【摘 要】
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Metal complexes of anthranilic acid derivatives that constitute a novel class of non-sugar-type aglucosidase inhibitors were synthesized and assessed in vitro f
【机 构】
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School of Chemistry and Chemical Engineering, Sun Yat-Sen University,
【出 处】
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Chinese Chemical Letters
论文部分内容阅读
Metal complexes of anthranilic acid derivatives that constitute a novel class of non-sugar-type aglucosidase inhibitors were synthesized and assessed in vitro for inhibitory activity. All of the Ag(I)complexes(9–16) inhibited a-glucosidase at the nanomolar scale, while 3,5-dichloroanthranilic acid silver(I)(9) was the most potent(IC_(50)= 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 they are discussed in this report.
Metal complexes of anthranilic acid derivatives that constitute a novel class of non-sugar-type aglucosidase inhibitors were synthesized and assessed in vitro for inhibitory activity. All of the Ag (I) complexes (9-16) inhibited a-glucosidase at the nanomolar scale , while 3,5-dichloroanthranilic acid silver (I) (9) was the most potent (IC 50 = 3.21 nmol / L). Analysis of the kinetics of enzyme inhibition indicating that the mechanism of the newly prepared silver complexes was noncompetitive The structure-activity relationships were also analyzed, and they are discussed in this report.
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