Inhibitory effects on HIV-1 protease of tri-p-coumaroylspermidine from Artemisia caruifolia and related amides

Chem Pharm Bull (Tokyo). 2001 Jul;49(7):915-7. doi: 10.1248/cpb.49.915.

Abstract

From a methanol extract of Artemisia caruifolia, which showed a moderate inhibitory activity on HIV-1 protease in a preliminary screening, N1,N5,N10-tri-p-coumaroylspermidine and three dicaffeoylquinic acids were isolated. The former compound was found to appreciably inhibit HIV-1 protease. Of related amides which were chemically synthesized, N1,N5,N10,N14-tetra-p-coumaroylspermine and N1,N4,N7,N10,N13-penta-p-coumaroylte-traethylenepentamine inhibited HIV-1 protease more potently than N1,N5,N10-tri-p-coumaroylspermidine.

MeSH terms

  • Amides / isolation & purification
  • Amides / pharmacology
  • Artemisia / chemistry*
  • Coumaric Acids / chemistry*
  • Coumaric Acids / pharmacology*
  • HIV Protease Inhibitors / isolation & purification*
  • HIV Protease Inhibitors / pharmacology*
  • Magnetic Resonance Spectroscopy
  • Plant Extracts / pharmacology
  • Spectrometry, Mass, Electrospray Ionization
  • Spermidine / analogs & derivatives
  • Spermidine / chemistry*
  • Spermidine / pharmacology*

Substances

  • Amides
  • Coumaric Acids
  • HIV Protease Inhibitors
  • N1,N5,N10-tris(4-coumaroyl)spermidine
  • Plant Extracts
  • Spermidine