Retatrutide 10mg

Retatrutide

01
Triple GLP-1 / GIP / Glucagon Agonist — 10mg
99% Purity Metabolic Flagship

Retatrutide is the most advanced metabolic compound of its generation. It acts simultaneously on three receptors: it suppresses appetite (GLP-1), optimizes insulin sensitivity and energy use (GIP), and activates hepatic thermogenesis to burn fat (Glucagon). In Phase 2 clinical trials (NEJM, 2023), participants achieved reductions of up to 24.2% in body weight over 48 weeks — the greatest reduction documented for a single agent.

Key Benefits
Powerful appetite suppression without food anxiety
Greatest documented fat loss in its class
Increased resting energy expenditure
Reduction of up to 81% in liver fat
Better preservation of lean muscle mass
Improved insulin sensitivity and triglycerides
Mechanism of Action
A 39-amino-acid peptide that activates three hormonal receptors in parallel. GLP-1 reduces appetite from the brain and delays gastric emptying. GIP improves nutrient partitioning. Glucagon activates fatty acid oxidation and hepatic ketogenesis. The hyperglycemic effect of glucagon is counterbalanced by GLP-1, resulting in a favorable net metabolic balance.
Usage Reference
RouteSubcutaneous, once weekly
Escalation0.5 mg → 1.0 → 2.0 → 4.0 → 6.0–8.0 mg (every 2 weeks)
Range1–12 mg/week
Reconstitution1 ml BAC per 10 mg vial = 10 mg/ml
Duration12–24 weeks with escalation and gradual taper
PrecautionsIncrease dose slowly, prioritize protein, stay well hydrated
Tirzepatide 10mg

Tirzepatide

02
Dual GLP-1 / GIP Agonist — 10mg
99% Purity Metabolic

Tirzepatide revolutionized the field by demonstrating that the combined activation of GLP-1 and GIP produces results superior to any single agonist. In the SURMOUNT-1 trial (NEJM, 2022), it achieved reductions of up to 22.5% in body weight. It offers better glycemic control, less metabolic fatigue, and greater energy efficiency than semaglutide.

Key Benefits
Greater fat loss than single GLP-1 agonists
Better glycemic control and insulin sensitivity
Less metabolic fatigue during calorie deficit
Greater energy efficiency and nutrient partitioning
Better adherence to nutrition plans
One weekly injection
Mechanism of Action
A dual agonist that acts on GLP-1 receptors (appetite suppression, delayed gastric emptying, improved insulin secretion) and GIP receptors (improved energy use, metabolic sensitivity, and nutrient partitioning). The combination of both pathways generates a synergy that clinically outperforms each receptor on its own.
Usage Reference
RouteSubcutaneous, once weekly
Escalation2.5 mg → 5.0 → 7.5 → 10.0 mg (every 4 weeks)
Range2.5–15 mg/week
Reconstitution1 ml BAC per 10 mg vial = 10 mg/ml
Duration12–24+ weeks
PrecautionsEscalate gradually, prioritize protein, stay hydrated
GHK-Cu 50mg

GHK-Cu

03
Copper Peptide — Regeneration and Anti-Aging — 50mg
99% Purity Anti-Aging Regeneration

GHK-Cu is a natural tripeptide (Glycine-Histidine-Lysine bound to copper) discovered in human plasma in the 1970s. Its levels decline with age, and reintroducing it activates cellular repair processes, collagen and elastin synthesis, and improvements in hair health. It is one of the most studied peptides in anti-aging and dermal regeneration.

