Carbonic anhydrase inhibitors based on sorafenib scaffold: Design, synthesis, crystallographic investigation and effects on primary breast cancer cells

  • M. Bozdag
  • , M. Ferraroni
  • , C. Ward
  • , Fabrizio Carta
  • , Silvia Bua
  • , Andrea Angeli
  • , Simon P. Langdon
  • , I. H. Kunkler
  • , Abdul Malek S. Al-Tamimi
  • , Claudiu T. Supuran

Research output: Contribution to journalArticlepeer-review

47 Scopus citations

Abstract

Carbonic anhydrase inhibitors (CAIs) of the sulfonamide, sulfamate and coumarin classes bearing the phenylureido tail found in the clinically used drug Sorafenib, a multikinase inhibitor actually used for the management of hepatocellular carcinomas, are reported. All compounds were assayed on human (h) CA isoforms I, II, VII and IX, involved in various pathologies. Among the sulfonamides, several compounds were selective for inhibiting hCA IX, with KI values in the low nanomolar ranges (i.e. 0.7–30.2 nM). We explored the binding modes of such compounds by means of X-ray crystallographic studies on isoform hCA I in adduct with one sulfonamide and a sulfamate inhibitor. Antiproliferative properties of some sulfamates on breast tumor cell lines were also investigated.

Original languageEnglish
Article number111600
JournalEuropean Journal of Medicinal Chemistry
Volume182
DOIs
StatePublished - 15 Nov 2019

UN SDGs

This output contributes to the following UN Sustainable Development Goals (SDGs)

  1. SDG 3 - Good Health and Well-being
    SDG 3 Good Health and Well-being

Keywords

  • Carbonic anhydrase
  • Coumarin
  • Enzyme inhibitor
  • Sorafenib
  • Sulfamate
  • Sulfonamide

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