从钙叶菊中分离出的抑制折叠蛋白反应的黄酮。

IF 3.3 2区 生物学 Q2 CHEMISTRY, MEDICINAL Journal of Natural Products Pub Date : 2024-06-13 DOI:10.1021/acs.jnatprod.4c00328
Marine Chambaud, Anne-Marie Le Ray, Racha Hamzi, Thomas Charpentier, Nadège Blon, Dimitri Bréard, Pierre Le Pogam, Marc Litaudon, Vincent Dumontet, Nelly Bataillé-Simoneau, Thomas Guillemette, Philippe Simoneau, Andreas Schinkovitz, David Guilet, Guillaume Viault* and Pascal Richomme*, 
{"title":"从钙叶菊中分离出的抑制折叠蛋白反应的黄酮。","authors":"Marine Chambaud,&nbsp;Anne-Marie Le Ray,&nbsp;Racha Hamzi,&nbsp;Thomas Charpentier,&nbsp;Nadège Blon,&nbsp;Dimitri Bréard,&nbsp;Pierre Le Pogam,&nbsp;Marc Litaudon,&nbsp;Vincent Dumontet,&nbsp;Nelly Bataillé-Simoneau,&nbsp;Thomas Guillemette,&nbsp;Philippe Simoneau,&nbsp;Andreas Schinkovitz,&nbsp;David Guilet,&nbsp;Guillaume Viault* and Pascal Richomme*,&nbsp;","doi":"10.1021/acs.jnatprod.4c00328","DOIUrl":null,"url":null,"abstract":"<p >The unfolded protein response (UPR) is a key component of fungal virulence. The prenylated xanthone γ-mangostin isolated from <i>Garcinia mangostana</i> (Clusiaceae) fruit pericarp, has recently been described to inhibit this fungal adaptative pathway. Considering that <i>Calophyllum caledonicum</i> (Calophyllaceae) is known for its high prenylated xanthone content, its stem bark extract was fractionated using a bioassay-guided procedure based on the cell-based anti-UPR assay. Four previously undescribed xanthone derivatives were isolated, caledonixanthones N–Q (<b>3</b>, <b>4</b>, <b>8</b>, and <b>12</b>), among which compounds <b>3</b> and <b>8</b> showed promising anti-UPR activities with IC<sub>50</sub> values of 11.7 ± 0.9 and 7.9 ± 0.3 μM, respectively.</p>","PeriodicalId":47,"journal":{"name":"Journal of Natural Products ","volume":null,"pages":null},"PeriodicalIF":3.3000,"publicationDate":"2024-06-13","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Xanthone Inhibitors of Unfolded Protein Response Isolated from Calophyllum caledonicum\",\"authors\":\"Marine Chambaud,&nbsp;Anne-Marie Le Ray,&nbsp;Racha Hamzi,&nbsp;Thomas Charpentier,&nbsp;Nadège Blon,&nbsp;Dimitri Bréard,&nbsp;Pierre Le Pogam,&nbsp;Marc Litaudon,&nbsp;Vincent Dumontet,&nbsp;Nelly Bataillé-Simoneau,&nbsp;Thomas Guillemette,&nbsp;Philippe Simoneau,&nbsp;Andreas Schinkovitz,&nbsp;David Guilet,&nbsp;Guillaume Viault* and Pascal Richomme*,&nbsp;\",\"doi\":\"10.1021/acs.jnatprod.4c00328\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p >The unfolded protein response (UPR) is a key component of fungal virulence. The prenylated xanthone γ-mangostin isolated from <i>Garcinia mangostana</i> (Clusiaceae) fruit pericarp, has recently been described to inhibit this fungal adaptative pathway. Considering that <i>Calophyllum caledonicum</i> (Calophyllaceae) is known for its high prenylated xanthone content, its stem bark extract was fractionated using a bioassay-guided procedure based on the cell-based anti-UPR assay. Four previously undescribed xanthone derivatives were isolated, caledonixanthones N–Q (<b>3</b>, <b>4</b>, <b>8</b>, and <b>12</b>), among which compounds <b>3</b> and <b>8</b> showed promising anti-UPR activities with IC<sub>50</sub> values of 11.7 ± 0.9 and 7.9 ± 0.3 μM, respectively.</p>\",\"PeriodicalId\":47,\"journal\":{\"name\":\"Journal of Natural Products \",\"volume\":null,\"pages\":null},\"PeriodicalIF\":3.3000,\"publicationDate\":\"2024-06-13\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Journal of Natural Products \",\"FirstCategoryId\":\"99\",\"ListUrlMain\":\"https://pubs.acs.org/doi/10.1021/acs.jnatprod.4c00328\",\"RegionNum\":2,\"RegionCategory\":\"生物学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q2\",\"JCRName\":\"CHEMISTRY, MEDICINAL\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of Natural Products ","FirstCategoryId":"99","ListUrlMain":"https://pubs.acs.org/doi/10.1021/acs.jnatprod.4c00328","RegionNum":2,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"CHEMISTRY, MEDICINAL","Score":null,"Total":0}
引用次数: 0

