Experimental research peptides

These compounds are classified research-only: no FDA approval, and no active clinical-trial programme behind them. Evidence is typically preclinical, and for many the human pharmacokinetics, effective dose, and safety profile are simply unknown. Profiles here document what the literature reports and where it is silent. Peptides currently in trials are listed under their use-case category instead.

116 profiles in this category. Browse all peptides. Research use only. Not medical advice.

Experimental research peptides (116)

Fat LossGLP-1/MetabolicExperimental

Fat Loss • Small Molecule / Metabolic • Experimental

Small-molecule nicotinamide N-methyltransferase (NNMT) inhibitor studied for NAD+ metabolism and body-composition research. Not an FDA-approved drug.

Mechanism: 5-Amino-1MQ is a small-molecule inhibitor of nicotinamide…

Half-life: 3.8-6.9 hours

MW: 286.11 g/mol

CosmeticExperimental

Cosmetic • Cosmetic SNARE-targeting peptide • Experimental

Topical hexapeptide (Argireline) used in cosmetics as a SNAP-25 fragment analog. Marketed to soften expression lines; not an FDA-approved drug.

Mechanism: Acetyl hexapeptide-8, commonly sold as Argireline, mimics…

Half-life: Topical; systemic PK not established

MW:

CosmeticExperimental

Cosmetic • Cosmetic SNARE-targeting peptide • Experimental

Elongated Argireline analog (SNAP-8) used in topical cosmetics. Not an FDA-approved drug; not WADA-prohibited as a cosmetic peptide.

Mechanism: Acetyl octapeptide-3, sold as SNAP-8, is an elongated ana…

Half-life: Topical; systemic PK not established

MW: ≈1075.2 g/mol

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CosmeticExperimental

Cosmetic • Cosmetic hair and skin matrikine • Experimental

Short acetylated tetrapeptide used topically in hair-density and skin-firmness formulations, commonly paired with red clover extract in commercial blends. Regulated as a cosmetic ingredient, not FDA-approved as a drug.

Mechanism: Acetyl tetrapeptide-3 is described as a matrikine — a pep…

MW: 509.6 g/mol

CognitiveExperimental

Cognitive • Synthetic Semax analog / nootropic research • Experimental

Adamantane-modified Semax analog researched for neurotrophic signaling and peptide stability. No FDA approval; human PK is not established.

Mechanism: Proposed Semax analog with an adamantane moiety intended …

Half-life: Not established; designed for improved stability compared with Semax

MW: ≈1033 g/mol

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Fat LossGLP-1/MetabolicExperimental

Fat Loss • Experimental fat-vasculature targeting peptide • Experimental

Experimental chimeric peptide designed to induce apoptosis in white-adipose vasculature via prohibitin targeting. Not FDA-approved; development did not yield a drug.

Mechanism: Adipotide is a peptidomimetic built from two functional p…

MW: 2557.2 g/mol

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CosmeticExperimental

Cosmetic • Copper tripeptide / cosmetic research • Experimental

Alanine-histidine-lysine copper complex used in hair- and skin-cosmetic research, related to GHK-Cu. Not an FDA-approved drug.

Mechanism: AHK-Cu is the copper complex of the tripeptide alanyl-his…

MW: 451.39 g/mol

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Fat LossMuscle/RecoveryGLP-1/Metabolic

Fat Loss • AMPK activator / research • Experimental

Adenosine analog studied as an AMP-activated protein kinase activator in metabolic and exercise-physiology research. Not FDA-approved. It is prohibited in sport under the WADA gene and metabolic modulators category.

Mechanism: AICAR is taken into cells and phosphorylated to ZMP, an A…

MW: 338.21 g/mol

Fat LossGLP-1/MetabolicExperimental

Fat Loss • Mas receptor agonist / research • Experimental

Synthetic Mas-receptor agonist related to angiotensin-(1-7) biology, studied in cardiometabolic and fibrosis models. Not FDA-approved.

Mechanism: Activates the Mas receptor (ACE2/Ang-(1-7)/Mas axis), opp…

Half-life: Short; orally active analog tested in rodents

MW: 902.0 g/mol

Fat LossMuscle/RecoveryGLP-1/Metabolic

Fat Loss • GH C-terminal fragment analog • Experimental

Modified C-terminal hGH fragment studied for lipolysis without GH-receptor growth effects. Not FDA-approved. WADA prohibits GH fragments including AOD-9604 (S2).

Mechanism: AOD-9604 is a synthetic analog of the C-terminal fragment…

Half-life: ~20-30 minutes

MW: 1815.1 g/mol

Fat LossGLP-1/MetabolicExperimental

Fat Loss • Mitochondrial uncoupler / small molecule • Experimental

Mitochondrial protonophore uncoupler used in metabolic research to increase energy expenditure independently of beta-oxidation stimulation. Not FDA-approved; not a peptide.

Mechanism: Increases inner-mitochondrial-membrane proton leak, uncou…

Half-life: Not established (limited public PK; primarily preclinical/in vitro characterization)

MW: 340.29 g/mol

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CosmeticExperimental

Cosmetic • Cosmetic hair peptide • Experimental

Biotin-conjugated tripeptide used in topical hair and lash products, typically as part of proprietary blends. Not FDA-approved as a drug; regulated as a cosmetic ingredient.

Mechanism: The peptide couples biotin to the GHK tripeptide, which h…

MW: 566.7 g/mol

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Experimental

Experimental • Khavinson peptide bioregulator / research • Experimental

Peptide preparation derived from bone marrow tissue and marketed as a tissue-specific bioregulator in the Khavinson tradition. Not FDA-approved for any indication. No controlled human efficacy trials of this specific preparation have been published; the available literature is class-level work on short peptide bioregulators.

Mechanism: The Khavinson bioregulator hypothesis holds that short pe…

Muscle/RecoveryExperimental

Muscle/Recovery • Healing / Regenerative • Experimental

Synthetic gastric pentadecapeptide widely sold as a research chemical for tissue-repair models. Not FDA-approved; FDA has flagged it for compounding risk. WADA prohibits BPC-157 under S0.