Key Benefits
Stimulates collagen and elastin: firmer, more elastic skin
Accelerates healing and repair of microlesions
Strengthens hair follicle and reduces shedding
Reduces chronic inflammation at cellular level
Activates genes related to repair and longevity
Versatile: topical, injectable, or microneedling
Mechanism of Action
GHK-Cu modulates the expression of more than 4,000 genes, stimulating the synthesis of collagen, glycosaminoglycans, and proteoglycans. It promotes angiogenesis, attracts repair cells to the site of damage, and reduces pro-inflammatory cytokines. Copper acts as an essential enzymatic cofactor in the formation of superoxide dismutase (SOD).
Usage Reference
RouteSubcutaneous, topical, or microneedling
SC Dose1–2 mg daily
Reconstitution1–2 ml BAC per 50 mg vial
Duration4–8 weeks, cyclic
CompatibilityAvoid combination with topical zinc (Cu-Zn antagonism)
PrecautionsModerate doses, cycle use, do not use continuously without a break
NAD+ 500mg

NAD+

04
Nicotinamide Adenine Dinucleotide — 500mg
99% Purity Longevity Cellular Energy

NAD+ is a fundamental coenzyme present in all living cells, essential for cellular energy production (ATP), DNA repair, and the activation of sirtuins (longevity proteins). Its levels decline significantly with age, and replenishment is associated with improvements in energy, cognitive function, and markers of aging.

Key Benefits
Increases cellular energy production (ATP)
Activates sirtuins: key longevity proteins
Supports the repair of damaged DNA
Improves cognitive function and mental clarity
Reduces chronic fatigue and improves recovery
Anti-aging support at the mitochondrial level
Mechanism of Action
NAD+ acts as an electron donor and acceptor in mitochondrial redox reactions, making it essential in the electron transport chain. It activates SIRT1-SIRT7 (sirtuins), which regulate gene expression, fat metabolism, and resistance to oxidative stress. It is also a substrate for PARP (DNA repair) and CD38 (immune regulation).
Usage Reference
RouteSubcutaneous or intravenous (IV)
SC Dose50–200 mg according to protocol
Frequency1–3 times per week
Duration4–12 weeks, cyclic
PrecautionsMay cause flushing (redness); start with low doses
TB-500 + BPC-157 Blend

TB-500 + BPC-157 Blend

05
High-Dose Tissue Repair Blend (10mg + 10mg) — 20mg
99% Purity Repair Recovery

A higher-concentration version of the TB-500 + BPC-157 repair blend, designed for longer protocols or injuries that require greater coverage. The same local + systemic repair synergy, with greater yield per vial and less frequent reconstitution.

Key Benefits
Greater yield per vial for extended protocols
Same repair synergy: local BPC + systemic TB
Ideal for chronic injuries or multiple sites
Reduction of inflammation and chronic pain
Better joint and connective tissue recovery
Lower cost per dose in long protocols
Mechanism of Action
BPC-157 promotes VEGF, EGF, and nitric oxide for local repair. TB-500 regulates actin for cell migration and systemic rebuilding. The higher concentration allows full 8-week protocols with a single vial.
Usage Reference
RouteSubcutaneous (local or abdominal)
Dose250–500 mcg of each component, once daily
Reconstitution2 ml BAC per 20 mg vial (10+10)
Duration6–8 weeks, then a 2–4 week break
PrecautionsRotate injection sites, use aseptic technique
IGF-1 LR3 1mg

IGF-1 LR3

06
Insulin-like Growth Factor 1 (Long R3 variant) — 1mg
99% Purity Growth Advanced

IGF-1 LR3 is a modified version of insulin-like growth factor with an extended half-life. It directly promotes hyperplasia (the creation of new muscle cells) and hypertrophy. It is one of the most powerful compounds for tissue growth, recovery, and advanced body composition.

Key Benefits
Promotes muscular hyperplasia (new fibers)
Improves hypertrophy and post-workout recovery
Powerful anti-catabolic effect
Improves nutrient partitioning toward muscle
Extended half-life vs. standard IGF-1
Synergy with GH protocols
Mechanism of Action
IGF-1 LR3 binds to IGF-1R receptors with lower affinity for binding proteins (IGFBPs), remaining free and active in circulation for longer. It activates the PI3K/Akt and MAPK/ERK pathways, stimulating protein synthesis, cell proliferation, and cell survival in skeletal muscle.
Usage Reference
RouteSubcutaneous or intramuscular
Dose20–80 mcg/day (split pre/post workout)
Reconstitution1 ml BAC per 1 mg vial = 1000 mcg/ml
Duration4–6 weeks maximum, mandatory break
PrecautionsMonitor glucose, do not use continuously, keep cycles short
GHRP-6 10mg

GHRP-6

07
Growth Hormone Releasing Peptide — 10mg
99% Purity Growth Hormone

GHRP-6 is a growth hormone secretagogue that stimulates the pituitary through activation of the ghrelin receptor. In addition to raising GH, it produces a marked increase in appetite, making it ideal for bulking phases or for people who struggle to eat enough.

