Peptide Guide
Research-backed profiles on 84 peptides. Mechanisms of action, dosing protocols, pricing, and the latest research — all in one place.
84 peptides
5-Amino-1MQ
5-Amino-1MQ is a small-molecule inhibitor of nicotinamide N-methyltransferase (NNMT), an enzyme strongly linked to obesity and metabolic dysfunction. By selectively blocking NNMT, it raises intracellular NAD+ levels and promotes fat cell shrinkage without suppressing appetite or stimulating the central nervous system. It has emerged as one of the most promising anti-obesity compounds in the peptide-adjacent research space, attracting attention for its unique non-stimulant mechanism of action.
Abaloparatide
Abaloparatide is a synthetic 34-amino-acid analog of parathyroid hormone-related protein (PTHrP) that potently stimulates new bone formation. FDA-approved in 2017 under the brand name Tymlos for the treatment of osteoporosis in postmenopausal women at high fracture risk, it represents a second-generation approach to anabolic bone therapy with advantages over teriparatide in certain clinical parameters.
ACE-031
ACE-031 is a recombinant fusion protein consisting of the extracellular domain of the activin receptor type IIB (ActRIIB) fused to a human IgG1 Fc domain. It functions as a soluble decoy receptor or 'myostatin trap,' intercepting myostatin and other TGF-β superfamily ligands before they can bind to muscle cells and inhibit growth. Originally developed by Acceleron Pharma for Duchenne muscular dystrophy, it produced remarkable muscle-building effects in early clinical trials before development was paused due to minor vascular side effects.
Adamax
Adamax is a modified derivative of Semax incorporating an adamantane moiety, designed for enhanced nootropic effects with improved blood-brain barrier penetration and extended half-life. It combines the neurotrophin-boosting properties of the ACTH(4-10) fragment with superior pharmacokinetic properties. Users in the nootropic community report improved focus, verbal fluency, mental clarity, and motivation, with effects often described as cleaner and more sustained than the parent compound Semax.
Adipotide (FTTP)
Adipotide (FTTP — Fat-Targeted Proapoptotic Peptide) is a peptidomimetic that selectively destroys the blood vessels feeding white adipose tissue, causing targeted fat cell death through vascular disruption. Originally developed at MD Anderson Cancer Center using cancer drug delivery technology repurposed for obesity, it produced dramatic fat loss in primate studies — 11% body weight reduction in 28 days. However, it carries significant renal risks and is considered one of the more aggressive fat loss compounds in the research peptide space.
AICAR
AICAR (5-aminoimidazole-4-carboxamide ribonucleoside, also known as Acadesine) is a potent AMP-activated protein kinase (AMPK) activator that mimics the metabolic effects of endurance exercise at the cellular level. Originally developed as a cardioprotective agent for coronary bypass surgery, it gained widespread attention after a landmark 2008 study showed it improved running endurance by 44% in sedentary mice. Banned by WADA in 2011, it remains one of the most studied exercise-mimetic compounds in metabolic research.
AOD-9604
AOD-9604 is a modified 16-amino-acid fragment of human growth hormone (corresponding to amino acids 176–191 of the hGH sequence) that retains the potent fat-metabolizing properties of growth hormone while completely lacking its growth-promoting, diabetogenic, and IGF-1-elevating effects. Developed at Monash University in Australia, it stimulates lipolysis and inhibits lipogenesis through a mechanism distinct from full-length GH, making it one of the most targeted and well-characterized anti-obesity peptides available. The Australian Therapeutic Goods Administration (TGA) has granted it GRAS (Generally Recognized as Safe) status for food use, and it has also shown promising cartilage-regenerative properties.
ARA-290
ARA-290 (cibinetide) is an 11-amino-acid synthetic peptide derived from the three-dimensional structure of erythropoietin (EPO) that selectively activates the innate repair receptor (IRR) without stimulating erythropoiesis or increasing red blood cell counts. It possesses potent anti-inflammatory, tissue-protective, and nerve-regenerative properties, with clinical trial data demonstrating benefits for small fiber neuropathy, sarcoidosis-associated neuropathy, and diabetic complications. It represents a paradigm shift in EPO-derived therapeutics — harnessing tissue protection without blood-thickening risks.
BAM-15
BAM-15 is a next-generation mitochondrial uncoupling agent that dissipates the proton gradient across the inner mitochondrial membrane, converting stored energy directly into heat rather than ATP. Unlike the notorious uncoupler DNP (2,4-dinitrophenol), BAM-15 selectively targets mitochondrial membranes without depolarizing the plasma membrane, providing a dramatically wider therapeutic window. In preclinical studies, it reduces body fat by up to 20%, improves insulin sensitivity, and reverses fatty liver disease — all without affecting food intake or lean mass.
