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Insulin Receptor

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Insulin Receptor

Chemical Structure Cat. No. Product Name CAS No.
KU14R Chemical Structure
BCP06499 KU14R 189224-48-4
A new I(3)-R antagonist, KU14R (2 (2-ethyl 2,3-dihydro-2-benzofuranyl)-2-imidazole), which selectively blocks the insulin secretory response to imidazolines.
GSK1838705A Chemical Structure
BCP02847 GSK1838705A 1116235-97-2
GSK1838705A is a potent small-molecule IGF-IR, the insulin receptor and anaplastic lymphoma kinase (ALK) inhibitor with IC50 of 2.0, 1.6 and 0.5 nM, respectively.
NVP-AEW541 Chemical Structure
BCP02417 NVP-AEW541 475489-16-8
NVP-AEW541 is an IGF-IR inhibitor with an IC50 of median 3.6 μM.
BMS-754807 Chemical Structure
BCP01926 BMS-754807 1001350-96-4
BMS-754807 is an orally bioavailable antagonist of human insulin-like growth factor type I receptor (IGF-1R) with potential antineoplastic activity.
Linsitinib Chemical Structure
BCP01831 Linsitinib 867160-71-2
Linsitinib is highly potent, orally efficacious and highly selective, dual ATP-competitive tyrosine kinase inhibitor of insulin-like growth factor-1 receptor (IGF-1R) (IC50: 35 nM) and insulin receptor (IR) (IC50: 75 nM).
Insulin degludec Chemical Structure
BCP23700 Insulin degludec 844439-96-9
Insulin degludec is an Insulin Analog. The chemical classification of insulin degludec is Insulin.
Human Insulin, Solution Chemical Structure
BCP08894 Human Insulin, Solution 11061-68-0
Insulin(human) is a peptide hormone that regulates the level of sugar (glucose) in the blood and that is produced by the beta cells of the pancreatic islets.
Insulin Chemical Structure
BCP13324 Insulin 11070-73-8
Insulin cattle is a kind of polypeptide hormone that regulates glucose metabolism in pancreatic islet B-cells.
MSDC-0160 Chemical Structure
BCP16099 MSDC-0160 146062-49-9
MSDC-0160 is a prototype mTOT-modulating insulin sensitizer being studied to treat diabetes and Alzheimer's disease.
NT-157 Chemical Structure
BCP29982 NT-157 1384426-12-3
NT157 is a selective inhibitor of IRS-1/2, IC50 values at sub-micromolar doses (ranging from 0.3 to 0.8 μM), has the potential to inhibit IGF-1R and STAT3 signaling pathways in cancer cells and stroma cells of TME leading to a decrease in cancer cell survival.
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