki/results/exp317?rev=1767843420&amp;do=diff</link>
        <description>Geldanamycin 0.015 to 0.05μM on day4 R07 exp317

Mechanism of Action

HSP90 inhibitor

	*  Class / Subclass 1: Proteostasis / Chaperone Inhibitor

Technical Notes

	*  PubChem Name: Geldanamycin
		*  Synonyms: N/A
		*  CAS #: 30562-34-6
		*  PubChem CID:</description>
    </item>
    <item rdf:about="https://crispr.tyerslab.com/wiki/results/exp318?rev=1767843420&amp;do=diff">
        <dc:format>text/html</dc:format>
        <dc:date>2026-01-08T03:37:00+00:00</dc:date>
        <dc:creator>Anonymous (anonymous@undisclosed.example.com)</dc:creator>
        <title>ABT-702 5μM R07 exp318</title>
        <link>https://crispr.tyerslab.com/wiki/results/exp318?rev=1767843420&amp;do=diff</link>
        <description>ABT-702 5μM R07 exp318

Mechanism of Action

Inhibits adenosine kinase (ADK)

	*  Class / Subclass 1: Metabolism / Metabolic Enzyme Inhibitor

Technical Notes

	*  PubChem Name: Adenosine Kinase Inhibitor
		*  Synonyms: N/A
		*  CAS #: 1188890-28-9</description>
    </item>
    <item rdf:about="https://crispr.tyerslab.com/wiki/results/exp319?rev=1767843420&amp;do=diff">
        <dc:format>text/html</dc:format>
        <dc:date>2026-01-08T03:37:00+00:00</dc:date>
        <dc:creator>Anonymous (anonymous@undisclosed.example.com)</dc:creator>
        <title>ABT-702 5μM plus Dimethyloxaloylglycine 11μM R07 exp319</title>
        <link>https://crispr.tyerslab.com/wiki/results/exp319?rev=1767843420&amp;do=diff</link>
        <description>ABT-702 5μM plus Dimethyloxaloylglycine 11μM R07 exp319

Mechanism of Action

Inhibits adenosine kinase (ADK)

	*  Class / Subclass 1: Metabolism / Metabolic Enzyme Inhibitor

Technical Notes

ABT-702



	*  PubChem Name: Adenosine Kinase Inhibitor</description>
    </item>
    <item rdf:about="https://crispr.tyerslab.com/wiki/results/exp320?rev=1767843420&amp;do=diff">
        <dc:format>text/html</dc:format>
        <dc:date>2026-01-08T03:37:00+00:00</dc:date>
        <dc:creator>Anonymous (anonymous@undisclosed.example.com)</dc:creator>
        <title>ABT-702 5μM plus CoCl2 18μM R07 exp320</title>
        <link>https://crispr.tyerslab.com/wiki/results/exp320?rev=1767843420&amp;do=diff</link>
        <description>ABT-702 5μM plus CoCl2 18μM R07 exp320

Mechanism of Action

Inhibits adenosine kinase (ADK)

	*  Class / Subclass 1: Metabolism / Metabolic Enzyme Inhibitor

Technical Notes

ABT-702



	*  PubChem Name: Adenosine Kinase Inhibitor
		*  Synonyms: N/A</description>
    </item>
    <item rdf:about="https://crispr.tyerslab.com/wiki/results/exp321?rev=1767843420&amp;do=diff">
        <dc:format>text/html</dc:format>
        <dc:date>2026-01-08T03:37:00+00:00</dc:date>
        <dc:creator>Anonymous (anonymous@undisclosed.example.com)</dc:creator>
        <title>ABT-702 5μM plus Deferoxamine 11μM R07 exp321</title>
        <link>https://crispr.tyerslab.com/wiki/results/exp321?rev=1767843420&amp;do=diff</link>
        <description>ABT-702 5μM plus Deferoxamine 11μM R07 exp321

Mechanism of Action

Inhibits adenosine kinase (ADK)

	*  Class / Subclass 1: Metabolism / Metabolic Enzyme Inhibitor

Technical Notes

ABT-702



	*  PubChem Name: Adenosine Kinase Inhibitor
		*  Synonyms:</description>
    </item>
    <item rdf:about="https://crispr.tyerslab.com/wiki/results/exp326?rev=1767843420&amp;do=diff">
        <dc:format>text/html</dc:format>
        <dc:date>2026-01-08T03:37:00+00:00</dc:date>
        <dc:creator>Anonymous (anonymous@undisclosed.example.com)</dc:creator>
        <title>CCT251545 20μM R07 exp326</title>
        <link>https://crispr.tyerslab.com/wiki/results/exp326?rev=1767843420&amp;do=diff</link>
        <description>CCT251545 20μM R07 exp326

Mechanism of Action

Inhibits CDK8 and CDK19 mediator-associated kinases

	*  Class / Subclass 1: Gene Regulation / Transcription Inhibitor
	*  Class / Subclass 2: Signal Transduction / Kinase Inhibitor

Technical Notes

	*</description>
    </item>
    <item rdf:about="https://crispr.tyerslab.com/wiki/results/exp329?rev=1767843420&amp;do=diff">
        <dc:format>text/html</dc:format>
        <dc:date>2026-01-08T03:37:00+00:00</dc:date>
        <dc:creator>Anonymous (anonymous@undisclosed.example.com)</dc:creator>
        <title>Hydroxyurea 100μM R07 exp329</title>
        <link>https://crispr.tyerslab.com/wiki/results/exp329?rev=1767843420&amp;do=diff</link>
        <description>Hydroxyurea 100μM R07 exp329

Mechanism of Action

Inhibits ribonucleotide reductase, scavenges tyrosyl radicals

	*  Class / Subclass 1: Metabolism / Metabolic Enzyme Inhibitor
	*  Class / Subclass 2: DNA Damage, Repair and Replication / Replication Inhibitor</description>
    </item>
    <item rdf:about="https://crispr.tyerslab.com/wiki/results/exp330?rev=1767843420&amp;do=diff">
        <dc:format>text/html</dc:format>
        <dc:date>2026-01-08T03:37:00+00:00</dc:date>
        <dc:creator>Anonymous (anonymous@undisclosed.example.com)</dc:creator>
        <title>5-Azacytidine 2μM R07 exp330</title>
        <link>https://crispr.tyerslab.com/wiki/results/exp330?rev=1767843420&amp;do=diff</link>
        <description>5-Azacytidine 2μM R07 exp330

Mechanism of Action

Analog of cytidine ribonucleoside, DNA methyltransferase inhibitor

	*  Class / Subclass 1: Metabolism / Antimetabolite
	*  Class / Subclass 2: Gene Regulation / Epigenetic Inhibitor
	*  Class / Subclass 3:</description>
    </item>
    <item rdf:about="https://crispr.tyerslab.com/wiki/results/exp331?rev=1767843420&amp;do=diff">
        <dc:format>text/html</dc:format>
        <dc:date>2026-01-08T03:37:00+00:00</dc:date>
        <dc:creator>Anonymous (anonymous@undisclosed.example.com)</dc:creator>
        <title>A-769662 20μM R07 exp331</title>
        <link>https://crispr.tyerslab.com/wiki/results/exp331?rev=1767843420&amp;do=diff</link>
        <description>A-769662 20μM R07 exp331

Mechanism of Action

Activates AMP-activated protein kinase (AMPK), allosteric

	*  Class / Subclass 1: Signal Transduction / Kinase Activator

Technical Notes

	*  PubChem Name: 4-Hydroxy-3-(2&#039;-hydroxy-1,1&#039;-biphenyl-4-yl)-6-oxo-6,7-dihydrothieno[2,3-b]pyridine-5-carbonitrile</description>
    </item>
    <item rdf:about="https://crispr.tyerslab.com/wiki/results/exp332?rev=1767843420&amp;do=diff">
        <dc:format>text/html</dc:format>
        <dc:date>2026-01-08T03:37:00+00:00</dc:date>
        <dc:creator>Anonymous (anonymous@undisclosed.example.com)</dc:creator>
        <title>Adefovir 20μM R07 exp332</title>
        <link>https://crispr.tyerslab.com/wiki/results/exp332?rev=1767843420&amp;do=diff</link>
        <description>Adefovir 20μM R07 exp332

Mechanism of Action

Nucleoside reverse transcriptase inhibitor (NRTI), active against HBV and HSV

	*  Class / Subclass 1: Infectious Disease / Antiviral
	*  Class / Subclass 2: DNA Damage, Repair and Replication / Reverse Transcriptase Inhibitor</description>
    </item>
    <item rdf:about="https://crispr.tyerslab.com/wiki/results/exp333?rev=1767843420&amp;do=diff">
        <dc:format>text/html</dc:format>
        <dc:date>2026-01-08T03:37:00+00:00</dc:date>
        <dc:creator>Anonymous (anonymous@undisclosed.example.com)</dc:creator>
        <title>All-trans-Retinoic-Acid 8μM R07 exp333</title>
        <link>https://crispr.tyerslab.com/wiki/results/exp333?rev=1767843420&amp;do=diff</link>
        <description>All-trans-Retinoic-Acid 8μM R07 exp333

Mechanism of Action

Ligand for retinoic acid receptor (RAR) and retinoid X receptor (RXR), metabolite of vitamin A1

	*  Class / Subclass 1: Gene Regulation / Nuclear Receptor Ligand
	*  Class / Subclass 2: Metabolism / Metabolite</description>
    </item>
    <item rdf:about="https://crispr.tyerslab.com/wiki/results/exp334?rev=1767843420&amp;do=diff">
        <dc:format>text/html</dc:format>
        <dc:date>2026-01-08T03:37:00+00:00</dc:date>
        <dc:creator>Anonymous (anonymous@undisclosed.example.com)</dc:creator>
        <title>All-trans-Retinoic-Acid 40μM R07 exp334</title>
        <link>https://crispr.tyerslab.com/wiki/results/exp334?rev=1767843420&amp;do=diff</link>
        <description>All-trans-Retinoic-Acid 40μM R07 exp334

Mechanism of Action

Ligand for retinoic acid receptor (RAR) and retinoid X receptor (RXR), metabolite of vitamin A1

	*  Class / Subclass 1: Gene Regulation / Nuclear Receptor Ligand
	*  Class / Subclass 2: Metabolism / Metabolite</description>
    </item>
    <item rdf:about="https://crispr.tyerslab.com/wiki/results/exp335?rev=1767843420&amp;do=diff">
        <dc:format>text/html</dc:format>
        <dc:date>2026-01-08T03:37:00+00:00</dc:date>
        <dc:creator>Anonymous (anonymous@undisclosed.example.com)</dc:creator>
        <title>Aminopterin 0.005μM R07 exp335</title>
        <link>https://crispr.tyerslab.com/wiki/results/exp335?rev=1767843420&amp;do=diff</link>
        <description>Aminopterin 0.005μM R07 exp335

Mechanism of Action

Inhibits dihydrofolate reductase (DHFR)

	*  Class / Subclass 1: Metabolism / Antimetabolite
	*  Class / Subclass 2: DNA Damage, Repair and Replication / Replication Inhibitor

Technical Notes

	*</description>
    </item>
    <item rdf:about="https://crispr.tyerslab.com/wiki/results/exp336?rev=1767843420&amp;do=diff">
        <dc:format>text/html</dc:format>
        <dc:date>2026-01-08T03:37:00+00:00</dc:date>
        <dc:creator>Anonymous (anonymous@undisclosed.example.com)</dc:creator>
        <title>Asunaprenir 3μM R07 exp336</title>
        <link>https://crispr.tyerslab.com/wiki/results/exp336?rev=1767843420&amp;do=diff</link>
        <description>Asunaprenir 3μM R07 exp336

Mechanism of Action

Block the enzymatic activity of the HCV NS3 protease

	*  Class / Subclass 1: Infectious Disease / Antiviral
	*  Class / Subclass 2: Proteostasis / Protease Inhibitor

Technical Notes

	*  PubChem Name:</description>
    </item>
    <item rdf:about="https://crispr.tyerslab.com/wiki/results/exp340?rev=1767843420&amp;do=diff">
        <dc:format>text/html</dc:format>
        <dc:date>2026-01-08T03:37:00+00:00</dc:date>
        <dc:creator>Anonymous (anonymous@undisclosed.example.com)</dc:creator>
        <title>BN82002 4μM R07 exp340</title>
        <link>https://crispr.tyerslab.com/wiki/results/exp340?rev=1767843420&amp;do=diff</link>
        <description>BN82002 4μM R07 exp340

Mechanism of Action

Inhibits CDC25 phosphatases, active against CDC25A/B/C isoforms

	*  Class / Subclass 1: Cell Cycle / Phosphatase inhibitor
	*  Class / Subclass 2: Signal Transduction / Phosphatase Inhibitor

Technical Notes</description>
    </item>
    <item rdf:about="https://crispr.tyerslab.com/wiki/results/exp341?rev=1767843420&amp;do=diff">
        <dc:format>text/html</dc:format>
        <dc:date>2026-01-08T03:37:00+00:00</dc:date>
        <dc:creator>Anonymous (anonymous@undisclosed.example.com)</dc:creator>
        <title>BRD2 inhibitor II 20μM R07 exp341</title>
        <link>https://crispr.tyerslab.com/wiki/results/exp341?rev=1767843420&amp;do=diff</link>
        <description>BRD2 inhibitor II 20μM R07 exp341

Mechanism of Action

Inhibits BRD2, blocks recognition of acetylated H4K12

	*  Class / Subclass 1: Gene Regulation / Epigenetic Inhibitor

Technical Notes

	*  PubChem Name: 1-[2-(1H-Benzimidazol-2-ylsulfanyl)ethyl]-3-methyl-1,3-dihydro-2H-benzimidazole-2-thione</description>
    </item>
    <item rdf:about="https://crispr.tyerslab.com/wiki/results/exp342?rev=1767843420&amp;do=diff">
        <dc:format>text/html</dc:format>
        <dc:date>2026-01-08T03:37:00+00:00</dc:date>
        <dc:creator>Anonymous (anonymous@undisclosed.example.com)</dc:creator>
        <title>Calcium Ionophore 0.4μM R07 exp342</title>
        <link>https://crispr.tyerslab.com/wiki/results/exp342?rev=1767843420&amp;do=diff</link>
        <description>Calcium Ionophore 0.4μM R07 exp342

Mechanism of Action

Calcium ionophore

	*  Class / Subclass 1: Infectious Disease / Antibiotic
	*  Class / Subclass 2: Organelle Function / Membrane Ionophore

Technical Notes

	*  PubChem Name: Calcium ionophore A23187</description>
    </item>
    <item rdf:about="https://crispr.tyerslab.com/wiki/results/exp343?rev=1767843420&amp;do=diff">
        <dc:format>text/html</dc:format>
        <dc:date>2026-01-08T03:37:00+00:00</dc:date>
        <dc:creator>Anonymous (anonymous@undisclosed.example.com)</dc:creator>
        <title>Centrinone 0.5μM R07 exp343</title>
        <link>https://crispr.tyerslab.com/wiki/results/exp343?rev=1767843420&amp;do=diff</link>
        <description>Centrinone 0.5μM R07 exp343

Mechanism of Action

Inhibits PLK4, blocks centriole duplication, causes p53-dependent G1 arrest

	*  Class / Subclass 1: Cell Cycle / Mitotic Inhibitor
	*  Class / Subclass 2: Signal Transduction / Kinase Inhibitor

Technical Notes</description>
    </item>
    <item rdf:about="https://crispr.tyerslab.com/wiki/results/exp344?rev=1767843420&amp;do=diff">
        <dc:format>text/html</dc:format>
        <dc:date>2026-01-08T03:37:00+00:00</dc:date>
        <dc:creator>Anonymous (anonymous@undisclosed.example.com)</dc:creator>
        <title>Chlorpromazine 10μM R07 exp344</title>
        <link>https://crispr.tyerslab.com/wiki/results/exp344?rev=1767843420&amp;do=diff</link>
        <description>Chlorpromazine 10μM R07 exp344

Mechanism of Action

Antipsychotic, pleiotropic antagonist for dopamine, seratonin, histamine, adrenergic, muscarinic receptors, potassium and sodium channels, also disrupts clathrin-mediated endocytosis

	*  Class / Subclass 1:</description>
    </item>
    <item rdf:about="https://crispr.tyerslab.com/wiki/results/exp345?rev=1767843420&amp;do=diff">
        <dc:format>text/html</dc:format>
        <dc:date>2026-01-08T03:37:00+00:00</dc:date>
        <dc:creator>Anonymous (anonymous@undisclosed.example.com)</dc:creator>
        <title>Cidofovir 10μM R07 exp345</title>
        <link>https://crispr.tyerslab.com/wiki/results/exp345?rev=1767843420&amp;do=diff</link>
        <description>Cidofovir 10μM R07 exp345

Mechanism of Action

Acyclic nucleoside phosphonate, inhibits DNA polymerase

	*  Class / Subclass 1: Infectious Disease / Antiviral
	*  Class / Subclass 2: Metabolism / Antimetabolite
	*  Class / Subclass 3: DNA Damage, Repair and Replication / Replication Inhibitor</description>
    </item>
    <item rdf:about="https://crispr.tyerslab.com/wiki/results/exp346?rev=1767843420&amp;do=diff">
        <dc:format>text/html</dc:format>
        <dc:date>2026-01-08T03:37:00+00:00</dc:date>
        <dc:creator>Anonymous (anonymous@undisclosed.example.com)</dc:creator>
        <title>CoCl2 18μM R07 exp346</title>
        <link>https://crispr.tyerslab.com/wiki/results/exp346?rev=1767843420&amp;do=diff</link>
        <description>CoCl2 18μM R07 exp346

Mechanism of Action

Hypoxia mimetic, inhibits VHL-HIF-1α interaction, induces HIF-1α accumulation

	*  Class / Subclass 1: Environmental Stresses / Heavy Metal
	*  Class / Subclass 2: Metabolism / Metabolic Enzyme Inhibitor</description>
    </item>
    <item rdf:about="https://crispr.tyerslab.com/wiki/results/exp347?rev=1767843420&amp;do=diff">
        <dc:format>text/html</dc:format>
        <dc:date>2026-01-08T03:37:00+00:00</dc:date>
        <dc:creator>Anonymous (anonymous@undisclosed.example.com)</dc:creator>
        <title>Cyclosporin-A 0.8μM R07 exp347</title>
        <link>https://crispr.tyerslab.com/wiki/results/exp347?rev=1767843420&amp;do=diff</link>
        <description>Cyclosporin-A 0.8μM R07 exp347

Mechanism of Action

Inhibits calcineurin, forms ternary complex with immunophilin (FBKP) and calcineurin

	*  Class / Subclass 1: Signal Transduction / Phosphatase Inhibitor

Technical Notes

	*  PubChem Name: Cyclosporin A</description>
    </item>
    <item rdf:about="https://crispr.tyerslab.com/wiki/results/exp348?rev=1767843420&amp;do=diff">
        <dc:format>text/html</dc:format>
        <dc:date>2026-01-08T03:37:00+00:00</dc:date>
        <dc:creator>Anonymous (anonymous@undisclosed.example.com)</dc:creator>
        <title>Cyclosporin-A 3μM R07 exp348</title>
        <link>https://crispr.tyerslab.com/wiki/results/exp348?rev=1767843420&amp;do=diff</link>
        <description>Cyclosporin-A 3μM R07 exp348

