
Insulin degludec
CAS No. 844439-96-9
Insulin degludec ( —— )
Catalog No. M25046 CAS No. 844439-96-9
Insulin degludec is an ultra-long-acting form of insulin used for the treatment of hyperglycemia caused by type 1 and type 2 dabetes. Insulin degludec shows binding efficiency with an IC50 value of 19.59 nM/L for insulin receptor. Insulin degludec can be used for the research of type 1 and type 2 diabetes.
Purity : >98% (HPLC)






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5MG | 298 | In Stock |
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10MG | 496 | In Stock |
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100MG | Get Quote | In Stock |
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Biological Information
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Product NameInsulin degludec
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NoteResearch use only, not for human use.
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Brief DescriptionInsulin degludec is an ultra-long-acting form of insulin used for the treatment of hyperglycemia caused by type 1 and type 2 dabetes. Insulin degludec shows binding efficiency with an IC50 value of 19.59 nM/L for insulin receptor. Insulin degludec can be used for the research of type 1 and type 2 diabetes.
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DescriptionInsulin degludec is an ultra-long-acting form of insulin used for the treatment of hyperglycemia caused by type 1 and type 2 dabetes. Insulin degludec shows binding efficiency with an IC50 value of 19.59 nM/L for insulin receptor. Insulin degludec can be used for the research of type 1 and type 2 diabetes.Insulin degludec (0.001-1000 nM; 12 h) binds with insulin receptor with an IC50 value of 19.59 nM/L.Insulin degludec (200 nM; 10 min) increases glucose uptake in HL-1 cells.
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In VitroInsulin degludec (0.001-1000 nM; 12 h) binds with insulin receptor with an IC50 value of 19.59 nM.Insulin degludec (200 nM; 10 min) increases glucose uptake in HL-1 cells. Western Blot Analysis Cell Line:HL-1 cardiomyocytes Concentration:200 nM Incubation Time:0-60 min Result:Decreased the level of Akt phosphorylation after 5 and 10min treatment.
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In VivoInsulin degludec (5 U/kg; s.c. once daily for 30 days) affects glucose homeostasis and liver metabolism in diabetic mice undergoing insulin-induced hypoglycemia. Animal Model:Male Swiss mice with diabetes Dosage:5 U/kg Administration:Subcutaneous injection; 5 U/kg once daily for 30 days Result:Showed a fast response to insulin-induced hypoglycemia with a glycemic level at or slightly under 100 mg/dl after 60 min and this response effect can be abolished by cortisol. Diminished rates of glucose production and showed a low lactate production in livers. Increased the number of hepatocytes.
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Synonyms——
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PathwayTyrosine Kinase
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TargetInsulin Receptor
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Recptor——
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Research Area——
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Indication——
Chemical Information
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CAS Number844439-96-9
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Formula Weight——
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Molecular Formula——
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Purity>98% (HPLC)
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Solubility0.1 M HCL : 50 mg/mL (ultrasonic and adjust pH to 2 with 0.1 M HCL)
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SMILESN/A
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Chemical Name——
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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S961
S961 is an high-affinity and selective insulin receptor (IR) antagonist with IC50s of 0.048, 0.027, and 630 nM for HIR-A, HIR-B, and human insulin-like growth factor I receptor (HIGF-IR) in SPA-assay, respectively.
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GIP (human)
Potent insulinotropic hormone synthesized by duodenal K-cells. High affinity GIP receptor agonist (EC50 = 0.81 nM) that inhibits gastric acid secretion and stimulates pancreatic insulin release in response to glucose. Also affects lipid metabolism and displays mitogenic and antiapoptotic effects in pancreatic β-cells.
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MSDC-0160
A new generation insulin sensitizer and mitochondrial target of thiazolidinediones (mTOT) modulator that has low affinity for binding and activation of PPARγ (EC50=23.7 uM).