Isoquinoline alkaloids from Thalictrum delavayi

Planta Med. 2001 Mar;67(2):189-90. doi: 10.1055/s-2001-11518.

Abstract

Two new protoberberine alkaloids, 2,3,9,10-dimethylenedioxy-8-oxoprotoberberine (1) and 2,3,9,10-dimethylenedioxy-1,8-dihydroxyprotoberberine (2), together with nine known isoquinoline-type alkaloids were isolated from the roots of Thalictrum delavayi. Their structures were elucidated by spectral methods. Among these compounds, pseudoprotopine showed competitive inhibition activity by DA receptor binding assay (D1) in vitro. The competitive inhibitions were 87.5% (10(-4) M) and 15.6% (10(-6) M), respectively.

Publication types

  • Comparative Study
  • Letter

MeSH terms

  • Alkaloids / chemistry
  • Alkaloids / isolation & purification*
  • Alkaloids / pharmacology
  • Isoquinolines / chemistry
  • Isoquinolines / isolation & purification*
  • Isoquinolines / pharmacology
  • Molecular Structure
  • Plant Roots / chemistry
  • Plants, Medicinal / chemistry*
  • Receptors, Dopamine / drug effects
  • Spectrophotometry, Ultraviolet

Substances

  • 2,3,9,10-dimethylenedioxy-1,8-dihydroxyprotoberberine
  • 2,3,9,10-dimethylenedioxy-8-oxoprotoberberine
  • Alkaloids
  • Isoquinolines
  • Receptors, Dopamine
  • pseudoprotopine