Key Benefits
Powerful growth hormone stimulation
Significant increase in appetite
Improves muscle recovery and deep sleep
Supports body composition during bulking
Fast action and natural pulsatile effect
Strong synergy with GHRH (CJC-1295)
Mechanism of Action
GHRP-6 activates the GH secretagogue receptor (GHS-R1a), the same receptor as endogenous ghrelin. This produces an acute pulse of GH from the pituitary, while also stimulating the hypothalamic hunger signal. It can also slightly raise cortisol and prolactin, unlike Ipamorelin.
Usage Reference
RouteSubcutaneous
Dose100–300 mcg per application, 1–3 times per day
TimingFasted, before sleep, or post-workout
Duration8–12 weeks, then a 4-week break
PrecautionsAvoid carbohydrates/sugar 30 min before and after
Ipamorelin 10mg

Ipamorelin

08
Selective Growth Hormone Secretagogue — 10mg
99% Purity Growth Hormone Clean Profile

Ipamorelin is the cleanest and most selective GH secretagogue available. Unlike GHRP-6, it does not significantly raise cortisol or prolactin, which makes it ideal for long-term protocols. It stimulates GH in a natural, pulsatile way, improving sleep, recovery, and body composition without adverse hormonal effects.

Key Benefits
Clean GH stimulation without cortisol/prolactin
Better deep sleep quality
Accelerated muscle recovery
Supports progressive fat loss
Exceptional safety profile for prolonged use
Excellent synergy with CJC-1295 No DAC
Mechanism of Action
Ipamorelin selectively activates the GHS-R1a receptor in the pituitary, generating a GH pulse that mimics the body's natural rhythm. Its selectivity means that, at normal doses, it does not produce the rise in cortisol, prolactin, or aldosterone seen with other secretagogues such as GHRP-2 or GHRP-6.
Usage Reference
RouteSubcutaneous
Dose100–300 mcg, 1–2 times per day
TimingBefore sleep (key) and/or fasted
Duration8–16 weeks
PrecautionsAvoid sugar before applying; do not combine with meals
BPC-157 2mg

BPC-157

09
Body Protection Compound — The Architect of Repair — 2mg
99% Purity Repair Neuroprotective

BPC-157 is a fragment of a natural gastric protein with one of the most extensive preclinical evidence bases in peptide research. It accelerates healing, improves local blood flow, protects nerves, and reduces inflammation. Its versatility makes it useful for everything from sports injuries to intestinal repair.

Key Benefits
Accelerated repair of tendons and ligaments
Healing of muscle injuries
Repair of leaky gut
Reduction of chronic pain and inflammation
Documented neuroprotective support
Improved post-workout recovery
Mechanism of Action
BPC-157 promotes the expression of VEGF (vascular endothelial growth factor) and EGF (epidermal growth factor), stimulating angiogenesis and tissue repair. It modulates nitric oxide synthesis and has documented effects on the dopamine system pathway. Its action is mainly local in the application area.
Usage Reference
RouteSubcutaneous (local to the affected area)
Dose250–500 mcg daily
Reconstitution1 ml BAC per 2 mg vial = 2000 mcg/ml
Duration2–4 weeks, pause and repeat
PrecautionsModerate dose, stay hydrated, do not prolong without breaks
Epithalon 10mg

Epithalon

10
Longevity and Telomeric Protection Peptide — 10mg
99% Purity Longevity Telomere

Epithalon (Epitalon) is a tetrapeptide developed in Russia focused on activating telomerase, the enzyme that protects telomeres and regulates cellular aging. It also optimizes circadian rhythm, melatonin production, and age-related hormonal functions. It is not cosmetic: it is deep aging biology.

