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Vial

5% RU-58841

Topical Non-Steroidal Anti-Androgen

RU-58841 is a non-steroidal anti-androgen developed for topical use, known for its ability to inhibit androgen receptors in hair follicles.

Usage:

Primarily researched for its effectiveness in preventing hair loss related to androgenic alopecia.

Mechanism of Action:

Blocks dihydrotestosterone (DHT) from binding to androgen receptors in scalp follicles, reducing miniaturization of hair follicles.

Benefits:

  • Reduces hair loss
  • Blocks DHT at receptor level
  • Topical application minimizes systemic effects

Side Effects:

  • Mild skin irritation
  • Dryness or redness
  • Rare hormonal imbalance (if absorbed systemically)

Suggested Dosage:

Not specified

Half-life: Around 5 hours (topical)

Delivery: Topical

No purchase links available
Vial

5-Amino-1MQ (10 mg)

Nicotinamide N-methyltransferase Inhibitor

5-Amino-1MQ is a potent and selective small-molecule inhibitor of nicotinamide N-methyltransferase (NNMT), an enzyme that methylates nicotinamide to 1-methylnicotinamide, thereby modulating NAD⁺ metabolism and influencing energy expenditure and adiposity.

Usage:

Used in research to study NNMT activity, NAD⁺ salvage pathways, obesity, type 2 diabetes, and metabolic regulation.

Mechanism of Action:

Binds to the active site of NNMT, preventing methylation of nicotinamide, which leads to increased intracellular NAD⁺ levels, enhanced mitochondrial function, and reduced lipogenesis.

Benefits:

  • Increased NAD⁺ levels
  • Enhanced mitochondrial function
  • Reduced adiposity in diet-induced obesity models
  • Improved glucose tolerance

Side Effects:

  • Not well characterized in humans
  • Potential off-target effects at high doses

Suggested Dosage:

Not specified

Half-life: Not well characterized

Delivery: Oral

Vial

9 Methyl β Carboline (15MG)

Dopaminergic Nootropic Compound

9-Me-BC (9-Methyl-β-carboline) is a nootropic compound with neuroprotective and dopaminergic properties, promoting the growth and survival of dopaminergic neurons.

Usage:

Used in research targeting cognitive enhancement, neuroprotection, and dopamine-related mood support.

Mechanism of Action:

Promotes dopaminergic neuron differentiation and mitochondrial function, enhancing dopamine signaling and brain plasticity.

Benefits:

  • Supports dopamine production
  • Enhances motivation and mood
  • Promotes neurogenesis
  • Neuroprotection against oxidative stress

Side Effects:

  • Mild headache
  • Irritability (with excess)
  • Insomnia (if taken late)

Suggested Dosage:

Not specified

Half-life: 12–16 hours (estimated)

Delivery: Oral or sublingual

No purchase links available
Vial

AOD 9604 (5Mg)

Lipolytic Fragment of Human Growth Hormone

AOD-9604 is a modified fragment of human growth hormone (176–191) developed to stimulate fat metabolism without the anabolic effects of full-length HGH.

Usage:

Primarily researched for fat loss and metabolic support without affecting blood sugar or insulin levels.

Mechanism of Action:

Mimics the fat-burning activity of natural HGH by stimulating lipolysis and inhibiting lipogenesis.

Benefits:

  • Accelerated fat loss
  • No effect on blood sugar or growth factors
  • Improved metabolic efficiency

Side Effects:

  • Mild injection site irritation
  • Rare headaches
  • Transient fatigue

Suggested Dosage:

Not specified

Half-life: 2–3 hours

Delivery: Subcutaneous injection

Vial

BPC 157

Regenerative Peptide

BPC-157 is a stable gastric peptide derived from body protection compound. It's known for accelerating healing across a wide variety of tissues.

Usage:

Used in studies on muscle and tendon repair, gut lining restoration, and even neurological healing.

Mechanism of Action:

Modulates the nitric oxide pathway, enhances angiogenesis, and promotes fibroblast migration and collagen synthesis.

Benefits:

  • Accelerated injury recovery
  • Anti-inflammatory effects
  • Gut healing
  • Tendon and ligament repair

Side Effects:

  • Mild nausea (oral)
  • Injection site irritation
  • Increased appetite (rare)

Suggested Dosage:

Not specified

Half-life: Short (estimated hours), but accumulates at injury sites

Delivery: Subcutaneous injection or oral (capsule/solution)

Vial

BPC 157 & TB 500 Blend

Regenerative Peptide Combination

This blend combines BPC-157 and TB-500, two peptides known for their potent tissue-regenerating properties. BPC-157 supports gut, tendon, and ligament healing, while TB-500 enhances angiogenesis and cell migration.

Usage:

Used in injury recovery, anti-inflammatory protocols, and full-body regenerative support in research settings.

Mechanism of Action:

BPC-157 accelerates angiogenesis and modulates inflammatory pathways; TB-500 promotes actin binding and tissue repair through enhanced cell migration.

Benefits:

  • Accelerated soft tissue healing
  • Reduced inflammation
  • Support for tendon, ligament, and nerve repair

Side Effects:

  • Mild dizziness
  • Flushing
  • Rare nausea

Suggested Dosage:

Not specified

Half-life: BPC-157: ~4–6 hours, TB-500: ~2–3 days

Delivery: Subcutaneous injection

Vial

Cagrilintide (10Mg)

Amylin Analog for Appetite Regulation

Cagrilintide is a long-acting amylin analog that mimics the effects of the natural hormone amylin, helping regulate appetite and food intake.

Usage:

Explored in weight loss studies due to its ability to enhance satiety and reduce caloric intake.

