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
Technical Notes
Compound References
- PubChem Name: Ixabepilone
- Synonyms: Azaepothilone B; BMS 247550; BMS 247550-1
- CAS #: 219989-84-1
- PubChem CID: 6445540
- IUPAC: (1S,3S,7S,10R,11S,12S,16R)-7,11-dihydroxy-8,8,10,12,16-pentamethyl-3-[(E)-1-(2-methyl-1,3-thiazol-4-yl)prop-1-en-2-yl]-17-oxa-4-azabicyclo[14.1.0]heptadecane-5,9-dione
- INCHI Name: InChI=1S/C27H42N2O5S/c1-15-9-8-10-27(7)22(34-27)12-20(16(2)11-19-14-35-18(4)28-19)29-23(31)13-21(30)26(5,6)25(33)17(3)24(15)32/h11,14-15,17,20-22,24,30,32H,8-10,12-13H2,1-7H3,(H,29,31)/b16-11+/t15-,17+,20-,21-,22-,24-,27+/m0/s1
- INCHI Key: FABUFPQFXZVHFB-PVYNADRNSA-N
- Molecular Weight: 506.7
- Canonical SMILES: CC1CCCC2(C(O2)CC(NC(=O)CC(C(C(=O)C(C1O)C)(C)C)O)C(=CC3=CSC(=N3)C)C)C
- Isomeric SMILES: C[C@H]1CCC[C@@]2([C@@H](O2)C[C@H](NC(=O)C[C@@H](C(C(=O)[C@@H]([C@H]1O)C)(C)C)O)/C(=C/C3=CSC(=N3)C)/C)C
- Molecular Formula: C27H42N2O5S
Compound Supplier
- Supplier Name: Toronto Research Chemicals
- Catalog #: I941990
- Lot #: N/A
Compound Characterization
- HRMS (ESI-TOF) m/z: (M+H)+ Calcd for C27H42N2O5S 507.28872; found 507.28672
Dose Response Curve
- Platform ID: Ixabepilone
- Min: -4.1980; Max: 87.9090
| IC | Concentration (µM) |
|---|---|
| IC10 | N/A |
| IC20 | 0.0030 |
| IC30 | 0.0036 |
| IC40 | 0.0043 |
| IC50 | 0.0050 |
| IC60 | N/A |
| IC70 | N/A |
| IC80 | N/A |
| IC90 | N/A |
Screen Summary
- Round: 04
- Dose: 0.004-0.005µM
- Days of incubation: 8
- Doublings: 6.1
- Numbers of reads: 21290000
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 |
|---|---|---|---|---|---|---|
| 35/7 | Scores |