BAY 38-7271  

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包装规格:25mg 50mg 100mg in glass bottle
产品简介:一个选择性、高效的大麻素受体CB1/CB2激动剂,对人重组CB1和CB2 作用的Ki值分别为1.85nM和5.96nM。BAY 38-7271具有很强的神经保护特性。
体外研究:BAY 38-7271 shows only minor interactions at the micromolar range with other binding sites such as adenosine A3 receptor(IC50=7.5 μM), peripheral GABAAbenzodiazepine receptor(IC50= 971 nM), melatonin ML1 receptor (IC50=3.3 μM), and at the monoamine transporter (IC50= 1.7 μM).
体内研究:BAY 38-7271 (Ed50 = 0.02 mg/kg; i.v. and 0.5 mg/kg; i.p.) induces a potent and dose-de-pendent reduction in core body temperature. BAY 38-7271 has low physical dependence liability and is not essentially different from that of other cannabinoid CB1 receptor agonists. BAY 38-7271 (1-1000 ng/kg/h; i.v. infusion; for 4 hours) shows neuroprotective efficacy in the rat SDH model. BAY 38-7271 also has neuroprotective efficacy in models of transient and permanent occlusion of the middle cerebral artery and brain edema models.
保存条件:-20℃
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