BPC-157
BPC-157 (Body Protection Compound-157) is a 15-amino-acid peptide derived from a protective protein found in human gastric juice. It exhibits extraordinary healing properties across virtually every tissue type studied — tendons, ligaments, muscles, bone, gut lining, brain, liver, and blood vessels. With over 100 peer-reviewed preclinical studies demonstrating robust therapeutic effects, it is arguably the most widely used and most extensively researched peptide in the biohacking and regenerative medicine communities. Its remarkable ability to accelerate healing whether administered locally near an injury or systemically has earned it a reputation as the single most versatile healing compound available.
BPC-157 + TB-500 Blend
The BPC-157 + TB-500 blend, commonly known as the 'Wolverine Stack,' combines the two most potent healing peptides available into a single vial for convenience and synergistic effect. BPC-157 drives angiogenesis, growth factor upregulation, and NO system stabilization while TB-500 (Thymosin Beta-4) promotes cell migration through actin regulation and provides potent systemic anti-inflammatory effects. Together they address the structural, vascular, inflammatory, and cellular components of tissue injury — making this the gold standard healing protocol in the peptide community.
Bronchogen
Bronchogen is a Khavinson bioregulator tripeptide (Ala-Glu-Asp) that specifically targets bronchial and pulmonary epithelial tissue. Developed at the St. Petersburg Institute of Bioregulation and Gerontology under Professor Vladimir Khavinson, it is designed to normalize respiratory mucosa function, support healthy bronchial epithelial cell turnover, and restore mucociliary clearance that declines with aging or chronic respiratory conditions. It is part of the broader family of short bioregulatory peptides with over 30 years of clinical use in Russian gerontology.
Cagrilintide
Cagrilintide is a long-acting acylated amylin analog developed by Novo Nordisk that reduces appetite and food intake by activating amylin receptors in the brainstem — a satiety pathway distinct from and complementary to GLP-1 signaling. When combined with semaglutide in the CagriSema formulation, it has produced the most potent weight loss of any pharmaceutical combination studied in Phase III trials, achieving a mean 22.7% body weight reduction. As a standalone agent, cagrilintide produces meaningful weight loss that validates amylin as a major therapeutic target in obesity.
Cagri-Sema Blend
The CagriSema blend combines cagrilintide (a long-acting amylin analog) with semaglutide (a GLP-1 receptor agonist) in a single formulation, targeting two anatomically and mechanistically distinct satiety pathways for unprecedented weight loss efficacy. This dual-mechanism approach — brainstem amylin signaling plus hypothalamic GLP-1 signaling — produced the most potent weight loss results of any pharmaceutical combination in Phase III clinical trials, with a mean 22.7% body weight reduction at 68 weeks and nearly half of participants losing over 20% of their body weight.
Cardiogen
Cardiogen is a Khavinson bioregulator tetrapeptide (Ala-Glu-Asp-Arg) that specifically targets cardiac muscle tissue, promoting cardiomyocyte repair, contractile function optimization, and resistance to ischemic stress. Developed at the St. Petersburg Institute of Bioregulation and Gerontology, it has been used for over 30 years in Russian gerontological practice to support cardiovascular health in aging populations and those recovering from cardiac events.
Cartalax
Cartalax is a Khavinson bioregulator tripeptide (Ala-Glu-Asp) targeting cartilage tissue and the musculoskeletal system. It promotes chondrocyte function, cartilage matrix synthesis, and the balance between cartilage degradation and regeneration. Used in Russian gerontological protocols to maintain joint integrity and counter age-related cartilage degeneration, it represents the bioregulatory approach to joint health.
Chonluten
Chonluten is a bioregulatory tripeptide (Glu-Asp-Gly) developed at the Khavinson Institute that targets bronchial mucosa and gastrointestinal epithelium. It normalizes mucosal barrier function, supports secretory immune defenses, and maintains the epithelial integrity essential for both respiratory and digestive health. Its dual-tissue targeting makes it particularly relevant for aging individuals experiencing concurrent decline in both respiratory and GI mucosal function.
CJC-1295 (No DAC)
CJC-1295 without DAC, also known as Modified GRF(1-29) or Mod GRF, is a synthetic 29-amino-acid analog of growth hormone-releasing hormone (GHRH) that stimulates pulsatile growth hormone release from the anterior pituitary. It is the most widely used GHRH analog in peptide therapy, prized for producing physiological GH pulses that mimic the body's natural secretory pattern. Its shorter half-life (~30 minutes vs. 8 days for the DAC version) allows discrete GH pulses rather than sustained elevation, which many consider more physiological and safer for long-term use. Almost always paired with a GHRP — typically Ipamorelin — for dramatically amplified GH output.
