5-Amino-1MQ
Preclinical ResearchA small molecule NNMT inhibitor researched for fat loss, metabolic improvement, and potential anti-aging effects at the cellular level.
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Showing 98 peptides
A small molecule NNMT inhibitor researched for fat loss, metabolic improvement, and potential anti-aging effects at the cellular level.
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A myostatin inhibitor targeting the activin type IIB receptor. Researched for muscle wasting diseases and potential muscle growth applications.
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A proapoptotic peptide that targets and destroys blood vessels feeding fat tissue. Researched for targeted fat loss with dramatic results in animal models.
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A copper-binding tripeptide (Ala-His-Lys) studied primarily in topical cosmetic research for hair follicle stimulation and dermal support.
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A GnRH agonist structurally similar to leuprolide. Researched for reproductive hormone regulation and studied as part of fertility and hormonal research protocols.
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A modified fragment of human growth hormone (amino acids 176-191) studied for fat metabolism. It holds FDA GRAS status as a food ingredient, which is not the same as FDA approval as a drug.
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A non-erythropoietic analog of erythropoietin researched for neuropathic pain, nerve repair, and metabolic benefits in type 2 diabetes research.
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A synthetic hexapeptide (Acetyl Hexapeptide-8) studied as a topical anti-wrinkle agent. Often called the 'topical Botox alternative' due to its muscle-relaxing skin effects.
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A single-chain peptide derived from relaxin-2, studied preclinically for anti-fibrotic effects in cardiac, renal, and lung tissue.
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The preserved sterile diluent used to reconstitute lyophilized peptides. Not a compound you dose — it is what everything else gets mixed with.
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A mitochondrial uncoupler researched for fat loss and metabolic improvement without the cardiovascular toxicity of older uncoupling agents.
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A synthetic peptide fragment famous in research circles for tissue repair and gut health.
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The most popular healing stack in the peptide research community. Combines BPC-157's localized healing with TB-500's systemic repair for comprehensive recovery support.
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A Khavinson bioregulator tetrapeptide targeting bronchial and lung tissue, researched for respiratory function.
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A long-acting amylin analog researched for weight loss, particularly in combination with semaglutide (the CagriSema combination).
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A Khavinson bioregulator peptide targeting cardiac tissue, researched for heart muscle function and cardiovascular aging.
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A naturally occurring dipeptide (beta-alanine + histidine) found in muscle and brain tissue. Researched for antioxidant effects, anti-aging, muscle endurance, and neuroprotection.
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A Khavinson bioregulator tripeptide studied for cartilage and connective tissue regulation.
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A mixture of low molecular weight neuropeptides derived from porcine brain. Researched for Alzheimer's disease, stroke recovery, and traumatic brain injury.
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The classic GH optimization stack. CJC-1295 triggers GH release while Ipamorelin amplifies it - together creating synergistic and sustained GH elevation.
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The short-acting GHRH analog commonly sold under the CJC-1295 name. Without the DAC moiety its half-life is roughly 30 minutes, producing a sharp GH pulse rather than sustained elevation.
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The long-acting GHRH analog: the DAC moiety binds albumin and extends the half-life to roughly 6-8 days, producing sustained GH elevation. This is NOT the same compound as the short-acting no-DAC version also sold as "CJC-1295".
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Hydrolyzed collagen-derived peptides researched for skin elasticity, joint health, bone density, and gut lining support. One of the most widely used and accessible peptide forms.
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A bioregulator peptide derived from cortical brain tissue. Researched for neuroprotection, cognitive function, and nervous system health.
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A Khavinson bioregulator tetrapeptide researched for immune system regulation and thymic function.
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An FDA-approved GnRH antagonist used for prostate cancer. Unlike GnRH agonists, it immediately suppresses testosterone without an initial flare.
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A highly experimental synthetic derivative of angiotensin IV studied for nootropic and neuroprotective effects. Evidence is largely preclinical.
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Delta Sleep-Inducing Peptide, discovered in 1974. Researched for improving sleep quality, particularly delta wave (deep) sleep and REM sleep.
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A synthetic pineal tetrapeptide researched for telomerase activation. Note: the commonly repeated 5-10 mg dose comes from Epithalamin, a crude extract — Epithalon itself is discussed in micrograms.
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A naturally occurring protein that inhibits myostatin and activin. Muscle and fat effects come from mechanistic and animal research, not established human outcomes.
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A senolytic peptide designed to selectively trigger apoptosis in senescent (zombie) cells. Researched as a potential anti-aging intervention.
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The fat-regulating tail fragment of human growth hormone. Studied for lipolysis (fat breakdown) without the growth-promoting effects of full GH.