Mechanism of Action:

Binds to amylin and calcitonin receptors in the brain to regulate appetite and slow gastric emptying.

Benefits:

  • Appetite suppression
  • Weight loss support
  • Improved satiety
  • Potential synergy with GLP-1 agonists

Side Effects:

  • Nausea
  • Constipation
  • Injection site reactions

Suggested Dosage:

Not specified

Half-life: 6–8 days

Delivery: Subcutaneous injection

Vial

Cagrisema Sodium (10Mg)

Peptide Compound for Metabolic Research

Cagrisema is a co-formulation of cagrilintide and semaglutide, combining the effects of amylin and GLP-1 receptor agonism for enhanced weight loss and glycemic control.

Usage:

Used in research on obesity, appetite regulation, and glucose metabolism. Promising results in weight loss and Type 2 diabetes models.

Mechanism of Action:

Combines GLP-1 receptor activation with amylin receptor activity to suppress appetite, slow gastric emptying, and improve metabolic parameters.

Benefits:

  • Appetite suppression
  • Weight reduction
  • Improved glucose control
  • Delayed gastric emptying

Side Effects:

  • Nausea
  • Constipation
  • Loss of appetite
  • Mild gastrointestinal discomfort

Suggested Dosage:

Not specified

Half-life: 5–7 days (approximate)

Delivery: Subcutaneous injection

Vial

CJC 1295 with Ipamorelin (5Mg)

GHRH Analog + Ghrelin Mimetic

This blend combines CJC-1295 (no DAC) with Ipamorelin to synergistically enhance growth hormone pulses while minimizing side effects.

Usage:

Supports muscle growth, recovery, and fat metabolism in research contexts.

Mechanism of Action:

Dual action: CJC triggers GHRH pathways, while Ipamorelin mimics ghrelin to stimulate GH release without affecting cortisol.

Benefits:

  • Synergistic GH release
  • Muscle growth
  • Tissue repair
  • No spike in prolactin/cortisol

Side Effects:

  • Mild flushing
  • Temporary hunger spike
  • Injection site reaction

Suggested Dosage:

Not specified

Half-life: CJC: ~30 min, Ipamorelin: ~2 hours

Delivery: Subcutaneous injection

Vial

CJC-1295 DAC (5Mg)

Growth Hormone-Releasing Hormone Analog

CJC-1295 DAC is a synthetic analog of growth hormone-releasing hormone (GHRH) with a drug affinity complex that significantly increases its half-life.

Usage:

Promotes long-term increase in growth hormone and IGF-1 levels. Used in anti-aging, fat loss, and muscle-building research.

Mechanism of Action:

Stimulates the pituitary gland to release growth hormone over an extended period due to its DAC attachment.

Benefits:

  • Increased growth hormone
  • Improved muscle mass
  • Fat metabolism
  • Enhanced recovery

Side Effects:

  • Water retention
  • Joint pain
  • Possible fatigue

Suggested Dosage:

Not specified

Half-life: 5–8 days

Delivery: Subcutaneous injection

Vial

CJC-1295 No DAC (2Mg)

Growth Hormone-Releasing Hormone Analog

CJC-1295 without DAC is a shorter-acting analog of GHRH designed for pulsatile stimulation of growth hormone release.

Usage:

Used in cycles requiring short bursts of GH release. Often paired with Ipamorelin for synergy.

Mechanism of Action:

Stimulates GH release in a short burst, mimicking natural secretion patterns.

Benefits:

  • Pulsatile GH release
  • Supports lean muscle
  • May enhance fat loss

Side Effects:

  • Injection site irritation
  • Mild flushing
  • Headaches

Suggested Dosage:

Not specified

Half-life: 30 minutes

Delivery: Subcutaneous injection

Vial

Delta Sleep-Inducing Peptide (5Mg)

Sleep-Regulating Neuropeptide

DSIP (Delta Sleep-Inducing Peptide) is a naturally occurring neuropeptide associated with promoting restful sleep and modulating biological rhythms.

Usage:

Used in research for improving sleep quality, reducing stress, and regulating hormonal cycles.

Mechanism of Action:

Influences the hypothalamus and pituitary axis, modulating cortisol, LH, and GH levels during sleep cycles.

Benefits:

  • Deeper, more restorative sleep
  • Reduced sleep onset latency
  • Stress and anxiety reduction

Side Effects:

  • Grogginess in high doses
  • Vivid dreams
  • Mild headache

Suggested Dosage:

Not specified

Half-life: Short, around 15–30 minutes

Delivery: Subcutaneous injection

Vial

Dihexa (5Mg)

Neurogenic Peptide

Dihexa is a potent cognitive-enhancing peptide developed from angiotensin IV, showing potential in promoting synaptogenesis and reversing cognitive decline.

Usage:

Studied for neurodegenerative diseases like Alzheimer’s and Parkinson’s, and for enhancing memory, focus, and learning ability.

Mechanism of Action:

Binds to HGF/c-Met receptor complex, promoting neural synapse formation and brain plasticity.

Benefits:

  • Enhanced memory and learning
  • Increased synaptic density
  • Neuroprotection
  • Potential Alzheimer's support

Side Effects:

  • Headache
  • Irritability
  • Unknown long-term effects

Suggested Dosage:

Not specified

Half-life: Unspecified (long-lasting cognitive effects)

Delivery: Oral (preferred) or sublingual

No purchase links available
Vial

Epitalon (10 mg)

Tetrapeptide

Epitalon (also known as epithalon or epithalone) is a synthetic tetrapeptide (Ala-Glu-Asp-Gly) derived from the bovine pineal gland extract epithalamin, studied for its ability to activate telomerase and exert geroprotective effects.

