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某些具有抗氧化活性的新型吗啉衍生物的降胆固醇和降血脂活性

Hypocholesterolemic and hypolipidemic activity of some novel morpholine derivatives with antioxidant activity.

作者信息

Chrysselis M C, Rekka E A, Kourounakis P N

机构信息

Department of Pharmaceutical Chemistry, School of Pharmacy, Aristotelian University of Thessaloniki, Thessaloniki 540 06, Greece.

出版信息

J Med Chem. 2000 Feb 24;43(4):609-12. doi: 10.1021/jm991039l.

Abstract

In this investigation, we study the synthesis and the evaluation of antioxidant and hypocholesterolemic activity of a number of 2-biphenylyl morpholine derivatives, which are structurally similar to some substituted morpholines possessing antioxidant activity, as well as to hypocholesterolemic 3-biaryl-quinuclidines. The novel derivatives are found to inhibit the ferrous/ascorbate induced lipid peroxidation of microsomal membrane lipids, the most potent derivative, 2-(4-biphenyl)-4-methyl-octahydro-1,4-benzoxazin-2-ol (compound 7), having an IC(50) value of 250 microM. In addition, these compounds demonstrate hypocholesterolemic and hypolipidemic action. The most active compound (7) decreases total cholesterol, low density lipoprotein, and triglycerides in plasma of Triton WR-1339 induced hyperlipidemic rats by 54%, 51%, and 49%, respectively, at 28 micromol/kg (ip). The above results indicate that the new molecules may be proven useful as leads for the design of novel compounds as potentially antiatherogenic factors.

摘要

在本研究中,我们研究了多种2-联苯基吗啉衍生物的合成及其抗氧化和降胆固醇活性的评估。这些衍生物在结构上与一些具有抗氧化活性的取代吗啉以及降胆固醇的3-联芳基奎宁环相似。发现这些新型衍生物可抑制亚铁/抗坏血酸诱导的微粒体膜脂质的脂质过氧化,其中最有效的衍生物2-(4-联苯基)-4-甲基-八氢-1,4-苯并恶嗪-2-醇(化合物7)的IC(50)值为250微摩尔。此外,这些化合物还表现出降胆固醇和降血脂作用。在28微摩尔/千克(腹腔注射)时,最具活性的化合物(7)可使Triton WR-1339诱导的高脂血症大鼠血浆中的总胆固醇、低密度脂蛋白和甘油三酯分别降低54%、51%和49%。上述结果表明,这些新分子可能被证明可作为设计新型化合物的先导物,作为潜在的抗动脉粥样硬化因子。

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