A new nemoralisin-type diterpenoid from Aglaia lawii.

IF 1.6 3区 化学 Q3 CHEMISTRY, APPLIED Natural Product Research Pub Date : 2025-03-08 DOI:10.1080/14786419.2025.2476204
Quan H Pham, Van T K Nguyen, Nguyen-Nguyen Pham-Tran, Binh T D Trinh, Ly T T Nguyen, Le-Thu T Nguyen, Ngoc T T Pham, Lien-Hoa D Nguyen, Ngoc T N Ngo
{"title":"A new nemoralisin-type diterpenoid from <i>Aglaia lawii</i>.","authors":"Quan H Pham, Van T K Nguyen, Nguyen-Nguyen Pham-Tran, Binh T D Trinh, Ly T T Nguyen, Le-Thu T Nguyen, Ngoc T T Pham, Lien-Hoa D Nguyen, Ngoc T N Ngo","doi":"10.1080/14786419.2025.2476204","DOIUrl":null,"url":null,"abstract":"<p><p>A new nemoralisin-type diterpenoid, nemoralisin O (<b>1</b>), along with ten previously identified compounds, was obtained from <i>Aglaia lawii</i> bark. Structural characterisation was performed using various spectroscopic techniques, with a focus on 1D and 2D NMR, and HR-ESI-MS analysis. The absolute stereochemistry of compound <b>1</b> was established by comparing its experimental ECD spectrum with theoretical ECD spectra of all eight possible stereoisomers using TD-DFT calculations, and by evaluating compatibility of calculated <sup>1</sup>H chemical shifts with experimental values using DP4 probability method. The cytotoxic effects of some isolated compounds on HepG2 human liver cancer cells and the inhibition of α-glucosidase were evaluated. Compounds <b>4</b>, <b>5</b>, and <b>6</b> exhibited weak cytotoxicity against HepG2 cells, and showed no inhibitory activity against α-glucosidase (IC<sub>50</sub> > 256 µg/ml).</p>","PeriodicalId":18990,"journal":{"name":"Natural Product Research","volume":" ","pages":"1-9"},"PeriodicalIF":1.6000,"publicationDate":"2025-03-08","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Natural Product Research","FirstCategoryId":"92","ListUrlMain":"https://doi.org/10.1080/14786419.2025.2476204","RegionNum":3,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q3","JCRName":"CHEMISTRY, APPLIED","Score":null,"Total":0}
引用次数: 0

Abstract

A new nemoralisin-type diterpenoid, nemoralisin O (1), along with ten previously identified compounds, was obtained from Aglaia lawii bark. Structural characterisation was performed using various spectroscopic techniques, with a focus on 1D and 2D NMR, and HR-ESI-MS analysis. The absolute stereochemistry of compound 1 was established by comparing its experimental ECD spectrum with theoretical ECD spectra of all eight possible stereoisomers using TD-DFT calculations, and by evaluating compatibility of calculated 1H chemical shifts with experimental values using DP4 probability method. The cytotoxic effects of some isolated compounds on HepG2 human liver cancer cells and the inhibition of α-glucosidase were evaluated. Compounds 4, 5, and 6 exhibited weak cytotoxicity against HepG2 cells, and showed no inhibitory activity against α-glucosidase (IC50 > 256 µg/ml).

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
一种新的麻豆霉素型二萜。
从白杨树皮中分离得到了一种新的线虫素型二萜类化合物nemoralisin O(1)和10个已鉴定的化合物。使用各种光谱技术进行结构表征,重点是1D和2D NMR以及HR-ESI-MS分析。利用TD-DFT计算将化合物1的实验ECD谱与所有8种可能的立体异构体的理论ECD谱进行比较,并利用DP4概率法评估计算的1H化学位移与实验值的相容性,建立了化合物1的绝对立体化学。研究了部分分离化合物对HepG2人肝癌细胞的细胞毒作用及α-葡萄糖苷酶的抑制作用。化合物4、5、6对HepG2细胞具有较弱的细胞毒性,对α-葡萄糖苷酶无抑制活性(IC50 ~ 256µg/ml)。
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
Natural Product Research
Natural Product Research 化学-医药化学
CiteScore
5.10
自引率
9.10%
发文量
605
审稿时长
2.1 months
期刊介绍: The aim of Natural Product Research is to publish important contributions in the field of natural product chemistry. The journal covers all aspects of research in the chemistry and biochemistry of naturally occurring compounds. The communications include coverage of work on natural substances of land and sea and of plants, microbes and animals. Discussions of structure elucidation, synthesis and experimental biosynthesis of natural products as well as developments of methods in these areas are welcomed in the journal. Finally, research papers in fields on the chemistry-biology boundary, eg. fermentation chemistry, plant tissue culture investigations etc., are accepted into the journal. Natural Product Research issues will be subtitled either ""Part A - Synthesis and Structure"" or ""Part B - Bioactive Natural Products"". for details on this , see the forthcoming articles section. All manuscript submissions are subject to initial appraisal by the Editor, and, if found suitable for further consideration, to peer review by independent, anonymous expert referees. All peer review is single blind and submission is online via ScholarOne Manuscripts.
期刊最新文献
The role of myristicin and gymnemasaponins in modern oncology: bridging natural products and cancer therapeutics Harnessing gene-encoded antioxidant peptides from amphibian skin secretions as a novel therapeutic strategy against influenza a virus Omphalotin peptide from Omphalotus olearius as a natural preservative against Fusarium mold contamination Bioactivity, chemical profiling, and validation of Moringa oleifera cultivated in Suncheon (KR) Exploring hesperidin: an effective naturalphytomedicine for combating breast cancer
×
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:604180095
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