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
- Class / Subclass 3: Environmental Stresses / Toxin
Technical Notes
Compound References
- PubChem Name: Cytochalasin B
- Synonyms: Phomin
- CAS #: 14930-96-2
- PubChem CID: 5311281
- IUPAC: (1S,4E,6R,10R,12E,14S,15S,17S,18S,19S)-19-benzyl-6,15-dihydroxy-10,17-dimethyl-16-methylidene-2-oxa-20-azatricyclo[12.7.0.01,18]henicosa-4,12-diene-3,21-dione
- INCHI Name: InChI=1S/C29H37NO5/c1-18-9-7-13-22(31)15-16-25(32)35-29-23(14-8-10-18)27(33)20(3)19(2)26(29)24(30-28(29)34)17-21-11-5-4-6-12-21/h4-6,8,11-12,14-16,18-19,22-24,26-27,31,33H,3,7,9-10,13,17H2,1-2H3,(H,30,34)/b14-8+,16-15+/t18-,19-,22-,23+,24+,26+,27-,29-/m1/s1
- INCHI Key: GBOGMAARMMDZGR-TYHYBEHESA-N
- Molecular Weight: 479.6
- Canonical SMILES: CC1CCCC(C=CC(=O)OC23C(C=CC1)C(C(=C)C(C2C(NC3=O)CC4=CC=CC=C4)C)O)O
- Isomeric SMILES: C[C@@H]1CCC[C@H](/C=C/C(=O)O[C@]23[C@@H](/C=C/C1)[C@@H](C(=C)[C@H]([C@H]2[C@@H](NC3=O)CC4=CC=CC=C4)C)O)O
- Molecular Formula: C29H37NO5
Compound Supplier
- Supplier Name: Sigma-Aldrich
- Catalog #: C6762
- Lot #: 086M4129V
Compound Characterization
- HRMS (ESI-TOF) m/z: (M+H)+ Calcd for C29H37NO5 480.27445; found 480.27738
Dose Response Curve
- Platform ID: Cytochalasin_B
- Min: -24.8534; Max: 80.8909
| IC | Concentration (µM) |
|---|---|
| IC10 | N/A |
| IC20 | 0.6851 |
| IC30 | 1.3466 |
| IC40 | 2.6729 |
| IC50 | 5.6719 |
| IC60 | N/A |
| IC70 | N/A |
| IC80 | N/A |
| IC90 | N/A |
Screen Summary
- Round: 07
- Dose: 5µM
- Days of incubation: 8
- Doublings: -0.1
- Numbers of reads: 21844473
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 |
|---|---|---|---|---|---|---|
| 0/71 | Scores |