Inhibition of soybean lipoxygenase-1 by 10-butyryl substituted 1,8-dihydroxy-9-anthrone (butantrone).

Medical biology Pub Date : 1986-01-01
S Laakso, L Römer, K K Mustakallio
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引用次数: 0

Abstract

10-Butyryl substituted 1,8-dihydroxyanthrone (butantrone) inhibited soybean lipoxygenase-1 irreversibly and more efficiently than its parent compound 1,8-dihydroxyanthrone (dithranol, anthralin) (IC50 values 0.090 mM and 1.1 mM, respectively). Intact butantrone rather than its hydrolysis product was the primary effector and the 10-butyryl moiety its site specific probe, probably directing the inhibitor to the proximity of the binding site of the lipid substrate/product.

10-丁酰基取代的 1,8-二羟基-9-蒽酮(丁蒽酮)对大豆脂氧合酶-1 的抑制作用。
10-丁酰基取代的 1,8-二羟基蒽酮(丁蒽酮)对大豆脂氧合酶-1 的抑制作用不可逆,且比其母体化合物 1,8-二羟基蒽酮(二蒽醇、蒽林)更有效(IC50 值分别为 0.090 mM 和 1.1 mM)。完整的丁蒽酮而非其水解产物是主要的效应物,而 10-丁酰基则是位点特异性探针,可能将抑制剂引向脂质底物/产物的结合位点附近。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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