Mechanism of Action

Inhibits calcineurin, forms ternary complex with immunophilin (FBKP) and calcineurin

	*  Class / Subclass 1: Signal Transduction / Phosphatase Inhibitor

Technical Notes

	*  PubChem Name: Cyclosporin A</description>
    </item>
    <item rdf:about="https://crispr.tyerslab.com/wiki/results/exp349?rev=1767843420&amp;do=diff">
        <dc:format>text/html</dc:format>
        <dc:date>2026-01-08T03:37:00+00:00</dc:date>
        <dc:creator>Anonymous (anonymous@undisclosed.example.com)</dc:creator>
        <title>Cytochalasin-B 5μM R07 exp349</title>
        <link>https://crispr.tyerslab.com/wiki/results/exp349?rev=1767843420&amp;do=diff</link>
        <description>Cytochalasin-B 5μM R07 exp349

Mechanism of Action

Binds fast-growing (barbed) end of F-actin filament, inhibits actin polymerization

	*  Class / Subclass 1: Cell Cycle / Cytokinesis Inhibitor
	*  Class / Subclass 2: Organelle Function / Cytoskeletal Inhibitor</description>
    </item>
    <item rdf:about="https://crispr.tyerslab.com/wiki/results/exp350?rev=1767843420&amp;do=diff">
        <dc:format>text/html</dc:format>
        <dc:date>2026-01-08T03:37:00+00:00</dc:date>
        <dc:creator>Anonymous (anonymous@undisclosed.example.com)</dc:creator>
        <title>Deferoxamine 11μM R07 exp350</title>
        <link>https://crispr.tyerslab.com/wiki/results/exp350?rev=1767843420&amp;do=diff</link>
        <description>Deferoxamine 11μM R07 exp350

Mechanism of Action

Iron chelator, hypoxia mimetic, induces HIF-1‘± accumulation

	*  Class / Subclass 1: Environmental Stresses / Metal Chelator
	*  Class / Subclass 2: Metabolism / Metabolic Enzyme Inhibitor

Technical Notes</description>
    </item>
    <item rdf:about="https://crispr.tyerslab.com/wiki/results/exp351?rev=1767843420&amp;do=diff">
        <dc:format>text/html</dc:format>
        <dc:date>2026-01-08T03:37:00+00:00</dc:date>
        <dc:creator>Anonymous (anonymous@undisclosed.example.com)</dc:creator>
        <title>Dexamethasone 0.006μM R07 exp351</title>
        <link>https://crispr.tyerslab.com/wiki/results/exp351?rev=1767843420&amp;do=diff</link>
        <description>Dexamethasone 0.006μM R07 exp351

Mechanism of Action

Glucocorticoid receptor agonist, anti-inflammatory

	*  Class / Subclass 1: Metabolism / Hormone Agonist
	*  Class / Subclass 2: Signal Transduction / GPCR Agonist

Technical Notes

	*  PubChem Name:</description>
    </item>
    <item rdf:about="https://crispr.tyerslab.com/wiki/results/exp352?rev=1767843420&amp;do=diff">
        <dc:format>text/html</dc:format>
        <dc:date>2026-01-08T03:37:00+00:00</dc:date>
        <dc:creator>Anonymous (anonymous@undisclosed.example.com)</dc:creator>
        <title>Dexamethasone 0.006 to 0.015μM on day4 R07 exp352</title>
        <link>https://crispr.tyerslab.com/wiki/results/exp352?rev=1767843420&amp;do=diff</link>
        <description>Dexamethasone 0.006 to 0.015μM on day4 R07 exp352

Mechanism of Action

Glucocorticoid receptor agonist, anti-inflammatory

	*  Class / Subclass 1: Metabolism / Hormone Agonist
	*  Class / Subclass 2: Signal Transduction / GPCR Agonist

Technical Notes</description>
    </item>
    <item rdf:about="https://crispr.tyerslab.com/wiki/results/exp354?rev=1767843420&amp;do=diff">
        <dc:format>text/html</dc:format>
        <dc:date>2026-01-08T03:37:00+00:00</dc:date>
        <dc:creator>Anonymous (anonymous@undisclosed.example.com)</dc:creator>
        <title>Diepoxybutane 3μM R07 exp354</title>
        <link>https://crispr.tyerslab.com/wiki/results/exp354?rev=1767843420&amp;do=diff</link>
        <description>Diepoxybutane 3μM R07 exp354

Mechanism of Action

DNA crosslinker, carcinogen

	*  Class / Subclass 1: DNA Damage, Repair and Replication / Inter/Intra-strand Crosslinker

Technical Notes

	*  PubChem Name: 2,2&#039;-Bioxirane
		*  Synonyms: N/A
		*  CAS #:</description>
    </item>
    <item rdf:about="https://crispr.tyerslab.com/wiki/results/exp355?rev=1767843420&amp;do=diff">
        <dc:format>text/html</dc:format>
        <dc:date>2026-01-08T03:37:00+00:00</dc:date>
        <dc:creator>Anonymous (anonymous@undisclosed.example.com)</dc:creator>
        <title>Dinaciclib 0.007μM R07 exp355</title>
        <link>https://crispr.tyerslab.com/wiki/results/exp355?rev=1767843420&amp;do=diff</link>
        <description>Dinaciclib 0.007μM R07 exp355

Mechanism of Action

Inhibits CDK2, CDK5, CDK1, CDK9

	*  Class / Subclass 1: Cell Cycle / Cell Cycle Inhibitor
	*  Class / Subclass 2: Signal Transduction / Kinase Inhibitor
	*  Class / Subclass 3: Gene Regulation / Transcription Inhibitor</description>
    </item>
    <item rdf:about="https://crispr.tyerslab.com/wiki/results/exp356?rev=1767843420&amp;do=diff">
        <dc:format>text/html</dc:format>
        <dc:date>2026-01-08T03:37:00+00:00</dc:date>
        <dc:creator>Anonymous (anonymous@undisclosed.example.com)</dc:creator>
        <title>Docosahexaenoic-acid 50μM R07 exp356</title>
        <link>https://crispr.tyerslab.com/wiki/results/exp356?rev=1767843420&amp;do=diff</link>
        <description>Docosahexaenoic-acid 50μM R07 exp356

Mechanism of Action

Essential omega-3 fatty acid

	*  Class / Subclass 1: Metabolism / Metabolite

Technical Notes

	*  PubChem Name: Docosahexaenoic acid
		*  Synonyms: DHA; Cervonic Acid; DHA;Cervonic Acid
		*</description>
    </item>
    <item rdf:about="https://crispr.tyerslab.com/wiki/results/exp357?rev=1767843420&amp;do=diff">
        <dc:format>text/html</dc:format>
        <dc:date>2026-01-08T03:37:00+00:00</dc:date>
        <dc:creator>Anonymous (anonymous@undisclosed.example.com)</dc:creator>
        <title>Dorsomorphin 5μM R07 exp357</title>
        <link>https://crispr.tyerslab.com/wiki/results/exp357?rev=1767843420&amp;do=diff</link>
        <description>Dorsomorphin 5μM R07 exp357

Mechanism of Action

Putative inhibitor of AMPK and BMP signalling

	*  Class / Subclass 1: Signal Transduction / Kinase Inhibitor

Technical Notes

	*  PubChem Name: Dorsomorphin
		*  Synonyms: BML-275; Compound C
		*</description>
    </item>
    <item rdf:about="https://crispr.tyerslab.com/wiki/results/exp358?rev=1767843420&amp;do=diff">
        <dc:format>text/html</dc:format>
        <dc:date>2026-01-08T03:37:00+00:00</dc:date>
        <dc:creator>Anonymous (anonymous@undisclosed.example.com)</dc:creator>
        <title>FK-506 5μM R07 exp358</title>
        <link>https://crispr.tyerslab.com/wiki/results/exp358?rev=1767843420&amp;do=diff</link>
        <description>FK-506 5μM R07 exp358

Mechanism of Action

Inhibits calcineurin

	*  Class / Subclass 1: Signal Transduction / Phosphatase Inhibitor

Technical Notes

	*  PubChem Name: Tacrolimus
		*  Synonyms: FK506; Fujimycin; FR900506
		*  CAS #: 104987-11-3
		*</description>
    </item>
    <item rdf:about="https://crispr.tyerslab.com/wiki/results/exp359?rev=1767843420&amp;do=diff">
        <dc:format>text/html</dc:format>
        <dc:date>2026-01-08T03:37:00+00:00</dc:date>
        <dc:creator>Anonymous (anonymous@undisclosed.example.com)</dc:creator>
        <title>FK-506 30μM R07 exp359</title>
        <link>https://crispr.tyerslab.com/wiki/results/exp359?rev=1767843420&amp;do=diff</link>
        <description>FK-506 30μM R07 exp359

Mechanism of Action

Inhibits calcineurin

	*  Class / Subclass 1: Signal Transduction / Phosphatase Inhibitor

Technical Notes

	*  PubChem Name: Tacrolimus
		*  Synonyms: FK506; Fujimycin; FR900506
		*  CAS #: 104987-11-3
		*</description>
    </item>
    <item rdf:about="https://crispr.tyerslab.com/wiki/results/exp360?rev=1767843420&amp;do=diff">
        <dc:format>text/html</dc:format>
        <dc:date>2026-01-08T03:37:00+00:00</dc:date>
        <dc:creator>Anonymous (anonymous@undisclosed.example.com)</dc:creator>
        <title>Genistein 15μM R07 exp360</title>
        <link>https://crispr.tyerslab.com/wiki/results/exp360?rev=1767843420&amp;do=diff</link>
        <description>Genistein 15μM R07 exp360

Mechanism of Action

Inhibits tyrosine kinases, phytoestrogen, toposiomerase II, pleiotropic effects

	*  Class / Subclass 1: Signal Transduction / Kinase Inhibitor
	*  Class / Subclass 2: Metabolism / Hormone Agonist
	*</description>
    </item>
    <item rdf:about="https://crispr.tyerslab.com/wiki/results/exp362?rev=1767843420&amp;do=diff">
        <dc:format>text/html</dc:format>
        <dc:date>2026-01-08T03:37:00+00:00</dc:date>
        <dc:creator>Anonymous (anonymous@undisclosed.example.com)</dc:creator>
        <title>GSK-J4 1μM R07 exp362</title>
        <link>https://crispr.tyerslab.com/wiki/results/exp362?rev=1767843420&amp;do=diff</link>
        <description>GSK-J4 1μM R07 exp362

Mechanism of Action

JMJD3/KDM6B, UTX/KDM6A histone demethylase inhibitor (H3K27me2/me3)

	*  Class / Subclass 1: Gene Regulation / Epigenetic Inhibitor

Technical Notes

	*  PubChem Name: GSK J4 HCl
		*  Synonyms: N/A
		*  CAS #:</description>
    </item>
    <item rdf:about="https://crispr.tyerslab.com/wiki/results/exp363?rev=1767843420&amp;do=diff">
        <dc:format>text/html</dc:format>
        <dc:date>2026-01-08T03:37:00+00:00</dc:date>
        <dc:creator>Anonymous (anonymous@undisclosed.example.com)</dc:creator>
        <title>GSK-J4 1-1.25μM to day4 R07 exp363</title>
        <link>https://crispr.tyerslab.com/wiki/results/exp363?rev=1767843420&amp;do=diff</link>
        <description>GSK-J4 1-1.25μM to day4 R07 exp363

Mechanism of Action

JMJD3/KDM6B, UTX/KDM6A histone demethylase inhibitor (H3K27me2/me3)

	*  Class / Subclass 1: Gene Regulation / Epigenetic Inhibitor

Technical Notes

	*  PubChem Name: GSK J4 HCl
		*  Synonyms:</description>
    </item>
    <item rdf:about="https://crispr.tyerslab.com/wiki/results/exp365?rev=1767843420&amp;do=diff">
        <dc:format>text/html</dc:format>
        <dc:date>2026-01-08T03:37:00+00:00</dc:date>
        <dc:creator>Anonymous (anonymous@undisclosed.example.com)</dc:creator>
        <title>I-BRD9 4μM R07 exp365</title>
        <link>https://crispr.tyerslab.com/wiki/results/exp365?rev=1767843420&amp;do=diff</link>
        <description>I-BRD9 4μM R07 exp365

Mechanism of Action

Inhibits BRD9 subunit of SWI/SNF complex

	*  Class / Subclass 1: Gene Regulation / Epigenetic Inhibitor

Technical Notes

	*  PubChem Name: N&#039;-(1,1-Dioxothian-4-yl)-5-ethyl-4-oxo-7-[3-(trifluoromethyl)phenyl]thieno[3,2-c]pyridine-2-carboximidamide</description>
    </item>
    <item rdf:about="https://crispr.tyerslab.com/wiki/results/exp372?rev=1767843420&amp;do=diff">
        <dc:format>text/html</dc:format>
        <dc:date>2026-01-08T03:37:00+00:00</dc:date>
        <dc:creator>Anonymous (anonymous@undisclosed.example.com)</dc:creator>
        <title>Ibrutinib 1μM R07 exp372</title>
        <link>https://crispr.tyerslab.com/wiki/results/exp372?rev=1767843420&amp;do=diff</link>
        <description>Ibrutinib 1μM R07 exp372

Mechanism of Action

Inhibits BTK

	*  Class / Subclass 1: Signal Transduction / Kinase Inhibitor

Technical Notes

	*  PubChem Name: Ibrutinib
		*  Synonyms: PCI-32765
		*  CAS #: 936563-96-1
		*  PubChem CID: 24821094
		*  IUPAC:</description>
    </item>
    <item rdf:about="https://crispr.tyerslab.com/wiki/results/exp374?rev=1767843420&amp;do=diff">
        <dc:format>text/html</dc:format>
        <dc:date>2026-01-08T03:37:00+00:00</dc:date>
        <dc:creator>Anonymous (anonymous@undisclosed.example.com)</dc:creator>
        <title>Latrunculin-B 10μM R07 exp374</title>
        <link>https://crispr.tyerslab.com/wiki/results/exp374?rev=1767843420&amp;do=diff</link>
        <description>Latrunculin-B 10μM R07 exp374

Mechanism of Action

Binds actin monomers, inhibits actin polymerization

	*  Class / Subclass 1: Cell Cycle / Cytokinesis Inhibitor
	*  Class / Subclass 2: Organelle Function / Cytoskeletal Inhibitor
	*  Class / Subclass 3:</description>
    </item>
    <item rdf:about="https://crispr.tyerslab.com/wiki/results/exp375?rev=1767843420&amp;do=diff">
        <dc:format>text/html</dc:format>
        <dc:date>2026-01-08T03:37:00+00:00</dc:date>
        <dc:creator>Anonymous (anonymous@undisclosed.example.com)</dc:creator>
        <title>Lenalidomide 20μM R07 exp375</title>
        <link>https://crispr.tyerslab.com/wiki/results/exp375?rev=1767843420&amp;do=diff</link>
        <description>Lenalidomide 20μM R07 exp375

Mechanism of Action

IMiD that targets IKZF1/3 for ubiquitination by CUL4-cereblon complex

	*  Class / Subclass 1: Proteostasis / Bivalent Ligand

Technical Notes

	*  PubChem Name: Lenalidomide
		*  Synonyms: CC-5013</description>
    </item>
    <item rdf:about="https://crispr.tyerslab.com/wiki/results/exp376?rev=1767843420&amp;do=diff">
        <dc:format>text/html</dc:format>
        <dc:date>2026-01-08T03:37:00+00:00</dc:date>
        <dc:creator>Anonymous (anonymous@undisclosed.example.com)</dc:creator>
        <title>Losmapimod 1μM R07 exp376</title>
        <link>https://crispr.tyerslab.com/wiki/results/exp376?rev=1767843420&amp;do=diff</link>
        <description>Losmapimod 1μM R07 exp376

Mechanism of Action

Inhibits p38‘±/‘_ MAP kinases

	*  Class / Subclass 1: Signal Transduction / Kinase Inhibitor

Technical Notes

	*  PubChem Name: Losmapimod
		*  Synonyms: GSK-AHAB; GW856553X; SB856553
		*  CAS #:</description>
    </item>
    <item rdf:about="https://crispr.tyerslab.com/wiki/results/exp379?rev=1767843420&amp;do=diff">
        <dc:format>text/html</dc:format>
        <dc:date>2026-01-08T03:37:00+00:00</dc:date>
        <dc:creator>Anonymous (anonymous@undisclosed.example.com)</dc:creator>
        <title>MSC2530818 10μM R07 exp379</title>
        <link>https://crispr.tyerslab.com/wiki/results/exp379?rev=1767843420&amp;do=diff</link>
        <description>MSC2530818 10μM R07 exp379

Mechanism of Action

Inhibits CDK8

	*  Class / Subclass 1: Gene Regulation / Transcription Inhibitor
	*  Class / Subclass 2: Signal Transduction / Kinase Inhibitor

Technical Notes

	*  PubChem Name: [(2s)-2-(4-Chlorophenyl)pyrrolidin-1-Yl](3-Methyl-1h-Pyrazolo[3,4-B]pyridin-5-Yl)methanone</description>
    </item>
    <item rdf:about="https://crispr.tyerslab.com/wiki/results/exp380?rev=1767843420&amp;do=diff">
        <dc:format>text/html</dc:format>
        <dc:date>2026-01-08T03:37:00+00:00</dc:date>
        <dc:creator>Anonymous (anonymous@undisclosed.example.com)</dc:creator>
        <title>NMS-873 0.07μM R07 exp380</title>
        <link>https://crispr.tyerslab.com/wiki/results/exp380?rev=1767843420&amp;do=diff</link>
        <description>NMS-873 0.07μM R07 exp380

Mechanism of Action

Inhibits p97 AAA-ATPase

	*  Class / Subclass 1: Proteostasis / Ubiquitin-Proteasome Inhibitor

Technical Notes

	*  PubChem Name: CID 71521142
		*  Synonyms: N/A
		*  CAS #: 1418013-75-8
		*  PubChem CID:</description>
    </item>
    <item rdf:about="https://crispr.tyerslab.com/wiki/results/exp382?rev=1767843420&amp;do=diff">
        <dc:format>text/html</dc:format>
        <dc:date>2026-01-08T03:37:00+00:00</dc:date>
        <dc:creator>Anonymous (anonymous@undisclosed.example.com)</dc:creator>
        <title>Palbociclib 1μM R07 exp382</title>
        <link>https://crispr.tyerslab.com/wiki/results/exp382?rev=1767843420&amp;do=diff</link>
        <description>Palbociclib 1μM R07 exp382

Mechanism of Action

Inhibits CDK4 and CDK6, causes G1 arrest

	*  Class / Subclass 1: Cell Cycle / Cyclin Dependent Kinase Inhibitor
	*  Class / Subclass 2: Signal Transduction / Kinase Inhibitor