CJC-1295 with DAC
CJC-1295 with DAC (Drug Affinity Complex) is a long-acting GHRH analog that uses a maleimidopropionic acid modification to covalently bind to circulating serum albumin after injection, extending its half-life to approximately 8 days. Unlike the no-DAC version which produces discrete GH pulses, CJC-1295 with DAC creates sustained, continuous GHRH receptor stimulation, resulting in chronically elevated GH and IGF-1 levels. This produces consistently high IGF-1 output with less frequent dosing (once or twice per week), but at the cost of natural pulsatility — a trade-off that divides the peptide community.
Cortagen
Cortagen is a Khavinson bioregulator peptide that targets cerebral cortex tissue, supporting cognitive function, neuroprotection, and cortical neuron health. Developed at the St. Petersburg Institute of Bioregulation and Gerontology, it modulates gene expression in cortical neurons to support memory, attention, and mental processing speed. It is used in Russian gerontological practice for age-related cognitive decline and as part of comprehensive brain health protocols.
Crystagen
Crystagen is a Khavinson bioregulator tripeptide (Thr-Glu-Asp) that targets the immune system, specifically T-cell function and thymic activity. It supports T-cell maturation, adaptive immune surveillance, and the thymic output that critically declines with age (thymic involution). Used in Russian anti-aging medicine to counteract immunosenescence, it helps maintain the immune competence that naturally erodes after age 40, leaving older adults increasingly vulnerable to infections, cancer, and autoimmune dysregulation.
DSIP (Delta Sleep-Inducing Peptide)
Delta Sleep-Inducing Peptide (DSIP) is a naturally occurring neuropeptide first isolated from rabbit brain in 1977. It plays a central role in modulating sleep architecture, particularly promoting delta-wave (slow-wave) sleep — the most restorative phase of the sleep cycle. DSIP also demonstrates stress-protective, analgesic, and neuroendocrine-regulatory properties. It is one of the most extensively studied sleep peptides and has been used clinically in Europe for insomnia and chronic pain syndromes.
Epitalon
Epitalon (Epithalon) is a synthetic tetrapeptide (Ala-Glu-Asp-Gly) based on the natural pineal gland peptide epithalamin, developed by Russian gerontologist Professor Vladimir Khavinson over three decades of research. It is the most extensively studied telomerase-activating peptide, shown to lengthen telomeres, restore melatonin production, and extend lifespan in multiple animal models. Epitalon occupies a unique position in anti-aging research as one of the few compounds with direct evidence of telomere elongation in human cell cultures.
FOXO4-DRI
FOXO4-DRI is a D-retro-inverso peptide that selectively induces apoptosis in senescent cells — making it a true senolytic agent. Developed by Peter de Keizer at Erasmus University Medical Center, it works by disrupting the interaction between FOXO4 and p53 that keeps senescent cells alive. In aged mice, it restored fitness, fur density, and renal function.
GHK-Cu
GHK-Cu (copper peptide, glycyl-L-histidyl-L-lysine:copper(II)) is a naturally occurring tripeptide-copper complex found in human plasma, saliva, and urine. Discovered by Dr. Loren Pickart in the 1970s, GHK-Cu declines dramatically with age — from ~200 ng/mL at age 20 to ~80 ng/mL by age 60. It is one of the most gene-modulating peptides known, influencing the expression of over 4,000 human genes — approximately 31% of the genome — with a broad shift toward regenerative, anti-inflammatory, and tissue-remodeling activity. GHK-Cu is studied for wound healing, skin rejuvenation, hair growth, bone repair, and systemic anti-aging.
GHRP-2
GHRP-2 (Growth Hormone Releasing Peptide-2, pralmorelin) is a synthetic hexapeptide that potently stimulates growth hormone release by activating the ghrelin receptor (GHS-R1a) in the anterior pituitary. It is one of the most potent GHRPs available, producing robust GH pulses comparable to GHRH stimulation tests. GHRP-2 also stimulates appetite, modulates cortisol and prolactin, and has demonstrated cytoprotective properties.
GHRP-6
GHRP-6 (Growth Hormone Releasing Peptide-6) is a synthetic hexapeptide and one of the original growth hormone secretagogues. It stimulates GH release via the ghrelin receptor and is known for producing the most pronounced hunger response among GHRPs. It also demonstrates gastroprotective and cardioprotective properties independent of GH release.
GLOW Blend
Glow Blend is a combination peptide product typically containing GHK-Cu and epithalon (or other skin-targeted peptides) designed for skin rejuvenation, anti-aging, and complexion improvement. The exact formulation varies by vendor but generally targets collagen production, antioxidant defense, and skin cell renewal in a single convenient preparation.
Glutathione
Glutathione (GSH) is a tripeptide (γ-glutamyl-cysteinyl-glycine) and the body's most abundant intracellular antioxidant. It plays critical roles in detoxification, immune function, and cellular redox balance. Injectable glutathione has become widely used for skin lightening, liver detoxification support, and systemic antioxidant therapy. Levels decline with age, illness, and environmental toxin exposure.
