Connecting to Pep Nation Lab's research database...
Select Up To Four Compounds To Review Their Evidence, Targets, And Handling Side By Side.
For Laboratory Research Only


| Attribute | ||
|---|---|---|
Research Summary | SS-31 acts like a mechanic that specifically repairs the engine inside your cells (the mitochondria). By fixing the engines, it brings dead, tired cells back to life, reversing aging at the deepest possible level. | NAD+ is the raw fuel your cells use to stay alive. As we get older, our gas tank runs low, causing us to feel tired and age faster. Giving the body NAD+ refills the tank, turning back the clock on aging and energy. |
Studied For | Primary mitochondrial diseaseBarth syndrome (cardiolipin deficiency)Heart failure / ischemia-reperfusion injuryDry AMD (age-related macular degeneration)Mitochondrial agingCardiac energeticsSkeletal muscle mitochondriaKidney ischemia-reperfusion modelsROS reduction at mitochondriaCardiolipin stabilizationRespiratory chain Complex I-V efficiencyATP production enhancementFrailty / aging mitochondriaChronic kidney disease modelsNeurodegenerative disease mitochondriaExercise intolerance researchenergy productionanti-agingmitochondrial repairheart failurecognitive declineischemia reperfusionkidney protection | Aging / cellular senescenceMitochondrial / metabolic dysfunctionNeurodegeneration modelsSirtuin activation (SIRT1-7)DNA repair (PARP activation)Addiction / substance withdrawal researchChronic fatigue / energy restorationAlzheimer's and Parkinson's researchAlcohol use disorder detoxMetabolic syndromeInsulin resistanceCardiovascular disease modelsExercise performance and enduranceInflammation modulationNAD metabolism optimizationLongevity researchNAMPT upregulationCognitive enhancementDepression researchenergy productionanti-aginglongevitymitochondrial functionsirtuin activatoraddiction recoverybrain fog |
Research Areas | LongevityMitochondrial FunctionImmune | LongevityMetabolicMitochondrial FunctionCognitiveImmune |
Best Stacked With | nad-plusmots-cepithalonbac-water | ss-31mots-cepithalonglutathioneb125-amino-1mq |
Overview | ||
Category | Anti-Aging & Longevity | Anti-Aging & Longevity |
Compound Class | Mitochondria-targeted tetrapeptide (D-Arg-dimethylTyr-Lys-Phe-NH2); cardiolipin-targeting | Essential coenzyme (dinucleotide); critical redox electron carrier in all living cells |
Molecular Target | Cardiolipin on inner mitochondrial membrane; scavenges mitochondrial ROS; stabilizes cristae architecture; restores respiratory chain efficiency | Sirtuin deacetylases (SIRT1-7); PARP1 for DNA repair; CD38/CD157 signaling; NADH/NAD+ redox balance in mitochondria |
Aliases / AKA | ElamipretideMTP-131BendaviaSS-31 peptideSzeto-Schiller 31D-Arg-dimethylTyr-Lys-Phe-NH2 | Nicotinamide adenine dinucleotideNADNAD+ coenzymeNAD plusBeta-nicotinamide adenine dinucleotideNAD IV therapy |
Parent Compound | Szeto-Schiller peptide series | Endogenous coenzyme |
Molecular Weight | 639.79 Da | 663.43 Da |
Amino Acid Sequence | D-Arg-Dmt-Lys-Phe-NH2 | dinucleotide |
CAS Number | 736992-21-5 | 53-84-9 |
Year Discovered | Not Listed | Not Listed |
Pro-Angiogenic | No | No |
GLP-1 Class | No | No |
Purity | Not Listed | Not Listed |
Identity | ||
Evidence Tier | ||
Risk Level | ||
PubMed Citations | 457 Good | 85,150 Extensive |
Clinical Trials | Not Listed | 281281 Active |
Regulatory Status | FDA-approved (Sept 2025) for Barth syndrome; investigational elsewhere. | Not FDA-approved (compounded injectable); oral precursors sold as supplements. |
Evidence & Regulatory | ||
Half-Life | ~4 hours | ~2-4 hours |
Typical Frequency | Not Listed | Not Listed |
Administration Route | Injection Only | Injection Only |
Mechanism / PK | Not Listed | Not Listed |
Reported Findings | The Barth-syndrome trial (TAZPOWER) supported a 2025 FDA accelerated approval for Barth syndrome; the primary mitochondrial myopathy program (MMPOWER-3) failed its endpoints, and several cardiac and dry-AMD endpoints were mixed or not met. Still the strongest human evidence in this group. | Animal and precursor human studies support raising NAD+ for mitochondrial and sirtuin function. Direct injectable NAD+ human efficacy is sparse and uncontrolled; preliminary. |
Side Effects Noted | Injection-site reactions, headache, gastrointestinal symptoms; generally tolerable at studied doses. | Rapid IV infusion commonly causes chest tightness, flushing, nausea, and cramping that are rate-dependent and eased by slow infusion. Injection-site reactions for subcutaneous use. |
Warnings | The 2025 approval is narrow (Barth syndrome); other uses remain investigational. Research use only outside approved labeling. | Compounded injectable; not FDA-approved; parenteral pharmacokinetics are poorly characterized. |
Pharmacology | ||
Form | lyophilized | lyophilized |
Diluent | sterile or bacteriostatic water | sterile water; dilute and infuse slowly for IV |
Storage Temp | cold, dark; avoid freeze-thaw | cold, dark, often -20C |
Light Sensitive | Yes | Yes |
Freeze / Thaw | avoid | avoid |
Handling Notes | Non-natural residues improve stability. | Hygroscopic; reconstituted solution is unstable. |
Reconstituted Shelf Life | 28 Days Refrigerated | 7 Days Refrigerated |
Handling & Storage | ||
Pep Nation Lab's comparison tool puts research-grade peptides and compounds head to head - mechanism of action, molecular target, evidence tier, molecular weight, sequence, half-life, and documented research focus - so qualified researchers can evaluate the differences that matter. Every data point is drawn from a referenced monograph. For in vitro laboratory research use only.
