[Des-His1,Glu9] Glucagon structure
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Common Name | [Des-His1,Glu9] Glucagon | ||
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CAS Number | 110121-11-4 | Molecular Weight | 3359.63 | |
Density | N/A | Boiling Point | N/A | |
Molecular Formula | C148H220N40O48S | Melting Point | N/A | |
MSDS | N/A | Flash Point | N/A |
Use of [Des-His1,Glu9] Glucagon[Des-His1,Glu9] Glucagon is a potent glucagon receptor system peptide antagonist. [Des-His1,Glu9] Glucagon enhances the glucose-stimulated release of insulin from pancreatic islet cells. [Des-His1,Glu9] Glucagon can be used to research diabetes[1]. |
Name | [Des-His1,Glu9] Glucagon |
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Description | [Des-His1,Glu9] Glucagon is a potent glucagon receptor system peptide antagonist. [Des-His1,Glu9] Glucagon enhances the glucose-stimulated release of insulin from pancreatic islet cells. [Des-His1,Glu9] Glucagon can be used to research diabetes[1]. |
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Related Catalog | |
Target |
Glucagon Receptor[1] |
In Vitro | [Des-His1,Glu9] Glucagon (1 pM-100 μM) does not activate membrane-bound adenylate cyclase up to a concentration of 2×10-4 molar in the cAMP assay on isolated rat liver membranes (from male Sprague Dawley rats)[1]. |
In Vivo | [Des-His1,Glu9] Glucagon (3.6-4.0 μg/kg for rabbits, 1 mg/kg for rats; i.v.; single dosage) suppresses hyperglycemic effects in rabbits and rats[1]. Animal Model: New Zealand rabbits (2.8-3.8 kg; fasted for 18 hours)[1] Dosage: 3.6-4.0 μg/kg Administration: i.v.; single dosage Result: Suppressed hyperglycemic response of glucagon. Animal Model: Male Wistar rats weighing [350-400 mg; hyperglycemia induced by i.p. injection of 65 mg/kg Streptozotocin (HY-13753)][1] Dosage: 1 mg/kg Administration: Intravenously administration through the tail vein; single dosage Result: Decreased blood glucose rapidly, and reduced hyperglycemic effect by 70% within 5 min. |
Molecular Formula | C148H220N40O48S |
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Molecular Weight | 3359.63 |