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Retatrutide (sodium salt)

(Synonyms: LY3437943) 目录号 : GC91869

Retatrutide is a triple agonist of the glucagon receptor (GCGR), glucagon-like peptide 1 receptor (GLP-1R), and gastric inhibitory polypeptide receptor (GIP receptor), also known as the glucose-dependent insulinotropic polypeptide receptor.

Retatrutide (sodium salt) Chemical Structure

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1 mg
¥798.00
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5 mg
¥3,794.00
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10 mg
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25 mg
¥13,972.00
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Sample solution is provided at 25 µL, 10mM.

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Retatrutide is a triple agonist of the glucagon receptor (GCGR), glucagon-like peptide 1 receptor (GLP-1R), and gastric inhibitory polypeptide receptor (GIP receptor), also known as the glucose-dependent insulinotropic polypeptide receptor.[1] It induces cAMP accumulation in HEK293 cells expressing the human GCGR, GLP-1R, or GIP receptor (EC50s = 5.79, 0.775, and 0.0643 nM, respectively). Retatrutide (0.1-30 nmol/kg) decreases plasma glucose levels in an intraperitoneal glucose tolerance test in mice. It decreases body weight, calorie intake, fat mass, and lean mass in a mouse model of diet-induced obesity in a dose-dependent manner. Acute administration of retatrutide (10 nmol/kg) delays gastric emptying and chronic administration for 10 days decreases food intake and body weight in mice.[2]

References:
[1].Coskun, T., Urva, S., Roell, W.C., et al.LY3437943, a novel triple glucagon, GIP, and GLP-1 receptor agonist for glycemic control and weight loss: From discovery to clinical proof of conceptCell Metab.34(9)1234-1247(2022).
[2].Urva, S., O'Farrell, L., Du, Y., et al.The novel GIP, GLP-1 and glucagon receptor agonist retatrutide delays gastric emptyingDiabetes Obes. Metab.25(9)2784-2788(2023).

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1 mg 5 mg 10 mg
1 mM 0.2114 mL 1.0568 mL 2.1136 mL
5 mM 0.0423 mL 0.2114 mL 0.4227 mL
10 mM 0.0211 mL 0.1057 mL 0.2114 mL
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