Ask sales for the Certificate of Analysis matched to the offered or supplied lot; it records the tests actually completed, applicable specifications, and reported results.
Review the matching batch COA for the analytical scope and results recorded for that lot.
Matching batch COA available.
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Khavinson bioregulator tetrapeptide (Ala-Glu-Asp-Leu, AEDL)
Overview
Bronchogen is a synthetic tetrapeptide bioregulator with the amino acid sequence Ala-Glu-Asp-Leu (AEDL, H-Ala-Glu-Asp-Leu-OH), developed by Professor Vladimir Khavinson's team at the St. Petersburg Institute of Bioregulation and Gerontology in Russia. It belongs to the Khavinson short-peptide (cytogen) family, specifically the member associated with bronchial-pulmonary tissue. The compound is listed in PubChem (CID 11690869, independently re-confirmed to exist in this pass; molecular formula C18H30N4O9); the molecular weight has been cross-checked and matches between PubChem (approximately 446.5 Da via the PUG-REST data interface) and independent third-party vendor technical data sheets (e.g., NovoProLabs, listing 446.44 Da). Note: PubChem also carries a second entry, CID 471572; independent structural verification (InChIKey comparison) in this pass found its N-terminus is glutamic acid rather than alanine (H-Glu-Asp-Leu-Ala-OH) — a distinct isomer with the same molecular formula but a different residue order, not a duplicate naming of the same compound. This entry is unrelated to any of Bronchogen's three core publications and may reflect a vendor-sourced mix-up; it should not be treated as an equivalent entry for Bronchogen. This class of short peptides is hypothesized to regulate gene expression by binding specific DNA motifs, and has been studied in vitro and in animal models for tissue-specific effects on bronchial epithelial cell differentiation. There are currently three core peer-reviewed publications (a 2011 DNA-binding mechanism study, a 2012 cell differentiation study, and a 2015 rat COPD model study), all independently re-verified to exist via PubMed/Springer Nature Link in this pass. All three originate from the Khavinson team and Russian/St. Petersburg research institutions; the evidence base remains limited in scale, and no double-blind human trials have been reported in the English-language literature. Bronchogen is offered as a lyophilized linear tetrapeptide with a ≥99.0% HPLC catalogue target. Ask sales for the matching batch COA; it records the analytical work actually completed. Any sequence evidence, water, residual-solvent, endotoxin, or raw-data requirement must be included in the agreed written scope before quotation.
Applications & buyer fit
Buyers for longevity-class peptides span research labs working on telomere, collagen, and circadian-rhythm models, plus cosmetic-formulation OEMs incorporating peptides like GHK-Cu into anti-aging finished products. Copper peptides in particular require attention to chelator-free water and EDTA-free buffers in downstream formulation work, incompatibility there is the most common cause of "the peptide didn't work" support tickets in this class.
Sourced for
Buyer fit
Documentation that ships
Procurement note: Copper peptides require chelator-free water and EDTA-free buffers in downstream formulation work.
Primary buyer fit: academic and contract research laboratories.
Specifications
Certificate of Analysis
Representative COA previews for Bronchogen; request the certificate matched to the offered or supplied lot from sales. These are previews — request the full high-resolution certificate for any lot.
Browse all published COAsRegulatory note
Research-use-only reference material; not for human or veterinary use.
Selected literature
Frequently asked questions
Use the receiving laboratory's approved protocol for vehicle, preservation, handling, and route-specific labelling. Record the supplied lot and the information actually stated on its batch COA so the preparation remains traceable.
The three tetrapeptides share the Ala-Glu-Asp core. Review the COA matched to the offered or supplied lot first. If the buyer's written acceptance procedure requires full sequence-level differentiation, agree LC-MS/MS or another appropriate method, reporting format, timing, and buyer-funded cost before testing.