Evaluation of secondary amide replacements in a series of CCR5 antagonists as a means to increase intrinsic membrane permeability. Part 1: Optimization of gem-disubstituted azacycles
作者:Rémy C. Lemoine、Ann C. Petersen、Lina Setti、Jutta Wanner、Andreas Jekle、Gabrielle Heilek、André deRosier、Changhua Ji、Pamela Berry、David Rotstein
DOI:10.1016/j.bmcl.2009.11.072
日期:2010.1
Replacement of a secondary amide with an N-acyl or N-sulfonyl gem-disubstituted azacyle in a series of CCR5 antagonists led to the identification of compounds with excellent in vitro HIV antiviral activity and increased intrinsic membrane permeability.
在一系列CCR5拮抗剂中,用N-酰基或N-磺酰基的宝石二取代的氮杂取代仲酰胺导致鉴定出具有出色的体外HIV抗病毒活性和增加的固有膜通透性的化合物。