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A copper-binding tripeptide famous for skin, hair, and wound-healing research.
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A synthetic ghrelin mimetic that strongly stimulates GH release. One of the original GHRPs with a robust research history.
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An early growth hormone releasing peptide known for its powerful appetite stimulation and GH release. One of the most studied GHRPs in research literature.
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A three-peptide blend of GHK-Cu, BPC-157 and TB-500 sold in a single vial and researched for skin, hair and soft-tissue repair.
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The body's master antioxidant, a tripeptide found in every cell. Researched for immune support, detoxification, liver health, and anti-aging.
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A synthetic version of GnRH that stimulates the release of LH and FSH. Used in research for testosterone support, fertility, and hormonal regulation.
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Human Chorionic Gonadotropin, an FDA-approved gonadotropin used clinically for hypogonadotropic hypogonadism, cryptorchidism, and ovulation induction. Widely researched for maintaining testicular function.
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One of the most potent synthetic GHRP compounds. Researched for GH release, muscle growth, and notably for cardioprotective effects.
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Recombinant human growth hormone (191 amino acid somatropin), FDA approved for growth hormone deficiency and several other named indications. The reference compound all GH secretagogues are compared against.
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Human Menopausal Gonadotropin (menotropins), an FDA-approved mixture of FSH and LH activity used in fertility treatment and researched for spermatogenesis support.
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A mitochondria-derived peptide researched for neuroprotection, metabolic health, and longevity. Levels decline with age and are studied as a longevity biomarker.
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A long-acting analog of insulin-like growth factor 1. Researched for muscle growth, fat loss, and anabolic effects independent of growth hormone.
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The most well-known peptide hormone. A 51 amino acid hormone produced by the pancreas that regulates blood sugar. Multiple forms are FDA-approved. Fundamental to metabolic health research.
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A selective GH secretagogue researched for GH release, with less activity at some off-target pathways than earlier GHRPs.
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A decapeptide that regulates reproductive hormones by modulating GnRH release. Researched for testosterone optimization and fertility.
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A four-peptide blend that adds KPV to the GLOW combination, researched for gut, skin and inflammatory conditions.
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A tripeptide fragment of alpha-MSH researched for its powerful anti-inflammatory and gut healing properties. Particularly promising for IBD and skin inflammation.
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A tight junction peptide regulator researched for leaky gut, celiac disease, and intestinal permeability. One of the most promising gut barrier research peptides.
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A GnRH agonist and one of the first peptide drugs widely used clinically. Used for prostate cancer, endometriosis, and hormonal regulation research.
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An FDA-approved GLP-1 receptor agonist. Developed by Novo Nordisk for type 2 diabetes, also approved for chronic weight management under the brand name Saxenda.
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The only human cathelicidin antimicrobial peptide. Researched for its broad-spectrum antimicrobial effects, wound healing, and immune modulation.
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A GLP-1 and glucagon dual receptor agonist from China's Innovent Biologics. Researched for weight loss and type 2 diabetes with promising Phase 3 trial data.
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A splice variant of IGF-1 that is locally produced in muscle tissue following exercise-induced damage. Researched for muscle repair and growth.
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A linear analog of alpha-MSH studied for skin tanning and photoprotection. More selective and considered lower risk than Melanotan II for sexual side effects.
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A synthetic analog of alpha-MSH studied for skin tanning, sexual function, and appetite regulation. One of the most well-known research peptides for pigmentation.
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An oral growth hormone secretagogue (technically a small molecule, not a peptide). Researched for GH and IGF-1 elevation, muscle mass, sleep quality, and bone density.
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A mitochondria-derived peptide that regulates metabolism at the cellular level. Researched for insulin sensitivity, fat regulation, exercise performance, and longevity.
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A modified, more stable form of the pineal tetrapeptide Epitalon, researched for telomerase activity and circadian/pineal regulation.
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An acetylated version of Selank with improved bioavailability and stability. Researched for anxiety relief, cognitive enhancement, and mood stabilization.
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An acetylated and amidated version of Semax with improved stability and potentially enhanced nootropic effects. Considered a more potent version.
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A coenzyme found in every cell that declines with age. Researched for energy production, DNA repair, cellular longevity, and neurological function.
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A hypothalamic neuropeptide involved in wakefulness, appetite, and energy homeostasis. Deficiency causes narcolepsy. Researched for sleep disorders, cognitive enhancement, and metabolic effects.
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The 'bonding hormone' - a naturally occurring peptide researched for social bonding, stress reduction, autism spectrum research, and metabolic effects.