Key Benefits
Telomerase activation: telomere protection
Regulation of circadian rhythm and melatonin
Improves deep, restorative sleep
Documented systemic anti-aging effect
Cardiovascular and immune support
Short protocols (1–2 times per year)
Mechanism of Action
Epithalon activates the telomerase reverse subunit (hTERT), the enzyme responsible for elongating telomeres at chromosomal ends. It also stimulates the pineal gland to normalize melatonin production and regulate neuroendocrine functions associated with aging.
Usage Reference
RouteSubcutaneous
Dose5–10 mg daily
Duration10–20 days, 1–2 times per year
Reconstitution1–2 ml BAC per 10 mg vial
PrecautionsShort cycles only, no continuous use, sleep well during protocol
CJC-1295 No DAC 5mg

CJC-1295 No DAC

11
Natural GH Stimulator — Pulsatile Version — 5mg
99% Purity Growth Hormone

CJC-1295 without DAC (also called Mod GRF 1-29) is an optimized version of natural GHRH that generates physiological pulses of growth hormone. Because it has a short half-life, it mimics the natural pulses of GH without saturating receptors or producing constant stimulation. It is the ideal complement to Ipamorelin.

Key Benefits
Stimulates GH naturally and in pulses
Respects the body's hormonal feedback
Improves deep sleep and recovery
Progressive fat loss
Better skin, hair, and tissue quality
Powerful synergy with Ipamorelin
Mechanism of Action
It binds to GHRH receptors in the pituitary, amplifying endogenous GH release with each natural pulse. Unlike the version with DAC, it does not artificially extend its half-life, preserving the physiological pattern of hormonal secretion.
Usage Reference
RouteSubcutaneous
Dose100–150 mcg per application, 1–3 times per day
TimingBefore sleep (key), fasted, post-workout
Duration8–16 weeks
PrecautionsAvoid sugar before applying; do not saturate receptors
Tesamorelin 10mg

Tesamorelin

12
Visceral Fat Reducer — Clinically Approved — 10mg
99% Purity Growth Hormone Clinically Approved

Tesamorelin is the only GH-stimulating peptide with formal clinical approval. It was specifically approved for the reduction of visceral (deep abdominal) fat associated with HIV lipodystrophy. Additional studies in adults without HIV show significant improvements in insulin sensitivity and metabolic profile.

Key Benefits
Specific reduction of deep abdominal fat
Improves insulin sensitivity
Natural increase in GH and IGF-1
Better overall metabolic profile
Does not suppress endogenous production
Only peptide in its class with clinical approval
Mechanism of Action
A synthetic GHRH analog that stimulates the pituitary to release GH in a sustained manner. Elevated GH activates lipolysis (especially visceral lipolysis) and raises IGF-1, improving body composition and lipid metabolism without the effects of exogenous GH.
Usage Reference
RouteSubcutaneous
Dose2 mg daily
TimingBefore sleep
Duration12–26 weeks
PrecautionsMonitor glucose and IGF-1; monitor sodium
MOTS-c 10mg

MOTS-c

13
Mitochondrial Peptide — Exercise Mimetic — 10mg
99% Purity Metabolic Mitochondrial

MOTS-c is a peptide derived from mitochondrial DNA that regulates mitochondria-to-nucleus communication. It is called an 'exercise mimetic' because it partially reproduces the metabolic effects of exercise: it improves insulin sensitivity, activates AMPK, and optimizes energy metabolism.

Key Benefits
Improves insulin sensitivity and glucose metabolism
AMPK activation (master energy sensor)
Reduction of body fat and prevention of obesity
Improves performance and physical capacity
Reduction of inflammatory markers
Promotes bone health and metabolic function
Mechanism of Action
MOTS-c is encoded by the mitochondrial genome (not the nuclear genome) and acts as a mitonuclear signal. It activates AMPK, the cell's master energy sensor, and inhibits MTHFR in the pentose phosphate pathway. It improves muscular glucose uptake and modulates one-carbon metabolism, simulating the effects of exercise at the molecular level.
Usage Reference
RouteSubcutaneous
Dose5 mg per injection, 3–5 times per week
TimingMorning or pre-physical activity
Duration4–8 weeks
PrecautionsAvoid combining with metformin without supervision
Selank 10mg

Selank

14
Intelligent Anxiolytic Peptide — 10mg
99% Purity Cognitive Anxiolytic

Selank was developed in Russia in the 1990s as a safe alternative to benzodiazepines: no addiction, no tolerance, no sedation, no cognitive impairment. It is a synthetic analog of tuftsin (an immune system peptide), optimized to act in the brain. It returns you to an optimal state of mental functioning.

