首页> 外文期刊>Journal of Medicinal Chemistry >Conjugation of a Nonspecific Antiviral Sapogenin with a Specific HIV Fusion Inhibitor: A Promising Strategy for Discovering New Antiviral Therapeutics
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Conjugation of a Nonspecific Antiviral Sapogenin with a Specific HIV Fusion Inhibitor: A Promising Strategy for Discovering New Antiviral Therapeutics

机译:非特异性抗病毒皂苷元与特定的HIV融合抑制剂的结合:发现新的抗病毒治疗药物的有前途的策略。

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摘要

Triterpene saponins are a major group of active components in natural products with nonspecific antiviral activities, while T20 peptide (enfuvirtide), which contains a helix zone-binding domain (HBD), is a gp41-specific HIV-1 fusion inhibitor. In this paper, we report the design, synthesis, and structure?activity relationship (SAR) of a group of hybrid molecules in which bioactive triterpene sapogenins were covalently attached to the HBD-containing peptides via click chemistry. We found that either the triterpenes or peptide part alone showed weak activity against HIV-1 Env-mediated cell?cell fusion, while the hybrids generated a strong cooperative effect. Among them, P26?BApc exhibited anti-HIV-1 activity against both T20-sensitive and -resistant HIV-1 strains and improved pharmacokinetic properties. These results suggest that this scaffold design is a promising strategy for developing new HIV-1 fusion inhibitors and possibly novel antiviral therapeutics against other viruses with class I fusion proteins.
机译:三萜皂苷是天然产物中具有非特异性抗病毒活性的主要活性成分,而包含螺旋区结合域(HBD)的T20肽(恩夫韦肽)是gp41特异性HIV-1融合抑制剂。在本文中,我们报告了一组杂化分子的设计,合成和结构活性关系(SAR),在杂化分子中,生物活性三萜皂苷元通过点击化学共价连接到含有HBD的肽上。我们发现,三萜或单独的肽部分对HIV-1 Env介导的细胞与细胞融合均显示出弱的活性,而杂种产生了很强的协同作用。其中,P26ΔBApc对T20敏感和耐药HIV-1菌株均具有抗HIV-1活性,并具有改善的药代动力学特性。这些结果表明,该支架设计是开发新的HIV-1融合抑制剂以及可能针对具有I类融合蛋白的其他病毒的新型抗病毒治疗剂的有前途的策略。

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