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Insulin Receptor

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Insulin Receptor

Chemical Structure Cat. No. Product Name CAS No.
MID-1 Chemical Structure
BCP48931 MID-1 312608-54-1
MID-1 is an inhibitor of MG53-IRS-1 (Mitsugumin 53-Insulin Receptor Substrate-1) interaction.
SU4984 Chemical Structure
BCP44116 SU4984 186610-89-9
SU4984 is a cell-permeable, reversible, and ATP-competitive inhibitor of the tyrosine kinase activity of fibroblast growth factor receptor 1 (FGFR1; IC50 = 10-20 µM).
NBI-31772 Chemical Structure
BCP42327 NBI-31772 374620-70-9
NBI-31772 is an potent insulin-like growth factor-1 binding protein (IGFBP) inhibitor.
Insulin Chemical Structure
BCP37517 Insulin 12584-58-6
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.
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