Gonadorelin Acetate
Gonadorelin is synthetic gonadotropin-releasing hormone (GnRH), identical to the naturally produced decapeptide from the hypothalamus. It stimulates the anterior pituitary to release luteinizing hormone (LH) and follicle-stimulating hormone (FSH). It is used clinically for fertility diagnostics and treatment, and in the peptide community for maintaining testicular function during testosterone replacement therapy (TRT) or anabolic steroid use.
Hexarelin
Hexarelin is a synthetic hexapeptide growth hormone secretagogue and one of the most potent GHRPs, producing the largest GH release of any peptide in its class. It acts through the ghrelin receptor and also exhibits significant cardioprotective properties independent of GH release. However, it is prone to desensitization with continuous use.
IGF-1 LR3
IGF-1 LR3 (Long R3 Insulin-like Growth Factor-1) is a modified version of IGF-1 with an arginine substitution at position 3 and a 13-amino-acid extension at the N-terminus. These modifications dramatically reduce binding to IGF-binding proteins (IGFBPs), increasing its bioavailability and half-life from ~15 minutes to 20–30 hours. It is the most potent anabolic peptide available for direct tissue growth.
Ipamorelin
Ipamorelin is a selective growth hormone secretagogue pentapeptide that stimulates GH release with remarkable specificity — it activates the ghrelin receptor without significantly affecting cortisol, prolactin, or appetite. This selectivity profile makes it the 'cleanest' GHRP and the most widely used growth hormone peptide for anti-aging, body composition, sleep enhancement, and recovery. Developed by Novo Nordisk in the 1990s, it has become the foundational GH peptide in clinical and self-directed protocols worldwide.
Ipamorelin/CJC-1295 Blend
The Ipamorelin/CJC-1295 blend combines two complementary GH-releasing peptides in a single vial: Ipamorelin (a GHRP acting on the ghrelin receptor) and CJC-1295 without DAC (a GHRH analog acting on the GHRH receptor). This combination is the gold standard for GH optimization, producing synergistic GH pulses 3–5 times greater than either peptide alone.
Ipamorelin/Tesamorelin Blend
The Ipamorelin/Tesamorelin blend combines Ipamorelin (GHRP) with Tesamorelin (a GHRH analog with FDA-approved status for visceral adiposity reduction). This blend is specifically popular for body composition optimization, particularly visceral fat reduction, leveraging the GHRH+GHRP synergy with Tesamorelin's demonstrated fat-targeting properties.
Kisspeptin-10
Kisspeptin-10 is a truncated bioactive fragment of the kisspeptin family of peptides, which are the master regulators of reproductive hormone release. It activates the KISS1R receptor on GnRH neurons in the hypothalamus, triggering a potent surge of gonadotropin-releasing hormone and downstream LH/FSH secretion. It is studied for fertility, hypogonadism, and sexual health applications.
KLOW Blend
KLOW Blend is a multi-peptide formulation typically containing KPV (anti-inflammatory tripeptide) and other complementary peptides targeting inflammation, gut health, and immune modulation. The exact composition varies by vendor but is generally designed for systemic inflammation reduction and mucosal healing.
KPV
KPV is a tripeptide (Lys-Pro-Val) derived from the C-terminal end of alpha-melanocyte-stimulating hormone (α-MSH), one of the body's most potent endogenous anti-inflammatory molecules. KPV retains the anti-inflammatory activity of the full α-MSH molecule while being small enough to penetrate tissues effectively and resist enzymatic degradation. It has demonstrated remarkable efficacy in inflammatory bowel disease models, skin inflammation, wound healing, and systemic inflammatory conditions. KPV is emerging as a cornerstone peptide for gut health protocols and chronic inflammation management.
L-Carnitine
L-Carnitine is a naturally occurring amino acid derivative essential for mitochondrial fatty acid transport. It shuttles long-chain fatty acids across the inner mitochondrial membrane for beta-oxidation — making it critical for fat metabolism and cellular energy production. Injectable L-Carnitine is used for enhanced fat burning, exercise performance, and metabolic support.
Livagen
Livagen is a synthetic tetrapeptide bioregulator (Lys-Glu-Asp-Ala) developed by Professor Khavinson's research group in Russia, designed to normalize liver function and hepatocyte gene expression. It belongs to the Khavinson bioregulator class of peptides that act on chromatin structure to restore youthful gene expression patterns in specific organ systems.
LL-37
LL-37 is the only human cathelicidin antimicrobial peptide — a 37-amino-acid peptide cleaved from the precursor protein hCAP-18 by proteinase 3 in neutrophils. It serves as a critical component of the innate immune system, providing broad-spectrum antimicrobial defense against bacteria, viruses, fungi, and biofilms. Beyond direct killing, LL-37 modulates immune cell recruitment, wound healing, angiogenesis, and inflammation resolution. It is expressed in neutrophils, macrophages, epithelial cells, and keratinocytes, and its deficiency is associated with recurrent infections, chronic wounds, and immune dysfunction. LL-37 is emerging as one of the most important peptides in immunology and infectious disease research.
