CT-996 is an orally active GLP-1RA agonist with an EC 50 of 0.49 nM. CT-996 reduces the recruitment of β-arrestin and the internalization of GLP-1R . CT-996 suppresses postprandial blood glucose in mice expressing human GLP-1 receptors and enhances glucose-stimulated insulin secretion (GSIS) in obese monkeys during intravenous glucose challenge. CT-996 can be used for the research of type 2 diabetes (T2D) and obesity.
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