Longevity and anti-aging peptides
Peptides here appear in research on mitochondrial function, telomere biology, senescence, and age-related decline. Much of the underlying evidence is preclinical or based on small human studies, and long-term safety data is generally absent. Treat the mechanism notes as descriptions of research, not established effects.
21 profiles in this category. Browse all peptides. Research use only. Not medical advice.
Longevity and anti-aging peptides (21)
Fat Loss • Oral small-molecule AMPK activator (investigational) • Emerging
Investigational oral small-molecule AMPK activator, formerly O304, tested in two small human trials in type 2 diabetes and in obesity with prediabetes. Not FDA-approved. Prohibited in sport as an AMPK activator under WADA S4.4.1.
Mechanism: ATX-304, first described as O304, raises AMP-activated pr…
Half-life: Long; plasma levels did not reach steady state until about day 14 of daily dosing. No numeric human half-life has been published.
MW: 380.2 g/mol
Longevity • FDA-approved calcitonin receptor agonist • Established
Synthetic 32-amino-acid polypeptide identical to salmon calcitonin, approved for Paget disease of bone, hypercalcaemia, and postmenopausal osteoporosis in women more than five years past menopause.
Mechanism: Calcitonin binds the calcitonin receptor on osteoclasts, …
MW: 3431.9 g/mol
Fat Loss • Long-acting GHRH analog • Experimental
GHRH analog. Catalog “CJC-1295” often means the DAC (Drug Affinity Complex) form that extends half-life via albumin binding. Not FDA-approved. WADA S2 (GHRH analogues).
Mechanism: CJC-1295 is a GHRH analog based on GRF(1-29) carrying fou…
Half-life: ~6–8 days (estimated 5.8–8.1 days in healthy adults after subcutaneous injection)
MW: 3647.2 g/mol
Cognitive • Sleep / neuropeptide research • Experimental
Nonapeptide first isolated from the cerebral venous blood of rabbits during induced slow-wave sleep and named for that association. Its physiological role remains genuinely unsettled: no specific receptor has been identified, reported effects on sleep architecture are inconsistent across studies, and its ability to cross the blood-brain barrier is debated. Research use only and not FDA-approved.
Mechanism: Delta sleep-inducing peptide is a nonapeptide first isola…
Half-life: ~7-15 minutes
MW: 848.81 g/mol
Fat Loss • FDA-approved mitochondria-targeted tetrapeptide • Established
Mitochondria-targeted tetrapeptide. FDA granted accelerated approval in September 2025 to Forzinity (elamipretide) to improve muscle strength in Barth syndrome patients ≥30 kg. Confirmatory trial required.
Mechanism: Elamipretide is a cell-permeable aromatic-cationic tetrap…
Half-life: ~4–5 h (iv) in human studies
MW: 639.8 g/mol
Longevity • Khavinson peptide bioregulator / research • Experimental
Peptide preparation derived from pineal tissue and marketed as a tissue-specific bioregulator in the Khavinson tradition. Not FDA-approved for any indication. No study of Endoluten itself is indexed in PubMed, controlled or otherwise; the studies cited here are class-level work on short peptide bioregulators.
Mechanism: The Khavinson bioregulator hypothesis holds that short pe…
Longevity • Pineal tetrapeptide / research • Experimental
Synthetic pineal tetrapeptide (AEDG) from Khavinson’s work on epithalamin. Studied for telomerase and circadian research; not FDA-approved.
Mechanism: Epitalon is Ala-Glu-Asp-Gly, a synthetic tetrapeptide der…
Half-life: Short (~10 min)
MW: 390.35 g/mol
Longevity • Senolytic FOXO4 peptide / research • Experimental
D-retro-inverso peptide designed to disrupt FOXO4–p53 binding and clear senescent cells in mice (2017 Cell paper). No CAS as a registered drug; not FDA-approved. Often sold as Proxofim.
Mechanism: FOXO4-DRI is a retro-inverso peptide — built from D-amino…
Half-life: Experimental; not established
MW: 5358 g/mol
Fat Loss • TGF-beta superfamily growth factor / research • Experimental
Circulating member of the TGF-beta superfamily that became prominent in ageing research after parabiosis experiments, and whose reported rejuvenative effects have since been actively disputed. Not FDA-approved; no human trials.
Mechanism: GDF-11 signals through activin type II receptors and ALK4…
Longevity • Endogenous tripeptide antioxidant • Experimental
Endogenous antioxidant tripeptide sold as an oral supplement and used IV in clinics. Not FDA-approved as a standalone drug for systemic “detox” or skin-lightening claims.
