Innocenti Alessio, Hilvo Mika, Scozzafava Andrea, Parkkila Seppo, Supuran Claudiu T
Università degli Studi di Firenze, Polo Scientifico, Laboratorio di Chimica Bioinorganica, Rm. 188, Via della Lastruccia 3, 50019 Sesto Fiorentino (Florence), Italy.
Bioorg Med Chem Lett. 2008 Jun 15;18(12):3593-6. doi: 10.1016/j.bmcl.2008.04.077. Epub 2008 May 4.
Inhibition of the newest isoform of the metalloenzyme carbonic anhydrase (CA, EC 4.2.1.1), CA XV, with a series of phenols was investigated. Murine CA XV showed an inhibition profile by phenols distinct of those of the cytosolic human isoforms CA I and II. Phenol and some of its 2-, 3-, and 4-substituted derivatives incorporating hydroxy, fluoro, carboxy, and acetamido moieties were effective CA XV inhibitors, with inhibition constants in the range of 7.20-11.30 microM, whereas compounds incorporating 4-amino-, 4-cyano, or 3-hydroxy groups were less effective (K(I)s of 335-434 microM). The best phenol inhibitor was clioquinol (K(I) of 2.33 microM). Phenols show a different inhibition mechanism as compared to sulfonamides and their isosteres, and may lead to the design of compounds with selectivity for inhibiting different CA isozymes with medicinal chemistry applications.
研究了一系列酚类物质对金属酶碳酸酐酶(CA,EC 4.2.1.1)的最新亚型CA XV的抑制作用。小鼠CA XV对酚类物质的抑制模式与胞质型人同工酶CA I和CA II不同。苯酚及其一些含有羟基、氟、羧基和乙酰氨基部分的2-、3-和4-取代衍生物是有效的CA XV抑制剂,抑制常数在7.20 - 11.30微摩尔范围内,而含有4-氨基、4-氰基或3-羟基的化合物效果较差(抑制常数为335 - 434微摩尔)。最佳的酚类抑制剂是氯碘羟喹(抑制常数为2.33微摩尔)。与磺胺类及其电子等排体相比,酚类表现出不同的抑制机制,并且可能导致设计出具有选择性抑制不同CA同工酶的化合物,用于药物化学应用。