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CATALOG NOPRODUCT NAMECASPURITYSTRUCTURE
122941Pacritinib(SB1518)937272-79-2≧98.0%
Pacritinib (puh-CRIT-i-nib) is an oral tyrosine kinase inhibitor (TKI) with activity
1662118MK-8931 ( Verubecestat )1286770-55-598% by HPLC/HNMR 
MK-8931(verubecestat)是一种BACE抑制剂,是由默沙东公司研制开发。主
6111110Nastorazepide209219-38-598% 
Nastorazepide (Z-360) is a selective, orally available, 1,5-benzodiazepine-derivative
6121401Vadadustat ( AKB-6548 )1000025-07-998% 
Vadadustat (AKB-6548), a novel, titratable, oral hypoxia-inducible factor prolyl hydr
71161SBI02069651884220-36-398% 
SBI0206965是一种有效的选择性自噬激酶ULK1抑制剂。许多肿瘤变得沉
2017889Roluperidone ( CYR-101 )359625-79-998.0% 
Roluperidone, also known as MIN-101, CYR-101, and MT-210, is a 5-HT2A and sigma 2 rec
121805L-778123 hydrochloride253863-00-298%
L-778123 hydrochloride is an inhibitor of FPTase and GGPTase-I with IC50 of 2 nM and
1711222Asciminib ( ABL001 )1492952-76-799.35%
Asciminib, 也叫ABL001,是一种有效的BCR-ABL的变构抑制剂。ABL001在与尼
181121AZD-5904 618913-30-7>98%
AZD5904是一个有效的口服生物利用率MPO抑制剂。在临床前研究中,AZ
185235Trilaciclib (G1T28)1374743-00-6>98%
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 /
188281Arimoclomol maleate289893-26-198%
Arimoclomol,也被称为BRX-220,能够潜在有用的治疗Niemann-Pick疾病C型
1810163BMS-9861651609392-27-9>99%
BMS-986165是具有选择性、强效、变构抑制剂的酪氨酸激酶2 (Tyk2)。