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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...
Autores principales: | , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2015
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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. |
format | Online Article Text |
id | pubmed-6272651 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
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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