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Design, Synthesis and Biological Evaluation of New Antioxidant and Neuroprotective Multitarget Directed Ligands Able to Block Calcium Channels
We report herein the design, synthesis and biological evaluation of new antioxidant and neuroprotective multitarget directed ligands (MTDLs) able to block Ca(2+) channels. New dialkyl 2,6-dimethyl-4-(4-(prop-2-yn-1-yloxy)phenyl)-1,4-dihydropyridine-3,5-dicarboxylate MTDLs 3a–t, resulting from the ju...
Autores principales: | , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7144121/ https://www.ncbi.nlm.nih.gov/pubmed/32183349 http://dx.doi.org/10.3390/molecules25061329 |
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author | Pachòn Angona, Irene Daniel, Solene Martin, Helene Bonet, Alexandre Wnorowski, Artur Maj, Maciej Jóźwiak, Krzysztof Silva, Tiago Barros Refouvelet, Bernard Borges, Fernanda Marco-Contelles, José Ismaili, Lhassane |
author_facet | Pachòn Angona, Irene Daniel, Solene Martin, Helene Bonet, Alexandre Wnorowski, Artur Maj, Maciej Jóźwiak, Krzysztof Silva, Tiago Barros Refouvelet, Bernard Borges, Fernanda Marco-Contelles, José Ismaili, Lhassane |
author_sort | Pachòn Angona, Irene |
collection | PubMed |
description | We report herein the design, synthesis and biological evaluation of new antioxidant and neuroprotective multitarget directed ligands (MTDLs) able to block Ca(2+) channels. New dialkyl 2,6-dimethyl-4-(4-(prop-2-yn-1-yloxy)phenyl)-1,4-dihydropyridine-3,5-dicarboxylate MTDLs 3a–t, resulting from the juxtaposition of nimodipine, a Ca(2+) channel antagonist, and rasagiline, a known MAO inhibitor, have been obtained from appropriate and commercially available precursors using a Hantzsch reaction. Pertinent biological analysis has prompted us to identify the MTDL 3,5-dimethyl-2,6–dimethyl–4-[4-(prop–2–yn–1-yloxy)phenyl]-1,4-dihydro- pyridine- 3,5-dicarboxylate (3a), as an attractive antioxidant (1.75 TE), Ca(2+) channel antagonist (46.95% at 10 μM), showing significant neuroprotection (38%) against H(2)O(2) at 10 μM, being considered thus a hit-compound for further investigation in our search for anti-Alzheimer’s disease agents. |
format | Online Article Text |
id | pubmed-7144121 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-71441212020-04-13 Design, Synthesis and Biological Evaluation of New Antioxidant and Neuroprotective Multitarget Directed Ligands Able to Block Calcium Channels Pachòn Angona, Irene Daniel, Solene Martin, Helene Bonet, Alexandre Wnorowski, Artur Maj, Maciej Jóźwiak, Krzysztof Silva, Tiago Barros Refouvelet, Bernard Borges, Fernanda Marco-Contelles, José Ismaili, Lhassane Molecules Communication We report herein the design, synthesis and biological evaluation of new antioxidant and neuroprotective multitarget directed ligands (MTDLs) able to block Ca(2+) channels. New dialkyl 2,6-dimethyl-4-(4-(prop-2-yn-1-yloxy)phenyl)-1,4-dihydropyridine-3,5-dicarboxylate MTDLs 3a–t, resulting from the juxtaposition of nimodipine, a Ca(2+) channel antagonist, and rasagiline, a known MAO inhibitor, have been obtained from appropriate and commercially available precursors using a Hantzsch reaction. Pertinent biological analysis has prompted us to identify the MTDL 3,5-dimethyl-2,6–dimethyl–4-[4-(prop–2–yn–1-yloxy)phenyl]-1,4-dihydro- pyridine- 3,5-dicarboxylate (3a), as an attractive antioxidant (1.75 TE), Ca(2+) channel antagonist (46.95% at 10 μM), showing significant neuroprotection (38%) against H(2)O(2) at 10 μM, being considered thus a hit-compound for further investigation in our search for anti-Alzheimer’s disease agents. MDPI 2020-03-14 /pmc/articles/PMC7144121/ /pubmed/32183349 http://dx.doi.org/10.3390/molecules25061329 Text en © 2020 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Communication Pachòn Angona, Irene Daniel, Solene Martin, Helene Bonet, Alexandre Wnorowski, Artur Maj, Maciej Jóźwiak, Krzysztof Silva, Tiago Barros Refouvelet, Bernard Borges, Fernanda Marco-Contelles, José Ismaili, Lhassane Design, Synthesis and Biological Evaluation of New Antioxidant and Neuroprotective Multitarget Directed Ligands Able to Block Calcium Channels |
title | Design, Synthesis and Biological Evaluation of New Antioxidant and Neuroprotective Multitarget Directed Ligands Able to Block Calcium Channels |
title_full | Design, Synthesis and Biological Evaluation of New Antioxidant and Neuroprotective Multitarget Directed Ligands Able to Block Calcium Channels |
title_fullStr | Design, Synthesis and Biological Evaluation of New Antioxidant and Neuroprotective Multitarget Directed Ligands Able to Block Calcium Channels |
title_full_unstemmed | Design, Synthesis and Biological Evaluation of New Antioxidant and Neuroprotective Multitarget Directed Ligands Able to Block Calcium Channels |
title_short | Design, Synthesis and Biological Evaluation of New Antioxidant and Neuroprotective Multitarget Directed Ligands Able to Block Calcium Channels |
title_sort | design, synthesis and biological evaluation of new antioxidant and neuroprotective multitarget directed ligands able to block calcium channels |
topic | Communication |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7144121/ https://www.ncbi.nlm.nih.gov/pubmed/32183349 http://dx.doi.org/10.3390/molecules25061329 |
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