Caged Xanthones and Biphenyls Isolated from the Tropical Plant Garcinia lateriflora

IF 3.3 2区 生物学 Q2 CHEMISTRY, MEDICINAL Journal of Natural Products Pub Date : 2024-01-22 DOI:10.1021/acs.jnatprod.3c00934
Ayano Kobayashi, Yohei Saito, Katsunori Miyake, Shuichi Fukuyoshi, David J. Newman, Barry R. O’Keefe, Kuo-Hsiung Lee and Kyoko Nakagawa-Goto*, 
{"title":"Caged Xanthones and Biphenyls Isolated from the Tropical Plant Garcinia lateriflora","authors":"Ayano Kobayashi,&nbsp;Yohei Saito,&nbsp;Katsunori Miyake,&nbsp;Shuichi Fukuyoshi,&nbsp;David J. Newman,&nbsp;Barry R. O’Keefe,&nbsp;Kuo-Hsiung Lee and Kyoko Nakagawa-Goto*,&nbsp;","doi":"10.1021/acs.jnatprod.3c00934","DOIUrl":null,"url":null,"abstract":"<p >Four cytotoxic heptacyclic caged-xanthones [gambogefic acids B–E (<b>1</b>–<b>4</b>)], a cytotoxic hexacyclic caged-xanthone [garcilatelic acid (<b>5</b>)], and four biphenyl derivatives [garcilatelibiphenyls A–D (<b>6</b>–<b>9</b>)] were newly isolated in a phytochemical study of a 50% MeOH/CH<sub>2</sub>Cl<sub>2</sub> extract of <i>Garcinia lateriflora</i> (Clusiaceae). The isolated compounds were evaluated for antiproliferative activity against five human tumor cell lines including a vincristine-resistant line. The new caged-xanthones displayed potent activity with IC<sub>50</sub> values from 0.5 to 6.7 μM against all tested tumor cell lines.</p>","PeriodicalId":47,"journal":{"name":"Journal of Natural Products ","volume":"87 2","pages":"266–275"},"PeriodicalIF":3.3000,"publicationDate":"2024-01-22","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.3c00934","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

Abstract

Four cytotoxic heptacyclic caged-xanthones [gambogefic acids B–E (14)], a cytotoxic hexacyclic caged-xanthone [garcilatelic acid (5)], and four biphenyl derivatives [garcilatelibiphenyls A–D (69)] were newly isolated in a phytochemical study of a 50% MeOH/CH2Cl2 extract of Garcinia lateriflora (Clusiaceae). The isolated compounds were evaluated for antiproliferative activity against five human tumor cell lines including a vincristine-resistant line. The new caged-xanthones displayed potent activity with IC50 values from 0.5 to 6.7 μM against all tested tumor cell lines.

Abstract Image

Abstract Image

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
从热带植物红花藤中分离出的笼黄酮和联苯。
在对红花藤(藤黄科)50% MeOH/CH2Cl2 提取物进行的植物化学研究中,新分离出四种细胞毒性七环笼黄酮[gambogefic acids B-E (1-4)]、一种细胞毒性六环笼黄酮[garcilatelic acid (5)]和四种联苯衍生物[garcilatelibiphenyls A-D (6-9)]。研究人员评估了这些化合物对五种人类肿瘤细胞系(包括一种耐长春新碱的细胞系)的抗增殖活性。新的笼黄酮类化合物对所有测试的肿瘤细胞系都显示出了很强的活性,其 IC50 值从 0.5 μM 到 6.7 μM。
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 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
The Paradox of Antimalarial Terpenoid Isonitrile Biosynthesis Explained. Proposal of Cyanoformate as an NC Delivery Vector. Pyridoxal 5'-Phosphate (PLP)-Dependent β- and γ-Substitution Reactions Forming Nonproteinogenic Amino Acids in Natural Product Biosynthesis. Cardenolides in Asclepias syriaca Seeds: Exploring the Legacy of Tadeus Reichstein. Breviane Spiroditerpenoids with Anti-inflammatory and Antiviral Activities from Deep-Sea-Derived Fungus Penicillium sp. F59. Chromones Featuring a [6,6]-Spiroketal Moiety Produced by Coculture of the Endophytic Fungi Chaetomium virescens and Xylaria Grammica.
×
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
×
提示
确定
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