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产品目录

编号化学名称Cas号纯度化学结构
17815022,6-二溴苄腈67197-53-998.0% 
2-(2,6-dibroMophenyl)acetonitrile 是有机合成反应中的一个重要合成砌块
90734RSM932A850807-63-5≧98.0%
Choline kinase α (CHKA; here designated as ChoKα) is the first enzyme in the CDP-ch
121805L-778123 hydrochloride253863-00-298%
L-778123 hydrochloride is an inhibitor of FPTase and GGPTase-I with IC50 of 2 nM and
90102Fevipiprant ( NVP-QAW039 )872365-14-5≧98.0%
Fevipiprant (QAW039; NVP-QAW039) is a selective, potent, reversible competitive CRTh2
2073106Lerociclib HCl (G1T38 HCl)2097938-59-3≧98.0%
Lerociclib HCl (G1T38 dihydrochloride)是一种分化型口服CDK4 / 6抑制剂,对
S510902Cenicriviroc ( TAK-652 )497223-25-398% Min.
Cenicriviroc(TAK-652, TBR-652) 是一种CCR2和CCR5受体抑制剂,临床上它被用
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
18381JPH203 HCl ( Nanvuranlat )1597402-27-1≧95.0%
JPH203,也称为KYT- 0353,是一个强有力的和选择性(l型氨基酸转运蛋白
18382eCF506 ( 别名:NXP 900 ) 1914078-41-3≧98.0%
eCF506靶向一种叫做Src酪氨酸激酶的分子,这是乳腺癌细胞生长和传
18435Ritlecitinib ( PF-06651600 )1792180-81-4≧98.0%
Ritlecitinib ( PF-06651600 )是一种有效的选择性JAK3抑制剂,是一种具有
184321Ensartinib ( X396 )1370651-20-9>98%
Ensartinib is an orally available small molecule inhibitor of the receptor tyrosine k
512194Lazertinib1903008-80-998% Min.
Description:Lazertinib is a an orally available third-generation, selective inhibi