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首页> 外文期刊>European Journal of Medicinal Chemistry: Chimie Therapeutique >Synthesis and evaluation of a series of benzopyran derivatives as PPAR alpha/gamma agonists.
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Synthesis and evaluation of a series of benzopyran derivatives as PPAR alpha/gamma agonists.

机译:一系列苯并吡喃衍生物作为PPARα/γ激动剂的合成和评估。

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摘要

A series of benzopyran derivatives were synthesized and evaluated for PPAR alpha/gamma agonist activities. Most of the compounds exhibit reasonable PPAR alpha and PPAR gamma agonist activities. In particular, compounds 7b, 8b, 8e and 8h with remarkable PPARg EC(50) values of 0.001muM are excellent full PPAR gamma agonists with the functional potency about 130, 20 times stronger than that of leading compound 5 and rosiglitazone, respectively. Compounds 7a, 7c, 7d and 8a are dual PPAR alpha/gamma agonists, and all of them gave comparable or stronger PPAR alpha/gamma agonist efficacy than that of the corresponding positive control.
机译:合成了一系列苯并吡喃衍生物,并评估了其对PPARα/γ激动剂的活性。大多数化合物表现出合理的PPARα和PPARγ激动剂活性。特别是,具有显着的PPARg EC(50)值为0.001μM的化合物7b,8b,8e和8h是出色的全PPARγ激动剂,其功能效价分别比前导化合物5和罗格列酮强130倍,20倍。化合物7a,7c,7d和8a是双重PPARα/γ激动剂,与相应的阳性对照相比,所有化合物均具有相当或更高的PPARα/γ激动剂功效。

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