作为碳酸酐酶选择性抑制剂的牛柳和野柳的沉淀:分离、结构解析、x射线晶体学。

IF 4.3 3区 医学 Q2 CHEMISTRY, MEDICINAL
Charikleia Paloukopoulou, Ogouschan Salim Ntagli, Luca Gherardi, Virginia Dourdouni, Glykeria Filippou, Vincenzo Alterio, Simone Giovannuzzi, Maria Luisa Massardi, Giuseppina De Simone, Roberto Ronca, Claudiu T. Supuran, Gennaro Pescitelli, Anastasia Karioti
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引用次数: 0

摘要

在本研究中,分离得到了4个深层蛋白。采用一维(1D)和二维(2D)核磁共振、高分辨率质谱和电子圆二色分析对药用植物及其结构进行了评价。本文首次报道的化合物1、丹酚酸p2、斜足酸i3和斜足酸o4均在体外表达的人(h)碳酸酐酶(CAs)上进行了谱图分析;EC 4.2.1.1)和肿瘤相关的人碳酸酐酶(hCA) IX和hCA XII优于组成型表达的hCA I和hCA II亚型。x射线晶体学使我们能够评估丹酚酸p2与hCA II的结合模式。这些化合物对人三阴性乳腺癌细胞系MDA-MB-231表现出显著的细胞毒作用,表明这类药物是未来研究的有前途的分子。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Depsides from Origanum dictamnus and Satureja pilosa as selective inhibitors of carbonic anhydrases: Isolation, structure elucidation, X-ray crystallography

In this study, four depsides were isolated from Origanum dictamnus L. and Satureja pilosa Velen. medicinal plants and their structures were assessed by means of one-dimensional (1D)- and two-dimensional (2D)-nuclear magnetic resonance, high resolution mass spectrometry, and electronic circular dichroism analyses. The compound 1, herein reported for the first time, salvianolic acid P 2, clinopodic acid I 3, and clinopodic acid O 4 were all profiled in vitro on a panel of human (h) expressed carbonic anhydrases (CAs; EC 4.2.1.1) and preferential inhibition for the tumor-associated human carbonic anhydrase (hCA) IX and hCA XII over the constitutively expressed hCA I and hCA II isoforms was observed. X-ray crystallography allowed us to assess the binding mode of salvianolic acid P 2 to hCA II. The compounds exhibited significant cytotoxic effects on the human triple-negative breast cancer cell line MDA-MB-231, suggesting that this class of depsides are promising molecules for future investigation.

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来源期刊
Archiv der Pharmazie
Archiv der Pharmazie 医学-化学综合
CiteScore
7.90
自引率
5.90%
发文量
176
审稿时长
3.0 months
期刊介绍: Archiv der Pharmazie - Chemistry in Life Sciences is an international journal devoted to research and development in all fields of pharmaceutical and medicinal chemistry. Emphasis is put on papers combining synthetic organic chemistry, structural biology, molecular modelling, bioorganic chemistry, natural products chemistry, biochemistry or analytical methods with pharmaceutical or medicinal aspects such as biological activity. The focus of this journal is put on original research papers, but other scientifically valuable contributions (e.g. reviews, minireviews, highlights, symposia contributions, discussions, and essays) are also welcome.
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