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Atropo/Tropo Flexibility: A Tool for Design and Synthesis of Self-Adaptable Inhibitors of Carbonic Anhydrases and Their Antiproliferative Effect

  • Jekateri̅na Ivanova
  • , Alessio Nocentini
  • , Kaspars Ta̅rs
  • , Ja̅nis Leita̅ns
  • , Elviss Dvinskis
  • , Andris Kazaks
  • , Ilona Domračeva
  • , Claudiu T. Supuran
  • , Raivis Žalubovskis*
  • *Corresponding author for this work
  • Latvian Institute of Organic Synthesis
  • University of Florence
  • Latvian Biomedical Research and Study Centre
  • Riga Technical University

Research output: Contribution to journalArticlepeer-review

16 Citations (Scopus)

Abstract

Here, we report for the first time a series of sulfonamide derivatives with scaffolds bearing flexible moieties, namely, rotamers or tropoisomers capable of adapting their geometry in the active center of enzymes thus being effective and selective carbonic anhydrase (CAs, EC 4.2.1.1) enzyme inhibitors. All compounds exhibited effective in vitro inhibition activity toward the main hCA isoforms related to cancer (i.e., hCA II, hCA IX, and hCA XII with KI values in the low nanomolar range). Three selected compounds showed a great cytotoxic effect on cancer cell lines ex vivo. X-ray crystallographic experiments assessed the binding modes of compound 35 with active centers of hCA IX and hCA XII.

Original languageEnglish
Pages (from-to)5703-5718
Number of pages16
JournalJournal of Medicinal Chemistry
Volume66
Issue number8
DOIs
Publication statusPublished - 27 Apr 2023
Externally publishedYes

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

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