GLP-1(7-37)
CAS No. 106612-94-6
GLP-1(7-37)( —— )
Catalog No. M30005 CAS No. 106612-94-6
GLP-1 (7-37) is a truncated, bioactive form of GLP-1 that is the product of proglucagon processing in intestinal endocrine L cells.
Purity : >98% (HPLC)
COA
Datasheet
HNMR
HPLC
MSDS
Handing Instructions
| Size | Price / USD | Stock | Quantity |
| 5MG | 320 | Get Quote |
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| 10MG | 490 | Get Quote |
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| 25MG | 745 | Get Quote |
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| 100MG | Get Quote | Get Quote |
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| 200MG | Get Quote | Get Quote |
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Biological Information
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Product NameGLP-1(7-37)
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NoteResearch use only, not for human use.
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Brief DescriptionGLP-1 (7-37) is a truncated, bioactive form of GLP-1 that is the product of proglucagon processing in intestinal endocrine L cells.
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DescriptionGLP-1 (7-37) is a truncated, bioactive form of GLP-1 that is the product of proglucagon processing in intestinal endocrine L cells.(In Vivo):GLP-1(7-37) (0.5, 5 or 50 pmol/min/kg) infused during the second hour of a 2-hour 11-mM hyperglycemic clamp produces a dose-related enhancement of the glucose-stimulated increase in plasma insulin concentration and an increased rate of glucose infusion in rats. Infusion of GLP-1(7-37) (5 pmol/min/kg) from 1 hour through 7 hours produces a sustained increase in plasma insulin concentration relative to levels in rats infused with vehicle in rats with maintained glucose concentration at 11 mM.
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In Vitro——
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In VivoGLP-1(7-37) (0.5, 5 or 50 pmol/min/kg) infused during the second hour of a 2-hour 11-mM hyperglycemic clamp produces a dose-related enhancement of the glucose-stimulated increase in plasma insulin concentration and an increased rate of glucose infusion in rats.Infusion of GLP-1(7-37) (5 pmol/min/kg) from 1 hour through 7 hours produces a sustained increase in plasma insulin concentration relative to levels in rats infused with vehicle in rats with maintained glucose concentration at 11 mM. Animal Model:Male Sprague-Dawley rats weighing 300 to 350 g with maintained plasma glucose concentration at 11 mM.Dosage:0.5, 5 or 50 pmol/min/kg.Administration:IV during the second hour of a 2-hour 11-mmol/L hyperglycemic clamp.Result:Produced a dose-related enhancement of the glucose-stimulated increase in plasma insulin concentration and an increased rate of glucose infusion.Animal Model:Male Sprague-Dawley rats weighing 300 to 350 g with glucose IV at a variable.rate for 7 hours to maintain plasma glucose concentration at 11 mM.Dosage:5 pmol/min/kg.Administration:IV from 1 hour through 7 hours.Result:Produced a sustained increase in plasma insulin concentration relative to levels in rats infused with vehicle.
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Synonyms——
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PathwayGPCR/G Protein
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TargetGlucagon Receptor
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Recptor——
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Research Area——
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Indication——
Chemical Information
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CAS Number106612-94-6
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Formula Weight3355.67
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Molecular FormulaC151H228N40O47
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Purity>98% (HPLC)
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SolubilityH2O : 30 mg/mL (8.94 mM; Need ultrasonic and warming)
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SMILES——
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Chemical NameSequence:His-Ala-Glu-Gly-Thr-Phe-Thr-Ser-Asp-Val-Ser-Ser-Tyr-Leu-Glu-Gly-Gln-Ala-Ala-Lys-Glu-Phe-Ile-Ala-Trp-Leu-Val-Lys-Gly-Arg-Gly
Shipping & Storage Information
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Storage(-20℃)
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ShippingWith Ice Pack
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Stability≥ 2 years
Reference
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des-His1-[Glu9]-Gluc...
Glucagon receptor antagonist (pA2 = 7.2 for inhibition of glucagon-induced adenylyl cyclase activation in rat liver membranes); displays no agonist activity. Enhances glucose-stimulated pancreatic insulin release in vitro. Blocks added glucagon-induced hyperglycemia in normal rabbits without affecting glycogenolysis in vivo. Also blocks endogenous glucagon-induced hyperglycemia in streptozocin diabetic rats.
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MK-0893
A potent, selective, reversible and competitive antagonist of glucagon receptor with high binding affinity (IC(=50=6.6 nM) and functional cAMP activity (IC50=15.7 nM).
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Taspoglutide
Taspoglutide is a glucagon-like peptide-1(GLP-1) agonist for treatment of type 2 diabetes.
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