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合成色酮的双席夫碱及其抗糖化活性。

Synthesis of bis-Schiff bases of isatins and their antiglycation activity.

机构信息

H.E.J. Research Institute of Chemistry, International Center for Chemical and Biological Sciences, University Karachi, Karachi 75270, Pakistan.

出版信息

Bioorg Med Chem. 2009 Nov 15;17(22):7795-801. doi: 10.1016/j.bmc.2009.09.028. Epub 2009 Sep 19.

DOI:10.1016/j.bmc.2009.09.028
PMID:19837595
Abstract

Bis-Schiff bases 1-27 have been synthesized and their in vitro antiglycation potential has been evaluated. Compounds 21 (IC(50)=243.95+/-4.59microM), 20 (IC(50)=257.61+/-5.63microM), and 7 (IC(50)=291.14+/-2.53microM) showed an excellent antiglycation activity better than the standard (rutin, IC(50)=294.46+/-1.50microM). This study has identified a series of potential molecules as antiglycation agents. A structure-activity relationship has been studied, and all the compounds were characterized by spectroscopic techniques.

摘要

已合成了双席夫碱 1-27,并评估了它们的体外抗糖化潜力。化合物 21(IC(50)=243.95+/-4.59μM)、20(IC(50)=257.61+/-5.63μM)和 7(IC(50)=291.14+/-2.53μM)表现出优异的抗糖化活性,优于标准品(芦丁,IC(50)=294.46+/-1.50μM)。本研究已经鉴定出一系列有潜力的作为抗糖化剂的分子。已经研究了构效关系,所有化合物均通过光谱技术进行了表征。

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