Two new resveratrol tetramers isolated from Cayratia japonica (Thunb.) Gagn. with strong inhibitory activity on fatty acid synthase and antioxidant activity

Chem Biodivers. 2010 Dec;7(12):2931-40. doi: 10.1002/cbdv.200900394.

Abstract

Two new resveratrol tetramers, cajyphenol A (1) and cajyphenol B (2), together with two known resveratrol dimers, quadrangularin A (3) and pallidol (4), and resveratrol (5) were isolated from the stems of Cayratia japonica (Thunb.) Gagn. Their structures were established by means of NMR (¹H,¹H-COSY, ¹H, ¹³C-HSQC, HMBC, and NOESY) and ESI-MS analyses. Compounds 1-5 showed fast-binding inhibitory activities on fatty acid synthase with the IC₅₀ values of 1.63±0.02, 1.49±0.03, 7.50±0.01, 11.1±0.01, and 10.2±0.01 μM, respectively. Compounds 1-5 also exhibited antioxidant activities in the ORAC assay.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Antioxidants / chemistry*
  • Antioxidants / isolation & purification
  • Antioxidants / pharmacology
  • Fatty Acid Synthases / antagonists & inhibitors*
  • Fatty Acid Synthases / metabolism
  • Indenes / chemistry*
  • Indenes / isolation & purification
  • Indenes / pharmacology
  • Magnetic Resonance Spectroscopy
  • Molecular Conformation
  • Resorcinols / chemistry*
  • Resorcinols / isolation & purification
  • Resorcinols / pharmacology
  • Resveratrol
  • Spectrometry, Mass, Electrospray Ionization
  • Stilbenes / chemistry*
  • Stilbenes / isolation & purification
  • Stilbenes / pharmacology
  • Vitaceae / chemistry*

Substances

  • Antioxidants
  • Indenes
  • Resorcinols
  • Stilbenes
  • cajyphenol A
  • cajyphenol B
  • Fatty Acid Synthases
  • Resveratrol