Peptide Protocol Library

Growth hormone releasing hormone (GHRH) analog with Drug Affinity Complex (DAC) that extends half-life to ~8 days. Stimulates pituitary to release GH in a pulsatile fashion.

GHRH analog without DAC. Shorter half-life (~30 min) creates more natural pulsatile GH release.

Selective ghrelin receptor agonist (GH secretagogue). Stimulates GH release from pituitary without significantly affecting cortisol, ACTH, or prolactin.

Synthetic GHRH analog. FDA-approved for HIV-associated lipodystrophy. Potent stimulator of endogenous GH production.

Oral ghrelin mimetic. Stimulates GH secretion via ghrelin receptor. Long-acting (24h half-life).

Synthetic hexapeptide GHRP. Acts on ghrelin receptor to stimulate GH release. More potent GH release than GHRP-6 but also increases cortisol and prolactin.

Potent growth hormone releasing peptide (GHRP) that binds ghrelin receptors to stimulate GH release. Stronger GH release than GHRP-2 but with more cortisol and prolactin elevation.

First-generation GHRP that stimulates ghrelin receptors to release growth hormone. Also strongly stimulates appetite via ghrelin pathway activation.

Bioidentical GHRH analog consisting of the first 29 amino acids of endogenous GHRH. Stimulates natural pulsatile GH release from the pituitary without suppressing endogenous production.

Modified IGF-1 with extended half-life (20-30 hours vs 15 minutes for native IGF-1). Binds IGF-1 receptors with reduced affinity for IGF binding proteins, resulting in higher bioavailability and potent anabolic effects.

Activin-binding glycoprotein that neutralizes myostatin, the primary negative regulator of muscle growth. By blocking myostatin, allows enhanced muscle hypertrophy and reduces adipose tissue.

PEGylated form of Mechano Growth Factor, a splice variant of IGF-1 produced in response to mechanical loading. PEGylation extends half-life. Activates satellite cells for muscle repair and hypertrophy.

Gastric pentadecapeptide that promotes angiogenesis, upregulates growth factor receptors (VEGF, FGF), modulates nitric oxide system, and promotes tendon and ligament healing. Cytoprotective for GI mucosa.

Synthetic fragment of Thymosin Beta-4. Promotes cell migration, angiogenesis, and reduces inflammation. Upregulates actin to promote cell motility for wound healing.

Naturally occurring copper-binding tripeptide. Activates wound healing, stimulates collagen and elastin synthesis, promotes stem cell activity, and has broad anti-aging gene expression effects.

Semi-synthetic heparinoid with anti-inflammatory and cartilage-protective properties. Stimulates proteoglycan synthesis in cartilage and inhibits complement activation.

Tetrapeptide fragment of Thymosin Beta-4 with potent anti-fibrotic and anti-inflammatory properties. Inhibits TGF-beta signaling, reduces fibrosis, and promotes angiogenesis without full TB-500 immune effects.

GLP-1 receptor agonist. Mimics incretin hormone to reduce appetite, slow gastric emptying, and improve insulin sensitivity. Acts on hypothalamic appetite centers.

Dual GIP/GLP-1 receptor agonist. Combines two incretin pathways for enhanced metabolic effects. Superior weight loss and glycemic control vs GLP-1 alone.

Modified fragment of human growth hormone (amino acids 177-191). Mimics fat-burning action of GH without affecting blood sugar or growth.

NNMT (nicotinamide N-methyltransferase) inhibitor. Blocks enzyme that contributes to fat storage and metabolic dysfunction. Increases NAD+ levels in fat cells.

Triple agonist targeting GLP-1, GIP, and glucagon receptors simultaneously. Provides superior weight loss through appetite reduction, increased energy expenditure, and improved glucose metabolism.

Mitochondria-derived peptide that activates AMPK pathway, enhances glucose uptake, improves insulin sensitivity, and promotes fatty acid oxidation. Acts as an exercise mimetic.

Fixed-ratio combination of cagrilintide (amylin analog) and semaglutide (GLP-1 agonist). Dual mechanism targets appetite, satiety, and gastric emptying through complementary pathways.

Melanocortin receptor agonist (MC3R/MC4R). Acts on central nervous system to increase sexual arousal and desire. Unlike PDE5 inhibitors, works on desire rather than mechanics.

Neuropeptide that stimulates GnRH release from hypothalamus. Key regulator of reproductive hormone axis. Increases LH and FSH.

Neuropeptide hormone that facilitates social bonding, trust, and sexual arousal. Enhances orgasm intensity and reduces refractory period. Also has anxiolytic and stress-reducing effects.

Non-selective melanocortin receptor agonist that stimulates melanogenesis (skin tanning) and activates MC4R in the brain to increase sexual arousal and libido. Also reduces appetite.

