Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
10592587 | Bioorganic & Medicinal Chemistry Letters | 2014 | 12 Pages |
Abstract
A novel, non-acid series of nitroquinoxalinone derivatives was synthesized and tested for their inhibitory activity against aldose reductase as targeting enzyme. All active compounds displayed an 8-nitro group, and showed significant activity in IC50 values ranging from 1.54 to 18.17 μM. Among them 6,7-dichloro-5,8-dinitro-3-phenoxyquinoxalin-2(1H)-one (7e), exhibited the strongest aldose reductase activity with an IC50 value of 1.54 μM and a good SAR (structure-activity relationship) profile.
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Authors
Saghir Hussain, Shagufta Parveen, Xiangyu Qin, Xin Hao, Shuzhen Zhang, Xin Chen, Changjin Zhu, Bing Ma,