The two most-studied research peptides for tissue repair and recovery.
Single GLP-1 versus dual GLP-1/GIP incretin agonists in metabolic research.
Dual versus triple incretin receptor agonists in weight-research models.
A GLP-1 agonist versus a triple-agonist incretin in metabolic research.
A GHRH analog versus a selective ghrelin-receptor secretagogue.
A ghrelin-receptor secretagogue versus a GHRH analog for growth-hormone research.
Two GHRH analogs studied on the growth-hormone axis.
The two first-generation growth-hormone releasing peptides.
An amylin analog versus a GLP-1 agonist in metabolic research.
A mitochondrial-derived peptide versus an HGH fragment in metabolic research.
Melanocortin versus kisspeptin pathways in reproductive research.
A telomerase-pathway peptide versus NAD+ metabolism in longevity research.
A potent versus a highly selective ghrelin-receptor secretagogue.
Two GHRH analogs with contrasting half-life profiles.
A direct IGF-1 analog versus a growth-hormone secretagogue.
The DAC versus non-DAC forms of the CJC-1295 GHRH analog.
Two Russian-developed nootropic and anxiolytic research peptides.
Two mitochondrial-targeted peptides in cellular-energy research.
Two immune-modulating research peptides with distinct mechanisms.
Two HGH-fragment analogs studied for fat-metabolism research.
Next-generation multi-receptor incretin agonists in metabolic research.
Two leading tissue-repair peptides with distinct healing mechanisms.
A systemic repair peptide versus a copper peptide for tissue and skin research.
A GHRH analog versus a selective ghrelin-receptor secretagogue on the GH axis.
A dual incretin agonist versus an amylin analog in metabolic research.
A triple incretin agonist versus an amylin analog in weight research.
Two metabolic research compounds targeting mitochondrial and NNMT pathways.
NAD+ metabolism versus a mitochondrial-derived peptide in longevity research.
Two copper research peptides studied for skin and hair.
A long-acting versus a short-acting GHRH analog.
A selective versus a first-generation ghrelin-receptor secretagogue.
A GLP-1 agonist versus a GLP-1/amylin combination in metabolic research.
Two peptides studied for gut and mucosal repair.
Melanocortin versus oxytocin pathways in intimacy and libido research.
Two thymic immune-modulating research peptides.
An anxiolytic nootropic versus a sleep-associated research peptide.
Direct IGF-1 signaling versus myostatin inhibition in muscle research.
A mitochondrial-targeted peptide versus NAD+ in cellular-energy research.
Browse the full research catalog or the A To Z index to compare any compound.
Any research-grade compound in the library can be placed side by side - up to four at a time. The tool compares mechanism of action, molecular target, evidence tier, molecular weight, amino acid sequence, reported half-life, and what each compound has been studied for, all drawn from referenced monographs.
The evidence tier reflects how extensively a compound has been studied in the referenced literature, from early preclinical signals through to compounds with human clinical data. It is a research-quality signal only, never a safety or efficacy endorsement.
Each comparison page is generated from the same referenced compound database - a genuine side-by-side of mechanism, identity, pharmacokinetics, and evidence, plus data-derived key differences. They are curated, not auto-generated thin pages.
No. Every comparison is for in vitro laboratory research use only. Nothing here is medical advice, a treatment recommendation, or dosing guidance, and no product is for human or animal consumption.