AZD-6482 |
AZD-6482 : ATP competitive inhibitor of PIK3CB
Probe Summary
Selectivity
Potency
In Vivo
Control Compounds
Chemical Information
References
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Probe Summary
| Targets | Biochemical/Biophysical Potency | Cellular Potency |
|---|---|---|
| PIK3CB |
|
|
ATP competitive
0.1 – 0.5 uM
Selectivity
In Vitro Selectivity Assessment
Potency: IC50 - PI3Ka 136 nM, PI3Kd 13.6 nM, PI3Kg 47.8 nM, DNA-PK 53.7 nM, PI3K-C2b 54.1 nM
Potency Assay Off-Target:
In Vitro kinase assay measurements against recombinant PI3Ks and PIKK using SelectScreen (Invitrogen ...
Selectivity Assessment Description:
In Vitro kinase assay showed that AZD-6482 has 200-, 20-, and 70-fold selectivity over p110α, p11 ...
In Cell Selectivity Assessment
Selectivity Assessment Description:
Tested cell proliferation on a large panel of 422 cancer cell lines using high-throughput tumor c ...
Potency Cellular
In Vitro
PIK3CB
Mode of Action: ATP competitive
Structure-Activity-Relationship data available? Yes
DOI Reference: 10.1158/2159-8290.CD-12-0003
In Vivo Validations
Swiss Albino Mice
Dose: 1 mg/Kg (IV), 10 mg/Kg (PO), 10 mg/Kg (IP)
Route of delivery:
Oral
Plasma half life:
2.75 h (IV), 1.1 h (IP)
Systemic clearance:
148 mL/min/Kg (IV)
DOI Reference: 10.1158/2159-8290.CD-12-0003
Chemical Information
| Molecular Formula | C22H24N4O4 |
| SMILEs | Cc1cc([C@@H](C)Nc2ccccc2C(=O)O)c2nc(N3CCOCC3)cc(=O)n2c1 |
| InChI | InChI=1S/C22H24N4O4/c1-14-11-17(15(2)23-18-6-4-3-5-16(18)22(28)29)21-24-19(12-20(27)26(21)13-14)25-7-9-30-10-8-25/h3-6,11-13,15,23H,7-10H2,1-2H3,(H,28,29)/t15-/m1/s1 |
| Molecular weight | 408.18 Da |
| AlogP | 2.710820000000001 |
| HBond acceptors | 8 |
| HBond donors | 2 |
| Atoms | 54 |
References
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