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Novel Orally Active Analgesic and Anti-Inflammatory Cyclohexyl-N-Acylhydrazone Derivatives

The N-acylhydrazone (NAH) moiety is considered a privileged structure, being present in many compounds with diverse pharmacological activities. Among the activities attributed to NAH derivatives anti-inflammatory and analgesic ones are recurrent. As part of a research program aiming at the design of...

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Autores principales: da Silva, Tiago Fernandes, Bispo Júnior, Walfrido, Alexandre-Moreira, Magna Suzana, Costa, Fanny Nascimento, Monteiro, Carlos Eduardo da Silva, Furlan Ferreira, Fabio, Barroso, Regina Cely Rodrigues, Noël, François, Sudo, Roberto Takashi, Zapata-Sudo, Gisele, Lima, Lídia Moreira, Barreiro, Eliezer J.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6272651/
https://www.ncbi.nlm.nih.gov/pubmed/25685912
http://dx.doi.org/10.3390/molecules20023067
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author da Silva, Tiago Fernandes
Bispo Júnior, Walfrido
Alexandre-Moreira, Magna Suzana
Costa, Fanny Nascimento
Monteiro, Carlos Eduardo da Silva
Furlan Ferreira, Fabio
Barroso, Regina Cely Rodrigues
Noël, François
Sudo, Roberto Takashi
Zapata-Sudo, Gisele
Lima, Lídia Moreira
Barreiro, Eliezer J.
author_facet da Silva, Tiago Fernandes
Bispo Júnior, Walfrido
Alexandre-Moreira, Magna Suzana
Costa, Fanny Nascimento
Monteiro, Carlos Eduardo da Silva
Furlan Ferreira, Fabio
Barroso, Regina Cely Rodrigues
Noël, François
Sudo, Roberto Takashi
Zapata-Sudo, Gisele
Lima, Lídia Moreira
Barreiro, Eliezer J.
author_sort da Silva, Tiago Fernandes
collection PubMed
description The N-acylhydrazone (NAH) moiety is considered a privileged structure, being present in many compounds with diverse pharmacological activities. Among the activities attributed to NAH derivatives anti-inflammatory and analgesic ones are recurrent. As part of a research program aiming at the design of new analgesic and anti-inflammatory lead-candidates, a series of cyclohexyl-N-acylhydrazones 10–26 were structurally designed from molecular modification on the prototype LASSBio-294, representing a new class of cycloalkyl analogues. Compounds 10–26 and their conformationally restricted analogue 9 were synthetized and evaluated as analgesic and anti-inflammatory agents in classical pharmacologic protocols. The cyclohexyl-N-acylhydrazones 10–26 and the cyclohexenyl analogue 9 showed great anti-inflammatory and/or analgesic activities, but compound 13 stood out as a new prototype to treat acute and chronic painful states due to its important analgesic activity in a neuropathic pain model.
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spelling pubmed-62726512018-12-13 Novel Orally Active Analgesic and Anti-Inflammatory Cyclohexyl-N-Acylhydrazone Derivatives da Silva, Tiago Fernandes Bispo Júnior, Walfrido Alexandre-Moreira, Magna Suzana Costa, Fanny Nascimento Monteiro, Carlos Eduardo da Silva Furlan Ferreira, Fabio Barroso, Regina Cely Rodrigues Noël, François Sudo, Roberto Takashi Zapata-Sudo, Gisele Lima, Lídia Moreira Barreiro, Eliezer J. Molecules Article The N-acylhydrazone (NAH) moiety is considered a privileged structure, being present in many compounds with diverse pharmacological activities. Among the activities attributed to NAH derivatives anti-inflammatory and analgesic ones are recurrent. As part of a research program aiming at the design of new analgesic and anti-inflammatory lead-candidates, a series of cyclohexyl-N-acylhydrazones 10–26 were structurally designed from molecular modification on the prototype LASSBio-294, representing a new class of cycloalkyl analogues. Compounds 10–26 and their conformationally restricted analogue 9 were synthetized and evaluated as analgesic and anti-inflammatory agents in classical pharmacologic protocols. The cyclohexyl-N-acylhydrazones 10–26 and the cyclohexenyl analogue 9 showed great anti-inflammatory and/or analgesic activities, but compound 13 stood out as a new prototype to treat acute and chronic painful states due to its important analgesic activity in a neuropathic pain model. MDPI 2015-02-12 /pmc/articles/PMC6272651/ /pubmed/25685912 http://dx.doi.org/10.3390/molecules20023067 Text en © 2015 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 license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
da Silva, Tiago Fernandes
Bispo Júnior, Walfrido
Alexandre-Moreira, Magna Suzana
Costa, Fanny Nascimento
Monteiro, Carlos Eduardo da Silva
Furlan Ferreira, Fabio
Barroso, Regina Cely Rodrigues
Noël, François
Sudo, Roberto Takashi
Zapata-Sudo, Gisele
Lima, Lídia Moreira
Barreiro, Eliezer J.
Novel Orally Active Analgesic and Anti-Inflammatory Cyclohexyl-N-Acylhydrazone Derivatives
title Novel Orally Active Analgesic and Anti-Inflammatory Cyclohexyl-N-Acylhydrazone Derivatives
title_full Novel Orally Active Analgesic and Anti-Inflammatory Cyclohexyl-N-Acylhydrazone Derivatives
title_fullStr Novel Orally Active Analgesic and Anti-Inflammatory Cyclohexyl-N-Acylhydrazone Derivatives
title_full_unstemmed Novel Orally Active Analgesic and Anti-Inflammatory Cyclohexyl-N-Acylhydrazone Derivatives
title_short Novel Orally Active Analgesic and Anti-Inflammatory Cyclohexyl-N-Acylhydrazone Derivatives
title_sort novel orally active analgesic and anti-inflammatory cyclohexyl-n-acylhydrazone derivatives
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6272651/
https://www.ncbi.nlm.nih.gov/pubmed/25685912
http://dx.doi.org/10.3390/molecules20023067
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