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新型口服活性镇痛和抗炎环己基-N-酰腙衍生物。

Novel orally active analgesic and anti-inflammatory cyclohexyl-N-acylhydrazone derivatives.

作者信息

da Silva Tiago Fernandes, Bispo Júnior Walfrido, Alexandre-Moreira Magna Suzana, Costa Fanny Nascimento, Monteiro Carlos Eduardo da Silva, Ferreira Fabio Furlan, Barroso Regina Cely Rodrigues, Noël François, Sudo Roberto Takashi, Zapata-Sudo Gisele, Lima Lídia Moreira, Barreiro Eliezer J

机构信息

Laboratório de Avaliação e Síntese de Substâncias Bioativas (LASSBio®), Instituto Nacional de Ciência e Tecnologia de Fármacos e Medicamentos (INCT-INOFAR), Universidade Federal do Rio de Janeiro, CCS, Cidade Universitária, P.O. Box 68024, Rio de Janeiro-RJ 21941-971, Brazil.

Programa de Pós-Graduação em Química, Instituto de Química, Universidade Federal do Rio de Janeiro, Rio de Janeiro-RJ 21941-909, Brazil.

出版信息

Molecules. 2015 Feb 12;20(2):3067-88. doi: 10.3390/molecules20023067.

Abstract

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.

摘要

N-酰腙(NAH)部分被认为是一种优势结构,存在于许多具有不同药理活性的化合物中。在归因于NAH衍生物的活性中,抗炎和镇痛活性反复出现。作为旨在设计新型镇痛和抗炎先导候选物的研究计划的一部分,通过对原型LASSBio-294进行分子修饰,在结构上设计了一系列环己基-N-酰腙10-26,代表了一类新型的环烷基类似物。合成了化合物10-26及其构象受限类似物9,并在经典药理学实验中作为镇痛和抗炎剂进行了评估。环己基-N-酰腙10-26和环己烯基类似物9表现出很强的抗炎和/或镇痛活性,但化合物13因其在神经性疼痛模型中的重要镇痛活性而脱颖而出,成为治疗急性和慢性疼痛状态的新原型。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/34fe/6272651/367bb0283ecf/molecules-20-03067-g001.jpg

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