Structure–activity relationship studies of SYA 013, a homopiperazine analog of haloperidol

Structure–activity relationship studies on 4-(4-(4-chlorophenyl)-1,4-diazepan-1-yl)-1-(4-fluorophenyl)butan-1-one (SYA 013), a homopiperazine analog of haloperidol has resulted in an understanding of the effect of structural modifications on binding affinity at dopamine and serotonin receptor subtyp...

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Veröffentlicht in:Bioorganic & medicinal chemistry 2012-03, Vol.20 (5), p.1671-1678
Hauptverfasser: Peprah, Kwakye, Zhu, Xue Y., Eyunni, Suresh V.K., Etukala, Jagan R., Setola, Vincent, Roth, Bryan L., Ablordeppey, Seth Y.
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Sprache:eng
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Zusammenfassung:Structure–activity relationship studies on 4-(4-(4-chlorophenyl)-1,4-diazepan-1-yl)-1-(4-fluorophenyl)butan-1-one (SYA 013), a homopiperazine analog of haloperidol has resulted in an understanding of the effect of structural modifications on binding affinity at dopamine and serotonin receptor subtypes. Further exploration, using bioisosteric replacement strategies has led to the identification of several new agents including compounds 7, 8, 11 and 12 which satisfy the initial criteria for further exploration as new antipsychotic agents. In addition, compound 18, a D3 selective tropanol, has been identified as having the potential for further optimization into a useful drug which may combat neuropsychiatric diseases.
ISSN:0968-0896
1464-3391
DOI:10.1016/j.bmc.2012.01.022