Mechanism: Preclinical work reports angiogenesis, nitric-oxide modul…

Half-life: ~30 minutes to 4 hours

MW: 1419.5 g/mol

Experimental

Experimental • Khavinson bioregulator / research • Experimental

Short peptide marketed as a Khavinson bronchial/lung bioregulator (often AEDL). Russian literature only; not FDA-approved.

Mechanism: Bronchogen is Ala-Glu-Asp-Leu, a synthetic tetrapeptide i…

Half-life: Not established (small tripeptide)

MW: 391.39 g/mol

Muscle/RecoveryExperimental

Muscle/Recovery • Khavinson bioregulator / research • Experimental

Short peptide sold as a cardiac bioregulator in the Khavinson series. No FDA approval; evidence is historical Russian literature.

Mechanism: Cardiogen is Ala-Glu-Asp-Arg, a synthetic tetrapeptide in…

Half-life: Not established (limited PK data; primarily research context)

MW: Low molecular weight peptide fraction

Muscle/RecoveryExperimental

Muscle/Recovery • Khavinson bioregulator / research • Experimental

Ala-Glu-Asp, a synthetic tripeptide in the Khavinson bioregulator series, marketed for cartilage and connective-tissue research. Like others in the series it is proposed to act by influencing transcription in the tissue it is associated with, a hypothesis supported almost entirely by cell-culture and cytogenetic work from one research group. No controlled clinical evidence exists for joint or cartilage outcomes, and it is not FDA-approved.

Mechanism: Cartalax is Ala-Glu-Asp, a synthetic tripeptide in the Kh…

Half-life: Short (hours)

MW: 317.3 g/mol

CognitiveExperimental

Cognitive • Peptide hydrolysate / nootropic research • Experimental

Peptide hydrolysate prepared from porcine brain tissue, supplied as a mixture of low-molecular-weight peptides and free amino acids rather than a single characterised compound. It is used in several countries in Europe and Asia for stroke, traumatic brain injury and dementia, where it is given by injection. Not FDA-approved in the United States, and because it is a mixture its composition is not standardised the way a single-entity drug would be.

Mechanism: Mixture of low-molecular-weight neuropeptides claimed to …

Half-life: Mixture; component PK not a single value

MW: Mixture of low-MW peptides

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CognitiveExperimental

Cognitive • Khavinson peptide bioregulator / research • Experimental

Peptide preparation derived from brain and central nervous system tissue and marketed as a tissue-specific bioregulator in the Khavinson tradition. Not FDA-approved for any indication. No controlled human efficacy trials of this specific preparation have been published; the available literature is class-level work on short peptide bioregulators.

Mechanism: The Khavinson bioregulator hypothesis holds that short pe…

Muscle/RecoveryExperimental

Muscle/Recovery • Bioregulator / research mixture • Experimental

Marketed cartilage-support peptide blend rather than a single characterised active ingredient, with composition varying between suppliers. Because it is a mixture, no single mechanism, sequence or pharmacokinetic profile applies to it, and no pivotal trial has evaluated any branded product under this name. Not FDA-approved and not a treatment for arthritis or joint disease.

Mechanism: Chondromix is a marketed blend rather than a defined sing…

Half-life: Not established

MW: 408.47 g/mol

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Experimental

Experimental • Khavinson lung bioregulator / research • Experimental

Glu-Asp-Gly, a synthetic tripeptide in the Khavinson bioregulator series, sold as a bronchial and lung bioregulator. The proposed tissue-specific activity rests on older Russian-language cytogenetic work that has not been independently replicated, and no receptor or signalling pathway has been characterised. There is no modern randomised trial evidence for respiratory outcomes, and it is not FDA-approved.

Mechanism: Chonluten is Glu-Asp-Gly, a synthetic tripeptide in the K…

Fat LossMuscle/RecoveryLongevity

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: ~8 hours

MW: 3647.2 g/mol

Fat LossMuscle/RecoveryExperimental

Fat Loss • Short-acting GHRH analog • Experimental

Modified GRF(1-29), a growth hormone-releasing hormone analog carrying four amino-acid substitutions that resist enzymatic breakdown but without the drug affinity complex group that makes the DAC version long-acting. It produces brief GH pulses lasting around thirty minutes rather than the multi-day elevation of DAC-CJC, and the two are pharmacologically distinct despite the shared name. Not FDA-approved. Prohibited in sport under WADA class S2.

Mechanism: This is modified GRF(1-29), a GHRH analog carrying four a…

Half-life: Short (hours) vs DAC variant

MW: ≈3368 g/mol

Fat LossMuscle/RecoveryExperimental

Fat Loss • GHRH + GHS combination • Experimental

Research blend combining a GHRH analog (usually Mod GRF / CJC no DAC) with ipamorelin to stimulate GH via two receptor classes. Not FDA-approved. Both components are WADA S2.

Mechanism: This combination pairs a GHRH receptor agonist with a ghr…

Half-life: CJC: ~30 min; Ipa: ~2 hours

MW: Varies

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CognitiveExperimental

Cognitive • Khavinson cortical bioregulator / research • Experimental

Ala-Glu-Asp-Pro, a synthetic tetrapeptide in the Khavinson bioregulator series associated with cerebral cortex tissue. Reported findings concern cortical neuron protein synthesis and nerve regeneration in animal models, published largely in Russian-language journals by a single research group without independent replication. No controlled human evidence exists, and it is not FDA-approved.

Mechanism: Cortagen is Ala-Glu-Asp-Pro, a synthetic tetrapeptide in …

MW: 430.4 g/mol

CognitiveExperimental

Cognitive • Brain polypeptide extract / research • Experimental

Cattle-cortex polypeptide extract used in some CIS countries as a nootropic. Not FDA-approved; composition is a hydrolysate, not a single peptide.

