Suppr超能文献

莪术根茎中倍半萜类化合物的精氨酸酶抑制活性。

Arginase inhibitory activities of guaiane sesquiterpenoids from Curcuma comosa rhizomes.

机构信息

Institute of Natural Medicine, University of Toyama, 2630-Sugitani, Toyama, 930-0194, Japan.

Department of Chemistry, University of Yangon, Yangon, 11041, Myanmar.

出版信息

J Nat Med. 2023 Sep;77(4):891-897. doi: 10.1007/s11418-023-01731-9. Epub 2023 Jul 18.

Abstract

Arginases are bimanganese enzymes involved in many human illnesses, and thus are targets for disease treatments. The screening of traditional medicinal plants demonstrated that an ethanol extract of Curcuma comosa rhizomes showed significant human arginase I and II inhibitory activity, and further fractionation led to the isolation of three known guaiane sesquiterpenoids, alismoxide (1), 7α,10α-epoxyguaiane-4α,11-diol (2) and guaidiol (3). Tests of their inhibitory activities on human arginases I and II revealed that 1 exhibited selective and potent competitive inhibition for human arginase I (IC = 30.2 μM), whereas the other compounds lacked inhibitory activities against human arginases. To the best of our knowledge, this is the first demonstration of human arginase I inhibitory activity by a sesquiterpenoid. Thus, 1 is a primary and specific inhibitory molecule against human arginase I.

摘要

精氨酸酶是参与许多人类疾病的双锰酶,因此是疾病治疗的靶点。对传统药用植物的筛选表明,菖蒲根茎的乙醇提取物对人精氨酸酶 I 和 II 具有显著的抑制活性,进一步的分离得到了三种已知的愈创木烷倍半萜,阿里莫德(1)、7α,10α-环氧愈创木烷-4α,11-二醇(2)和愈创木醇(3)。它们对人精氨酸酶 I 和 II 的抑制活性测试表明,1 对人精氨酸酶 I 表现出选择性和强效的竞争性抑制作用(IC=30.2μM),而其他化合物对人精氨酸酶没有抑制活性。据我们所知,这是倍半萜对人精氨酸酶 I 抑制活性的首次证明。因此,1 是一种针对人精氨酸酶 I 的主要和特异性抑制分子。

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验