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Intranasal oxytocin delivery for social anxiety, autism spectrum, PTSD, and bonding research. The nasal route allows direct access to the brain via the olfactory pathway.
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A synthetic peptide derived from the neurotrophic factor CNTF, studied preclinically for neurogenesis and cognitive effects.
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A palmitoyl-conjugated pentapeptide marketed under the name Matrixyl. One of the most studied cosmetic peptides for collagen stimulation and anti-aging skin care.
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A novel synthetic peptide targeting TREK-1 potassium channels. Researched for rapid antidepressant effects with a unique mechanism distinct from SSRIs.
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A pegylated version of Mechano Growth Factor, a splice variant of IGF-1. Extended half-life version studied for muscle repair, growth, and recovery.
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A semi-synthetic polysaccharide researched for joint health, cartilage repair, and as a potential treatment for Maculopathy. Not technically a peptide but widely studied alongside peptide protocols.
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A bioregulator peptide derived from the pineal gland. Researched for cognitive protection, anti-aging, and neurological health.
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An experimental anticancer peptide designed to bind HDM-2 and form membrane pores in cancer cells. Evidence is entirely preclinical.
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Also known as Bremelanotide, PT-141 is an FDA-approved peptide for sexual dysfunction. It works centrally in the brain rather than on the vascular system like traditional treatments.
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A triple receptor agonist targeting GLP-1, GIP, and glucagon receptors simultaneously. Investigational compound with some of the most dramatic weight loss data ever seen in clinical trials.
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A synthetic analog of tuftsin, Selank is an anxiolytic peptide approved in Russia. Researched for anxiety reduction, cognitive enhancement, and mood stabilization.
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An amidated version of Selank with potentially improved stability and bioavailability. Same anxiolytic and cognitive benefits with modifications for enhanced delivery.
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A GLP-1 receptor agonist approved for type 2 diabetes and chronic weight management.
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A synthetic peptide based on ACTH fragment. Approved in Russia for neuroprotection and cognitive enhancement. Studied for focus, memory, and stroke recovery.
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An amidated version of Semax offering improved stability, longer duration of action, and potentially enhanced cognitive effects.
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The first 29 amino acids of GHRH. Was FDA approved for growth hormone deficiency and remains one of the most studied GHRH analogs for body composition and anti-aging.
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An ERR agonist (exercise mimetic) that activates the same pathways as endurance exercise without physical activity. Researched for metabolic improvement and heart failure.
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An octapeptide extension of Argireline designed to reduce wrinkles more effectively. Inhibits muscle contractions responsible for expression lines.
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A mitochondria-targeting peptide that reduces oxidative stress and improves mitochondrial function. FDA approved for Barth syndrome. Researched for heart failure, aging, and energy.
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A dual GLP-1 and glucagon receptor agonist from Boehringer Ingelheim researched for obesity and NASH (non-alcoholic steatohepatitis / liver fat disease).
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A synthetic fragment of Thymosin Beta-4, studied for its role in cellular migration and repair.
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An FDA-approved PTH analog researched for bone density improvement. One of the few anabolic bone treatments that actually builds new bone rather than just preventing loss.
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An FDA-approved GHRH analog indicated for the reduction of excess abdominal fat in HIV-infected adults with lipodystrophy. FDA labeling states it is NOT indicated for weight-loss management.
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A triple monoamine reuptake inhibitor originally researched for Parkinson's and Alzheimer's. Repurposed for obesity research showing significant weight loss in trials.
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A Khavinson bioregulator tetrapeptide studied for testicular tissue function and reproductive hormone regulation.
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A polypeptide bioregulator derived from the thymus gland. Researched for immune restoration, anti-aging effects, and longevity in elderly populations.
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A key immune regulator derived from the thymus gland. Researched extensively for immune support, antiviral effects, and as a vaccine adjuvant.
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The parent compound of TB-500. A naturally occurring 43 amino acid peptide involved in cell migration, wound healing, and tissue repair. More expensive and less stable than TB-500.
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A dual GIP and GLP-1 receptor agonist. FDA approved for type 2 diabetes, with remarkable weight loss data showing up to 20% body weight reduction in trials.
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A GnRH agonist that initially stimulates and then suppresses testosterone production. Used clinically for prostate cancer and researched for post-cycle testosterone restoration.
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A Khavinson bioregulator tripeptide targeting vascular endothelium, researched for blood vessel health.
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A dipeptide bioregulator (Lys-Glu) researched for immune regulation, anti-aging, and cellular health. One of the simplest bioregulator peptides.
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A naturally occurring neuropeptide with powerful anti-inflammatory and immune-modulating properties. Researched for CIRS, autoimmune conditions, and gut health.
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