BIX-02565 |
Inhibitor of RPS6KA3
Probe Summary
Selectivity
Potency
In Vivo
Control Compounds
Chemical Information
References
Vendors
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Probe Summary
| Targets | Biochemical/Biophysical Potency | Cellular Potency |
|---|---|---|
| RPS6KA3 |
|
|
Inhibitor
20 nM
Selectivity
In Vitro Selectivity Assessment
Potency: IC50 - LRRK2 16 nM, PRKD1 35 nM
Potency Assay Off-Target:
In a panel of 20 kinases, BIX-02565 inhibited six of them with IC50 < 1 uM.
In an expanded panel of ...
Selectivity Assessment Description:
Outside target family: Tested in a panel of 68 receptors, ion channels, and protein targets for o ...
Potency Cellular
In Vitro
RPS6KA3
Mode of Action: Inhibitor
Structure-Activity-Relationship data available? No
In Vivo Validations
Rat
Dose: 1,3, 10 (IV) mg/Kg; , 30, 100, 300 (PO) mg/Kg
Route of delivery:
Intravenous, Oral
Reference: --
Orthogonal Probes def
BI-D1870
Chemical Information
| Molecular Formula | C26H30N6O2 |
| SMILEs | C[C@@H]1CCNC(=O)c2cc3ccc(C(=O)Nc4nc5ccccc5n4CCCN(C)C)cc3n21 |
| InChI | InChI=1S/C26H30N6O2/c1-17-11-12-27-25(34)23-15-18-9-10-19(16-22(18)32(17)23)24(33)29-26-28-20-7-4-5-8-21(20)31(26)14-6-13-30(2)3/h4-5,7-10,15-17H,6,11-14H2,1-3H3,(H,27,34)(H,28,29,33)/t17-/m1/s1 |
| Molecular weight | 458.24 Da |
| AlogP | 0.0 |
| HBond acceptors | 8 |
| HBond donors | 2 |
| Atoms | 64 |
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