Technical Notes

	*  PubChem Name:</description>
    </item>
    <item rdf:about="https://crispr.tyerslab.com/wiki/results/exp389?rev=1767843420&amp;do=diff">
        <dc:format>text/html</dc:format>
        <dc:date>2026-01-08T03:37:00+00:00</dc:date>
        <dc:creator>Anonymous (anonymous@undisclosed.example.com)</dc:creator>
        <title>PF-06409577 20μM R07 exp389</title>
        <link>https://crispr.tyerslab.com/wiki/results/exp389?rev=1767843420&amp;do=diff</link>
        <description>PF-06409577 20μM R07 exp389

Mechanism of Action

Activates AMPK, lowers cholesterol levels in NAFLD/NASH preclinical models

	*  Class / Subclass 1: Signal Transduction / Kinase Activator

Technical Notes

	*  PubChem Name: 6-Chloro-5-(4-(1-hydroxycyclobutyl)phenyl)-1H-indole-3-carboxylic acid</description>
    </item>
    <item rdf:about="https://crispr.tyerslab.com/wiki/results/exp390?rev=1767843420&amp;do=diff">
        <dc:format>text/html</dc:format>
        <dc:date>2026-01-08T03:37:00+00:00</dc:date>
        <dc:creator>Anonymous (anonymous@undisclosed.example.com)</dc:creator>
        <title>Pifithrin-alpha 20μM R07 exp390</title>
        <link>https://crispr.tyerslab.com/wiki/results/exp390?rev=1767843420&amp;do=diff</link>
        <description>Pifithrin-alpha 20μM R07 exp390

Mechanism of Action

Claimed to inhibit p53 but has p53-independent effects, cyclic form may increase stem cell reprogramming

	*  Class / Subclass 1: Signal Transduction / Apoptosis Inhibitor

Technical Notes

	*  PubChem Name:</description>
    </item>
    <item rdf:about="https://crispr.tyerslab.com/wiki/results/exp391?rev=1767843420&amp;do=diff">
        <dc:format>text/html</dc:format>
        <dc:date>2026-01-08T03:37:00+00:00</dc:date>
        <dc:creator>Anonymous (anonymous@undisclosed.example.com)</dc:creator>
        <title>Pomalidomide 20μM R07 exp391</title>
        <link>https://crispr.tyerslab.com/wiki/results/exp391?rev=1767843420&amp;do=diff</link>
        <description>Pomalidomide 20μM R07 exp391

Mechanism of Action

IMiD that targets neo-substrates IKZF1/3 for ubiquitination by CUL4A-DDB1-cereblon complex

	*  Class / Subclass 1: Proteostasis / Ubiquitin-Proteasome Activator

Technical Notes

	*  PubChem Name:</description>
    </item>
    <item rdf:about="https://crispr.tyerslab.com/wiki/results/exp392?rev=1767843420&amp;do=diff">
        <dc:format>text/html</dc:format>
        <dc:date>2026-01-08T03:37:00+00:00</dc:date>
        <dc:creator>Anonymous (anonymous@undisclosed.example.com)</dc:creator>
        <title>PT-1 25μM R07 exp392</title>
        <link>https://crispr.tyerslab.com/wiki/results/exp392?rev=1767843420&amp;do=diff</link>
        <description>PT-1 25μM R07 exp392

Mechanism of Action

Activates AMPK, selectivefor ‘_1-complexes, may antagonize autoinhibition

	*  Class / Subclass 1: Signal Transduction / Kinase Activator

Technical Notes

	*  PubChem Name: 2-Chloro-5-[[(5Z)-5-[[5-(4,5-dimethyl-2-nitrophenyl)furan-2-yl]methylidene]-4-oxo-1,3-thiazolidin-2-ylidene]amino]benzoic acid</description>
    </item>
    <item rdf:about="https://crispr.tyerslab.com/wiki/results/exp393?rev=1767843420&amp;do=diff">
        <dc:format>text/html</dc:format>
        <dc:date>2026-01-08T03:37:00+00:00</dc:date>
        <dc:creator>Anonymous (anonymous@undisclosed.example.com)</dc:creator>
        <title>Resminostat 0.5μM R07 exp393</title>
        <link>https://crispr.tyerslab.com/wiki/results/exp393?rev=1767843420&amp;do=diff</link>
        <description>Resminostat 0.5μM R07 exp393

Mechanism of Action

Inhibits HDAC 1, HDAC3, HDAC6

	*  Class / Subclass 1: Gene Regulation / Epigenetic Inhibitor

Technical Notes

	*  PubChem Name: Resminostat (hydrochloride)
		*  Synonyms: RAS2410 hydrochloride; 4SC-201 hydrochloride</description>
    </item>
    <item rdf:about="https://crispr.tyerslab.com/wiki/results/exp399?rev=1767843420&amp;do=diff">
        <dc:format>text/html</dc:format>
        <dc:date>2026-01-08T03:37:00+00:00</dc:date>
        <dc:creator>Anonymous (anonymous@undisclosed.example.com)</dc:creator>
        <title>Salubrinal 20μM R07 exp399</title>
        <link>https://crispr.tyerslab.com/wiki/results/exp399?rev=1767843420&amp;do=diff</link>
        <description>Salubrinal 20μM R07 exp399

Mechanism of Action

Inhibits eIF2‘± phosphatase, indirectly inhibits eIF2‘±

	*  Class / Subclass 1: Proteostasis / Translation Inhibitor

Technical Notes

	*  PubChem Name: Salubrinal
		*  Synonyms: N/A
		*  CAS #:</description>
    </item>
    <item rdf:about="https://crispr.tyerslab.com/wiki/results/exp400?rev=1767843420&amp;do=diff">
        <dc:format>text/html</dc:format>
        <dc:date>2026-01-08T03:37:00+00:00</dc:date>
        <dc:creator>Anonymous (anonymous@undisclosed.example.com)</dc:creator>
        <title>Senexin-A 25μM R07 exp400</title>
        <link>https://crispr.tyerslab.com/wiki/results/exp400?rev=1767843420&amp;do=diff</link>
        <description>Senexin-A 25μM R07 exp400

Mechanism of Action

Inhibits CDK8, suppresses induction of gene expression

	*  Class / Subclass 1: Signal Transduction / Kinase Inhibitor
	*  Class / Subclass 2: Gene Regulation / Transcription Inhibitor

Technical Notes</description>
    </item>
    <item rdf:about="https://crispr.tyerslab.com/wiki/results/exp401?rev=1767843420&amp;do=diff">
        <dc:format>text/html</dc:format>
        <dc:date>2026-01-08T03:37:00+00:00</dc:date>
        <dc:creator>Anonymous (anonymous@undisclosed.example.com)</dc:creator>
        <title>SNS-032 25μM R07 exp401</title>
        <link>https://crispr.tyerslab.com/wiki/results/exp401?rev=1767843420&amp;do=diff</link>
        <description>SNS-032 25μM R07 exp401

Mechanism of Action

Inhibits CDK2, CDK7, CDK9

	*  Class / Subclass 1: Cell Cycle / Cyclin Dependent Kinase Inhibitor
	*  Class / Subclass 2: Signal Transduction / Kinase Inhibitor

Technical Notes

	*  PubChem Name: Sns-032</description>
    </item>
    <item rdf:about="https://crispr.tyerslab.com/wiki/results/exp405?rev=1767843420&amp;do=diff">
        <dc:format>text/html</dc:format>
        <dc:date>2026-01-08T03:37:00+00:00</dc:date>
        <dc:creator>Anonymous (anonymous@undisclosed.example.com)</dc:creator>
        <title>Tenofovir 10μM R07 exp405</title>
        <link>https://crispr.tyerslab.com/wiki/results/exp405?rev=1767843420&amp;do=diff</link>
        <description>Tenofovir 10μM R07 exp405

Mechanism of Action

Nucleoside reverse transcriptase inhibitor, chain terminator

	*  Class / Subclass 1: Infectious Disease / Antiviral

Technical Notes

	*  PubChem Name: Tenofovir
		*  Synonyms: GS 1278; PMPA; TDF
		*</description>
    </item>
    <item rdf:about="https://crispr.tyerslab.com/wiki/results/exp406?rev=1767843420&amp;do=diff">
        <dc:format>text/html</dc:format>
        <dc:date>2026-01-08T03:37:00+00:00</dc:date>
        <dc:creator>Anonymous (anonymous@undisclosed.example.com)</dc:creator>
        <title>Thalidomide 20μM R07 exp406</title>
        <link>https://crispr.tyerslab.com/wiki/results/exp406?rev=1767843420&amp;do=diff</link>
        <description>Thalidomide 20μM R07 exp406

Mechanism of Action

IMiD that targets neo-substrates IKZF1/3 for ubiquitination by CUL4A-DDB1-cereblon complex

	*  Class / Subclass 1: Proteostasis / Bivalent Ligand

Technical Notes

	*  PubChem Name: Thalidomide
		*</description>
    </item>
    <item rdf:about="https://crispr.tyerslab.com/wiki/results/exp407?rev=1767843420&amp;do=diff">
        <dc:format>text/html</dc:format>
        <dc:date>2026-01-08T03:37:00+00:00</dc:date>
        <dc:creator>Anonymous (anonymous@undisclosed.example.com)</dc:creator>
        <title>Thapsigargin 0.005μM R07 exp407</title>
        <link>https://crispr.tyerslab.com/wiki/results/exp407?rev=1767843420&amp;do=diff</link>
        <description>Thapsigargin 0.005μM R07 exp407

Mechanism of Action

Inhibits sarco/endoplasmic reticulum Ca2+ ATPase (SERCA), non-competitive inhibitor, raises intracellular calcium concentration

	*  Class / Subclass 1: Organelle Function / Membrane Transport Inhibitor</description>
    </item>
    <item rdf:about="https://crispr.tyerslab.com/wiki/results/exp409?rev=1767843420&amp;do=diff">
        <dc:format>text/html</dc:format>
        <dc:date>2026-01-08T03:37:00+00:00</dc:date>
        <dc:creator>Anonymous (anonymous@undisclosed.example.com)</dc:creator>
        <title>THZ531 0.11μM R07 exp409</title>
        <link>https://crispr.tyerslab.com/wiki/results/exp409?rev=1767843420&amp;do=diff</link>
        <description>THZ531 0.11μM R07 exp409

Mechanism of Action

Inhibits CDK12 and CDK13, forms covalent adduct, more selective analog of THZ1, blocks phosphorylation of the C-terminal domain of RNA polymerase II

	*  Class / Subclass 1: Gene Regulation / Transcription Inhibitor</description>
    </item>
    <item rdf:about="https://crispr.tyerslab.com/wiki/results/exp410?rev=1767843420&amp;do=diff">
        <dc:format>text/html</dc:format>
        <dc:date>2026-01-08T03:37:00+00:00</dc:date>
        <dc:creator>Anonymous (anonymous@undisclosed.example.com)</dc:creator>
        <title>THZ531 0.11 to 0.125μM on day4 R07 exp410</title>
        <link>https://crispr.tyerslab.com/wiki/results/exp410?rev=1767843420&amp;do=diff</link>
        <description>THZ531 0.11 to 0.125μM on day4 R07 exp410

Mechanism of Action

Inhibits CDK12 and CDK13, forms covalent adduct, more selective analog of THZ1, blocks phosphorylation of the C-terminal domain of RNA polymerase II

	*  Class / Subclass 1: Gene Regulation / Transcription Inhibitor</description>
    </item>
    <item rdf:about="https://crispr.tyerslab.com/wiki/results/exp412?rev=1767843420&amp;do=diff">
        <dc:format>text/html</dc:format>
        <dc:date>2026-01-08T03:37:00+00:00</dc:date>
        <dc:creator>Anonymous (anonymous@undisclosed.example.com)</dc:creator>
        <title>THZ531 0.11 to 0.125 to 0.35μM on day4 then day6 R07 exp412</title>
        <link>https://crispr.tyerslab.com/wiki/results/exp412?rev=1767843420&amp;do=diff</link>
        <description>THZ531 0.11 to 0.125 to 0.35μM on day4 then day6 R07 exp412

Mechanism of Action

Inhibits CDK12 and CDK13, forms covalent adduct, more selective analog of THZ1, blocks phosphorylation of the C-terminal domain of RNA polymerase II

	*  Class / Subclass 1:</description>
    </item>
    <item rdf:about="https://crispr.tyerslab.com/wiki/results/exp413?rev=1767843420&amp;do=diff">
        <dc:format>text/html</dc:format>
        <dc:date>2026-01-08T03:37:00+00:00</dc:date>
        <dc:creator>Anonymous (anonymous@undisclosed.example.com)</dc:creator>
        <title>THZ531 0.11 to 0.175μM on day4 R07 exp413</title>
        <link>https://crispr.tyerslab.com/wiki/results/exp413?rev=1767843420&amp;do=diff</link>
        <description>THZ531 0.11 to 0.175μM on day4 R07 exp413

Mechanism of Action

Inhibits CDK12 and CDK13, forms covalent adduct, more selective analog of THZ1, blocks phosphorylation of the C-terminal domain of RNA polymerase II

	*  Class / Subclass 1: Gene Regulation / Transcription Inhibitor</description>
    </item>
    <item rdf:about="https://crispr.tyerslab.com/wiki/results/exp414?rev=1767843420&amp;do=diff">
        <dc:format>text/html</dc:format>
        <dc:date>2026-01-08T03:37:00+00:00</dc:date>
        <dc:creator>Anonymous (anonymous@undisclosed.example.com)</dc:creator>
        <title>Tozasertib 0.1μM R07 exp414</title>
        <link>https://crispr.tyerslab.com/wiki/results/exp414?rev=1767843420&amp;do=diff</link>
        <description>Tozasertib 0.1μM R07 exp414

Mechanism of Action

Inhibits Aurora A,B,C kinases, blocks cytokinesis, also inhibits RIPK1 and blocks necroptosis

	*  Class / Subclass 1: Cell Cycle / Cytokinesis Inhibitor
	*  Class / Subclass 2: Signal Transduction / Kinase Inhibitor</description>
    </item>
    <item rdf:about="https://crispr.tyerslab.com/wiki/results/exp415?rev=1767843420&amp;do=diff">
        <dc:format>text/html</dc:format>
        <dc:date>2026-01-08T03:37:00+00:00</dc:date>
        <dc:creator>Anonymous (anonymous@undisclosed.example.com)</dc:creator>
        <title>Trichostatin-A 0.06μM R07 exp415</title>
        <link>https://crispr.tyerslab.com/wiki/results/exp415?rev=1767843420&amp;do=diff</link>
        <description>Trichostatin-A 0.06μM R07 exp415

Mechanism of Action

Inhibits class I and II HDAC enzymes

	*  Class / Subclass 1: Gene Regulation / Epigenetic Inhibitor
	*  Class / Subclass 2: Infectious Disease / Antifungal

Technical Notes

	*  PubChem Name: Trichostatin A</description>
    </item>
    <item rdf:about="https://crispr.tyerslab.com/wiki/results/exp416?rev=1767843420&amp;do=diff">
        <dc:format>text/html</dc:format>
        <dc:date>2026-01-08T03:37:00+00:00</dc:date>
        <dc:creator>Anonymous (anonymous@undisclosed.example.com)</dc:creator>
        <title>Tubacin 1.6μM R07 exp416</title>
        <link>https://crispr.tyerslab.com/wiki/results/exp416?rev=1767843420&amp;do=diff</link>
        <description>Tubacin 1.6μM R07 exp416

Mechanism of Action

Inhibits HDAC6 selectively

	*  Class / Subclass 1: Gene Regulation / Epigenetic Inhibitor

Technical Notes

	*  PubChem Name: Tubacin
		*  Synonyms: N/A
		*  CAS #: 537049-40-4
		*  PubChem CID: 6675804
		*</description>
    </item>
    <item rdf:about="https://crispr.tyerslab.com/wiki/results/exp417?rev=1767843420&amp;do=diff">
        <dc:format>text/html</dc:format>
        <dc:date>2026-01-08T03:37:00+00:00</dc:date>
        <dc:creator>Anonymous (anonymous@undisclosed.example.com)</dc:creator>
        <title>Tubastatin-A 2.5μM R07 exp417</title>
        <link>https://crispr.tyerslab.com/wiki/results/exp417?rev=1767843420&amp;do=diff</link>
        <description>Tubastatin-A 2.5μM R07 exp417

Mechanism of Action

Inhibits HDAC6 selectively

	*  Class / Subclass 1: Gene Regulation / Epigenetic Inhibitor

Technical Notes

	*  PubChem Name: Tubastatin A
		*  Synonyms: N/A
		*  CAS #: 1252003-15-8
		*  PubChem CID:</description>
    </item>
    <item rdf:about="https://crispr.tyerslab.com/wiki/results/exp418?rev=1767843420&amp;do=diff">
        <dc:format>text/html</dc:format>
        <dc:date>2026-01-08T03:37:00+00:00</dc:date>
        <dc:creator>Anonymous (anonymous@undisclosed.example.com)</dc:creator>
        <title>Tunicamycin 0.04μM R07 exp418</title>
        <link>https://crispr.tyerslab.com/wiki/results/exp418?rev=1767843420&amp;do=diff</link>
        <description>Tunicamycin 0.04μM R07 exp418

Mechanism of Action

Inhibits GlcNAc phosphotransferase (GPT), blocks N-linked glycoslylation, induces protein unfolding in ER, nucleoside antibiotic

	*  Class / Subclass 1: Proteostasis / Unfolded Protein Response Activator</description>
    </item>
    <item rdf:about="https://crispr.tyerslab.com/wiki/results/exp419?rev=1767843420&amp;do=diff">
        <dc:format>text/html</dc:format>
        <dc:date>2026-01-08T03:37:00+00:00</dc:date>
        <dc:creator>Anonymous (anonymous@undisclosed.example.com)</dc:creator>
        <title>Tunicamycin 0.04 to 0.075μM  on day4 R07 exp419</title>
        <link>https://crispr.tyerslab.com/wiki/results/exp419?rev=1767843420&amp;do=diff</link>
        <description>Tunicamycin 0.04 to 0.075μM  on day4 R07 exp419

Mechanism of Action

Inhibits GlcNAc phosphotransferase (GPT), blocks N-linked glycoslylation, induces protein unfolding in ER, nucleoside antibiotic

	*  Class / Subclass 1: Proteostasis / Unfolded Protein Response Activator</description>
    </item>
    <item rdf:about="https://crispr.tyerslab.com/wiki/results/exp420?rev=1767843420&amp;do=diff">
        <dc:format>text/html</dc:format>
        <dc:date>2026-01-08T03:37:00+00:00</dc:date>
        <dc:creator>Anonymous (anonymous@undisclosed.example.com)</dc:creator>
        <title>Tunicamycin 0.04 to 0.125μM  on day4 R07 exp420</title>
        <link>https://crispr.tyerslab.com/wiki/results/exp420?rev=1767843420&amp;do=diff</link>
        <description>Tunicamycin 0.04 to 0.125μM  on day4 R07 exp420