Synthetic analog of tuftsin (immunomodulatory peptide). Modulates GABA, serotonin, dopamine, and norepinephrine. Anxiolytic without sedation. Increases BDNF.

Synthetic analog of ACTH(4-10). Neuroprotective peptide that increases BDNF, NGF, and modulates dopamine/serotonin. Enhances attention and memory formation.

Angiotensin IV analog. Activates hepatocyte growth factor (HGF) system. Promotes synaptogenesis and neuronal connectivity. ~10 million times more potent than BDNF at forming new synapses.

Endogenous neuropeptide that promotes delta wave sleep. Modulates cortisol and has stress-protective effects. Normalizes sleep architecture.

TREK-1 potassium channel blocker. Produces rapid antidepressant effects similar to mechanism of action proposed for some novel antidepressants.

Complex of low-molecular-weight neuropeptides derived from cerebral cortex. Provides neurotrophic support, enhances neuronal metabolism, and improves cognitive function through GABAergic and glutamatergic modulation.

Benzylpiperazine-aminopyridine compound that stimulates neurogenesis in the hippocampus. Increases hippocampal volume and enhances synaptic plasticity, potentially reversing depression-related brain atrophy.

Small molecule derivative of ciliary neurotrophic factor (CNTF). Enhances neurogenesis and inhibits tau hyperphosphorylation by increasing BDNF and inhibiting leukemia inhibitory factor (LIF) signaling.

Thymic peptide hormone that enhances T-cell maturation, dendritic cell function, and immune surveillance. Modulates both innate and adaptive immunity.

Synthetic tetrapeptide based on epithalamin (pineal gland extract). Activates telomerase, promoting telomere elongation. Regulates melatonin production and circadian rhythm.

Human cathelicidin antimicrobial peptide. Part of innate immune system. Directly kills bacteria, fungi, and viruses. Also modulates inflammation and promotes wound healing.

C-terminal tripeptide of alpha-MSH. Potent anti-inflammatory effects via NF-kB pathway inhibition. Modulates gut inflammation.

Polypeptide complex extracted from calf thymus. Restores thymic function, modulates T-cell immunity, and has demonstrated anti-aging effects through immune system rejuvenation.

Mitochondria-targeted peptide that binds cardiolipin in the inner mitochondrial membrane. Stabilizes cristae structure, improves electron transport chain efficiency, and reduces reactive oxygen species.

Senolytic peptide that disrupts the FOXO4-p53 interaction in senescent cells. Forces senescent cells to undergo apoptosis while sparing healthy cells, effectively clearing "zombie cells" from tissues.

Mitochondria-derived peptide that protects cells from apoptosis and oxidative stress. Activates STAT3 and ERK signaling, improves insulin sensitivity, and has potent cytoprotective effects on neurons and cardiomyocytes.

Pharmaceutical-grade Thymosin Alpha-1. Enhances dendritic cell maturation, T-cell differentiation, and NK cell activity. Modulates immune response without immunosuppression — upregulates when needed, calms when overactive.

Direct precursor to NAD+ (nicotinamide adenine dinucleotide). Rapidly converted to NAD+ via the salvage pathway, restoring cellular energy metabolism, DNA repair, sirtuin activation, and mitochondrial function that decline with age.

Direct intravenous infusion of NAD+ bypasses oral absorption limitations, rapidly elevating cellular NAD+ levels. Supports mitochondrial function, DNA repair, sirtuin activation, and cellular energy production.

Tripeptide-copper complex that stimulates hair follicle growth by increasing follicle size and prolonging anagen phase. Also promotes wound healing and collagen synthesis through copper-dependent enzyme activation.

Signal peptide that mimics collagen breakdown products (matrikines). Stimulates fibroblasts to produce collagen I, III, and IV, fibronectin, and glycosaminoglycans in the skin matrix.

Biotin-conjugated peptide that strengthens hair follicle anchoring in the dermal papilla. Reduces follicle aging by improving metabolic activity and blood flow to hair follicles.

Synthetic GnRH (gonadotropin-releasing hormone). Stimulates pituitary to release LH and FSH. Used to maintain fertility during TRT.

Full-length kisspeptin that activates GPR54 receptors in the hypothalamus to stimulate GnRH release. Potent stimulator of the entire HPG axis including LH, FSH, and downstream sex hormones.

Selective estrogen receptor modulator (SERM) — the active trans-isomer of clomiphene. Blocks estrogen feedback at the hypothalamus/pituitary, increasing LH and FSH to boost endogenous testosterone production.

Potent non-steroidal aromatase inhibitor that blocks conversion of testosterone to estradiol. Used in HRT protocols to manage estrogen levels in men on testosterone therapy.