Cartalax

Cartalax (AED) is a synthetic tripeptide bioregulator that modulates fibroblast function across multiple tissues, studied for its geroprotective effects on skin, cartilage, and kidney tissue. Research demonstrates it increases cell proliferation and reduces senescence markers through regulation of Ki-67, p53, and SIRT-6 pathways.

Cartalax is a synthetic tripeptide (Ala-Glu-Asp) classified as a polyfunctional bioregulatory peptide with primary effects on fibroblasts across multiple tissue types. Its geroprotective properties have been demonstrated in skin, cartilage-related connective tissue, and renal cell cultures, where it reduces markers of cellular senescence and restores more youthful patterns of gene expression.

Overview

Cartalax is one of several short bioregulatory peptides characterized as polyfunctional due to its effects on processes common to many tissue types. Because fibroblasts are ubiquitous cells found in skin, cartilage, blood vessels, and kidneys, Cartalax exerts broad systemic influence. Research indicates the peptide increases cell proliferation rates and beneficially alters levels of cytokines and signaling molecules associated with senescence. It is classified as a geroprotective bioregulator because it reduces cellular aging markers, restores function to senescent cells, and appears to slow overall tissue deterioration.

Mechanism of Action

Cartalax affects multiple molecular pathways involved in cell proliferation, apoptosis, and extracellular matrix homeostasis:

  • Proliferation: Increases Ki-67 and CD98hc expression, both of which decline during cellular aging
  • Anti-apoptotic: Decreases p53 signaling and suppresses caspase-mediated apoptosis
  • Senescence markers: Reduces p16 and p21 protein levels in aging cells
  • SIRT-6 activation: Increases SIRT-6 expression, low levels of which are thought to trigger cellular senescence
  • NF-kB modulation: Activates NF-kB signaling pathways involved in immune regulation and cell survival
  • MMP regulation: Inhibits MMP-9 synthesis (which increases during skin aging) while balancing MMP-1, MMP-3, and MMP-8 activity to normalize extracellular matrix turnover

This combination of effects makes Cartalax a balancing agent for fibroblast function, normalizing the equilibrium between tissue breakdown and regeneration, with the most pronounced effects observed in older cells.

Reconstitution Calculator

Cartalax

Cartalax is a synthetic tripeptide (Ala-Glu-Asp) classified as a polyfunctional

Draw Volume
0.100mL
Syringe Units
10units
Concentration
10,000mcg/mL
Doses / Vial
20doses
Vial Total
20mg
Waste / Vial
0mcg
Syringe Cap.
100units · 1mL
Recommended Schedule
M
T
W
T
F
S
S
FrequencyOnce daily (subcutaneous injection or oral capsul…
TimingSubcutaneous injection in the morning
Cycle10-30 days per cycle; may repeat after 3-6 month break
NoteCartalax is a synthetic tripeptide bioregulator (Ala-Glu-Asp) developed by Professor Vladimir Khavinson at the St.
How to reconstitute
Gather & prepare
1/6Gather & prepare

Set up a clean workspace with all supplies ready.

1.Wash hands thoroughly, put on disposable gloves
2.Your 20mg peptide vial (lyophilized powder)
3.Bacteriostatic water (you'll need 2mL)
4.A 3–5mL syringe with 21–25 gauge needle for reconstitution
5.Alcohol swabs (70% isopropyl)
Use bacteriostatic water (0.9% benzyl alcohol) for multi-dose vials. Sterile water is only safe for single-use.
Supply Planner

7x / week for weeks

·
40%
2vials
28 doses20 days/vial12 leftover
Cost Breakdown
Vial price
$0.00per dose
$0.00 /week$0 /month
Store 2-8°C30 day shelf lifeSwirl gentlyFor research purposes only

Research

Skin Fibroblast Regulation

Cartalax boosts proliferation, tissue regeneration, and extracellular matrix remodeling in skin, particularly in older animals, while decreasing apoptosis. Lin'kova et al. (2016) demonstrated that Cartalax and similar peptides inhibit MMP-9 synthesis in aging skin while enhancing Ki-67 and CD98hc expression and suppressing caspase-mediated apoptosis. The peptide has been shown to stimulate skin cell proliferation, improve microcirculation, and increase functional activity of skin fibroblasts, leading to improvements in carnosine, collagen, cytokine, and growth factor production.

Cartilage and Connective Tissue

While no studies have tested Cartalax directly in cartilage, its broad effects on fibroblasts are highly relevant to cartilage health. Fibroblasts are the primary regulators of cartilage homeostasis (Ellman et al., 2013), and Cartalax modulates many of the key signaling molecules involved, including AP-1, NF-kB, c-jun, CCN1, TGF-B, TNF-a, and multiple MMPs. By normalizing fibroblast function and balancing the equilibrium between collagen deposition and breakdown, Cartalax is being investigated in conditions including arthritis, osteoporosis, degenerative disc disease, and gout.

Kidney Cell Renewal

Research in renal tissue cultures revealed that polypeptide isolates from calf kidneys containing Cartalax (AED) and T-35 (EDL) stimulated cell renewal in older rat kidneys by increasing Ki-67 and decreasing p53 (Chalisova et al., 2015). Further studies in renal cell cultures confirmed that Cartalax increases cell proliferation while decreasing senescence markers p16, p21, and p53, and importantly increases SIRT-6 expression, which is heavily correlated with cellular aging.

Gene Expression and Aging

Studies on human mesenchymal stem cell cultures demonstrated that Cartalax and other short bioregulators affect expression of genes central to the aging process, including IGF1, FOXO1, TERT, TNKS2, and NF-kB, with changes ranging from 1.6- to 5.6-fold (Ashapkin et al., 2020).

