Activity-guided isolation of constituents of Cerbera manghas with antiproliferative and antiestrogenic activities

Bioorg Med Chem Lett. 2000 Nov 6;10(21):2431-4. doi: 10.1016/s0960-894x(00)00477-7.

Abstract

Two new cardenolides, (-)-14-hydroxy-3beta-(3-O-methyl-6-deoxy-alpha-L-rhamnosyl)-11a lpha, 12alpha-epoxy-(5beta,14beta,17betaH)-card-20 (22)-enolide (1), (-)-14-hydroxy-3beta-(3-O-methyl-6-deoxy-alpha-L-glucopyranosyl)-11al pha,12alpha-epoxy-(5beta,14beta,17betaH)-card -20(22)-enolide (2), and a known cardenolide, (-)-17beta-neriifolin (3), were isolated from the roots of Cerbera manghas as antiproliferative and antiestrogenic principles when evaluated against a human colon cancer cell line (Col2) and the Ishikawa cell line, respectively. Two known lignans, (-)-olivil (4) and (-)-cycloolivil (5), were also isolated but were inactive in the assay systems used.

Publication types

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

MeSH terms

  • Antineoplastic Agents, Phytogenic / isolation & purification*
  • Antineoplastic Agents, Phytogenic / pharmacology
  • Cardenolides / isolation & purification*
  • Cardenolides / pharmacology*
  • Drug Screening Assays, Antitumor
  • Estrogen Receptor Modulators / isolation & purification*
  • Estrogen Receptor Modulators / pharmacology
  • Flow Cytometry
  • Humans
  • Magnoliopsida / chemistry
  • Molecular Structure
  • Plant Roots / chemistry*
  • Trees*
  • Tumor Cells, Cultured

Substances

  • Antineoplastic Agents, Phytogenic
  • Cardenolides
  • Estrogen Receptor Modulators