MOTS-c
Compoundable (Rx)Metabolic Peptides · Mitochondrial
MOTS-c is a mitochondrial-derived peptide encoded within the 12S rRNA gene.
What is MOTS-c?
MOTS-c is a mitochondrial-derived peptide encoded within the 12S rRNA gene. It functions as an exercise mimetic, activating AMPK pathways similar to physical exercise. It has shown promise for improving insulin sensitivity, fat metabolism, exercise capacity, and cellular energy production.
Also known as: Mitochondrial ORF of the Twelve S rRNA Type-C
How Does MOTS-c Work?
Activates AMPK (AMP-activated protein kinase), the master metabolic regulator, similar to exercise. Enhances glucose uptake, improves insulin sensitivity, promotes fatty acid oxidation, and stimulates mitochondrial biogenesis. Translocates to the nucleus to regulate gene expression in response to metabolic stress.
What is MOTS-c Used For?
- Exercise mimetic
- Metabolic optimization
- Insulin sensitivity
- Fat metabolism
- Longevity
Potential Side Effects
- Injection site irritation
- Mild nausea
- Headache (uncommon)
Contraindications
- Pregnancy
- Active cancer
- Children
FDA Legal Status
United States — FDA
Compoundable (Rx)Category 1 (restored 2026)
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Frequently Asked Questions
Is MOTS-c really an exercise mimetic?
How is MOTS-c different from other fat loss peptides?
Quick Facts
- Legal Status (USA)
- Compoundable (Rx)
- FDA Category
- Category 1 (restored 2026)
- Evidence Rating
- CPreliminary Evidence (Mostly Preclinical)
- Class / Subclass
- Metabolic Peptides / Mitochondrial
- Administration
- subcutaneous
- Typical Dosage
- 5-10mg weekly
- Half-Life
- ~4-6 hours
- Year Discovered
- 2015
Sources
Last updated: 2026-04-01
Sources & references
Primary sources used for the dosing, mechanism, side-effect, and regulatory claims on this page. Verify time-sensitive information (regulatory status, prescribing details) on the source before relying on it for medical decisions. See our disclaimer.
- PubMed PMID 25738459 — peer-reviewed primary literature on MOTS-c.
- FDA Federal Register — official notice record for FDA regulatory actions and Category 1 / 503A bulk-substance updates.