编号 | 化学名称 | Cas号 | 纯度 | 化学结构 |
---|---|---|---|---|
20518 | BMS-986141 | 1478711-48-6 | 98% Min. | |
BMS-986141 is an Orally-Active Small-Molecule Antagonist of the Platelet Protease-Act | ||||
20519 | BMS-986120 | 1478712-37-6 | 98% Min. | |
BMS-986120 is a potent and selective oral antagonist of protease-activated receptor-4 | ||||
20618 | Pirtobrutinib | 2101700-15-4 | 98% Min. | |
20650 | Sonrotoclax (BGB-11417) | 2383086-06-2 | ≧98.0% | |
Sonrotoclax is an antineoplastic. | ||||
24004 | T-1095 | 209746-59-8 | ≧96.0% | |
T-1095 is a potent and selective inhibitor of Na+-glucose cotransporters (SGLTs). | ||||
20635 | ERAS-801 ( JGK-068S ) | 2490431-16-6 | ≧98.0% | |
ERAS-801 ( JGK-068S ) 是一种有效的 EGFR 抑制剂。 | ||||
24008 | RNK-05047 | 2503036-46-0 | ≧98.0% | |
RNK-05047 为BRD4降解剂,其在小鼠荷瘤异种移植模型中展现出显著抑 | ||||
24009 | Asengeprast (FT011) | 1001288-58-9 | ≧98.0% | |
Asengeprast (FT011) 是一种抗纤维化剂,降低胶原蛋白 I 和 III 的 mRNA | ||||
24010 | Zasocitinib | 2272904-53-5 | ≧98.0% | |
Zasocitinib是一种作用于非受体酪氨酸蛋白激酶 (TYK2)靶点的抑制 | ||||
24011 | Zongertinib ( BI 1810631 ) | 2728667-27-2 | ≧98.0% | |
Zongertinib [BI 1810631] 是一种人表皮生长因子受体 2 (HER2) 抑制剂。 | ||||
24012 | Zunsemetinib | 1640282-42-3 | ≧98.0% | |
Zunsemetinib是一种在研口服丝裂原活化蛋白激酶活化蛋白激酶2(MK2 | ||||
24013 | Ziftomenib ( KO-539 ) | 2134675-36-6 | ≧98.0% | |
Ziftomenib 是一种口服、有效、选择性的小分子抑制剂,针对 menin 和 |