Bowman Michael J, Chmielewski Jean
Department of Chemistry, 560 Oval Drive, Purdue University, West Lafayette, IN 47907, USA.
Bioorg Med Chem. 2009 Feb 1;17(3):967-76. doi: 10.1016/j.bmc.2008.02.060. Epub 2008 Mar 11.
There is a great need for alternative modes of inhibition for the design of anti-HIV therapies, due to the increased resistance of HIV to currently approved drugs. A novel strategy for generating potent dimerization inhibitors of HIV-1 protease is described based on sidechain-linked interfacial peptides. In a number of cases the activity of these agents against HIV-1 protease was found to be among the most potent reported, with inhibitory constants in the low nM range.
由于HIV对目前已批准药物的耐药性增加,因此迫切需要用于抗HIV疗法设计的替代抑制模式。本文描述了一种基于侧链连接的界面肽生成HIV-1蛋白酶强效二聚化抑制剂的新策略。在许多情况下,发现这些药物对HIV-1蛋白酶的活性是报道中最有效的之一,其抑制常数在低纳摩尔范围内。