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MOTS-c vs SS-31

Research material comparison: purity standards, available formats, molecular data, batch COA documentation, and regulatory status. For in vitro research use only.

MOTS-c: DSS-31: A
AttributeMOTS-cSS-31
CategoryMetabolic / MitochondrialMetabolic / Mitochondrial
Evidence RatingDPreclinicalAFDA Approved
Clinical StatusResearch-only / No human clinical trials completed (Phase 1 of analog CB4211 only)FDA-approved (Forzinity, September 2025) for Barth syndrome. Phase II (heart failure, renal dysfunction, age-related macular degeneration).
MechanismMOTS-c activates AMPK by inhibiting the folate cycle, causing accumulation of AICAR (an AMP analog). Activated AMPK shifts cells into energy-efficient mode: enhancing glucose uptake, fatty-acid oxidation, and mitochondrial respiration while downregulating fat storage and gluconeogenesis. Under stres...SS-31 is a cell-permeable peptide with an alternating aromatic-cationic motif (D-Arg-Dmt-Lys-Phe-NH2) that allows it to cross membranes without a carrier. It concentrates >1000-fold in mitochondria, where it binds to cardiolipin on the inner mitochondrial membrane. This stabilizes the electron trans...
Half-LifeSeveral hours; tissue effects may persist longer~4 hours
Bioavailability
Molecular Weight~2174.6 g/mol~639.8 g/mol
WADA StatusNot ListedNot Listed
Research Half-LifeSeveral hours; tissue effects may persist longer~4 hours
Key Use Cases
  • Metabolic Health
  • Anti-Aging
  • Anti-Aging
  • Metabolic Health
Safety Concerns
  • No adverse effects reported in preclinical animal studies
  • Human tolerability is completely unknown for native MOTS-c (no completed human trials)
  • Modified analog CB4211 showed good tolerability in Phase 1
  • Generally well-tolerated in clinical trials at tested doses
  • Common: injection site reactions (pain, redness)
  • Mild headache, dizziness, and nausea reported
Contraindications
  • No established contraindications due to absence of human clinical data
  • Caution in diabetics on glucose-lowering medication (potential additive hypoglycemia based on mechanism)
  • Pregnancy and breastfeeding (no data)
  • Active cancer (AMPK modulation has complex effects on tumor biology)
  • Pregnancy and breastfeeding (insufficient data)
  • Severe renal impairment (limited pharmacokinetic data)
  • Hypersensitivity to any component
Regulatory (US)Not FDA-approved. Removed from FDA Category 2 on April 15, 2026. PCAC review scheduled July 23-24, 2026. Research chemical.FDA-approved (September 2025) as Forzinity for Barth syndrome — first FDA-approved mitochondria-targeted therapeutic. Accelerated approval pathway. FDA Fast Track and Orphan Drug designation.

Research Material Specifications

Catalog specifications for the corresponding research materials, including batch documentation coverage.

SpecificationMOTS-cSS-31
Purity Standard≥98%≥98%
CAS Number1627580-64-6736992-21-5
Molecular FormulaC₁₀₁H₁₅₂N₂₈O₂₂S₂N/A
Available Formats20mg10mg
Batch COAs Published1 on file
Stock StatusIn stockOut of stock

Research Disclaimer: This comparison is provided for educational purposes only. All products are sold exclusively for in vitro research use. The information presented is based on published preclinical and clinical research and does not constitute medical advice. Consult a qualified healthcare professional before making any decisions regarding peptide use.

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