TC2
TC2 is an efficient GIPR-preferring monomeric quadruple agonist that can respectively activate GIPR, GLP-1R, GcgR, and Y2R with IC50 values of 0.47, 2.1, 30, and 55 nM respectively. TC2 exhibits a significant GLP-1R preference, with a significant reduction in β-inhibitory protein 2 (βArr2) recruitment, while maintaining a strong cAMP signal. TC2 can be used for research on obesity and diabetes[1].
Product Specifications
UNSPSC
12352209
Target
GCGR; GLP Receptor; Neuropeptide Y Receptor
Related Pathways
GPCR/G Protein; Neuronal Signaling
Applications
Metabolism-protein/nucleotide metabolism
Field of Research
Metabolic Disease
Smiles
Molecular Formula
C263H407N67O72
Molecular Weight
5659.45
References & Citations
[1]Dinsmore TC, et al. Molecular Design of Unimolecular Tetra-Receptor Agonists. J Am Chem Soc. 2025 Jun 18;147 (24) :20819-20832.
Shipping Conditions
Room temperature
Scientific Category
Peptides
Clinical Information
No Development Reported
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