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Non-peptide entry inhibitors of HIV-1 that target the gp41 coiled coil pocket

Authors :
Steve Anderson
Akhter Molla
Robert J Carrick
Jeffrey R. Huth
Karl A. Walter
Leo W. Barrett
Robert P. Meadows
Kent D. Stewart
Dale J. Kempf
Paul L. Richardson
Clarence J. Maring
Vincent S. Stoll
Edmund D. Matayoshi
Teresa I. Ng
Edward T. Olejniczak
William E. Kohlbrenner
Renaldo Mendoza
Jean M. Severin
Hongmei Mo
Keith F. McDaniel
Rebecca Hutchinson
Source :
Bioorganicmedicinal chemistry letters. 20(2)
Publication Year :
2009

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 3–41 μM. 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.

Details

ISSN :
14643405
Volume :
20
Issue :
2
Database :
OpenAIRE
Journal :
Bioorganicmedicinal chemistry letters
Accession number :
edsair.doi.dedup.....8d5d850f797b63ddc2ee55406990346b