Characterisation of new oligoglycosidic compounds in two Chinese medicinal herbs

Phytochem Anal. 2002 Jul-Aug;13(4):202-6. doi: 10.1002/pca.642.

Abstract

A series of caffeic acid derivatives (3,5-dicaffeoyl-quinic acid, 3,4-dicaffeoyl-quinic acid, and 4,5-dicaffeoyl-quinic acid), and the new compound beta,3,4-trihydroxyphenethyl-O-[beta-apiofuranosyl-(1-->4)-alpha- rhamnopyranosyl-(1-->3)]-(4-O-caffeoyl)-beta-glucopyranoside (wedelosin), as well as three known flavonoid glycosides (quercetin 3-O-beta-glucoside, kaempferol 3-O-beta-apiosyl-(1-2)-beta-glucoside, and astragalin or kaempferol 3-O-beta-glucoside) were isolated from the Chinese medicinal herb Wedelia chinensis. Wedelosin showed an inhibitory activity on both the classical and the alternative activation pathway of the complement system. Another Chinese medicinal herb, Kyllinga brevifolia, yielded two known flavonoid glycosides [kaempferol 3-O-beta-apiosyl-(1-2)-beta-glucoside and isorhamnetin 3-O-beta-apiosyl-(1-2)-beta-glucoside], and a new quercetin triglycoside [quercetin 3-O-beta-apiofuranosyl-(1-->2)-beta-glucopyranoside 7-O-alpha-rhamnopyranoside]. The latter compound showed a moderate anti-viral activity.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Antiviral Agents / analysis
  • Antiviral Agents / pharmacology
  • Complement Inactivator Proteins / analysis
  • Complement Inactivator Proteins / pharmacology
  • Drugs, Chinese Herbal / chemistry*
  • Glycosides / analysis*
  • Glycosides / pharmacology
  • Magnetic Resonance Spectroscopy
  • Spectrophotometry, Ultraviolet

Substances

  • Antiviral Agents
  • Complement Inactivator Proteins
  • Drugs, Chinese Herbal
  • Glycosides