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作 者:Jing-wei Zheng Lin Ma
机构地区:[1]School of Chemistry and Chemical Engineering, Sun Yat-Sen University, Guangzhou 510275, China
出 处:《Chinese Chemical Letters》2016年第5期627-630,共4页中国化学快报(英文版)
摘 要:Metal complexes of anthranilic acid derivatives that constitute a novel class of non-sugar-type α- glucosidase inhibitors were synthesized and assessed in vitro for inhibitory activity. All of the AgO) complexes (9-16) inhibited α-glucosidase at the nanomolar scale, while 3,5-dichloroanthranilic acid silver(1) (9) was the most potent (ICso = 3.21 nmol/L). Analysis of the kinetics of enzyme inhibition indicated that the mechanism of the newly prepared silver complexes was noncompetitive. The structure-activity relationships were also analyzed, and thev are discussed in this report.Metal complexes of anthranilic acid derivatives that constitute a novel class of non-sugar-type α- glucosidase inhibitors were synthesized and assessed in vitro for inhibitory activity. All of the AgO) complexes (9-16) inhibited α-glucosidase at the nanomolar scale, while 3,5-dichloroanthranilic acid silver(1) (9) was the most potent (ICso = 3.21 nmol/L). Analysis of the kinetics of enzyme inhibition indicated that the mechanism of the newly prepared silver complexes was noncompetitive. The structure-activity relationships were also analyzed, and thev are discussed in this report.
关 键 词:α-Glucosidase Anthranilic acid derivatives Metal complexes Noncompetitive inhibitors
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