摘要

未折叠蛋白反应(UPR)是真菌毒力的关键组成部分。最近有报道称,从芒果属(Garcinia mangostana)果皮中分离出的前炔化黄酮γ-芒果苷(prenylated xanthone γ-mangostin)可抑制这种真菌适应途径。考虑到 Calophyllum caledonicum(Calophyllaceae)以其高前基化氧杂蒽酮含量而闻名,我们采用基于细胞抗 UPR 检测的生物测定指导程序对其茎皮提取物进行了分馏。其中化合物 3 和 8 显示出良好的抗 UPR 活性,其 IC50 值分别为 11.7 ± 0.9 和 7.9 ± 0.3 μM。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

摘要图片

查看原文
分享 分享
微信好友 朋友圈 QQ好友 复制链接
本刊更多论文
Xanthone Inhibitors of Unfolded Protein Response Isolated from Calophyllum caledonicum

The unfolded protein response (UPR) is a key component of fungal virulence. The prenylated xanthone γ-mangostin isolated from Garcinia mangostana (Clusiaceae) fruit pericarp, has recently been described to inhibit this fungal adaptative pathway. Considering that Calophyllum caledonicum (Calophyllaceae) is known for its high prenylated xanthone content, its stem bark extract was fractionated using a bioassay-guided procedure based on the cell-based anti-UPR assay. Four previously undescribed xanthone derivatives were isolated, caledonixanthones N–Q (3, 4, 8, and 12), among which compounds 3 and 8 showed promising anti-UPR activities with IC50 values of 11.7 ± 0.9 and 7.9 ± 0.3 μM, respectively.

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
9.10
自引率
5.90%
发文量
294
审稿时长
2.3 months
期刊介绍: The Journal of Natural Products invites and publishes papers that make substantial and scholarly contributions to the area of natural products research. Contributions may relate to the chemistry and/or biochemistry of naturally occurring compounds or the biology of living systems from which they are obtained. Specifically, there may be articles that describe secondary metabolites of microorganisms, including antibiotics and mycotoxins; physiologically active compounds from terrestrial and marine plants and animals; biochemical studies, including biosynthesis and microbiological transformations; fermentation and plant tissue culture; the isolation, structure elucidation, and chemical synthesis of novel compounds from nature; and the pharmacology of compounds of natural origin. When new compounds are reported, manuscripts describing their biological activity are much preferred. Specifically, there may be articles that describe secondary metabolites of microorganisms, including antibiotics and mycotoxins; physiologically active compounds from terrestrial and marine plants and animals; biochemical studies, including biosynthesis and microbiological transformations; fermentation and plant tissue culture; the isolation, structure elucidation, and chemical synthesis of novel compounds from nature; and the pharmacology of compounds of natural origin.
期刊最新文献
Discovery of Uncommon Tryptophan-Containing Diketopiperazines from Aspergillus homomorphus CBS 101889 Using an Aspergillus nidulans Heterologous Expression System. NMR-Guided Isolation of Anti-inflammatory Carabranolides from the Fruits of Carpesium abrotanoides L. Characterization of Sesquiterpene Dimers from the Flowers of Inula japonica and the Structural Revisions of Related Compounds. Genome-Driven Discovery of Antiviral Atralabdans A-C from the Soil-Dwelling Streptomyces atratus. Isolation, Characterization, and Antiproliferative Activity of Terpenoids from the Tropical Plant Turraea delphinensis.
×
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
现在去查看 取消
0
微信
客服QQ
Book学术公众号 扫码关注我们
反馈
×
意见反馈
请填写您的意见或建议
请填写您的手机或邮箱
已复制链接
已复制链接
快去分享给好友吧!
我知道了
×
扫码分享
扫码分享
Book学术官方微信
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术
文献互助 智能选刊 最新文献 互助须知 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 Book学术 All rights reserved.
ghs 京公网安备 11010802042870号 京ICP备2023020795号-1