
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

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

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

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

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)

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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)

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

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

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)

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

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

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

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

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)

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

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

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)

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

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

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

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

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

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

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

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

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

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)

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

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

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