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Glucagon Receptor

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Glucagon Receptor

Chemical Structure Cat. No. Product Name CAS No.
GLP-1 receptor agonist 5 Chemical Structure
BCP31389 GLP-1 receptor agonist 5 1246826-07-2
GLP-1 receptor agonist 5 is a GLP-1 receptor agonist extracted from patent WO2010114824A1, Example 179, with an EC50 of 5 nM.
PF-06882961 Chemical Structure
BCP31501 PF-06882961 2230198-02-2
PF-06882961 is a Glucagon-like peptide-1 (GLP-1) receptor.
GLP-1 receptor agonist 1 Chemical Structure
BCP31425 GLP-1 receptor agonist 1 2212020-52-3
GLP-1 receptor agonist 1 is a glucagon-like peptide-1 (GLP-1) receptor agonist extracted from patent WO2018056453A1, Compound 67.
Albiglutide Chemical Structure
BCP17376 Albiglutide 782500-75-8
Albiglutide is a recombinant DNA produced polypeptide analogue of human glucagon-like peptide-1 (GLP-1) which is used in combination with diet and exercise in the therapy of type 2 diabetes, either alone or in combination with other antidiabetic agents. There have been no published reports of hepatotoxicity attributed to albiglutide therapy.
PF-06291874 Chemical Structure
BCP24856 PF-06291874 1393124-08-7
PF-06291874 is a highly potent glucagon receptor antagonist. It displays low in vivo clearance and excellent oral bioavailability in both rats and dogs.
BETP Chemical Structure
BCP19312 BETP 1371569-69-5
BETP is an agonist of glucagon-like peptide-1 (GLP-1) receptor, with EC50s of 0.66 and 0.755 μM for human and rat GLP-1 receptor, respectively.
Semaglutide Chemical Structure
BCP24773 Semaglutide 910463-68-2
Semaglutide, Long-acting human GLP-1 analog. Semaglutide seems to be more effective the other GLP-1Ras.
GRA Ex-25 Chemical Structure
BCP18873 GRA Ex-25 307983-31-9
GRA Ex-25 is an inhibitor of glucagon receptor, with IC50 of 56 and 55 nM for rat and human glucagon receptors, respectively.
Dulaglutide Chemical Structure
BCP24327 Dulaglutide 923950-08-7
Dulaglutide is a glucagon-like peptide-1 (GLP-1) receptor agonist.
Lixisenatide Chemical Structure
BCP24030 Lixisenatide 320367-13-3
Lixisenatide inhibit glucagon release, markedly reduce postprandial glucago.
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