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Nitrophenyl derivatives as aldose reductase inhibitors

L Costantino, AM Ferrari, MC Gamberini…

文献索引:Costantino, Luca; Ferrari, Anna Maria; Gamberini, Maria Cristina; Rastelli, Giulio Bioorganic and Medicinal Chemistry, 2002 , vol. 10, # 12 p. 3923 - 3931

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被引用次数: 21

摘要

Nitrophenyl derivatives were recently discovered as a new class of ALR2 inhibitors by means of docking and database screening of the National Cancer Institute database of organic molecules. The nitro group was predicted to bind to the Tyr48 and His110 active site residues of the enzyme, the site where acidic ALR2 inhibitors such as carboxylic acids bind in their anionic form. Given the novelty of these compounds, we decided to expand their ...