从海绵黄潜藻(Suberea ianthelliformis)中发现黄潜藻胺 D-G,以及黄潜藻胺 D 的全合成。

IF 2.2 4区 化学 Q2 CHEMISTRY, ORGANIC
Beilstein Journal of Organic Chemistry Pub Date : 2024-12-09 eCollection Date: 2024-01-01 DOI:10.3762/bjoc.20.266
Sasha Hayes, Yaoying Lu, Bernd H A Rehm, Rohan A Davis
{"title":"从海绵黄潜藻(Suberea ianthelliformis)中发现黄潜藻胺 D-G,以及黄潜藻胺 D 的全合成。","authors":"Sasha Hayes, Yaoying Lu, Bernd H A Rehm, Rohan A Davis","doi":"10.3762/bjoc.20.266","DOIUrl":null,"url":null,"abstract":"<p><p>The marine sponge <i>Suberea ianthelliformis</i> was investigated for new chemistry after the recent discovery that polyamines ianthelliformisamines A-C (<b>1</b>-<b>3</b>) - originally sourced from this Australian sponge - act as <i>Pseudomonas aeruginosa</i> biofilm inhibitors and antibiotic enhancers. Large-scale extraction and isolation studies resulted in the discovery of four new and minor natural products, ianthelliformisamines D-G (<b>4</b>-<b>7</b>) and the known steroid, aplysterol (<b>8</b>). Compounds <b>4</b>-<b>7</b> were fully characterised following 1D/2D NMR, MS and UV data analyses. All compounds were assessed for their inhibition on planktonic growth of <i>P. aeruginosa</i> PAO1 in addition to their ability to inhibit the formation of biofilms. None of the tested natural products inhibited planktonic growth or biofilm formation of PAO1 when screened at 50 µM. Ianthelliformisamine D (<b>4</b>) contains a rare <i>N</i>-(3-aminopropyl)-2-pyrrolidone moiety only found in <30 natural products. Owing to the novelty of compound <b>4</b>, we undertook the first total synthesis of this natural product, which was achieved in three steps.</p>","PeriodicalId":8756,"journal":{"name":"Beilstein Journal of Organic Chemistry","volume":"20 ","pages":"3205-3214"},"PeriodicalIF":2.2000,"publicationDate":"2024-12-09","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11650616/pdf/","citationCount":"0","resultStr":"{\"title\":\"Discovery of ianthelliformisamines D-G from the sponge <i>Suberea ianthelliformis</i> and the total synthesis of ianthelliformisamine D.\",\"authors\":\"Sasha Hayes, Yaoying Lu, Bernd H A Rehm, Rohan A Davis\",\"doi\":\"10.3762/bjoc.20.266\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><p>The marine sponge <i>Suberea ianthelliformis</i> was investigated for new chemistry after the recent discovery that polyamines ianthelliformisamines A-C (<b>1</b>-<b>3</b>) - originally sourced from this Australian sponge - act as <i>Pseudomonas aeruginosa</i> biofilm inhibitors and antibiotic enhancers. Large-scale extraction and isolation studies resulted in the discovery of four new and minor natural products, ianthelliformisamines D-G (<b>4</b>-<b>7</b>) and the known steroid, aplysterol (<b>8</b>). Compounds <b>4</b>-<b>7</b> were fully characterised following 1D/2D NMR, MS and UV data analyses. All compounds were assessed for their inhibition on planktonic growth of <i>P. aeruginosa</i> PAO1 in addition to their ability to inhibit the formation of biofilms. None of the tested natural products inhibited planktonic growth or biofilm formation of PAO1 when screened at 50 µM. Ianthelliformisamine D (<b>4</b>) contains a rare <i>N</i>-(3-aminopropyl)-2-pyrrolidone moiety only found in <30 natural products. Owing to the novelty of compound <b>4</b>, we undertook the first total synthesis of this natural product, which was achieved in three steps.</p>\",\"PeriodicalId\":8756,\"journal\":{\"name\":\"Beilstein Journal of Organic Chemistry\",\"volume\":\"20 \",\"pages\":\"3205-3214\"},\"PeriodicalIF\":2.2000,\"publicationDate\":\"2024-12-09\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11650616/pdf/\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Beilstein Journal of Organic Chemistry\",\"FirstCategoryId\":\"92\",\"ListUrlMain\":\"https://doi.org/10.3762/bjoc.20.266\",\"RegionNum\":4,\"RegionCategory\":\"化学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"2024/1/1 0:00:00\",\"PubModel\":\"eCollection\",\"JCR\":\"Q2\",\"JCRName\":\"CHEMISTRY, ORGANIC\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Beilstein Journal of Organic Chemistry","FirstCategoryId":"92","ListUrlMain":"https://doi.org/10.3762/bjoc.20.266","RegionNum":4,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2024/1/1 0:00:00","PubModel":"eCollection","JCR":"Q2","JCRName":"CHEMISTRY, ORGANIC","Score":null,"Total":0}
引用次数: 0

摘要

本文章由计算机程序翻译,如有差异,请以英文原文为准。
Discovery of ianthelliformisamines D-G from the sponge Suberea ianthelliformis and the total synthesis of ianthelliformisamine D.

The marine sponge Suberea ianthelliformis was investigated for new chemistry after the recent discovery that polyamines ianthelliformisamines A-C (1-3) - originally sourced from this Australian sponge - act as Pseudomonas aeruginosa biofilm inhibitors and antibiotic enhancers. Large-scale extraction and isolation studies resulted in the discovery of four new and minor natural products, ianthelliformisamines D-G (4-7) and the known steroid, aplysterol (8). Compounds 4-7 were fully characterised following 1D/2D NMR, MS and UV data analyses. All compounds were assessed for their inhibition on planktonic growth of P. aeruginosa PAO1 in addition to their ability to inhibit the formation of biofilms. None of the tested natural products inhibited planktonic growth or biofilm formation of PAO1 when screened at 50 µM. Ianthelliformisamine D (4) contains a rare N-(3-aminopropyl)-2-pyrrolidone moiety only found in <30 natural products. Owing to the novelty of compound 4, we undertook the first total synthesis of this natural product, which was achieved in three steps.

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
CiteScore
4.90
自引率
3.70%
发文量
167
审稿时长
1.4 months
期刊介绍: The Beilstein Journal of Organic Chemistry is an international, peer-reviewed, Open Access journal. It provides a unique platform for rapid publication without any charges (free for author and reader) – Platinum Open Access. The content is freely accessible 365 days a year to any user worldwide. Articles are available online immediately upon publication and are publicly archived in all major repositories. In addition, it provides a platform for publishing thematic issues (theme-based collections of articles) on topical issues in organic chemistry. The journal publishes high quality research and reviews in all areas of organic chemistry, including organic synthesis, organic reactions, natural product chemistry, structural investigations, supramolecular chemistry and chemical biology.
×
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