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Carbonic anhydrase activation profile of indole-based derivatives
Carbonic Anhydrase Activators (CAAs) could represent a novel approach for the treatment of Alzheimer’s disease, ageing, and other conditions that require remedial achievement of spatial learning and memory therapy. Within a research project aimed at developing novel CAAs selective for certain isofor...
Autores principales: | , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Taylor & Francis
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8344252/ https://www.ncbi.nlm.nih.gov/pubmed/34340630 http://dx.doi.org/10.1080/14756366.2021.1959573 |
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author | Barresi, Elisabetta Ravichandran, Rahul Germelli, Lorenzo Angeli, Andrea Baglini, Emma Salerno, Silvia Marini, Anna Maria Costa, Barbara Da Pozzo, Eleonora Martini, Claudia Da Settimo, Federico Supuran, Claudiu Cosconati, Sandro Taliani, Sabrina |
author_facet | Barresi, Elisabetta Ravichandran, Rahul Germelli, Lorenzo Angeli, Andrea Baglini, Emma Salerno, Silvia Marini, Anna Maria Costa, Barbara Da Pozzo, Eleonora Martini, Claudia Da Settimo, Federico Supuran, Claudiu Cosconati, Sandro Taliani, Sabrina |
author_sort | Barresi, Elisabetta |
collection | PubMed |
description | Carbonic Anhydrase Activators (CAAs) could represent a novel approach for the treatment of Alzheimer’s disease, ageing, and other conditions that require remedial achievement of spatial learning and memory therapy. Within a research project aimed at developing novel CAAs selective for certain isoforms, three series of indole-based derivatives were investigated. Enzyme activation assay on human CA I, II, VA, and VII isoforms revealed several effective micromolar activators, with promising selectivity profiles towards the brain-associated cytosolic isoform hCA VII. Molecular modelling studies suggested a theoretical model of the complex between hCA VII and the new activators and provide a possible explanation for their modulating as well as selectivity properties. Preliminary biological evaluations demonstrated that one of the most potent CAA 7 is not cytotoxic and is able to increase the release of the brain-derived neurotrophic factor (BDNF) from human microglial cells, highlighting its possible application in the treatment of CNS-related disorders. |
format | Online Article Text |
id | pubmed-8344252 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Taylor & Francis |
record_format | MEDLINE/PubMed |
spelling | pubmed-83442522021-08-09 Carbonic anhydrase activation profile of indole-based derivatives Barresi, Elisabetta Ravichandran, Rahul Germelli, Lorenzo Angeli, Andrea Baglini, Emma Salerno, Silvia Marini, Anna Maria Costa, Barbara Da Pozzo, Eleonora Martini, Claudia Da Settimo, Federico Supuran, Claudiu Cosconati, Sandro Taliani, Sabrina J Enzyme Inhib Med Chem Research Paper Carbonic Anhydrase Activators (CAAs) could represent a novel approach for the treatment of Alzheimer’s disease, ageing, and other conditions that require remedial achievement of spatial learning and memory therapy. Within a research project aimed at developing novel CAAs selective for certain isoforms, three series of indole-based derivatives were investigated. Enzyme activation assay on human CA I, II, VA, and VII isoforms revealed several effective micromolar activators, with promising selectivity profiles towards the brain-associated cytosolic isoform hCA VII. Molecular modelling studies suggested a theoretical model of the complex between hCA VII and the new activators and provide a possible explanation for their modulating as well as selectivity properties. Preliminary biological evaluations demonstrated that one of the most potent CAA 7 is not cytotoxic and is able to increase the release of the brain-derived neurotrophic factor (BDNF) from human microglial cells, highlighting its possible application in the treatment of CNS-related disorders. Taylor & Francis 2021-08-02 /pmc/articles/PMC8344252/ /pubmed/34340630 http://dx.doi.org/10.1080/14756366.2021.1959573 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 | Research Paper Barresi, Elisabetta Ravichandran, Rahul Germelli, Lorenzo Angeli, Andrea Baglini, Emma Salerno, Silvia Marini, Anna Maria Costa, Barbara Da Pozzo, Eleonora Martini, Claudia Da Settimo, Federico Supuran, Claudiu Cosconati, Sandro Taliani, Sabrina Carbonic anhydrase activation profile of indole-based derivatives |
title | Carbonic anhydrase activation profile of indole-based derivatives |
title_full | Carbonic anhydrase activation profile of indole-based derivatives |
title_fullStr | Carbonic anhydrase activation profile of indole-based derivatives |
title_full_unstemmed | Carbonic anhydrase activation profile of indole-based derivatives |
title_short | Carbonic anhydrase activation profile of indole-based derivatives |
title_sort | carbonic anhydrase activation profile of indole-based derivatives |
topic | Research Paper |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8344252/ https://www.ncbi.nlm.nih.gov/pubmed/34340630 http://dx.doi.org/10.1080/14756366.2021.1959573 |
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