Key Benefits
Reduces anxiety without sedation or dulling
Greater focus and mental clarity
Better working memory and decision-making
Improves sleep quality (indirectly)
Neuroprotective and reduces oxidative stress
Does not produce dependence or tolerance
Mechanism of Action
It modulates the GABAergic system (the brain's natural brake), regulates serotonin and dopamine, reduces neuronal hyperactivity associated with anxiety, and improves communication between neurons. It does not force relaxation: it restores neurochemical balance.
Usage Reference
RouteIntranasal (primary) or subcutaneous
Nasal Dose250–300 mcg, 1–2 times per day
SC Dose250–500 mcg, once daily
Duration10–14 days, then a 1–2 week break
PrecautionsMorning or early day; avoid night if it activates mental clarity
Semax 10mg

Semax

15
Nootropic and Neuroprotective Peptide — 10mg
99% Purity Cognitive Nootropic

Semax is a synthetic heptapeptide analogous to the ACTH 4-10 fragment, with no real hormonal activity. Developed in Russia to treat ischemic brain damage, it is now used for its powerful nootropic effects: it improves memory, learning, and attention. It entered the Russian Federation's List of Vital Medicines in 2011.

Key Benefits
Enhances memory, learning, and attention
Increases BDNF (brain neurotrophic factor)
Neuroprotection against ischemia and stress
Improves mood without sedative effects
Greater resilience to stress and mental fatigue
Reduces anxiety in high cognitive-demand settings
Mechanism of Action
It increases the expression of BDNF (Brain-Derived Neurotrophic Factor), which is essential for neuronal survival and synaptic plasticity. It modulates neurotransmitters such as dopamine and serotonin. It protects neurons against damage from oxidative stress, ischemia, and excitotoxicity.
Usage Reference
RouteIntranasal (primary) or subcutaneous
Nasal Dose250–1000 mcg, 1–3 times per day
SC Dose300–600 mcg, once daily
Duration10–14 intensive days or 2–4 cognitive weeks
PrecautionsMorning only; avoid night (may cause insomnia)
GLOW Blend 70mg

GLOW Blend

16
BPC-157 + TB-500 + GHK-Cu — Total Regeneration — 70mg
99% Purity Premium Blend Regeneration

GLOW is a triple blend that combines three regenerative peptides: BPC-157 for local tissue repair, TB-500 for systemic regeneration, and GHK-Cu for cellular rejuvenation, collagen support, and dermal health. It is the all-in-one protocol for recovery, aesthetics, and anti-aging in a single solution.

Key Benefits
Triple synergy: repair + regeneration + rejuvenation
Improvement of skin, hair, and connective tissue
Accelerated injury recovery
Stimulation of collagen and elastin (GHK-Cu)
Reduction of systemic inflammation
Simplified protocol: one vial, multiple benefits
Mechanism of Action
BPC-157 activates VEGF/EGF for local repair. TB-500 regulates actin for systemic cell migration. GHK-Cu modulates more than 4,000 genes linked to collagen, antioxidation, and cellular longevity. The combination covers repair, regeneration, and rejuvenation in a single protocol.
Usage Reference
RouteSubcutaneous (also compatible with microneedling for GHK-Cu)
DoseAccording to the blend ratio, 0.3–0.5 ml daily
Reconstitution2–3 ml BAC per 70 mg vial
Duration6–8 weeks, then a 2–4 week break
PrecautionsAvoid topical zinc with GHK-Cu, rotate sites, use aseptic technique

Important Notice

This catalog is for educational purposes only. It does not constitute medical advice or a therapeutic recommendation of any kind. The use of research compounds should be carried out under medical supervision.