Department of Medicinal Chemistry, School of Pharmaceutical Sciences, Shandong University, 44, West Culture Road, 250012 Ji'nan, Shandong, PR China.
Bioorg Med Chem. 2012 Jun 15;20(12):3856-64. doi: 10.1016/j.bmc.2012.04.030. Epub 2012 Apr 21.
A novel series of piperidine-linked amino-triazine derivatives were designed, synthesized and evaluated for in vitro anti-HIV activity as non-nucleoside reverse transcriptase inhibitors on the basis of our previous work. Screening results indicated that most compounds showed excellent activity against wild-type HIV-1 with EC(50) values in low nanomolar concentration range (especially compound 6b3, EC(50) = 4.61 nM, SI = 5945) and high activity against K103N/Y181C resistant mutant strain of HIV-1 with EC(50) values in low micromolar concentration range. In addition, preliminary structure-activity relationship and molecular modeling of these new analogs were detailed in this manuscript.
基于我们之前的工作,设计、合成了一系列新型哌啶连接的氨基三嗪衍生物,并将其作为非核苷类逆转录酶抑制剂进行了体外抗 HIV 活性评价。筛选结果表明,大多数化合物对野生型 HIV-1 表现出优异的活性,半数有效浓度(EC(50))值处于纳摩尔浓度范围内(特别是化合物 6b3,EC(50)=4.61 nM,SI=5945),对 K103N/Y181C 耐药突变株 HIV-1 的活性也很高,半数有效浓度(EC(50))值处于微摩尔浓度范围内。此外,本文还详细描述了这些新类似物的初步构效关系和分子模拟。