Mechanism of Action

Inhibits GlcNAc phosphotransferase (GPT), blocks N-linked glycoslylation, induces protein unfolding in ER, nucleoside antibiotic

	*  Class / Subclass 1: Proteostasis / Unfolded Protein Response Activator</description>
    </item>
    <item rdf:about="https://crispr.tyerslab.com/wiki/results/exp421?rev=1767843420&amp;do=diff">
        <dc:format>text/html</dc:format>
        <dc:date>2026-01-08T03:37:00+00:00</dc:date>
        <dc:creator>Anonymous (anonymous@undisclosed.example.com)</dc:creator>
        <title>VHL-ligand-1 20μM R07 exp421</title>
        <link>https://crispr.tyerslab.com/wiki/results/exp421?rev=1767843420&amp;do=diff</link>
        <description>VHL-ligand-1 20μM R07 exp421

Mechanism of Action

Binds VHL, targeting moiety for PROTACs

	*  Class / Subclass 1: Proteostasis / Bivalent Ligand

Technical Notes

	*  PubChem Name: Protein degrader 1 hydrochloride
		*  Synonyms: N/A
		*  CAS #: 1448189-80-7</description>
    </item>
    <item rdf:about="https://crispr.tyerslab.com/wiki/results/exp422?rev=1767843420&amp;do=diff">
        <dc:format>text/html</dc:format>
        <dc:date>2026-01-08T03:37:00+00:00</dc:date>
        <dc:creator>Anonymous (anonymous@undisclosed.example.com)</dc:creator>
        <title>Wiskostatin 3μM R07 exp422</title>
        <link>https://crispr.tyerslab.com/wiki/results/exp422?rev=1767843420&amp;do=diff</link>
        <description>Wiskostatin 3μM R07 exp422

Mechanism of Action

Inhibits N-WASP, blocks actin polymerization

	*  Class / Subclass 1: Organelle Function / Cytoskeletal Inhibitor
	*  Class / Subclass 2: Cell Cycle / Actin Inhibitor

Technical Notes

	*  PubChem Name:</description>
    </item>
    <item rdf:about="https://crispr.tyerslab.com/wiki/results/exp423?rev=1767843420&amp;do=diff">
        <dc:format>text/html</dc:format>
        <dc:date>2026-01-08T03:37:00+00:00</dc:date>
        <dc:creator>Anonymous (anonymous@undisclosed.example.com)</dc:creator>
        <title>Zebularine 20μM R07 exp423</title>
        <link>https://crispr.tyerslab.com/wiki/results/exp423?rev=1767843420&amp;do=diff</link>
        <description>Zebularine 20μM R07 exp423

Mechanism of Action

Inhibits cytidine deaminase, transition state analog, also inhibits DNMT1 via reversible covalent complex

	*  Class / Subclass 1: Gene Regulation / Epigenetic Inhibitor

Technical Notes

	*  PubChem Name:</description>
    </item>
    <item rdf:about="https://crispr.tyerslab.com/wiki/results/exp425?rev=1767843420&amp;do=diff">
        <dc:format>text/html</dc:format>
        <dc:date>2026-01-08T03:37:00+00:00</dc:date>
        <dc:creator>Anonymous (anonymous@undisclosed.example.com)</dc:creator>
        <title>Beta-Estradiol 0.55μM R07 exp425</title>
        <link>https://crispr.tyerslab.com/wiki/results/exp425?rev=1767843420&amp;do=diff</link>
        <description>Beta-Estradiol 0.55μM R07 exp425

Mechanism of Action

Agonist for estrogen receptor (ER), inactive control for 2-Methoxyestradiol

	*  Class / Subclass 1: Gene Regulation / Transcription Activator
	*  Class / Subclass 2: Metabolism / Hormone Agonist</description>
    </item>
    <item rdf:about="https://crispr.tyerslab.com/wiki/results/exp426?rev=1767843420&amp;do=diff">
        <dc:format>text/html</dc:format>
        <dc:date>2026-01-08T03:37:00+00:00</dc:date>
        <dc:creator>Anonymous (anonymous@undisclosed.example.com)</dc:creator>
        <title>FBS-Wisent 0.1 R07 exp426</title>
        <link>https://crispr.tyerslab.com/wiki/results/exp426?rev=1767843420&amp;do=diff</link>
        <description>FBS-Wisent 0.1 R07 exp426

Mechanism of Action

Unknown, poor batch of FBS

	*  Class / Subclass 1: Environmental Stresses / Toxin

Screen Summary

	*  Round: 07
		*  Dose: 10%
		*  Days of incubation: 8
		*  Doublings: 5.4
		*  Numbers of reads: 23344123</description>
    </item>
    <item rdf:about="https://crispr.tyerslab.com/wiki/results/exp429?rev=1767843420&amp;do=diff">
        <dc:format>text/html</dc:format>
        <dc:date>2026-01-08T03:37:00+00:00</dc:date>
        <dc:creator>Anonymous (anonymous@undisclosed.example.com)</dc:creator>
        <title>Rapamycin 0.001μM R08 exp429</title>
        <link>https://crispr.tyerslab.com/wiki/results/exp429?rev=1767843420&amp;do=diff</link>
        <description>Rapamycin 0.001μM R08 exp429

Mechanism of Action

Allosteric mTORC1 inhibitor, forms ternary complex with FKBP12 and mTOR, attenuates protein synthesis and metabolism

	*  Class / Subclass 1: Signal Transduction / Kinase Inhibitor
	*  Class / Subclass 2:</description>
    </item>
    <item rdf:about="https://crispr.tyerslab.com/wiki/results/exp430?rev=1767843420&amp;do=diff">
        <dc:format>text/html</dc:format>
        <dc:date>2026-01-08T03:37:00+00:00</dc:date>
        <dc:creator>Anonymous (anonymous@undisclosed.example.com)</dc:creator>
        <title>Rifampicin 30μM R08 exp430</title>
        <link>https://crispr.tyerslab.com/wiki/results/exp430?rev=1767843420&amp;do=diff</link>
        <description>Rifampicin 30μM R08 exp430

Mechanism of Action

Inhibits bacterial RNA polymerase, induces hepatic cytochrome P450 enzymes

	*  Class / Subclass 1: Infectious Disease / Antibiotic

Technical Notes

	*  PubChem Name: Rifampicin
		*  Synonyms: Rifampin; Rifamycin AMP</description>
    </item>
    <item rdf:about="https://crispr.tyerslab.com/wiki/results/exp431?rev=1767843420&amp;do=diff">
        <dc:format>text/html</dc:format>
        <dc:date>2026-01-08T03:37:00+00:00</dc:date>
        <dc:creator>Anonymous (anonymous@undisclosed.example.com)</dc:creator>
        <title>Rotenone 0.07μM R08 exp431</title>
        <link>https://crispr.tyerslab.com/wiki/results/exp431?rev=1767843420&amp;do=diff</link>
        <description>Rotenone 0.07μM R08 exp431

Mechanism of Action

Inhibits complex I, blocks electron transfer from iron-sulfur centers to ubiquinone, generates ROS, also inhibits microtubule assembly

	*  Class / Subclass 1: Organelle Function / Mitochondrial Inhibitor</description>
    </item>
    <item rdf:about="https://crispr.tyerslab.com/wiki/results/exp432?rev=1767843420&amp;do=diff">
        <dc:format>text/html</dc:format>
        <dc:date>2026-01-08T03:37:00+00:00</dc:date>
        <dc:creator>Anonymous (anonymous@undisclosed.example.com)</dc:creator>
        <title>YM155 0.001μM R08 exp432</title>
        <link>https://crispr.tyerslab.com/wiki/results/exp432?rev=1767843420&amp;do=diff</link>
        <description>YM155 0.001μM R08 exp432

Mechanism of Action

Inhibits expression of survivin, amongst other ascribed mechanisms

	*  Class / Subclass 1: Gene Regulation / Transcription Inhibitor
	*  Class / Subclass 2: Signal Transduction / Apoptosis Activator

Technical Notes</description>
    </item>
    <item rdf:about="https://crispr.tyerslab.com/wiki/results/exp433?rev=1767843420&amp;do=diff">
        <dc:format>text/html</dc:format>
        <dc:date>2026-01-08T03:37:00+00:00</dc:date>
        <dc:creator>Anonymous (anonymous@undisclosed.example.com)</dc:creator>
        <title>LJH685 50μM R08 exp433</title>
        <link>https://crispr.tyerslab.com/wiki/results/exp433?rev=1767843420&amp;do=diff</link>
        <description>LJH685 50μM R08 exp433

Mechanism of Action

Inhibits p90 ribosomal S6 kinase (RSK)

	*  Class / Subclass 1: Signal Transduction / Kinase Inhibitor

Technical Notes

	*  PubChem Name: 2,6-Difluoro-4-{4-[4-(4-Methylpiperazin-1-Yl)phenyl]pyridin-3-Yl}phenol</description>
    </item>
    <item rdf:about="https://crispr.tyerslab.com/wiki/results/exp434?rev=1767843420&amp;do=diff">
        <dc:format>text/html</dc:format>
        <dc:date>2026-01-08T03:37:00+00:00</dc:date>
        <dc:creator>Anonymous (anonymous@undisclosed.example.com)</dc:creator>
        <title>Vemurafenib 6.6μM R08 exp434</title>
        <link>https://crispr.tyerslab.com/wiki/results/exp434?rev=1767843420&amp;do=diff</link>
        <description>Vemurafenib 6.6μM R08 exp434

Mechanism of Action

Inhibits BRAF-V300E, paradoxical RAF activation by stabilization of CRAF/BRAF heterodimer

	*  Class / Subclass 1: Signal Transduction / Kinase Inhibitor

Technical Notes

	*  PubChem Name: Vemurafenib</description>
    </item>
    <item rdf:about="https://crispr.tyerslab.com/wiki/results/exp435?rev=1767843420&amp;do=diff">
        <dc:format>text/html</dc:format>
        <dc:date>2026-01-08T03:37:00+00:00</dc:date>
        <dc:creator>Anonymous (anonymous@undisclosed.example.com)</dc:creator>
        <title>JQ1 0.8μM R08 exp435</title>
        <link>https://crispr.tyerslab.com/wiki/results/exp435?rev=1767843420&amp;do=diff</link>
        <description>JQ1 0.8μM R08 exp435

Mechanism of Action

Inhibits BET bromodomain proteins BRD2, BRD3, BRD4, BRDT

	*  Class / Subclass 1: Gene Regulation / Epigenetic Inhibitor

Technical Notes

	*  PubChem Name: JQ1 compound
		*  Synonyms: JQ1
		*  CAS #: 1268524-70-4</description>
    </item>
    <item rdf:about="https://crispr.tyerslab.com/wiki/results/exp436?rev=1767843420&amp;do=diff">
        <dc:format>text/html</dc:format>
        <dc:date>2026-01-08T03:37:00+00:00</dc:date>
        <dc:creator>Anonymous (anonymous@undisclosed.example.com)</dc:creator>
        <title>Dynasore 7μM R08 exp436</title>
        <link>https://crispr.tyerslab.com/wiki/results/exp436?rev=1767843420&amp;do=diff</link>
        <description>Dynasore 7μM R08 exp436

Mechanism of Action

Putative dynamin GTPase inhibitor, blocks endocytosis

	*  Class / Subclass 1: Organelle Function / Vesicule Trafficking Inhibitor

Technical Notes

	*  PubChem Name: Dynasore
		*  Synonyms: N/A
		*  CAS #:</description>
    </item>
    <item rdf:about="https://crispr.tyerslab.com/wiki/results/exp437?rev=1767843420&amp;do=diff">
        <dc:format>text/html</dc:format>
        <dc:date>2026-01-08T03:37:00+00:00</dc:date>
        <dc:creator>Anonymous (anonymous@undisclosed.example.com)</dc:creator>
        <title>Ethanol 0.003 R08 exp437</title>
        <link>https://crispr.tyerslab.com/wiki/results/exp437?rev=1767843420&amp;do=diff</link>
        <description>Ethanol 0.003 R08 exp437

Mechanism of Action

Pleiotropic effects on membranes, ion channels, enzymes, receptors

	*  Class / Subclass 1: Environmental Stresses / Solvent

Technical Notes

	*  PubChem Name: Ethanol
		*  Synonyms: N/A
		*  CAS #: 64-17-5</description>
    </item>
    <item rdf:about="https://crispr.tyerslab.com/wiki/results/exp438?rev=1767843420&amp;do=diff">
        <dc:format>text/html</dc:format>
        <dc:date>2026-01-08T03:37:00+00:00</dc:date>
        <dc:creator>Anonymous (anonymous@undisclosed.example.com)</dc:creator>
        <title>NN-Diethyl-meta-toluamide 500μM R08 exp438</title>
        <link>https://crispr.tyerslab.com/wiki/results/exp438?rev=1767843420&amp;do=diff</link>
        <description>NN-Diethyl-meta-toluamide 500μM R08 exp438

Mechanism of Action

Insect repellent

	*  Class / Subclass 1: Environmental Stresses / Environmental Contaminant

Technical Notes

	*  PubChem Name: N,N-Diethyl-3-methylbenzamide
		*  Synonyms: DEET; N,N-Diethyl-m-toluamide; DEET;N,N-Diethyl-m-toluamide</description>
    </item>
    <item rdf:about="https://crispr.tyerslab.com/wiki/results/exp439?rev=1767843420&amp;do=diff">
        <dc:format>text/html</dc:format>
        <dc:date>2026-01-08T03:37:00+00:00</dc:date>
        <dc:creator>Anonymous (anonymous@undisclosed.example.com)</dc:creator>
        <title>QNZ 0.01μM R08 exp439</title>
        <link>https://crispr.tyerslab.com/wiki/results/exp439?rev=1767843420&amp;do=diff</link>
        <description>QNZ 0.01μM R08 exp439

Mechanism of Action

Inhibits NF-κB activation, TNF-α production

	*  Class / Subclass 1: Gene Regulation / Transcription Inhibitor
	*  Class / Subclass 2: Signal Transduction / Apoptosis Inhibitor

Technical Notes

	*  PubChem Name:</description>
    </item>
    <item rdf:about="https://crispr.tyerslab.com/wiki/results/exp440?rev=1767843420&amp;do=diff">
        <dc:format>text/html</dc:format>
        <dc:date>2026-01-08T03:37:00+00:00</dc:date>
        <dc:creator>Anonymous (anonymous@undisclosed.example.com)</dc:creator>
        <title>Aphidicolin 0.4μM R08 exp440</title>
        <link>https://crispr.tyerslab.com/wiki/results/exp440?rev=1767843420&amp;do=diff</link>
        <description>Aphidicolin 0.4μM R08 exp440

Mechanism of Action

Inhibits DNA polymerases Polα, Polδ, Polϵ and Polζ

	*  Class / Subclass 1: DNA Damage, Repair and Replication / Replication Inhibitor
	*  Class / Subclass 2: Cell Cycle / Replication Inhibitor</description>
    </item>
    <item rdf:about="https://crispr.tyerslab.com/wiki/results/exp441?rev=1767843420&amp;do=diff">
        <dc:format>text/html</dc:format>
        <dc:date>2026-01-08T03:37:00+00:00</dc:date>
        <dc:creator>Anonymous (anonymous@undisclosed.example.com)</dc:creator>
        <title>GSK-J4 1.5μM R08 exp441</title>
        <link>https://crispr.tyerslab.com/wiki/results/exp441?rev=1767843420&amp;do=diff</link>
        <description>GSK-J4 1.5μM R08 exp441

Mechanism of Action

JMJD3/KDM6B, UTX/KDM6A histone demethylase inhibitor (H3K27me2/me3)

	*  Class / Subclass 1: Gene Regulation / Epigenetic Inhibitor

Technical Notes

	*  PubChem Name: GSK J4 HCl
		*  Synonyms: N/A
		*</description>
    </item>
    <item rdf:about="https://crispr.tyerslab.com/wiki/results/exp442?rev=1767843420&amp;do=diff">
        <dc:format>text/html</dc:format>
        <dc:date>2026-01-08T03:37:00+00:00</dc:date>
        <dc:creator>Anonymous (anonymous@undisclosed.example.com)</dc:creator>
        <title>Ibrutinib 10μM R08 exp442</title>
        <link>https://crispr.tyerslab.com/wiki/results/exp442?rev=1767843420&amp;do=diff</link>
        <description>Ibrutinib 10μM R08 exp442

Mechanism of Action

Inhibits BTK

	*  Class / Subclass 1: Signal Transduction / Kinase Inhibitor

Technical Notes

	*  PubChem Name: Ibrutinib
		*  Synonyms: PCI-32765
		*  CAS #: 936563-96-1
		*  PubChem CID: 24821094
		*  IUPAC:</description>
    </item>
    <item rdf:about="https://crispr.tyerslab.com/wiki/results/exp443?rev=1767843420&amp;do=diff">
        <dc:format>text/html</dc:format>
        <dc:date>2026-01-08T03:37:00+00:00</dc:date>
        <dc:creator>Anonymous (anonymous@undisclosed.example.com)</dc:creator>
        <title>SNS-032 15μM R08 exp443</title>
        <link>https://crispr.tyerslab.com/wiki/results/exp443?rev=1767843420&amp;do=diff</link>
        <description>SNS-032 15μM R08 exp443

Mechanism of Action

Inhibits CDK2, CDK7, CDK9

	*  Class / Subclass 1: Cell Cycle / Cyclin Dependent Kinase Inhibitor
	*  Class / Subclass 2: Signal Transduction / Kinase Inhibitor

Technical Notes

	*  PubChem Name: Sns-032</description>
    </item>
    <item rdf:about="https://crispr.tyerslab.com/wiki/results/exp444?rev=1767843420&amp;do=diff">
        <dc:format>text/html</dc:format>
        <dc:date>2026-01-08T03:37:00+00:00</dc:date>
        <dc:creator>Anonymous (anonymous@undisclosed.example.com)</dc:creator>
        <title>THZ531 0.225μM R08 exp444</title>
        <link>https://crispr.tyerslab.com/wiki/results/exp444?rev=1767843420&amp;do=diff</link>
        <description>THZ531 0.225μM R08 exp444

Mechanism of Action

Inhibits CDK12 and CDK13, forms covalent adduct, more selective analog of THZ1, blocks phosphorylation of the C-terminal domain of RNA polymerase II

	*  Class / Subclass 1: Gene Regulation / Transcription Inhibitor</description>
    </item>
    <item rdf:about="https://crispr.tyerslab.com/wiki/results/exp445?rev=1767843420&amp;do=diff">
        <dc:format>text/html</dc:format>
        <dc:date>2026-01-08T03:37:00+00:00</dc:date>
        <dc:creator>Anonymous (anonymous@undisclosed.example.com)</dc:creator>
        <title>∆-9-Tetrahydrocannabinol 30μM R08 exp445</title>
        <link>https://crispr.tyerslab.com/wiki/results/exp445?rev=1767843420&amp;do=diff</link>
        <description>∆-9-Tetrahydrocannabinol 30μM R08 exp445

