UTG-4 is a GLP-1R, GIPR, and GCGR agonist with EC50 values of 126.3 pM, 29.2 pM, and 250.2 pM, respectively. UTG-4 binds to HSA (Kd = 14.6 µM). UTG-4 effectively alleviates endothelial-mesenchymal transition. UTG-4 promotes weight loss, inhibits food intake, improves glucose tolerance, and has a significant anti-atherosclerotic effect[1].
Molekulargewicht:
4920.52
Formel:
C230H349N49O70
Target-Kategorie:
GCGR,GLP Receptor
Anwendungsbeschreibung:
MCE Product type: Peptides
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