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首页> 外文期刊>Die Pharmazie >Novel oxazole containing phenylpropane derivatives as peroxisome proliferator activated receptor agonists with hypolipidemic activity.
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Novel oxazole containing phenylpropane derivatives as peroxisome proliferator activated receptor agonists with hypolipidemic activity.

机译:新型的恶唑,含有苯基丙烷衍生物作为过氧化物酶体增殖物激活的具有降血脂活性的受体激动剂。

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摘要

alpha-Alkoxy arylpropanoic acids containing 2-phenyloxazole-4yl-alkyl moiety are found to be potent hypolipidemic agents. These compounds were potent activators of the peroxisome proliferator activated receptor gamma (PPARgamma), with moderate PPARalpha activity and known to cause adverse effects such as weight gain and edema, which are essentially attributed to PPARgamma activation. Although extensive work has been done on the phenylpropanoic acid class of compounds, other phenyl propane derivatives such as alcohols, amines, ethers etc. have not received much attention. In order to develop predominant PPARalpha agonists as hypolipidemic agents with minor chemical modifications on compound III, we have synthesised few (2S)-ethoxyphenylpropane derivatives containing a 2-phenyl-5-methyloxazole-4ylalkoxy moiety of the general formula IV and evaluated by PPARalpha and gamma transactivation assay in conjugation with in vivo studies in male Swiss albino mice model. Compounds 3c and 3d showed the desired predominant PPARalpha activity and excellent tryiglyceride reduction in vivo and were selected as lead compounds for further development as hypolipidemic agents.
机译:发现含有2-苯基恶唑-4基-烷基部分的α-烷氧基芳基丙酸是有效的降血脂药。这些化合物是过氧化物酶体增殖物激活的受体γ(PPARgamma)的有效激活剂,具有中等的PPARalpha活性,已知会引起不良影响,例如体重增加和浮肿,这主要归因于PPARgamma激活。尽管已经对苯基丙酸类化合物进行了广泛的研究,但是其他苯基丙烷衍生物,例如醇,胺,醚等,并未受到太多关注。为了开发作为降血脂药的主要PPARalpha激动剂,并对化合物III进行较小的化学修饰,我们合成了很少的含有通式IV的2-苯基-5-甲基恶唑-4基烷氧基部分的(2S)-乙氧基苯基丙烷衍生物,并通过PPARalpha和γ激活试验与瑞士白化病雄性小鼠模型的体内研究相结合。化合物3c和3d在体内显示出所需的主要PPARalpha活性和出色的甘油三酸酯还原性,因此被选作先导化合物作为降血脂药进一步开发。

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