Usage:

Used in research on aging, telomere lengthening, antioxidant defense, mitochondrial function, and immune modulation.

Mechanism of Action:

Upregulates telomerase reverse transcriptase expression and telomerase activity in somatic cells, promotes heterochromatin decondensation, and modulates antioxidant enzyme activity and mitochondrial health.

Benefits:

  • Telomere elongation and surpassing the Hayflick limit in cell cultures
  • Reduction of oxidative stress via increased SOD and GPx activities
  • Improved mitochondrial membrane potential and function
  • Enhanced immune cell proliferation and function
  • Potential oncostatic and anti-metastatic effects in animal models

Side Effects:

  • Minimal adverse effects reported in preclinical and limited clinical studies
  • Possible mild injection-site irritation

Suggested Dosage:

Not specified

Half-life: 30 minutes

Delivery: Subcutaneous injection

Vial

Epithalon (10Mg)

Telomerase Activator Peptide

Epithalon is a synthetic tetrapeptide derived from epithalamin, which regulates the production of telomerase and may play a role in aging reversal.

Usage:

Used in research to delay cellular aging, increase lifespan in animals, and restore circadian rhythm.

Mechanism of Action:

Activates telomerase enzyme to lengthen telomeres, enhances melatonin secretion, and restores hypothalamic regulation.

Benefits:

  • Telomere lengthening
  • Improved sleep quality
  • Enhanced longevity markers
  • Immune system support

Side Effects:

  • Mild fatigue
  • Drowsiness
  • Irritation at injection site

Suggested Dosage:

Not specified

Half-life: 2–10 hours

Delivery: Subcutaneous injection

Vial

Follistatin 344 (1Mg)

Myostatin Inhibitor Peptide

Follistatin 344 is a protein-based peptide known for its ability to inhibit myostatin, a negative regulator of muscle growth. By suppressing myostatin, it can promote hypertrophy and increased muscle mass.

Usage:

Used in research related to muscle-wasting conditions, muscle regeneration, and performance enhancement.

Mechanism of Action:

Binds to and inhibits myostatin, thus allowing muscle tissue to grow beyond normal physiological limits.

Benefits:

  • Increased muscle growth
  • Reduced muscle degradation
  • Potential support in sarcopenia or cachexia research

Side Effects:

  • Potential muscle stiffness
  • Unverified long-term safety
  • Possible organ enlargement if misused

Suggested Dosage:

Not specified

Half-life: Several hours (exact data varies)

Delivery: Subcutaneous or intramuscular injection

No purchase links available
Vial

GHK-Cu

Copper-Binding Peptide

GHK-Cu is a naturally occurring copper-binding tripeptide involved in wound healing, tissue regeneration, and skin remodeling.

Usage:

Commonly used in skin care and research for anti-aging, hair regrowth, and tissue repair.

Mechanism of Action:

Binds copper ions to activate regenerative pathways, improve collagen synthesis, and modulate inflammation.

Benefits:

  • Improves skin texture and elasticity
  • Promotes wound healing
  • Stimulates hair growth
  • Reduces inflammation

Side Effects:

  • Mild irritation at injection or application site
  • Rare allergic reactions

Suggested Dosage:

Not specified

Half-life: 30 minutes (systemic), longer for topical effects

Delivery: Subcutaneous injection or topical application

Vial

GHRP-2 (5 mg)

Growth Hormone Releasing Peptide

GHRP-2 is a synthetic hexapeptide that acts as a ghrelin receptor agonist to potently stimulate the release of growth hormone from the pituitary.

Usage:

Used in research to evaluate GH secretagogue activity, body composition changes, and metabolic effects.

Mechanism of Action:

Binds to the growth hormone secretagogue receptor (GHSR-1a) in the hypothalamus and pituitary, triggering G-protein–coupled signaling that increases pulsatile GH secretion.

Benefits:

  • Enhanced pulsatile growth hormone release
  • Improved lean muscle mass
  • Accelerated fat metabolism
  • Increased appetite (via ghrelin receptor activation)

Side Effects:

  • Transient increase in cortisol and prolactin
  • Mild water retention
  • Increased hunger
  • Possible tingling or numbness at injection site

Suggested Dosage:

Not specified

Half-life: ≈15–60 minutes

Delivery: Subcutaneous or intramuscular injection

Vial

GHRP-6 (5 mg)

Growth Hormone Releasing Peptide

GHRP-6 is a synthetic hexapeptide ghrelin receptor agonist that potently stimulates growth hormone release from the pituitary.

Usage:

Used in research to assess GH secretagogue activity, body composition changes, metabolic regulation, and wound healing effects.

Mechanism of Action:

Binds to and activates the growth hormone secretagogue receptor (GHSR-1a) in the hypothalamus and pituitary, triggering G-protein–coupled signaling and increased pulsatile GH secretion.

Benefits:

  • Robust pulsatile growth hormone release
  • Improved lean muscle mass
  • Enhanced fat metabolism
  • Potential wound healing and tissue repair support

Side Effects:

  • Transient increases in cortisol and prolactin
  • Increased appetite
  • Mild water retention
  • Possible injection-site discomfort

Suggested Dosage:

Not specified

Half-life: ≈2.5 hours

Delivery: Subcutaneous or intramuscular injection

Vial

Glow (GHK-CU TB-500 & BPC-157)

Multi-Peptide Regenerative Blend

GHK-CU TB-500 & BPC-157 aka Glow is a synergistic blend of GHK-Cu, TB-500, and BPC-157, designed to support advanced tissue regeneration, healing, and anti-inflammatory activity.

Usage:

Used in research for skin repair, injury recovery, collagen stimulation, and systemic healing.

