Suppr超能文献

对产生头皮屑的真菌球形马拉色菌β-碳酸酐酶MgCA的阴离子抑制研究。

Anion inhibition studies of the dandruff-producing fungus Malassezia globosa β-carbonic anhydrase MgCA.

作者信息

Del Prete Sonia, Vullo Daniela, Osman Sameh M, AlOthman Zeid, Capasso Clemente, Supuran Claudiu T

机构信息

Università degli Studi di Firenze, Dipartimento Neurofarba, Sezione di Scienze Farmaceutiche, Polo Scientifico, Sesto Fiorentino, Firenze, Italy; Istituto di Biochimica delle Proteine-CNR, Via P. Castellino 111, 80131 Napoli, Italy.

Università degli Studi di Firenze, Polo Scientifico, Laboratorio di Chimica Bioinorganica, Rm. 188, Via della Lastruccia 3, 50019 Sesto Fiorentino (Florence), Italy.

出版信息

Bioorg Med Chem Lett. 2015 Nov 15;25(22):5194-8. doi: 10.1016/j.bmcl.2015.09.068. Epub 2015 Oct 3.

Abstract

The genome of the fungal parasite Malassezia globosa, the causative agent of dandruff, contains a single gene annotated as encoding a carbonic anhydrase (CAs, EC 4.2.1.1) belonging to the β-class (MgCA). In an earlier work (J. Med. Chem. 2012, 55, 3513) we have validated this enzyme as an anti-dandruff drug target, reporting that sulfonamide inhibitors show in vitro and in vivo effects, in an animal model of Malassezia infection. However, few classes of compounds apart the sulfonamides, were investigated for their activity against MgCA. Here we present an anion inhibition study of this enzyme, reporting that metal complexing anions such as cyanate, thiocyanate, cyanide, azide are weak MgCA inhibitors (KIs ranging between 6.81 and 45.2 mM) whereas bicarbonate (KI of 0.59 mM) and diethyldithiocarbamate (KI of 0.30 mM) together with sulfamide, sulfamate, phenylboronic acid and phenylarsonic acid were the most effective inhibitors detected so far, with KIs ranging between 83 and 94 μM. This study may help a better understanding of the inhibition profile of this enzyme and may offer the possibility to design new such modulators of activity belonging to different chemical classes.

摘要

引起头皮屑的真菌寄生虫球形马拉色菌的基因组中含有一个注释为编码属于β类碳酸酐酶(CAs,EC 4.2.1.1)的单一基因(MgCA)。在早期的一项研究(《药物化学杂志》,2012年,第55卷,第3513页)中,我们已证实该酶是一种抗头皮屑药物靶点,报道了磺胺类抑制剂在马拉色菌感染动物模型中显示出体外和体内效应。然而,除磺胺类化合物外,很少有其他类别的化合物针对其对MgCA的活性进行研究。在此,我们展示了对该酶的阴离子抑制研究,报道金属络合阴离子如氰酸盐、硫氰酸盐、氰化物、叠氮化物是较弱的MgCA抑制剂(抑制常数KIs在6.81至45.2 mM之间),而碳酸氢盐(抑制常数KI为0.59 mM)和二乙基二硫代氨基甲酸盐(抑制常数KI为0.30 mM)以及磺胺、氨基磺酸、苯硼酸和苯胂酸是迄今为止检测到的最有效的抑制剂,抑制常数KIs在83至94 μM之间。这项研究可能有助于更好地理解该酶的抑制特征,并可能提供设计属于不同化学类别的新型活性调节剂的可能性。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验