SS-31
Also known as Elamipretide
Last reviewed September 26, 2026
SS-31, also known as elamipretide, is studied for its affinity for the inner mitochondrial membrane. Research focuses on cardiolipin, a phospholipid central to mitochondrial efficiency.
Mechanism of action
Research describes SS-31 as concentrating in the inner mitochondrial membrane and interacting with cardiolipin, studied for effects on electron-transport efficiency and oxidative stress.
- Cardiolipin AffinityStudied for selective binding to a phospholipid that shapes the structure of the inner mitochondrial membrane.
- Redox BalanceExplored for effects on electron-transport efficiency and the oxidative by-products of energy production.
- Route studied
- Subcutaneous
- Research status
- Approved analog
Elamipretide (SS-31) has been evaluated in a phase 3 randomized clinical trial in primary mitochondrial myopathy, and a 2026 review titled 'Elamipretide: First Approval' reports its first regulatory approval.
What the research covers
What research examines
- Cardiolipin binding in the inner mitochondrial membrane
- Electron-transport efficiency and oxidative stress
- Primary mitochondrial myopathy in a phase 3 clinical trial
- Mitochondrial dysfunction in heart failure research
- Synaptic and memory impairment in mouse models of inflammation
- Cardiomyocyte hypoxia/reoxygenation injury in cell models
Reported effects in studies
- Safety was an evaluated endpoint in the MMPOWER-3 phase 3 trial in primary mitochondrial myopathy
- Specific adverse events are not summarized in the cited study titles
- Much of the mechanistic evidence comes from animal and cell studies
What research protocols have used
Research protocols have used 1–10 mg per administration, 3 times per week (morning), in 8-week blocks with 4 weeks off.
For research use only. These figures summarize published research protocols. They are not instructions or medical advice.
Every CoreX order ships with a per-lot protocol guide.
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Cited research
- Elamipretide: First Approval.
Drugs · 2026 · Review · PubMed 41335372
- Efficacy and Safety of Elamipretide in Individuals With Primary Mitochondrial Myopathy: The MMPOWER-3 Randomized Clinical Trial.
Neurology · 2023 · RCT · PubMed 37268435
- Elamipretide: A Review of Its Structure, Mechanism of Action, and Therapeutic Potential.
International journal of molecular sciences · 2025 · Review · PubMed 39940712
- Targeting mitochondrial dysfunction with elamipretide.
Heart failure reviews · 2022 · Review · PubMed 35037146
- Elamipretide (SS-31) improves mitochondrial dysfunction, synaptic and memory impairment induced by lipopolysaccharide in mice.
Journal of neuroinflammation · 2019 · PubMed 31747905
Questions about SS-31
SS-31, also known as elamipretide, is a peptide studied for its affinity for the inner mitochondrial membrane. Research centers on its interaction with cardiolipin, a phospholipid central to mitochondrial structure and efficiency. It has been investigated in preclinical models and in human clinical trials, including a phase 3 trial in primary mitochondrial myopathy, and a 2026 review reports its first regulatory approval.
Research describes SS-31 as concentrating in the inner mitochondrial membrane and interacting with cardiolipin, a phospholipid that shapes the membrane's structure. Through this interaction, it has been studied for effects on electron-transport efficiency and on the oxidative by-products generated during cellular energy production. These mechanistic descriptions come largely from laboratory and animal research and are summarized in published reviews of its structure and mechanism of action.
Studies have examined SS-31 in several settings. A phase 3 randomized trial, MMPOWER-3, assessed its efficacy and safety in primary mitochondrial myopathy. Reviews discuss targeting mitochondrial dysfunction in heart failure. Mouse research examined mitochondrial dysfunction, synaptic function and memory impairment induced by lipopolysaccharide, and cell studies have explored mitochondria-targeted formulations in cardiomyocyte hypoxia/reoxygenation injury. Findings vary by model and should be interpreted within each study's design.
Safety was formally assessed as an endpoint in the MMPOWER-3 phase 3 trial in individuals with primary mitochondrial myopathy, and regulatory approval implies a safety review for at least one indication. However, specific adverse events are not summarized in the cited study titles, and much of the mechanistic literature comes from animal and cell models. Researchers should consult the full clinical publications for detailed safety findings.
Research protocols have used 1–10 mg per administration by the subcutaneous route, 3 times per week in the morning, in 8-week blocks followed by 4 weeks off. These figures describe protocols reported in research settings and are not recommendations. Each CoreX order ships with a protocol guide for laboratory reference. SS-31 is supplied for laboratory research use only.
Ask about SS-31
Our research assistant answers questions about the science, the studied ranges, and our products. It can be wrong, and it does not give medical advice.
SS-31 at CoreX
Every batch is independently tested for identity and purity, and the certificate of analysis is tied to the lot number on your label.
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