SSTR5 antagonist 2 TFA structure
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Common Name | SSTR5 antagonist 2 TFA | ||
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CAS Number | 1254733-98-6 | Molecular Weight | 660.65 | |
Density | N/A | Boiling Point | N/A | |
Molecular Formula | C34H36F4N2O7 | Melting Point | N/A | |
MSDS | N/A | Flash Point | N/A |
Use of SSTR5 antagonist 2 TFASSTR5 Antagonist 1 (compound 10) is a highly potent, oral active and selective somatostatin (receptor) subtype 5 (SSTR5) antagonist and has potential to treat type 2 diabetes mellitus (T2DM)[1]. |
Name | SSTR5 antagonist 2 TFA |
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Description | SSTR5 Antagonist 1 (compound 10) is a highly potent, oral active and selective somatostatin (receptor) subtype 5 (SSTR5) antagonist and has potential to treat type 2 diabetes mellitus (T2DM)[1]. |
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Related Catalog | |
Target |
SSTR5[1]. |
In Vivo | SSTR5 antagonist 2 (10 mg/kg, orally) increases both total and active circulating incretin hormone GLP1 levels in mice at a dose of 10 mg/kg[1]. SSTR5 antagonist 2 increases pancreatic insulin secretion as well as total and active GLP1 release, and demonstrates synergistic effects in combination with DPP4 inhibitors[1]. Animal Model: Rodent diabetic model without risk of hypoglycemia[1]. Dosage: 10 mg/kg. Administration: Orally. Result: Increased both total and active circulating incretin hormone GLP1 levels. |
References |
Molecular Formula | C34H36F4N2O7 |
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Molecular Weight | 660.65 |