a -78773:选择性,有效的5-脂氧合酶抑制剂。

Journal of lipid mediators Pub Date : 1993-03-01
R L Bell, D W Brooks, P R Young, C Lanni, A O Stewart, J Bouska, P E Malo, G W Carter
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引用次数: 0

摘要

研究了新发现的5-脂氧合酶抑制剂a -78773的效价和选择性。该化合物在抑制游离细胞裂解物和分离的人中性粒细胞中白三烯的形成方面明显比zileuton更有效。a -78773抑制RBL细胞裂解物5-脂氧合酶的浓度比抑制兔网织细胞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。该化合物也是一种有效的、持久的、口服活性的白三烯在狗体内和在大鼠体内形成的抑制剂。在白三烯形成被完全抑制的实验中,没有观察到其他途径的类二十烷醇的增加。a -78773应被证明是治疗白三烯介导性疾病的有价值的临床工具。
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A-78773: a selective, potent 5-lipoxygenase inhibitor.

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.

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