Mazdutide
Mazdutide (LY3305677/IBI362) is a novel dual GLP-1/glucagon receptor agonist developed by Eli Lilly (licensed to Innovent Biologics for China). Unlike tirzepatide (which targets GLP-1/GIP), mazdutide adds glucagon receptor agonism to enhance energy expenditure and fat oxidation alongside appetite suppression. It represents the next frontier in metabolic peptide therapeutics.
Melanotan 1
Melanotan-1 (afamelanotide) is a synthetic analog of alpha-melanocyte-stimulating hormone (α-MSH) that stimulates melanogenesis, producing a protective tan without UV exposure. It is FDA-approved under the brand name Scenesse for the prevention of phototoxicity in adults with erythropoietic protoporphyria (EPP). Unlike Melanotan-2, it is highly selective for the MC1 receptor and does not produce significant sexual or appetite-related side effects.
Melanotan 2
Melanotan-2 (MT-2) is a synthetic cyclic peptide analog of alpha-melanocyte-stimulating hormone (α-MSH) that produces skin tanning, enhances sexual arousal, and suppresses appetite through broad melanocortin receptor activation. It is one of the most widely used research peptides globally, known for its potent multi-receptor activity across MC1R through MC5R. Unlike Melanotan-1, its non-selective binding profile produces a diverse range of physiological effects beyond melanogenesis.
Methylene Blue
Methylene blue is a synthetic phenothiazine dye that has been repurposed as a mitochondrial enhancer and neuroprotective agent. Originally used as a medical dye and antimalarial, it functions as an alternative electron carrier in the mitochondrial electron transport chain, enhancing cellular energy production and reducing oxidative stress. It is one of the oldest synthetic drugs in medicine, with a history dating back to 1876.
MOTS-c
MOTS-c (Mitochondrial Open Reading Frame of the 12S rRNA Type-c) is a mitochondrial-derived peptide that functions as a systemic exercise mimetic and metabolic regulator. Discovered in 2015 by Dr. Changhan David Lee's lab at USC, it is the first peptide shown to be encoded in the mitochondrial genome yet act on the nuclear genome, fundamentally challenging the traditional view of mitochondria as passive energy producers. MOTS-c activates AMPK, regulates metabolic homeostasis, and has demonstrated remarkable anti-aging and exercise-mimetic effects in both preclinical and early human studies.
N-Acetyl Semax Amidate
N-Acetyl Semax Amidate (NASA) is a modified form of Semax, a synthetic heptapeptide analog of ACTH(4-10), with enhanced stability and blood-brain barrier penetration. The N-acetyl and C-terminal amide modifications protect the peptide from enzymatic degradation, extending its half-life and nootropic potency. It is widely regarded as one of the most effective peptide nootropics for focus, memory, and neuroprotection.
NA-Epitalon
N-Acetyl Epitalon is a modified form of Epitalon (epithalon), a synthetic tetrapeptide (Ala-Glu-Asp-Gly) that activates telomerase and is studied for anti-aging properties. The N-acetyl modification enhances its bioavailability and resistance to enzymatic degradation compared to standard Epitalon. It was originally developed based on the work of Dr. Vladimir Khavinson on pineal gland peptide bioregulators.
NA-Selank Amidate
N-Acetyl Selank Amidate is an enhanced version of Selank, a synthetic heptapeptide analog of the naturally occurring immunomodulatory peptide tuftsin. The N-acetyl and amide modifications significantly improve its stability, half-life, and blood-brain barrier penetration. It is primarily used as an anxiolytic nootropic, providing calm focus without sedation, and has immunomodulatory properties that distinguish it from conventional anxiolytic drugs.
NAD+
NAD+ (nicotinamide adenine dinucleotide) is a critical coenzyme found in every living cell that plays essential roles in energy metabolism, DNA repair, gene expression regulation, and cellular signaling. NAD+ levels decline significantly with age — by age 60, levels are roughly half of what they were at age 20 — and this decline is implicated in numerous age-related diseases. Supplementation via IV infusion, subcutaneous injection, or precursors aims to restore youthful NAD+ levels and support cellular function.
Noopept
Noopept (N-phenylacetyl-L-prolylglycine ethyl ester, GVS-111) is a synthetic dipeptide-derived nootropic developed in Russia that is estimated to be 1,000 times more potent than piracetam by weight. It enhances memory, learning, and neuroprotection through BDNF and NGF upregulation, AMPA receptor modulation, and antioxidant effects. It is one of the most widely used and well-studied nootropic compounds globally.
