编号 | 化学名称 | Cas号 | 纯度 | 化学结构 |
---|---|---|---|---|
52004 | Belnacasan | 273404-37-8 | 98% | |
Belnacasan (VX-765) 是 VRT-043198 的口服生物活性前药,VRT-043198 是有效 | ||||
2071401 | Pimodivir ( VX-787 ) | 1629869-44-8 | 98% Min. | |
Pimodivir (VX-787) 是一种可口服的甲型流感病毒聚合酶抑制剂,通过 | ||||
2073107 | Trilaciclib hydrochloride (G1T28 hydrochloride) | 1977495-97-8 | 98% Min. | |
Trilaciclib是一种小分子竞争性细胞周期蛋白依赖性激酶4和6(CDK4 / | ||||
2073108 | PF-06802861 ( ARRY 371797 ; ARRY-797 ) | 1034189-82-6 | ≧98.0% | |
ARRY 797(也称为ARRY 371797或PF 06802861)是一种具有口服活性,选择性 | ||||
208191 | OATD-01 (GLPG-4716) | 2088453-21-6 | ≧98.0% | |
OATD-01 (GLPG-4716)是一种有效的酸性哺乳动物几丁质酶(AMCase)和壳 | ||||
2091501 | AB-680 | 2105904-82-1 | 98% Min. | |
AB-680一种是高效、可逆和选择性CD73抑制剂。AB-680是第一个临床使 | ||||
2091502 | 5-(chloromethyl)-1-propyl-1H-imidazole hydrochloride | 497223-15-1 | ≧95.0% | |
5-(chloromethyl)-1-propyl-1H-imidazole hydrochloride 是合成 Cenicriviroc ( TAK-652 | ||||
2091906 | BAY-2416964 | 2242464-44-2 | 98% Min. | |
BAY-2416964 is a potent and orally active aryl hydrocarbon receptor (AHR) antagonist | ||||
20103001 | ASN007 | 2055597-12-9 | ≧98.0% | |
ASN007 , a novel oral ERK inhibitor , has shown anti-tumor activity in both solid tum | ||||
20103002 | Senaparib | 1401682-78-7 | ≧98.0% | |
Senaparib (IMP4297) is a novel agent targeting PARP (poly-ADP ribose polymerase) with | ||||
20103004 | 2,6-二氟-3,5-二甲氧基苯胺 | 651734-54-2 | ≧98.0% | |
2,6-difluoro-3,5-dimethoxybenzeneamine is a key intermeidate ofPemigatinib.1Kg~10Kg s | ||||
201221 | Razuprotafib sodium | 1809275-69-1 | ≧98.0% | |
Razuprotafib,也称为AKB-9778,是血管内皮蛋白酪氨酸磷酸酶(VE-PTP) |