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pubmed-article:20639110pubmed:abstractTextA series of novel benzimidazole derivatives were synthesized and evaluated for their anti-hepatitis B virus (HBV) activity and cytotoxicity in the HepG2.2.15 cell line. The preliminary SAR was discussed. Compound 12a, with IC50<0.41 microM and SI>81.2, was the most promising compound and selected as the benchmark compound for further optimization.lld:pubmed
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pubmed-article:20639110pubmed:authorpubmed-author:YangLiLlld:pubmed
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pubmed-article:20639110pubmed:authorpubmed-author:WangGui-FengG...lld:pubmed
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pubmed-article:20639110pubmed:copyrightInfoCopyright (c) 2010 Elsevier Ltd. All rights reserved.lld:pubmed
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pubmed-article:20639110pubmed:year2010lld:pubmed
pubmed-article:20639110pubmed:articleTitleDesign and synthesis of novel benzimidazole derivatives as inhibitors of hepatitis B virus.lld:pubmed
pubmed-article:20639110pubmed:affiliationDepartment of Chemistry, East China Normal University, 3663 North Zhongshan Road, Shanghai 200062, PR China.lld:pubmed
pubmed-article:20639110pubmed:publicationTypeJournal Articlelld:pubmed
pubmed-article:20639110pubmed:publicationTypeResearch Support, Non-U.S. Gov'tlld:pubmed
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