武汉永璨生物科技有限公司
+86-17702719238 sales@sun-shinechem.com

新产品

编号化学名称Cas号纯度化学结构
S510901Cenicriviroc Mesylate497223-28-698% Min.
Cenicriviroc(代号TAK-652,TBR-652)是用于治疗HIV感染的实验候选药物
512193ITI-214磷酸盐1642303-38-598% Min.
ITI-214 is a potent and selective phosphodiesterase 1 (PDE1) inhibitor. As the clinic
6111901UNC25411612782-86-198% Min.
UNC2541 is a potent and MerTK-specific inhibitor and exhibits sub-micro molar inhibit
112591U-73343142878-12-498% Min.
U-73343 is a negative control (or inactive analogue) of U73122, which is a putative p
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
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,
S-2030414-(2,2,2-三氟乙氧基)苯基硼酸886536-37-495%
g scale to Kg scale may be provided.
2623242-(3-Fluoro-4-isopropoxyphenyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane1350426-06-098% Min.
52004Belnacasan273404-37-898%
Belnacasan (VX-765) 是 VRT-043198 的口服生物活性前药,VRT-043198 是有效
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 /
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