Mechanism: Cortexin is a preparation of low-molecular-weight polypep…

Half-life: Mixture; not a single PK value

MW: Mixture

CognitiveExperimental

Cognitive • Khavinson bioregulator / research • Experimental

Peptide preparation extracted from brain tissue and sold as a central nervous system bioregulator in the Khavinson tradition. It is a complex of low-molecular-weight peptides rather than a single defined molecule, so no specific sequence or mechanism can be assigned and batch composition is not standardised. Evidence is limited to older bioregulator literature, and it is not FDA-approved.

Mechanism: Cranoluten is a peptide preparation extracted from brain …

Half-life: Not established

MW: 393.39 g/mol

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CosmeticExperimental

Cosmetic • Cosmetic tyrosinase-inhibiting peptide • Experimental

Synthetic decapeptide used topically in pigmentation products as a non-hydroquinone alternative. Regulated as a cosmetic ingredient; not FDA-approved as a drug.

Mechanism: Decapeptide-12 was identified by screening for peptides t…

MW: 1395.5 g/mol

CognitiveLongevityExperimental

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

CognitiveExperimental

Cognitive • Angiotensin IV analog / nootropic research • Experimental

Orally active angiotensin IV analog that potentiates HGF/c-Met signaling in animal memory models. Not FDA-approved; human safety is not established.

Mechanism: Dihexa is a small orally active molecule derived from ang…

Half-life: Oral; long CNS residence reported in animals

MW: 504.70 g/mol

CosmeticExperimental

Cosmetic • Cosmetic nicotinic antagonist mimetic • Experimental

Waglerin-1–inspired tripeptide used in cosmetics to reduce expression-line appearance. Topical cosmetic active, not an FDA drug.

Mechanism: This dipeptide is a synthetic mimetic of waglerin-1, a co…

Half-life: Topical; systemic PK not established

MW:

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LongevityExperimental

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 controlled human efficacy trials of this specific preparation have been published; the available literature is class-level work on short peptide bioregulators.

Mechanism: The Khavinson bioregulator hypothesis holds that short pe…

LongevityExperimental

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

Fat LossMuscle/RecoveryExperimental

Fat Loss • Myostatin-binding glycoprotein / research • Experimental

Isoform of follistatin that binds myostatin/activin. Gene-therapy and research-peptide forms exist; no FDA-approved follistatin drug. WADA prohibits myostatin inhibitors (S4).

Mechanism: Follistatin-344 is a glycoprotein that acts as a high-aff…

Half-life: Varies; protein biologic

MW: ≈38–40 kDa (glycosylation dependent)

LongevityExperimental

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

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Fat LossMuscle/RecoveryLongevity

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…

Fat LossMuscle/RecoveryGLP-1/Metabolic

Fat Loss • GH C-terminal fragment / research • Experimental

C-terminal fragment of human GH studied for lipolysis. Closely related to AOD-9604. Not FDA-approved. WADA S2 (GH fragments).

Mechanism: This is the C-terminal fragment of human growth hormone s…

Half-life: Short (minutes–hours; animal PK)

MW: ≈1729 g/mol

Muscle/RecoveryCosmeticExperimental

Muscle/Recovery • Copper tripeptide / cosmetic and research • Experimental

Endogenous glycyl-L-histidyl-L-lysine copper complex used widely in cosmetics for skin remodeling. Injectable research use is unapproved. USADA lists GHK (tripeptide-1) as not prohibited.

Mechanism: GHK is a naturally occurring tripeptide (glycyl-L-histidy…

Half-life: Short; typically used topically

MW: 403.92 g/mol

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Fat LossMuscle/RecoveryExperimental

Fat Loss • Growth hormone-releasing peptide / research • Experimental

Synthetic hexapeptide growth hormone secretagogue from the same series as GHRP-2 and GHRP-6. Not FDA-approved and less studied than either. Human pharmacokinetic data is limited.

Mechanism: GHRP-1 is a synthetic enkephalin-derived peptide that bin…

MW: 955.1 g/mol

Fat LossMuscle/RecoveryExperimental

Fat Loss • GHS combination / research • Experimental

Blend of two ghrelin-receptor agonists. Both GHRP-2 (pralmorelin) and ipamorelin are WADA S2. Not FDA-approved as a combination.

Mechanism: This blend combines two agonists at the same receptor, gr…

Half-life: Short; both ~1–2 h combined activity

MW: Mixture

Fat LossMuscle/RecoveryExperimental

Fat Loss • Ghrelin-receptor agonist / research • Experimental

Synthetic hexapeptide growth hormone secretagogue and one of the earliest compounds in its class. It raises growth hormone through the ghrelin receptor, and because that is the receptor ghrelin uses to signal hunger it also produces marked appetite stimulation and increased gastric motility, along with rises in cortisol and prolactin. Those off-target effects prompted development of more selective agents such as ipamorelin. Not FDA-approved. Prohibited in sport under WADA class S2.

Mechanism: GHRP-6 is a synthetic hexapeptide agonist at growth hormo…

Half-life: ~30 minutes

MW: 873.0 g/mol

Muscle/RecoveryCosmeticExperimental

Muscle/Recovery • Regenerative-cosmetic blend • Experimental

Vendor blend typically combining GHK-Cu, BPC-157, and TB-500 for cosmetic/regenerative research. Not a single API; BPC-157 and TB-500 are WADA issues if the blend contains them.

Mechanism: Glow is a compounded blend rather than a single compound,…

Half-life: Varies by component

MW: Varies

LongevityCosmeticExperimental

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

Fat LossMuscle/RecoveryExperimental

Fat Loss • GHRP / research • Experimental

Potent GHRP (examorelin) that raises GH and can desensitize with frequent use. Also studied for cardiac GHSR effects. Not FDA-approved. WADA S2.