Mechanism of Action:

Combines copper peptide (GHK-Cu) for tissue repair, TB-500 for cell migration and healing, and BPC-157 for gut and tendon regeneration.

Benefits:

  • Enhanced wound healing
  • Reduced inflammation
  • Improved collagen production
  • Tissue and joint regeneration

Side Effects:

  • Mild redness or swelling at injection site
  • Possible fatigue
  • Rare allergic reactions

Suggested Dosage:

Not specified

Half-life: Varies by peptide: GHK-Cu (30 min), TB-500 (~2–3 hours), BPC-157 (~4–6 hours)

Delivery: Subcutaneous or localized injection

Vial

Glutathione (1500 mg)

Tripeptide Antioxidant

Glutathione is a tripeptide composed of glutamate, cysteine, and glycine; it serves as the body's principal endogenous antioxidant and detoxifier.

Usage:

Used in research to study oxidative stress, detoxification pathways, immune function, and skin health.

Mechanism of Action:

Acts as an electron donor to neutralize reactive oxygen species and participates in phase II detoxification by conjugating to xenobiotics via glutathione S-transferases.

Benefits:

  • Reduction of oxidative stress
  • Support for phase II detoxification
  • Enhanced immune cell function
  • Potential skin-brightening effects

Side Effects:

  • Generally well tolerated
  • High oral doses may cause gastrointestinal discomfort
  • Rare allergic reactions

Suggested Dosage:

Not specified

Half-life: ≈1.5–2 hours (intravenous); oral bioavailability is low and variable

Delivery: Oral, liposomal, intravenous, or intramuscular injection

Vial

HCG

Hormonal Peptide for Fertility and Testosterone Support

Human Chorionic Gonadotropin (HCG) is a hormone produced during pregnancy that mimics luteinizing hormone (LH), stimulating the testes to produce testosterone.

Usage:

Used in research related to fertility, testosterone preservation during anabolic cycles, and hormone replacement therapy (HRT).

Mechanism of Action:

Binds to LH receptors in the Leydig cells of the testes, triggering endogenous testosterone production.

Benefits:

  • Stimulates natural testosterone production
  • Prevents testicular atrophy
  • Supports fertility and spermatogenesis

Side Effects:

  • Gynecomastia (with high doses)
  • Water retention
  • Mood swings or hormonal fluctuations

Suggested Dosage:

Not specified

Half-life: Approximately 24–36 hours

Delivery: Subcutaneous or intramuscular injection

Vial

HGH Frag 176-191 (5Mg)

Fat-Loss Fragment of Human Growth Hormone

HGH Fragment 176–191 is a truncated form of the human growth hormone molecule specifically engineered to enhance fat-burning properties.

Usage:

Commonly researched for targeted fat loss and improved body composition, especially in stubborn fat areas.

Mechanism of Action:

Activates beta-3 adrenergic receptors in adipose tissue to increase lipolysis and block lipogenesis.

Benefits:

  • Targeted fat reduction
  • Preserves lean muscle mass
  • No spike in blood sugar or IGF-1

Side Effects:

  • Temporary redness at injection site
  • Mild restlessness
  • Occasional dry mouth

Suggested Dosage:

Not specified

Half-life: 1–2 hours

Delivery: Subcutaneous injection

Vial

HMG 75IU

Human Menopausal Gonadotropin

HMG is a blend of follicle-stimulating hormone (FSH) and luteinizing hormone (LH) derived from postmenopausal women, used in fertility and hormone production research.

Usage:

Commonly used in studies on ovulation induction, spermatogenesis, and testosterone support.

Mechanism of Action:

Stimulates gonadal activity by promoting follicle development in females and spermatogenesis and testosterone production in males.

Benefits:

  • Increased fertility hormone levels
  • Boosts natural testosterone (males)
  • Supports ovulation (females)

Side Effects:

  • Abdominal discomfort
  • Breast tenderness
  • Possible mood changes
  • Ovarian hyperstimulation (in females)

Suggested Dosage:

Not specified

Half-life: Approximately 24–36 hours

Delivery: Subcutaneous or intramuscular injection

Vial

IGF LR3 (1Mg)

Insulin-like Growth Factor Analog

IGF-1 LR3 is a synthetic analog of insulin-like growth factor-1 (IGF-1), modified to extend its half-life and potency in stimulating cellular growth.

Usage:

Commonly used in research for promoting muscle growth, recovery, and tissue repair by enhancing protein synthesis and nutrient uptake.

Mechanism of Action:

Binds to IGF-1 receptors in muscle and other tissues, promoting anabolic activity and inhibiting programmed cell death.

Benefits:

  • Accelerated muscle growth
  • Enhanced recovery
  • Improved nitrogen retention
  • Increased protein synthesis

Side Effects:

  • Joint pain
  • Hypoglycemia
  • Water retention

Suggested Dosage:

Not specified

Half-life: 20–30 hours

Delivery: Subcutaneous or intramuscular injection

Vial

Ipamorelin (5Mg)

Selective Growth Hormone Secretagogue

Ipamorelin is a selective growth hormone secretagogue and ghrelin receptor agonist that stimulates GH release without affecting cortisol or prolactin.

Usage:

Commonly used in research for promoting growth hormone release, recovery, anti-aging, and body composition improvement.

Mechanism of Action:

Binds to ghrelin receptors, stimulating GH release from the pituitary gland without raising other hormone levels like cortisol.

Benefits:

  • Increased natural GH levels
  • Enhanced recovery
  • Improved sleep quality
  • Minimal side effects

Side Effects:

  • Temporary hunger spike
  • Mild flushing
  • Injection site irritation

Suggested Dosage:

Not specified

Half-life: About 2 hours

Delivery: Subcutaneous injection

Vial

Kisspeptin 10 (10Mg)

Reproductive Hormone Regulator

Kisspeptin-10 is a short peptide derived from the full-length Kisspeptin protein, critical for initiating the release of gonadotropin-releasing hormone (GnRH).

