未描述的细胞毒性丁烯内酯;从黄花蒿内生真菌土曲霉中分离得到的曲霉烯内酯A-E。

IF 3.2 2区 生物学 Q2 BIOCHEMISTRY & MOLECULAR BIOLOGY
Mamdouh Nabil Samy , Eman Zekry Attia , Basmaa Ali Khalifa , Ahmed G. Darwish , Ahmed A. Al-Karmalawy , Radwan Alnajjar , Usama Ramadan Abdelmohsen , Mohamed Ali Ibrahim , Samir Anis Ross
{"title":"未描述的细胞毒性丁烯内酯;从黄花蒿内生真菌土曲霉中分离得到的曲霉烯内酯A-E。","authors":"Mamdouh Nabil Samy ,&nbsp;Eman Zekry Attia ,&nbsp;Basmaa Ali Khalifa ,&nbsp;Ahmed G. Darwish ,&nbsp;Ahmed A. Al-Karmalawy ,&nbsp;Radwan Alnajjar ,&nbsp;Usama Ramadan Abdelmohsen ,&nbsp;Mohamed Ali Ibrahim ,&nbsp;Samir Anis Ross","doi":"10.1016/j.phytochem.2024.114377","DOIUrl":null,"url":null,"abstract":"<div><div>Chemical investigation of the ethyl acetate extract of the endophytic fungus <em>Aspergillus terreus</em> AArEF2 found in the fresh leaves of <em>Artemisia arborescens</em> L. led to isolation of five previously undescribed butenolides, asperterreunolides A-E (<strong>1-5</strong>), along with the known metabolite butyrolactone IV (<strong>6</strong>). The structure elucidation of these metabolites was established by detailed spectroscopic analyses (1D, 2D NMR and HR-ESI-MS analyses). The absolute configuration of compounds <strong>4</strong> and <strong>5</strong> was determined using the modified Mosher's method. The isolated metabolites (<strong>1</strong>–<strong>6</strong>) were evaluated for their cytotoxic activity against A-431, C4–2B, and MDA PCa 2b cell lines by MTT assay using a 96-well microplate. The findings revealed that all the isolated compounds had notable cytotoxic properties with IC<sub>50</sub> values ranging from 3.72 to 6.27 μmol/L. Moreover, molecular docking was applied to propose the mechanism of action for the potential antitumor activity of the five previously undescribed butenolides, asperterreunolides A-E (<strong>1</strong>–<strong>5</strong>), along with known metabolite butyrolactone IV (<strong>6</strong>) to be attributed to type IIA topoisomerase inhibition. Furthermore, molecular dynamic simulations were implemented for 200 ns to study the stability of the asperterreunolides A-E (<strong>1</strong>–<strong>5</strong>) and butyrolactone IV (<strong>6</strong>) inside the active site of the type IIA topoisomerase.</div></div>","PeriodicalId":20170,"journal":{"name":"Phytochemistry","volume":"232 ","pages":"Article 114377"},"PeriodicalIF":3.2000,"publicationDate":"2024-12-30","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Undescribed cytotoxic butenolides; asperterreunolides A-E, isolated from endophytic fungus Aspergillus terreus derived from Artemisia arborescens L. supported with in silico study\",\"authors\":\"Mamdouh Nabil Samy ,&nbsp;Eman Zekry Attia ,&nbsp;Basmaa Ali Khalifa ,&nbsp;Ahmed G. Darwish ,&nbsp;Ahmed A. Al-Karmalawy ,&nbsp;Radwan Alnajjar ,&nbsp;Usama Ramadan Abdelmohsen ,&nbsp;Mohamed Ali Ibrahim ,&nbsp;Samir Anis Ross\",\"doi\":\"10.1016/j.phytochem.2024.114377\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><div>Chemical investigation of the ethyl acetate extract of the endophytic fungus <em>Aspergillus terreus</em> AArEF2 found in the fresh leaves of <em>Artemisia arborescens</em> L. led to isolation of five previously undescribed butenolides, asperterreunolides A-E (<strong>1-5</strong>), along with the known metabolite butyrolactone IV (<strong>6</strong>). The structure elucidation of these metabolites was established by detailed spectroscopic analyses (1D, 2D NMR and HR-ESI-MS analyses). The absolute configuration of compounds <strong>4</strong> and <strong>5</strong> was determined using the modified Mosher's method. The isolated metabolites (<strong>1</strong>–<strong>6</strong>) were evaluated for their cytotoxic activity against A-431, C4–2B, and MDA PCa 2b cell lines by MTT assay using a 96-well microplate. The findings revealed that all the isolated compounds had notable cytotoxic properties with IC<sub>50</sub> values ranging from 3.72 to 6.27 μmol/L. Moreover, molecular docking was applied to propose the mechanism of action for the potential antitumor activity of the five previously undescribed butenolides, asperterreunolides A-E (<strong>1</strong>–<strong>5</strong>), along with known metabolite butyrolactone IV (<strong>6</strong>) to be attributed to type IIA topoisomerase inhibition. Furthermore, molecular dynamic simulations were implemented for 200 ns to study the stability of the asperterreunolides A-E (<strong>1</strong>–<strong>5</strong>) and butyrolactone IV (<strong>6</strong>) inside the active site of the type IIA topoisomerase.</div></div>\",\"PeriodicalId\":20170,\"journal\":{\"name\":\"Phytochemistry\",\"volume\":\"232 \",\"pages\":\"Article 114377\"},\"PeriodicalIF\":3.2000,\"publicationDate\":\"2024-12-30\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Phytochemistry\",\"FirstCategoryId\":\"99\",\"ListUrlMain\":\"https://www.sciencedirect.com/science/article/pii/S003194222400414X\",\"RegionNum\":2,\"RegionCategory\":\"生物学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q2\",\"JCRName\":\"BIOCHEMISTRY & MOLECULAR BIOLOGY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Phytochemistry","FirstCategoryId":"99","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S003194222400414X","RegionNum":2,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"BIOCHEMISTRY & MOLECULAR BIOLOGY","Score":null,"Total":0}
引用次数: 0

