298708-81-3

298708-81-3

中文名称298708-81-3
中文同义词化合物 T10480L
英文名称Bay 41-4109
英文同义词Bay 41-4109;methyl (R)-4-(2-chloro-4-fluorophenyl)-2-(3,5-difluoropyridin-2-yl)-6-methyl-1,4-dihydropyrimidine-5-carboxylate;BAY41-4109; BAY-41-4109; BAYER 41-4109;Bayer 41-4109;5-Pyrimidinecarboxylic acid, 4-(2-chloro-4-fluorophenyl)-2-(3,5-difluoro-2-pyridinyl)-1,4-dihydro-6-methyl-, methyl ester, (4R)-;BAY-41-4109 (R-isomer);Bay 41 4109,Bay 414109
CAS号298708-81-3
分子式C18H13ClF3N3O2
分子量395.76
EINECS号
相关类别
Mol文件298708-81-3.mol
结构式298708-81-3 结构式

298708-81-3 性质

沸点475.3±45.0 °C(Predicted)
密度1.46±0.1 g/cm3(Predicted)
储存条件Store at -20°C
溶解度DMSO:100 mg/mL (252.68 mM);水:< 0.1 mg/mL(不溶)
酸度系数(pKa)5.43±0.60(Predicted)
形态固体
颜色浅黄至黄色

298708-81-3 用途与合成方法

BAY 41-4109是人乙型肝炎病毒 (HBV) 的有效抑制剂,IC50值为 53 nM。

IC50&Target: 53 nM (HBV)

BAY 41-4109 is able to both accelerate and misdirect capsid assembly in vitro . Preformed capsids are stabilized by BAY 41-4109, up to a ratio of one inhibitor molecule per two dimers. BAY 41-4109 is equally effective at inhibiting HBV DNA release and the cytoplasmic HBcAg level, with IC 50 s of 32.6 and 132 nM in HepG2.2.15 cells, respectively. HBV DNA and HBcAg are inhibited in a dose-dependent manner, indicating that the anti-HBV mechanisms are associated with and dependent on the rate of HBcAg inhibition.

BAY 41-4109 reduces viral DNA in the liver and in the plasma dose-dependently with efficacy comparable to 3TC. BAY 41 -4109 reduces hepatitis B virus core antigen (HBcAg) in livers of HBV-transgenic mice. Pharmacokinetic studies in mice have shown rapid absorption, a bioavailability of 30% and dose-proportional plasma concentrations, about 60% in rats and dogs.BAY41-4109 inhibits virus production in vivo by a mechanism that targets the viral capsid.

安全信息

MSDS信息

更新日期产品编号产品名称CAS号包装价格
2024/04/30HY-100029298708-81-3
Bay 41-4109
298708-81-35mg1300元
2024/04/30HY-100029298708-81-3
Bay 41-4109
298708-81-310mg2200元

298708-81-3 上下游产品信息

"298708-81-3"相关产品信息
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