Mechanism of Action

Agonist of CB1 and CB2 cannabinoid receptors

	*  Class / Subclass 1: Environmental Stresses / Controlled Substance
	*  Class / Subclass 2: Signal Transduction / GPCR Agonist

Technical Notes</description>
    </item>
    <item rdf:about="https://crispr.tyerslab.com/wiki/results/exp446?rev=1767843420&amp;do=diff">
        <dc:format>text/html</dc:format>
        <dc:date>2026-01-08T03:37:00+00:00</dc:date>
        <dc:creator>Anonymous (anonymous@undisclosed.example.com)</dc:creator>
        <title>4-Nitroquinoline-1-oxide 0.5μM R08 exp446</title>
        <link>https://crispr.tyerslab.com/wiki/results/exp446?rev=1767843420&amp;do=diff</link>
        <description>4-Nitroquinoline-1-oxide 0.5μM R08 exp446

Mechanism of Action

UV mimetic, metabolized to electrohpile that forms stable quinolone monoadducts

	*  Class / Subclass 1: DNA Damage, Repair and Replication / Helix-Distorting Adduct

Technical Notes

	*</description>
    </item>
    <item rdf:about="https://crispr.tyerslab.com/wiki/results/exp447?rev=1767843420&amp;do=diff">
        <dc:format>text/html</dc:format>
        <dc:date>2026-01-08T03:37:00+00:00</dc:date>
        <dc:creator>Anonymous (anonymous@undisclosed.example.com)</dc:creator>
        <title>Amiloride 100μM R08 exp447</title>
        <link>https://crispr.tyerslab.com/wiki/results/exp447?rev=1767843420&amp;do=diff</link>
        <description>Amiloride 100μM R08 exp447

Mechanism of Action

Inhibits epithelial sodium channel (ENaC) and other Na+/H+ channels, also inhibits urokinase-type plasminogen activator (uPA)

	*  Class / Subclass 1: Signal Transduction / Ion Channel Inhibitor

Technical Notes</description>
    </item>
    <item rdf:about="https://crispr.tyerslab.com/wiki/results/exp448?rev=1767843420&amp;do=diff">
        <dc:format>text/html</dc:format>
        <dc:date>2026-01-08T03:37:00+00:00</dc:date>
        <dc:creator>Anonymous (anonymous@undisclosed.example.com)</dc:creator>
        <title>Ammonium tetrathiomolybdate 10μM R08 exp448</title>
        <link>https://crispr.tyerslab.com/wiki/results/exp448?rev=1767843420&amp;do=diff</link>
        <description>Ammonium tetrathiomolybdate 10μM R08 exp448

Mechanism of Action

Inhibits cuproenzymes superoxide dismutase 1 (SOD1) and cytochrome c oxidase (COX)

	*  Class / Subclass 1: Environmental Stresses / Metal Chelator
	*  Class / Subclass 2: Metabolism / Metabolic Enzyme Inhibitor</description>
    </item>
    <item rdf:about="https://crispr.tyerslab.com/wiki/results/exp449?rev=1767843420&amp;do=diff">
        <dc:format>text/html</dc:format>
        <dc:date>2026-01-08T03:37:00+00:00</dc:date>
        <dc:creator>Anonymous (anonymous@undisclosed.example.com)</dc:creator>
        <title>Arsenic trioxide 60μM R08 exp449</title>
        <link>https://crispr.tyerslab.com/wiki/results/exp449?rev=1767843420&amp;do=diff</link>
        <description>Arsenic trioxide 60μM R08 exp449

Mechanism of Action

Induces degradation of aberrant PML-RAR‘± fusion protein in acute promyelocytic leukemia

	*  Class / Subclass 1: Environmental Stresses / Heavy Metal
	*  Class / Subclass 2: Signal Transduction / Apoptosis Inducer</description>
    </item>
    <item rdf:about="https://crispr.tyerslab.com/wiki/results/exp450?rev=1767843420&amp;do=diff">
        <dc:format>text/html</dc:format>
        <dc:date>2026-01-08T03:37:00+00:00</dc:date>
        <dc:creator>Anonymous (anonymous@undisclosed.example.com)</dc:creator>
        <title>Artemisinin 50μM R08 exp450</title>
        <link>https://crispr.tyerslab.com/wiki/results/exp450?rev=1767843420&amp;do=diff</link>
        <description>Artemisinin 50μM R08 exp450

Mechanism of Action

Sesquiterpene endoperoxide activated by heme, kills malaria parasite through oxidative damage

	*  Class / Subclass 1: Infectious Disease / Antimalarial

Technical Notes

	*  PubChem Name: Artemisinin</description>
    </item>
    <item rdf:about="https://crispr.tyerslab.com/wiki/results/exp451?rev=1767843420&amp;do=diff">
        <dc:format>text/html</dc:format>
        <dc:date>2026-01-08T03:37:00+00:00</dc:date>
        <dc:creator>Anonymous (anonymous@undisclosed.example.com)</dc:creator>
        <title>Atovaquone 15μM R08 exp451</title>
        <link>https://crispr.tyerslab.com/wiki/results/exp451?rev=1767843420&amp;do=diff</link>
        <description>Atovaquone 15μM R08 exp451

Mechanism of Action

Ubiquinone analog, inhibits mitochondrial complex III, induces DNA strand breaks

	*  Class / Subclass 1: Infectious Disease / Antimalarial
	*  Class / Subclass 2: Organelle Function / Mitochondrial Inhibitor</description>
    </item>
    <item rdf:about="https://crispr.tyerslab.com/wiki/results/exp452?rev=1767843420&amp;do=diff">
        <dc:format>text/html</dc:format>
        <dc:date>2026-01-08T03:37:00+00:00</dc:date>
        <dc:creator>Anonymous (anonymous@undisclosed.example.com)</dc:creator>
        <title>Azithromycin 100μM R08 exp452</title>
        <link>https://crispr.tyerslab.com/wiki/results/exp452?rev=1767843420&amp;do=diff</link>
        <description>Azithromycin 100μM R08 exp452

Mechanism of Action

Binds 50S subunit of bacterial ribosome, inhibits translation

	*  Class / Subclass 1: Infectious Disease / Antibiotic
	*  Class / Subclass 2: Proteostasis / Translation Inhibitor

Technical Notes</description>
    </item>
    <item rdf:about="https://crispr.tyerslab.com/wiki/results/exp453?rev=1767843420&amp;do=diff">
        <dc:format>text/html</dc:format>
        <dc:date>2026-01-08T03:37:00+00:00</dc:date>
        <dc:creator>Anonymous (anonymous@undisclosed.example.com)</dc:creator>
        <title>B02 10μM R08 exp453</title>
        <link>https://crispr.tyerslab.com/wiki/results/exp453?rev=1767843420&amp;do=diff</link>
        <description>B02 10μM R08 exp453

Mechanism of Action

Inhibits RAD51 recombinase, blocks homologous recombination

	*  Class / Subclass 1: DNA Damage, Repair and Replication / Repair Protein Inhibitor

Technical Notes

	*  PubChem Name: RAD51 inhibitor B02
		*</description>
    </item>
    <item rdf:about="https://crispr.tyerslab.com/wiki/results/exp454?rev=1767843420&amp;do=diff">
        <dc:format>text/html</dc:format>
        <dc:date>2026-01-08T03:37:00+00:00</dc:date>
        <dc:creator>Anonymous (anonymous@undisclosed.example.com)</dc:creator>
        <title>Bafilomycin-A1 0.009μM R08 exp454</title>
        <link>https://crispr.tyerslab.com/wiki/results/exp454?rev=1767843420&amp;do=diff</link>
        <description>Bafilomycin-A1 0.009μM R08 exp454

Mechanism of Action

Inhibits vacuolar-type H+ ATPase, blocks acidification of lysosome

	*  Class / Subclass 1: Signal Transduction / Ion Channel Inhibitor
	*  Class / Subclass 2: Organelle Function / Membrane Transport Inhibitor</description>
    </item>
    <item rdf:about="https://crispr.tyerslab.com/wiki/results/exp455?rev=1767843420&amp;do=diff">
        <dc:format>text/html</dc:format>
        <dc:date>2026-01-08T03:37:00+00:00</dc:date>
        <dc:creator>Anonymous (anonymous@undisclosed.example.com)</dc:creator>
        <title>Benzoate 10000μM R08 exp455</title>
        <link>https://crispr.tyerslab.com/wiki/results/exp455?rev=1767843420&amp;do=diff</link>
        <description>Benzoate 10000μM R08 exp455

Mechanism of Action

Food additive (E211), bacteriostatic and fungistatic

	*  Class / Subclass 1: Environmental Stresses / Food Preservative

Technical Notes

	*  PubChem Name: Sodium benzoate
		*  Synonyms: N/A
		*  CAS #:</description>
    </item>
    <item rdf:about="https://crispr.tyerslab.com/wiki/results/exp456?rev=1767843420&amp;do=diff">
        <dc:format>text/html</dc:format>
        <dc:date>2026-01-08T03:37:00+00:00</dc:date>
        <dc:creator>Anonymous (anonymous@undisclosed.example.com)</dc:creator>
        <title>Benzoate 20000μM R08 exp456</title>
        <link>https://crispr.tyerslab.com/wiki/results/exp456?rev=1767843420&amp;do=diff</link>
        <description>Benzoate 20000μM R08 exp456

Mechanism of Action

Food additive (E211), bacteriostatic and fungistatic

	*  Class / Subclass 1: Environmental Stresses / Food Preservative

Technical Notes

	*  PubChem Name: Sodium benzoate
		*  Synonyms: N/A
		*  CAS #:</description>
    </item>
    <item rdf:about="https://crispr.tyerslab.com/wiki/results/exp457?rev=1767843420&amp;do=diff">
        <dc:format>text/html</dc:format>
        <dc:date>2026-01-08T03:37:00+00:00</dc:date>
        <dc:creator>Anonymous (anonymous@undisclosed.example.com)</dc:creator>
        <title>Bisphenol F 50μM R08 exp457</title>
        <link>https://crispr.tyerslab.com/wiki/results/exp457?rev=1767843420&amp;do=diff</link>
        <description>Bisphenol F 50μM R08 exp457

Mechanism of Action

BPA analog and substitute, endocrine disrupter

	*  Class / Subclass 1: Environmental Stresses / Industrial Chemical

Technical Notes

	*  PubChem Name: 4,4&#039;-Methylenediphenol
		*  Synonyms: N/A
		*</description>
    </item>
    <item rdf:about="https://crispr.tyerslab.com/wiki/results/exp458?rev=1767843420&amp;do=diff">
        <dc:format>text/html</dc:format>
        <dc:date>2026-01-08T03:37:00+00:00</dc:date>
        <dc:creator>Anonymous (anonymous@undisclosed.example.com)</dc:creator>
        <title>Bisphenol S 100μM R08 exp458</title>
        <link>https://crispr.tyerslab.com/wiki/results/exp458?rev=1767843420&amp;do=diff</link>
        <description>Bisphenol S 100μM R08 exp458

Mechanism of Action

BPA analog and substitute in BPA-free plastics, endocrine disrupter

	*  Class / Subclass 1: Environmental Stresses / Industrial Chemical

Technical Notes

	*  PubChem Name: 4,4&#039;-Sulfonyldiphenol
		*</description>
    </item>
    <item rdf:about="https://crispr.tyerslab.com/wiki/results/exp459?rev=1767843420&amp;do=diff">
        <dc:format>text/html</dc:format>
        <dc:date>2026-01-08T03:37:00+00:00</dc:date>
        <dc:creator>Anonymous (anonymous@undisclosed.example.com)</dc:creator>
        <title>Bleomycin 5μM R08 exp459</title>
        <link>https://crispr.tyerslab.com/wiki/results/exp459?rev=1767843420&amp;do=diff</link>
        <description>Bleomycin 5μM R08 exp459

Mechanism of Action

Induces DNA strand breaks, possibly by iron chelation and ROS generation, or generation of alkali-labile lesions

	*  Class / Subclass 1: DNA Damage, Repair and Replication / Clastogen

Technical Notes</description>
    </item>
    <item rdf:about="https://crispr.tyerslab.com/wiki/results/exp460?rev=1767843420&amp;do=diff">
        <dc:format>text/html</dc:format>
        <dc:date>2026-01-08T03:37:00+00:00</dc:date>
        <dc:creator>Anonymous (anonymous@undisclosed.example.com)</dc:creator>
        <title>BML-284 0.09μM R08 exp460</title>
        <link>https://crispr.tyerslab.com/wiki/results/exp460?rev=1767843420&amp;do=diff</link>
        <description>BML-284 0.09μM R08 exp460

Mechanism of Action

Wnt agonist, GSK3-‘_ dependent, activates ‘_-catenin/TCF-dependent transcription

	*  Class / Subclass 1: Signal Transduction / GPCR Agonist
	*  Class / Subclass 2: Gene Regulation / Transcription Activator</description>
    </item>
    <item rdf:about="https://crispr.tyerslab.com/wiki/results/exp461?rev=1767843420&amp;do=diff">
        <dc:format>text/html</dc:format>
        <dc:date>2026-01-08T03:37:00+00:00</dc:date>
        <dc:creator>Anonymous (anonymous@undisclosed.example.com)</dc:creator>
        <title>BS-181 20μM R08 exp461</title>
        <link>https://crispr.tyerslab.com/wiki/results/exp461?rev=1767843420&amp;do=diff</link>
        <description>BS-181 20μM R08 exp461

Mechanism of Action

Inhibits CDK7, causes G1 arrest and apoptosis

	*  Class / Subclass 1: Gene Regulation / Transcription Inhibitor
	*  Class / Subclass 2: Signal Transduction / Kinase Inhibitor

Technical Notes

	*  PubChem Name:</description>
    </item>
    <item rdf:about="https://crispr.tyerslab.com/wiki/results/exp462?rev=1767843420&amp;do=diff">
        <dc:format>text/html</dc:format>
        <dc:date>2026-01-08T03:37:00+00:00</dc:date>
        <dc:creator>Anonymous (anonymous@undisclosed.example.com)</dc:creator>
        <title>Cadmium 60μM R08 exp462</title>
        <link>https://crispr.tyerslab.com/wiki/results/exp462?rev=1767843420&amp;do=diff</link>
        <description>Cadmium 60μM R08 exp462

Mechanism of Action

Widely used metal in manufacturing and pigments, known carcinogen

	*  Class / Subclass 1: Environmental Stresses / Heavy Metal

Technical Notes

	*  PubChem Name: Cadmium chloride
		*  Synonyms: N/A
		*</description>
    </item>
    <item rdf:about="https://crispr.tyerslab.com/wiki/results/exp463?rev=1767843420&amp;do=diff">
        <dc:format>text/html</dc:format>
        <dc:date>2026-01-08T03:37:00+00:00</dc:date>
        <dc:creator>Anonymous (anonymous@undisclosed.example.com)</dc:creator>
        <title>Caffeine 2600μM R08 exp463</title>
        <link>https://crispr.tyerslab.com/wiki/results/exp463?rev=1767843420&amp;do=diff</link>
        <description>Caffeine 2600μM R08 exp463

Mechanism of Action

CNS stimulant, antagonist of adenosine receptors, inhibits phosphodiesterases, modulates intracellular calcium

	*  Class / Subclass 1: Signal Transduction / GPCR Antagonist
	*  Class / Subclass 2: Environmental Stresses / Food Additive</description>
    </item>
    <item rdf:about="https://crispr.tyerslab.com/wiki/results/exp464?rev=1767843420&amp;do=diff">
        <dc:format>text/html</dc:format>
        <dc:date>2026-01-08T03:37:00+00:00</dc:date>
        <dc:creator>Anonymous (anonymous@undisclosed.example.com)</dc:creator>
        <title>Calcipotriol 5μM R08 exp464</title>
        <link>https://crispr.tyerslab.com/wiki/results/exp464?rev=1767843420&amp;do=diff</link>
        <description>Calcipotriol 5μM R08 exp464

Mechanism of Action

Synthetic vitamin D3 analog, binds vitamin D nuclear hormone receptor

	*  Class / Subclass 1: Metabolism / Vitamin
	*  Class / Subclass 2: Signal Transduction / Nuclear Receptor Ligand

Technical Notes</description>
    </item>
    <item rdf:about="https://crispr.tyerslab.com/wiki/results/exp465?rev=1767843420&amp;do=diff">
        <dc:format>text/html</dc:format>
        <dc:date>2026-01-08T03:37:00+00:00</dc:date>
        <dc:creator>Anonymous (anonymous@undisclosed.example.com)</dc:creator>
        <title>Cannabidiol 13μM R08 exp465</title>
        <link>https://crispr.tyerslab.com/wiki/results/exp465?rev=1767843420&amp;do=diff</link>
        <description>Cannabidiol 13μM R08 exp465

Mechanism of Action

Negative allosteric modulator of cannabinoid CB1 receptor

	*  Class / Subclass 1: Environmental Stresses / Psychoactive Drug
	*  Class / Subclass 2: Signal Transduction / GPCR Antagonist

Technical Notes</description>
    </item>
    <item rdf:about="https://crispr.tyerslab.com/wiki/results/exp466?rev=1767843420&amp;do=diff">
        <dc:format>text/html</dc:format>
        <dc:date>2026-01-08T03:37:00+00:00</dc:date>
        <dc:creator>Anonymous (anonymous@undisclosed.example.com)</dc:creator>
        <title>Cannabidiol 20μM R08 exp466</title>
        <link>https://crispr.tyerslab.com/wiki/results/exp466?rev=1767843420&amp;do=diff</link>
        <description>Cannabidiol 20μM R08 exp466

Mechanism of Action

Negative allosteric modulator of cannabinoid CB1 receptor

	*  Class / Subclass 1: Environmental Stresses / Psychoactive Drug
	*  Class / Subclass 2: Signal Transduction / GPCR Antagonist

Technical Notes</description>
    </item>
    <item rdf:about="https://crispr.tyerslab.com/wiki/results/exp467?rev=1767843420&amp;do=diff">
        <dc:format>text/html</dc:format>
        <dc:date>2026-01-08T03:37:00+00:00</dc:date>
        <dc:creator>Anonymous (anonymous@undisclosed.example.com)</dc:creator>
        <title>CAY10603 0.55μM R08 exp467</title>
        <link>https://crispr.tyerslab.com/wiki/results/exp467?rev=1767843420&amp;do=diff</link>
        <description>CAY10603 0.55μM R08 exp467

Mechanism of Action

Inhibits HDAC6, selective over other HDACs

	*  Class / Subclass 1: Gene Regulation / Epigenetic Inhibitor

Technical Notes

	*  PubChem Name: HDAC6 Inhibitor
		*  Synonyms: BML-281
		*  CAS #: 1045792-66-2</description>
    </item>
    <item rdf:about="https://crispr.tyerslab.com/wiki/results/exp468?rev=1767843420&amp;do=diff">
        <dc:format>text/html</dc:format>
        <dc:date>2026-01-08T03:37:00+00:00</dc:date>
        <dc:creator>Anonymous (anonymous@undisclosed.example.com)</dc:creator>
        <title>CB-5083 0.4μM R08 exp468</title>
        <link>https://crispr.tyerslab.com/wiki/results/exp468?rev=1767843420&amp;do=diff</link>
        <description>CB-5083 0.4μM R08 exp468