Safety Profile

Cartalax has been studied in cell cultures and animal models with no significant adverse effects reported. Its mechanism as a balancing agent for fibroblast function, rather than a unidirectional stimulator, may contribute to a favorable safety profile. The peptide normalizes rather than overdrives cellular processes, with effects most pronounced in senescent cells. However, formal human clinical trials and toxicology data remain limited in the published literature.

Pharmacokinetic Profile

Half-life
Minutes (short peptide); effects persist via epigenetic changes

Quick Start

Typical Dose
100-200mcg oral (1-2 capsules) or 700-1400mcg injectable
Frequency
1-2 times daily with meals (oral) or once daily (injectable)
Route
Oral, Subcutaneous
Cycle Length
1-3 months depending on application
Storage
Oral capsules: room temperature; Injectable lyophilized: 2-8°C; Reconstituted: 2-8°C refrigerated

Molecular Structure

2D Structure
Cartalax molecular structure
Molecular Properties
Formula
C12H19N3O8
Weight
333.29 Da
Length
3 amino acids
CAS
Not available
PubChem CID
87815447
Exact Mass
333.1172 Da
LogP
-4.9
TPSA
196 Ų
H-Bond Donors
6
H-Bond Acceptors
9
Rotatable Bonds
10
Complexity
493
Identifiers (SMILES, InChI)
InChI
InChI=1S/C12H19N3O8/c1-5(13)10(20)14-6(2-3-8(16)17)11(21)15-7(12(22)23)4-9(18)19/h5-7H,2-4,13H2,1H3,(H,14,20)(H,15,21)(H,16,17)(H,18,19)(H,22,23)/t5-,6-,7-/m0/s1
InChIKeyKXEVYGKATAMXJJ-ACZMJKKPSA-N

Research Indications

Joint Health

Good Evidence
Osteoarthritis

Clinical efficacy shown in osteochondrosis, osteoarthritis, and osteoporosis treatment.

Moderate Evidence
Degenerative Joint Disease Prevention

Supports cartilage maintenance and joint function.

Moderate Evidence
Post-Fracture Recovery

Supports bone and connective tissue healing.

Skin Health

Good Evidence
Fibroblast Activation

Increased Ki-67 expression with suppressed apoptosis in young and aged cells.

Good Evidence
Collagen Production

Enhances collagen synthesis in connective tissue.

Moderate Evidence
Cellular Senescence Reduction

Inhibited MMP-9 synthesis; maintained extracellular matrix integrity.

Research Protocols

oral

Capsule form; do not chew, swallow whole with water during meals.

GoalDoseFrequency
Joint Support100-200mcg (1-2 capsules)1-2x daily with meals

subcutaneous Injection

Cartilage/musculoskeletal bioregulator. Higher dose protocol with titration.

GoalDoseFrequency
Loading phase2,000 mcg (2 mg)Once daily
Escalation 13,000 mcg (3 mg)Once daily
Escalation 24,000 mcg (4 mg)Once daily
Full dose5,000 mcg (5 mg)Once daily
Reconstitution Guide (20mg vial + 3mL BAC water)
  1. Wipe vial tops with alcohol swab
  2. Draw 3.0 mL bacteriostatic water into syringe
  3. Inject slowly down the inside wall of the peptide vial
  4. Gently swirl to dissolve — never shake
  5. Resulting concentration: 6.67 mg/mL
  6. For 2,000 mcg (2 mg) dose: draw 30 units (0.30 mL)
  7. For 3,000 mcg (3 mg) dose: draw 45 units (0.45 mL)
  8. For 5,000 mcg (5 mg) dose: draw 75 units (0.75 mL)
  9. Store reconstituted vial refrigerated at 2-8°C

topical

Solution applied to face, neck, hands, or superficial joint areas.

GoalDoseFrequency
Skin Rejuvenation0.5-1ml solution2x daily

Interactions

Peptide Interactions

BPC-157compatible

Different mechanisms; no direct interaction.

TB-500compatible

Distinct action pathways; may complement effects.

What to Expect

What to Expect

Week 1-2

Establishing baseline; minimal noticeable changes

Week 3-4

Gradual improvement in joint comfort

Month 2

Noticeable mobility improvements

Month 3

Maximum therapeutic effect achieved

Safety Profile

Common Side Effects

  • No reported side effects in Russian clinical use when taken properly
  • Well-tolerated in elderly patients

Contraindications

  • Pregnancy and breastfeeding
  • Active cancer (theoretical proliferation risk)

Discontinue If

  • Allergic reactions
  • Digestive upset (rare with proper administration)
  • No improvement after 3 months
  • Unexpected symptoms

Quality Indicators

What to look for

  • Professional Russian packaging with holographic seals
  • Exactly 0.1mg (100mcg) AC-4 peptide complex per capsule
  • Clear Russian/English instructions specifying 'with meals'

Caution

  • Proper documentation required for authenticity
  • Import verification needed

Red flags

  • Missing holographic seals or professional packaging
  • Unclear dosing instructions

Frequently Asked Questions

References (9)

  1. [1]
    Fibroblast Proliferation Study (2019)
  2. [2]
    Kidney Cell Culture Research (2020)
  3. [3]
    Clinical Spine & Joint Study (Russia)
  4. [4]
    Matrix Metalloproteinase Research (2020)
  5. [1]
    [Lin'kova NS et al. (2016). Peptide Regulation of Skin Fibroblast Functions during Their Aging In Vitro. Bull Exp Biol Med (2016)
  6. [2]
    [Ellman MB et al. (2013). Fibroblast growth factor control of cartilage homeostasis. J Cell Biochem (2013)
  7. [3]
  8. [5]
  9. [4]
Updated 2026-03-08Sources: jabronistore-wiki, peptide-wiki-mdx, pep-pedia, pubchem, peptide-wiki-mdx-v2

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