Compound Library

A long-acting growth hormone releasing hormone (GHRH) analog that stimulates sustained, pulsatile GH release from the pituitary gland.

A highly selective growth hormone secretagogue that stimulates GH release without significantly affecting cortisol, prolactin, or appetite.

A bioidentical GHRH analog representing the first 29 amino acids of natural GHRH, providing the most physiologically natural approach to GH stimulation.

An orally active, non-peptide growth hormone secretagogue that mimics ghrelin signaling to produce sustained elevations in GH and IGF-1.

An FDA-approved GHRH analog specifically indicated for reducing visceral adipose tissue, with potent effects on body composition.

One of the most potent GH-releasing peptides available, with unique cardioprotective properties that distinguish it from other secretagogues.

A modified, long-acting form of IGF-1 with 3x the potency of natural IGF-1, capable of promoting muscle hyperplasia and enhanced nutrient partitioning.

The master hormone for growth, repair, and regeneration — FDA-approved for growth hormone deficiency, with extensive research supporting its role in body composition, recovery, and anti-aging.

A 15-amino-acid peptide derived from human gastric juice that demonstrates remarkable healing properties across virtually every tissue type studied.

A synthetic version of the naturally occurring 43-amino-acid peptide Thymosin Beta-4, essential for tissue repair, cell migration, and reducing inflammation.

A naturally occurring copper-binding tripeptide that activates over 4,000 genes, promoting tissue remodeling, anti-aging, and regeneration at the genetic level.

A tripeptide fragment of alpha-melanocyte stimulating hormone (α-MSH) with potent anti-inflammatory and antimicrobial properties, especially for gut health.

A non-erythropoietic EPO-derived peptide that activates the innate repair receptor, providing tissue-protective and anti-inflammatory effects without blood thickening.

An FDA-approved GLP-1 receptor agonist that has revolutionized weight management, producing average weight loss of 15-17% of body weight in clinical trials.

A first-in-class dual GIP/GLP-1 receptor agonist that has demonstrated the most potent weight loss results of any pharmaceutical agent, averaging 20-26% body weight reduction.

A modified fragment of human growth hormone (amino acids 176-191) that retains the fat-burning properties of HGH without its growth-promoting or diabetogenic effects.

A mitochondrial-derived peptide that acts as an exercise mimetic, improving metabolic homeostasis, insulin sensitivity, and reducing age-related metabolic decline.

A first-in-class triple incretin receptor agonist (GLP-1/GIP/Glucagon) demonstrating up to 24% weight loss in clinical trials — the most effective anti-obesity compound tested to date.

A mitochondrial protonophore uncoupler that dissipates the proton gradient to burn calories as heat, promoting fat loss without affecting body temperature or food intake.

A long-acting amylin analog that reduces appetite and enhances satiety, being developed in combination with semaglutide (CagriSema) for unprecedented weight loss.

A selective thyroid hormone receptor beta agonist that enhances metabolic rate and fat oxidation without the cardiac side effects of traditional thyroid hormones.

A dual GLP-1/glucagon receptor agonist demonstrating significant weight loss and metabolic improvements, with a unique glucagon component for enhanced energy expenditure.

A dual GLP-1/glucagon receptor agonist showing remarkable liver fat reduction and weight loss, particularly promising for MASH/NASH treatment.

A triple monoamine reuptake inhibitor that reduces appetite and increases metabolic rate by enhancing dopamine, norepinephrine, and serotonin signaling.

A synthetic heptapeptide analog of ACTH(4-10) that enhances cognitive function, memory, and neuroprotection through BDNF upregulation.

A synthetic analog of the immunomodulatory peptide tuftsin, providing anxiolytic and nootropic effects without sedation, addiction potential, or cognitive impairment.

An extraordinarily potent nootropic peptide reported to be 10 million times more potent than BDNF at forming new neural connections.

A novel nootropic beta-carboline compound that enhances dopaminergic neurotransmission, promotes neurogenesis, and protects against neurotoxicity.