Mechanism of Action

Inhibits p97 AAA-ATPase

	*  Class / Subclass 1: Proteostasis / Unfoldase Inhibitor

Technical Notes

	*  PubChem Name: CB-5083
		*  Synonyms: N/A
		*  CAS #: 1542705-92-9
		*  PubChem CID: 73051434
		*  IUPAC:</description>
    </item>
    <item rdf:about="https://crispr.tyerslab.com/wiki/results/exp469?rev=1767843420&amp;do=diff">
        <dc:format>text/html</dc:format>
        <dc:date>2026-01-08T03:37:00+00:00</dc:date>
        <dc:creator>Anonymous (anonymous@undisclosed.example.com)</dc:creator>
        <title>CFI-400945 25μM R08 exp469</title>
        <link>https://crispr.tyerslab.com/wiki/results/exp469?rev=1767843420&amp;do=diff</link>
        <description>CFI-400945 25μM R08 exp469

Mechanism of Action

Inhibits PLK4, blocks centriole duplication, induces mitotic defects and cell death

	*  Class / Subclass 1: Signal Transduction / Kinase Inhibitor
	*  Class / Subclass 2: Cell Cycle / Mitotic Inhibitor</description>
    </item>
    <item rdf:about="https://crispr.tyerslab.com/wiki/results/exp470?rev=1767843420&amp;do=diff">
        <dc:format>text/html</dc:format>
        <dc:date>2026-01-08T03:37:00+00:00</dc:date>
        <dc:creator>Anonymous (anonymous@undisclosed.example.com)</dc:creator>
        <title>Chloroquine 32μM R08 exp470</title>
        <link>https://crispr.tyerslab.com/wiki/results/exp470?rev=1767843420&amp;do=diff</link>
        <description>Chloroquine 32μM R08 exp470

Mechanism of Action

Lysosomotropic agent, prevents sequestration of heme into hemozoin, forms toxic complex with heme, enhances hematin-induced red blood cell lysis, also intercalates into DNA

	*  Class / Subclass 1: Infectious Disease / Antimalarial</description>
    </item>
    <item rdf:about="https://crispr.tyerslab.com/wiki/results/exp471?rev=1767843420&amp;do=diff">
        <dc:format>text/html</dc:format>
        <dc:date>2026-01-08T03:37:00+00:00</dc:date>
        <dc:creator>Anonymous (anonymous@undisclosed.example.com)</dc:creator>
        <title>Cholesterol 0.003 to 0.006 to 0.1μM on day2 then day6 R08 exp471</title>
        <link>https://crispr.tyerslab.com/wiki/results/exp471?rev=1767843420&amp;do=diff</link>
        <description>Cholesterol 0.003 to 0.006 to 0.1μM on day2 then day6 R08 exp471

Mechanism of Action

Major membrane lipid, precursor for the biosynthesis of steroid hormones, bile acids, and vitamin D

	*  Class / Subclass 1: Metabolism / Metabolite

Technical Notes</description>
    </item>
    <item rdf:about="https://crispr.tyerslab.com/wiki/results/exp472?rev=1767843420&amp;do=diff">
        <dc:format>text/html</dc:format>
        <dc:date>2026-01-08T03:37:00+00:00</dc:date>
        <dc:creator>Anonymous (anonymous@undisclosed.example.com)</dc:creator>
        <title>CI-1040 9.5μM R08 exp472</title>
        <link>https://crispr.tyerslab.com/wiki/results/exp472?rev=1767843420&amp;do=diff</link>
        <description>CI-1040 9.5μM R08 exp472

Mechanism of Action

Inhibits MEK1, blocks ERK1/2 activation

	*  Class / Subclass 1: Signal Transduction / Kinase Inhibitor

Technical Notes

	*  PubChem Name: 2-(2-Chloro-4-iodophenylamino)-N-cyclopropylmethoxy-3,4-difluorobenzamide</description>
    </item>
    <item rdf:about="https://crispr.tyerslab.com/wiki/results/exp473?rev=1767843420&amp;do=diff">
        <dc:format>text/html</dc:format>
        <dc:date>2026-01-08T03:37:00+00:00</dc:date>
        <dc:creator>Anonymous (anonymous@undisclosed.example.com)</dc:creator>
        <title>Cincreasin 100μM R08 exp473</title>
        <link>https://crispr.tyerslab.com/wiki/results/exp473?rev=1767843420&amp;do=diff</link>
        <description>Cincreasin 100μM R08 exp473

Mechanism of Action

Inhibits budding yeast Mps1 but not human MPS1 (TTK), overrides spindle checkpoint

	*  Class / Subclass 1: Signal Transduction / Kinase Inhibitor
	*  Class / Subclass 2: Organelle Function / Cytoskeletal Inhibitor</description>
    </item>
    <item rdf:about="https://crispr.tyerslab.com/wiki/results/exp474?rev=1767843420&amp;do=diff">
        <dc:format>text/html</dc:format>
        <dc:date>2026-01-08T03:37:00+00:00</dc:date>
        <dc:creator>Anonymous (anonymous@undisclosed.example.com)</dc:creator>
        <title>CR131-b 0.005μM R08 exp474</title>
        <link>https://crispr.tyerslab.com/wiki/results/exp474?rev=1767843420&amp;do=diff</link>
        <description>CR131-b 0.005μM R08 exp474

Mechanism of Action

Inhibits EIF4A, blocks translation by trapping EIF4A on mRNA at poly-purine sites

	*  Class / Subclass 1: Proteostasis / Translation Inhibitor

Technical Notes

	*  PubChem Name: (1R,2R,3S,3Ar,8bS)-1,8b-dihydroxy-N,6,8-trimethoxy-3a-(4-methoxyphenyl)-3-phenyl-2,3-dihydro-1H-cyclopenta[b][1]benzofuran-2-carboxamide</description>
    </item>
    <item rdf:about="https://crispr.tyerslab.com/wiki/results/exp475?rev=1767843420&amp;do=diff">
        <dc:format>text/html</dc:format>
        <dc:date>2026-01-08T03:37:00+00:00</dc:date>
        <dc:creator>Anonymous (anonymous@undisclosed.example.com)</dc:creator>
        <title>CyclicAMP 200μM R08 exp475</title>
        <link>https://crispr.tyerslab.com/wiki/results/exp475?rev=1767843420&amp;do=diff</link>
        <description>CyclicAMP 200μM R08 exp475

Mechanism of Action

Second messenger, activates PKA, ion channels, cyclic nucleotide-binding proteins

	*  Class / Subclass 1: Metabolism / Metabolite
	*  Class / Subclass 2: Signal Transduction / Kinase Activator

Technical Notes</description>
    </item>
    <item rdf:about="https://crispr.tyerslab.com/wiki/results/exp476?rev=1767843420&amp;do=diff">
        <dc:format>text/html</dc:format>
        <dc:date>2026-01-08T03:37:00+00:00</dc:date>
        <dc:creator>Anonymous (anonymous@undisclosed.example.com)</dc:creator>
        <title>Dihydrosphingosine 8μM R08 exp476</title>
        <link>https://crispr.tyerslab.com/wiki/results/exp476?rev=1767843420&amp;do=diff</link>
        <description>Dihydrosphingosine 8μM R08 exp476

Mechanism of Action

Inhibits cytosolic phospholipase A2α (cPLA2α) activity

	*  Class / Subclass 1: Metabolism / Metabolite

Technical Notes

	*  PubChem Name: Sphinganine
		*  Synonyms: N/A
		*  CAS #: 764-22-7</description>
    </item>
    <item rdf:about="https://crispr.tyerslab.com/wiki/results/exp477?rev=1767843420&amp;do=diff">
        <dc:format>text/html</dc:format>
        <dc:date>2026-01-08T03:37:00+00:00</dc:date>
        <dc:creator>Anonymous (anonymous@undisclosed.example.com)</dc:creator>
        <title>DKK1 89ng/ml R08 exp477</title>
        <link>https://crispr.tyerslab.com/wiki/results/exp477?rev=1767843420&amp;do=diff</link>
        <description>DKK1 89ng/ml R08 exp477

Mechanism of Action

Dickkopf1 (DKK1), recombinant protein inhibitor of WNT signaling, binds LRP5/LRP6 co-receptor and KRM1

	*  Class / Subclass 1: Signal Transduction / GPCR Antagonist

Technical Notes

	*  PubChem Name: N/A</description>
    </item>
    <item rdf:about="https://crispr.tyerslab.com/wiki/results/exp478?rev=1767843420&amp;do=diff">
        <dc:format>text/html</dc:format>
        <dc:date>2026-01-08T03:37:00+00:00</dc:date>
        <dc:creator>Anonymous (anonymous@undisclosed.example.com)</dc:creator>
        <title>Doxorubicin 0.02μM R08 exp478</title>
        <link>https://crispr.tyerslab.com/wiki/results/exp478?rev=1767843420&amp;do=diff</link>
        <description>Doxorubicin 0.02μM R08 exp478

Mechanism of Action

DNA intercalator, traps topoisomerase II complex

	*  Class / Subclass 1: DNA Damage, Repair and Replication / Topoisomerase II Inhibitor
	*  Class / Subclass 2: Infectious Disease / Antibiotic

Technical Notes</description>
    </item>
    <item rdf:about="https://crispr.tyerslab.com/wiki/results/exp480?rev=1767843420&amp;do=diff">
        <dc:format>text/html</dc:format>
        <dc:date>2026-01-08T03:37:00+00:00</dc:date>
        <dc:creator>Anonymous (anonymous@undisclosed.example.com)</dc:creator>
        <title>ETC-159 50μM R08 exp480</title>
        <link>https://crispr.tyerslab.com/wiki/results/exp480?rev=1767843420&amp;do=diff</link>
        <description>ETC-159 50μM R08 exp480

Mechanism of Action

Inhibits PORCN palmitoyl transferase that modifies WNT ligands

	*  Class / Subclass 1: Signal Transduction / Other Inhibitor

Technical Notes

	*  PubChem Name: Etc-159
		*  Synonyms: ETC-1922159
		*  CAS #:</description>
    </item>
    <item rdf:about="https://crispr.tyerslab.com/wiki/results/exp481?rev=1767843420&amp;do=diff">
        <dc:format>text/html</dc:format>
        <dc:date>2026-01-08T03:37:00+00:00</dc:date>
        <dc:creator>Anonymous (anonymous@undisclosed.example.com)</dc:creator>
        <title>Ethambutol 25μM R08 exp481</title>
        <link>https://crispr.tyerslab.com/wiki/results/exp481?rev=1767843420&amp;do=diff</link>
        <description>Ethambutol 25μM R08 exp481

Mechanism of Action

Inhibits arabinosyl transferase, interferes with cell wall formation

	*  Class / Subclass 1: Infectious Disease / Antibiotic

Technical Notes

	*  PubChem Name: Ethambutol Hydrochloride
		*  Synonyms:</description>
    </item>
    <item rdf:about="https://crispr.tyerslab.com/wiki/results/exp482?rev=1767843420&amp;do=diff">
        <dc:format>text/html</dc:format>
        <dc:date>2026-01-08T03:37:00+00:00</dc:date>
        <dc:creator>Anonymous (anonymous@undisclosed.example.com)</dc:creator>
        <title>Fas-L 44ng/ml R08 exp482</title>
        <link>https://crispr.tyerslab.com/wiki/results/exp482?rev=1767843420&amp;do=diff</link>
        <description>Fas-L 44ng/ml R08 exp482

Mechanism of Action

Ligand for Fas receptor, triggers apoptosis

	*  Class / Subclass 1: Signal Transduction / Other Receptor Agonist

Technical Notes

	*  PubChem Name: N/A
		*  Synonyms: N/A
		*  CAS #: N/A
		*  PubChem CID:</description>
    </item>
    <item rdf:about="https://crispr.tyerslab.com/wiki/results/exp483?rev=1767843420&amp;do=diff">
        <dc:format>text/html</dc:format>
        <dc:date>2026-01-08T03:37:00+00:00</dc:date>
        <dc:creator>Anonymous (anonymous@undisclosed.example.com)</dc:creator>
        <title>FTY720 3μM R08 exp483</title>
        <link>https://crispr.tyerslab.com/wiki/results/exp483?rev=1767843420&amp;do=diff</link>
        <description>FTY720 3μM R08 exp483

Mechanism of Action

Agonist of sphingosine 1-phosphate receptor-1 (S1P1), derived from myriocin

	*  Class / Subclass 1: Metabolism / Metabolic Enzyme Inhibitor

Technical Notes

	*  PubChem Name: Fingolimod hydrochloride
		*</description>
    </item>
    <item rdf:about="https://crispr.tyerslab.com/wiki/results/exp484?rev=1767843420&amp;do=diff">
        <dc:format>text/html</dc:format>
        <dc:date>2026-01-08T03:37:00+00:00</dc:date>
        <dc:creator>Anonymous (anonymous@undisclosed.example.com)</dc:creator>
        <title>GSK-J5 1.5μM R08 exp484</title>
        <link>https://crispr.tyerslab.com/wiki/results/exp484?rev=1767843420&amp;do=diff</link>
        <description>GSK-J5 1.5μM R08 exp484

Mechanism of Action

Inactive isomer of GSKJ4

	*  Class / Subclass 1: Gene Regulation / Epigenetic Inhibitor

Technical Notes

	*  PubChem Name: Ethyl 3-[[2-pyridin-3-yl-6-(1,2,4,5-tetrahydro-3-benzazepin-3-yl)pyrimidin-4-yl]amino]propanoate;hydrochloride</description>
    </item>
    <item rdf:about="https://crispr.tyerslab.com/wiki/results/exp485?rev=1767843420&amp;do=diff">
        <dc:format>text/html</dc:format>
        <dc:date>2026-01-08T03:37:00+00:00</dc:date>
        <dc:creator>Anonymous (anonymous@undisclosed.example.com)</dc:creator>
        <title>GSK626616 14μM R08 exp485</title>
        <link>https://crispr.tyerslab.com/wiki/results/exp485?rev=1767843420&amp;do=diff</link>
        <description>GSK626616 14μM R08 exp485

Mechanism of Action

Inhibits DYRK3, prevents stress granule dissolution, mTORC1 release

	*  Class / Subclass 1: Signal Transduction / Kinase Inhibitor

Technical Notes

	*  PubChem Name: 4(5H)-Thiazolone, 2-((2,6-dichlorophenyl)amino)-5-(6-quinoxalinylmethylene)-, (5Z)-</description>
    </item>
    <item rdf:about="https://crispr.tyerslab.com/wiki/results/exp486?rev=1767843420&amp;do=diff">
        <dc:format>text/html</dc:format>
        <dc:date>2026-01-08T03:37:00+00:00</dc:date>
        <dc:creator>Anonymous (anonymous@undisclosed.example.com)</dc:creator>
        <title>Heregulin-B 44ng/ml R08 exp486</title>
        <link>https://crispr.tyerslab.com/wiki/results/exp486?rev=1767843420&amp;do=diff</link>
        <description>Heregulin-B 44ng/ml R08 exp486

Mechanism of Action

EGF family ligand for ErbB receptors, a.k.a. neuregulin-1

	*  Class / Subclass 1: Signal Transduction / Receptor Ligand

Technical Notes

	*  PubChem Name: N/A
		*  Synonyms: N/A
		*  CAS #: N/A
		*</description>
    </item>
    <item rdf:about="https://crispr.tyerslab.com/wiki/results/exp487?rev=1767843420&amp;do=diff">
        <dc:format>text/html</dc:format>
        <dc:date>2026-01-08T03:37:00+00:00</dc:date>
        <dc:creator>Anonymous (anonymous@undisclosed.example.com)</dc:creator>
        <title>Hinokiflavone 12μM R08 exp487</title>
        <link>https://crispr.tyerslab.com/wiki/results/exp487?rev=1767843420&amp;do=diff</link>
        <description>Hinokiflavone 12μM R08 exp487

Mechanism of Action

Putative splicing inhibitor, ROS generation

	*  Class / Subclass 1: Uncharacterized Mechanism / Natural Product
	*  Class / Subclass 2: Gene Regulation / Splicing Inhibitor

Technical Notes

	*  PubChem Name:</description>
    </item>
    <item rdf:about="https://crispr.tyerslab.com/wiki/results/exp488?rev=1767843420&amp;do=diff">
        <dc:format>text/html</dc:format>
        <dc:date>2026-01-08T03:37:00+00:00</dc:date>
        <dc:creator>Anonymous (anonymous@undisclosed.example.com)</dc:creator>
        <title>Hippuristanol 0.12μM R08 exp488</title>
        <link>https://crispr.tyerslab.com/wiki/results/exp488?rev=1767843420&amp;do=diff</link>
        <description>Hippuristanol 0.12μM R08 exp488

Mechanism of Action

Inhibits translation by trapping EIF4A on mRNA at poly-purine sites

	*  Class / Subclass 1: Proteostasis / Translation Inhibitor

Technical Notes

	*  PubChem Name: Hippuristanol
		*  Synonyms: N/A</description>
    </item>
    <item rdf:about="https://crispr.tyerslab.com/wiki/results/exp489?rev=1767843420&amp;do=diff">
        <dc:format>text/html</dc:format>
        <dc:date>2026-01-08T03:37:00+00:00</dc:date>
        <dc:creator>Anonymous (anonymous@undisclosed.example.com)</dc:creator>
        <title>Hippuristanol 0.12μM R08 exp489 no dilution day6</title>
        <link>https://crispr.tyerslab.com/wiki/results/exp489?rev=1767843420&amp;do=diff</link>
        <description>Hippuristanol 0.12μM R08 exp489 no dilution day6

Mechanism of Action

Inhibits translation by trapping EIF4A on mRNA at poly-purine sites

	*  Class / Subclass 1: Proteostasis / Translation Inhibitor

Technical Notes

	*  PubChem Name: Hippuristanol</description>
    </item>
    <item rdf:about="https://crispr.tyerslab.com/wiki/results/exp490?rev=1767843420&amp;do=diff">
        <dc:format>text/html</dc:format>
        <dc:date>2026-01-08T03:37:00+00:00</dc:date>
        <dc:creator>Anonymous (anonymous@undisclosed.example.com)</dc:creator>
        <title>Hydroxychloroquine 30μM R08 exp490</title>
        <link>https://crispr.tyerslab.com/wiki/results/exp490?rev=1767843420&amp;do=diff</link>
        <description>Hydroxychloroquine 30μM R08 exp490

Mechanism of Action

Lysosomotropic agent, prevents sequestration of heme into hemozoin, forms toxic complex with heme, also inhibits TLR 7/9

