Functionalized azirine based scaffolds as endothelin inhibitors for the selective anti-angiogenic activity

Eur J Med Chem. 2024 Aug 5:274:116510. doi: 10.1016/j.ejmech.2024.116510. Epub 2024 May 25.

Abstract

Anti-angiogenic therapy has long been used as an adjunct therapy for the resolution of tumor burden. The current findings describe the synthesis of novel marine-based azirine-containing compounds that exhibit anti-angiogenic mediated anti-tumor activity. Azirine-2-carboxylate inhibited HUVEC-mediated tubulogenesis without causing cell death in a dose-dependent manner. Ex-vivo CAM, in-vivo Matrigel implantation, and ear angiogenesis experiments have all shown that azirine-2-carboxylate effectively inhibits angiogenesis. Furthermore, azirine-2-carboxylate inhibits the migration of ECs without disrupting the preformed tubule network. Azirine-2-carboxylate had adequate intramuscular systemic exposure and inhibited tumor growth in a xenograft mouse model. DARTS analysis, competitive binding assay, and gene expression investigations revealed that azirine-2-carboxylate inhibits endothelin-1-mediated angiogenesis. Overall, the discovery of azirine-2-carboxylate demonstrated a potent inhibition of angiogenesis targeting ET1 and a possible application in anti-angiogenic therapy.

Keywords: Anti-angiogenic property; Azirines; Cancer; Endothelial cells; Endothelin 1 inhibitor.

MeSH terms

  • Angiogenesis Inhibitors* / chemical synthesis
  • Angiogenesis Inhibitors* / chemistry
  • Angiogenesis Inhibitors* / pharmacology
  • Animals
  • Antineoplastic Agents / chemical synthesis
  • Antineoplastic Agents / chemistry
  • Antineoplastic Agents / pharmacology
  • Azirines* / chemical synthesis
  • Azirines* / chemistry
  • Azirines* / pharmacology
  • Cell Movement / drug effects
  • Cell Proliferation / drug effects
  • Dose-Response Relationship, Drug
  • Human Umbilical Vein Endothelial Cells* / drug effects
  • Humans
  • Mice
  • Molecular Structure
  • Neovascularization, Pathologic / drug therapy
  • Structure-Activity Relationship

Substances

  • Angiogenesis Inhibitors
  • Azirines
  • Antineoplastic Agents