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Incretin

GIP

GIP (glucose-dependent insulinotropic polypeptide) is a 42-amino-acid incretin hormone released from intestinal K-cells after meals, where it helps stimulate glucose-dependent insulin secretion.

By The Peptides Codex Editorial TeamIndividual review date not recorded

Page data last changed: . Chemistry registry snapshot: . Registry refreshes and identity assessments are separate from scientific content review.

Length
42 aa
Class
Incretin
Function
Incretin hormone that stimulates insulin secretion after eating
Context
Endogenous hormone; one of the two receptors targeted by dual agonists like tirzepatide

The 'other incretin' — the GIP receptor is the second half of GIP/GLP-1 dual agonists.

Also known as: glucose-dependent insulinotropic polypeptide · gastric inhibitory polypeptide

Part of the Metabolic & GLP-1 peptides cluster

Overview

GIP (glucose-dependent insulinotropic polypeptide) is a 42-amino-acid incretin hormone released from intestinal K-cells after meals, where it helps stimulate glucose-dependent insulin secretion. Long overshadowed by GLP-1, its receptor is now a deliberate target in dual-agonist peptides such as tirzepatide.

Source & context

Biological / chemical source: Intestinal K-cells

Primary research or clinical context: Endogenous hormone; one of the two receptors targeted by dual agonists like tirzepatide

Incretin biology

GIP and GLP-1 are the two classical incretins: gut hormones that amplify insulin release specifically when glucose is present. GIP is secreted by K-cells in the upper small intestine, while GLP-1 comes from L-cells further down. Together they explain why oral glucose triggers more insulin than the same glucose given intravenously.

From overlooked to central

For years GIP received far less attention than GLP-1. The success of GIP/GLP-1 dual agonists renewed interest in its receptor pharmacology, and GIP biology is now a core topic in metabolic peptide education. This page describes that physiology; it does not offer treatment guidance.

Sequence

One-letter sequence commonly cited for GIP (educational; isoforms and modifications may differ):

YAEGTFISDYSIAMDKIHQQDFVNWLLAQKGKKNDWKHNITQ

YAEGTFISDYSIAMDKIHQQDFVNWLLAQKGKKNDWKHNITQ

GIP42 aaPEPTIDESCODEX.COMN-terminus →→ C-terminusY1A2E−3G4T5F6I7S8D−9Y10S11I12A13M14D−15K+16I17H18Q19Q20D−21F22V23N24W25L26L27A28Q29K+30G31K+32K+33N34D−35W36K+37H38N39I40T41Q42nonpolarpolaracidicbasicGly / Pronon-canonical (X)Hydropathy (Kyte–Doolittle): ▮ hydrophobic (cyan) / ▮ hydrophilic (rose) · Side-chain charge at pH 7: + / −
GIP — Structure cardDownload SVG
Y1A2E3G4T5F6I7S8D9Y10S11I12A13M14D15K16I17H18Q19Q20D21F22V23N24W25L26L27A28Q29K30G31K32K33N34D35W36K37H38N39I40T41Q42
Helical wheel projection

Residues plotted ~100° apart around an α-helix — clustering of one color reveals an amphipathic face.

Analyze sequences in the playground →

Structure & chemistry

Molecular identity & reference confidence

Reference mass unavailable

Reference values are taken from the cited molecular record or curated profile. A database match is not independent laboratory verification; modifications, counter-ions, and formulations can change the measured mass.

Molecular form
GIP (source record; form not independently established)
Species
Not established by this molecular identity audit
Termini (N / C)
Not specified / Not specified

Average reference mass

Reference policy updated: 2026-10-05

Identifiers
  • IUPHAR ligand: 3542
  • CAS RN: 100040-31-1

Chemistry values: IUPHAR/BPS Guide to Pharmacology · fetched 2026-09-06.

Clinical development snapshot

ClinicalTrials.gov lists 255 registered studies with “GIP” as an intervention (snapshot 2026-10-01). A registry footprint is not evidence of efficacy or approval.

