A novel potential therapeutic avenue for autism: Design, synthesis and pharmacophore generation of SSRIs with dual action

Authors
Ghoneim, Ola M.Ibrahim, Diaa A.El-Deeb, Ibrahim M.Lee, So HaBooth, Raymond G.
Issue Date
2011-11-15
Publisher
Pergamon Press Ltd.
Citation
Bioorganic & Medicinal Chemistry Letters, v.21, no.22, pp.6714 - 6723
Abstract
Autism symptoms are currently modulated by Selective Serotonin Reuptake Inhibitors (SSRIs). SSRIs slow onset of action limits their efficiency. The established synergistic activity of SSRIs and 5HT(1B/1D) autoreceptors antagonists motivated us to incorporate SSRIs and 5HT(1B/1D) antagonists in one 'hybrid' molecule. A library of virtual 'hybrid' molecules was designed using the tethering technique. A pharmacophore model was generated derived from 16 structurally diverse SSRIs (K-i = 0.013-5000 nM) and used as 3D query. Compounds with fit values (>= 2) were chosen for synthesis and subsequent in vitro biological evaluation. Our pharmacophore model is a promising milestone to a class of SSRIs with dual action. (C) 2011 Elsevier Ltd. All rights reserved.
Keywords
SEROTONIN REUPTAKE INHIBITORS; BIOLOGICAL EVALUATION; RECEPTOR; DERIVATIVES; ANTAGONISTS; PIPERAZINES; DISRUPTION; ACTIVATION; SEROTONIN REUPTAKE INHIBITORS; BIOLOGICAL EVALUATION; RECEPTOR; DERIVATIVES; ANTAGONISTS; PIPERAZINES; DISRUPTION; ACTIVATION; Autism; Selective Serotonin Reuptake Inhibitors (SSRIs); Pharmacophore
ISSN
0960-894X
URI
https://pubs.kist.re.kr/handle/201004/129806
DOI
10.1016/j.bmcl.2011.09.046
Appears in Collections:
KIST Article > 2011
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