Mechanism: Hexarelin is a synthetic hexapeptide agonist at growth ho…

Half-life: ~56–76 minutes (human PK studies)

MW: 887.0 g/mol

CognitiveLongevityExperimental

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

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LongevityExperimental

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…

Fat LossMuscle/RecoveryExperimental

Fat Loss • IGF-1 / prescription (mecasermin) • Experimental

Endogenous growth factor. Recombinant mecasermin (Increlex) is FDA-approved for severe primary IGF-1 deficiency. Research vials are unapproved. WADA S2.

Mechanism: Insulin-like growth factor 1 is a 70-amino-acid peptide p…

Half-life: ~10–16 hours (bound); minutes unbound

MW: 7649 Da

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Fat LossMuscle/RecoveryExperimental

Fat Loss • Truncated IGF-1 analog / research • Experimental

IGF-1 lacking the first three amino acids, with reduced IGFBP binding and higher local potency in research models. Not FDA-approved. WADA S2.

Mechanism: IGF-1 DES(1-3) is native IGF-1 with the first three N-ter…

Fat LossMuscle/RecoveryExperimental

Fat Loss • Modified IGF-1 analog / research • Experimental

Modified analog of insulin-like growth factor 1 carrying an arginine substitution at position 3 plus a thirteen-residue N-terminal extension, both of which reduce binding to IGF binding proteins. With less of the peptide sequestered, a larger free fraction remains available to the IGF-1 receptor and activity persists longer than native IGF-1. It is a research reagent with no approved use and no controlled human safety data. Prohibited in sport under WADA class S2.

Mechanism: IGF-1 LR3 is a modified analog carrying an arginine subst…

Half-life: Longer than native IGF-1 in vitro; human PK not established in labels

MW: Reported ≈9.1 kDa (supplier-dependent)

Fat LossMuscle/RecoveryExperimental

Fat Loss • Selective GHS / research • Experimental

Pentapeptide ghrelin-receptor agonist noted for GH release with relatively less ACTH/cortisol than older GHRPs. Not FDA-approved. WADA S2 (named).

Mechanism: Ipamorelin is a synthetic pentapeptide agonist at growth …

Half-life: ~2 hours

MW: 711.9 g/mol

Experimental

Experimental • Kisspeptin fragment / research • Experimental

Decapeptide KISS1 fragment that stimulates GnRH release. Used in reproductive-endocrine research. WADA lists kisspeptin and agonists as S2. Not FDA-approved.

Mechanism: Kisspeptin-10 is the C-terminal decapeptide fragment of t…

Half-life: ~4 minutes

MW: 1302.5 g/mol

Experimental

Experimental • Full-length kisspeptin / research • Experimental

Full-length product of the KISS1 gene, originally described as metastin for its reported suppression of tumour metastasis. It acts on hypothalamic neurons upstream of GnRH release and is a gatekeeper of puberty and reproductive axis function; loss-of-function mutations in its receptor cause failure of puberty. It has been used in human reproductive-endocrine research, where its longer sequence gives a somewhat greater duration of action than kisspeptin-10. Not FDA-approved. Prohibited in sport under WADA class S2.

Mechanism: Kisspeptin-54 is the full-length product of the KISS1 gen…

Half-life: Short; study-dependent

MW: ≈5857 g/mol

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CognitiveLongevityExperimental

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)

Muscle/RecoveryCosmeticExperimental

Muscle/Recovery • Regenerative blend • Experimental

Vendor regenerative blend (commonly BPC-157, TB-500, GHK-Cu, and KPV). Not a single drug; several components are WADA-prohibited or unapproved.

Mechanism: KLOW is a compounded blend of GHK-Cu, KPV, BPC-157 and TB…

Half-life: Varies

MW: Varies

KPV

CosmeticExperimental

Cosmetic • Anti-inflammatory MSH fragment / research • Experimental

C-terminal α-MSH tripeptide with anti-inflammatory activity in gut and skin models without strong melanotropic tanning. Not FDA-approved.

Mechanism: KPV is Lys-Pro-Val, the C-terminal tripeptide of alpha-me…

Half-life: Short; topical and research injectable use

MW: 342.44 g/mol

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Experimental

Experimental • Khavinson peptide bioregulator / research • Experimental

Peptide preparation derived from prostate tissue and marketed as a tissue-specific bioregulator in the Khavinson tradition. Not FDA-approved for any indication. No controlled human efficacy trials of this specific preparation have been published; the available literature is class-level work on short peptide bioregulators.

Mechanism: The Khavinson bioregulator hypothesis holds that short pe…

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Fat LossGLP-1/MetabolicExperimental

Fat Loss • Khavinson liver bioregulator / research • Experimental

Short synthetic peptide marketed as a hepatic bioregulator in the Khavinson tradition. Not FDA-approved for any indication. Published work is largely Russian-language and class-level, and no controlled human trials evaluating this specific peptide for liver outcomes have been indexed.

Mechanism: Livagen is Lys-Glu-Asp-Ala, a synthetic tetrapeptide in t…

MW: 461.5 g/mol

CosmeticExperimental

Cosmetic • Human cathelicidin / research • Experimental

Human host-defense peptide (cathelicidin) with antimicrobial and immunomodulatory activity. Not FDA-approved as a drug; excess LL-37 is implicated in rosacea/psoriasis biology.

Mechanism: LL-37 is the only human cathelicidin, released by proteol…

Half-life: ~1-2 hours

MW: 4493 Da

CosmeticExperimental

Cosmetic • Unapproved melanocortin agonist • Experimental

Cyclic α-MSH analog used illicitly for tanning and libido. Not FDA-approved. FDA and EMA have warned against its use. WADA S0 as a non-approved substance.

Mechanism: Melanotan II is a cyclic lactam analog of alpha-melanocyt…

Half-life: ~36 hours

MW: 1024.2 g/mol

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MGF

Fat LossMuscle/RecoveryExperimental

Fat Loss • IGF-1 splice variant / research • Experimental

Mechano growth factor is the IGF-1Ec splice variant induced by muscle loading. Research MGF peptides are not an FDA drug. WADA S2.

