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Bay 41-4109

Bay 41-4109

产品编号 T10480L   CAS 298708-81-3

BAY 41-4109 is a potent inhibitor of human hepatitis B virus (HBV)(IC50 : 53 nM).

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Bay 41-4109 Chemical Structure
Bay 41-4109, CAS 298708-81-3
规格 价格/CNY 货期 数量
2 mg ¥ 2,720 5日内发货
25 mg ¥ 17,100 6-8周
50 mg ¥ 22,300 6-8周
100 mg ¥ 34,700 6-8周

Bay 41-4109 的其他形式现货产品:

Bay 41-4109 racemate
其他形式的 Bay 41-4109:
千万补贴 助力科研
BCA蛋白浓度测定试剂盒限时半价
Venetoclax限时半价
产品目录号及名称: Bay 41-4109 (T10480L)
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生物活性
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存储 & 溶解度
参考文献
产品描述 BAY 41-4109 is a potent inhibitor of human hepatitis B virus (HBV)(IC50 : 53 nM).
靶点活性 HBV:53 nM
体外活性 BAY 41-4109 is able to both accelerate and misdirect capsid assembly in vitro and it is equally effective at inhibiting HBV DNA release and the cytoplasmic HBcAg level, with IC50s 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[3]. Preformed capsids are stabilized by BAY 41-4109, up to a ratio of one inhibitor molecule per two dimers[2].
体内活性 BAY41-4109 inhibits virus production in vivo by a mechanism that targets the viral capsid[2]. BAY 41-4109 reduces viral DNA in the liver and in the plasma dose-dependently with efficacy comparable to 3TC and it also 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[1].
分子量 395.76
分子式 C18H13ClF3N3O2
CAS No. 298708-81-3

存储

Powder: -20°C for 3 years | In solvent: -80°C for 1 year

溶解度

DMSO: 100 mg/mL (252.68 mM), Sonication is recommended.

溶液配制表

可选溶剂 浓度 体积 质量 1 mg 5 mg 10 mg 25 mg
DMSO 1 mM 2.5268 mL 12.6339 mL 25.2678 mL 63.1696 mL
5 mM 0.5054 mL 2.5268 mL 5.0536 mL 12.6339 mL
10 mM 0.2527 mL 1.2634 mL 2.5268 mL 6.317 mL
20 mM 0.1263 mL 0.6317 mL 1.2634 mL 3.1585 mL
50 mM 0.0505 mL 0.2527 mL 0.5054 mL 1.2634 mL
100 mM 0.0253 mL 0.1263 mL 0.2527 mL 0.6317 mL

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TargetMol Library Books参考文献

1. Weber O, et al. Inhibition of human hepatitis B virus (HBV) by a novel non-nucleosidic compound in a transgenic mouse model. Antiviral Res. 2002 May;54(2):69-78. 2. Stray SJ, et al. BAY 41-4109 has multiple effects on Hepatitis B virus capsid assembly. J Mol Recognit. 2006 Nov-Dec;19(6):542-8. 3. Wu GY, et al. Inhibition of hepatitis B virus replication by Bay 41-4109 and its association with nucleocapsid disassembly. J Chemother. 2008 Aug;20(4):458-67.

TargetMol Library Books文献引用

1. Yang Y, Yan Y, Yin J, et al. Structure-Based Discovery of N-Sulfonylpiperidine-3-carboxamides as Novel Capsid Assembly Modulators for Potent Inhibition of HBV Replication. Viruses. 2022, 14(2): 348. 2. Yin J, Feng Z, Li Z, et al.Synthesis and evaluation of N-sulfonylpiperidine-3-carboxamide derivatives as capsid assembly modulators inhibiting HBV in vitro and in HBV-transgenic mice.European Journal of Medicinal Chemistry.2023: 115141.
Tenofovir Vonafexor Entecavir monohydrate Paederoside Alisol F Dihydrodehydrodiconiferyl alcohol 9-O-α-L-rhamnopyranoside AT-130 Herpetone

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母液配置方法:2 mg 药物溶于 50 μL DMSO (母液浓度为 40 mg/mL), 如您需要配置的浓度超过该产品的溶解度,请先与我们联系。

体内配方的制备方法:取 50 μL DMSO 主液,加入 300 μL PEG300, 混匀澄清,再加 50 μL Tween 80,混匀澄清,再加 600 μL ddH2O, 混匀澄清。

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Keywords

Bay 41-4109 298708-81-3 Microbiology/Virology HBV Bay 41 4109 Bay 414109 Inhibitor inhibitor inhibit

 

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