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首页> 外文期刊>Chemical biology and drug design >Design, Synthesis, and Biological Evaluation of 1-(thiophen-2-yl)-9H-pyrido[3,4-b]indole Derivatives as Anti-HIV-1 Agents
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Design, Synthesis, and Biological Evaluation of 1-(thiophen-2-yl)-9H-pyrido[3,4-b]indole Derivatives as Anti-HIV-1 Agents

机译:1-(噻吩-2-基)-9H-吡啶并[3,4-b]吲哚衍生物作为抗HIV-1试剂的设计,合成及生物学评价

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摘要

A novel series of 1-(thiophen-2-yl)-9H-pyrido [3,4-b]indole derivatives were synthesized using DL-tryptophan as starting material. All the compounds were characterized by spectral analysis such as H-1 NMR, Mass, IR, elemental analysis and evaluated for inhibitory potency against HIV-1 replication. Among the reported analogues, compound 7g exhibited significant anti-HIV activity with EC50 0.53m and selectivity index 483; compounds 7e, 7i, and 7o displayed moderate activity with EC50 3.8, 3.8, and 2.8m and selectivity index >105, >105, and 3.85, respectively. Interestingly, compound 7g inhibited p24 antigen expression in acute HIV-1(IIIB) infected cell line C8166 with EC50 1.1m. In this study, we also reported the Lipinski rule of 5 parameters, predicted toxicity profile, drug-likeness, and drug score of the synthesized analogues.
机译:以DL-色氨酸为起始原料合成了一系列新型的1-(噻吩-2-基)-9H-吡啶并[3,4-b]吲哚衍生物。所有化合物均通过光谱分析(例如H-1 NMR,质谱,IR,元素分析)进行表征,并评估其对HIV-1复制的抑制能力。在报道的类似物中,化合物7g表现出显着的抗HIV活性,EC50为0.53m,选择性指数为483。化合物7e,7i和7o表现出中等活性,EC50为3.8、3.8和2.8m,选择性指数分别为> 105,> 105和3.85。有趣的是,化合物7g以EC50 1.1m抑制了急性HIV-1(IIIB)感染的C8166细胞株中p24抗原的表达。在这项研究中,我们还报告了合成类似物的5个参数的Lipinski规则,预测的毒性概况,药物相似性和药物得分。

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