Mechanism: Mechano growth factor is a splice variant of the IGF-1 ge…

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Fat LossMuscle/RecoveryGLP-1/Metabolic

Fat Loss • Oral ghrelin-mimetic small molecule • Experimental

Oral non-peptide GH secretagogue (ibutamoren) that raises GH and IGF-1. Not FDA-approved. WADA S2 names ibutamoren (MK-677).

Mechanism: MK-677, also called ibutamoren, is an orally bioavailable…

Half-life: ~24 hours

MW: 624.8 g/mol

Fat LossLongevityGLP-1/Metabolic

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

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CosmeticExperimental

Cosmetic • Cosmetic lash and brow peptide • Experimental

Lipidated pentapeptide used in eyelash and eyebrow conditioning products. Regulated as a cosmetic ingredient; not FDA-approved as a drug and not equivalent to prostaglandin analog lash treatments.

Mechanism: Attachment of a myristoyl fatty acid chain increases lipo…

MW: 796.1 g/mol

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CognitiveExperimental

Cognitive • Modified Selank analog / research • Experimental

Chemically modified analog of Selank with N-terminal acetylation and C-terminal amidation, sold as a research chemical and commonly used intranasally. Not FDA-approved. Published research on this modified form specifically is very limited; most available data concerns Selank itself.

Mechanism: The parent peptide Selank is a synthetic analog of the im…

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CognitiveExperimental

Cognitive • Modified Semax analog / research • Experimental

N-acetylated, C-amidated Semax analog sold for nootropic research, intended to resist peptidases versus standard Semax. Not FDA-approved.

Mechanism: This is Semax carrying two standard medicinal-chemistry m…

MW: 855 g/mol

Fat LossLongevityGLP-1/Metabolic

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

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CognitiveExperimental

Cognitive • Dipeptide nootropic / research • Experimental

Synthetic dipeptide developed in Russia and marketed there as a nootropic. It is not FDA-approved and is not a lawful dietary supplement ingredient in the United States. Most published research is Russian-language and preclinical.

Mechanism: Noopept is a proline-containing dipeptide structurally re…

MW: 318.4 g/mol

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CognitiveExperimental

Cognitive • Endogenous wake-promoting neuropeptide / research • Experimental

Endogenous 33-amino-acid hypothalamic neuropeptide central to arousal and wakefulness. Loss of orexin-producing neurons causes narcolepsy type 1. Studied as an intranasal research compound; not FDA-approved.

Mechanism: Orexin-A is produced by a small population of lateral hyp…

MW: 3561.1 g/mol

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Fat LossGLP-1/MetabolicExperimental

Fat Loss • Khavinson bioregulator / research • Experimental

Peptide preparation sold in the Khavinson bioregulator tradition, supplied as a complex of low-molecular-weight peptides extracted from animal tissue rather than a single characterised compound. Sources disagree on which organ it is intended to support, which is itself a reason for caution when interpreting product claims. No controlled human evidence exists and it is not FDA-approved.

Mechanism: Ovagen is a peptide preparation marketed in the Khavinson…

MW: 375.37 g/mol

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Fat LossGLP-1/MetabolicExperimental

Fat Loss • Endogenous dual GLP-1/glucagon receptor agonist • Experimental

Naturally occurring 37-amino-acid gut hormone that activates both GLP-1 and glucagon receptors. It is the endogenous template for the dual-agonist drug class and is studied rather than marketed. Not FDA-approved.

Mechanism: Oxyntomodulin is produced from proglucagon in intestinal …

MW: 4422 g/mol

CognitiveExperimental

Cognitive • Neurotrophic fragment / research • Experimental

Short nootropic peptide associated with Cerebrolysin-derived fragments in research catalogs. Distinct from the p21 CDK inhibitor protein. Not FDA-approved.

Mechanism: P21 is sold as a peptide acting on the brain-derived neur…

Half-life: Unknown (preclinical)

MW: ≈2292 g/mol

Fat LossCognitiveGLP-1/Metabolic

Fat Loss • Endogenous neuropeptide / research • Experimental

38-aa neuropeptide that activates PAC1/VPAC receptors. Research tool in migraine, neuroprotection, and metabolic models. Not FDA-approved as a drug.

Mechanism: Pituitary adenylate cyclase-activating polypeptide is a 3…

Half-life: Very short; rapidly degraded by peptidases

MW: ≈4534 g/mol

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CosmeticExperimental

Cosmetic • Cosmetic matrikine • Experimental

Palmitoylated hexapeptide used in topical anti-ageing formulations, frequently combined with other matrikines. Regulated as a cosmetic ingredient; not FDA-approved as a drug.

Mechanism: The peptide portion corresponds to a repeating motif of e…

MW: 737 g/mol

CosmeticExperimental

Cosmetic • Cosmetic matrikine • Experimental

Palmitoylated KTTKS matrikine (Matrixyl) used in anti-wrinkle cosmetics. Not an FDA drug. Not WADA-prohibited as a cosmetic peptide.

Mechanism: Palmitoyl pentapeptide-4 is the KTTKS sequence, a fragmen…

Half-life: Topical; systemic PK not established

MW: ≈802.07 g/mol

CosmeticExperimental

Cosmetic • Cosmetic matrikine • Experimental

Palmitoylated GQPR tetrapeptide used to reduce IL-6 in stressed skin models and paired with pal-tripeptide-1 in Matrixyl 3000.

Mechanism: Palmitoyl tetrapeptide-7 is a short peptide with a palmit…

Half-life: Topical; systemic PK not established

MW: ≈694.9 g/mol

CosmeticExperimental

Cosmetic • Cosmetic copper-free GHK analog • Experimental

The GHK tripeptide supplied with a palmitic acid chain attached to improve penetration through the outer skin barrier, and without the bound copper of GHK-Cu. It is used topically as a matrikine, a peptide fragment that signals matrix turnover to dermal fibroblasts, and is most often formulated alongside palmitoyl tetrapeptide-7. Regulated as a cosmetic ingredient rather than a drug, and not FDA-approved for any therapeutic use.

