Synthesis and in vitro antitumoral activity of new N-phenyl-3-pyrrolecarbothioamides

Bioorg Med Chem. 2003 Feb 20;11(4):495-503. doi: 10.1016/s0968-0896(02)00465-0.

Abstract

A new series of N-phenylpyrrolecarbothioamides were obtained from base catalyzed intramolecular cyclization of 3-amino-3-(alkyl or arylamino)propenethioamides. Pyrrole derivatives were evaluated for their in vitro anticancer activity toward cell lines of nine different types of human cancer. Some of newly prepared compounds demonstrated inhibitory effects on the growth of a wide range of cancer cell lines generally at 10(-6) M level and in some case at 10(-8) M concentrations.

MeSH terms

  • Antineoplastic Agents / chemical synthesis*
  • Antineoplastic Agents / pharmacology
  • Cell Division / drug effects
  • Cyclization
  • Drug Screening Assays, Antitumor
  • Humans
  • Magnetic Resonance Spectroscopy
  • Spectrophotometry, Infrared
  • Structure-Activity Relationship
  • Thioamides / chemical synthesis*
  • Thioamides / pharmacology
  • Tumor Cells, Cultured

Substances

  • Antineoplastic Agents
  • Thioamides