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10005913-10A potent antagonist for the human IP (prostacyclin) receptor that antagonizes the carbaprostacyclin-induced activation of human neuroblastoma adenylate cyclase, blocking cAMP accumulation in a dose-dependent manner inhibits the binding of tritiated
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10005913-25A potent antagonist for the human IP (prostacyclin) receptor that antagonizes the carbaprostacyclin-induced activation of human neuroblastoma adenylate cyclase, blocking cAMP accumulation in a dose-dependent manner inhibits the binding of tritiated
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10005913-5A potent antagonist for the human IP (prostacyclin) receptor that antagonizes the carbaprostacyclin-induced activation of human neuroblastoma adenylate cyclase, blocking cAMP accumulation in a dose-dependent manner inhibits the binding of tritiated
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10075-1A celecoxib analog that retains potent, selective COX-2 inhibitory activity (IC50 = 32 nM).
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10075-10A celecoxib analog that retains potent, selective COX-2 inhibitory activity (IC50 = 32 nM).
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10075-25A celecoxib analog that retains potent, selective COX-2 inhibitory activity (IC50 = 32 nM).
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10075-5A celecoxib analog that retains potent, selective COX-2 inhibitory activity (IC50 = 32 nM).
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10005072-1A labeled analog of AEA that is non-fluorescent when outside the cell but upon transport into the cell, is cleaved by esterases to give a bright fluorescence at 530 nm used as an alternative substrate to study AEA transport via the AEA transporter.
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10005072-100A labeled analog of AEA that is non-fluorescent when outside the cell but upon transport into the cell, is cleaved by esterases to give a bright fluorescence at 530 nm used as an alternative substrate to study AEA transport via the AEA transporter.
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10005072-500A labeled analog of AEA that is non-fluorescent when outside the cell but upon transport into the cell, is cleaved by esterases to give a bright fluorescence at 530 nm used as an alternative substrate to study AEA transport via the AEA transporter.
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10006400-1CAY10462 is the hydrochloride salt of CAY10434 and selective inhibitor of the 20-HETE synthase CYP4A11 exhibiting an IC50 of 8.8 nM when tested in human renal microsomes.
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10006400-10CAY10462 is the hydrochloride salt of CAY10434 and selective inhibitor of the 20-HETE synthase CYP4A11 exhibiting an IC50 of 8.8 nM when tested in human renal microsomes.