Design, synthesis, and antitumor activity of desmosdumotin C analogues

J Asian Nat Prod Res. 2019 Jul;21(7):702-715. doi: 10.1080/10286020.2018.1473383. Epub 2018 Dec 30.

Abstract

Desmosdumotin C (Des C), a natural product isolated from the roots of Desmos dumosus, has shown good antitumor activity. A three dimensional quantitative structure-activity relationship (QSAR) study using the comparative molecular field analysis (CoMFA) method was performed on 32 Des C analogues. Based on the QSAR, 18 new Des C analogues were designed and synthesized. An efficient three-step synthetic strategy toward Des C and its analogues was developed from commercial available 2, 4, 6-trihydroxyacetophenone. All synthesized compounds were evaluated against a panel of human cancer cell lines and showed ED50 values ranging from 1.1 to 25.1 µΜ.

Keywords: CoMFA; QSAR; antitumor; desmosdumotin C analogues; human cancer cell Lines.

MeSH terms

  • Alkenes / chemical synthesis*
  • Alkenes / pharmacology*
  • Annonaceae / chemistry*
  • Antineoplastic Agents, Phytogenic / chemical synthesis*
  • Antineoplastic Agents, Phytogenic / pharmacology*
  • Cell Line, Tumor
  • Cell Proliferation / drug effects
  • Drug Design
  • Drug Screening Assays, Antitumor
  • Humans
  • Ketones / chemical synthesis*
  • Ketones / pharmacology*
  • Molecular Structure
  • Quantitative Structure-Activity Relationship

Substances

  • Alkenes
  • Antineoplastic Agents, Phytogenic
  • Ketones
  • desmosdumotin C