Mechanism: Palmitoyl tripeptide-1 delivers the GHK sequence with a s…

Half-life: Topical; systemic PK not established

MW: ≈578.8 g/mol

CosmeticExperimental

Cosmetic • Cosmetic TGF-β mimetic tripeptide • Experimental

Lipidated tripeptide marketed under the Syn-Coll name and used topically in firming and anti-ageing formulations. It is described as a thrombospondin-1 mimetic, intended to promote activation of transforming growth factor beta already present in the dermis rather than to supply new growth factor. Evidence comes predominantly from supplier research and small cosmetic studies. A cosmetic active, not a drug, and not FDA-approved.

Mechanism: Palmitoyl tripeptide-5 is a lipidated tripeptide used top…

Half-life: Topical; systemic PK not established

MW:

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Fat LossGLP-1/MetabolicExperimental

Fat Loss • Khavinson pancreatic bioregulator / research • Experimental

Lys-Glu-Asp-Trp, a synthetic tetrapeptide in the Khavinson bioregulator series associated with pancreatic tissue, with reported effects on carbohydrate metabolism markers in animal models. It should not be confused with Suprefort, the tissue extract marketed for the same organ. The supporting literature is regional and uncontrolled, and it is not FDA-approved or a treatment for diabetes.

Mechanism: Pancragen is Lys-Glu-Asp-Trp, a synthetic tetrapeptide in…

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CognitiveExperimental

Cognitive • TREK-1 research peptide • Experimental

Shortened analog of spadin, a peptide derived from sortilin maturation, which blocks the TREK-1 potassium channel. Because mice lacking TREK-1 show a depression-resistant phenotype, the channel became an antidepressant target, and PE-22-28 produces antidepressant-like effects in rodents within days rather than the weeks required by monoamine reuptake inhibitors. Preclinical only, with no human trials, and not FDA-approved.

Mechanism: PE-22-28 is a shortened analog of spadin, a peptide deriv…

MW: 773.9 g/mol

Fat LossMuscle/RecoveryExperimental

Fat Loss • PEGylated IGF-1 splice variant / research • Experimental

PEGylated mechano-growth-factor (IGF-1Ec) analog sold for muscle-repair research. Not FDA-approved. WADA S2 (IGF / MGF).

Mechanism: PEG-MGF is the mechano growth factor E-peptide with polye…

Half-life: Extended vs native MGF; no validated human PK

MW: ≈8–10 kDa (PEG dependent)

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Muscle/RecoveryExperimental

Muscle/Recovery • BPC-157 arginate salt / research • Experimental

Arginate salt form of the BPC-157 pentadecapeptide, marketed as a more stable alternative to the acetate salt. Not FDA-approved. Published research on the arginate form specifically is minimal; nearly all available evidence concerns BPC-157 itself.

Mechanism: The peptide sequence is the same as BPC-157, so the propo…

CognitiveLongevityExperimental

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

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Experimental

Experimental • Experimental anticancer peptide / research • Experimental

Experimental peptide containing a p53 motif designed to lyse cancer-cell membranes in preclinical papers. Not FDA-approved; not a cancer treatment.

Mechanism: PNC-27 is a synthetic peptide joining a p53 -derived HDM-…

MW: 4032 g/mol

Fat LossMuscle/RecoveryExperimental

Fat Loss • GHRP-2 / diagnostic GH secretagogue • Experimental

Pralmorelin is GHRP-2, used as a GH-stimulation diagnostic in Japan. Research vials are not that approved diagnostic. WADA S2 names GHRP-2 (pralmorelin).

Mechanism: Pralmorelin, also called GHRP-2, is a synthetic agonist a…

Half-life: Reported short; human diagnostic use in Japan

MW: 801.98 g/mol

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Experimental

Experimental • Khavinson prostate bioregulator / research • Experimental

Peptide preparation derived from prostate tissue and sold as a prostate bioregulator in the Khavinson tradition. It is a mixture of low-molecular-weight peptides rather than a single characterised compound, so no specific mechanism can be attributed to it. It is not a treatment for benign prostatic hyperplasia or any other prostate condition, has no controlled trial evidence, and is not FDA-approved.

Mechanism: Prostamax is a peptide preparation derived from prostate …

MW: 487.5 g/mol

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CosmeticExperimental

Cosmetic • Hair-follicle Wnt research peptide • Experimental

Cell-penetrating peptide designed to block CXXC5–Dishevelled binding and enhance Wnt signaling in hair-growth mouse models. Not FDA-approved.

Mechanism: PTD-DBM is a fusion of a protein transduction domain, whi…

MW: 3082.6 g/mol

Muscle/RecoveryExperimental

Muscle/Recovery • PTH fragment / research or compounded • Experimental

PTH(1–34) analog class. The FDA-approved drug is teriparatide (Forteo/Bonsity). Research or compounded vials are not those products.

Mechanism: This entry covers generic and compounded preparations of …

Half-life: ~1 h (sc); same as Forteo reference

MW: ≈4118 g/mol

CognitiveExperimental

Cognitive • Anxiolytic tuftsin analog / research • Experimental

Synthetic heptapeptide combining the immunomodulatory tetrapeptide tuftsin with a stabilising tail, developed in Russia as an anxiolytic and most often used intranasally. It has been studied for anxiety without the sedation or dependence associated with benzodiazepines, and retains some immune-modulating activity from its tuftsin origin. Not FDA-approved; the supporting clinical literature is largely Russian-language.

