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90120-50ETYA is a nonspecific inhibitor of cyclooxygenases and lipoxygenases. ETYA inhibits human platelet 12-LO and COX-1 with IC<sub>50</sub> values of 4 µM and 8 µM, respectively.
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18128-1A dual inhibitor of MRP-1 and BCRP maximally inhibits MRP-1 in isolated human peripheral blood leukocytes at 200 nM effective against both human BCRP and the mouse homolog, Bcrp1.
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18128-10A dual inhibitor of MRP-1 and BCRP maximally inhibits MRP-1 in isolated human peripheral blood leukocytes at 200 nM effective against both human BCRP and the mouse homolog, Bcrp1.
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18128-5A dual inhibitor of MRP-1 and BCRP maximally inhibits MRP-1 in isolated human peripheral blood leukocytes at 200 nM effective against both human BCRP and the mouse homolog, Bcrp1.
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18128-50A dual inhibitor of MRP-1 and BCRP maximally inhibits MRP-1 in isolated human peripheral blood leukocytes at 200 nM effective against both human BCRP and the mouse homolog, Bcrp1.
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90250-100Elaidic acid is the 9-trans isomer of oleic acid. It is a monounsaturated trans-fatty acid which can be found in partially hydrogenated cooking oils.
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90250-1000Elaidic acid is the 9-trans isomer of oleic acid. It is a monounsaturated trans-fatty acid which can be found in partially hydrogenated cooking oils.
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90250-250Elaidic acid is the 9-trans isomer of oleic acid. It is a monounsaturated trans-fatty acid which can be found in partially hydrogenated cooking oils.
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90250-50Elaidic acid is the 9-trans isomer of oleic acid. It is a monounsaturated trans-fatty acid which can be found in partially hydrogenated cooking oils.
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15583-1A macrodiolide antibiotic that displays anti-protozoal activity against both Plasmodium and Trypanosoma (IC<sub>50</sub>s = 370 and 460 ng/ml, respectively) and cytotoxicity against MRC-5 cells (IC<sub>50</sub> = 870 ng/ml) enhances the anti-fungal
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15583-5A macrodiolide antibiotic that displays anti-protozoal activity against both Plasmodium and Trypanosoma (IC<sub>50</sub>s = 370 and 460 ng/ml, respectively) and cytotoxicity against MRC-5 cells (IC<sub>50</sub> = 870 ng/ml) enhances the anti-fungal
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18398-1A non-competitive NMDA receptor antagonist that inhibits neuronal calcium channel currents selective for NR2B subunit-containing receptors (IC<sub>50</sub> = 1 µM), displaying greater than 100-fold selectivity for NR2B over NR2A and NR2C