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Complete guide to RAD-140, LGD-4033, MK-2866 and research SARMs — androgen receptor selectivity, tissue-specific activity and published pharmacokinetic research.
Selective Androgen Receptor Modulators (SARMs) are a class of research compounds that bind to the androgen receptor with tissue selectivity, distinguishing them from traditional anabolic steroids in research models.
Mechanism of Action: SARMs act as partial or full agonists at the androgen receptor. Their selectivity arises from differential receptor conformation changes upon binding in different tissues — muscle and bone versus liver and other androgen-sensitive tissues. This tissue-selective activity makes them valuable research tools for examining androgen receptor biology.
Key Research SARMs: RAD-140 (Testolone) shows high binding affinity and has been studied for potential neuroprotective properties alongside anabolic effects. LGD-4033 (Ligandrol) has one of the most extensive published pharmacokinetic profiles among research SARMs, with clinical studies examining dose-response and half-life. MK-2866 (Ostarine) is the most published SARM with research examining muscle preservation and bone density effects. GW-501516 (Cardarine) is technically a PPARδ agonist rather than a SARM — research examines fatty acid oxidation and endurance capacity. YK-11 is unique as both a SARM and myostatin inhibitor, studied for dual anabolic mechanism. S4 (Andarine) and S23 have been studied for receptor binding selectivity and anabolic activity.
All research SARMs from UK Peptides are supplied in capsule form at 99%+ purity with HPLC verification. For research use only.
81 compounds. 99%+ purity. COA verified. Min. £100 order. Next-day UK delivery.
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