Inhibition of human immunodeficiency virus type-1 integrase by curcumin

Biochem Pharmacol. 1995 Apr 18;49(8):1165-70. doi: 10.1016/0006-2952(95)98514-a.

Abstract

Curcumin (diferuloylmethane) is the yellow pigment in turmeric (Curcuma longa L.) that is widely used as a spice, food coloring (curry) and preservative. Curcumin exhibits a variety of pharmacological effects including antitumor, anti-inflammatory, and anti-infectious activities and is currently in clinical trials for AIDS patients. The effects of curcumin have been determined on purified human immunodeficiency virus type 1 (HIV-1) integrase. Curcumin has an inhibitory concentration50 (IC50) for strand transfer of 40 microM. Inhibition of an integrase deletion mutant containing only amino acids 50-212 suggests that curcumin interacts with the integrase catalytic core. Two structural analogs, methyl cinnamate and chlorogenic acid, were inactive. Energy minimization studies suggest that the anti-integrase activity of curcumin could be due to an intramolecular stacking of two phenyl rings that brings the hydroxyl groups into close proximity. The present data suggest that HIV-1 integrase inhibition may contribute to the antiviral activity of curcumin. These observations suggest new strategies for antiviral drug development that could be based upon curcumin as a lead compound for the development of inhibitors of HIV-1 integrase.

Publication types

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

MeSH terms

  • Antiviral Agents / pharmacology*
  • Base Sequence
  • Binding Sites
  • Curcumin / pharmacology*
  • DNA Nucleotidyltransferases / antagonists & inhibitors*
  • DNA Nucleotidyltransferases / genetics
  • Dose-Response Relationship, Drug
  • HIV-1 / enzymology*
  • Integrases
  • Molecular Sequence Data
  • Structure-Activity Relationship

Substances

  • Antiviral Agents
  • DNA Nucleotidyltransferases
  • Integrases
  • Curcumin