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No human trial data

MOTS-c Side Effects

Animal and cell data only for MOTS-c itself; a company-reported Phase 1 of an analogue (CB4211) is the nearest human data

MOTS-c is a mitochondrial-encoded peptide identified in 2015 that improves metabolic markers and exercise capacity in mice through AMPK signalling. No controlled human trial of MOTS-c has been published. The closest human data are from CohBar's 2020–2021 Phase 1a/1b of CB4211, a modified analogue, which the company described as well tolerated with injection-site reactions; that description was a press release, not a paper.

Research-use information only. Research-grade MOTS-c is not an approved medicine; where trial or label figures appear below they belong to the pharmaceutical product studied, not to any research vial. This page does not give dosing or medical advice.

What is reported

Every rate carries its source. Where no source exists, no rate is printed.

EffectRate (sourced)DetailSource
Injection-site reactionsnot quantifiedReported by the developer as the main adverse event in the CB4211 (analogue) Phase 1; unquantified in any publication.CohBar company statements 2021 (not peer-reviewed)
Adverse effects in animal studiesnot quantifiedNot reported as a specific finding in the primary mouse studies; the studies were not designed as toxicology.Lee et al. 2015; Reynolds et al. 2021

What is not known

  • •Any human adverse-effect rate for MOTS-c itself.
  • •Long-term consequences of AMPK activation by an exogenous peptide.
  • •Identity and dose of any research vial.

Mechanism-based cautions

  • •MOTS-c lowers blood glucose and improves insulin sensitivity in mice — additive effects with glucose-lowering agents are plausible and unstudied.
  • •Endogenous MOTS-c levels are being studied as a disease biomarker; exogenous dosing could confound such measurements.

Regulatory status: Not approved anywhere; MOTS-c is on the WADA prohibited list (S4.4 metabolic modulators).

References

  1. Lee C, et al. The mitochondrial-derived peptide MOTS-c promotes metabolic homeostasis and reduces obesity and insulin resistance. Cell Metabolism, 2015. PMID 25738459.
  2. Reynolds JC, et al. MOTS-c is an exercise-induced mitochondrial-encoded regulator of age-dependent physical decline and muscle homeostasis. Nature Communications, 2021. PMID 33473109.
  3. Kim SJ, et al. Mitochondrially derived peptides as novel regulators of metabolism. Journal of Physiology, 2017. PMID 28574175.

What is actually in a research vial

Everything above describes MOTS-c the molecule. The risk specific to a research vial is different: it may not contain MOTS-c at the labelled amount, and it may contain what the synthesis left behind. Identity (mass spectrometry), purity (HPLC), measured net content and an endotoxin result are the four lines on a certificate that bear on adverse effects, and only a certificate you can check at the laboratory tells you any of them. This is what we have verified for MOTS-c so far.

Who sells MOTS-c, and what they document

14 of the 77 vendors on our scoreboard list MOTS-c with a price we read on the product page (11 Sept 2026–2 Oct 2026). Of those, 11 name their testing laboratory, 7 publish certificates that resolve on the lab's own site, and 10 publish measured milligrams against the label. The full ranking, with every dated price, is on Best MOTS-c Vendors.

VendorRubricLab namedPrice read
MyPurePeptidepartner10/10Janoshik Analytical$45.00 · 40mg · 30 Sept 2026
Purgo Labspartner10/10SteriGenix · Freedom Diagnostics$49.99 · 10mg · 2 Oct 2026
Amino Clubpartner9/10ILS Labs$39.99 · 10mg · 2 Oct 2026
Mile High Compounds8/10Kovera Labs · Chromate$49.99 · 10mg · 11 Sept 2026
Oros Research8/10Ethos Analytics$39.99 · 10mg · 29 Sept 2026

Top 5 by rubric score; 9 more on the ranking page.

MOTS-c certificates we have opened

None yet for MOTS-c specifically. The COA library holds the certificates we have read for each vendor on other compounds, which is the next best signal of how that vendor documents a lot.

Frequently asked

Has MOTS-c been tested in people?

Not in a published controlled trial. A modified analogue (CB4211) went through Phase 1 in 2020–2021; the developer reported it as well tolerated with injection-site reactions, but no paper followed and the programme was later discontinued.