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19648-1A biscoclaurine alkaloid that can decrease the fluidity of biological membranes exhibits antiparasitic, antimalarial, antiviral, anti-inflammatory, antimetastatic, and anticancer activities in various cell and animal models.
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19648-100A biscoclaurine alkaloid that can decrease the fluidity of biological membranes exhibits antiparasitic, antimalarial, antiviral, anti-inflammatory, antimetastatic, and anticancer activities in various cell and animal models.
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19648-50A biscoclaurine alkaloid that can decrease the fluidity of biological membranes exhibits antiparasitic, antimalarial, antiviral, anti-inflammatory, antimetastatic, and anticancer activities in various cell and animal models.
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19648-500A biscoclaurine alkaloid that can decrease the fluidity of biological membranes exhibits antiparasitic, antimalarial, antiviral, anti-inflammatory, antimetastatic, and anticancer activities in various cell and animal models.
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11092-10A non-lipid inhibitor of cellular ceramidase activity (IC50 = 28 &muM in a cell-based assay) induces the accumulation of endogenous ceramide species and decreases intracellular levels of sphingosine and S1P inhibits cell proliferation of ovarian
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11092-25A non-lipid inhibitor of cellular ceramidase activity (IC50 = 28 &muM in a cell-based assay) induces the accumulation of endogenous ceramide species and decreases intracellular levels of sphingosine and S1P inhibits cell proliferation of ovarian
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11092-5A non-lipid inhibitor of cellular ceramidase activity (IC50 = 28 &muM in a cell-based assay) induces the accumulation of endogenous ceramide species and decreases intracellular levels of sphingosine and S1P inhibits cell proliferation of ovarian
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11092-50A non-lipid inhibitor of cellular ceramidase activity (IC50 = 28 &muM in a cell-based assay) induces the accumulation of endogenous ceramide species and decreases intracellular levels of sphingosine and S1P inhibits cell proliferation of ovarian
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15500-2.5A natural antifungal phytotoxin that selectively and potently inhibits fungal Pkc1, which are central to cell wall integrity (IC<sub>50</sub> = 25 nM for Candida Pkc1) potently inhibits MAPK-interacting kinases Mnk1 and Mnk2 (IC<sub>50</sub> = 115
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15500-500A natural antifungal phytotoxin that selectively and potently inhibits fungal Pkc1, which are central to cell wall integrity (IC<sub>50</sub> = 25 nM for Candida Pkc1) potently inhibits MAPK-interacting kinases Mnk1 and Mnk2 (IC<sub>50</sub> = 115
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19374-1An inhibitor of ALK with an IC<sub>50</sub> value of 200 pM in enzymatic assays inhibits ALK in cells (IC<sub>50</sub> = 25 nM) and in vivo, producing tumor regression in a rat xenograft model.
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19374-10An inhibitor of ALK with an IC<sub>50</sub> value of 200 pM in enzymatic assays inhibits ALK in cells (IC<sub>50</sub> = 25 nM) and in vivo, producing tumor regression in a rat xenograft model.