RO2468 |
Antagonist of MDM2
Probe Summary
Selectivity
Potency
In Vivo
Control Compounds
Chemical Information
References
Vendors
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Probe Summary
| Targets | Biochemical/Biophysical Potency | Cellular Potency |
|---|---|---|
| MDM2 |
|
|
Antagonist
up to 1 uM
Selectivity
Potency Cellular
In Vitro
MDM2
Mode of Action: Antagonist
Structure-Activity-Relationship data available? No
In Vivo Validations
Male C57 mice, Female nude mice
Dose: 10 mg/Kg QD
Route of delivery:
Intravenous, Oral
Plasma half life:
3 h (IV)
Systemic clearance:
1,8 mL/min/kg (IV)
Organ of interest (O):
SJSA-1 xenografts (nude mice, 3-20 mg/kg)
Reference: --
Chemical Information
| Molecular Formula | C30H30Cl2FN5O4 |
| SMILEs | COc1cc(C(N)=O)ccc1NC(=O)[C@@H]1N[C@@H](CC(C)(C)C)[C@@]2(C(=O)Nc3cc(Cl)ncc32)[C@H]1c1cccc(Cl)c1F |
| InChI | InChI=1S/C30H30Cl2FN5O4/c1-29(2,3)12-21-30(16-13-35-22(32)11-19(16)37-28(30)41)23(15-6-5-7-17(31)24(15)33)25(38-21)27(40)36-18-9-8-14(26(34)39)10-20(18)42-4/h5-11,13,21,23,25,38H,12H2,1-4H3,(H2,34,39)(H,36,40)(H,37,41)/t21-,23-,25+,30+/m0/s1 |
| Molecular weight | 613.17 Da |
| AlogP | 5.024 |
| HBond acceptors | 9 |
| HBond donors | 5 |
| Atoms | 72 |