Design, synthesis and biological evaluation of new parbendazole derivatives for the treatment of HNSCC

Eur J Med Chem. 2022 Aug 5:238:114450. doi: 10.1016/j.ejmech.2022.114450. Epub 2022 May 11.

Abstract

Head and neck squamous cell carcinoma (HNSCC) is a lethal disease with a terrible prognosis, accounting for more than 900,000 new cases and 500,000 deaths each year, nevertheless, its pharmacotherapy is rather limited. Parbendazole was previously identified as a potential HNSCC therapy candidate in our research. Herein, we report the discovery of two series of parbendazole derivatives as tubulin inhibitors. Structure-activity relationship (SAR) analyses led to the discovery of compound 9q with the best pharmacological activities and pharmacokinetic properties. This compound exhibited reasonable inhibition activity on cell proliferation (HN6, CAL-27, Fadu) and tubulin polymerization, induced cell apoptosis, blocked cell cycle and suppressed cell migration and invasion. Compound 9q also displayed low toxicity and a favorable therapeutic effect on a xenograft tumor, indicating that it is a promising starting point for further research.

Keywords: HNSCC; Parbendazole; Tubulin polymerization inhibitors.

MeSH terms

  • Apoptosis
  • Benzimidazoles / pharmacology
  • Cell Line, Tumor
  • Cell Proliferation
  • Head and Neck Neoplasms* / drug therapy
  • Humans
  • Squamous Cell Carcinoma of Head and Neck / drug therapy

Substances

  • Benzimidazoles
  • parbendazole