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19870-100A natural anthraquinone with antibacterial, antiviral, anti-inflammatory, and anticancer activity in various research models inhibits hepatitis B viral DNA production diminishes the expression of iNOS and COX-2 induces necrosis in cancer cells.
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19870-50A natural anthraquinone with antibacterial, antiviral, anti-inflammatory, and anticancer activity in various research models inhibits hepatitis B viral DNA production diminishes the expression of iNOS and COX-2 induces necrosis in cancer cells.
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19870-500A natural anthraquinone with antibacterial, antiviral, anti-inflammatory, and anticancer activity in various research models inhibits hepatitis B viral DNA production diminishes the expression of iNOS and COX-2 induces necrosis in cancer cells.
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11021-10An inhibitor of Nampt and NF-&kappaB pathway activity potent cytotoxic effects in human breast (IC50 = 7.3 nM) and lung cancer (IC50 = 0.
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11021-25An inhibitor of Nampt and NF-&kappaB pathway activity potent cytotoxic effects in human breast (IC50 = 7.3 nM) and lung cancer (IC50 = 0.
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11021-5An inhibitor of Nampt and NF-&kappaB pathway activity potent cytotoxic effects in human breast (IC50 = 7.3 nM) and lung cancer (IC50 = 0.
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11021-50An inhibitor of Nampt and NF-&kappaB pathway activity potent cytotoxic effects in human breast (IC50 = 7.3 nM) and lung cancer (IC50 = 0.
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15114-10A potent inhibitor of chymotrypsin and chymase (Ki = 9.36 and 13.1 nM, respectively), that less effectively blocks the activity of cathepsins, papain, and leukocyte elastase.
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15114-25A potent inhibitor of chymotrypsin and chymase (Ki = 9.36 and 13.1 nM, respectively), that less effectively blocks the activity of cathepsins, papain, and leukocyte elastase.
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15114-5A potent inhibitor of chymotrypsin and chymase (Ki = 9.36 and 13.1 nM, respectively), that less effectively blocks the activity of cathepsins, papain, and leukocyte elastase.
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11580-10A potent inhibitor of MEK in (IC50 = 2.3 nM Kd = 74 nM when activated with ATP) that suppresses phosphorylation of ERK in mouse colon 26 tumors (IC50 = 35 nM).
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11580-25A potent inhibitor of MEK in (IC50 = 2.3 nM Kd = 74 nM when activated with ATP) that suppresses phosphorylation of ERK in mouse colon 26 tumors (IC50 = 35 nM).