COMPOUND WIKI
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Tissue RepairUnregulated/Therapeutic

Larazotide Acetate

Synonyms: AT-1001, Zonulin Antagonist

Sequence: Gly-Gly-Val-Leu-Val-Gln-Pro-Gly

History & Discovery Timeline

Larazotide Acetate (AT-1001) was identified by Dr. Alessio Fasano and colleagues from a sequence near the carboxyl terminus of the Vibrio cholerae Zonula Occludens Toxin (Zot). What it is: It is a synthetic octapeptide that acts as a tight junction regulator. It is classified under the Tissue Repair/Immune category. Proposed Mechanisms & Research Findings: It acts as a tight junction antagonist, preventing the opening of tight junctions in the intestinal mucosa, thereby blocking the passage of inflammatory antigens like gluten. Regulatory & Safety Status: It is not FDA approved and has been evaluated in Phase III clinical trials for celiac disease. Gray-market forms are highly risky due to lack of dosage control. Athletic & Anti-Doping Status: It is not prohibited by WADA, as it acts locally in the gut and does not enhance physical performance.

Understanding Larazotide Acetate Key Facts

Primary Target System:IMMUNE
Residue Count / Length:8 Amino Acids
Primary Action & Category:Tight Junction Regulator (Tissue Repair)
Primary Receptors:Zonulin Receptor
Larazotide Acetate mechanism diagram
Figure 1: Detailed molecular mechanism pathways of Larazotide Acetate (click to enlarge).
Larazotide Acetate (AT-1001, Zonulin Antagonist) | Clinical Research & Mechanism | Peptide Compendium