Design and synthesis of novel potent antinociceptive agents:: Methyl-imidazolyl N-acylhydrazone derivatives

被引:62
作者
Figueiredo, JM
Câmara, CD
Amarante, EG
Miranda, ALP
Santos, FM
Rodrigues, CR
Fraga, CAM
Barreiro, EJ
机构
[1] Univ Fed Rio de Janeiro, CCS, Fac Farm, LASSBio, BR-21944970 Rio de Janeiro, Brazil
[2] Univ Fed Rio de Janeiro, Inst Quim, BR-21944970 Rio de Janeiro, Brazil
关键词
D O I
10.1016/S0968-0896(00)00152-8
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
This paper describes recent results of design, synthesis and pharmacological evaluation of new N-heterocyclic functionalized N-acylhydrazone compounds, belonging to the 2-methyl-imidazolyl-3-acylhydrazone class (4a-e). These compounds were planned by applying the molecular simplification strategy to propose the structural modifications on the previously described functionalized imidazo[1,2-a]pyridine 3-acylhydrazone series (2), which presented an important analgesic profile. This new series (4) was synthesized in order to investigate the possible pharmacophoric contribution of the N-heteroaromatic ring and N-acylhydrazone moieties to the analgesic activity. Compounds 4a-b are the most potent antinociceptive agents from this series. (C) 2000 Elsevier Science Ltd. All rights reserved.
引用
收藏
页码:2243 / 2248
页数:6
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