Abstract
The ectodomain of HIV-1 gp41 mediates the fusion of viral and host cellular membranes. The peptide-based drug Enfuvirtide(1) is precedent that antagonists of this fusion activity may act as anti HIV-agents. Here, NMR screening was used to discover non-peptide leads against this target and resulted in the discovery of a new benzamide 1 series. This series is non-peptide, low molecular weight, and analogs have activity in a cell fusion assay with EC50 values ranging 3-41microM. Structural work on the gp41/benzamide 1 complex was determined by NMR spectroscopy using a designed model peptide system that mimics an open pocket of the fusogenic form of the protein.
Copyright 2009 Elsevier Ltd. All rights reserved.
MeSH terms
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Anti-HIV Agents / chemical synthesis
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Anti-HIV Agents / chemistry*
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Anti-HIV Agents / pharmacology
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Benzamides / chemical synthesis
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Benzamides / chemistry*
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Benzamides / pharmacology
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Crystallography, X-Ray
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Enfuvirtide
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HIV Envelope Protein gp41 / chemistry*
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HIV Envelope Protein gp41 / metabolism
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HIV Envelope Protein gp41 / pharmacology
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HIV Fusion Inhibitors / chemical synthesis
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HIV Fusion Inhibitors / chemistry*
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HIV Fusion Inhibitors / pharmacology
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Humans
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Magnetic Resonance Spectroscopy
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Models, Molecular
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Peptide Fragments / chemistry
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Peptide Fragments / pharmacology
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Protein Binding
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Structure-Activity Relationship
Substances
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Anti-HIV Agents
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Benzamides
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HIV Envelope Protein gp41
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HIV Fusion Inhibitors
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Peptide Fragments
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Enfuvirtide
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benzamide