FDA
No application listedNo application naming MOTS-c as an active ingredient is listed in Drugs@FDA. Checked 2026-10-05; the control lookup (semaglutide) returned 6 applications.
Drugs@FDA via openFDAResearch-use information. This page summarises published literature and regulator records. It is not guidance for use, not medical advice, and not a statement that any material is suitable for use in people or animals.
MOTS-c is a 16-residue peptide encoded by a short open reading frame in the mitochondrial 12S rRNA gene. Research describes it as a mitochondrial-derived signalling peptide that can enter the nucleus under metabolic stress. It is supplied here as a research material for laboratory use only.
C101H152N28O22S2 (matches the formula computed from the sequence)1627580-64-6 (confirmed in PubChem)Chemistry checked against PubChem on 2026-10-05. Where the formula can be computed from the listed sequence, it was, and the two routes agree.
Receptor and pathway background: Mitochondria-linked peptides.
4 studies are cited for MOTS-c. Each is labelled by design below, and each entry says what the paper measured.
PubMed returns 262 records for the search terms published on the method page (57 of them with a review publication type, 8 with a clinical-trial publication type), checked 5 October 2026. ClinicalTrials.gov lists 5 registered studies whose intervention matches the name (2 interventional), checked 5 October 2026.
Studies are listed by what they measured. Papers whose titles state an amount or schedule, or describe a clinical outcome of an approved medicine, are not listed. This is a wording rule, not a quality filter; see the method page.
No application naming MOTS-c as an active ingredient is listed in Drugs@FDA. Checked 2026-10-05; the control lookup (semaglutide) returned 6 applications.
Drugs@FDA via openFDANo centrally authorised procedure in the EMA medicines database (checked 5 October 2026) names MOTS-c as an active substance. National authorisations are not in this dataset.
EMA medicines dataNo SmPC, PIL or PAR document in MHRA Products matches the exact name "MOTS-c". Checked 2026-10-05; the control lookup (semaglutide) returned 271 documents.
MHRA ProductsThe WADA 2026 Prohibited List, in force 1 January 2026 names MOTS-c under S4.4 (metabolic modulators). A WADA entry is a sporting rule, not a statement about legality outside sport.
WADA Prohibited List 2026A regulator record is information about a database entry. It is not advice and not a statement that any use is lawful or unlawful in any country. How regulators approach research peptides.
Data dates: regulatory records 2026-10-05; WADA list 2026-10-05.
[1] Rice MC, Imun M, Jung SW, Park CY, Kim JS, Lai RW, et al.. MOTS-c is a mitochondrial-encoded interferon-linked host defense peptide. Elife. 2026;12.
Identified MOTS-c as a mitochondria-encoded host defense peptide and tested its antimicrobial and interferon-linked activity.
[2] Kim KH, Son JM, Benayoun BA, Lee C. The Mitochondrial-Encoded Peptide MOTS-c Translocates to the Nucleus to Regulate Nuclear Gene Expression in Response to Metabolic Stress. Cell Metab. 2018;28:516-524.e7.
Showed that MOTS-c translocates to the nucleus under metabolic stress and regulates nuclear gene expression.
[3] Lee C, Kim KH, Cohen P. MOTS-c: A novel mitochondrial-derived peptide regulating muscle and fat metabolism. Free Radic Biol Med. 2016;100:182-187.
Review of MOTS-c as a mitochondrial-derived peptide in muscle and fat metabolism.
[4] Lee C, Zeng J, Drew BG, Sallam T, Martin-Montalvo A, Wan J, et al.. The mitochondrial-derived peptide MOTS-c promotes metabolic homeostasis and reduces obesity and insulin resistance. Cell Metab. 2015;21:443-54.
Identified the MOTS-c open reading frame in mitochondrial DNA and reported its metabolic effects in cells and mice.
Data dates: citations read from PubMed 2026-10-05.
Peptency editorial team, last reviewed 5 October 2026. Citations are read back from PubMed, chemistry is checked against PubChem, and regulator records are read from each regulator's own database on the dates shown. The method page lists every source, search term and rule. Corrections are welcome through the contact details on the About page.
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