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C351074-100mgA selective inhibitor of the 20-HETE synthase CYP4A11 displaying an IC|50|value of 8.8 nM when tested in human renal microsomes. Less potent as an inhibitor of 1A, 1C, and 3A CYP450 enzymes.
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C351074-10mgA selective inhibitor of the 20-HETE synthase CYP4A11 displaying an IC|50|value of 8.8 nM when tested in human renal microsomes. Less potent as an inhibitor of 1A, 1C, and 3A CYP450 enzymes.
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C351074-25mgA selective inhibitor of the 20-HETE synthase CYP4A11 displaying an IC|50|value of 8.8 nM when tested in human renal microsomes. Less potent as an inhibitor of 1A, 1C, and 3A CYP450 enzymes.
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C351074-50mgA selective inhibitor of the 20-HETE synthase CYP4A11 displaying an IC|50|value of 8.8 nM when tested in human renal microsomes. Less potent as an inhibitor of 1A, 1C, and 3A CYP450 enzymes.
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C351074-5mgA selective inhibitor of the 20-HETE synthase CYP4A11 displaying an IC|50|value of 8.8 nM when tested in human renal microsomes. Less potent as an inhibitor of 1A, 1C, and 3A CYP450 enzymes.
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C350984-100μgA PGF2α analog containing a thio-fluorobenzene substituent in the lower side chain. Has an IC|50|of about 30 nM when tested for binding to recombinant human FP receptors.
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C350984-500μgA PGF2α analog containing a thio-fluorobenzene substituent in the lower side chain. Has an IC|50|of about 30 nM when tested for binding to recombinant human FP receptors.
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