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11679-100A diterpenoid compound that inhibits NF-&kappaB binding to DNA promoters and induces expression of the CYP1A enzymes to produce immunosuppressant, antithrombotic, anti-inflammatory, antineoplastic, antiviral, antibacterial, antidiabetic,
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11679-250A diterpenoid compound that inhibits NF-&kappaB binding to DNA promoters and induces expression of the CYP1A enzymes to produce immunosuppressant, antithrombotic, anti-inflammatory, antineoplastic, antiviral, antibacterial, antidiabetic,
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11679-50A diterpenoid compound that inhibits NF-&kappaB binding to DNA promoters and induces expression of the CYP1A enzymes to produce immunosuppressant, antithrombotic, anti-inflammatory, antineoplastic, antiviral, antibacterial, antidiabetic,
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11679-500A diterpenoid compound that inhibits NF-&kappaB binding to DNA promoters and induces expression of the CYP1A enzymes to produce immunosuppressant, antithrombotic, anti-inflammatory, antineoplastic, antiviral, antibacterial, antidiabetic,
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15872-1A steroid hormone produced in the body from 5&alpha-reduced metabolites of dehydroepiandrosterone that possesses 7-fold weaker androgen potency compared to that of testosterone excreted in urine and used as the international reference standard for
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15872-100A steroid hormone produced in the body from 5&alpha-reduced metabolites of dehydroepiandrosterone that possesses 7-fold weaker androgen potency compared to that of testosterone excreted in urine and used as the international reference standard for
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15872-250A steroid hormone produced in the body from 5&alpha-reduced metabolites of dehydroepiandrosterone that possesses 7-fold weaker androgen potency compared to that of testosterone excreted in urine and used as the international reference standard for
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15872-500A steroid hormone produced in the body from 5&alpha-reduced metabolites of dehydroepiandrosterone that possesses 7-fold weaker androgen potency compared to that of testosterone excreted in urine and used as the international reference standard for
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82230-10A classical nitroxyl (NO-) donor dissociates in a pH-dependent, first order process with a half-life of 2.3 minutes at 37°C, pH 7.4, to liberate 0.54 moles for NO per mole of parent compound.
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82230-100A classical nitroxyl (NO-) donor dissociates in a pH-dependent, first order process with a half-life of 2.3 minutes at 37°C, pH 7.4, to liberate 0.54 moles for NO per mole of parent compound.
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82230-5A classical nitroxyl (NO-) donor dissociates in a pH-dependent, first order process with a half-life of 2.3 minutes at 37°C, pH 7.4, to liberate 0.54 moles for NO per mole of parent compound.
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82230-50A classical nitroxyl (NO-) donor dissociates in a pH-dependent, first order process with a half-life of 2.3 minutes at 37°C, pH 7.4, to liberate 0.54 moles for NO per mole of parent compound.