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Tandospirone
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Tandospirone
CAS No. : 87760-53-0
MCE 站:Tandospirone
产品活性:Tandospirone (SM-3997) 是一种高效、选择性的 5-HT1A 受体部分激动剂,其 Ki 值为 27 nM。Tandospirone 具有抗焦虑和抗抑郁作用。Tandospirone 可用于中枢神经系统疾病及其潜在机制的研究。
研究领域:GPCR/G Protein | Neuronal Signaling
作用靶点:5-HT Receptor
In Vitro: Tandospirone is approximately two to three orders of magnitude less potent at 5-HT2, 5-HT1C, α1-adrenergic, α2-adrenergic and dopamine D1 and D2 receptors (Ki values ranging from 1300 to 41000 nM) than 5-HT1A.
Tandospirone is essentially inactive at 5-HT1B receptors; 5-HT uptake sites; beta-adrenergic, muscarinic cholinergic, and benzodiazepine receptors.
Tandospirone activats postsynaptic 5-HT1A receptor coupled with G-protein (Gi/o), resulting in inhibition of protein kinase A (PKA)-mediated protein phosphorylation and neuronal activity.
In Vivo: Tandospirone (10-80 mg/kg; i.p.) inhibits freezing behavior in the conditioned fear stress-induced freezing behavior rat model.
Tandospirone exhibits the anxiolytic effect dependent on the plasma concentration of at 0.5 hours but not 4 hours.
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