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CAS No. : 132810-10-7
MCE 国际站:Blonanserin
产品活性:Blonanserin (AD-5423) 是一种有效的 5-HT2A (Ki = 0.812 nM) 和多巴胺 D2 受体 (Ki = 0.142 nM) 拮抗剂。Blonanserin 通常作为一种非典型的抗精神病试剂,可用于锥体外系症状、过度镇静或低血压的研究。
研究领域:GPCR/G Protein | Neuronal Signaling
作用靶点:5-HT Receptor | Dopamine Receptor | Adrenergic Receptor | Sigma Receptor
In Vitro: Blonanserin exerts some blockade of α1-adrenergic receptors (Ki=26.7 nM) and also shows significant affinity for the D3 receptor (Ki=0.494 nM). Blonanserin possesses low affinity for the sigma receptor (IC50=286 nM), but lacks significant affinity for numerous other sites including the 5-HT1A, 5-HT3, D1, α2-adrenergic, β-adrenergic, H1, and mACh receptors and the monoamine transporters.
In Vivo: Blonanserin (oral gavage; 1 mg/kg; 14 days) significantly ameliorates the social deficit observed in PCP-administered mice and inhibits the decrease in the levels of Ser897-phosphorylation, but preatment with blonanserin does not affect the social behaviors in saline-administered mice.
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