For laboratory research use only. Not for human or animal consumption.
BioIntegrityResearch

Metabolic Signaling

GLP-2 Dual Agonist

Dual GIP/GLP-1 receptor agonist

Dual GIP / GLP-1 Receptor Agonist

Research context

This compound is a 39-residue synthetic peptide derived from the GIP sequence, engineered for activity at both the GIP and GLP-1 receptors with reported imbalance favouring GIP. Research examines relative receptor potency, β-arrestin recruitment profiles, and biased agonism at each receptor.

Common assays: GIPR/GLP-1R dual binding · cAMP accumulation · β-arrestin recruitment · Receptor internalisation

Specification

DesignationDual GIP/GLP-1 receptor agonist
Full nameDual GIP / GLP-1 Receptor Agonist
SequenceSynthetic 39-residue peptide based on the GIP sequence with Aib substitutions
CAS number2023788-19-2
Molecular formulaC225H348N48O68
Molecular weight4813.45 g/mol
Formats10 mL Vial · 15 mL Nasal Spray · 15 mL Oral Spray
SolubilityBacteriostatic water, sterile water
StorageLyophilised: 2–8 °C, protected from light. Reconstituted: 2–8 °C.
Current lotTIR40N1125

Published literature

Selected peer-reviewed references describing research involving this compound. Listed for reference only; inclusion is not a claim about any outcome.

  1. Coskun T, Sloop KW, Loghin C, et al.LY3298176, a novel dual GIP and GLP-1 receptor agonist for the treatment of type 2 diabetes mellitus: from discovery to clinical proof of conceptMolecular Metabolism · 2018 Find on PubMed ↗
  2. Willard FS, Douros JD, Gabe MB, et al.Tirzepatide is an imbalanced and biased dual GIP and GLP-1 receptor agonistJCI Insight · 2020 Find on PubMed ↗

Common questions

What makes this a dual agonist?

It is based on the GIP sequence but engineered to also activate the GLP-1 receptor. Published characterisation reports differing potency at the two receptors rather than balanced activity.

What is biased agonism in the dual-agonist literature?

It refers to a ligand preferentially activating one downstream pathway over another at the same receptor — here, reported differences between cAMP signalling and β-arrestin recruitment at GLP-1R.

Same pathway

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