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CARDARINE 10 mg – 60 Tablets – Oral Administration
(0)$50.00Add to cartCardarine is a PPAR-delta modulator that activates mitochondrial lipid oxidation and enhances aerobic endurance capacity, without stimulating the central nervous system or suppressing the hormonal axis. It accelerates visceral fat burning, dramatically improves cardiovascular performance, optimizes lipid profile and protects endothelial vascular function, being useful in extreme cutting phases, sports performance optimization and metabolic sensitivity improvement.
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IBUTAMOREN 15 mg 50 Tablets – Oral Administration
(0)$60.00Add to cartIbutamoren MK-677 is a non-peptide growth hormone secretagogue that mimics ghrelin’s action to enhance endogenous pulsatile GH and IGF-1 secretion, without suppressing the hypothalamic-pituitary axis or compromising natural testosterone production. It promotes anabolic protein synthesis, speeds up tissue recovery and deep restorative sleep, improves bone mineral density and body composition, and boosts the clean appetite needed for bulking phases, making it useful in hypertrophy protocols, post-injury recovery, metabolic anti-aging, and overall wellness optimization.
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LIGANDROL 5 mg – 60 Tablets – Oral Administration
(0)$60.00Add to cartLigandrol (LGD-4033) 5mg is a selective androgen receptor modulator (SARM) that activates the AR anabolic pathway in muscle and bone tissue with high tissue affinity, without converting to estrogens or chronically suppressing the hypothalamic-pituitary-gonadal axis. It enhances myofibrillar protein synthesis, accelerates quality lean mass gain, improves bone density and functional strength, and facilitates recovery between workouts. It is useful in clean bulking phases, body recomposition, muscle atrophy prevention, and structural strengthening protocols without the hepatotoxic burden or androgenic side effects of traditional steroids.
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OSTARINE 10 mg – 60 Tablets – Oral Administration
(0)$60.00Add to cartOstarine (MK2866) 10mg is a highly bioavailable selective androgen receptor modulator (SARM) that activates the anabolic AR pathway in muscle and bone with superior tissue specificity, without aromatization to estrogens or significant hepatotoxicity. It preserves and builds functional lean mass, speeds up joint and tissue recovery, improves bone mineral density, and maintains strength in a calorie deficit, making it useful for conservative cutting phases, body recomposition, post-injury musculoskeletal recovery, mild hormone replacement therapy, and sarcopenia prevention—without severe suppression or classic androgenic side effects.
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TESTOLONE 10 mg – 50 Tablets – Oral Administration
(0)$60.00Add to cartTestolone RAD-140 is a high anabolic potency selective androgen receptor modulator (SARM) that activates the AR pathway in muscle and neuronal tissue with superior affinity to endogenous testosterone, without aromatic conversion to estrogens or direct hepatotoxic load. It enhances dense lean muscle hypertrophy, accelerates neuromuscular recovery, improves cognitive neuroprotection and bone density, and optimizes explosive strength and functional endurance, being useful in aggressive bulking stages, advanced recomp, sports neuroprotection, and maximum anabolic optimization protocols with minimal water retention and an attenuated androgenic side effect profile compared to traditional steroids.
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YK11 5 mg – 60 Tablets – Oral Administration
(0)$60.00Add to cartYK-11 5mg is a steroidal selective androgen receptor modulator (SARM) with myostatin inhibitory activity that enhances muscle hypertrophy through AR activation and blocking the growth-limiting factor, without estrogen aromatization or significant water retention. Induces superior quality lean mass gains and density, accelerates satellite cell differentiation for tissue recovery, improves absolute strength and muscle hardness, and optimizes bone mineralization; useful in advanced bulking stages, overcoming anabolic plateaus, extreme recomp, and protocols for maximum muscle phenotypic expression with genetic potential unlocked via epigenetic inhibition of GDF-8.
