1. GPCR/G Protein
  2. Glucagon Receptor
  3. GLP-2(3-33)


Cat. No.: HY-P2625
Handling Instructions

GLP-2(3-33), generated naturally by dipeptidylpeptidase IV (DPPIV), acts as a partial agonist on GLP-2 receptor (EC50=5.8 nM).

For research use only. We do not sell to patients.

Custom Peptide Synthesis

GLP-2(3-33) Chemical Structure

GLP-2(3-33) Chemical Structure

CAS No. : 275801-62-2

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GLP-2(3-33), generated naturally by dipeptidylpeptidase IV (DPPIV), acts as a partial agonist on GLP-2 receptor (EC50=5.8 nM)[1][2].

In Vitro

GLP-2 is secreted as a 33-amino acid peptide, but is rapidly degraded at an N-terminus site to GLP-2(3-33) in circulation, in large part, by dipeptidylpeptidase IV (DPPIV). GLP-2 (3-33) acts as a partial agonist with potential competitive antagonistic properties on the GLP-2 receptor. In the GLP-2 receptor-binding assay, the binding IC50 for GLP-2 1–33 was 3.1 nM, and it was 41 nM for GLP-2 3-33. Thus, GLP-2 3–33 had 7.5% binding affinity compared to GLP-2 1-33[1].

In Vivo

GLP-2(3-33) (60 ng; once a day i.p. for 4 weeks) increases dyslipidemia and hepatic lipid accumulation in HFD-fed mice[2].

Animal Model: Male C57BL/6J (B6) mice (HFD)[2]
Dosage: 60 ng
Administration: Once a day i.p. for 4 weeks
Result: Significantly affected plasma lipids; Showed increase of triglycerides and cholesterol and reduction of HDL; Significantly increased plasma ALT and AST and intrahepatic lipid concentration.
Molecular Weight






Sequence Shortening



Room temperature in continental US; may vary elsewhere.


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GLP-2(3-33)Glucagon ReceptorGCGRDPPIVHFD-fedcompetitivecirculationInhibitorinhibitorinhibit

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