Design and synthesis of 4H-3-(2-phenoxy)phenyl-1,2,4-triazole derivatives as benzodiazepine receptor agonists

被引:67
作者
Akbarzadeh, T
Tabatabai, SA
Khoshnoud, MJ
Shafaghi, B
Shafiee, A [1 ]
机构
[1] Univ Tehran Med Sci, Dept Med Chem, Fac Pharm, Tehran, Iran
[2] Shaheed Beheshti Univ Med Sci, Fac Pharm, Dept Med Chem, Tehran, Iran
[3] Shaheed Beheshti Univ Med Sci, Fac Pharm, Dept Pharmacol & Toxicol, Tehran, Iran
关键词
D O I
10.1016/S0968-0896(02)00469-8
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
A series of new 5-substituted analogues of 4H-3-(2-phenoxy)phenyl-1,2,4-triazole and its chlorinated derivatives was designed and prepared. Conformational analysis and superimposition of energy minima conformers of the compounds on estazolam, a known benzodiazepine receptor agonist, revealed that the main proposed benzodiazepine pharmacophores were well matched. Rotarod and pentylenetetrazole-induced lethal convulsion tests showed that the introduction of an amino group in position 5 of 1,2,4-triazole ring especially in chlorinated derivatives had the best effect which was comparable with diazepam. (C) 2002 Elsevier Science Ltd. All rights reserved.
引用
收藏
页码:769 / 773
页数:5
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