Novel thiazolidinone-containing compounds, without the well-known sulphonamide zinc-binding group acting as human carbonic anhydrase IX inhibitors-Reference-Cited by-同舟云学术

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Novel thiazolidinone-containing compounds, without the well-known sulphonamide zinc-binding group acting as human carbonic anhydrase IX inhibitors

Published:2018-01-01 Issue:1 Volume:33 Page:1299-1308
ISSN:1475-6366
Container-title:Journal of Enzyme Inhibition and Medicinal Chemistry
language:en
Short-container-title:Journal of Enzyme Inhibition and Medicinal Chemistry

Author:

Güzel-Akdemir Özlen¹,Angeli Andrea²,Demir Kübra¹,Supuran Claudiu T.²^ORCID,Akdemir Atilla³^ORCID

Affiliation:

1. Department of Pharmaceutical Chemistry, Faculty of Pharmacy, Istanbul University, Istanbul, Turkey;

2. Department of NEUROFARBA, Sezione di Scienze Farmaceutiche Universita degli Studi di Firenze, Sesto Fiorentino, Florence, Italy;

3. Computer-Aided Drug Discovery Laboratory, Department of Pharmacology, Faculty of Pharmacy, Bezmialem Vakif University, Istanbul, Turkey

Funder

Istanbul University Scientific Research Projects Department

Publisher

Informa UK Limited

Subject

Drug Discovery,Pharmacology,General Medicine

Link

https://www.tandfonline.com/doi/pdf/10.1080/14756366.2018.1499628

Reference41 articles.

1. Carbonic anhydrases: novel therapeutic applications for inhibitors and activators

2. Interfering with pH regulation in tumours as a therapeutic strategy

3. Hypoxia activates the capacity of tumor-associated carbonic anhydrase IX to acidify extracellular pH

4. Biochemical Characterization of CA IX, One of the Most Active Carbonic Anhydrase Isozymes

5. Carbonic Anhydrase IX as a Target for Designing Novel Anticancer Drugs

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1. In silico study of five new sulfonamide derivatives bearing a thiazolidine-4-one moiety: targeting carbonic anhydrase IX;Review of Clinical Pharmacology and Pharmacokinetics - International Edition;2024-07-02

2. Tumor associated carbonic anhydrase inhibitors: Rational approaches, design strategies, structure activity relationship and mechanistic insights;European Journal of Medicinal Chemistry Reports;2024-04

3. Mandelic acid-based spirothiazolidinones targeting M. tuberculosis: Synthesis, in vitro and in silico investigations;Bioorganic Chemistry;2022-04

4. Thiazolidin-4-Ones as Potential Antimicrobial Agents: Experimental and In Silico Evaluation;Molecules;2022-03-16

5. Synthesis and potential antitumor activities of mandelic acid linked 2-aryl-1,3-thiazolidin-4-ones;J RES PHARM;2022

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