编号 | 化学名称 | Cas号 | 纯度 | 化学结构 |
---|---|---|---|---|
51603 | AZD6482 | 1173900-33-8 | ≧98.0% | |
AZD6482 is aPI3Kinhibitor withIC50of 10 nM, 8-, 87- and 109-fold more selective to PI | ||||
51905 | CPI-613(Devimistat ) | 95809-78-2 | ≧98.0% | |
CPI-613( Devimistat ) is an E1 pyruvate dehydrogenase (PDH) modulator that prevents c | ||||
52023 | DCC-2036(Rebastinib) | 1020172-07-9 | 98% | |
Rebastinib(DCC-2036;DCC2036) is an inhibitor of tyrosine kinases TIE2 and ABL1.Rebast | ||||
52019 | GSK 2656157 | 1337532-29-2 | 98% | |
GSK2656157 is an ATP-competitive and highly selective inhibitor ofPERKwithIC50of 0.9 | ||||
51608 | SSR128129E | 848318-25-2 | 98% | |
SSR128129E is an orally-active and allostericFGFR1inhibitor withIC50of 1.9 M, while n | ||||
51607 | VE-822 ( Berzosertib ) | 1232416-25-9 | ≧98.0% | |
VE-822(Berzosertib), an analogue of VE-821 with increased potency and selectivity aga | ||||
52003 | Zosuquidar trihydrochloride | 167465-36-3 | 99% | |
zosuquidar trihydrochloride is adifluorocyclopropyl quinoline. Zosuquidar trihydrochl | ||||
52105 | SNS-032 ( BMS-387032 ) | 345627-80-7 | 98% | |
SNS-032 has firstly been described as a selective inhibitor ofCDK2withIC50of 48 nM an | ||||
51614 | AMG-925 | 1401033-86-0 | 98% | |
AMG-925 is a potent and orally bioavailable dual inhibitor of CDK4 and FLT3, includin | ||||
52026 | AMG-319 | 1608125-21-8 | 98% | |
AMG 319 is an investigational, highly selective, small molecule inhibitor of PI3K tha | ||||
71805 | Capivasertib ( AZD5363 ) | 1143532-39-1 | 98% | |
Capivasertib是一种新型的吡咯并嘧啶衍生物,是一种可口服的丝氨酸 | ||||
90731 | GDC-0810 ( Brilanestrant , ARN-810 ) | 1365888-06-7 | ≧98.0% | |
GDC-0810 (Brilanestrant, ARN-810, RG6046) is a selective estrogen receptor degrader ( |