O-304 (ATX-304)
O-304 is a novel small-molecule AMPK activator developed by Betagenon AB that directly activates AMPK by preventing its dephosphorylation. Unlike indirect AMPK activators, O-304 maintains AMPK in its active phosphorylated state, producing exercise-mimetic and glucose-lowering effects. It has completed Phase IIa clinical trials for type 2 diabetes with promising results.
Ovagen
Ovagen is a hepatoprotective bioregulator peptide (Lys-Glu-Asp) developed by the Khavinson laboratory in Russia. It is designed to support liver function and regeneration by regulating gene expression in hepatocytes. As a short peptide bioregulator, it works at the epigenetic level to restore normal protein synthesis patterns in aged or damaged liver tissue.
Oxytocin
Oxytocin is a naturally occurring neuropeptide produced in the hypothalamus and released by the posterior pituitary gland. Known as the 'bonding hormone,' it plays critical roles in social attachment, trust, empathy, and pair bonding. It also has well-established roles in labor induction, lactation, and stress regulation. Intranasal oxytocin is being actively researched for autism spectrum disorder, social anxiety, PTSD, and depression.
P21
P21 is a synthetic peptide derived from the active region of ciliary neurotrophic factor (CNTF) that promotes neurogenesis in the hippocampus. It was developed to capture CNTF's neurotrophic benefits while being small enough to cross the blood-brain barrier. P21 increases neurogenesis and synaptic plasticity without the appetite-suppressing and weight-loss effects of full-length CNTF.
Pancragen
Pancragen is a bioregulator peptide (Lys-Glu-Asp-Trp) developed by the Khavinson laboratory that targets pancreatic tissue. It is designed to support normal pancreatic function, including both exocrine (digestive enzyme) and endocrine (insulin/glucagon) activity. It works at the epigenetic level to normalize gene expression in aging or damaged pancreatic cells.
PE-22-28
PE-22-28 is a synthetic peptide derived from the spadin family that acts as a blocker of the TREK-1 potassium channel. TREK-1 inhibition produces rapid antidepressant and cognitive-enhancing effects, making PE-22-28 a novel nootropic with mood-elevating properties. It represents a fundamentally different approach to cognitive enhancement and mood regulation compared to traditional monoamine-targeting compounds.
PEG-MGF
PEG-MGF (PEGylated Mechano Growth Factor) is a PEGylated version of the MGF splice variant of IGF-1 (IGF-1Ec in humans). The addition of polyethylene glycol (PEG) extends its half-life from minutes to hours, enabling systemic administration. MGF is naturally produced in response to mechanical stress on muscle tissue and plays a critical role in activating satellite cells for muscle repair and growth.
Pinealon
Pinealon is a tripeptide bioregulator (Glu-Asp-Arg) developed by the Khavinson laboratory that targets brain tissue, particularly the pineal gland and central nervous system neurons. It is designed to normalize neuronal function, improve sleep quality through melatonin regulation, and provide neuroprotection in aging brain tissue. As a bioregulator, it works through epigenetic modulation of gene expression.
PNC-27
PNC-27 is a synthetic anticancer peptide consisting of an HDM-2 (MDM2) binding domain fused to a cell-penetrating peptide leader sequence. It selectively targets and kills cancer cells that overexpress HDM-2 on their surface while sparing normal cells. It represents a targeted approach to cancer-cell destruction based on exploiting the differential expression of MDM2 between cancerous and healthy tissue.
Prostamax
Prostamax is a bioregulator peptide complex developed by the Khavinson laboratory that targets prostate tissue. It is designed to normalize prostate gland function, reduce inflammation, and support healthy cell differentiation in aging prostate tissue. As a bioregulator, it works through epigenetic modulation of gene expression in prostatic cells.
PT-141
PT-141 (bremelanotide) is a synthetic melanocortin peptide and the only FDA-approved on-demand treatment for hypoactive sexual desire disorder (HSDD) in premenopausal women, marketed as Vyleesi. Originally derived from Melanotan-2 during clinical development, PT-141 was the first centrally-acting sexual dysfunction drug — it works in the brain rather than on peripheral blood flow, making it effective for desire-based dysfunction rather than purely mechanical arousal problems. It activates melanocortin-4 receptors (MC4R) in the hypothalamus to increase sexual desire and arousal in both men and women.
Retatrutide
Retatrutide (LY3437943) is a novel triple-agonist peptide developed by Eli Lilly that simultaneously activates GLP-1, GIP, and glucagon receptors — the first 'triagonist' in its class. In Phase II clinical trials, retatrutide produced unprecedented weight loss of up to 24.2% of body weight at 48 weeks, surpassing all existing anti-obesity medications including semaglutide and tirzepatide. It represents the cutting edge of incretin-based metabolic therapy and is currently in Phase III trials for obesity, type 2 diabetes, and metabolic dysfunction-associated steatohepatitis (MASH/NASH).
