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新型 4-羟基二苯并吡喃酮类化合物作为自由基清除剂和链终止抗氧化剂的构效关系。

Structure-activity relationships of new 4-hydroxy bis-coumarins as radical scavengers and chain-breaking antioxidants.

机构信息

Institute of Organic Chemistry with Centre of Phytochemistry, Bulgarian Academy of Sciences, Acad. G. Bonchev Str., Bl.9, 1113 Sofia, Bulgaria.

出版信息

Biochimie. 2010 Sep;92(9):1138-46. doi: 10.1016/j.biochi.2010.02.033. Epub 2010 Mar 6.

Abstract

The main antioxidant properties of five new 4-hydroxy-bis-coumarins during bulk lipid autoxidation at 80 degrees C and 0.1 mM and 1.0 mM concentrations were studied and compared with 4-hydroxy-2H-chromen-2-one (1). These compounds are: 3,3'-((3,4-dihydroxy-phenyl) methylene) bis (4-hydroxy-2H-chromen-2-one) (2), 3,3'-((3,4-dimethoxyphenyl) methylene) bis (4-hydroxy-2H-chromen-2-one) (3), 3,3'-((4-hydroxy-3,5-dimethoxy-phenyl) methylene) bis(4-hydroxy-2H-chromen-2-one) (4) 3,3'-((3,4,5- trimethoxyphenyl) methylene) bis (4-hydroxy-2H-chromen-2-one) (5) 3,3'-((4-hydroxy-3-methoxy-5-nitrophenyl) methylene) bis (4-hydroxy-2H-chromen-2-one) (6), It was found that compound 2 with a catecholic structure in the aromatic nucleus showed the strongest antioxidant activity. Compound 4 showed a moderate antioxidant activity, and all the other compounds didn't show any capacity as chain-breaking antioxidants. Both 4-hydroxy-bis-coumarins (2 and 4) demonstrated also stronger radical scavenging activity towards DPPH radical by using TLC DPPH rapid test, than compound 1. The other compounds (3, 5, 6) didn't show any capacity as radical scavengers. The structure-activity relationship was discussed on the base of comparable kinetic analysis of studied 4-hydroxy-bis-coumarins with the known and standard antioxidants as alpha-tocopherol (TOH), caffeic acid (CA), sinapic acid (SA), ferulic acid (FA), and p-coumaric acid (p-CumA). In order to study the possible synergism between two phenolic antioxidants, the antioxidant efficiency and reactivity of two equimolar binary mixtures of coumarins and TOH (2+TOH and 4+TOH) and of corresponding cinnamic acid with TOH (CA+TOH and SA+TOH) were also tested and compared. The oxidation stability of the lipid substrate in presence of binary mixtures CA+TOH, SA+TOH and 2+TOH appeared to be higher than that of the individual antioxidants. However, no synergism was obtained for all tested binary mixtures.

摘要

五种新的 4-羟基二苯甲酰基甲烷在 80°C 和 0.1mM 和 1.0mM 浓度下的批量脂质自氧化过程中的主要抗氧化性能进行了研究,并与 4-羟基-2H-色烯-2-酮(1)进行了比较。这些化合物是:3,3'-((3,4-二羟基-苯基)亚甲基)双(4-羟基-2H-色烯-2-酮)(2),3,3'-((3,4-二甲氧基-苯基)亚甲基)双(4-羟基-2H-色烯-2-酮)(3),3,3'-((4-羟基-3,5-二甲氧基-苯基)亚甲基)双(4-羟基-2H-色烯-2-酮)(4),3,3'-((3,4,5-三甲氧基-苯基)亚甲基)双(4-羟基-2H-色烯-2-酮)(5),3,3'-((4-羟基-3-甲氧基-5-硝基-苯基)亚甲基)双(4-羟基-2H-色烯-2-酮)(6)。研究发现,具有芳核中环己二烯结构的化合物 2 表现出最强的抗氧化活性。化合物 4 表现出中等的抗氧化活性,而其他所有化合物都没有表现出作为链断裂抗氧化剂的能力。两种 4-羟基二苯甲酰基甲烷(2 和 4)在使用 TLC DPPH 快速测试法对 DPPH 自由基的清除活性方面也表现出比化合物 1 更强的活性。其他化合物(3、5、6)没有表现出任何清除自由基的能力。在比较了研究的 4-羟基二苯甲酰基甲烷与已知和标准抗氧化剂(α-生育酚(TOH)、咖啡酸(CA)、芥子酸(SA)、阿魏酸(FA)和对香豆酸(p-CumA)的动力学分析的基础上,讨论了构效关系。为了研究两种酚类抗氧化剂之间可能存在的协同作用,还测试并比较了两种等摩尔二元混合物(2+TOH 和 4+TOH)和相应肉桂酸与 TOH(CA+TOH 和 SA+TOH)的抗氧化效率和反应性。在存在二元混合物 CA+TOH、SA+TOH 和 2+TOH 的情况下,脂质底物的氧化稳定性似乎高于单独的抗氧化剂。然而,所有测试的二元混合物都没有获得协同作用。

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