	*  Class / Subclass 1: Infectious Disease / Antimalarial
	*  Class / Subclass 2:</description>
    </item>
    <item rdf:about="https://crispr.tyerslab.com/wiki/results/exp492?rev=1767843420&amp;do=diff">
        <dc:format>text/html</dc:format>
        <dc:date>2026-01-08T03:37:00+00:00</dc:date>
        <dc:creator>Anonymous (anonymous@undisclosed.example.com)</dc:creator>
        <title>iCRT14 30μM R08 exp492</title>
        <link>https://crispr.tyerslab.com/wiki/results/exp492?rev=1767843420&amp;do=diff</link>
        <description>iCRT14 30μM R08 exp492

Mechanism of Action

Inhibits β-catenin-dependent transcription, may alter interaction of β-catenin with TCF4

	*  Class / Subclass 1: Gene Regulation / Transcription Inhibitor

Technical Notes

	*  PubChem Name: CID 5967294</description>
    </item>
    <item rdf:about="https://crispr.tyerslab.com/wiki/results/exp493?rev=1767843420&amp;do=diff">
        <dc:format>text/html</dc:format>
        <dc:date>2026-01-08T03:37:00+00:00</dc:date>
        <dc:creator>Anonymous (anonymous@undisclosed.example.com)</dc:creator>
        <title>IL-3 9ng/ml R08 exp493</title>
        <link>https://crispr.tyerslab.com/wiki/results/exp493?rev=1767843420&amp;do=diff</link>
        <description>IL-3 9ng/ml R08 exp493

Mechanism of Action

Ligand for IL3RA receptor, induces myeloid lineage proliferation and differentiation

	*  Class / Subclass 1: Signal Transduction / Receptor Ligand

Technical Notes

	*  PubChem Name: N/A
		*  Synonyms: N/A</description>
    </item>
    <item rdf:about="https://crispr.tyerslab.com/wiki/results/exp494?rev=1767843420&amp;do=diff">
        <dc:format>text/html</dc:format>
        <dc:date>2026-01-08T03:37:00+00:00</dc:date>
        <dc:creator>Anonymous (anonymous@undisclosed.example.com)</dc:creator>
        <title>Isoniazid 100μM R08 exp494</title>
        <link>https://crispr.tyerslab.com/wiki/results/exp494?rev=1767843420&amp;do=diff</link>
        <description>Isoniazid 100μM R08 exp494

Mechanism of Action

Inhibits fatty acid synthases, pro-drug activated by catalase-peroxidase KatG

	*  Class / Subclass 1: Infectious Disease / Antibiotic

Technical Notes

	*  PubChem Name: Isoniazid
		*  Synonyms: INH; Isonicotinic acid hydrazide; Isonicotinic hydrazide</description>
    </item>
    <item rdf:about="https://crispr.tyerslab.com/wiki/results/exp495?rev=1767843420&amp;do=diff">
        <dc:format>text/html</dc:format>
        <dc:date>2026-01-08T03:37:00+00:00</dc:date>
        <dc:creator>Anonymous (anonymous@undisclosed.example.com)</dc:creator>
        <title>IWR1 50μM R08 exp495</title>
        <link>https://crispr.tyerslab.com/wiki/results/exp495?rev=1767843420&amp;do=diff</link>
        <description>IWR1 50μM R08 exp495

Mechanism of Action

Stabilizes axin complex, inhibits Wnt/β-catenin signaling, also inhibits tankyrase

	*  Class / Subclass 1: Signal Transduction / Other Inhibitor

Technical Notes

	*  PubChem Name: IWR-1-endo
		*  Synonyms:</description>
    </item>
    <item rdf:about="https://crispr.tyerslab.com/wiki/results/exp496?rev=1767843420&amp;do=diff">
        <dc:format>text/html</dc:format>
        <dc:date>2026-01-08T03:37:00+00:00</dc:date>
        <dc:creator>Anonymous (anonymous@undisclosed.example.com)</dc:creator>
        <title>Lead acetate 990μM R08 exp496</title>
        <link>https://crispr.tyerslab.com/wiki/results/exp496?rev=1767843420&amp;do=diff</link>
        <description>Lead acetate 990μM R08 exp496

Mechanism of Action

Industrial pollutant, heavy metal toxin

	*  Class / Subclass 1: Environmental Stresses / Heavy Metal

Technical Notes

	*  PubChem Name: Lead acetate trihydrate
		*  Synonyms: N/A
		*  CAS #: 6080-56-4</description>
    </item>
    <item rdf:about="https://crispr.tyerslab.com/wiki/results/exp497?rev=1767843420&amp;do=diff">
        <dc:format>text/html</dc:format>
        <dc:date>2026-01-08T03:37:00+00:00</dc:date>
        <dc:creator>Anonymous (anonymous@undisclosed.example.com)</dc:creator>
        <title>Lead acetate 2000μM R08 exp497</title>
        <link>https://crispr.tyerslab.com/wiki/results/exp497?rev=1767843420&amp;do=diff</link>
        <description>Lead acetate 2000μM R08 exp497

Mechanism of Action

Industrial pollutant, heavy metal toxin

	*  Class / Subclass 1: Environmental Stresses / Heavy Metal

Technical Notes

	*  PubChem Name: Lead acetate trihydrate
		*  Synonyms: N/A
		*  CAS #: 6080-56-4</description>
    </item>
    <item rdf:about="https://crispr.tyerslab.com/wiki/results/exp498?rev=1767843420&amp;do=diff">
        <dc:format>text/html</dc:format>
        <dc:date>2026-01-08T03:37:00+00:00</dc:date>
        <dc:creator>Anonymous (anonymous@undisclosed.example.com)</dc:creator>
        <title>Lead acetate 2000μM R08 exp498 no dilution day6</title>
        <link>https://crispr.tyerslab.com/wiki/results/exp498?rev=1767843420&amp;do=diff</link>
        <description>Lead acetate 2000μM R08 exp498 no dilution day6

Mechanism of Action

Industrial pollutant, heavy metal toxin

	*  Class / Subclass 1: Environmental Stresses / Heavy Metal

Technical Notes

	*  PubChem Name: Lead acetate trihydrate
		*  Synonyms: N/A</description>
    </item>
    <item rdf:about="https://crispr.tyerslab.com/wiki/results/exp499?rev=1767843420&amp;do=diff">
        <dc:format>text/html</dc:format>
        <dc:date>2026-01-08T03:37:00+00:00</dc:date>
        <dc:creator>Anonymous (anonymous@undisclosed.example.com)</dc:creator>
        <title>LY2090314 0.003μM R08 exp499</title>
        <link>https://crispr.tyerslab.com/wiki/results/exp499?rev=1767843420&amp;do=diff</link>
        <description>LY2090314 0.003μM R08 exp499

Mechanism of Action

Inhibits glycogen synthase kinase-3 (GSK-3), activates Wnt signalling

	*  Class / Subclass 1: Signal Transduction / Kinase Inhibitor

Technical Notes

	*  PubChem Name: 3-[6-Fluoro-10-(piperidine-1-carbonyl)-1,10-diazatricyclo[6.4.1.04,13]trideca-2,4,6,8(13)-tetraen-3-yl]-4-imidazo[1,2-a]pyridin-3-ylpyrrole-2,5-dione</description>
    </item>
    <item rdf:about="https://crispr.tyerslab.com/wiki/results/exp500?rev=1767843420&amp;do=diff">
        <dc:format>text/html</dc:format>
        <dc:date>2026-01-08T03:37:00+00:00</dc:date>
        <dc:creator>Anonymous (anonymous@undisclosed.example.com)</dc:creator>
        <title>LY2090314 0.003μM R08 exp500 no dilution day6</title>
        <link>https://crispr.tyerslab.com/wiki/results/exp500?rev=1767843420&amp;do=diff</link>
        <description>LY2090314 0.003μM R08 exp500 no dilution day6

Mechanism of Action

Inhibits glycogen synthase kinase-3 (GSK-3), activates Wnt signalling

	*  Class / Subclass 1: Signal Transduction / Kinase Inhibitor

Technical Notes

	*  PubChem Name: 3-[6-Fluoro-10-(piperidine-1-carbonyl)-1,10-diazatricyclo[6.4.1.04,13]trideca-2,4,6,8(13)-tetraen-3-yl]-4-imidazo[1,2-a]pyridin-3-ylpyrrole-2,5-dione</description>
    </item>
    <item rdf:about="https://crispr.tyerslab.com/wiki/results/exp501?rev=1767843420&amp;do=diff">
        <dc:format>text/html</dc:format>
        <dc:date>2026-01-08T03:37:00+00:00</dc:date>
        <dc:creator>Anonymous (anonymous@undisclosed.example.com)</dc:creator>
        <title>Methotrexate 0.01μM R08 exp501</title>
        <link>https://crispr.tyerslab.com/wiki/results/exp501?rev=1767843420&amp;do=diff</link>
        <description>Methotrexate 0.01μM R08 exp501

Mechanism of Action

Inhibits dihydrofolate reductase (DHFR)

	*  Class / Subclass 1: Metabolism / Antimetabolite
	*  Class / Subclass 2: DNA Damage, Repair and Replication / Replication Inhibitor

Technical Notes

	*</description>
    </item>
    <item rdf:about="https://crispr.tyerslab.com/wiki/results/exp502?rev=1767843420&amp;do=diff">
        <dc:format>text/html</dc:format>
        <dc:date>2026-01-08T03:37:00+00:00</dc:date>
        <dc:creator>Anonymous (anonymous@undisclosed.example.com)</dc:creator>
        <title>Milciclib 2μM R08 exp502</title>
        <link>https://crispr.tyerslab.com/wiki/results/exp502?rev=1767843420&amp;do=diff</link>
        <description>Milciclib 2μM R08 exp502

Mechanism of Action

Inhibits CDK2, also TRKA, CDK1, CDK4

	*  Class / Subclass 1: Cell Cycle / Cyclin Dependent Kinase Inhibitor
	*  Class / Subclass 2: Signal Transduction / Kinase Inhibitor

Technical Notes

	*  PubChem Name:</description>
    </item>
    <item rdf:about="https://crispr.tyerslab.com/wiki/results/exp503?rev=1767843420&amp;do=diff">
        <dc:format>text/html</dc:format>
        <dc:date>2026-01-08T03:37:00+00:00</dc:date>
        <dc:creator>Anonymous (anonymous@undisclosed.example.com)</dc:creator>
        <title>Mitomycin-C 0.06μM R08 exp503</title>
        <link>https://crispr.tyerslab.com/wiki/results/exp503?rev=1767843420&amp;do=diff</link>
        <description>Mitomycin-C 0.06μM R08 exp503

Mechanism of Action

DNA crosslinker, reductive activation forms a mitosene that N-alkylates successively DNA bases

	*  Class / Subclass 1: DNA Damage, Repair and Replication / Inter/Intra-strand Crosslinker

Technical Notes</description>
    </item>
    <item rdf:about="https://crispr.tyerslab.com/wiki/results/exp504?rev=1767843420&amp;do=diff">
        <dc:format>text/html</dc:format>
        <dc:date>2026-01-08T03:37:00+00:00</dc:date>
        <dc:creator>Anonymous (anonymous@undisclosed.example.com)</dc:creator>
        <title>MK2206 4μM R08 exp504</title>
        <link>https://crispr.tyerslab.com/wiki/results/exp504?rev=1767843420&amp;do=diff</link>
        <description>MK2206 4μM R08 exp504

Mechanism of Action

Inhibit Akt1, Akt2, Akt3

	*  Class / Subclass 1: Signal Transduction / Kinase Inhibitor

Technical Notes

	*  PubChem Name: MK-2206 dihydrochloride
		*  Synonyms: N/A
		*  CAS #: 1032350-13-2
		*  PubChem CID:</description>
    </item>
    <item rdf:about="https://crispr.tyerslab.com/wiki/results/exp505?rev=1767843420&amp;do=diff">
        <dc:format>text/html</dc:format>
        <dc:date>2026-01-08T03:37:00+00:00</dc:date>
        <dc:creator>Anonymous (anonymous@undisclosed.example.com)</dc:creator>
        <title>ML-792 0.2μM R08 exp505</title>
        <link>https://crispr.tyerslab.com/wiki/results/exp505?rev=1767843420&amp;do=diff</link>
        <description>ML-792 0.2μM R08 exp505

Mechanism of Action

Inhibits SUMO-activating enzyme (SAE)

	*  Class / Subclass 1: Proteostasis / SUMOylation Inhibitor

Technical Notes

	*  PubChem Name: [(1R,2S,4R)-4-[[5-[1-[(3-Bromophenyl)methyl]pyrazole-3-carbonyl]pyrimidin-4-yl]amino]-2-hydroxycyclopentyl]methyl sulfamate</description>
    </item>
    <item rdf:about="https://crispr.tyerslab.com/wiki/results/exp506?rev=1767843420&amp;do=diff">
        <dc:format>text/html</dc:format>
        <dc:date>2026-01-08T03:37:00+00:00</dc:date>
        <dc:creator>Anonymous (anonymous@undisclosed.example.com)</dc:creator>
        <title>Momordin-Ic 10μM R08 exp506</title>
        <link>https://crispr.tyerslab.com/wiki/results/exp506?rev=1767843420&amp;do=diff</link>
        <description>Momordin-Ic 10μM R08 exp506

Mechanism of Action

Triterpenoid saponin, putative SUMO-specific protease 1 (SENP1) inhibitor

	*  Class / Subclass 1: Uncharacterized Mechanism / Traditional Medicine
	*  Class / Subclass 2: Proteostasis / SUMOylation Inhibitor</description>
    </item>
    <item rdf:about="https://crispr.tyerslab.com/wiki/results/exp507?rev=1767843420&amp;do=diff">
        <dc:format>text/html</dc:format>
        <dc:date>2026-01-08T03:37:00+00:00</dc:date>
        <dc:creator>Anonymous (anonymous@undisclosed.example.com)</dc:creator>
        <title>Monensin 0.3μM R08 exp507</title>
        <link>https://crispr.tyerslab.com/wiki/results/exp507?rev=1767843420&amp;do=diff</link>
        <description>Monensin 0.3μM R08 exp507

Mechanism of Action

Polyether antibiotic, binds monovalent cations, Na+/H+ antiporter, blocks Golgi transport

	*  Class / Subclass 1: Infectious Disease / Antibiotic
	*  Class / Subclass 2: Organelle Function / Membrane Ionophore</description>
    </item>
    <item rdf:about="https://crispr.tyerslab.com/wiki/results/exp508?rev=1767843420&amp;do=diff">
        <dc:format>text/html</dc:format>
        <dc:date>2026-01-08T03:37:00+00:00</dc:date>
        <dc:creator>Anonymous (anonymous@undisclosed.example.com)</dc:creator>
        <title>NN-Dimethylsphingosine 2.5μM R08 exp508</title>
        <link>https://crispr.tyerslab.com/wiki/results/exp508?rev=1767843420&amp;do=diff</link>
        <description>NN-Dimethylsphingosine 2.5μM R08 exp508

Mechanism of Action

Inhibits sphingosine kinase, blocks sphingosine 1-phosphate (SPP) formation

	*  Class / Subclass 1: Metabolism / Metabolite
	*  Class / Subclass 2: Signal Transduction / Kinase Inhibitor</description>
    </item>
    <item rdf:about="https://crispr.tyerslab.com/wiki/results/exp510?rev=1767843420&amp;do=diff">
        <dc:format>text/html</dc:format>
        <dc:date>2026-01-08T03:37:00+00:00</dc:date>
        <dc:creator>Anonymous (anonymous@undisclosed.example.com)</dc:creator>
        <title>Nicotine 3000μM R08 exp510</title>
        <link>https://crispr.tyerslab.com/wiki/results/exp510?rev=1767843420&amp;do=diff</link>
        <description>Nicotine 3000μM R08 exp510

Mechanism of Action

Agonist for nicotinic acetylcholine receptors (nAChRs)

	*  Class / Subclass 1: Environmental Stresses / Psychoactive Drug
	*  Class / Subclass 2: Signal Transduction / Other Receptor Agonist

Technical Notes</description>
    </item>
    <item rdf:about="https://crispr.tyerslab.com/wiki/results/exp512?rev=1767843420&amp;do=diff">
        <dc:format>text/html</dc:format>
        <dc:date>2026-01-08T03:37:00+00:00</dc:date>
        <dc:creator>Anonymous (anonymous@undisclosed.example.com)</dc:creator>
        <title>Olaparib 4μM R08 exp512</title>
        <link>https://crispr.tyerslab.com/wiki/results/exp512?rev=1767843420&amp;do=diff</link>
        <description>Olaparib 4μM R08 exp512

Mechanism of Action

Inhibits PARP1 and PARP2, blocks ssDNA break repair, selectively toxic to BRCA1/2 negative cancers

	*  Class / Subclass 1: DNA Damage, Repair and Replication / PARP Inhibitor

Technical Notes

	*  PubChem Name:</description>
    </item>
    <item rdf:about="https://crispr.tyerslab.com/wiki/results/exp513?rev=1767843420&amp;do=diff">
        <dc:format>text/html</dc:format>
        <dc:date>2026-01-08T03:37:00+00:00</dc:date>
        <dc:creator>Anonymous (anonymous@undisclosed.example.com)</dc:creator>
        <title>ONC212 0.15μM R08 exp513</title>
        <link>https://crispr.tyerslab.com/wiki/results/exp513?rev=1767843420&amp;do=diff</link>
        <description>ONC212 0.15μM R08 exp513

Mechanism of Action

Inhibits mitochondrial CLPP protease, more potent derivative of TIC10/ONC201, possible agonist of GPR132

	*  Class / Subclass 1: Proteostasis / Protease Inhibitor
	*  Class / Subclass 2: Signal Transduction / GPCR Agonist</description>
    </item>
    <item rdf:about="https://crispr.tyerslab.com/wiki/results/exp514?rev=1767843420&amp;do=diff">
        <dc:format>text/html</dc:format>
        <dc:date>2026-01-08T03:37:00+00:00</dc:date>
        <dc:creator>Anonymous (anonymous@undisclosed.example.com)</dc:creator>
        <title>Phorbol-12-myristate-13-acetate 0.57μM R08 exp514</title>
        <link>https://crispr.tyerslab.com/wiki/results/exp514?rev=1767843420&amp;do=diff</link>
        <description>Phorbol-12-myristate-13-acetate 0.57μM R08 exp514

Mechanism of Action

Activates PKC isoforms, potent tumour promoter

	*  Class / Subclass 1: Signal Transduction / Kinase Activator

Technical Notes

	*  PubChem Name: Phorbol 12-myristate 13-acetate</description>
    </item>
    <item rdf:about="https://crispr.tyerslab.com/wiki/results/exp515?rev=1767843420&amp;do=diff">
        <dc:format>text/html</dc:format>
        <dc:date>2026-01-08T03:37:00+00:00</dc:date>
        <dc:creator>Anonymous (anonymous@undisclosed.example.com)</dc:creator>
        <title>PU-H71 1μM R08 exp515</title>
        <link>https://crispr.tyerslab.com/wiki/results/exp515?rev=1767843420&amp;do=diff</link>
        <description>PU-H71 1μM R08 exp515

