One new ten-membered macrolide and one new pyridinone derivative from the mangrove endophytic fungus Alternaria porri #25.

IF 1.6 3区 化学 Q3 CHEMISTRY, APPLIED
Fengting Tang, Namei Zheng, Yuhui Wang, Jinjun Li, Ronglan Tan, Zhiyun Du, Huarong Huang, Guangying Chen
{"title":"One new ten-membered macrolide and one new pyridinone derivative from the mangrove endophytic fungus <i>Alternaria porri #</i>25.","authors":"Fengting Tang, Namei Zheng, Yuhui Wang, Jinjun Li, Ronglan Tan, Zhiyun Du, Huarong Huang, Guangying Chen","doi":"10.1080/14786419.2025.2570894","DOIUrl":null,"url":null,"abstract":"<p><p>One new ten-membered macrolide derivative, porriolide (<b>1</b>), and one new 2(1H)-pyridinone derivative (±)-porripyridone (<b>2</b>), together with seven known compounds alternariol 4-methyl ether (<b>3</b>), alternariol (<b>4</b>), 5'-methoxy-6-methylbiphenyl-3,4,3'-triol (<b>5</b>), altenusinoide A (<b>6</b>), harziano pyridone (<b>7</b>), penicilloxalone A (<b>8</b>), and cytosporin D (<b>9</b>) were obtained from mangrove endophytic fungus <i>Alternaria porri</i> #25. Their structures were elucidated using comprehensive spectroscopic methods, and the absolute configuration of the new compounds were further confirmed by ECD spectra and single-crystal X-ray diffraction analysis, respectively. Compounds <b>2</b> and <b>7</b> exhibited cytotoxic activities against prostate cancer VCap and PC-3 cells with IC<sub>50</sub> values ranging from 22.94 ± 0.53 μmol/L to 38.13 ± 0.93 μmol/L, while compound <b>1</b> showed no cytotoxic activity.</p>","PeriodicalId":18990,"journal":{"name":"Natural Product Research","volume":" ","pages":"1-6"},"PeriodicalIF":1.6000,"publicationDate":"2025-10-07","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/10.1080/14786419.2025.2570894","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

One new ten-membered macrolide derivative, porriolide (1), and one new 2(1H)-pyridinone derivative (±)-porripyridone (2), together with seven known compounds alternariol 4-methyl ether (3), alternariol (4), 5'-methoxy-6-methylbiphenyl-3,4,3'-triol (5), altenusinoide A (6), harziano pyridone (7), penicilloxalone A (8), and cytosporin D (9) were obtained from mangrove endophytic fungus Alternaria porri #25. Their structures were elucidated using comprehensive spectroscopic methods, and the absolute configuration of the new compounds were further confirmed by ECD spectra and single-crystal X-ray diffraction analysis, respectively. Compounds 2 and 7 exhibited cytotoxic activities against prostate cancer VCap and PC-3 cells with IC50 values ranging from 22.94 ± 0.53 μmol/L to 38.13 ± 0.93 μmol/L, while compound 1 showed no cytotoxic activity.

一个新的十元大环内酯和一个新的吡啶酮衍生物从红树林内生真菌褐孢#25。
从红树林内生真菌Alternaria porri #25中获得了一个新的十元大环内酯衍生物porriolide(1)和一个新的2(1H)-吡啶酮衍生物(±)- porriridone(2),以及七个已知化合物alternariol 4-甲基醚(3)、alternariol(4)、5'-甲氧基-6-甲基联苯-3,4,3'-三醇(5)、altenusinoide A(6)、harziano pyridone(7)、penicilloxalone A(8)和cytosporin D(9)。用综合光谱方法对其结构进行了表征,并分别用ECD光谱和单晶x射线衍射分析进一步确定了新化合物的绝对构型。化合物2和7对前列腺癌VCap和PC-3细胞具有细胞毒活性,IC50值为22.94±0.53 ~ 38.13±0.93 μmol/L,而化合物1无细胞毒活性。
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