Synthesis and antiproliferative in-vitro activity of natural flavans and related compounds

Arch Pharm (Weinheim). 2007 Dec;340(12):650-5. doi: 10.1002/ardp.200700077.

Abstract

The total synthesis of natural flavan racemates (+/-) 1, (+/-) 2 and natural flavones 3, 4 had thus been achieved. A straightforward synthetic procedure of flavans via the Pd-C catalyzed hydrogenation/hydrogenolysis of corresponding flavones was developed. Furthermore, the antiproliferative activities of racemic flavans (+/-) 1, (+/-) 2, flavones 3, 4, and five synthetic intermediates toward human SGC-7901, BEL-7402, HeLa, and HL-60 cell lines in vitro were evaluated by MTT assay, and the racemic flavans (+/-) 1 were found to have significant antiproliferative activity against all four cell lines.

MeSH terms

  • Antineoplastic Agents / chemical synthesis*
  • Antineoplastic Agents / chemistry
  • Antineoplastic Agents / pharmacology
  • Cell Line, Tumor
  • Cell Proliferation / drug effects
  • Cell Survival / drug effects
  • Drug Screening Assays, Antitumor
  • Flavones / chemical synthesis*
  • Flavones / chemistry
  • Flavones / pharmacology
  • Humans
  • Stereoisomerism
  • Structure-Activity Relationship
  • Tetrazolium Salts
  • Thiazoles

Substances

  • Antineoplastic Agents
  • Flavones
  • Tetrazolium Salts
  • Thiazoles
  • thiazolyl blue