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Multitargeting approaches involving carbonic anhydrase inhibitors: hybrid drugs against a variety of disorders

Carbonic anhydrases (CAs, EC 4.2.1.1) are enzymes involved in a multitude of diseases, and their inhibitors are in clinical use as drugs for the management of glaucoma, epilepsy, obesity, and tumours. In the last decade, multitargeting approaches have been proposed by hybridisation of CA inhibitors...

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Autor principal: Supuran, Claudiu T.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Taylor & Francis 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8330743/
https://www.ncbi.nlm.nih.gov/pubmed/34325588
http://dx.doi.org/10.1080/14756366.2021.1945049
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author Supuran, Claudiu T.
author_facet Supuran, Claudiu T.
author_sort Supuran, Claudiu T.
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description Carbonic anhydrases (CAs, EC 4.2.1.1) are enzymes involved in a multitude of diseases, and their inhibitors are in clinical use as drugs for the management of glaucoma, epilepsy, obesity, and tumours. In the last decade, multitargeting approaches have been proposed by hybridisation of CA inhibitors (CAIs) of sulphonamide, coumarin, and sulphocoumarin types with NO donors, CO donors, prostaglandin analogs, β-adrenergic blockers, non-steroidal anti-inflammatory drugs, and a variety of anticancer agents (cytotoxic drugs, kinase/telomerase inhibitors, P-gp and thioredoxin inhibitors). Many of the obtained hybrids showed enhanced efficacy compared to the parent drugs, making multitargeting an effective and innovative approach for various pharmacological applications.
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spelling pubmed-83307432021-08-09 Multitargeting approaches involving carbonic anhydrase inhibitors: hybrid drugs against a variety of disorders Supuran, Claudiu T. J Enzyme Inhib Med Chem Review Article Carbonic anhydrases (CAs, EC 4.2.1.1) are enzymes involved in a multitude of diseases, and their inhibitors are in clinical use as drugs for the management of glaucoma, epilepsy, obesity, and tumours. In the last decade, multitargeting approaches have been proposed by hybridisation of CA inhibitors (CAIs) of sulphonamide, coumarin, and sulphocoumarin types with NO donors, CO donors, prostaglandin analogs, β-adrenergic blockers, non-steroidal anti-inflammatory drugs, and a variety of anticancer agents (cytotoxic drugs, kinase/telomerase inhibitors, P-gp and thioredoxin inhibitors). Many of the obtained hybrids showed enhanced efficacy compared to the parent drugs, making multitargeting an effective and innovative approach for various pharmacological applications. Taylor & Francis 2021-07-30 /pmc/articles/PMC8330743/ /pubmed/34325588 http://dx.doi.org/10.1080/14756366.2021.1945049 Text en © 2021 The Author(s). Published by Informa UK Limited, trading as Taylor & Francis Group. https://creativecommons.org/licenses/by/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) ), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Review Article
Supuran, Claudiu T.
Multitargeting approaches involving carbonic anhydrase inhibitors: hybrid drugs against a variety of disorders
title Multitargeting approaches involving carbonic anhydrase inhibitors: hybrid drugs against a variety of disorders
title_full Multitargeting approaches involving carbonic anhydrase inhibitors: hybrid drugs against a variety of disorders
title_fullStr Multitargeting approaches involving carbonic anhydrase inhibitors: hybrid drugs against a variety of disorders
title_full_unstemmed Multitargeting approaches involving carbonic anhydrase inhibitors: hybrid drugs against a variety of disorders
title_short Multitargeting approaches involving carbonic anhydrase inhibitors: hybrid drugs against a variety of disorders
title_sort multitargeting approaches involving carbonic anhydrase inhibitors: hybrid drugs against a variety of disorders
topic Review Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8330743/
https://www.ncbi.nlm.nih.gov/pubmed/34325588
http://dx.doi.org/10.1080/14756366.2021.1945049
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