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Synthesis and anti-HIV-1 activity of the conjugates of gossypol with oligopeptides and D-glucosamine 被引量:6
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作者 Jian Yang Ju-Rong Li +4 位作者 Jing-Xiang Yang Long-Long Li wen-jie ouyang Shu-Wen Wu Fang Zhang 《Chinese Chemical Letters》 SCIE CAS CSCD 2014年第7期1052-1056,共5页
A series of novel gossypol derivatives were synthesized and screened for their in vitro anti-HIV- 1I activity. The results showed that replacing the aldehyde groups of gossypol with certain oligopeptides and Dglucosam... A series of novel gossypol derivatives were synthesized and screened for their in vitro anti-HIV- 1I activity. The results showed that replacing the aldehyde groups of gossypol with certain oligopeptides and Dglucosamine not only reduced the cytotoxicity of gossypol derivatives but also enhanced their antiviral activity against HIV-1. Interestingly, D-glucosamine derivative of gossypol that lacked the COONa group also exhibited the same potent anti-HIV-1 activity as oligopeptide derivatives with the COONa group. These compounds blocked the entry of HIV-1ⅢB into target cell. which was similar to T20. Furthermore, the molecular docking analysis rationalized their anti-HIV-1 activity. The results also implied that certain oligopeptides and D-glucosamine were important moities to prepare gossypol derivatives as HIV- 1 entry inhibitors besides certain amino acids. 展开更多
关键词 GOSSYPOL D-Glucosamine derivative Oligopeptide derivative ANTI-HIV-1
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