Informational only. Not medical advice.INFORMATIONAL PLATFORM ONLY — NOT MEDICAL ADVICE, DIAGNOSIS, OR TREATMENT
Head-to-head comparison of GHK and MOTS-c — mechanism, dosing, side effects, legal status, and pricing.
GHK is the parent tripeptide Gly-His-Lys, originally isolated from human plasma by Loren Pickart (1973) as an activity that caused aged hepatocytes to synthesize proteins like younger tissue. It is DISTINCT from GHK-Cu, the 1:1 copper(II) complex tracked as a separate entry — but GHK binds copper readily in vivo, so in physiological environments the bare peptide rapidly associates with available Cu(II). Not FDA-approved for any indication; used in cosmetic and research contexts only.
MOTS-c is a 16-amino-acid mitochondrial-derived peptide (MDP) encoded within the mitochondrial 12S rRNA, discovered by Lee and Cohen at USC in 2015 (sequence: MRWQEMGYIFYPRKLR). It is an investigational, research-only peptide studied as a metabolic regulator; it has not been approved by the FDA for any indication.
GHK
MOTS-c
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Legal Status
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COA-verified vendors · trust score ≥70 required · single-vial price — bulk/bundle deals may be lower
GHK
MOTS-c
COA corpus from Disclosed Labs — independently tested batches only.
GHK
No COA data yet.
Submit testing data →MOTS-c
193
COAs
99.5%
Avg purity
16
Labs
GHK is among peptides under FDA review for the Category 1 (503A) list; if added, it would require a prescription to be compounded by registered 503A/503B pharmacies — not yet authorized. MOTS-c remains research-only. In April 2026 the FDA removed 12 peptides from Category 2, which does not place them on the Category 1 list or authorize compounding. The FDA's Pharmacy Compounding Advisory Committee is advisory and meets July 23–24, 2026 to review nominations and make recommendations to the FDA.
The overwhelming majority of GHK research uses the GHK-Cu complex; direct studies of copper-free GHK are limited. Pickart (J Biomater Sci Polym Ed, 2008, PMID 18644225) reviewed GHK's role in tissue remodeling and wound healing. Pickart et al. (Oxid Med Cell Longev, 2012, PMID 22666519) reviewed GHK-Cu in oxidative stress and cognitive aging. Pickart, Vasquez-Soltero & Margolina (BioMed Res Int, 2014, PMID 25302294; 'GHK and DNA: Resetting the Human Genome to Health') summarized microarray data indicating GHK modulates expression of thousands of human genes. No human clinical trials exist for injected bare GHK; cosmetic formulations typically use topical GHK or GHK-Cu at ~50–200 ppm.
Key references
Lee et al. (Cell Metabolism, 2015; PMID 25738459) identified MOTS-c and showed that exogenous administration in mice prevented diet-induced obesity and insulin resistance via AMPK activation in skeletal muscle. Kim et al. (Cell Metabolism, 2018; PMID 29983246) demonstrated that MOTS-c translocates to the nucleus under metabolic stress and regulates antioxidant response element (ARE) genes. Reynolds et al. (Nature Communications, 2021; PMID 33473109) reported that exercise induces MOTS-c in human skeletal muscle and that MOTS-c treatment improved physical capacity in young, middle-aged, and aged mice. Human clinical data are limited to CohBar's Phase 1a/1b study of the analog CB4211 in healthy volunteers and obese NAFLD subjects, which reported acceptable tolerability and exploratory signals on ALT/AST and glucose; CohBar wound down the program in 2023. No completed Phase 2 or Phase 3 trials exist for MOTS-c or its analogs, and grey-market dosing (typically ~10 mg SubQ 2-3x/week) is not clinically validated.
GHK (Cosmetic) and MOTS-c (Metabolic) are in different categories and target different biological pathways. This is a common pattern in multi-compound research protocols. Researchers should monitor the biomarkers from both profiles and watch for interactions listed in each compound’s contraindications. Consult a licensed healthcare provider before combining any research compounds.
This platform provides informational tools only, not medical advice. This comparison is for educational purposes only. Consult a licensed provider.
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Key references