Cargando…

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...

Descripción completa

Detalles Bibliográficos
Autores principales: 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
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2020
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
_version_ 1783519774143152128
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
work_keys_str_mv AT pachonangonairene designsynthesisandbiologicalevaluationofnewantioxidantandneuroprotectivemultitargetdirectedligandsabletoblockcalciumchannels
AT danielsolene designsynthesisandbiologicalevaluationofnewantioxidantandneuroprotectivemultitargetdirectedligandsabletoblockcalciumchannels
AT martinhelene designsynthesisandbiologicalevaluationofnewantioxidantandneuroprotectivemultitargetdirectedligandsabletoblockcalciumchannels
AT bonetalexandre designsynthesisandbiologicalevaluationofnewantioxidantandneuroprotectivemultitargetdirectedligandsabletoblockcalciumchannels
AT wnorowskiartur designsynthesisandbiologicalevaluationofnewantioxidantandneuroprotectivemultitargetdirectedligandsabletoblockcalciumchannels
AT majmaciej designsynthesisandbiologicalevaluationofnewantioxidantandneuroprotectivemultitargetdirectedligandsabletoblockcalciumchannels
AT jozwiakkrzysztof designsynthesisandbiologicalevaluationofnewantioxidantandneuroprotectivemultitargetdirectedligandsabletoblockcalciumchannels
AT silvatiagobarros designsynthesisandbiologicalevaluationofnewantioxidantandneuroprotectivemultitargetdirectedligandsabletoblockcalciumchannels
AT refouveletbernard designsynthesisandbiologicalevaluationofnewantioxidantandneuroprotectivemultitargetdirectedligandsabletoblockcalciumchannels
AT borgesfernanda designsynthesisandbiologicalevaluationofnewantioxidantandneuroprotectivemultitargetdirectedligandsabletoblockcalciumchannels
AT marcocontellesjose designsynthesisandbiologicalevaluationofnewantioxidantandneuroprotectivemultitargetdirectedligandsabletoblockcalciumchannels
AT ismaililhassane designsynthesisandbiologicalevaluationofnewantioxidantandneuroprotectivemultitargetdirectedligandsabletoblockcalciumchannels