Development of HIV entry inhibitors targeted to the coiled-coil regions of gp41

Biochem Biophys Res Commun. 2000 Mar 24;269(3):641-6. doi: 10.1006/bbrc.1999.1972.

Abstract

The discoveries that synthetic peptides corresponding to the N- and C-terminal heptad repeat (HR) regions of gp41 have potent anti-HIV activity opened a new avenue to identification of small molecule HIV entry inhibitors targeted to the HIV gp41 coiled-coil regions. Based on the structural information of the HIV gp41 core, three distinct approaches to develop small molecule anti-HIV agents have been reported. Each of these approaches has specific advantages, which will have complementary effects on the design of new strategies for identification of more potent HIV entry inhibitors. It is expected that novel antiviral drugs targeted to the HIV gp41 coiled-coil regions will be developed in the near future for the chemotherapy and/or prophylaxis of HIV infection and AIDS.

Publication types

  • Research Support, Non-U.S. Gov't
  • Research Support, U.S. Gov't, P.H.S.
  • Review

MeSH terms

  • Amino Acid Sequence
  • Anti-HIV Agents / chemistry*
  • Anti-HIV Agents / pharmacology*
  • Drug Design
  • HIV Envelope Protein gp41 / chemistry*
  • HIV Envelope Protein gp41 / drug effects
  • HIV Envelope Protein gp41 / physiology*
  • HIV-1 / drug effects
  • HIV-1 / physiology*
  • Humans
  • Molecular Sequence Data
  • Peptides / chemistry
  • Peptides / pharmacology*

Substances

  • Anti-HIV Agents
  • HIV Envelope Protein gp41
  • Peptides