Chemical Structure : CT-996
CAS No.: 2810808-95-6
Catalog No.: PC-26360Not For Human Use, Lab Use Only.
Tifeglipron (CT-996, RO7795081, RG6652) is a potent, selective and orally active glucagon-like peptide 1 receptor (GLP-1R) agonist with EC50 of 0.49 nM.
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| 5 mg | $258 | In stock | |
| 10 mg | $398 | In stock | |
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Tifeglipron (CT-996, RO7795081, RG6652) is a potent, selective and orally active glucagon-like peptide 1 receptor (GLP-1R) agonist with EC50 of 0.49 nM.
CT-996 reduces the β-arrestin recruitment and GLP-1R internalization.
CT-996 suppresses postprandial blood glucose following a mixed meal tolerance test (MMTT) in mice expressing the human GLP-1 receptor and enhances glucose stimulated insulin secretion (GSIS) during an intravenous glucose challenge in obese monkeys.
| M.Wt | 579.60 | |
| Formula | C30H31F2N5O5 | |
| Appearance | Solid | |
| Storage |
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| Solubility |
10 mM in DMSO |
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| Chemical Name/SMILES |
2-(((2S,4S)-4-((2-((2,4-difluorophenoxy)methyl)pyrimidin-4-yl)oxy)-2-methylpiperidin-1-yl)methyl)-1-(((S)-oxetan-2-yl)methyl)-1H-benzo[d]imidazole-6-carboxylic acid |
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1. Drucker DJ. GLP-1-based therapies for diabetes, obesity and beyond. Nat Rev Drug Discov. 2025 Aug;24(8):631-650.
2. JIAN LUO, et al. Diabetes 14 June 2024; 73 (Supplement_1): 771–P.

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