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Vilazodone
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Vilazodone
CAS No. : 163521-12-8
MCE 站:Vilazodone
产品活性:Vilazodone (EMD 68843;SB 659746A) 是一种有效的,具有口服活性的,选择性 5 -羟色胺再摄取抑制剂 (SSRI) 和部分 5-HT1A 受体激动剂。Vilazodone 在动物体内表现出抗抑郁作用,可用于抑郁症 (MDD) 和情绪性疾病的研究。
研究领域:GPCR/G Protein | Neuronal Signaling
作用靶点:5-HT Receptor | Serotonin Transporter
In Vitro: Vilazodone shows an IC50 of 0.2 nM at the human 5-HT1A receptor and 0.5 nM for the SERT. Vilazodone preferentially binds to the high agonist affinity state of human 5-HT1A?receptors, and it displays high affinity (pKi≥9.3) for human recombinant and rat, guinea pig, mouse, and marmoset native tissue 5-HT1A?receptors.Vilazodone acts as a high efficacy partial agonist at 5-HT1A?receptors. In [35S]GTPγS binding studies in Sf9 cells expressing h5-HT1A?receptors, a single concentration of Vilazodone (100nM) increases basal binding by approximately 70% of that produced by the full 5-HT1A?receptor agonist, 8‐OH‐PIPAT.In [35S]GTPγS binding studies in rat hippocampal membranes, Vilazodone acts as a potent 5‐HT1A?receptor partial agonist with a pEC50?of 8.1 and an intrinsic activity of 0.61.Vilazodone acts as a potent 5‐HT reuptake inhibitor in rat and guinea pig cortex. In LLCPK cells expressing human SERT, whereby vilazodone inhibits [3H]5‐HT uptake with a pIC50?of 8.8.
In Vivo: Vilazodone (intraperitoneal injection; 3 mg/kg ; single dose) produces increases in extracellular levels of 5‐HT in both the frontal cortex (FC) and ventral hippocampus (vHipp) of rats in vivo?microdialysis studies. Maximum increases are observed at 3 mg/kg and reaches 527% and 558% of preinjection baseline values in the FC and vHipp, respectively.Vilazodone (oral gavage ;55 mg/kg ; single dose) inhibits stress‐induced vocalizations in the rat ultrasonic vocalizations test at 120 and 210 min post dose.
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