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新型噻唑并苯并咪唑衍生物的合成及抗乙型肝炎病毒活性。

Synthesis and anti-hepatitis B virus activity of a novel class of thiazolylbenzimidazole derivatives.

机构信息

Department of Chemistry, East China Normal University, Shanghai, PR China.

出版信息

Arch Pharm (Weinheim). 2011 Feb;344(2):78-83. doi: 10.1002/ardp.201000167. Epub 2010 Dec 22.

Abstract

Recently, heterocyclic benzimidazole derivatives have been investigated and validated as a promising class of antiviral agents. In this paper, a series of novel thiazolylbenzimidazole derivatives was synthesized and evaluated for their anti-hepatitis B virus (HBV) activity and cytotoxicity on the HepG2.2.15 cell line. Afterwards, the preliminary structure-activity relationship (SAR) was discussed. Compound 8b, with IC(50)  = 1.1 µM and SI > 90.9, was the most promising compound and could be selected as a benchmark compound for further investigation.

摘要

最近,杂环苯并咪唑衍生物已被研究并验证为一类有前途的抗病毒药物。本文合成了一系列新型噻唑基苯并咪唑衍生物,并在 HepG2.2.15 细胞系上评价了它们抗乙型肝炎病毒 (HBV) 的活性和细胞毒性。随后,讨论了初步的构效关系 (SAR)。化合物 8b 的 IC50 为 1.1 μM,SI > 90.9,是最有前途的化合物,可作为进一步研究的基准化合物。

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