Usage:

Studied for its role in regulating puberty, fertility, and reproductive hormone cycles. May have applications in treating hypogonadism and infertility.

Mechanism of Action:

Stimulates the hypothalamus to release GnRH, which then promotes LH and FSH secretion from the pituitary gland.

Benefits:

  • Restores reproductive hormone function
  • Enhances LH and FSH secretion
  • Supports testosterone or estrogen production
  • Potential fertility aid

Side Effects:

  • Hormonal fluctuations
  • Mild headaches
  • Mood changes

Suggested Dosage:

Not specified

Half-life: Approximately 30 minutes

Delivery: Subcutaneous injection

Vial

KLOW (GHK-CU TB-500 BPC-157 & KPV)

Regenerative Peptide Blend

KLOW is a proprietary blend of regenerative peptides typically including GHK-Cu, BPC-157, and TB-500, designed to support skin rejuvenation, tissue healing, and inflammation reduction.

Usage:

Used in research focused on wound healing, recovery from soft tissue injuries, and aesthetic rejuvenation.

Mechanism of Action:

Combines copper ion transport, angiogenesis stimulation, and anti-inflammatory signaling to promote accelerated tissue repair.

Benefits:

  • Enhanced skin tone and elasticity
  • Accelerated injury recovery
  • Reduced inflammation

Side Effects:

  • Mild irritation at injection site
  • Temporary redness or swelling

Suggested Dosage:

Not specified

Half-life: Varies by blend — typically 2–12 hours per peptide

Delivery: Subcutaneous or intradermal injection

Vial

KPV (10Mg)

Anti-Inflammatory Tripeptide

KPV is a naturally occurring tripeptide derived from alpha-MSH, noted for its strong anti-inflammatory properties and low toxicity profile.

Usage:

Used in research for inflammatory bowel diseases, autoimmune conditions, and skin inflammation.

Mechanism of Action:

Acts as an alpha-MSH analog, modulating inflammation by inhibiting pro-inflammatory cytokines without affecting melanogenesis.

Benefits:

  • Reduces systemic inflammation
  • Supports gut health
  • May help with skin and joint inflammation
  • Non-stimulatory and well-tolerated

Side Effects:

  • Mild headache
  • Temporary injection site irritation
  • Rare nausea

Suggested Dosage:

Not specified

Half-life: Variable depending on formulation, ~30–60 minutes for injectable form

Delivery: Subcutaneous injection or oral capsule (research use)

Vial

Melanotan 2 (10Mg)

Tanning and Libido Peptide

Melanotan II is a synthetic analog of alpha-MSH that promotes melanin production and has aphrodisiac effects by stimulating melanocortin receptors.

Usage:

Used in research for sunless tanning, libido enhancement, and photoprotection in fair-skinned individuals.

Mechanism of Action:

Binds to melanocortin receptors to increase melanin production and stimulate sexual arousal pathways.

Benefits:

  • Darker skin pigmentation
  • Improved libido
  • Potential protection against UV damage

Side Effects:

  • Facial flushing
  • Nausea (dose-dependent)
  • Appetite suppression
  • Darkening of moles or freckles

Suggested Dosage:

Not specified

Half-life: 33–37 hours

Delivery: Subcutaneous injection

Vial

MOTS C (10Mg)

Mitochondrial-Derived Peptide

MOTS-c is a peptide encoded by mitochondrial DNA, involved in metabolic regulation, cellular protection, and potentially anti-aging effects.

Usage:

Studied for its role in metabolic health, mitochondrial function, and physical endurance enhancement.

Mechanism of Action:

Activates AMPK signaling and regulates mitochondrial respiration to improve insulin sensitivity and reduce oxidative stress.

Benefits:

  • Improved insulin sensitivity
  • Enhanced energy metabolism
  • Increased endurance

Side Effects:

  • Temporary fatigue
  • Minor site irritation
  • Mild nausea (rare)

Suggested Dosage:

Not specified

Half-life: Approx. 2–3 hours

Delivery: Subcutaneous injection

Vial

NAD

Cellular Energy Cofactor

NAD (Nicotinamide Adenine Dinucleotide) is a coenzyme found in all living cells. It plays a central role in energy metabolism, mitochondrial function, and cellular repair.

Usage:

Used in research related to anti-aging, neuroprotection, and metabolic health. Often administered to support energy production and cellular recovery.

Mechanism of Action:

Acts as a coenzyme in redox reactions, supporting ATP production and DNA repair. Influences sirtuin activity and mitochondrial health.

Benefits:

  • Enhanced cellular energy
  • Improved mitochondrial function
  • Neuroprotective properties
  • Supports healthy aging

Side Effects:

  • Flushing
  • Mild nausea
  • Headache (at high doses)

Suggested Dosage:

Not specified

Half-life: 1–2 hours (active form)

Delivery: IV infusion, subcutaneous injection, oral (low bioavailability)

No purchase links available
Vial

NAD+

Oxidized Cellular Cofactor

NAD+ is the oxidized form of NAD and is essential for redox reactions, sirtuin activation, and mitochondrial energy production.

Usage:

Studied for its role in aging, energy regulation, and DNA repair. Administered in IV therapy and supplement form to enhance cellular health.

Mechanism of Action:

Functions as a key electron transporter in cellular respiration, enabling efficient ATP generation and regulating gene expression via sirtuins.

