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A - 78773:一种选择性、强效的5 - 脂氧合酶抑制剂。

A-78773: a selective, potent 5-lipoxygenase inhibitor.

作者信息

Bell R L, Brooks D W, Young P R, Lanni C, Stewart A O, Bouska J, Malo P E, Carter G W

机构信息

Immunosciences Research Area, Abbott Park, IL 60064.

出版信息

J Lipid Mediat. 1993 Mar-Apr;6(1-3):259-64.

PMID:8395248
Abstract

The potency and selectivity of A-78773, a newly discovered 5-lipoxygenase inhibitor, were examined. The compound was significantly more potent than zileuton in inhibiting leukotriene formation in cell free lysates and in isolated human neutrophils. A-78773 inhibited a RBL cell lysate 5-lipoxygenase at concentrations 2 orders of magnitude lower than those required to inhibit rabbit reticulocyte 15-lipoxygenase or human platelet 12-lipoxygenase. The compound was also a potent, long lasting, orally active inhibitor of leukotriene formation ex vivo in dogs and in vivo in the rat. In experiments where leukotriene formation was completely inhibited, no increase in eicosanoids from other pathways was observed. A-78773 should prove to be a valuable clinical tool in treating leukotriene mediated diseases.

摘要

对新发现的5-脂氧合酶抑制剂A-78773的效力和选择性进行了研究。该化合物在抑制无细胞裂解液和分离的人中性粒细胞中的白三烯形成方面比齐留通效力显著更强。A-78773抑制RBL细胞裂解液5-脂氧合酶的浓度比抑制兔网织红细胞15-脂氧合酶或人血小板12-脂氧合酶所需的浓度低2个数量级。该化合物也是犬体内外和大鼠体内白三烯形成的强效、长效、口服活性抑制剂。在白三烯形成被完全抑制的实验中,未观察到其他途径类花生酸的增加。A-78773应被证明是治疗白三烯介导疾病的一种有价值的临床工具。

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