Mechanism of Action

Inhibits HSP90

	*  Class / Subclass 1: Proteostasis / Chaperone Inhibitor

Technical Notes

	*  PubChem Name: 9H-Purine-9-propanamine, 6-amino-8-((6-iodo-1,3-benzodioxol-5-yl)thio)-N-(1-methylethyl)-
		*</description>
    </item>
    <item rdf:about="https://crispr.tyerslab.com/wiki/results/exp516?rev=1767843420&amp;do=diff">
        <dc:format>text/html</dc:format>
        <dc:date>2026-01-08T03:37:00+00:00</dc:date>
        <dc:creator>Anonymous (anonymous@undisclosed.example.com)</dc:creator>
        <title>Pyrazinamide 100μM R08 exp516</title>
        <link>https://crispr.tyerslab.com/wiki/results/exp516?rev=1767843420&amp;do=diff</link>
        <description>Pyrazinamide 100μM R08 exp516

Mechanism of Action

Inhibits growth of Mycobacterium tuberculosis in combination with isoniazid, ethambutanol and rifampicin, converted to active pyrazinamide by pyrazinamidase

	*  Class / Subclass 1: Infectious Disease / Antibiotic</description>
    </item>
    <item rdf:about="https://crispr.tyerslab.com/wiki/results/exp517?rev=1767843420&amp;do=diff">
        <dc:format>text/html</dc:format>
        <dc:date>2026-01-08T03:37:00+00:00</dc:date>
        <dc:creator>Anonymous (anonymous@undisclosed.example.com)</dc:creator>
        <title>Quercetin 20μM R08 exp517</title>
        <link>https://crispr.tyerslab.com/wiki/results/exp517?rev=1767843420&amp;do=diff</link>
        <description>Quercetin 20μM R08 exp517

Mechanism of Action

General kinase inhibitor, may inhibit NF-‘_B, anti-oxidant, putative senolytic

	*  Class / Subclass 1: Signal Transduction / Kinase Inhibitor
	*  Class / Subclass 2: Gene Regulation / Transcription Inhibitor</description>
    </item>
    <item rdf:about="https://crispr.tyerslab.com/wiki/results/exp518?rev=1767843420&amp;do=diff">
        <dc:format>text/html</dc:format>
        <dc:date>2026-01-08T03:37:00+00:00</dc:date>
        <dc:creator>Anonymous (anonymous@undisclosed.example.com)</dc:creator>
        <title>RK-33 8μM R08 exp518</title>
        <link>https://crispr.tyerslab.com/wiki/results/exp518?rev=1767843420&amp;do=diff</link>
        <description>RK-33 8μM R08 exp518

Mechanism of Action

Inhibits DDX3 RNA helicase, causes G1 arrest and apoptosis, broad spectrum anti-viral

	*  Class / Subclass 1: Proteostasis / Translation Inhibitor
	*  Class / Subclass 2: Infectious Disease / Antiviral

Technical Notes</description>
    </item>
    <item rdf:about="https://crispr.tyerslab.com/wiki/results/exp519?rev=1767843420&amp;do=diff">
        <dc:format>text/html</dc:format>
        <dc:date>2026-01-08T03:37:00+00:00</dc:date>
        <dc:creator>Anonymous (anonymous@undisclosed.example.com)</dc:creator>
        <title>RS-1 10μM R08 exp519</title>
        <link>https://crispr.tyerslab.com/wiki/results/exp519?rev=1767843420&amp;do=diff</link>
        <description>RS-1 10μM R08 exp519

Mechanism of Action

Activates DNA binding by RAD51

	*  Class / Subclass 1: DNA Damage, Repair and Replication / Repair Protein Activator

Technical Notes

	*  PubChem Name: 3-(Benzylsulfamoyl)-4-bromo-N-(4-bromophenyl)benzamide</description>
    </item>
    <item rdf:about="https://crispr.tyerslab.com/wiki/results/exp520?rev=1767843420&amp;do=diff">
        <dc:format>text/html</dc:format>
        <dc:date>2026-01-08T03:37:00+00:00</dc:date>
        <dc:creator>Anonymous (anonymous@undisclosed.example.com)</dc:creator>
        <title>Rucaparib 6.5μM R08 exp520</title>
        <link>https://crispr.tyerslab.com/wiki/results/exp520?rev=1767843420&amp;do=diff</link>
        <description>Rucaparib 6.5μM R08 exp520

Mechanism of Action

PARP1/2/3 inhibitor (Clovis), PARP1 mediates single-strand break repair, which can lead to replication-induced double strand breaks to form if not repaired; specifically target cancer with BRCA1, BRCA2 or PALB2 mutations; FDA granted an accelerated approval for use in cases of pretreated advanced ovarian cancer</description>
    </item>
    <item rdf:about="https://crispr.tyerslab.com/wiki/results/exp521?rev=1767843420&amp;do=diff">
        <dc:format>text/html</dc:format>
        <dc:date>2026-01-08T03:37:00+00:00</dc:date>
        <dc:creator>Anonymous (anonymous@undisclosed.example.com)</dc:creator>
        <title>Salinomycin 3.5μM R08 exp521</title>
        <link>https://crispr.tyerslab.com/wiki/results/exp521?rev=1767843420&amp;do=diff</link>
        <description>Salinomycin 3.5μM R08 exp521

Mechanism of Action

Potassium ionophore antibiotic, has activity against cancer stem cells

	*  Class / Subclass 1: Organelle Function / Membrane Ionophore

Technical Notes

	*  PubChem Name: Salinomycin
		*  Synonyms:</description>
    </item>
    <item rdf:about="https://crispr.tyerslab.com/wiki/results/exp524?rev=1767843420&amp;do=diff">
        <dc:format>text/html</dc:format>
        <dc:date>2026-01-08T03:37:00+00:00</dc:date>
        <dc:creator>Anonymous (anonymous@undisclosed.example.com)</dc:creator>
        <title>Staurosporine 0.02μM R08 exp524</title>
        <link>https://crispr.tyerslab.com/wiki/results/exp524?rev=1767843420&amp;do=diff</link>
        <description>Staurosporine 0.02μM R08 exp524

Mechanism of Action

Inhibits many protein kinases including PKC, PKA, tyrosine kinases, CDKs, others

	*  Class / Subclass 1: Signal Transduction / Kinase Inhibitor

Technical Notes

	*  PubChem Name: Staurosporine</description>
    </item>
    <item rdf:about="https://crispr.tyerslab.com/wiki/results/exp525?rev=1767843420&amp;do=diff">
        <dc:format>text/html</dc:format>
        <dc:date>2026-01-08T03:37:00+00:00</dc:date>
        <dc:creator>Anonymous (anonymous@undisclosed.example.com)</dc:creator>
        <title>Sulforaphane 9μM R08 exp525</title>
        <link>https://crispr.tyerslab.com/wiki/results/exp525?rev=1767843420&amp;do=diff</link>
        <description>Sulforaphane 9μM R08 exp525

Mechanism of Action

Organosulfur compound, found in cruciferous plants

	*  Class / Subclass 1: Uncharacterized Mechanism / Natural Product

Technical Notes

	*  PubChem Name: Sulforaphane
		*  Synonyms: N/A
		*  CAS #:</description>
    </item>
    <item rdf:about="https://crispr.tyerslab.com/wiki/results/exp526?rev=1767843420&amp;do=diff">
        <dc:format>text/html</dc:format>
        <dc:date>2026-01-08T03:37:00+00:00</dc:date>
        <dc:creator>Anonymous (anonymous@undisclosed.example.com)</dc:creator>
        <title>Sulforaphane 9μM R08 exp526 no dilution day6</title>
        <link>https://crispr.tyerslab.com/wiki/results/exp526?rev=1767843420&amp;do=diff</link>
        <description>Sulforaphane 9μM R08 exp526 no dilution day6

Mechanism of Action

Organosulfur compound, found in cruciferous plants

	*  Class / Subclass 1: Uncharacterized Mechanism / Natural Product

Technical Notes

	*  PubChem Name: Sulforaphane
		*  Synonyms:</description>
    </item>
    <item rdf:about="https://crispr.tyerslab.com/wiki/results/exp527?rev=1767843420&amp;do=diff">
        <dc:format>text/html</dc:format>
        <dc:date>2026-01-08T03:37:00+00:00</dc:date>
        <dc:creator>Anonymous (anonymous@undisclosed.example.com)</dc:creator>
        <title>Tanespimycin 14μM R08 exp527</title>
        <link>https://crispr.tyerslab.com/wiki/results/exp527?rev=1767843420&amp;do=diff</link>
        <description>Tanespimycin 14μM R08 exp527

Mechanism of Action

Inhibits HSP90, derivative of geldanamycin, a.k.a 17-AAG

	*  Class / Subclass 1: Proteostasis / Chaperone Inhibitor
	*  Class / Subclass 2: Infectious Disease / Antibiotic

Technical Notes

	*  PubChem Name:</description>
    </item>
    <item rdf:about="https://crispr.tyerslab.com/wiki/results/exp528?rev=1767843420&amp;do=diff">
        <dc:format>text/html</dc:format>
        <dc:date>2026-01-08T03:37:00+00:00</dc:date>
        <dc:creator>Anonymous (anonymous@undisclosed.example.com)</dc:creator>
        <title>TGF-beta1 44ng/ml R08 exp528</title>
        <link>https://crispr.tyerslab.com/wiki/results/exp528?rev=1767843420&amp;do=diff</link>
        <description>TGF-beta1 44ng/ml R08 exp528

Mechanism of Action

Ligand for TGF-β1 receptor

	*  Class / Subclass 1: Signal Transduction / Other Receptor Agonist

Technical Notes

	*  PubChem Name: N/A
		*  Synonyms: N/A
		*  CAS #: N/A
		*  PubChem CID: N/A
		*</description>
    </item>
    <item rdf:about="https://crispr.tyerslab.com/wiki/results/exp529?rev=1767843420&amp;do=diff">
        <dc:format>text/html</dc:format>
        <dc:date>2026-01-08T03:37:00+00:00</dc:date>
        <dc:creator>Anonymous (anonymous@undisclosed.example.com)</dc:creator>
        <title>Thimerosal 0.85μM R08 exp529</title>
        <link>https://crispr.tyerslab.com/wiki/results/exp529?rev=1767843420&amp;do=diff</link>
        <description>Thimerosal 0.85μM R08 exp529

Mechanism of Action

Organomercury compound, antiseptic and antifungal, approved preservative in vaccines

	*  Class / Subclass 1: Infectious Disease / Antifungal

Technical Notes

	*  PubChem Name: Thimerosal
		*  Synonyms:</description>
    </item>
    <item rdf:about="https://crispr.tyerslab.com/wiki/results/exp530?rev=1767843420&amp;do=diff">
        <dc:format>text/html</dc:format>
        <dc:date>2026-01-08T03:37:00+00:00</dc:date>
        <dc:creator>Anonymous (anonymous@undisclosed.example.com)</dc:creator>
        <title>Thioridazine 5μM R08 exp530</title>
        <link>https://crispr.tyerslab.com/wiki/results/exp530?rev=1767843420&amp;do=diff</link>
        <description>Thioridazine 5μM R08 exp530

Mechanism of Action

DRD2/4 selectivity, causes cardiac arrhythmia, also has antibiotic activity against M. tuberculosis

	*  Class / Subclass 1: Signal Transduction / GPCR Antagonist

Technical Notes

	*  PubChem Name:</description>
    </item>
    <item rdf:about="https://crispr.tyerslab.com/wiki/results/exp531?rev=1767843420&amp;do=diff">
        <dc:format>text/html</dc:format>
        <dc:date>2026-01-08T03:37:00+00:00</dc:date>
        <dc:creator>Anonymous (anonymous@undisclosed.example.com)</dc:creator>
        <title>THZ1 0.06μM R08 exp531</title>
        <link>https://crispr.tyerslab.com/wiki/results/exp531?rev=1767843420&amp;do=diff</link>
        <description>THZ1 0.06μM R08 exp531

Mechanism of Action

Inhibits CDK7, forms covalent adduct, blocks phosphorylation of the C-terminal domain of RNA polymerase II

	*  Class / Subclass 1: Gene Regulation / Transcription Inhibitor
	*  Class / Subclass 2: Signal Transduction / Kinase Inhibitor</description>
    </item>
    <item rdf:about="https://crispr.tyerslab.com/wiki/results/exp532?rev=1767843420&amp;do=diff">
        <dc:format>text/html</dc:format>
        <dc:date>2026-01-08T03:37:00+00:00</dc:date>
        <dc:creator>Anonymous (anonymous@undisclosed.example.com)</dc:creator>
        <title>TIC10 10μM R08 exp532</title>
        <link>https://crispr.tyerslab.com/wiki/results/exp532?rev=1767843420&amp;do=diff</link>
        <description>TIC10 10μM R08 exp532

Mechanism of Action

Inhibits mitochondrial CLPP protease, a.k.a. ONC201, parent of ONC212, possible agonist of GPR132

	*  Class / Subclass 1: Proteostasis / Protease Inhibitor
	*  Class / Subclass 2: Signal Transduction / GPCR Agonist</description>
    </item>
    <item rdf:about="https://crispr.tyerslab.com/wiki/results/exp533?rev=1767843420&amp;do=diff">
        <dc:format>text/html</dc:format>
        <dc:date>2026-01-08T03:37:00+00:00</dc:date>
        <dc:creator>Anonymous (anonymous@undisclosed.example.com)</dc:creator>
        <title>TNF-alpha 44ng/ml R08 exp533</title>
        <link>https://crispr.tyerslab.com/wiki/results/exp533?rev=1767843420&amp;do=diff</link>
        <description>TNF-alpha 44ng/ml R08 exp533

Mechanism of Action

Ligand for TNFR1, induces apoptosis or necrosis

	*  Class / Subclass 1: Signal Transduction / Other Receptor Agonist

Technical Notes

	*  PubChem Name: N/A
		*  Synonyms: N/A
		*  CAS #: N/A
		*  PubChem CID:</description>
    </item>
    <item rdf:about="https://crispr.tyerslab.com/wiki/results/exp534?rev=1767843420&amp;do=diff">
        <dc:format>text/html</dc:format>
        <dc:date>2026-01-08T03:37:00+00:00</dc:date>
        <dc:creator>Anonymous (anonymous@undisclosed.example.com)</dc:creator>
        <title>Trientine 500μM R08 exp534</title>
        <link>https://crispr.tyerslab.com/wiki/results/exp534?rev=1767843420&amp;do=diff</link>
        <description>Trientine 500μM R08 exp534

Mechanism of Action

Copper-selective chelator, enhances renal excretion of copper

	*  Class / Subclass 1: Environmental Stresses / Metal Chelator

Technical Notes

	*  PubChem Name: Triethylenetetramine
		*  Synonyms: N/A</description>
    </item>
    <item rdf:about="https://crispr.tyerslab.com/wiki/results/exp535?rev=1767843420&amp;do=diff">
        <dc:format>text/html</dc:format>
        <dc:date>2026-01-08T03:37:00+00:00</dc:date>
        <dc:creator>Anonymous (anonymous@undisclosed.example.com)</dc:creator>
        <title>Trimetrexate 0.03μM R08 exp535</title>
        <link>https://crispr.tyerslab.com/wiki/results/exp535?rev=1767843420&amp;do=diff</link>
        <description>Trimetrexate 0.03μM R08 exp535

Mechanism of Action

Inhibits bacterial, protozoan, and mammalian dihydrofolate reductase (DHFR), methotrexate analog

	*  Class / Subclass 1: Metabolism / Antimetabolite
	*  Class / Subclass 2: DNA Damage, Repair and Replication / Replication Inhibitor</description>
    </item>
    <item rdf:about="https://crispr.tyerslab.com/wiki/results/exp536?rev=1767843420&amp;do=diff">
        <dc:format>text/html</dc:format>
        <dc:date>2026-01-08T03:37:00+00:00</dc:date>
        <dc:creator>Anonymous (anonymous@undisclosed.example.com)</dc:creator>
        <title>Vitamin-D3 40μM R08 exp536</title>
        <link>https://crispr.tyerslab.com/wiki/results/exp536?rev=1767843420&amp;do=diff</link>
        <description>Vitamin-D3 40μM R08 exp536

Mechanism of Action

Steroid hormone, converted to active 1,25-dihydroxycholecalciferol (calcitriol), role in calcium homeostasis

	*  Class / Subclass 1: Metabolism / Vitamin
	*  Class / Subclass 2: Metabolism / Metabolite</description>
    </item>
    <item rdf:about="https://crispr.tyerslab.com/wiki/results/exp537?rev=1767843420&amp;do=diff">
        <dc:format>text/html</dc:format>
        <dc:date>2026-01-08T03:37:00+00:00</dc:date>
        <dc:creator>Anonymous (anonymous@undisclosed.example.com)</dc:creator>
        <title>WNT3A 44ng/ml R08 exp537</title>
        <link>https://crispr.tyerslab.com/wiki/results/exp537?rev=1767843420&amp;do=diff</link>
        <description>WNT3A 44ng/ml R08 exp537

Mechanism of Action

Ligand for Frizzled receptor complex, stabilizes ‘_-catenin, induces TCS/LEF-dependent transcription

	*  Class / Subclass 1: Signal Transduction / GPCR Agonist

Technical Notes

	*  PubChem Name: N/A</description>
    </item>
    <item rdf:about="https://crispr.tyerslab.com/wiki/results/exp538?rev=1767843420&amp;do=diff">
        <dc:format>text/html</dc:format>
        <dc:date>2026-01-08T03:37:00+00:00</dc:date>
        <dc:creator>Anonymous (anonymous@undisclosed.example.com)</dc:creator>
        <title>ZLN024 50μM R08 exp538</title>
        <link>https://crispr.tyerslab.com/wiki/results/exp538?rev=1767843420&amp;do=diff</link>
        <description>ZLN024 50μM R08 exp538

Mechanism of Action

Activates AMPK, allosteric

	*  Class / Subclass 1: Signal Transduction / Kinase Activator

Technical Notes

	*  PubChem Name: ZLN024 hydrochloride
		*  Synonyms: N/A
		*  CAS #: 1883548-91-1
		*  PubChem CID:</description>
    </item>
    <item rdf:about="https://crispr.tyerslab.com/wiki/results/exp539?rev=1767843420&amp;do=diff">
        <dc:format>text/html</dc:format>
        <dc:date>2026-01-08T03:37:00+00:00</dc:date>
        <dc:creator>Anonymous (anonymous@undisclosed.example.com)</dc:creator>
        <title>42°C R08 exp539</title>
        <link>https://crispr.tyerslab.com/wiki/results/exp539?rev=1767843420&amp;do=diff</link>
        <description>42°C R08 exp539

Mechanism of Action

Elevated growth temperature

	*  Class / Subclass 1: Environmental Stresses / Stress Condition

Screen Summary

	*  Round: 08
		*  Dose: N/A
		*  Days of incubation: 8
		*  Doublings: -0.5
		*  Numbers of reads: 18691098</description>
    </item>
</rdf:RDF>