A short bioregulatory peptide (EDR) that supports pineal gland function, melatonin synthesis, circadian rhythm regulation, and neuroprotection.

A naturally occurring nonapeptide that promotes delta wave (deep) sleep, modulates stress hormones, and normalizes disrupted sleep patterns.

A synthetic tetrapeptide that activates telomerase, the enzyme responsible for maintaining telomere length — a key biomarker of biological aging.

An FDA-approved melanocortin receptor agonist that treats sexual dysfunction by acting on the central nervous system rather than the vascular system.

The master regulator of the reproductive hormone axis that stimulates GnRH release, supporting natural testosterone/estrogen production and sexual function.

A naturally occurring thymic peptide that enhances immune function by activating dendritic cells and T-lymphocytes, approved in over 35 countries.

The only human cathelicidin antimicrobial peptide, providing broad-spectrum defense against bacteria, viruses, and fungi while modulating immune responses.

A neuropeptide with potent anti-inflammatory, immune-modulating, and vasodilatory properties, studied for CIRS, pulmonary conditions, and autoimmune disorders.

The primary male sex hormone and anabolic steroid, essential for muscle mass, bone density, libido, mood, and overall vitality in both men and women.

The primary female sex hormone critical for reproductive health, bone density, cardiovascular protection, brain function, and skin health in women — and important for men's health at optimal levels.

A critical neurosteroid and reproductive hormone that supports sleep, mood, neuroprotection, bone health, and is essential for balancing estrogen in HRT protocols.

The most abundant circulating steroid hormone and a precursor to both testosterone and estrogen, declining significantly with age and linked to immune function, mood, and longevity.

The master precursor steroid hormone from which all other steroid hormones are derived, with direct neurosteroid properties supporting memory, mood, and cognitive function.

A glycoprotein hormone that mimics LH to maintain testicular function, fertility, and intratesticular testosterone production during TRT.

Thyroid hormones that regulate metabolic rate, energy production, body temperature, cognitive function, and virtually every organ system in the body.

A 19-nortestosterone derivative used therapeutically for joint health, collagen synthesis, and lean tissue preservation — one of the most studied anabolic compounds in clinical medicine.

One of the mildest anabolic steroids with a strong safety profile, valued in longevity protocols for lean tissue preservation, immune support, and minimal side effects.

A DHT-derived anabolic with anti-estrogenic properties, used in wellness protocols for estrogen management, body composition, and mood enhancement alongside TRT.

A long-acting PDE5 inhibitor originally developed for erectile dysfunction, now widely used for cardiovascular health, blood flow optimization, prostate health, and exercise performance.

A mild oral anabolic steroid with a high anabolic-to-androgenic ratio, used medically for muscle wasting and increasingly studied for its effects on body composition and recovery.

A selective estrogen receptor modulator (SERM) that stimulates endogenous testosterone production while preserving fertility, used as an alternative to TRT.

A potent aromatase inhibitor that reduces estrogen conversion from testosterone, used to manage estradiol levels during TRT and hormone optimization.

The world's most prescribed diabetes medication, now studied as a potential anti-aging drug through AMPK activation, mTOR inhibition, and mitochondrial effects.

The only compound proven to extend lifespan in every organism tested, from yeast to mammals, through inhibition of the mTOR pathway — the master regulator of cellular aging.

NAD+ precursors that restore declining cellular energy levels, activate sirtuins and PARPs, and support DNA repair — central to the biology of aging.

A polyphenol compound found in red wine and grapes that activates SIRT1, enhances mitochondrial function, and provides cardiovascular and neuroprotective benefits.

A mitochondria-targeted tetrapeptide that restores cellular energy production by stabilizing cardiolipin, reversing age-related mitochondrial dysfunction within hours.

An anti-inflammatory and antioxidant compound studied for its potential to modulate aging pathways, reduce chronic inflammation, and support cellular health.

A senolytic peptide that selectively induces apoptosis in senescent cells by disrupting the FOXO4-p53 interaction, effectively clearing 'zombie cells' that drive aging.

