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
Technical Notes
Compound References
- PubChem Name: Etoposide
- Synonyms: VP-16; VP-16-213
- CAS #: 33419-42-0
- PubChem CID: 36462
- IUPAC: (5S,5aR,8aR,9R)-5-[[(2R,4aR,6R,7R,8R,8aS)-7,8-dihydroxy-2-methyl-4,4a,6,7,8,8a-hexahydropyrano[3,2-d][1,3]dioxin-6-yl]oxy]-9-(4-hydroxy-3,5-dimethoxyphenyl)-5a,6,8a,9-tetrahydro-5H-[2]benzofuro[6,5-f][1,3]benzodioxol-8-one
- INCHI Name: InChI=1S/C29H32O13/c1-11-36-9-20-27(40-11)24(31)25(32)29(41-20)42-26-14-7-17-16(38-10-39-17)6-13(14)21(22-15(26)8-37-28(22)33)12-4-18(34-2)23(30)19(5-12)35-3/h4-7,11,15,20-22,24-27,29-32H,8-10H2,1-3H3/t11-,15+,20-,21-,22+,24-,25-,26-,27-,29+/m1/s1
- INCHI Key: VJJPUSNTGOMMGY-MRVIYFEKSA-N
- Molecular Weight: 588.6
- Canonical SMILES: CC1OCC2C(O1)C(C(C(O2)OC3C4COC(=O)C4C(C5=CC6=C(C=C35)OCO6)C7=CC(=C(C(=C7)OC)O)OC)O)O
- Isomeric SMILES: C[C@@H]1OC[C@@H]2[C@@H](O1)[C@@H]([C@H]([C@@H](O2)O[C@H]3[C@H]4COC(=O)[C@@H]4[C@@H](C5=CC6=C(C=C35)OCO6)C7=CC(=C(C(=C7)OC)O)OC)O)O
- Molecular Formula: C29H32O13
Compound Supplier
- Supplier Name: Sigma-Aldrich
- Catalog #: E1383
- Lot #: N/A
Compound Characterization
- HRMS (ESI-TOF) m/z: (M+H)+ Calcd for C29H32O13 589.19157; found 589.19262
Dose Response Curve
- Platform ID: Etoposide
- Min: -33.3567; Max: 88.0314
| IC | Concentration (µM) |
|---|---|
| IC10 | N/A |
| IC20 | 0.1877 |
| IC30 | 0.2644 |
| IC40 | 0.3501 |
| IC50 | 0.4531 |
| IC60 | N/A |
| IC70 | N/A |
| IC80 | N/A |
| IC90 | N/A |
Screen Summary
- Round: 05
- Dose: 100nM
- Days of incubation: 8
- Doublings: 2.5
- Numbers of reads: 14351214
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 |
|---|---|---|---|---|---|---|
| 30/46 | Scores |