Biochemical Pharmacology

dc.contributor.authorReddy, G.R.
dc.contributor.authorUeda, N
dc.contributor.authorHada, T
dc.contributor.authorSackeyfio, A.C.
dc.contributor.authorYamamoto, S
dc.contributor.authorHano, Y
dc.contributor.authorNomura, T
dc.date.accessioned2013-06-21T13:41:54Z
dc.date.accessioned2017-10-16T11:43:36Z
dc.date.available2013-06-21T13:41:54Z
dc.date.available2017-10-16T11:43:36Z
dc.date.issued1991
dc.description.abstractSeveral naturally occurring prenylflavones were tested for their inhibitory actions on arachidonate 5-lipoxygenase purified from porcine leukocytes. Of the compounds tested, artonin E (5'-hydroxymorusin) exhibited the most potent inhibition on arachidonate 5-lipoxygenase (IC50 = 0.36 microM). Arachidonate 12-lipoxygenase purified from porcine leukocytes and human platelets, 15-lipoxygenase from rabbit reticulocytes and fatty acid cyclooxygenase from bovine vesicular glands were inhibited by the compound only at higher concentrations (IC50 = 2.3, 11, 5.2 and 2.5 microM, respectively).en_US
dc.identifier.citationReddy, G. R., Ueda, N., Hada, T., Sackeyfio, A. C., Yamamoto, S., Hano, Y., . . . Nomura, T. (1991). A prenylflavone, artonin E, as arachidonate 5-lipoxygenase inhibitor. Biochemical Pharmacology, 41(1), 115-118.en_US
dc.identifier.urihttp://197.255.68.203/handle/123456789/3838
dc.language.isoenen_US
dc.publisherBiochemical Pharmacologyen_US
dc.titleBiochemical Pharmacologyen_US
dc.typeArticleen_US

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