Synthesis and in vitro anticancer activities of selenium N-heterocyclic carbene compounds

Chem Biol Drug Des. 2021 Sep;98(3):435-444. doi: 10.1111/cbdd.13900. Epub 2021 Jul 7.

Abstract

Fourteen novel selenium N-heterocyclic carbene (Se-NHC) compounds derived from 4,5-diarylimidazole were designed, synthesized, and evaluated as antiproliferative agents. Most of them were more effective toward A2780 ovarian cancer cells than HepG2 hepatocellular carcinoma cells. Among them, the most active compound 2b was about fourfold more active than the positive control ebselen against A2780 cells. In addition, this compound displayed twofold higher cytotoxicity to A2780 cells than to IOSE80 normal ovarian epithelial cells. Further studies revealed that 2b could induce reactive oxygen species production, damage mitochondrial membrane potential, block the cells in the G0/G1 phase, and finally promote A2780 cell apoptosis.

Keywords: N-heterocyclic carbene; antitumor; apoptosis; ovarian cancer; selenium compounds.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Antineoplastic Agents / chemical synthesis*
  • Antineoplastic Agents / pharmacology
  • Apoptosis / drug effects
  • Cell Line, Tumor
  • Cell Survival / drug effects
  • Coordination Complexes / chemistry*
  • Coordination Complexes / pharmacology
  • Drug Screening Assays, Antitumor
  • G1 Phase Cell Cycle Checkpoints / drug effects
  • Heterocyclic Compounds / chemistry
  • Humans
  • Methane / analogs & derivatives*
  • Methane / chemistry
  • Reactive Oxygen Species / metabolism
  • Selenium / chemistry*
  • Structure-Activity Relationship

Substances

  • Antineoplastic Agents
  • Coordination Complexes
  • Heterocyclic Compounds
  • Reactive Oxygen Species
  • carbene
  • Selenium
  • Methane