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产品目录

编号化学名称Cas号纯度化学结构
20732Lanraplenib1800046-95-098%
GS-9876(lanraplenib)是一种高度选择性的口服SYK抑制剂,主要用于狼
52004Belnacasan273404-37-898%
Belnacasan (VX-765) 是 VRT-043198 的口服生物活性前药,VRT-043198 是有效
2071401Pimodivir ( VX-787 )1629869-44-898% 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
2073107Trilaciclib hydrochloride (G1T28 hydrochloride)1977495-97-898% 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 /
2073108PF-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
208191OATD-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
2091501AB-6802105904-82-198% 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
20915025-(chloromethyl)-1-propyl-1H-imidazole hydrochloride497223-15-1≧95.0%
5-(chloromethyl)-1-propyl-1H-imidazole hydrochloride 是合成 Cenicriviroc ( TAK-652
2091906BAY-24169642242464-44-298% Min.
BAY-2416964 is a potent and orally active aryl hydrocarbon receptor (AHR) antagonist
20103001ASN0072055597-12-9≧98.0%
ASN007 , a novel oral ERK inhibitor , has shown anti-tumor activity in both solid tum
20103002Senaparib1401682-78-7≧98.0%
Senaparib (IMP4297) is a novel agent targeting PARP (poly-ADP ribose polymerase) with
201030042,6-二氟-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