摘要

对从青蒿鲜叶中提取的内生真菌土曲霉AArEF2的乙酸乙酯提取物进行化学研究,分离出5种以前未描述过的丁烯内酯,asperterreunolides A-E(1-5),以及已知的代谢物丁内酯IV(6)。通过详细的光谱分析(1D、2D NMR和HR-ESI-MS分析)确定了这些代谢物的结构。用改进的Mosher法确定了化合物4和5的绝对构型。分离的代谢物(1-6)对a -431、C4-2B和MDA - PCa 2b细胞系的细胞毒活性采用96孔微孔板MTT法进行评估。结果表明,所有化合物均具有显著的细胞毒性,IC50值在3.72 ~ 6.27 μmol/L之间。此外,应用分子对接提出了先前描述的五种丁烯内酯,asperterreunolides A-E(1-5),以及已知的代谢物丁内酯IV(6)的潜在抗肿瘤活性的作用机制,该机制归因于IIA型拓扑异构酶抑制。此外,通过200 ns的分子动力学模拟,研究了曲霉烯内酯A-E(1-5)和丁内酯IV(6)在IIA型拓扑异构酶活性位点内的稳定性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Undescribed cytotoxic butenolides; asperterreunolides A-E, isolated from endophytic fungus Aspergillus terreus derived from Artemisia arborescens L. supported with in silico study

Undescribed cytotoxic butenolides; asperterreunolides A-E, isolated from endophytic fungus Aspergillus terreus derived from Artemisia arborescens L. supported with in silico study
Chemical investigation of the ethyl acetate extract of the endophytic fungus Aspergillus terreus AArEF2 found in the fresh leaves of Artemisia arborescens L. led to isolation of five previously undescribed butenolides, asperterreunolides A-E (1-5), along with the known metabolite butyrolactone IV (6). The structure elucidation of these metabolites was established by detailed spectroscopic analyses (1D, 2D NMR and HR-ESI-MS analyses). The absolute configuration of compounds 4 and 5 was determined using the modified Mosher's method. The isolated metabolites (16) were evaluated for their cytotoxic activity against A-431, C4–2B, and MDA PCa 2b cell lines by MTT assay using a 96-well microplate. The findings revealed that all the isolated compounds had notable cytotoxic properties with IC50 values ranging from 3.72 to 6.27 μmol/L. Moreover, molecular docking was applied to propose the mechanism of action for the potential antitumor activity of the five previously undescribed butenolides, asperterreunolides A-E (15), along with known metabolite butyrolactone IV (6) to be attributed to type IIA topoisomerase inhibition. Furthermore, molecular dynamic simulations were implemented for 200 ns to study the stability of the asperterreunolides A-E (15) and butyrolactone IV (6) inside the active site of the type IIA topoisomerase.
求助全文
通过发布文献求助,成功后即可免费获取论文全文。 去求助
来源期刊
Phytochemistry
Phytochemistry 生物-植物科学
CiteScore
6.40
自引率
7.90%
发文量
443
审稿时长
39 days
期刊介绍: Phytochemistry is a leading international journal publishing studies of plant chemistry, biochemistry, molecular biology and genetics, structure and bioactivities of phytochemicals, including ''-omics'' and bioinformatics/computational biology approaches. Phytochemistry is a primary source for papers dealing with phytochemicals, especially reports concerning their biosynthesis, regulation, and biological properties both in planta and as bioactive principles. Articles are published online as soon as possible as Articles-in-Press and in 12 volumes per year. Occasional topic-focussed special issues are published composed of papers from invited authors.
×
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:481959085
Book学术官方微信