Journal of Enzyme Inhibition and Medicinal Chemistry (Dec 2022)

Biological investigation of N-methyl thiosemicarbazones as antimicrobial agents and bacterial carbonic anhydrases inhibitors

  • Ilaria D’Agostino,
  • Githa Elizabeth Mathew,
  • Paola Angelini,
  • Roberto Venanzoni,
  • Giancarlo Angeles Flores,
  • Andrea Angeli,
  • Simone Carradori,
  • Beatrice Marinacci,
  • Luigi Menghini,
  • Mohamed A. Abdelgawad,
  • Mohammed M. Ghoneim,
  • Bijo Mathew,
  • Claudiu T. Supuran

DOI
https://doi.org/10.1080/14756366.2022.2055009
Journal volume & issue
Vol. 37, no. 1
pp. 986 – 993

Abstract

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The enormous burden of the COVID-19 pandemic in economic and healthcare terms has cast a shadow on the serious threat of antimicrobial resistance, increasing the inappropriate use of antibiotics and shifting the focus of drug discovery programmes from antibacterial and antifungal fields. Thus, there is a pressing need for new antimicrobials involving innovative modes of action (MoAs) to avoid cross-resistance rise. Thiosemicarbazones (TSCs) stand out due to their easy preparation and polypharmacological application, also in infectious diseases. Recently, we reported a small library of TSCs (1–9) that emerged for their non-cytotoxic behaviour. Inspired by their multifaceted activity, we investigated the antibacterial, antifungal, and antidermatophytal profiles of derivatives 1–9, highlighting a new promising research line. Furthermore, the ability of these compounds to inhibit selected microbial and human carbonic anhydrases (CAs) was assessed, revealing their possible involvement in the MoA and a good selectivity index for some derivatives.

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