Synthesis, docking and pharmacological evaluation of novel indole based potential atypical antipsychotics

被引:14
作者
Bali, Alka [1 ]
Sen, Umesh [1 ]
Peshin, Tania [1 ]
机构
[1] Panjab Univ, Univ Inst Pharmaceut Sci, UGC Ctr Adv Study, Chandigarh 160014, India
关键词
Atypical antipsychotics; Indole derivatives; Log BB; D-2/5-HT2A antagonists; In silico; Docking studies; 1-(ARYLOXYPROPYL)-4-(CHLOROARYL) PIPERAZINES; PIPERIDINE DERIVATIVES; DOPAMINE; RECEPTOR; SERIES; SCHIZOPHRENIA; AFFINITY;
D O I
10.1016/j.ejmech.2013.09.020
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
A series of substituted indole derivatives have been synthesized and the target compounds evaluated for atypical antipsychotic activity in apomorphine induced mesh climbing and stereotypy assays in mice. The compounds 11 and 12 have emerged as important lead compounds showing potential atypical antipsychotic profile. In silico (docking studies) have been carried out to postulate a hypothetical binding model for the target compounds with respect to the dopaminergic D-2 and 5-HT2A receptors. Theoretical ADME profiling of the compounds based on selected physicochemical parameters has suggested an excellent compliance with Lipinski's rules. The potential of these compounds to penetrate the blood brain barrier (log BB) was computed through an online software program and the values obtained for the compounds suggest good potential for brain permeation. (C) 2013 Elsevier Masson SAS. All rights reserved.
引用
收藏
页码:477 / 490
页数:14
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