Benefits:

  • Increased energy levels
  • Enhanced cognitive performance
  • Anti-aging support
  • Improved metabolic efficiency

Side Effects:

  • Flushing or tingling
  • Digestive upset
  • Rare fatigue during infusion

Suggested Dosage:

Not specified

Half-life: 1–2 hours

Delivery: IV infusion, subcutaneous, oral

Vial

NSI-189 Phosphate (20Mg)

Neurogenic Research Compound

NSI-189 is a neurogenic compound developed to stimulate neurogenesis in the hippocampus and has been studied for depression and cognitive impairment.

Usage:

Investigated for its potential in treating major depressive disorder (MDD) and cognitive decline. Also explored for stroke recovery.

Mechanism of Action:

Stimulates neurogenesis and increases hippocampal volume. May modulate BDNF and other neurotrophic pathways.

Benefits:

  • Mood elevation
  • Cognitive support
  • Potential neurogenesis

Side Effects:

  • Mild headaches
  • Fatigue
  • GI discomfort (rare)

Suggested Dosage:

Not specified

Half-life: 17–20 hours

Delivery: Oral

No purchase links available
Vial

Oxytocin

Peptide Hormone

Oxytocin is a naturally occurring neuropeptide produced in the hypothalamus and released by the posterior pituitary; it plays key roles in uterine contraction, milk ejection, and social bonding.

Usage:

Used in research to study parturition (labor induction), lactation, social behavior, and anxiety modulation.

Mechanism of Action:

Binds to oxytocin receptors (OXTR) in target tissues, triggering G-protein coupled signaling that leads to uterine smooth muscle contraction, milk let-down, and modulation of central nervous system pathways involved in social cognition.

Benefits:

  • Induction of uterine contractions
  • Promotion of milk ejection
  • Enhancement of social bonding and trust
  • Reduction of anxiety in behavioral studies

Side Effects:

  • Uterine hyperstimulation (when used in labor)
  • Fluid retention
  • Hypotension
  • Headache

Suggested Dosage:

Not specified

Half-life: ≈3–5 minutes

Delivery: Intravenous or intramuscular injection; intranasal spray for central effects

Vial

PEG MGF (2Mg)

Muscle Repair Growth Factor Analog

PEG-MGF (Pegylated Mechano Growth Factor) is a modified form of IGF-1 that plays a key role in muscle repair and growth, especially after resistance training or injury.

Usage:

Commonly studied in muscle regeneration, athletic recovery, and performance research.

Mechanism of Action:

Stimulates satellite cell proliferation and muscle fiber repair. The PEG modification increases its half-life.

Benefits:

  • Accelerated muscle recovery
  • Muscle hypertrophy support
  • Localized growth potential

Side Effects:

  • Muscle tightness
  • Injection site irritation
  • Water retention

Suggested Dosage:

Not specified

Half-life: 24–36 hours (due to PEGylation)

Delivery: Subcutaneous or intramuscular injection

Vial

Phenylpiracetam Hydrazide (150Mg)

Cognitive-Enhancing Compound

Phenylpiracetam Hydrazide is a modified version of phenylpiracetam, known for enhanced bioavailability and potential nootropic effects with reduced tolerance build-up.

Usage:

Studied for improving memory, focus, and physical performance under stress. Popular in nootropic research for neurostimulation.

Mechanism of Action:

Modulates AMPA and NMDA receptors and may enhance dopamine and norepinephrine signaling.

Benefits:

  • Enhanced focus and alertness
  • Increased stamina under stress
  • Improved working memory

Side Effects:

  • Irritability
  • Insomnia
  • Headache (especially without choline)

Suggested Dosage:

Not specified

Half-life: 3–5 hours

Delivery: Oral (capsule or powder)

No purchase links available
Vial

Pinealon (10 mg)

Neuroprotective Peptide

Pinealon is a synthetic tetrapeptide derived from the pineal gland, studied for its neuroprotective and cognition‐enhancing properties.

Usage:

Used in research on memory consolidation, learning, neurodegenerative models, and age‐related cognitive decline.

Mechanism of Action:

Modulates neurotransmitter release, protects against oxidative stress in neuronal cells, and promotes neurotrophic factor expression.

Benefits:

  • Improved learning and memory in animal models
  • Neuroprotection against oxidative damage
  • Enhanced synaptic plasticity
  • Potential anti‐aging effects in the central nervous system

Side Effects:

  • Generally well tolerated in preclinical studies
  • Possible mild injection‐site irritation

Suggested Dosage:

Not specified

Half-life: ≈20–40 minutes

Delivery: Subcutaneous or intramuscular injection

Vial

PT 141 (10Mg)

Melanocortin Receptor Agonist

PT-141 (Bremelanotide) is a synthetic peptide developed from melanotan II that activates melanocortin receptors, influencing libido and sexual function.

Usage:

Used in research related to sexual arousal disorders, both male and female.

Mechanism of Action:

Stimulates MC-3 and MC-4 receptors in the brain, enhancing sexual arousal via the central nervous system.

Benefits:

  • Enhanced libido
  • Improved sexual arousal
  • Potential treatment for erectile dysfunction

Side Effects:

  • Nausea
  • Facial flushing
  • Increased blood pressure

Suggested Dosage:

Not specified

Half-life: 2.7 hours

Delivery: Subcutaneous injection

Vial

Reta - GLP-3

Investigational Multi-Agonist Peptide

Reta GLP-3 is a triple agonist targeting GLP-1, GIP, and glucagon receptors, being explored for its powerful metabolic effects, especially in obesity and type 2 diabetes.

Usage:

Used in clinical trials and investigational studies for significant body fat reduction, appetite control, and glucose management.

Mechanism of Action:

Acts on GLP-1, GIP, and glucagon receptors to enhance insulin sensitivity, reduce appetite, and increase energy expenditure.

