Polygodial and Ophiobolin A Analogues for Covalent Crosslinking of Anticancer Targets

Int J Mol Sci. 2021 Oct 19;22(20):11256. doi: 10.3390/ijms222011256.

Abstract

In a search of small molecules active against apoptosis-resistant cancer cells, including glioma, melanoma, and non-small cell lung cancer, we previously prepared α,β- and γ,δ-unsaturated ester analogues of polygodial and ophiobolin A, compounds capable of pyrrolylation of primary amines and demonstrating double-digit micromolar antiproliferative potencies in cancer cells. In the current work, we synthesized dimeric and trimeric variants of such compounds in an effort to discover compounds that could crosslink biological primary amine containing targets. We showed that such compounds retain the pyrrolylation ability and possess enhanced single-digit micromolar potencies toward apoptosis-resistant cancer cells. Target identification studies of these interesting compounds are underway.

Keywords: Wittig reaction; anticancer activity; apoptosis resistance; ophiobolin A; polygodial.

MeSH terms

  • A549 Cells
  • Animals
  • 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
  • Humans
  • MCF-7 Cells
  • Mice
  • Molecular Structure
  • Sesquiterpenes / chemistry*
  • Sesterterpenes / chemistry*
  • Structure-Activity Relationship
  • Terpenes / chemical synthesis*
  • Terpenes / chemistry
  • Terpenes / pharmacology

Substances

  • Antineoplastic Agents
  • Sesquiterpenes
  • Sesterterpenes
  • Terpenes
  • ophiobolin A
  • polygodial