New bis-catechols 5-lipoxygenase inhibitors

被引:17
|
作者
Dupont, R
Goossens, JF
Cotelle, N
Vrielynck, L
Vezin, H
Hénichart, JP
Cotelle, P [1 ]
机构
[1] USTL, CNRS, UPRESA 8009, Lab Chim Organ & Macromol, F-59655 Villeneuve Dascq, France
[2] Univ Lille 2, Inst Chim Pharmaceut Albert Lespagnol, F-59006 Lille, France
[3] USTL, CNRS, UMR 8516, Spectrochim Infrarouge & Raman Lab, F-59655 Villeneuve Dascq, France
关键词
D O I
10.1016/S0968-0896(00)00258-3
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Three polyhydroxy-2-phenylnaphthalenes (1-3) and the oxy analogue of tetrahydroxypavinan (4) were prepared and evaluated for their antioxidant properties (inhibition of diphenylpycrylhydrazyl radical (DPPH), reduction of iron (III) ion) and inhibition of 5-lipoxygenase (5-LO) activity. Their three-dimensional structures were established on the basis of spectroscopic data and semi-empirical calculations. Compounds 1 and 2 were found as potent 5-LO inhibitors as nordihydroguaiaretic acid (NDGA), whereas 4 is 2.5 times less potent than NDGA. The reliability of the 3-D structures with the 5-LO inhibition properties is discussed. Their antioxidant properties show that tested compounds are expected to act as redox inhibitors. (C) 2001 Elsevier Science Ltd. All rights reserved.
引用
收藏
页码:229 / 235
页数:7
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