biohacking$bioLLM CA: TBA

database / healing

Larazotide

also known as AT-1001

in clinical study healing gastrointestinalimmune mass-verified
OOOOOOOOOONNNNNNNNNHHHHHHHHHHH
51 heavy atoms · 106 bonds · drag to pan, scroll to zoom C32O10N9

Skeletal structure drawn from the computed atomic coordinates in PubChem CID 9810532. Carbons are implicit vertices; hydrogens on carbon are suppressed, as in any structural formula. Nothing here is estimated — every atom sits where PubChem placed it.

Research reference only. The observations below are recorded in the cited literature. Nothing here is advice or a recommendation, and no dosing information is published on this site.

Sequence

GGVLVQPG

Gly-Gly-Val-Leu-Val-Gln-Pro-Gly

1. Gly — Glycine · glycine · hydropathy -0.4 · charge 0G12. Gly — Glycine · glycine · hydropathy -0.4 · charge 0G3. Val — Valine · hydrophobic · hydropathy 4.2 · charge 0V4. Leu — Leucine · hydrophobic · hydropathy 3.8 · charge 0L5. Val — Valine · hydrophobic · hydropathy 4.2 · charge 0V6. Gln — Glutamine · polar · hydropathy -3.5 · charge 0Q67. Pro — Proline · proline · hydropathy -1.6 · charge 0P8. Gly — Glycine · glycine · hydropathy -0.4 · charge 0G8

Computed backbone mass 725.84 Da agrees with PubChem's reported 725.8 Da (Δ 0.04 Da). Two independent sources agree on the primary structure.

Molecular data

Chemical fields come from the PubChem compound record; computed values are derived from the sequence shown above.
molecular formulaC32H55N9O10
molecular weight725.8 Da (PubChem)
computed backbone mass725.84 Da
length8 residues
net charge (pH 7.4)0
mean hydropathy0.74
half-lifenot characterised
delivery routeoral
PubChem CID9810532
PDBnot characterised
UniProt parentnot characterised

Mechanism

Tight-junction regulator studied as a zonulin antagonist in intestinal permeability.

Reported targets: tight junction complex

Experimental structure

No experimental structure of this peptide is deposited in the PDB. Nothing is rendered here — a predicted fold would not be a structure, and this site does not draw one.

Reported effects

Each row is an outcome described in the literature indexed for this peptide. Reported in the cited work — not a claim, not a recommendation.

Reported observations and the corpus they are drawn from.
reported outcomewhere it appears
intestinal permeability reductionPreventive effects of Larazotide acetate (AT-1001) on non-alcoholic fatty li… Pediatrics and neonatology 2026

Registered trials

Records from ClinicalTrials.gov. Listed for reference — this project sponsors no trial and is not involved in any of them.
NCTtitlestatusphase
NCT05022303AT1001 for the Treatment of COVID-19 Related MIS-CTERMINATEDPHASE2
NCT01218659Study to Compare the Efficacy and Safety of Oral AT1001 and Enzyme Replacement Therapy in PaCOMPLETEDPHASE3
NCT01853852A Phase I, Randomized, Single-Blind, Four-Period Cross-Over, Placebo-Controlled, Dose-EscalaCOMPLETEDPHASE1
NCT00386490Safety of Larazotide Acetate in Healthy VolunteersCOMPLETEDPHASE1
NCT01730482A Study to Assess the Absorption, Metabolism and Excretion of Migalastat Hydrochloride (AT10COMPLETEDPHASE1

Literature (3)

Preventive effects of Larazotide acetate (AT-1001) on non-alcoholic fatty liver diseases (NAFLD) in a mouse model — Pediatrics and neonatology 2026

abstract not reproduced — this record is not open-access, so it is linked rather than copied.

publisher record ↗ · PMID 40562584 · DOI 10.1016/j.pedneo.2025.01.016

Viral spike antigen clearance and augmented recovery in children with post-COVID multisystem inflammatory syndrome treated with larazotide — Science translational medicine 2025

abstract not reproduced — this record is not open-access, so it is linked rather than copied.

publisher record ↗ · PMID 40737433 · DOI 10.1126/scitranslmed.adu4284

The PAR2 Antagonist Larazotide Can Mitigate Acute Histamine-Stimulated Epithelial Barrier Disruption in Keratinocytes: A Potential Adjunct Treatment for Atopic Dermatitis — JID innovations : skin science from molecules to population health 2025

Atopic dermatitis (AD) is a chronic inflammatory skin condition with evidence of defects in the barrier properties of the epidermis. Changes in the permeability properties of the tight junction have been reported in AD, and reversing this leaky tight junction may be a potential treatment for AD. This study aimed to determine the effect of larazotide, an antagonist of the protease-activated receptor 2, on the permeability and barrier properties of the tight junctions in keratinocyte monolayers. Normal human epithelial keratinocytes were grown in culture on permeable supports. The effects of larazotide on transepithelial resistance and permeability properties of keratinocyte monolayers were studied before and after histamine challenge. Larazotide mitigated the disruptive effect of histamine on epithelial permeability by increasing the electrical resistance and decreasing epithelial permeab…

open access ↗ · PMID 40330848 · DOI 10.1016/j.xjidi.2025.100369

Related

BPC-157

healing · 8 citations

TB-500

healing · 8 citations

Thymosin β4

healing · 8 citations

GHK

healing · 8 citations