Mechanism: Selank is a synthetic heptapeptide combining the immunomo…

Half-life: Not established (varies by route; nasal studied in RU)

MW: ≈751.9 g/mol

CognitiveExperimental

Cognitive • ACTH fragment nootropic / research • Experimental

Synthetic analog of the ACTH(4-10) fragment with a stabilising tail added, developed in Russia and used there as an intranasal nootropic and neuroprotective agent for stroke and cognitive indications. It has no corticotropic activity despite its ACTH origin. Reported activity centres on brain-derived neurotrophic factor expression and monoamine modulation. Not FDA-approved, and the clinical literature is almost entirely Russian-language with limited independent replication.

Mechanism: Semax is a synthetic analog of ACTH(4-10) with a Pro-Gly-…

Half-life: ~20-30 minutes (nasal)

MW: 813.92 g/mol

Fat LossMuscle/RecoveryExperimental

Fat Loss • GHRH(1-29) / discontinued US brand • Experimental

GHRH(1-29), the shortest fragment of growth hormone-releasing hormone that retains full activity at the pituitary GHRH receptor. It was marketed in the United States as Geref for paediatric growth hormone deficiency and as a diagnostic agent; the brand was discontinued in 2008 for commercial rather than safety reasons, and it remains available through compounding pharmacies. Because it stimulates the pituitary rather than replacing the hormone, it requires an intact somatotroph axis. Prohibited in sport under WADA class S2.

Mechanism: Sermorelin is GRF(1-29), the shortest N-terminal fragment…

Half-life: ~11-12 minutes

MW: 3357.96 g/mol

CosmeticExperimental

Cosmetic • Cosmetic EGF / research • Experimental

Recombinant or fragment EGF used in cosmetics as sh-oligopeptide-1. Topical cosmetic; injectable EGF is a different, unapproved proposition.

Mechanism: Human epidermal growth factor is a 53-amino-acid protein …

Half-life: Topical; systemic PK not applicable

MW: ≈6.2 kDa (protein growth factor)

Fat LossMuscle/RecoveryGLP-1/Metabolic

Fat Loss • ERR agonist / small molecule research • Experimental

Pan-estrogen-related-receptor agonist studied as an exercise mimetic in mice (2023). Not a peptide and not FDA-approved.

Mechanism: SLU-PP-332 is a synthetic pan-agonist of the estrogen-rel…

Half-life: Not established

MW: 467.5 g/mol

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LongevityExperimental

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

Fat LossGLP-1/MetabolicExperimental

Fat Loss • Khavinson bioregulator / research • Experimental

Peptide preparation derived from pancreatic tissue and marketed as a pancreatic bioregulator in the Khavinson tradition. Not FDA-approved for any indication, and no controlled human efficacy trials have been published; the available literature is class-level work on short peptide bioregulators rather than studies of this specific preparation.

Mechanism: Suprefort is a peptide preparation derived from pancreati…

Half-life: Not established (small tripeptide)

MW: 391.39 g/mol

NEW
LongevityExperimental

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 controlled human efficacy trials of this specific preparation have been published; the available literature is class-level work on short peptide bioregulators.

Mechanism: The Khavinson bioregulator hypothesis holds that short pe…

Muscle/RecoveryExperimental

Muscle/Recovery • Thymosin β4 fragment / research • Experimental

Usually sold as an acetylated thymosin-β4 actin-binding fragment (LKKTETQ), not full-length Tβ4. Not FDA-approved. Related to prohibited thymosin-β4 use in sport.

Mechanism: TB-500 is a synthetic peptide corresponding to the actin-…

Half-life: Hours; not well defined for research fragments

MW: ~889 Da (heptapeptide fragment forms vary)

Experimental

Experimental • Khavinson endocrine bioregulator / research • Experimental

Short peptide sold as a testicular/endocrine bioregulator. Not FDA-approved; not a testosterone secretagogue with modern RCT evidence.

Mechanism: Testagen is Lys-Glu-Asp-Gly, a synthetic tetrapeptide in …

Half-life: Not established (limited public PK data; primarily research context)

MW: 447.44 g/mol

Experimental

Experimental • Khavinson bioregulator / research • Experimental

Peptide preparation derived from testicular tissue and sold as a male endocrine bioregulator in the Khavinson tradition. It is a complex of low-molecular-weight peptides rather than a single defined molecule, and is distinct from Testagen, the synthetic tetrapeptide associated with the same tissue. It is not a treatment for hypogonadism or a substitute for testosterone therapy, and it is not FDA-approved.

Mechanism: Testoluten is a peptide preparation derived from testicul…

Half-life: Not established

MW: 319.27 g/mol

Experimental

Experimental • Thymic polypeptide extract / research • Experimental

Thymus-derived polypeptide preparation used in some countries as an immunomodulator. Not FDA-approved; composition is an extract, not a single sequence.

Mechanism: Thymalin is a preparation of low-molecular-weight peptide…

Half-life: Not established (polypeptide complex)

MW: Mixture

Experimental

Experimental • Thymic dipeptide / research • Experimental

Glu-Trp, a synthetic dipeptide identified as the active fragment of thymopoietin and also known as oglufanide. Despite its very small size it has been studied as an immunomodulator affecting T-cell differentiation and innate immune function, and is used in some CIS markets for that purpose. Its plasma half-life is measured in minutes, which constrains how it can be given. Not FDA-approved.

Mechanism: Thymogen is Glu-Trp, a synthetic dipeptide identified as …

Half-life: Not firmly established (small dipeptide)

MW: 333.34 g/mol

Experimental

Experimental • Thymic peptide / research • Experimental

Vendor thymic-immune peptide listing; identity may overlap thymulin/thymogen/thymalin depending on supplier. Not FDA-approved.

Mechanism: Thymolin is marketed as a thymic immunomodulator, but the…

Half-life: Not established

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Experimental

Experimental • Thymopoietin fragment / research • Experimental

Synthetic pentapeptide corresponding to residues 32 to 36 of thymopoietin, the fragment that carries its immunologically active sequence. Used in some countries as an immunomodulator; not FDA-approved.

