1,2,4-Triazole Derivatives Inhibiting the Human Immunodeficiency Virus Type 1 (HIV-1) in vitro
作者:Irene M. Lagoja、Christophe Pannecouque、Laura Musumeci、Matheus Froeyen、Arthur Van Aerschot、Jan Balzarini、Piet Herdewijn、Erik De Clercq
DOI:10.1002/1522-2675(200207)85:7<1883::aid-hlca1883>3.0.co;2-r
日期:2002.7
A novel series of selective 1,2,4-triazole nonnucleoside reverse transcriptase inhibitors (NNRTIs) is described. In MT-4 cells compound, U inhibited human immunodeficiency virus type I (HIV-1) induced cytopathology at an IC50 of 9.98 muM with a selectivity index of 18.6. The hypothetical docking model of RUM derived from X-ray crystallographic structure of capravirine complex with HIV-1 RT links the activity profile to the H-bonding network.