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Details

Autor(en) / Beteiligte
Titel
Second generation N-(1,2-diphenylethyl)piperazines as dual serotonin and noradrenaline reuptake inhibitors: Improving metabolic stability and reducing ion channel activity
Ist Teil von
  • Bioorganic & medicinal chemistry letters, 2010-06, Vol.20 (12), p.3788-3792
Ort / Verlag
Amsterdam: Elsevier Ltd
Erscheinungsjahr
2010
Quelle
ScienceDirect
Beschreibungen/Notizen
  • New N-(1,2-diphenylethyl)piperazines 6 are disclosed as dual serotonin and noradrenaline reuptake inhibitors (SNRI). Piperazine (−)-6a was identified as a potent and selective dual SNRI with improved metabolic stability and reduced ion channel activity when compared to previous examples. New N-(1,2-diphenylethyl)piperazines 6 are disclosed as dual serotonin and noradrenaline reuptake inhibitors (SNRI) which may have potential in treating stress urinary incontinence (SUI). In this Letter, we present new data for SNRI PF-526014 (4) including performance in a canine in vivo model of SUI, cardiovascular assessment, pharmacokinetics in dog and determination of the primary routes of metabolism in vitro. Starting from 4, detailed structure activity relationships established that potent dual SNRIs could be achieved by appropriate substitution of the phenyl rings (6: R; R1) combined with a preferred stereochemistry. From this set of compounds, piperazine (−)-6a was identified as a potent and selective dual SNRI with improved metabolic stability and reduced ion channel activity when compared to 4. Based on this profile, (−)-6a was selected for further evaluation in a preclinical model of SUI.

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