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Calculated reference model · not an experimental or batch-certified structure. Backbone view: 33 of 51 atoms.

Model data & sources
  • Heavy atoms only; hydrogens are omitted from the reference display.
  • Source-defined atom stereochemistry is checked against the calculated coordinates; no energy-minimum or observed-fold claim is made.
  • Reference molecular species only; batch counterions, excipients and material composition are not certified.
Sequence
GGVLVQPG
Formula
C32H55N9O10
Method
RDKit ETKDGv3 / MMFF94s calculated reference conformer
Batch 1 of 2
KC-LZT-01
Batch 2 of 2
KC-LZT-02
The forms on this page come off different batches, so more than one code is shipping. Each has its own certificate, and the code printed on your label is the one you have.

Larazotide

Peptides

Published formats

  • Standard Reference Vial

Supplementary product details from the published catalog, checked 2026-10-07. These reference details do not establish current availability.

Pricing

Pricing and order placement are reserved for reviewed research accounts. Log in or submit an account application to view current product pricing.

Technical Specifications

Batch COA Database ↗
CAS Registry Number258818-34-7
Molecular FormulaC₃₂H₅₅N₉O₁₀
Molecular Weight725.8
IUPAC Designationglycyl-glycyl-L-valyl-L-leucyl-L-valyl-L-glutaminyl-L-prolyl-glycine acetic acid
Physical FormRefer to product documentation
Storage RequirementsRefer to product documentation
Other NamesAT-1001

Identity fields from the published product record, checked 2026-10-07. Reference information is not a batch identity certificate.

Research Overview

Larazotide Research Standard

Larazotide (CAS 258818-34-7) is a synthetic octapeptide supplied as dry-fill capsules at 500 mcg per capsule, 60 count, 30 mg total. It is a zonulin antagonist, and it acts on a target most research peptides do not touch: the paracellular space between epithelial cells rather than a receptor on their surface.[1]

Mechanism of Action & Research Context

The target is the zonulin pathway, which regulates intestinal tight junctions and therefore paracellular permeability.

  • Zonulin opens tight junctions; larazotide antagonises it. Zonulin family peptide is a potent regulator of intestinal tight junctions. Larazotide acetate is described as a zonulin antagonist that specifically increases intestinal barrier integrity — it tightens rather than loosens.[1]

  • The pathway is inducible by a defined trigger. Gliadin, the prolamine fraction of gluten, disassembles intercellular junctional proteins by upregulating the zonulin pathway, and that disassembly is inhibited by larazotide acetate. So the system has a clean agonist/antagonist pair for experimental use.[2]

  • Barrier integrity as a measurable checkpoint. In a mouse model, elevated serum zonulin accompanied a leaky intestinal barrier, dysbiosis and inflammation, and restoring barrier integrity before disease onset — including with larazotide acetate — reduced arthritis onset. Barrier function is treated there as a discrete, manipulable variable rather than a downstream consequence.[1]

  • A caution on the wider hypothesis. The review covering this area notes that attribution of many human diseases to increased paracellular permeability rested for decades on tenuous evidence, and that the supporting work is comparatively recent. The tight-junction mechanism is well defined; the breadth of what it explains is not.[2]

Research Applications

Primary fields of in vitro and preclinical laboratory investigation include:

  • Transepithelial electrical resistance and paracellular flux assays in intestinal epithelial monolayers such as Caco-2.[1]

  • Tight junction protein localisation by immunofluorescence.[2]

  • Gliadin challenge models, using the antagonist against a defined trigger.[2]

  • Serum zonulin quantification as a barrier-integrity readout.[1]

  • Gut-systemic axis studies linking barrier function to distant inflammation.[1]

Analytical Documentation

Purity and identity vary by manufacturing lot. Kimera Chems does not publish a single fixed purity figure for this item; refer to the batch-specific Certificate of Analysis (COA) issued for the lot received, which reflects third-party analytical testing for that lot.

References

  1. Tajik N, Frech M, Schulz O, et al. Targeting zonulin and intestinal epithelial barrier function to prevent onset of arthritis. Nat Commun. 2020;11(1):1995. doi:10.1038/s41467-020-15831-7
  2. Valitutti F, Fasano A. Breaking down barriers: how understanding celiac disease pathogenesis informed the development of novel treatments. Dig Dis Sci. 2019;64(7):1748–1758. doi:10.1007/s10620-019-05646-y

Storage & Handling

Store at controlled room temperature. Keep tightly closed.

Storage guidance is a house recommendation. Analytical documentation is per-lot release testing.

Related Research Compounds

Research Use Only Disclaimer: This product is labeled and sold "For Research Use Only - NOT FOR HUMAN CONSUMPTION." It is not a drug, dietary supplement, food, cosmetic, or medical device, and it is not approved by the FDA or any other regulator for human or veterinary use. It is supplied to approved account holders as a research chemical for laboratory use and must be handled in accordance with applicable law.

Certificates of Analysis

Currently shipping from batches KC-LZT-01 and KC-LZT-02. The code printed on your label says which one you have.

Kimera Chems

Compounds That Survive Scrutiny

Research use only. Not for human or veterinary use.