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Antiviral activity of GW678248, a novel benzophenone nonnucleoside reverse transcriptase inhibitor.

Authors :
Ferris RG
Hazen RJ
Roberts GB
St Clair MH
Chan JH
Romines KR
Freeman GA
Tidwell JH
Schaller LT
Cowan JR
Short SA
Weaver KL
Selleseth DW
Moniri KR
Boone LR
Source :
Antimicrobial agents and chemotherapy [Antimicrob Agents Chemother] 2005 Oct; Vol. 49 (10), pp. 4046-51.
Publication Year :
2005

Abstract

The compound GW678248 is a novel benzophenone nonnucleoside reverse transcriptase inhibitor (NNRTI). Preclinical assessment of GW678248 indicates that this compound potently inhibits wild-type (WT) and mutant human immunodeficiency virus type 1 (HIV-1) reverse transcriptase in biochemical assays, with 50% inhibitory concentrations (IC(50)s) between 0.8 and 6.8 nM. In HeLa CD4 MAGI cell culture virus replication assays, GW678248 has an IC(50) of < or =21 nM against HIV-1 isogenic strains with single or double mutations known to be associated with NNRTI resistance, including L100I, K101E, K103N, V106A/I/M, V108I, E138K, Y181C, Y188C, Y188L, G190A/E, P225H, and P236L and various combinations. An IC(50) of 86 nM was obtained with a mutant virus having V106I, E138K, and P236L mutations that resulted from serial passage of WT virus in the presence of GW678248. The presence of 45 mg/ml human serum albumin plus 1 mg/ml alpha-1 acid glycoprotein increased the IC(50) approximately sevenfold. Cytotoxicity studies with GW678248 indicate that the 50% cytotoxicity concentration is greater than the level of compound solubility and provides a selectivity index of >2,500-fold for WT, Y181C, or K103N HIV-1. This compound exhibits excellent preclinical antiviral properties and, as a prodrug designated GW695634, is being developed as a new generation of NNRTI for the treatment of HIV-1 in combination with other antiretroviral agents.

Details

Language :
English
ISSN :
0066-4804
Volume :
49
Issue :
10
Database :
MEDLINE
Journal :
Antimicrobial agents and chemotherapy
Publication Type :
Academic Journal
Accession number :
16189079
Full Text :
https://doi.org/10.1128/AAC.49.10.4046-4051.2005