Repair & Recovery Peptides
Oral mode
Cartalax
Peptide type: Cartilage & Connective Tissue Support

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Not FDA approved

This peptide is not FDA approved for human use, and because peptides are often incompletely studied you should not use or self-experiment with it outside qualified medical supervision.

Overview

Cartalax is a Russian-marketed product built around the AED tripeptide, which PubChem lists as alanyl-glutamyl-aspartic acid. The strongest indexed literature for AED is not robust human cartilage-trial evidence.

Instead, the reviewed papers mainly cover cell-aging, fibroblast (a repair cell that builds connective tissue), mesenchymal-stem-cell, and kidney-tissue models from Khavinson-associated research groups. That means the common cartilage-support marketing story is much stronger than the underlying clinical evidence.

Reported benefits

  • Exploratory effects on gene-expression markers in aging cell models.
  • Exploratory fibroblast and extracellular-matrix findings in vitro.
  • Exploratory kidney-tissue renewal findings in organotypic culture.
  • Product is commonly marketed for joints and cartilage, but that use-case is not strongly established by the reviewed indexed human evidence.

Mechanism of action

The main published hypothesis is short-peptide bioregulation of gene expression (how strongly cells make specific proteins). AED has been studied at nanomolar concentrations in cell systems and has been reported to affect markers linked to proliferation, apoptosis, extracellular-matrix remodeling, and aging-related signaling.

Those findings are experimental and do not establish a proven cartilage-specific therapeutic mechanism in humans.

Reported Use

Oral mode

No FDA dosing guidance

This peptide is not covered by FDA-labeled dosing guidance on this page. Peptides are often investigational or incompletely studied. Do not self-experiment; use only with a doctor or qualified clinician.

Typical dose

Commercial capsule directions exist on retailer product pages, but they should not be treated as evidence-backed clinical dosing

Frequency

Product instructions vary by seller and are not the same as trial-validated dosing

Administration sites

Marketed products are oral capsules rather than a verified FDA-approved drug format

Best timing

Product instructions vary; no clinical timing recommendation was identified

Effects timeline

No source-backed clinical timeline identified

Storage

Product-specific

Cycle length

No source-backed clinical cycle established

Break between

No source-backed clinical repeat schedule established

Sequence

3 aa

AED

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Quick Signals

At A Glance

A faster read on evidence, focus, structure, and status.

Evidence

Mostly preclinical

Preclinical / Limited evidence.

6 indexed studies

Current level

Preclinical

Scale: low evidence to established use

Most discussed for

Joint healthAnti-aging

Cartalax is a Russian-marketed product built around the AED tripeptide (Ala-Glu-Asp), which PubChem lists as alanyl-glutamyl-aspartic acid.

Status

Regulatory and sport context

Not approved

No FDA-approved label is surfaced for this entry. Compounding and prescribing status can differ from FDA approval status.

Sport review

This compound is not specifically named by WADA, but athlete-specific review is still advised before use in competition.

Safety

Side Effects And Safety

Switch between common side-effect notes and stop criteria to keep safety context visible.

Key cautions

  • A robust controlled human safety dataset for Cartalax was not identified in the reviewed sources.
  • Seller claims such as no side effects should not be treated as clinical safety evidence.
  • If used as a commercial oral supplement product, intolerance or allergy to the peptide or excipients is still possible.
  • Because the evidence base is limited and product formats vary, unexpected symptoms should be treated more seriously than marketing copy suggests.

Molecule

Molecular Information

Core structure fields that help explain what kind of peptide this is and how much sequence detail is available.

Molecular weight

333.29 Da

Chain length

3 amino acids

Sequence type

Linear tripeptide

Derived from

Synthetic tripeptide record listed by PubChem as alanyl-glutamyl-aspartic acid

Amino acid sequence source string

AED

None identified in the reviewed PubChem record

Context

Important Context

The main context that changes how confidently this peptide should be interpreted.

