Diterpenoid and phenolic constituents from corn silk (Zea mays) with PTP1B inhibitory activity.

IF 1.9 3区 化学 Q3 CHEMISTRY, APPLIED Natural Product Research Pub Date : 2025-01-01 Epub Date: 2023-10-11 DOI:10.1080/14786419.2023.2265038
Pham Thi Mai Huong, Tran Thi Hong Hanh, Tran Hong Quang, Nguyen Xuan Cuong, Dong-Sung Lee, Nguyen Hoai Nam, Chau Van Minh
{"title":"Diterpenoid and phenolic constituents from corn silk (<i>Zea mays</i>) with PTP1B inhibitory activity.","authors":"Pham Thi Mai Huong, Tran Thi Hong Hanh, Tran Hong Quang, Nguyen Xuan Cuong, Dong-Sung Lee, Nguyen Hoai Nam, Chau Van Minh","doi":"10.1080/14786419.2023.2265038","DOIUrl":null,"url":null,"abstract":"<p><p>Chemical investigation of corn silk resulted in the isolation of nine secondary metabolites, including a new <i>ent</i>-kaurane diterpenoid, zeamaysditerpene A (<b>1</b>) and eight known compounds, stigmaydene A (<b>2</b>), stigmaydene J (<b>3</b>), stigmaydene L (<b>4</b>), stigmane D (<b>5</b>), demethyltorosaflavone D (<b>6</b>), chrysoeriol 6-<i>C</i>-<i>β</i>-boivinopyranosyl-7-<i>O</i>-<i>β</i>-D-glucopyranoside (<b>7</b>), deoxypodophyllotoxin (<b>8</b>), and <i>α</i>-peltatin glucoside (<b>9</b>). Their structures were elucidated using a combination of spectroscopic methods, including 1D and 2D NMR and HRESIQTOF mass spectra. The absolute configuration of <b>1</b> was deduced by applying electronic circular dichroism (ECD) calculation method. Among the isolates, only <b>6</b> displayed significant inhibition against PTP1B activity in a dose-dependent manner, with an IC<sub>50</sub> value of 10.7 ± 0.1 µM. Furthermore, molecular docking simulation was carried out to explore the action perspective of <b>6</b> inside the enzyme PTP1B. This finding suggests that <b>6</b> might be a potential lead for the development of a new anti-diabetic agent.</p>","PeriodicalId":18990,"journal":{"name":"Natural Product Research","volume":" ","pages":"323-330"},"PeriodicalIF":1.9000,"publicationDate":"2025-01-01","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/10.1080/14786419.2023.2265038","RegionNum":3,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2023/10/11 0:00:00","PubModel":"Epub","JCR":"Q3","JCRName":"CHEMISTRY, APPLIED","Score":null,"Total":0}
引用次数: 0

Abstract

Chemical investigation of corn silk resulted in the isolation of nine secondary metabolites, including a new ent-kaurane diterpenoid, zeamaysditerpene A (1) and eight known compounds, stigmaydene A (2), stigmaydene J (3), stigmaydene L (4), stigmane D (5), demethyltorosaflavone D (6), chrysoeriol 6-C-β-boivinopyranosyl-7-O-β-D-glucopyranoside (7), deoxypodophyllotoxin (8), and α-peltatin glucoside (9). Their structures were elucidated using a combination of spectroscopic methods, including 1D and 2D NMR and HRESIQTOF mass spectra. The absolute configuration of 1 was deduced by applying electronic circular dichroism (ECD) calculation method. Among the isolates, only 6 displayed significant inhibition against PTP1B activity in a dose-dependent manner, with an IC50 value of 10.7 ± 0.1 µM. Furthermore, molecular docking simulation was carried out to explore the action perspective of 6 inside the enzyme PTP1B. This finding suggests that 6 might be a potential lead for the development of a new anti-diabetic agent.

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
玉米丝中具有PTP1B抑制活性的二萜类和酚类成分。
对玉米丝进行化学研究,分离出9种次生代谢产物,包括一种新的铀烷二萜,玉米糖苷酶a(1)和8种已知化合物,豆甾醇a(2)、豆甾醇J(3)、豆烯醇L(4)、豆烷D(5)、去甲基环黄黄酮D(6)、黄甾醇6-C-β-博伊文吡喃糖基-7-O-β-D-吡喃葡糖苷(7)、脱氧鬼臼毒素(8),和α-peltatin葡糖苷(9)。使用包括1D和2D NMR以及HRESIQTOF质谱在内的光谱方法的组合来阐明它们的结构。应用电子圆二色性(ECD)计算方法推导了1的绝对构型。在分离株中,只有6株以剂量依赖的方式对PTP1B活性表现出显著的抑制作用,IC50值为10.7 ± 0.1 µM。此外,还进行了分子对接模拟,以探索6在酶PTP1B内的作用前景。这一发现表明,6可能是开发一种新的抗糖尿病药物的潜在线索。
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
Evaluation of the antiulcer activity of ethanolic extract and solvent fractions of Calendula tripterocarpa Rupr. in experimental rats and their DART-ToF-MS profiling. Generation of glucosylantimycins by heterologous expression of a promiscuous glycosyltransferase in a deepsea-derived Streptomyces. Antifungal activity of different extractions of drone larvae (apilarnil). Phenylpropanoids and polyacetylenes from the roots of Adenophora triphylla. Sophaline B inhibits non-small cell lung cancer by activating NLRP3/caspase-1/GSDMD-dependent pyroptosis and PI3K/AKT/mTOR-mediated autophagy.
×
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