Retatrutide + Cagrilintide Blend
Reta-Cagri Blend combines retatrutide, a triple-agonist GLP-1/GIP/glucagon receptor peptide, with cagrilintide, a long-acting amylin analog. This combination targets multiple metabolic pathways simultaneously — appetite suppression, insulin sensitization, glucagon-mediated fat oxidation, and gastric emptying regulation. The blend represents a next-generation approach to obesity pharmacotherapy, leveraging synergistic mechanisms that individually have shown dramatic weight loss in clinical trials.
RU-58841
RU-58841 is a non-steroidal anti-androgen developed for topical treatment of androgenetic alopecia (male pattern baldness). It works by competitively binding to androgen receptors in the scalp, blocking the hair-miniaturizing effects of dihydrotestosterone (DHT) without systemic anti-androgenic effects. Though never brought to market, it remains one of the most discussed experimental hair loss treatments in the research community.
Selank
Selank is a synthetic analog of the naturally occurring immunomodulatory peptide tuftsin, developed at the Institute of Molecular Genetics of the Russian Academy of Sciences. It is approved in Russia as an anxiolytic and nootropic medication. Selank combines potent anti-anxiety effects with cognitive enhancement and immune modulation, making it one of the most versatile peptides in the research community. Unlike benzodiazepines, it produces anxiolysis without sedation, addiction potential, or cognitive impairment.
Semaglutide
Semaglutide is a GLP-1 receptor agonist that has revolutionized the treatment of type 2 diabetes and obesity. FDA-approved as Ozempic (injectable, diabetes), Wegovy (injectable, obesity), and Rybelsus (oral, diabetes), it is the most widely prescribed and clinically validated peptide for metabolic disease. Semaglutide produces unprecedented weight loss of 15–17% in clinical trials and has demonstrated cardiovascular, renal, and potentially neuroprotective benefits beyond glycemic control.
Sermorelin
Sermorelin is a synthetic analog of growth hormone-releasing hormone (GHRH) consisting of the first 29 amino acids of the native 44-amino acid GHRH sequence. It is the shortest fragment of GHRH that retains full biological activity at the pituitary. Sermorelin was FDA-approved for the diagnosis and treatment of growth hormone deficiency in children and has become one of the most widely used growth hormone secretagogues in anti-aging and peptide therapy. Unlike exogenous GH, sermorelin stimulates natural pulsatile GH release, preserving the body's feedback mechanisms.
SLU-PP-332
SLU-PP-332 is a small-molecule agonist of the estrogen-related receptor (ERR) family, particularly ERRα, ERRβ, and ERRγ. Dubbed an 'exercise mimetic,' it activates the same transcriptional programs induced by endurance exercise — mitochondrial biogenesis, fatty acid oxidation, and oxidative muscle fiber gene expression. In preclinical studies, it dramatically improved exercise endurance and fatigue resistance without physical training.
SNAP-8
SNAP-8 (Acetyl Octapeptide-3) is a cosmetic peptide that reduces the appearance of expression wrinkles by modulating neuromuscular junction signaling. It is a longer, more potent version of Argireline (Acetyl Hexapeptide-3) and works by partially inhibiting the SNARE complex responsible for vesicular neurotransmitter release. Often called 'topical Botox,' it offers a non-invasive approach to wrinkle reduction.
SS-31 (Elamipretide)
SS-31 (Elamipretide, Bendavia, MTP-131) is a mitochondria-targeted tetrapeptide that selectively concentrates in the inner mitochondrial membrane and restores bioenergetic function. It binds to cardiolipin, a phospholipid unique to mitochondria that is essential for electron transport chain efficiency. SS-31 represents a first-in-class approach to treating mitochondrial dysfunction, with clinical trials in heart failure, Barth syndrome, and age-related mitochondrial decline.
Survodutide
Survodutide (BI 456906) is a dual glucagon/GLP-1 receptor agonist developed by Boehringer Ingelheim. Unlike tirzepatide (GLP-1/GIP), survodutide pairs GLP-1 receptor agonism with glucagon receptor agonism, specifically targeting hepatic fat metabolism and energy expenditure. It has shown remarkable efficacy for both obesity and MASH (metabolic dysfunction-associated steatohepatitis), with Phase II data demonstrating up to 19% weight loss and dramatic liver fat reduction.
TB-500 (Thymosin Beta-4)
TB-500 is a synthetic version of the active region (amino acids 17-23) of Thymosin Beta-4, a 43-amino acid protein naturally produced in high concentrations by platelets, wound fluid, and most tissues in the body. It is one of the most widely used healing and recovery peptides, known for promoting tissue repair, reducing inflammation, and accelerating wound healing across multiple tissue types including muscle, tendon, ligament, skin, and cardiac tissue. TB-500 has gained enormous popularity in both the athletic and clinical research communities for its versatile regenerative properties.
