Documentation
Vendor-supplied data
COA stated as available
Not independently documented
Checked
Jul 18, 2026
Recovery / Regeneration
Also known as: Ala-Glu-Asp Β· AED Β· AED peptide
A synthetic Khavinson-type tripeptide (Ala-Glu-Asp) marketed for cartilage and connective-tissue support. Published data are limited to in vitro and mechanistic work from a single research tradition; there are no clinical trials, and the marketed joint/cartilage use is essentially unsupported.
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Cartalax is a synthetic short peptide with the sequence Ala-Glu-Asp (AED), one of the 'peptide bioregulators' associated with the research group led by Vladimir Khavinson. It is sold on the research-chemical market for cartilage and connective-tissue applications and is not an approved drug in any jurisdiction.
There are no controlled human trials of Cartalax. The peer-reviewed work on the AED peptide is in vitro and comes largely from one research group. No published clinical evidence supports the marketed cartilage or joint-repair claims.
Human safety data are lacking. As an unapproved peptide sold for research use, its purity, long-term effects, and interactions are not established.
Not approved as a drug in any jurisdiction (no FDA, EMA, or comparable marketing authorisation). Sold as a 'research chemical' / peptide bioregulator.
Vendor comparison
The table lists only product-specific offers that were checked and for which a real destination exists. Missing prices, quantities, stock and laboratory details are not inferred.
Documentation
Vendor-supplied data
COA stated as available
Not independently documented
Checked
Jul 18, 2026
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Cartalax is a synthetic short peptide with the sequence Ala-Glu-Asp (AED), one of the 'peptide bioregulators' associated with the research group led by Vladimir Khavinson. It is sold on the research-chemical market for cartilage and connective-tissue applications and is not an approved drug in any jurisdiction.
Cartalax is a synthetic tripeptide with the sequence alanine-glutamic acid-aspartic acid, usually written Ala-Glu-Asp and abbreviated AED. It belongs to the family of short peptide bioregulators associated with the research group led by Vladimir Khavinson, and it is sold on the research-chemical market for cartilage and connective-tissue support. It is not an approved drug in any jurisdiction: no FDA, EMA, or comparable marketing authorisation exists for it. peptides.cx catalogues it under Recovery / Regeneration with an evidence grade of C, which here reflects a thin and one-sided literature rather than a body of mixed clinical results.
What exists in the peer-reviewed record is in vitro work, drawn largely from a single research tradition. Published studies report that the AED peptide can influence the differentiation of cultured human stem cells, and Khavinson-group papers hypothesise that short peptides of this kind interact with DNA and chromatin to modulate gene transcription. That remains a hypothesis rather than a demonstrated mechanism. No specific, validated action in cartilage or chondrocytes has been shown in the peer-reviewed literature, there are no controlled human trials of Cartalax, and independently replicated animal efficacy studies for cartilage are scarce to absent in the indexed literature. The gap between what Cartalax is marketed for and what has actually been measured is wide, and the joint-repair claim is best read as essentially unsupported.
Human safety data are lacking for the same reason efficacy data are lacking. As an unapproved peptide sold for research use, its purity, long-term effects, and interactions are not established, and no adverse-effect profile has been characterised in people. Cartalax is often discussed alongside related bioregulators such as AEDG, better known as Epitalon, in longevity and joint-health circles, and it shares their central problem: an appealing theory with very little outcome data behind it. This page is an educational reference summarising what the science does and does not show; it is not medical advice, and it does not provide dosing, protocols, or sourcing guidance.
Evidence grade: C
There are no controlled human trials of Cartalax. The peer-reviewed work on the AED peptide is in vitro and comes largely from one research group. No published clinical evidence supports the marketed cartilage or joint-repair claims. Direct, independently replicated animal efficacy studies of Cartalax for cartilage are scarce to absent in the indexed literature; most supporting material is mechanistic or review-level rather than controlled in vivo data.
There are no controlled human trials of Cartalax. The peer-reviewed work on the AED peptide is in vitro and comes largely from one research group. No published clinical evidence supports the marketed cartilage or joint-repair claims.
Direct, independently replicated animal efficacy studies of Cartalax for cartilage are scarce to absent in the indexed literature; most supporting material is mechanistic or review-level rather than controlled in vivo data.
Human safety data are lacking. As an unapproved peptide sold for research use, its purity, long-term effects, and interactions are not established.
Not approved as a drug in any jurisdiction (no FDA, EMA, or comparable marketing authorisation). Sold as a 'research chemical' / peptide bioregulator.