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产品目录

编号化学名称Cas号纯度化学结构
512193ITI-214磷酸盐1642303-38-598% Min.
ITI-214 is a potent and selective phosphodiesterase 1 (PDE1) inhibitor. As the clinic
52001Selisistat ( EX-527 )49843-98-3≧98.0%
Selisistat 是第一个确定的有效且可渗透细胞的 SIRT1 特异性抑制剂,
6111901UNC25411612782-86-198% Min.
UNC2541 is a potent and MerTK-specific inhibitor and exhibits sub-micro molar inhibit
6111904Lemborexant (E-2006)1369764-02-298% Min.
Lemborexant( E-2006, CAS 1369764-02-2)是食欲素OX 1和OX 2受体的双重拮抗
111891ONC2061638178-87-698% Min.
ONC206 is a chemical analogue of ONC201. ONC206 is a benzyl-flurobenzyl imipridone th
112191Aprocitentan1103522-45-798% Min.
Aprocitentan is an orally active, dual endothelin (ET) receptor antagonist developed
112591U-73343142878-12-498% Min.
U-73343 is a negative control (or inactive analogue) of U73122, which is a putative p
203071CC-900091860875-51-998%
CC-90009 是一种 cereblon (CRBN) E3 连接酶调节剂。CC-90009 与 CRBN 特异性
204302Lerociclib1628256-23-4 (free base)98%
Lerociclib,也称为G1T38,是一种口服,有效和选择性的CDK4 / 6抑制剂
204305ICEC0942 HCl1805789-54-1 (HCl)98% Min.
ICEC0942, also known as PPDA-001 and CT7001, is a potent, orally active and selective
204504Zegocractin ( CM-4620 )1713240-67-5≧98.0%
Zegocractin (CM-4620, Auxora(TM)) 是钙释放激活钙通道蛋白 1(CRAC 通道,
2041232-oxo-5,5-diphenyltetrahydro-4-furancarboxylic acid79371-39-4≧96.0%