Research Use Only - Important Disclaimer
All products listed on this website are intended for laboratory research use only and are not for human consumption, medical, veterinary, or household use. These products should only be handled by qualified professionals. We do not provide any dosage information, and the products must not be used as food additives, drugs, cosmetics, or for any other inappropriate applications. By purchasing, you acknowledge and agree to these terms.

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
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
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

Adipotide
Peptide for Research
Adipotide, also known as FTPP (Fat Targeted Proapoptotic Peptide), is an experimental peptide designed to induce targeted apoptosis of fat cells, potentially resulting in rapid reduction of body fat in animal studies.
Usage:
Primarily used in research settings to investigate its effects on body weight reduction, fat loss, and metabolic health. Not approved for human use.
Mechanism of Action:
Adipotide targets specific proteins on the surface of fat cell blood vessels (Prohibitin and ANXA2), causing apoptosis (cell death) in the blood vessels supplying white adipose tissue. This leads to fat cell death and subsequent reduction of fat mass.
Benefits:
- Rapid fat loss observed in animal studies
- Reduces white adipose tissue
- Potential metabolic improvements (e.g., insulin sensitivity)
- Non-stimulant fat loss mechanism
Side Effects:
- Dehydration
- Mild to moderate kidney stress (noted in primate studies)
- Electrolyte imbalance
- Potential for nausea, lethargy, and other systemic effects
Suggested Dosage:
Not specified
Half-life: 2–4 hours (in animal studies; human data not established)
Delivery: Subcutaneous injection (for research use only)

AOD 9604
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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)

Lipo-C with B12
Lipotropic Injectable Formula
Lipo-C with B12 is a compounded injectable formula designed to support fat metabolism, liver health, and energy production. It combines lipotropic nutrients and B vitamins to promote efficient fat utilization and metabolic health.
Usage:
Used in research and wellness settings to study weight management, liver detoxification, and energy enhancement. Often administered intramuscularly for maximum absorption.
Mechanism of Action:
Works synergistically by supplying essential nutrients for fat transport, methylation, and cellular energy production. L-carnitine assists in fatty acid transport into mitochondria; choline, inositol, and methionine support liver fat processing; B vitamins help optimize metabolism and energy yield.
Benefits:
- Supports fat metabolism and weight management
- Enhances liver detoxification
- Promotes higher energy levels
- May aid in mood and cognitive function
- Provides comprehensive B vitamin support
Side Effects:
- Mild injection site discomfort
- Possible digestive upset (rare)
- Allergic reaction (rare, mostly with repeated exposure)
- Mild headache (occasionally reported)
Suggested Dosage:
Not specified
Half-life: Varies by ingredient; B12 (up to several days), other B vitamins and lipotropics (generally hours)
Delivery: Intramuscular injection (IM)

Melanotan 2
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

Methylene Blue 500g Liquid
Redox Indicator / Nootropic Compound
Methylene Blue is a heterocyclic aromatic chemical compound historically used as a dye, redox indicator, and medication. In research and nootropic contexts, it is investigated for its neuroprotective, mitochondrial-support, and cognitive-enhancing effects.
Usage:
Used in research for its antioxidant properties, mitochondrial support, neuroprotection, and as a stain in various biological protocols. Studied as a potential cognitive enhancer and for memory support.
Mechanism of Action:
Acts as an electron donor and acceptor in cellular respiration, enhancing mitochondrial function, reducing oxidative stress, and potentially improving cognitive function by supporting cellular energy metabolism.
Benefits:
- Supports mitochondrial energy production
- May enhance memory and cognitive function
- Neuroprotective effects against oxidative damage
- Acts as an antioxidant
- Used as a biological stain and diagnostic tool
Side Effects:
- Urine/feces discoloration (blue/green tint)
- Nausea (at high doses)
- Headache
- Dizziness
- Serotonin syndrome (risk if combined with SSRIs/MAOIs at high doses)
Suggested Dosage:
Not specified
Half-life: 5–24 hours (dose-dependent)
Delivery: Oral (liquid or capsule), intravenous (clinical use)

MOTS C
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

Myostatin Inhibitor (1mg)
Peptide for Research
Myostatin inhibitors are experimental peptides designed to block the activity of myostatin, a protein that restricts muscle growth. Inhibition of myostatin has been shown in animal studies to result in significant increases in muscle mass and strength.
Usage:
Used in research to study muscle hypertrophy, muscle wasting disorders, sarcopenia, and athletic performance. Not approved for human use.
Mechanism of Action:
Binds to myostatin or its receptors, preventing myostatin from signaling muscle cells to limit growth. This removal of inhibition leads to increased muscle fiber size and number.
Benefits:
- Promotes muscle growth and hypertrophy
- Potential treatment for muscle wasting diseases
- Enhances muscle recovery
- May improve physical performance
Side Effects:
- Unknown long-term safety profile
- Potential for muscle cramps
- Possible tendon stress or joint discomfort
- Risk of off-target effects due to broad biological impact
Suggested Dosage:
Not specified
Half-life: Varies depending on peptide structure; typically several hours in animal models
Delivery: Subcutaneous injection (for research use only)

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
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
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
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
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
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
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
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
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
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
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
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
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