Research status

Preclinical / Limited evidence. Indexed AED literature exists, but it is mainly experimental cell-aging, fibroblast (a repair cell that builds connective tissue), stem-cell, and kidney research rather than robust human cartilage-trial evidence.

Regulatory and sport status

FDA review shows it is not FDA approved. based on an openFDA Drugs@FDA no-match query. Sport review: Cartalax was not found by name in the reviewed 2026 WADA prohibited-list PDF, so athlete-specific review is still advised.

Blend composition

Single compound

Single active ingredient: AED (alanyl-glutamyl-aspartic acid).

Route Notes

Route-Specific Notes

Only shown when the source material adds route-specific details beyond the quick-start guide.

Oral

  • Administration: Marketed products are oral capsules rather than a verified FDA-approved drug format.
  • Absorption: No clinical PK or exposure framework was identified in the reviewed sources.
  • Cycle: No source-backed clinical cycle established.
  • Additional: Commercial capsule directions exist, but they should not be treated as proof of therapeutic dosing.

Compare

How Well Documented Is It?

A quick five-point snapshot of how visible and well-documented this peptide is. Higher values mean more coverage or clearer status in that area, not better medical performance.

ResearchRegulatorySportBreadthSequence

Research

How much published research coverage this peptide has in the linked sources, with an approval-context floor for clearly established drug products.

Source: PubMed

Score: 4

Regulatory

How clearly the approval or regulatory status is documented for this entry.

Source: openFDA drugsfda API

Score: 10

Sport

How clearly sports or competition status is documented in the linked review sources.

Source: 2026 WADA Prohibited List PDF

Score: 78

Breadth

How broadly this peptide appears across discussion topics and use-case groupings in the catalog.

Source: Curated site taxonomy

Score: 72

Sequence

How much structure or residue-sequence detail is available for this entry.

Source: Sequence

Score: 6

Protocols

Research Protocols

Common protocol-style rows shown in a consistent table layout so every peptide page is easy to compare.

GoalDoseRouteFrequency
Aging mesenchymal stem-cell gene-expression researchNanomolar concentrationsIn vitro cell cultureProtocol-specific laboratory exposure
Skin-fibroblast aging researchLaboratory peptide exposureIn vitro cell cultureProtocol-specific laboratory exposure

Research

What It Has Been Studied For

Plain-language summaries of the main health areas where this peptide shows up in the linked research.

AED modulated aging-related gene-expression markers in experimental stem-cell models.
AED affected proliferation, apoptosis, and matrix-remodeling markers in cultured skin fibroblasts.
The reviewed indexed source set did not establish robust human cartilage-trial evidence for the marketed joint-support claims.

Stacking

What People Commonly Stack It With

A plain-language view of compounds that are commonly discussed alongside this peptide in the source material.

Co-marketing is common, but controlled interaction data were not identified.
No verified interaction framework was identified in the reviewed evidence.

Practical

Preparation, Quality, And Expectations

Operational checklist blocks designed for quick scanning and repeatable page structure.

How to reconstitute

  1. Oral capsule products do not require reconstitution.
  2. Do not assume a standard injectable Cartalax or BAC-water protocol, because a verified standardized injectable product was not identified.
  3. Handling should follow the exact marketed product format rather than generic peptide-vial assumptions.

Quality indicators

Good signs

  • Product clearly identifies the AED peptide content
  • Lot-specific identity or purity documentation is available
  • Product distinguishes supplement marketing from drug approval

Avoid

  • No documentation of AED content
  • Claims of proven cartilage repair or no side effects without controlled evidence
  • Vague peptide-complex labeling that does not clearly identify the active ingredient

What to expect

Laboratory exposure window

Published effects were measured in cell or tissue models rather than a clinical symptom timeline.

Human use

No source-backed clinical expectation timeline was identified.

Marketed supplement timeline

Seller timelines should be treated as marketing claims rather than established evidence.

References

Research And Source List

Structured reference cards with source metadata and a direct link so users can inspect the original study/source.