Isolation and identification of diverse steroids as Escherichia coli β-glucuronidase inhibitors from the Submerge-cultured mycelia of Hirsutella sinensis.

IF 1.6 3区 化学 Q3 CHEMISTRY, APPLIED
Youmin Ying, Xiaoxiao Chen, Ling Li, Jianwei Wang, Yun Zhang, Wei Mao, Weiguang Shan, Sha Xu
{"title":"Isolation and identification of diverse steroids as <i>Escherichia coli β</i>-glucuronidase inhibitors from the Submerge-cultured mycelia of <i>Hirsutella sinensis</i>.","authors":"Youmin Ying, Xiaoxiao Chen, Ling Li, Jianwei Wang, Yun Zhang, Wei Mao, Weiguang Shan, Sha Xu","doi":"10.1080/14786419.2025.2571857","DOIUrl":null,"url":null,"abstract":"<p><p>The ethanol extract of the submerge-cultured mycelia of <i>Hirsutella sinensis</i> (SCMHS) inhibited the <i>Escherichia coli β</i>-glucuronidase (EcGUS) <i>in vitro</i>. In-depth chemical investigation furnished 26 steroids, including a new compound hirsusterol A (<b>1</b>) featuring a rare 14,15-<i>seco</i> steroidal moiety and 25 known compounds with varied chemical diversity. The plausible biosynthetic pathway for hirsusterol A (<b>1</b>) was proposed. Except for ergosterol (<b>22</b>) and ergosterol peroxide (<b>23</b>), all the other compounds have never been obtained from <i>H. sinensis</i> previously. Compounds <b>8</b> and <b>23</b> were found to be potent uncompetitive inhibitors of EcGUS. This is the first report of these two steroids as EcGUS inhibitors. The findings of this study preliminary clarified the active ingredient underlying the EcGUS inhibition activity of SMCHS and provided potential drug leads for the development of new EcGUS inhibitors.</p>","PeriodicalId":18990,"journal":{"name":"Natural Product Research","volume":" ","pages":"1-9"},"PeriodicalIF":1.6000,"publicationDate":"2025-10-10","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Natural Product Research","FirstCategoryId":"92","ListUrlMain":"https://doi.org/10.1080/14786419.2025.2571857","RegionNum":3,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q3","JCRName":"CHEMISTRY, APPLIED","Score":null,"Total":0}
引用次数: 0

Abstract

The ethanol extract of the submerge-cultured mycelia of Hirsutella sinensis (SCMHS) inhibited the Escherichia coli β-glucuronidase (EcGUS) in vitro. In-depth chemical investigation furnished 26 steroids, including a new compound hirsusterol A (1) featuring a rare 14,15-seco steroidal moiety and 25 known compounds with varied chemical diversity. The plausible biosynthetic pathway for hirsusterol A (1) was proposed. Except for ergosterol (22) and ergosterol peroxide (23), all the other compounds have never been obtained from H. sinensis previously. Compounds 8 and 23 were found to be potent uncompetitive inhibitors of EcGUS. This is the first report of these two steroids as EcGUS inhibitors. The findings of this study preliminary clarified the active ingredient underlying the EcGUS inhibition activity of SMCHS and provided potential drug leads for the development of new EcGUS inhibitors.

从中华毛杆菌菌丝体中分离鉴定多种甾体类大肠杆菌β-葡萄糖醛酸酶抑制剂。
毛杆菌菌丝体乙醇提取物对大肠杆菌β-葡萄糖醛酸酶(EcGUS)有体外抑制作用。深入的化学研究提供了26种类固醇,包括一种具有罕见的14,15秒类固醇片段的新化合物hirsusterol a(1)和25种具有不同化学多样性的已知化合物。提出了毛甾醇A(1)的生物合成途径。除麦角甾醇(22)和麦角甾醇过氧化物(23)外,其余化合物均未从中华棉铃虫中分离得到。化合物8和23是有效的非竞争性EcGUS抑制剂。这是首次报道这两种类固醇作为EcGUS抑制剂。本研究结果初步阐明了SMCHS抑制EcGUS活性的有效成分,为开发新的EcGUS抑制剂提供了潜在的药物线索。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 求助全文
来源期刊
Natural Product Research
Natural Product Research 化学-医药化学
CiteScore
5.10
自引率
9.10%
发文量
605
审稿时长
2.1 months
期刊介绍: The aim of Natural Product Research is to publish important contributions in the field of natural product chemistry. The journal covers all aspects of research in the chemistry and biochemistry of naturally occurring compounds. The communications include coverage of work on natural substances of land and sea and of plants, microbes and animals. Discussions of structure elucidation, synthesis and experimental biosynthesis of natural products as well as developments of methods in these areas are welcomed in the journal. Finally, research papers in fields on the chemistry-biology boundary, eg. fermentation chemistry, plant tissue culture investigations etc., are accepted into the journal. Natural Product Research issues will be subtitled either ""Part A - Synthesis and Structure"" or ""Part B - Bioactive Natural Products"". for details on this , see the forthcoming articles section. All manuscript submissions are subject to initial appraisal by the Editor, and, if found suitable for further consideration, to peer review by independent, anonymous expert referees. All peer review is single blind and submission is online via ScholarOne Manuscripts.
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:604180095
Book学术官方微信