Literature DB >> 8086132

In vitro susceptibility of clinical isolates of HIV-1 to XM323, a non-peptidyl HIV protease inhibitor.

D L Winslow1, D Mayers, H Scarnati, J Lane, A Bincsik, M J Otto.   

Abstract

OBJECTIVE: To determine the in vitro susceptibility of primary clinical isolates and laboratory strains of HIV-1 to XM323.
METHODS: The AIDS Clinical Trials Group/US Department of Defense p24 antigen-based consensus assay was used to determine in vitro susceptibility of 57 primary clinical isolates and three laboratory strains of HIV-1 to XM323, zidovudine, zalcitabine (ddC), and didanosine (ddI).
RESULTS: The concentrations of compound required to inhibit viral p24 antigen production by 50% [median inhibitory concentration (IC50)] for nucleosides were as follows: zidovudine, 0.001-->5 microM; ddC, < 0.01-0.23 microM; ddI, 0.2-->25 microM). Against both nucleoside susceptible and resistant isolates XM323 exhibited potent inhibition with IC50 values of < 0.02-0.27 microM and IC90 values of 0.03-1.17 microM.
CONCLUSIONS: XM323 is a potent inhibitor of diverse clinical isolates of HIV-1 in vitro and represents a novel class of non-peptidyl inhibitors of HIV-1 protease.

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Year:  1994        PMID: 8086132     DOI: 10.1097/00002030-199406000-00005

Source DB:  PubMed          Journal:  AIDS        ISSN: 0269-9370            Impact factor:   4.177


  2 in total

1.  SPC3, a nontoxic peptide inhibitor of HIV infection.

Authors:  J M Sabatier; S Baghdiguian; N Yahi; H Rochat; J Van Rietschoten; J Fantini
Journal:  In Vitro Cell Dev Biol Anim       Date:  1995-06       Impact factor: 2.416

2.  Autoprocessing: an essential step for the activation of HIV-1 protease.

Authors:  M Wan; M Takagi; B N Loh; X Z Xu; T Imanaka
Journal:  Biochem J       Date:  1996-06-01       Impact factor: 3.857

  2 in total

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