Polyoxygenated cyclohexenes from the stems of Uvaria calamistrata

IF 3.2 2区 生物学 Q2 BIOCHEMISTRY & MOLECULAR BIOLOGY Phytochemistry Pub Date : 2025-01-30 DOI:10.1016/j.phytochem.2025.114421
Lihang Niu , Jiahang Li , Qiang Zhang , Haoxuan Jin , Chunfeng Xie , Cheng Yang
{"title":"Polyoxygenated cyclohexenes from the stems of Uvaria calamistrata","authors":"Lihang Niu ,&nbsp;Jiahang Li ,&nbsp;Qiang Zhang ,&nbsp;Haoxuan Jin ,&nbsp;Chunfeng Xie ,&nbsp;Cheng Yang","doi":"10.1016/j.phytochem.2025.114421","DOIUrl":null,"url":null,"abstract":"<div><div>Nine previously undescribed polyoxygenated cyclohexenes uvacalols L–T (<strong>1</strong>–<strong>9</strong>), together with five known analogues (<strong>10</strong>–<strong>14</strong>) were obtained from the stems of <em>Uvaria calamistrata</em>. Their structures were established through spectroscopic data analysis, circular dichroism calculations and single-crystal X-ray diffraction. Uvacalols L–N (<strong>1</strong>–<strong>3</strong>) are chlorinated analogues. Some compounds were measured for their anti-inflammatory activities through NO generation inhibition in RAW 264.7 cells. Compound <strong>8</strong> had the best inhibitory activity with an IC<sub>50</sub> value of 4.49 ± 0.38 μM.</div></div>","PeriodicalId":20170,"journal":{"name":"Phytochemistry","volume":"234 ","pages":"Article 114421"},"PeriodicalIF":3.2000,"publicationDate":"2025-01-30","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Phytochemistry","FirstCategoryId":"99","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S0031942225000445","RegionNum":2,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"BIOCHEMISTRY & MOLECULAR BIOLOGY","Score":null,"Total":0}
引用次数: 0

Abstract

Nine previously undescribed polyoxygenated cyclohexenes uvacalols L–T (19), together with five known analogues (1014) were obtained from the stems of Uvaria calamistrata. Their structures were established through spectroscopic data analysis, circular dichroism calculations and single-crystal X-ray diffraction. Uvacalols L–N (13) are chlorinated analogues. Some compounds were measured for their anti-inflammatory activities through NO generation inhibition in RAW 264.7 cells. Compound 8 had the best inhibitory activity with an IC50 value of 4.49 ± 0.38 μM.

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
求助全文
约1分钟内获得全文 去求助
来源期刊
Phytochemistry
Phytochemistry 生物-植物科学
CiteScore
6.40
自引率
7.90%
发文量
443
审稿时长
39 days
期刊介绍: Phytochemistry is a leading international journal publishing studies of plant chemistry, biochemistry, molecular biology and genetics, structure and bioactivities of phytochemicals, including ''-omics'' and bioinformatics/computational biology approaches. Phytochemistry is a primary source for papers dealing with phytochemicals, especially reports concerning their biosynthesis, regulation, and biological properties both in planta and as bioactive principles. Articles are published online as soon as possible as Articles-in-Press and in 12 volumes per year. Occasional topic-focussed special issues are published composed of papers from invited authors.
期刊最新文献
Editorial Board Anti-inflammatory sesquiterpenoids from Chloranthus japonicus. Megastigmane glycosides from Heterosmilax yunnanensis and their neuroprotective activity. Undescribed alkaloids, peptides and polyketides from marine sediment-derived fungus Aspergillus terreus PPS1. Editorial Board
×
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