作者:You Seok Hwang、Jean Chmielewski
DOI:10.1021/jm049581j
日期:2005.3.1
The role of HIV protease in viral replication has made it a significant target for inhibition. The focus of our studies is to target the dimerization interface of HIV-1 protease because disruption of the dimer will inhibit enzymatic activity. The initial strategy began with cross-linked peptides derived from the interface of HIV protease. Herein we describe the design of a focused library of agents
HIV蛋白酶在病毒复制中的作用使其成为重要的抑制靶标。我们研究的重点是针对HIV-1蛋白酶的二聚界面,因为二聚体的破坏会抑制酶的活性。最初的策略始于源自HIV蛋白酶界面的交联肽。在本文中,我们描述了基于HIV-1蛋白酶二聚化抑制作用的最小药效基团的试剂集中库的设计。