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产品目录

编号化学名称Cas号纯度化学结构
19381Abrocitinib 1622902-68-4>98%
Abrocitinib(PF-04965842)是Pifzer研发的是一种Janus激酶抑制剂药物,目
20294Paltusotine ( CRN-00808 )2172870-89-0≧98.0%
Paltusotine 是一类新型的、口服、选择性、非肽类2型生长抑素受体
51703Luminespib ( NVP-AUY922 ; VER-52296 )747412-49-398%
NVP-AUY922 is an experimental drug candidate for the treatment of cancer. It was disc
51902AT131481056901-62-2≧98%
AT13148, a first-in-class multi-AGC kinase inhibitor, against gastric cancer cells. A
51702AZD12081204144-28-498%
AZD1208 is a potent, highly selective, and orally available Pim kinase inhibitor that
51603AZD64821173900-33-8≧98.0%
AZD6482 is aPI3Kinhibitor withIC50of 10 nM, 8-, 87- and 109-fold more selective to PI
51905CPI-613(Devimistat )95809-78-2≧98.0%
CPI-613( Devimistat ) is an E1 pyruvate dehydrogenase (PDH) modulator that prevents c
52023DCC-2036(Rebastinib)1020172-07-998%
Rebastinib(DCC-2036;DCC2036) is an inhibitor of tyrosine kinases TIE2 and ABL1.Rebast
52021Ganetespib(STA-9090)888216-25-998% 
Ganetespib blocked the ability of HSP90 to bind to biotinylated geldanamycin and disr
52019GSK 26561571337532-29-298% 
GSK2656157 is an ATP-competitive and highly selective inhibitor ofPERKwithIC50of 0.9
2073103Remibrutinib ( LOU064 )1787294-07-898% Min.
Remibrutinib ( LOU064 ) is a Potent and Highly Selective Covalent Inhibitor of Bruton
51608SSR128129E848318-25-298% 
SSR128129E is an orally-active and allostericFGFR1inhibitor withIC50of 1.9 M, while n