A century-old pharmaceutical with remarkable mitochondrial-enhancing and neuroprotective properties, acting as an alternative electron carrier in the mitochondrial ETC.

Direct injectable form of NAD+ that bypasses oral bioavailability limitations, rapidly restoring cellular NAD+ levels to support mitochondrial function, DNA repair, and sirtuin activation.

A small molecule NNMT inhibitor that boosts cellular energy metabolism, promotes fat loss, and may reverse diet-induced obesity by restoring NAD+ levels.

A highly bioavailable choline source that crosses the blood-brain barrier, supporting acetylcholine synthesis, cognitive function, and growth hormone release.

Injectable vitamin B12 provides superior bioavailability for energy production, methylation support, neurological function, and red blood cell formation.

A naturally occurring nootropic that provides both choline and cytidine for acetylcholine synthesis, neuroprotection, and enhanced phospholipid membrane repair.

Injectable Coenzyme Q10 delivers this essential mitochondrial electron carrier directly to tissues, supporting cellular energy production and providing potent antioxidant protection.

A 70mg compounded peptide blend containing 50mg GHK-Cu, 10mg BPC-157, and 10mg TB-4 — designed for tissue repair, skin rejuvenation, and accelerated healing.

The body's master antioxidant — a tripeptide essential for detoxification, immune function, and protection against oxidative stress, delivered via injection for maximum bioavailability.

An 80mg compounded peptide blend containing 50mg GHK-Cu, 10mg BPC-157, 10mg Thymosin Beta-4, and 10mg KPV — designed for tissue repair, skin rejuvenation, gut healing, and anti-inflammatory support.

An amino acid derivative essential for transporting fatty acids into mitochondria for energy production, supporting fat metabolism, exercise performance, and cognitive function.

A lipotropic injection blend containing methionine, inositol, choline, and B vitamins that supports liver function, fat metabolism, and energy production.

A compounded blend combining NAD+ precursors with L-Carnitine and amino acids for comprehensive mitochondrial support, energy production, and exercise performance.

A methyl donor essential for homocysteine metabolism, increasingly used alongside NAD+ precursors to prevent methyl group depletion and support cardiovascular and liver health.

A water-soluble bile acid with potent liver-protective, neuroprotective, and anti-apoptotic properties — essential support for protocols involving hepatotoxic compounds.

An AMPK activator known as an 'exercise mimetic' that triggers the same metabolic pathways as endurance exercise, enhancing fat oxidation and glucose uptake.

A PPARdelta agonist that dramatically enhances endurance, fat oxidation, and metabolic efficiency by reprogramming muscle fibers to preferentially burn fat.

A naturally occurring glycoprotein that inhibits myostatin and activin, removing the genetic brake on muscle growth and enabling enhanced muscle development.

A synthetic allosteric effector of hemoglobin that enhances oxygen delivery to tissues, improving endurance, recovery, and potentially combating tumor hypoxia.

A PEGylated form of Mechano Growth Factor that promotes muscle repair and growth by activating satellite cells, with extended half-life for sustained anabolic signaling.

A novel ERR (estrogen-related receptor) agonist that mimics the molecular effects of exercise, enhancing endurance, fat oxidation, and muscle fiber type switching.

A steroidal SARM that acts as both an androgen receptor partial agonist and a myostatin inhibitor, providing a dual mechanism for muscle growth.

The most potent anabolic-androgenic steroid available, with powerful effects on body composition and nutrient partitioning — carries significant health risks and requires careful consideration.

A DHT-derived anabolic steroid with unique collagen synthesis and joint-related properties, used in some therapeutic protocols for hereditary angioedema and connective tissue conditions.

A testosterone derivative with enhanced anabolic properties and strong effects on red blood cell production, collagen synthesis, and appetite — originally developed for veterinary use.

An FDA-approved synthetic melanocortin analog that stimulates melanin production for UV-independent tanning and photoprotection in certain skin conditions.

A non-selective melanocortin agonist that produces rapid tanning, appetite suppression, and enhanced sexual function through activation of multiple MC receptors.