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Hinokitiol, a selective inhibitor of the platelet-type isozyme of arachidonate 12-lipoxygenase
Authors:Suzuki H  Ueda T  Juránek I  Yamamoto S  Katoh T  Node M  Suzuki T
Institution:Department of Biochemistry, Tokushima University School of Medicine, Kuramoto-cho, Tokushima, 770-8503, Japan. suzuki@basic.med.tokushima-u.ac.jp
Abstract:Hinokitiol (4-isopropyltropolone), a constituent of Japanese cypress, reversibly inhibited platelet-type 12-lipoxygenase with an IC(50) of 0.1 microM, and the enzyme activity was almost lost at 1 microM. The compound was much less active with other lipoxygenase enzymes with higher IC(50) values (leukocyte-type 12-lipoxygenase, 50 microM; soybean lipoxygenase, 17 microM; 15-lipoxygenase-1, >100 microM; 5-lipoxygenase, 17 microM). Hinokitiol up to 100 microM had almost no effect on cyclooxygenases-1 and -2. Their structure-activity relationship examined with various tropolone derivatives indicated the requirements of the 2-hydroxyl group and 4-alkyl group for the potent and selective inhibition of platelet-type 12-lipoxygenase.
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