Mechanism: Glutathione is a tripeptide of glutamate, cysteine and gl…
Half-life: ~1.5 hours (IV); oral bioavailability limited
MW: 307.32 g/mol
Cognitive • Mitochondrial-derived peptide / research • Experimental
A 24-amino-acid peptide encoded within the mitochondrial 16S ribosomal RNA gene and one of the first mitochondrial-derived peptides described. It has been studied for cytoprotective signalling, particularly resistance to apoptosis and to oxidative and amyloid stress, and for effects on insulin sensitivity. Circulating concentrations decline with age, which drives much of the interest in it. Research use only, with no human interventional trials and no FDA-approved use.
Mechanism: Humanin is a 24-amino-acid peptide encoded within the mit…
Half-life: ~2-4 hours
MW: 2687.3 g/mol
Longevity • Potent humanin analog / research • Experimental
Analog of the mitochondrial-derived peptide humanin carrying a serine-to-glycine substitution at position 14, reported in preclinical work to be substantially more potent than the parent peptide. Not FDA-approved; no human trials.
Mechanism: Humanin is encoded within the mitochondrial 16S rRNA gene…
Cognitive • Longevity protein / research • Experimental
Transmembrane and soluble anti-aging protein that is an FGF23 co-receptor. Shop “Klotho” vials are not an FDA-approved drug and are often fragments or poorly characterized proteins.
Mechanism: Alpha-Klotho is a single-pass transmembrane protein expre…
MW: ~130 kDa (full-length protein)
Cognitive • Phenothiazine redox agent / approved for methaemoglobinaemia • Established
Phenothiazine dye approved as an intravenous treatment for acquired methaemoglobinaemia. It is separately sold as a research chemical and studied at low doses for mitochondrial and cognitive endpoints, which are not approved uses.
Mechanism: At therapeutic doses methylene blue is reduced to leucome…
MW: 319.9 g/mol
Fat Loss • Mitochondrial-derived peptide / research • Experimental
A 16-amino-acid peptide encoded in the mitochondrial 12S ribosomal RNA gene, notable as an example of the mitochondrion signalling to the rest of the cell rather than only receiving instructions. It has been studied for effects on glucose utilisation and fatty-acid oxidation through AMPK activation in metabolic models. Circulating concentrations fall with age and rise with exercise. Research use only; no human trials have been published and it is not FDA-approved.
Mechanism: MOTS-c is a 16-amino-acid peptide encoded in the mitochon…
Half-life: ~2-4 hours
MW: 2174.6 g/mol
Fat Loss • Redox coenzyme / supplement • Experimental
Essential redox cofactor sold as IV clinic infusions and oral precursors (NR/NMN). NAD+ itself is not FDA-approved as a drug for anti-aging.
Mechanism: Nicotinamide adenine dinucleotide is a redox coenzyme tha…
Half-life: Minutes to hours (rapidly metabolized)
MW: 663.43 g/mol
Cognitive • Khavinson pineal tripeptide / research • Experimental
Glu-Asp-Arg tripeptide from the Khavinson pineal series, studied for neuroprotection in older literature. Not FDA-approved.
Mechanism: Pinealon is Glu-Asp-Arg, a synthetic tripeptide in the Kh…
Half-life: Not established in humans
MW: 450.41 g/mol
Longevity • Mitochondria-targeted tetrapeptide / research • Experimental
Mitochondria-targeted tetrapeptide from the same Szeto-Schiller series as elamipretide, distinguished by lacking the dimethyltyrosine residue that gives elamipretide its cardiolipin affinity. Not FDA-approved; preclinical only.
Mechanism: Like other Szeto-Schiller peptides, SS-20 concentrates in…
MW: 595.7 g/mol
Longevity • Khavinson peptide bioregulator / research • Experimental
Peptide preparation derived from liver tissue and marketed as a tissue-specific bioregulator in the Khavinson tradition. Not FDA-approved for any indication. No study of Svetinorm itself is indexed in PubMed, controlled or otherwise; the studies cited here are class-level work on short peptide bioregulators.
Mechanism: The Khavinson bioregulator hypothesis holds that short pe…
Longevity • Khavinson dipeptide / research • Experimental
Lys-Glu, a synthetic dipeptide and one of the shortest members of the Khavinson bioregulator series, studied for immune and geroprotective endpoints. Reported findings include effects on lymphocyte proliferation and on chromatin structure in ageing cells, largely from one research group in Russian-language journals. As a dipeptide its proposed nuclear access is more plausible on size grounds than for longer peptides, but no controlled human trials exist and it is not FDA-approved.
Mechanism: Vilon is Lys-Glu, a synthetic dipeptide and one of the sh…
Half-life: Not established in humans
MW: 275.30 g/mol
Longevity • Khavinson peptide bioregulator / research • Experimental
Peptide preparation derived from female reproductive tissue and marketed as a tissue-specific bioregulator in the Khavinson tradition. Not FDA-approved for any indication. No study of Zhenoluten itself is indexed in PubMed, controlled or otherwise; the studies cited here are class-level work on short peptide bioregulators.
Mechanism: The Khavinson bioregulator hypothesis holds that short pe…