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Vendor-supplied data
COA stated as available
Not independently documented
Checked
Jul 18, 2026
Mitochondrial
Also known as: Elamipretide · MTP-131
A mitochondria-targeting peptide studied in clinical trials for mitochondrial disease.
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SS-31 is a cell-permeable peptide that targets cardiolipin in mitochondrial membranes.
Studied in controlled clinical trials with mixed results; not approved.
Investigational; research-market material is not the studied clinical product.
Investigational; studied in clinical trials. Not an approved general-use medicine.
Vendor comparison
The table lists only product-specific offers that were checked and for which a real destination exists. Missing prices, quantities, stock and laboratory details are not inferred.
Documentation
Vendor-supplied data
COA stated as available
Not independently documented
Checked
Jul 18, 2026
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SS-31 is a cell-permeable peptide that targets cardiolipin in mitochondrial membranes.
SS-31, also known as Elamipretide or MTP-131, is a cell-permeable, mitochondria-targeting peptide studied primarily for its role in supporting mitochondrial function. It belongs to a class of small aromatic-cationic peptides that concentrate in the inner mitochondrial membrane. There, its proposed mechanism centers on binding and stabilizing cardiolipin, a phospholipid essential to the structure and efficiency of the electron transport chain. By associating with cardiolipin, SS-31 is thought to help preserve mitochondrial cristae architecture and support cellular energy production, which is why it has attracted interest in the study of conditions linked to mitochondrial dysfunction.
SS-31 is researched because mitochondria sit at the center of cellular energy metabolism, and their decline is implicated in a wide range of age-related and disease processes. In laboratory and animal studies, the peptide has been reported to produce protective mitochondrial effects, and it advanced into controlled human clinical trials investigating mitochondrial and cardiac-related conditions. It is important to be evidence-honest here: the human trial results have been mixed, and SS-31 has not been approved as a general-use medicine. Much of the most striking data comes from preclinical (animal and in-vitro) models, which do not always translate into demonstrated benefit in people. SS-31 remains an investigational compound under active scientific study rather than an established therapy.
Because SS-31 is investigational, its safety profile in humans is still being characterized. In clinical trials, injection-site reactions have been among the reported side effects, and long-term outcomes remain incompletely understood. A further important distinction is that material sold on the research-chemical market is not the same as the studied clinical product; purity, identity, and formulation are not guaranteed outside of a regulated trial setting. This page is an educational reference summarizing the current evidence picture for SS-31 and is not medical advice. Anyone considering questions about mitochondrial health should consult a qualified healthcare professional.
Evidence grade: B
Studied in controlled clinical trials with mixed results; not approved. Protective mitochondrial effects reported.
Studied in controlled clinical trials with mixed results; not approved.
Protective mitochondrial effects reported.
Investigational; research-market material is not the studied clinical product.
Investigational; studied in clinical trials. Not an approved general-use medicine.
Early 2000s
SS-31 emerged from the Szeto-Schiller family of aromatic-cationic peptides, first described by academic researchers as small cell-permeable molecules that concentrate in mitochondria.
2000s
Preclinical work characterised its interaction with cardiolipin in the inner mitochondrial membrane and reported cytoprotective effects in cell and animal models of oxidative and ischemic stress.
Early 2010s
A biotech developer advanced the compound into human trials under the names elamipretide, MTP-131 and Bendavia, studying it in cardiac and mitochondrial conditions.
Mid 2010s
A trial in cardiac ischemia-reperfusion (heart attack setting) did not meet its primary endpoints, tempering early cardiovascular expectations.
Late 2010s to early 2020s
A phase 3 study in primary mitochondrial myopathy did not meet its primary endpoints; parallel investigation continued in rare conditions such as Barth syndrome and certain eye diseases with mixed results.
Early-to-mid 2020s
The compound remained investigational, with regulatory review focused on narrow rare-disease indications and no general-use approval in place.