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Semaglutide TFA

CAS No. :

MCE 站：Semaglutide TFA

产品活性：Semaglutide TFA 是人胰高血糖素样肽-1 的一个长效类似物，是人胰高血糖素样肽-1 (GLP-1) 受体激动剂。Semaglutide TFA 有潜力用于 2 型糖尿病的研究。

研究领域：GPCR/G Protein

作用靶点：GCGR

In Vitro: Semaglutide has two amino acid substitutions compared to human GLP-1 (Aib⁸, Arg³⁴) ａnd is derivatized at lysine 26. The GLP-1R affinity of Semaglutide is 0.38±0.06 nM. Semaglutide is a GLP-1 analogue with 94% sequence omology to human GLP-1.

In Vivo: The plasma half-life of Semaglutide is 46h in mini-pigs following i.v. administration ａnd semaglutide has an MRT of 63.6h after s.c. dosing to mini-pigs. Semaglutide improves 1-methyl-4-phenyl-1,2,3,6- tetrahydropyridine (MPTP)-induced motor impairments. In addition, Semaglutide rescues the decrease of tyrosine hydroxylase (TH) levels, alleviates the inflammation response, reduces lipid peroxidation, inhibits the apoptosis pathway, ａnd also increases autophagy- related protein expression, to protect dopaminergic neurons in the substantia nigra ａnd striatum. Moreover, the long-acting GLP-1 analogue semaglutide is superior to liraglutide in most parameters. Semaglutide lowers blood glucose by stimulating the release of insulin ａnd also lowers body weight.

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