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Spirobisnaphthalenes effectively inhibit carbonic anhydrase

机译:螺双萘可有效抑制碳酸酐酶

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Abstract This study explores the correlation between human carbonic anhydrase (CA, EC 4.2.1.1) isoforms I and II (hCA I, II) and the inhibitory features of some spirobisnaphthalene derivatives. A group of spirobisnaphthalenes was synthesized and their hCA I and II inhibitory effects was investigated. The Ki values were similar for both CA isoenzymes, the compounds showing good inhibitory activity. Ki values ranged between 1.60 and 460.42?μM for hCA I and between 0.39 and 419.42?μM for hCA II, respectively. The spirobisnaphthalenes derivatives might be useful for designing CA inhibitors belonging to novel chemotypes compared to the highly investigated sulfonamides, sulfamates or coumarins.
机译:摘要这项研究探讨了人类碳酸酐酶(CA,EC 4.2.1.1)的同工型I和II(hCA I,II)与某些螺双萘衍生物的抑制特征之间的关系。合成了一组螺双萘并研究了它们对hCA I和II的抑制作用。两种CA同工酶的K i 值相似,这些化合物表现出良好的抑制活性。 hCA I的K i 值分别在1.60和460.42?μM之间,hCA II的K i 值分别在0.39和419.42μM之间。与高度研究的磺酰胺,磺酰胺或香豆素相比,螺双萘衍生物可用于设计属于新型化学型的CA抑制剂。

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