Alkaloids and Styryl Lactones from Goniothalamus tortilipetalus and Their Biological Activities.

IF 3.3 2区 生物学 Q2 CHEMISTRY, MEDICINAL Journal of Natural Products Pub Date : 2024-11-07 DOI:10.1021/acs.jnatprod.4c00933
Sorraya Champakam, Brian O Patrick, Natcha Injan, Somkiat Nokbin, Sarot Cheenpracha, Zi Han Loh, Tharakorn Maneerat, Panom Winyayong, Phunrawie Promnart, Siau Hui Mah, Raymond J Andersen, Surat Laphookhieo
{"title":"Alkaloids and Styryl Lactones from <i>Goniothalamus tortilipetalus</i> and Their Biological Activities.","authors":"Sorraya Champakam, Brian O Patrick, Natcha Injan, Somkiat Nokbin, Sarot Cheenpracha, Zi Han Loh, Tharakorn Maneerat, Panom Winyayong, Phunrawie Promnart, Siau Hui Mah, Raymond J Andersen, Surat Laphookhieo","doi":"10.1021/acs.jnatprod.4c00933","DOIUrl":null,"url":null,"abstract":"<p><p>Phytochemical investigations of the twig and leaf extracts of <i>Goniothalamus tortilipetalus</i> resulted in the isolation and identification of two new alkaloids, goniotortiline (<b>1</b>) and goniotortilactam (<b>2</b>), three new styryl lactone derivatives, goniotortilactone (<b>3</b>) and goniotortilols A (<b>4</b>) and B (<b>5</b>), and 25 known compounds. Their structures were elucidated by spectroscopic methods and HRESITOFMS data. Compounds <b>5</b>, <b>13</b>, <b>15</b>, <b>16</b>, <b>22</b>, and <b>30</b> inhibited nitric oxide (NO) production with IC<sub>50</sub> values ranging from 8.7 ± 0.1 to 17 ± 1 μM, revealing stronger effects than the standard drug, dexamethasone (IC<sub>50</sub> 16.9 ± 2.2 μM), and compound <b>30</b> possessed the most potent NO production inhibition. Compounds <b>12</b> and <b>29</b> demonstrated notable efficacy in enhancing glucose consumption with IC<sub>50</sub> values of 77 ± 4 and 66 ± 4 μM, respectively, while their glucose uptakes were 1.7- and 2-fold, respectively.</p>","PeriodicalId":47,"journal":{"name":"Journal of Natural Products ","volume":null,"pages":null},"PeriodicalIF":3.3000,"publicationDate":"2024-11-07","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://doi.org/10.1021/acs.jnatprod.4c00933","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

Phytochemical investigations of the twig and leaf extracts of Goniothalamus tortilipetalus resulted in the isolation and identification of two new alkaloids, goniotortiline (1) and goniotortilactam (2), three new styryl lactone derivatives, goniotortilactone (3) and goniotortilols A (4) and B (5), and 25 known compounds. Their structures were elucidated by spectroscopic methods and HRESITOFMS data. Compounds 5, 13, 15, 16, 22, and 30 inhibited nitric oxide (NO) production with IC50 values ranging from 8.7 ± 0.1 to 17 ± 1 μM, revealing stronger effects than the standard drug, dexamethasone (IC50 16.9 ± 2.2 μM), and compound 30 possessed the most potent NO production inhibition. Compounds 12 and 29 demonstrated notable efficacy in enhancing glucose consumption with IC50 values of 77 ± 4 and 66 ± 4 μM, respectively, while their glucose uptakes were 1.7- and 2-fold, respectively.

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
来自 Goniothalamus tortilipetalus 的生物碱和苯乙烯内酯及其生物活性。
通过对 Goniothalamus tortilipetalus 的树枝和叶提取物进行植物化学研究,分离并鉴定出了两种新生物碱--goniotortiline (1) 和 goniotortilactam (2),三种新苯乙烯内酯衍生物--goniotortilactone (3) 和 goniotortilols A (4) 和 B (5),以及 25 种已知化合物。通过光谱方法和 HRESITOFMS 数据阐明了这些化合物的结构。化合物 5、13、15、16、22 和 30 抑制了一氧化氮(NO)的产生,其 IC50 值从 8.7 ± 0.1 到 17 ± 1 μM,比标准药物地塞米松(IC50 16.9 ± 2.2 μM)的效果更强,其中化合物 30 对一氧化氮产生的抑制作用最强。化合物 12 和 29 在增强葡萄糖消耗方面具有显著疗效,IC50 值分别为 77 ± 4 和 66 ± 4 μM,而它们的葡萄糖摄取量分别为 1.7 倍和 2 倍。
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
Alkaloids and Styryl Lactones from Goniothalamus tortilipetalus and Their Biological Activities. Combining the Strengths of MS and NMR in Biochemometrics: A Case Study on Buddleja officinalis. Structurally Diverse Duclauxins from a Coral-Derived Talaromyces sp. and Insight into Determining the Configuration at C-1 of Heptacyclic Duclauxins by 1H NMR. Doubly Homologated Tyrosine-Containing Peptides from the Cyanobacterium Microcystis aeruginosa NIES-4285 and Their Biosynthesis. Natural Products with Potential for the Treatment of Pain: Global Evidence from the NAPRALERT Database.
×
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