首页> 外文期刊>Journal of biochemical and molecular toxicology >Purification of glutathione S‐transferase enzyme from quail liver tissue and inhibition effects of (3a R R ,4 S S ,7 R R ,7a S S )‐2‐(4‐(( E E )‐3‐(aryl)acryloyl)phenyl)‐3a,4,7,7a‐tetrahydro‐1 H H ‐4,7‐methanoisoindole‐1,3(2 H H )‐dione derivatives on the enzyme activity
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Purification of glutathione S‐transferase enzyme from quail liver tissue and inhibition effects of (3a R R ,4 S S ,7 R R ,7a S S )‐2‐(4‐(( E E )‐3‐(aryl)acryloyl)phenyl)‐3a,4,7,7a‐tetrahydro‐1 H H ‐4,7‐methanoisoindole‐1,3(2 H H )‐dione derivatives on the enzyme activity

机译:从鹌鹑肝组织纯化谷胱甘肽S-转移酶和抑制(3ar,4 ss,7 rr,7a ss)-2-(4-((ee)-3-(芳基)丙烯酰基)苯基)-3a的抑制作用 ,4,7,7A-四氢-1HH-4,7-甲基异吲哚-1,3(2 HH) - 二氧化硫衍生物对酶活性

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摘要

Abstract The use of quail meat and eggs has made this animal important in recent years, with its low cost and high yields. Glutathione S‐transferases (GST, E.C.2.5.1.18) are an important enzyme family, which play a critical role in detoxification system. In our study, GST was purified from quail liver tissue with 47.88‐fold purification and 12.33% recovery by glutathione agarose affinity chromatography. The purity of enzyme was checked by SDS‐PAGE method and showed a single band. In addition, inhibition effects of (3a R ,4 S ,7 R ,7a S )‐2‐(4‐(( E )‐3‐(aryl)acryloyl)phenyl)‐3a,4,7,7a‐tetrahydro‐1 H ‐4,7methanoisoindole‐1,3(2 H )‐dion derivatives ( 1a–g ) were investigated on the enzyme activity. The inhibition parameters (IC 50 and K i values) were calculated for these compounds. IC 50 values of these derivatives ( 1a–e ) were found as 23.00, 15.75, 115.50, 10.00, and 28.75?μM, respectively. K i values of these derivatives ( 1a–e ) were calculated in the range of 3.04?±?0.50 to 131.50?±?32.50?μM. However, for f and g compounds, the inhibition effects on the enzyme were not found.
机译:摘要近年来,使用鹌鹑肉和鸡蛋的使用很重要,成本低,产量高。谷胱甘肽S-转移酶(GST,E.C.2.5.1.18)是一个重要的酶家族,其在排毒系统中发挥着关键作用。在我们的研究中,GST从鹌鹑肝组织中纯化,纯化47.88倍净化和12.33%的谷胱甘肽亲和层析。通过SDS-PAGE方法检查酶的纯度并显示单个带。此外,(3a r,4 s,7 r,7a s)-2-(4-((e)-3-(芳基)丙烯酰基)苯基)-3a,4,7,7a-四氢 - 的抑制作用研究了1 H -4,7methanoisoIndole-1,3(2h) - 分枝衍生物(1A-G)对酶活性进行研究。计算这些化合物的抑制参数(IC 50和k i值)。将这些衍生物(1A-E)的IC 50值分别为23.00,15.75,115.50,10.00和28.75Ωμm。这些衍生物(1A-E)的k I值计算在3.04Ω±±0.50至131.50?±32.50Ωμm的范围内。然而,对于F和G化合物,未发现对酶的抑制作用。

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