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BMS-564929 is an investigational selective androgen receptor modulator (SARM) developed by Bristol-Myers Squibb for the treatment of age-related decline in androgen levels in men ("andropause"). It is a highly potent, orally active, nonsteroidal tissue selective modulator that binds to the androgen receptor with a Ki value of 2.11 nM. The compound is approximately 400-fold selective for androgen receptors versus progesterone receptors and more than 1000-fold selective versus glucocorticoid, mineralocorticoid, and estrogen receptors. In preclinical studies, BMS-564929 demonstrated substantially higher potency than testosterone in promoting muscle growth while showing high selectivity for muscle versus prostate tissue, potentially offering a more favorable safety profile than traditional testosterone therapy.
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