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
Compound References
- PubChem Name: N-(3-Aminopropyl)-N-[(1R)-1-(3-benzyl-7-chloro-4-oxochromen-2-yl)-2-methylpropyl]-4-methylbenzamide;hydrochloride
- Synonyms: N/A
- CAS #: 940929-33-9
- PubChem CID: 49867937
- IUPAC: N-(3-aminopropyl)-N-[(1R)-1-(3-benzyl-7-chloro-4-oxochromen-2-yl)-2-methylpropyl]-4-methylbenzamide;hydrochloride
- INCHI Name: InChI=1S/C31H33ClN2O3.ClH/c1-20(2)28(34(17-7-16-33)31(36)23-12-10-21(3)11-13-23)30-26(18-22-8-5-4-6-9-22)29(35)25-15-14-24(32)19-27(25)37-30;/h4-6,8-15,19-20,28H,7,16-18,33H2,1-3H3;1H/t28-;/m1./s1
- INCHI Key: MLMZVWABFOLFGV-LNLSOMNWSA-N
- Molecular Weight: 553.5
- Canonical SMILES: CC1=CC=C(C=C1)C(=O)N(CCCN)C(C2=C(C(=O)C3=C(O2)C=C(C=C3)Cl)CC4=CC=CC=C4)C(C)C.Cl
- Isomeric SMILES: CC1=CC=C(C=C1)C(=O)N(CCCN)[C@@H](C2=C(C(=O)C3=C(O2)C=C(C=C3)Cl)CC4=CC=CC=C4)C(C)C.Cl
- Molecular Formula: C31H34Cl2N2O3
Compound Supplier
- Supplier Name: N/A
- Catalog #: N/A
- Lot #: N/A
Compound Characterization
Characterization data not available.
Dose Response Curve
- Platform ID: SB743921
- Min: -3.7906; Max: 93.6518
| IC | Concentration (µM) |
|---|---|
| IC10 | N/A |
| IC20 | 0.0006 |
| IC30 | 0.0007 |
| IC40 | 0.0007 |
| IC50 | 0.0008 |
| IC60 | N/A |
| IC70 | N/A |
| IC80 | N/A |
| IC90 | N/A |
Screen Summary
- Round: 05
- Dose: 1nM
- Days of incubation: 8
- Doublings: -0.0
- Numbers of reads: 22832707
Screen Results
| Sensitive/Resistant hits (FDR<0.05) | CRANKS | Score Plot | Top 30 Genes | Screen Similarity | Top 30 Sensitive GO terms | Top 30 Resistant GO terms |
|---|---|---|---|---|---|---|
| 0/155 | Scores |