首页> 外文期刊>Journal of enzyme inhibition and medicinal chemistry. >Investigation of the in vitro antioxidant behaviour of some 2-phenylindole derivatives: discussion on possible antioxidant mechanisms and comparison with melatonin.
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Investigation of the in vitro antioxidant behaviour of some 2-phenylindole derivatives: discussion on possible antioxidant mechanisms and comparison with melatonin.

机译:一些2-苯基吲哚衍生物的体外抗氧化行为研究:可能的抗氧化机理的讨论以及与褪黑激素的比较。

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摘要

Oxidative stress has been implicated in the development of many neurodegenerative diseases and also responsible from aging and some cancer types. Indolic compounds are a broad family of substances present in microorganisms, plants and animals. They are mainly related to tryptophan metabolism, and present particular properties that depend on their respective chemical structures. Due to free radical scavenger and antioxidant properties of indolic derivatives such as indolinic nitroxides and melatonin, a series of 2-phenyl indole derivatives were prepared and their in vitro effects on rat liver lipid peroxidation levels, superoxide formation and DPPH stable radical scavenging activities were determined against melatonin, BHT and alpha-tocopherol. The compounds significantly inhibited (72-98%) lipid peroxidation at 10(-3) M. These values were similar to that observed with BHT (88%). Possible structure-activity relationships of the compounds were discussed.
机译:氧化应激与许多神经退行性疾病的发展有关,并且也与衰老和某些癌症类型有关。吲哚化合物是存在于微生物,植物和动物中的多种物质。它们主要与色氨酸代谢有关,并呈现取决于其各自化学结构的特定性质。由于吲哚啉氮氧化物和褪黑激素等吲哚衍生物的自由基清除剂和抗氧化性能,制备了一系列2-苯基吲哚衍生物,并测定了它们对大鼠肝脏脂质过氧化水平,超氧化物形成和DPPH稳定自由基清除活性的影响。对抗褪黑激素,BHT和α-生育酚。这些化合物在10(-3)M时显着抑制(72-98%)脂质过氧化。这些值与BHT(88%)观察到的值相似。讨论了化合物之间可能的构效关系。

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