Registered studies
255
Highest phase reached
Phase 4
Active in latest 100
79
Most recent update
2026-10-01
Most recently updated studies
NCTTitlePhaseStatusUpdated
NCT07793929A Study to Evaluate the Impact of Renal Impairment on the Pharmacokinetics (PK) of RibupatidePhase 1recruiting2026-10-01
NCT07734792Tirzepatide in Thrombectomy-Treated Acute Ischemic Stroke: A Randomized TrialPhase 3not yet recruiting2026-10-01
NCT06790225Glucose-dependent INsulinotropic Polypeptide: Effect on Bone Remodelling and Cell Activity (GINEBRA)Not applicablecompleted2026-10-01
NCT07846865Tirzepatide Versus Positive Airway Pressure for the Treatment of Obstructive Sleep Apnoea: A Randomised ComparPhase 3not yet recruiting2026-09-29
NCT06923839Testing the Potential Metabolic Effect of the Human Gut Bacterial Peptide, RUCILP, in Healthy MenPhase 1completed2026-09-29
NCT07685808Study of Olatorepatide in Adult Participants Living With Overweight or Obesity Without DiabetesPhase 2recruiting2026-09-29
See all on ClinicalTrials.gov →

Change log

Dated observations from the data pipeline (registry flags, trial footprints, identifiers) and editorial reviews of this profile.

  1. Trials8 registered studies added on ClinicalTrials.gov (now 255).

FAQ about GIP

What is GIP?+

GIP (glucose-dependent insulinotropic polypeptide) is a 42-amino-acid incretin hormone released from intestinal K-cells after meals, where it helps stimulate glucose-dependent insulin secretion. Long overshadowed by GLP-1, its receptor is now a deliberate target in dual-agonist peptides such as tirzepatide.

What Canadian product status is recorded for GIP?+

Canadian product status for GIP has not been verified in this profile. No verified record here does not mean no authorization exists. Status depends on the product, formulation and use; consult Health Canada's product records.

What is the typical length of GIP?+

GIP is commonly described as approximately 42 amino acids (Incretin).

Related peptides

References & further reading

  1. 1.Müller et al. (2025). Glucose-dependent insulinotropic polypeptide (GIP). Mol Metab
  2. 2.Zhang et al. (2021). The glucose-dependent insulinotropic polypeptide (GIP) regulates body weight and food intake via CNS-GIPR signaling. Cell Metab
  3. 3.Fisman et al. (2021). The dual glucose-dependent insulinotropic polypeptide (GIP) and glucagon-like peptide-1 (GLP-1) receptor agonist tirzepatide: a novel cardiometabolic therapeutic prospect. Cardiovasc Diabetol
  4. 4.Müller et al. (2026). Glucose-dependent insulinotropic polypeptide (GIP). Trends Endocrinol Metab
  5. 5.Heimbürger et al. (2020). Glucose-dependent insulinotropic polypeptide (GIP) and cardiovascular disease. Peptides
  6. 6.McIntosh et al. (2009). Glucose-dependent insulinotropic polypeptide (Gastric Inhibitory Polypeptide; GIP). Vitam Horm
  7. 7.Emanuelsson et al. (2026). Genetic variants of glucose-dependent insulinotropic polypeptide (GIP) signalling as proxy for body weight reduction and cardiovascular risk. Eur Heart J
  8. 8.Gasbjerg et al. (2018). Glucose-dependent insulinotropic polypeptide (GIP) receptor antagonists as anti-diabetic agents. Peptides
  9. 9.UniProt — GIP, Gastric inhibitory polypeptide, human (P09681)
  10. 10.Wikipedia — Gastric inhibitory polypeptide (GIP)
Disclaimer: Educational content only. Not medical advice. Not instructions for human use. Research peptides and unapproved products may be restricted or illegal to market for human consumption in your jurisdiction. Consult qualified professionals and applicable law.
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