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LGD-4033 (Ligandrol) is a highly potent non-steroidal SARM with a 24-36 hour half-life and an exceptionally favorable anabolic-to-androgenic ratio. It selectively drives skeletal muscle protein synthesis with minimal impact on secondary androgenic organs.
GW-501516 (Cardarine) is a high-affinity PPAR-delta agonist that recruits PGC-1alpha co-activators to upregulate fatty acid oxidation, mitochondrial biogenesis, and Type I oxidative fiber conversion. An excellent endurance-enhancing research compound.
MK-677 (Ibutamoren) is a potent non-peptide ghrelin receptor agonist that stimulates endogenous pulsatile GH release from the pituitary without desensitization. It also elevates IGF-1 levels for full-scale somatotropic axis activation.
MK-2866 (Ostarine) is a non-steroidal SARM that selectively agonizes androgen receptors in muscle and bone tissue with a Ki of 3.8 nM. Its 24-hour half-life provides steady receptor occupancy for investigating lean tissue preservation and muscle wasting prevention.
RAD140 is a potent non-steroidal SARM with a 60-hour half-life that selectively agonizes skeletal muscle androgen receptors with minimal prostate or sebaceous gland activity. It drives myofibrillar protein synthesis and exhibits neuroprotective properties.
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.
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.
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