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14408-25A cell-permeable, cyclic nucleotide derivative that mimics the action of endogenous cAMP and is a phosphodiesterase inhibitor.
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14408-250A cell-permeable, cyclic nucleotide derivative that mimics the action of endogenous cAMP and is a phosphodiesterase inhibitor.
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14408-50A cell-permeable, cyclic nucleotide derivative that mimics the action of endogenous cAMP and is a phosphodiesterase inhibitor.
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15407-100A glucocorticoid steroid that activates the glucorcorticoid receptor with an EC<sub>50</sub> value of 12.4 nM reduces inflammation and has utility in inflammatory diseases, like asthma and inflammatory bowel disease may be abused by athletes.
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15407-250A glucocorticoid steroid that activates the glucorcorticoid receptor with an EC<sub>50</sub> value of 12.4 nM reduces inflammation and has utility in inflammatory diseases, like asthma and inflammatory bowel disease may be abused by athletes.
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15407-50A glucocorticoid steroid that activates the glucorcorticoid receptor with an EC<sub>50</sub> value of 12.4 nM reduces inflammation and has utility in inflammatory diseases, like asthma and inflammatory bowel disease may be abused by athletes.
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15407-500A glucocorticoid steroid that activates the glucorcorticoid receptor with an EC<sub>50</sub> value of 12.4 nM reduces inflammation and has utility in inflammatory diseases, like asthma and inflammatory bowel disease may be abused by athletes.
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15725-10A cardiotonic steroid that inhibits theNa+/K+-ATPase transporter (Kds = 42, 45, and 40 nM for the &alpha1, &alpha2, and &alpha3 subunits, respectively) inhibits SRC-1 and SRC-3 at doses as low as 5 nM, promotes the degradation of SRC-3 protein,
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15725-25A cardiotonic steroid that inhibits theNa+/K+-ATPase transporter (Kds = 42, 45, and 40 nM for the &alpha1, &alpha2, and &alpha3 subunits, respectively) inhibits SRC-1 and SRC-3 at doses as low as 5 nM, promotes the degradation of SRC-3 protein,
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15725-5A cardiotonic steroid that inhibits theNa+/K+-ATPase transporter (Kds = 42, 45, and 40 nM for the &alpha1, &alpha2, and &alpha3 subunits, respectively) inhibits SRC-1 and SRC-3 at doses as low as 5 nM, promotes the degradation of SRC-3 protein,
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15725-50A cardiotonic steroid that inhibits theNa+/K+-ATPase transporter (Kds = 42, 45, and 40 nM for the &alpha1, &alpha2, and &alpha3 subunits, respectively) inhibits SRC-1 and SRC-3 at doses as low as 5 nM, promotes the degradation of SRC-3 protein,
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18507-100A biguanide that exhibits antihyperglycemic activity by increasing glucose utilization and inhibiting hepatic gluconeogenesis inhibits the mitochondrial respiratory complex I and the mitochondrial ATP synthase disrupts the unfolded protein