BYL-719 |
BYL-719 : ATP competitive inhibitor of PIK3CA
Probe Summary
Selectivity
Potency
In Vivo
Control Compounds
Chemical Information
References
Vendors
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Probe Summary
| Targets | Biochemical/Biophysical Potency | Cellular Potency |
|---|---|---|
| PIK3CA |
|
|
ATP competitive
10 nM - 1 uM
Selectivity
In Vitro Selectivity Assessment
Potency: IC50 - PIK3CB 1200 nM, PIK3CD 290 nM, PIK3CG 250 nM
Potency Assay Off-Target:
In vitro kinase assay.
BYL-719 was >50-fold selective of PIK3CA over 442 kinases in vitro (Ambit). ...
Selectivity Assessment Description:
IC50 for CYP450A > 10 uM
In Cell Selectivity Assessment
Potency: IC50 - PI3KCB 2200 nM, PI3KCD 1200 nM
Potency Cellular
In Vitro
PIK3CA
Mode of Action: ATP competitive
Structure-Activity-Relationship data available? Yes
PMID Reference: 23726034
In Vivo Validations
Rat
Dose: 1 mg/kg
Route of delivery:
Intravenous
Plasma half life:
2. 9 hr
Systemic clearance:
10 mL/min/kg
PMID Reference: 23726034
Orthogonal Probes def
Pictilisib
Chemical Information
| Molecular Formula | C19H22F3N5O2S |
| SMILEs | Cc1nc(NC(=O)N2CCC[C@H]2C(N)=O)sc1-c1ccnc(C(C)(C)C(F)(F)F)c1 |
| InChI | InChI=1S/C19H22F3N5O2S/c1-10-14(11-6-7-24-13(9-11)18(2,3)19(20,21)22)30-16(25-10)26-17(29)27-8-4-5-12(27)15(23)28/h6-7,9,12H,4-5,8H2,1-3H3,(H2,23,28)(H,25,26,29)/t12-/m0/s1 |
| Molecular weight | 441.14 Da |
| AlogP | 3.835020000000002 |
| HBond acceptors | 7 |
| HBond donors | 3 |
| Atoms | 52 |
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