Synthesis of new sulfonamide derivatives: Investigation of their interactions with carbonic anhydrase and cholinesterase enzymes by in vitro and in silico evaluations-Reference-Cited by-同舟云学术

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Synthesis of new sulfonamide derivatives: Investigation of their interactions with carbonic anhydrase and cholinesterase enzymes by in vitro and in silico evaluations

Published:2024-10 Issue: Volume:1314 Page:138798
ISSN:0022-2860
Container-title:Journal of Molecular Structure
language:en
Short-container-title:Journal of Molecular Structure

Author:

Kurban Muhammet Gürkan^ORCID,Çakmak Reşit^ORCID,Başaran Eyüp^ORCID,Türkmenoğlu Burçin^ORCID,Şentürk Murat^ORCID

Publisher

Elsevier BV

Reference80 articles.

1. Targeting carbonic anhydrase IX and XII isoforms with small molecule inhibitors and monoclonal antibodies;Kciuk;J. Enzyme Inhib. Med. Chem.,2022

2. Carbonic anhydrase inhibitors-Part 94. 1, 3, 4-Thiadiazole-2-sulfonamide derivatives as antitumor agents?;Supuran;Eur. J. Med. Chem.,2000

3. Design, synthesis, and biological activity studies of carbonic anhydrase inhibitors;Erzurum;Z. Naturforsch. C.,2023

4. Application of the dual-tail approach for the design and synthesis of novel thiopyrimidine–benzenesulfonamide hybrids as selective carbonic anhydrase inhibitors;Abdel-Mohsen;Eur. J. Med. Chem.,2022

5. Carbonic anhydrases as drug targets-an overview;Supuran;Curr. Top. Med. Chem.,2007

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