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PI3K/Akt/mTOR

编号化学名称Cas号纯度化学结构
20633STX-4782883540-92-7≧98.0%
STX-478 是第二代突变体选择性口服 PI3Ka 小分子变构抑制剂。
51802TIC10 ( ONC201 )1616632-77-999.85% 
ONC201 / TIC10是人类TRAIL基因的新型小分子诱导剂,可改善重组TRAIL的
51902AT131481056901-62-2≧98%
AT13148, a first-in-class multi-AGC kinase inhibitor, against gastric cancer cells. A
102703AZD-88351620576-64-8≧98.0%
AZD8835 is a potent and selective inhibitor ofPI3KαandPI3KδwithIC50s of 6.2 and 5.7
161227116Afuresertib HCl1047645-82-8≧98.0%
Afuresertib,也称为GSK2110183,是一种具有潜在抗肿瘤活性的丝氨酸/
21248Giredestrant1953133-47-5≧98.0%
Giredestrant, also known as GDC-9545 and RG6171, is a SERD. GDC-9545 is an orally ava
20618Pirtobrutinib2101700-15-498% Min.
24069Tuvusertib1613200-51-3≧98.0%
Tuvusertib, also known as M-1774 and ATR inhibitor 1, is a ATR inhibitor. M1774 selec
25094Nedisertib ( peposertib )1637542-33-6≧98.0%
Nedisertib,也称为M-3814,MSC2490484A,是一种口服的DNA依赖性蛋白激酶