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effect collection

Gut Healing Research Peptides

7 peptides with demonstrated gut healing effects in research. Sorted by evidence quality from strongest to exploratory.

Overview

7 research peptides demonstrate gut healing properties. This collection covers their mechanisms, evidence base, and research applications.

BPC-157

Phase I–II Clinical Trials | Healing & Recovery

BPC-157 is a synthetic 15-amino-acid peptide (sequence: Gly-Glu-Pro-Pro-Pro-Gly-Lys-Pro-Ala-Asp-Asp-Ala-Gly-Leu-Val, MW ~1419.5 g/mol) derived from a protein found in human gastric juice.

Mechanism: BPC-157 acts through multiple overlapping pathways. It promotes angiogenesis by upregulating VEGFR2 and VEGF expression, and activates nitric oxide synthesis via the Src kinase-caveolin-1 pathway and...

KPV

Preclinical | Anti-Inflammatory / Immune

KPV is a naturally occurring tripeptide (Lys-Pro-Val, MW ~342.4 g/mol) derived from the C-terminal region (positions 11–13) of alpha-melanocyte-stimulating hormone (α-MSH).

Mechanism: KPV exerts anti-inflammatory effects through a mechanism distinct from the parent α-MSH hormone. Rather than acting through melanocortin receptors (which would trigger pigmentation), KPV is...

Larazotide

Phase III / NDA Filed | Healing & Recovery

Larazotide (AT-1001) is a synthetic 8-amino acid peptide that acts as a tight junction regulator. It is being developed as an oral adjunct therapy for celiac disease, designed to reduce intestinal permeability ("leaky gut") triggered by gluten...

Mechanism: Larazotide acts as a zonulin antagonist, blocking the zonulin pathway that opens tight junctions in the intestinal epithelium.

Teduglutide

FDA Approved | Gastrointestinal / GLP-2 Analog

Teduglutide is a 33-amino-acid recombinant analog of human glucagon-like peptide-2 (GLP-2) (MW ~3752 g/mol) with a single amino acid substitution (Ala2 to Gly) that confers resistance to dipeptidyl peptidase-4 (DPP-4) degradation.

Mechanism: Teduglutide binds to the GLP-2 receptor expressed on intestinal subepithelial myofibroblasts, enteric neurons, and enteroendocrine cells.

Plecanatide

FDA Approved | Gastrointestinal / GC-C Agonist

Plecanatide is a 16-amino-acid synthetic peptide (MW ~1681.9 g/mol) that is a structural analog of uroguanylin, an endogenous intestinal peptide.

Mechanism: Plecanatide binds to and activates guanylate cyclase-C (GC-C) receptors on the luminal surface of intestinal epithelial cells, primarily in the proximal small intestine.

Linaclotide

FDA Approved | Gastrointestinal / GC-C Agonist

Linaclotide is a 14-amino-acid synthetic peptide (MW ~1526.8 g/mol) structurally related to the endogenous guanylin and uroguanylin peptides, containing three intramolecular disulfide bonds.

Mechanism: Linaclotide binds to and activates GC-C on the luminal surface of intestinal epithelial cells, stimulating intracellular cGMP production.

Uroguanylin

Preclinical (for uroguanylin itself) / A for GC-C pathway | GI / Metabolic

Uroguanylin is a 16-amino-acid intestinal peptide hormone that activates guanylate cyclase C (GC-C) receptors on intestinal epithelial cells.

Mechanism: Uroguanylin binds to GC-C receptors on the luminal surface of intestinal epithelial cells, stimulating intracellular cGMP production.

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BPC-157 5mg
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BPC-157 5mg

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$34 USD
BPC-157 10mg
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KPV 10mg
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KPV 10mg

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BPC-157 + TB-500 Wolverine 10mg (5+5)
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BPC-157 + TB-500 Wolverine 10mg (5+5)

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Research Use Only. The information on this page is compiled from published research literature and is provided for educational purposes only. It does not constitute medical advice. All compounds referenced are intended for in vitro research use by qualified laboratories and institutions.

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