Benefits:

  • Substantial weight loss
  • Improved glycemic control
  • Enhanced metabolic rate

Side Effects:

  • Nausea
  • Gastrointestinal discomfort
  • Possible increased heart rate

Suggested Dosage:

Not specified

Half-life: Approximately 5–7 days

Delivery: Subcutaneous injection (weekly)

Vial

S23 (10Mg)

Selective Androgen Receptor Modulator (SARM)

S23 is a potent SARM known for its anabolic effects and potential as a male contraceptive by suppressing sperm production.

Usage:

Explored for its ability to increase lean muscle mass and reduce fat without significant androgenic side effects.

Mechanism of Action:

Binds to androgen receptors in muscle and bone tissues, promoting growth while reducing activity in reproductive tissues.

Benefits:

  • Promotes lean muscle gains
  • Reduces body fat
  • Preserves bone density
  • Potential male contraception research

Side Effects:

  • Testosterone suppression
  • Mood changes
  • Aggression (in some cases)

Suggested Dosage:

Not specified

Half-life: 12 hours (approx.)

Delivery: Oral

No purchase links available
Vial

Selank (10Mg)

Synthetic Anxiolytic Peptide

Selank is a synthetic peptide derived from the immune molecule tuftsin, developed for its anti-anxiety, nootropic, and immune-modulating properties.

Usage:

Used in studies targeting anxiety, cognitive performance, and neuroprotection.

Mechanism of Action:

Modulates the expression of serotonin and dopamine, influencing mood and cognitive function without sedative effects.

Benefits:

  • Reduces anxiety
  • Improves memory and focus
  • Supports immune regulation
  • Neuroprotective effects

Side Effects:

  • Rare nasal irritation
  • Mild fatigue or headache

Suggested Dosage:

Not specified

Half-life: 3–10 minutes in plasma, longer central nervous effects

Delivery: Intranasal administration

Vial

Sema GLP-1

GLP-1 Receptor Agonist

Semaglutide is a GLP-1 receptor agonist that mimics the effects of glucagon-like peptide-1, helping regulate blood sugar and suppress appetite.

Usage:

Commonly studied for weight loss, appetite control, and blood glucose regulation in individuals with metabolic conditions such as Type 2 diabetes and obesity.

Mechanism of Action:

Activates GLP-1 receptors to enhance insulin secretion, slow gastric emptying, suppress appetite, and reduce glucagon secretion.

Benefits:

  • Appetite suppression
  • Weight loss
  • Improved blood sugar control
  • Reduced risk of cardiovascular events

Side Effects:

  • Nausea
  • Constipation
  • Headache
  • Loss of appetite

Suggested Dosage:

Not specified

Half-life: About 7 days

Delivery: Subcutaneous injection

Vial

Semax (10Mg)

Neuroprotective Peptide

Semax is a synthetic heptapeptide developed from a fragment of ACTH, known for its neuroprotective and cognitive-enhancing properties.

Usage:

Used in research focused on memory enhancement, neuroprotection, and stroke recovery support.

Mechanism of Action:

Modulates expression of neurotrophins like BDNF and improves cerebral blood flow, especially in hypoxic or ischemic conditions.

Benefits:

  • Enhanced memory and learning
  • Neuroprotection under stress
  • Improved focus and mental clarity

Side Effects:

  • Irritation in nasal passages
  • Mild headache
  • Rare anxiety or overstimulation

Suggested Dosage:

Not specified

Half-life: Several hours (short-acting)

Delivery: Intranasal

Vial

Sermorelin (5Mg)

Growth Hormone-Releasing Peptide

Sermorelin is a synthetic peptide that mimics growth hormone-releasing hormone (GHRH), stimulating the pituitary gland to release endogenous growth hormone.

Usage:

Commonly researched for growth hormone deficiency, anti-aging therapies, and performance enhancement through natural GH pathways.

Mechanism of Action:

Binds to GHRH receptors in the pituitary gland to stimulate pulsatile GH secretion, supporting downstream IGF-1 production.

Benefits:

  • Stimulates natural growth hormone production
  • Improves sleep and recovery
  • Supports lean muscle and fat metabolism
  • May promote skin and tissue repair

Side Effects:

  • Temporary flushing
  • Dizziness
  • Injection site irritation

Suggested Dosage:

Not specified

Half-life: 10–20 minutes

Delivery: Subcutaneous injection

Vial

SLU PP 332

Experimental Research Peptide

SLU-PP-332 is an experimental peptide under early-stage investigation for its effects on metabolic regulation and potential nootropic effects.

Usage:

Studied for potential impacts on mitochondrial function, endurance capacity, and cognitive processes in preclinical models.

Mechanism of Action:

Believed to influence metabolic signaling, possibly via modulation of PGC-1α and mitochondrial biogenesis pathways.

Benefits:

  • Enhanced energy regulation
  • May support mitochondrial health
  • Potential cognitive benefits

Side Effects:

  • Not well-documented
  • Unknown long-term effects

Suggested Dosage:

Not specified

Half-life: Undocumented; suspected to be short-acting

Delivery: Subcutaneous injection

No purchase links available
Vial

SS-31 (10 mg)

Mitochondria-Targeted Peptide

SS-31 (also known as Elamipretide or Bendavia) is a synthetic tetrapeptide that selectively targets cardiolipin on the inner mitochondrial membrane to improve mitochondrial function and reduce oxidative stress.

Usage:

Used in research on mitochondrial dysfunction, ischemia-reperfusion injury, heart failure, neurodegenerative diseases, and age-related decline in bioenergetics.

