Design and synthesis of new tetrandrine derivatives and their antitumor activities

J Asian Nat Prod Res. 2016 Oct;18(10):966-75. doi: 10.1080/10286020.2016.1188085. Epub 2016 May 31.

Abstract

A series of tetrandrine derivatives were designed and synthesized using Suzuki coupling reaction. Eleven targeted compounds with over 50% inhibition against HL60 and A549 human cancer cell lines at 10 μM were further evaluated for the in vitro antitumor activities by MTT or SRB assay. The biological results revealed that some compounds exhibited potent antitumor activities. Thiophene derivative 6 and acetylphenyl derivative 5 were the most active ones against HL60 and A549 cell lines, with IC50 values less than 5 μM, which thus could be considered as useful candidate for further development of new antitumor agents.

Keywords: Suzuki coupling; Tetrandrine; antitumor activity; structure–activity relationship; synthesis.

MeSH terms

  • Antineoplastic Agents / chemical synthesis*
  • Antineoplastic Agents / chemistry
  • Antineoplastic Agents / pharmacology
  • Benzylisoquinolines / chemical synthesis*
  • Benzylisoquinolines / chemistry
  • Benzylisoquinolines / pharmacology*
  • Cell Proliferation / drug effects
  • Drug Design*
  • Drug Screening Assays, Antitumor
  • HL-60 Cells
  • Humans
  • Molecular Structure
  • Structure-Activity Relationship

Substances

  • Antineoplastic Agents
  • Benzylisoquinolines
  • tetrandrine