Mechanism: Thymopentin reproduces the active site of thymopoietin, a…

MW: 679.8 g/mol

Experimental

Experimental • Thymic peptide / approved outside US • Experimental

28-aa thymic peptide (thymalfasin). Approved in several countries (Zadaxin) for hepatitis B and as an immune adjuvant; not FDA-approved in the US.

Mechanism: Thymosin alpha-1 is a 28-amino-acid acetylated peptide cl…

Half-life: ~2 hours

MW: 3108.3 g/mol

Muscle/RecoveryCosmeticExperimental

Muscle/Recovery • Actin-sequestering peptide / research • Experimental

43-aa G-actin-sequestering peptide studied for wound healing and cardiac repair (timbetasin programs). Not FDA-approved. Distinct from the shorter TB-500 fragment.

Mechanism: Thymosin beta-4 is a 43-amino-acid peptide and the princi…

Half-life: Not well established in humans

MW: ≈4963 g/mol

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Experimental

Experimental • Thymic nonapeptide / research • Experimental

Zinc-dependent thymic nonapeptide, also called facteur thymique serique, secreted by thymic epithelial cells. It is biologically inactive until zinc binds and fixes it in the active conformation, so its activity tracks zinc status as well as peptide concentration. It has been studied for T-cell differentiation and, separately, for anti-inflammatory and antinociceptive effects in animal models. Circulating levels fall with age as the thymus involutes. Not FDA-approved as a drug.

Mechanism: Thymulin is a nonapeptide secreted by thymic epithelial c…

MW: 858.9 g/mol

NEW
Experimental

Experimental • Khavinson peptide bioregulator / research • Experimental

Peptide preparation derived from thyroid tissue and marketed as a tissue-specific bioregulator in the Khavinson tradition. Not FDA-approved for any indication. No controlled human efficacy trials of this specific preparation have been published; the available literature is class-level work on short peptide bioregulators.

Mechanism: The Khavinson bioregulator hypothesis holds that short pe…

NEW
CosmeticExperimental

Cosmetic • Cosmetic firming peptide • Experimental

Fluorinated tripeptide marketed in topical firming products, sold commercially under the Progeline name. Regulated as a cosmetic ingredient; not FDA-approved as a drug.

Mechanism: Supplier research describes inhibition of progerin, a tru…

MW: 475.5 g/mol

NEW
Experimental

Experimental • Endogenous immunostimulatory tetrapeptide • Experimental

Naturally occurring tetrapeptide derived from the Fc region of immunoglobulin G, studied for effects on phagocytes. It is the structural parent of Selank. Not FDA-approved.

Mechanism: Tuftsin is released by enzymatic cleavage of the IgG heav…

MW: 500.6 g/mol

Fat LossGLP-1/MetabolicExperimental

Fat Loss • Endogenous neuropeptide / research • Experimental

28-aa neuropeptide vasodilator and VPAC agonist. Aviptadil (synthetic VIP) has been studied in pulmonary settings but VIP itself is not an FDA-approved general-use drug.

Mechanism: Vasoactive intestinal peptide is a 28-amino-acid neuropep…

Half-life: Not established (rapid enzymatic degradation; route dependent)

MW: 3325.8 g/mol

Muscle/RecoveryExperimental

Muscle/Recovery • Khavinson vascular bioregulator / research • Experimental

Peptide preparation derived from vascular tissue and sold as a cardiovascular bioregulator in the Khavinson tradition. It is a mixture of low-molecular-weight peptides rather than a single characterised compound, and is distinct from Vesugen, the synthetic tripeptide associated with the same tissue. Supporting evidence is historical, regional and uncontrolled, and it is not FDA-approved.

Mechanism: Ventfort is a peptide preparation derived from vascular t…

Half-life: Not established in humans

MW: 405.36 g/mol

Muscle/RecoveryExperimental

Muscle/Recovery • Khavinson vascular tripeptide / research • Experimental

Lys-Glu-Asp, a synthetic tripeptide in the Khavinson bioregulator series associated with vascular tissue and endothelial function. It is distinct from Ventfort, the tissue extract marketed for the same purpose. The proposed activity rests on cell-culture and cytogenetic work from one research group published mainly in Russian, without independent replication or controlled human evidence. Not FDA-approved.

Mechanism: Vesugen is Lys-Glu-Asp, a synthetic tripeptide in the Kha…

Half-life: Not established (limited public PK data; primarily research context)

MW: ≈390.4 g/mol

LongevityExperimental

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

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Experimental

Experimental • Khavinson peptide bioregulator / research • Experimental

Peptide preparation derived from thymus tissue and marketed as a tissue-specific bioregulator in the Khavinson tradition. Not FDA-approved for any indication. No controlled human efficacy trials of this specific preparation have been published; the available literature is class-level work on short peptide bioregulators.

Mechanism: The Khavinson bioregulator hypothesis holds that short pe…

NEW
Muscle/RecoveryExperimental

Muscle/Recovery • Regenerative blend • Experimental

Common shop blend of BPC-157 plus TB-500. Not a single API. Both components are unapproved and WADA-relevant (BPC-157 is S0; TB-500/Tβ4 is prohibited-class).

Mechanism: The Wolverine stack is a compounded combination of BPC-15…

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LongevityExperimental

Longevity • Khavinson peptide bioregulator / research • Experimental

Peptide preparation derived from female reproductive tissue tissue and marketed as a tissue-specific bioregulator in the Khavinson tradition. Not FDA-approved for any indication. No controlled human efficacy trials of this specific preparation have been published; the available literature is class-level work on short peptide bioregulators.

Mechanism: The Khavinson bioregulator hypothesis holds that short pe…

NEW
CosmeticExperimental

Cosmetic • Zinc-bound thymic nonapeptide / research • Experimental

Zinc-complexed form of thymulin, the thymic nonapeptide that requires bound zinc for biological activity. Investigated for immune modulation and, topically, for hair growth. Not FDA-approved.

Mechanism: Thymulin is biologically inactive without a bound zinc io…