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All peptides
Research vial labelled MOTS-c, a Mitochondrial and metabolic peptide studied in preclinical and clinical literature

MOTS-c

A mitochondrial-derived peptide with promising exercise-mimetic signalling work in animals.

General profile

Class
Mitochondrial and metabolic
Evidence
Early or preclinical only
Studied dose range
5–10 mg
Frequency in protocols
2–3× weekly
Route
Subcutaneous
Half life
~3 hours
Reconstitution
2 mL bacteriostatic water per 10 mg vial
Storage
Refrigerated, ~30 days

Timing and cycling in the literature

Usually dosed in the morning window, fasted

Two to three times weekly

Acts as an exercise-mimetic on metabolic signalling, so trial protocols pair it with the fasted, pre-activity window.

Reported cycle: 4 weeks on, 4 weeks off

Mitochondrial signalling protocols are described in four week blocks paired with training, then an equal break.

Watch for: Blood glucose behaviour if you already track it, and unexpected fatigue.

What it conflicts with

Three separate questions, kept separate. A hard stop means the mechanisms must not run together at all and timing does not fix it. A syringe rule means the same day is fine but one barrel is not. Redundancy is not dangerous, it is paying twice to hit one target.

No named pair conflicts are on file for this compound. That is missing data, not clearance: with no compatibility data the default is separate syringes, and you still introduce one new compound at a time.

Most syringe compatibility claims here are practice and expert consensus, not peer reviewed mixing studies. A clear liquid after mixing does not prove the compounds are still active, and cloudiness, particles or gelling means discard. Active cancer, pregnancy, major cardiac care and heavy immunosuppression override every stack preference on this page.

See how MOTS-c fits your week

The injection scheduler spaces doses using the clinical timing data, flags the pairs above before you draw them, and tells you why.

Model this in the injection scheduler

The studies

Human trials: Observational human association studies, no efficacy trials.

Open questions: Everything about human dosing is extrapolated.

Published papers

Indexed from Europe PMC and refreshed weekly. Each link opens the paper itself.

Search the full literature