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Leukotriene biosynthesis inhibition by aryl and aroyl substituted naphthoquinones.

作者信息

Roland D M, Macchia W M, Grim K S, Kimble E F, White D H, Kowalski T J

机构信息

Research Department, CIBA-GEIGY Corp., Summit, NJ 07901.

出版信息

Agents Actions. 1991 Sep;34(1-2):145-7. doi: 10.1007/BF01993262.

Abstract

Naphthoquinones are known to inhibit 5-lipoxygenase. In particular, CGS 8515 (methyl 2-[(3,4-dihydro-3,4-dioxo-1-naphthalenyl)amino]benzoate) has been studied in detail. However this potent and selective 5-lipoxygenase inhibitor has a short duration of action and poor bioavailability. To improve the duration of action we have prepared a series of carbon substituted naphthoquinones. Several members of this series have demonstrated potent in vitro inhibition of 5-LO (IC50's less than 10(-6) M) and at doses of 1 mg/kg iv completely inhibited LTB4 production measured in ex vivo A23187-stimulated blood from dogs. The duration of action measured by the ex vivo assay was improved up to threefold over CGS 8515.

摘要

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