Mechanism of Action:

Binds to cardiolipin in the inner mitochondrial membrane, stabilizing cristae structure, enhancing electron transport chain efficiency, reducing reactive oxygen species production, and preventing cytochrome c peroxidase activity.

Benefits:

  • Improved mitochondrial bioenergetics
  • Reduced reactive oxygen species (ROS) production
  • Protection against ischemia-reperfusion injury
  • Improved cardiac and skeletal muscle function
  • Neuroprotective effects in models of neurodegeneration

Side Effects:

  • Injection-site reactions
  • Nausea
  • Headache
  • Possible mild hypotension

Suggested Dosage:

Not specified

Half-life: ≈2 hours

Delivery: Subcutaneous or intravenous injection

Vial

TB 500 w/ Thymosin Beta 4

Wound Healing and Recovery Peptide

TB-500 is the synthetic version of a segment of thymosin beta-4, a natural peptide involved in tissue repair and regeneration.

Usage:

Applied in research on soft tissue recovery, angiogenesis, and inflammation reduction.

Mechanism of Action:

Promotes cell migration, angiogenesis, and reduces inflammation by regulating actin binding and cellular remodeling.

Benefits:

  • Accelerated muscle and tendon healing
  • Improved flexibility
  • Anti-fibrotic effects
  • Angiogenesis support

Side Effects:

  • Fatigue
  • Headaches
  • Possible lethargy post-injection

Suggested Dosage:

Not specified

Half-life: 2–3 hours (biological activity may persist longer)

Delivery: Subcutaneous or intramuscular injection

Vial

Tesamorelin (5Mg)

Growth Hormone-Releasing Peptide

Tesamorelin is a synthetic analog of GHRH that promotes the natural release of growth hormone and has shown clinical effectiveness in reducing visceral fat.

Usage:

Commonly used in research focused on lipodystrophy, particularly in HIV patients, and explored for cognitive and metabolic benefits.

Mechanism of Action:

Stimulates the pituitary gland to secrete growth hormone by binding to GHRH receptors.

Benefits:

  • Reduces visceral adipose tissue
  • Enhances GH secretion
  • May improve lipid profiles
  • Supports cognitive function

Side Effects:

  • Injection site redness
  • Water retention
  • Tingling or numbness in extremities

Suggested Dosage:

Not specified

Half-life: Approximately 20–30 minutes

Delivery: Subcutaneous injection

Vial

Tesofensine Powder

Triple Monoamine Reuptake Inhibitor

Tesofensine is a serotonin–noradrenaline–dopamine reuptake inhibitor (SNDRI) that was originally developed for neurodegenerative diseases and later studied for its potent weight loss effects.

Usage:

Used in research focused on appetite suppression and weight loss. May enhance energy expenditure and reduce food cravings.

Mechanism of Action:

Blocks the reuptake of serotonin, norepinephrine, and dopamine, increasing their levels and thereby reducing appetite and promoting satiety.

Benefits:

  • Appetite suppression
  • Potential weight loss
  • Enhanced mood and energy

Side Effects:

  • Dry mouth
  • Increased heart rate
  • Insomnia
  • Elevated blood pressure

Suggested Dosage:

Not specified

Half-life: Approximately 8 days

Delivery: Oral (capsule or powder form)

No purchase links available
Vial

Thymosin Alpha 1

Immunomodulatory Peptide

Thymosin Alpha 1 is a naturally occurring peptide fragment derived from prothymosin alpha, known for its immune-boosting properties.

Usage:

Used in research related to immune enhancement, chronic infections, and adjunctive cancer therapy. Shown to increase T-cell function.

Mechanism of Action:

Enhances T-cell maturation and function, modulates cytokine production, and improves the innate immune response.

Benefits:

  • Immune system support
  • Antiviral and antibacterial effects
  • Potential anti-tumor activity
  • Improved vaccine response

Side Effects:

  • Mild injection site reactions
  • Fatigue
  • Irritability (rare)

Suggested Dosage:

Not specified

Half-life: 2 hours (approx.)

Delivery: Subcutaneous injection

Vial

Tirz GLP-2 (10Mg)

Dual GIP and GLP-1 Receptor Agonist

Tirzepatide is a novel investigational peptide that acts as a dual agonist of GIP and GLP-1 receptors, enhancing insulin secretion and improving glycemic control while reducing appetite.

Usage:

Primarily studied in the treatment of Type 2 diabetes and obesity. Research also explores its cardiovascular and metabolic benefits.

Mechanism of Action:

Activates both glucose-dependent insulinotropic polypeptide (GIP) and glucagon-like peptide-1 (GLP-1) receptors to regulate blood sugar and appetite.

Benefits:

  • Improved insulin sensitivity
  • Appetite suppression
  • Significant weight loss
  • Better glycemic control

Side Effects:

  • Nausea
  • Vomiting
  • Constipation
  • Fatigue (in early dosing phase)

Suggested Dosage:

Not specified

Half-life: 5 days

Delivery: Subcutaneous injection

Vial

YK 11

Myostatin-Inhibiting SARM

YK-11 is a selective androgen receptor modulator (SARM) known for its ability to inhibit myostatin, potentially leading to extreme muscle growth.

Usage:

Used in research to explore muscle-building potential through myostatin suppression without traditional androgenic side effects.

Mechanism of Action:

Binds to androgen receptors and increases follistatin expression, which inhibits myostatin and promotes muscle cell growth.

Benefits:

  • Significant muscle hypertrophy
  • Inhibition of myostatin
  • Improved strength
  • Minimal androgenic activity

Side Effects:

  • Potential testosterone suppression
  • Joint discomfort
  • Liver strain at high doses

Suggested Dosage:

Not specified

Half-life: 6–10 hours (estimated)

Delivery: Oral

No purchase links available