YK11 Oral Steroids Tablets 10mg 100pcs
Original price was: $100.00.$70.00Current price is: $70.00.Myostatin inhibitor SARM for muscle growth research. Study follistatin upregulation and AR activation.
Showing 97–112 of 114 resultsSorted by popularity
Myostatin inhibitor SARM for muscle growth research. Study follistatin upregulation and AR activation.
Andarine (S4) is a tissue-selective SARM that binds the androgen receptor with high affinity and preferentially activates androgen response elements in skeletal muscle and bone over prostate tissue. Its 4-hour half-life requires optimized dosing protocols.
AICAR is a cell-permeable nucleoside analog that converts intracellularly to ZMP, potently activating AMPK to mimic exercise-induced metabolic stress. An oral formulation for investigating mitochondrial biogenesis and insulin-independent glucose disposal.
SR9009 is a Rev-ErbA nuclear receptor agonist that suppresses BMAL1 and CLOCK gene transcription to reprogram circadian metabolic rhythms. It upregulates mitochondrial biogenesis and fatty acid oxidation in skeletal muscle, functioning as an exercise mimetic.
MAST Blend-200 is a dual-ester Drostanolone formulation combining Propionate (rapid) and Enanthate (sustained) esters for staggered androgen receptor activation. The 2-methyl modification prevents aromatization, delivering pure DHT-derivative signaling.
DHB (1-Testosterone) is a potent 5-alpha reduced androgen with a 1-ene double bond that enhances anabolic potency while being immune to aromatization and 5-alpha reductase conversion. It delivers pure, dry myofibrillar protein synthesis signaling.
Primary androgen for AR activation and anabolic signaling research. Study protein synthesis and nitrogen retention.
Turinabol (4-Chlorodehydromethyltestosterone) is a Dianabol derivative with a 4-chloro substitution that prevents aromatization while preserving potent anabolic signaling. It drives clean, dry lean tissue accrual without estrogenic water retention.
T3 (Liothyronine Sodium) is the synthetic form of the active thyroid hormone triiodothyronine that directly binds nuclear thyroid receptors to dramatically accelerate basal metabolic rate and cellular oxygen consumption. A fundamental tool for thermogenesis and metabolic research.
Primobolan (Methenolone Acetate) is a mild oral DHT derivative with a 1-methyl group that resists hepatic deactivation without C17-alkylation. It delivers clean, estrogen-free anabolic signaling with minimal hepatotoxicity, ideal for lean tissue preservation research.
Primobolan (Methenolone Acetate) is a mild oral DHT derivative with a 1-methyl group that resists hepatic deactivation without C17-alkylation. It delivers clean, estrogen-free anabolic signaling with minimal hepatotoxicity, ideal for lean tissue preservation research.
Proviron (Mesterolone) is a 1-methyl DHT derivative with exceptionally high affinity for SHBG, effectively displacing endogenous testosterone to increase free androgen concentrations. It provides oral androgen receptor activation without significant hepatic strain from C17-alkylation.
Exemestane (Aromasin) is a steroidal Type I aromatase inhibitor that acts as a suicide substrate, irreversibly binding and permanently deactivating the CYP19A1 enzyme. With a 24-hour half-life, it produces marked and sustained estrogen suppression.
Winstrol (Stanozolol) Aqueous Suspension 50mg/ml is a water-based injectable DHT derivative that provides rapid non-genomic signaling through microsomal androgen receptors. It inhibits SHBG to increase free androgen bioavailability for lean tissue research.
19-nor androgen for potent AR activation and anti-catabolic research. Study nitrogen retention pathways.
MENT (Trestolone Acetate) is a potent 7-alpha-methyl-19-nortestosterone injectable androgen that binds the androgen receptor with affinity significantly exceeding testosterone. The acetate ester provides rapid bioavailability for investigating acute myogenic transcription.
End of content
End of content
No products in the cart.