Xylazine

本公司产品仅用于科研实验，不得用于人体或动物的临床与诊断

Xylazine 是 α2-肾上腺素能受体激动剂。

Xylazine is α2-adrenergic receptor agonist.

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Xylazine (5.2 mg/kg; intraperitoneal injection; for 10-60 minutes; male Sprague-Dawley rats) administration alters mRNA expression and protein phosphorylation levels of AMPK signaling molecules, suggesting that the LKB1-AMPK pathway plays a role in the sedative and tranquilizing effects in the CNS caused by Xylazine treatment. Animal Model:Male Sprague-Dawley rats (160-180 g)Dosage:5.2 mg/kg Administration:Intraperitoneal injection; for 10 minutes, 20 minutes, 40 minutesor 60 minutes Result:Increased in AMPK activity in the cerebral cortex, hippocampus, thalamus and cerebellum. Phosphorylated LKB1 and AMPKα protein levels were decreased.

BAY 1470

Metabolic Enzyme/Protease

P450

α2-adrenergic receptor

Neurological Disease

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7361-61-7

220.33

C12H16N2S

>98% (HPLC)

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Cc1cccc(C)c1NC1=NCCCS1

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(-20℃)

With Ice Pack

≥ 2 years