Tesamorelin
Tesamorelin is a synthetic analog of human growth hormone-releasing hormone (GHRH) with a trans-3-hexenoic acid modification at the N-terminus that enhances receptor binding and enzymatic stability. It is FDA-approved (as Egrifta) for the reduction of excess abdominal fat in HIV-infected patients with lipodystrophy, making it one of the few peptides with specific FDA approval for a body composition indication. Tesamorelin is the most potent GHRH analog in clinical use and has shown remarkable specificity for visceral fat reduction.
Tesofensine
Tesofensine is a triple monoamine reuptake inhibitor (serotonin, norepinephrine, and dopamine) originally developed for Alzheimer's and Parkinson's disease that was repurposed for obesity treatment after clinical trials revealed dramatic weight loss as a side effect. It is one of the most potent appetite suppressants studied in clinical trials, with Phase II data showing over 10% weight loss — far exceeding other centrally-acting anti-obesity agents.
Testagen
Testagen is a synthetic bioregulator tetrapeptide (Asp-Glu-Asp-Leu) developed by the St. Petersburg Institute of Bioregulation and Gerontology under the leadership of Professor Vladimir Khavinson. It is classified as a testicular bioregulator, designed to support testicular function and normalize testosterone production through gene-level regulation rather than direct hormonal supplementation.
Thymogen
Thymogen (Glu-Trp) is a synthetic dipeptide bioregulator designed to mimic the immunomodulatory activity of thymic peptides. Developed at the Russian Institute of Bioregulation and Gerontology, it is used clinically in Russia as an immunostimulant for treating immunodeficiency states, chronic infections, and as an adjunct in post-surgical recovery. It represents the simplest active thymic peptide fragment.
Thymosin Alpha-1
Thymosin Alpha-1 (Tα1) is a 28-amino acid peptide naturally produced by the thymus gland that serves as a master regulator of immune function. It is one of the most clinically validated immunomodulatory peptides, approved in over 35 countries for the treatment of hepatitis B, hepatitis C, and as an immune adjuvant. Marketed as Zadaxin, it has been studied in over 90 clinical trials involving thousands of patients. Tα1 enhances both innate and adaptive immunity while maintaining immune homeostasis — stimulating underactive immune systems without over-activating already functional ones, a property that distinguishes it from crude immunostimulants.
Thymulin
Thymulin (facteur thymique serique, FTS) is a zinc-dependent nonapeptide hormone produced by thymic epithelial cells. It is the only thymic hormone that requires a metal cofactor (zinc) for biological activity. Thymulin plays a critical role in T-cell differentiation and maturation, and its levels decline dramatically with age as the thymus involutes — making it a target for immune reconstitution in aging.
Tirzepatide
Tirzepatide is a first-in-class dual GLP-1/GIP receptor agonist that has redefined the treatment landscape for type 2 diabetes and obesity. FDA-approved as Mounjaro (diabetes, 2022) and Zepbound (obesity, 2023), tirzepatide produces the most dramatic weight loss ever seen in a pharmaceutical — up to 22.5% in the SURMOUNT-1 trial. Its dual incretin mechanism activates both GLP-1 and GIP receptors, producing superior metabolic effects compared to GLP-1-only agonists like semaglutide. Tirzepatide has also shown groundbreaking results in obstructive sleep apnea, heart failure with preserved ejection fraction, and MASH.
Vesilute
Vesilute is a synthetic tripeptide bioregulator (Lys-Glu-Asp) from the Khavinson bioregulator family, designed to support vascular endothelial function and normalize blood vessel wall health. It targets the endothelial lining of blood vessels at the gene expression level, promoting vascular repair and homeostasis. It is used in Russian anti-aging medicine as part of comprehensive vascular health protocols.
Vesugen
Vesugen is a synthetic tripeptide bioregulator (Lys-Glu-Asp) developed by the Khavinson group targeting vascular tissue. It is classified as a vessel wall bioregulator peptide designed to support and normalize vascular function at the gene expression level. Used in Russian gerontological medicine, vesugen is part of comprehensive vascular health programs for age-related circulatory decline.
Vilon
Vilon (Lys-Glu) is the shortest bioregulator peptide in the Khavinson family — a dipeptide designed to support immune function and thymic activity. Despite its minimal size (just two amino acids), research suggests it can modulate gene expression in immune cells. It is used as a thymic bioregulator in Russian anti-aging and immunological protocols.
VIP (Vasoactive Intestinal Peptide)
Vasoactive Intestinal Peptide (VIP) is a 28-amino acid neuropeptide with broad physiological functions including vasodilation, immunomodulation, neuroprotection, and regulation of circadian rhythms. It is found throughout the central and peripheral nervous systems, the gastrointestinal tract, and the immune system. VIP has gained attention for its potential therapeutic applications in chronic inflammatory conditions, mast cell activation syndrome (MCAS), mold illness (CIRS), and neurodegenerative diseases.
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