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分析皂苷和酚类化合物作为α-碳酸酐酶同工酶抑制剂。

Analysis of saponins and phenolic compounds as inhibitors of α-carbonic anhydrase isoenzymes.

机构信息

Department of Chemistry, Faculty of Science, Ege University, Bornova, İzmir, Turkey.

出版信息

J Enzyme Inhib Med Chem. 2013 Apr;28(2):412-7. doi: 10.3109/14756366.2011.651464. Epub 2012 Feb 3.

Abstract

A series of phenolic and saponin type natural products such as quercetin, rutin, catechin, epicatechin, silymarin, trojanoside H, astragaloside IV, astragaloside VIII and astrasieversianin X, were investigated for their inhibitory effects against the metalloenzyme carbonic anhydrase (CA, EC 4.2.1.1). We here report inhibitory effects of these compounds against five α-CA isozymes (hCA I, hCA II, bCA III, hCA IV and hCA VI). Most of the phenolic and saponin type compounds inhibited the isoenzymes quite effectively at low micromolar K(I)-s ranging between 0.1 and 4 µM, whereas a few derivatives were ineffective (K(I)-s > 100 µM). The results were remarkable which might lead to design of novel CAIs with a diverse inhibition mechanism compared to sulfonamide/sulfamate inhibitors.

摘要

研究了一系列酚类和皂苷类天然产物,如槲皮素、芦丁、儿茶素、表儿茶素、水飞蓟素、水飞蓟宾 H、黄芪甲苷 IV、黄芪皂苷 VIII 和 astrasieversianin X,以评估它们对金属酶碳酸酐酶(CA,EC 4.2.1.1)的抑制作用。我们在此报告了这些化合物对五种α-CA 同工酶(hCA I、hCA II、bCA III、hCA IV 和 hCA VI)的抑制作用。大多数酚类和皂苷类化合物在低微摩尔 K(I)范围内(0.1 到 4 µM 之间)对同工酶有相当有效的抑制作用,而少数衍生物则无效(K(I)> 100 µM)。结果非常显著,这可能导致设计出与磺酰胺/磺酸盐抑制剂具有不同抑制机制的新型 CAIs。

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