异叶毛蕊叶挥发油的化学成分和对映选择性分析

IF 2.2 3区 农林科学 Q3 CHEMISTRY, APPLIED
Katherine Vivanco, José Vinicio Montesinos, Nixon Cumbicus, Omar Malagón, Gianluca Gilardoni
{"title":"异叶毛蕊叶挥发油的化学成分和对映选择性分析","authors":"Katherine Vivanco, José Vinicio Montesinos, Nixon Cumbicus, Omar Malagón, Gianluca Gilardoni","doi":"10.1080/10412905.2023.2266430","DOIUrl":null,"url":null,"abstract":"ABSTRACTThe first chemical and enantioselective analyses of the essential oil from the leaves of Mauria heterophylla Kunth were carried out. The dry plant materialproduced an essential oil with a 0.09 ± 0.05% yield by weight. The volatile fraction was submitted to GC-MS (qualitative) and GC-FID (quantitative) analyses, on two different stationary phases. A total of forty-four constituents were detected and quantified with at least one column, corresponding to about 85.5% of the whole oil mass. Limonene (15.2%), (E)-β-caryophyllene (11.1%), α-phellandrene (10.9%), germacrene D (6.6%), α-pinene (6.4%), myrcene (3.9%), β-phellandrene (2.8%), bicyclogermacrene (2.8%), (E)-β-farnesene (2.2%) and δ-cadinene (1.2%) were major components. Furthermore, the study was complemented with the enantioselective analysis of eleven common chiral terpenes, carried out on two β-cyclodextrin-based chiral selectors. Among the chiral metabolites, (1R,4S)-(+)-camphene, (1R,5R)-(+)-β-pinene, (S)-(+)-α-phellandrene and (S)-(+)-β-phellandrene were enantiomerically pure, whereas α-pinene, sabinene, limonene, linalool, terpinen-4-ol, α-terpineol and germacrene D were present as scalemic mixtures.KEYWORDS: Mauria heterophyllagas chromatographymass spectrometryenantiomersβ-cyclodextrinEcuador Disclosure statementNo potential conflict of interest was reported by the author(s).","PeriodicalId":15782,"journal":{"name":"Journal of Essential Oil Research","volume":"17 1","pages":"0"},"PeriodicalIF":2.2000,"publicationDate":"2023-10-08","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"The essential oil from leaves of <i>Mauria heterophylla</i> Kunth (Anacardiaceae): chemical and enantioselective analyses\",\"authors\":\"Katherine Vivanco, José Vinicio Montesinos, Nixon Cumbicus, Omar Malagón, Gianluca Gilardoni\",\"doi\":\"10.1080/10412905.2023.2266430\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"ABSTRACTThe first chemical and enantioselective analyses of the essential oil from the leaves of Mauria heterophylla Kunth were carried out. The dry plant materialproduced an essential oil with a 0.09 ± 0.05% yield by weight. The volatile fraction was submitted to GC-MS (qualitative) and GC-FID (quantitative) analyses, on two different stationary phases. A total of forty-four constituents were detected and quantified with at least one column, corresponding to about 85.5% of the whole oil mass. Limonene (15.2%), (E)-β-caryophyllene (11.1%), α-phellandrene (10.9%), germacrene D (6.6%), α-pinene (6.4%), myrcene (3.9%), β-phellandrene (2.8%), bicyclogermacrene (2.8%), (E)-β-farnesene (2.2%) and δ-cadinene (1.2%) were major components. Furthermore, the study was complemented with the enantioselective analysis of eleven common chiral terpenes, carried out on two β-cyclodextrin-based chiral selectors. Among the chiral metabolites, (1R,4S)-(+)-camphene, (1R,5R)-(+)-β-pinene, (S)-(+)-α-phellandrene and (S)-(+)-β-phellandrene were enantiomerically pure, whereas α-pinene, sabinene, limonene, linalool, terpinen-4-ol, α-terpineol and germacrene D were present as scalemic mixtures.KEYWORDS: Mauria heterophyllagas chromatographymass spectrometryenantiomersβ-cyclodextrinEcuador Disclosure statementNo potential conflict of interest was reported by the author(s).\",\"PeriodicalId\":15782,\"journal\":{\"name\":\"Journal of Essential Oil Research\",\"volume\":\"17 1\",\"pages\":\"0\"},\"PeriodicalIF\":2.2000,\"publicationDate\":\"2023-10-08\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Journal of Essential Oil Research\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.1080/10412905.2023.2266430\",\"RegionNum\":3,\"RegionCategory\":\"农林科学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q3\",\"JCRName\":\"CHEMISTRY, APPLIED\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of Essential Oil Research","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1080/10412905.2023.2266430","RegionNum":3,"RegionCategory":"农林科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q3","JCRName":"CHEMISTRY, APPLIED","Score":null,"Total":0}
引用次数: 0

摘要

摘要对野毛蕊叶挥发油进行了化学和对映选择性分析。干燥的植物原料产生的精油重量产率为0.09±0.05%。挥发分在两种不同的固定相上进行GC-MS(定性)和GC-FID(定量)分析。至少一根色谱柱共检测到44种成分,约占整个油团的85.5%。主要成分为柠檬烯(15.2%)、(E)-β-石竹烯(11.1%)、α-茶树烯(10.9%)、木香烯D(6.6%)、α-蒎烯(6.4%)、月桂烯(3.9%)、β-茶树烯(2.8%)、双环茶树烯(2.8%)、(E)-β-法尼烯(2.2%)和δ-木香烯(1.2%)。此外,本研究还对11种常见手性萜烯进行了对映选择性分析,并对两种基于β-环糊精的手性选择物进行了分析。手性代谢物中,(1R、4S)-(+)-莰烯、(1R、5R)-(+)-β-蒎烯、(S)-(+)-α-茶树烯和(S)-(+)-β-茶树烯是对映体纯产物,而α-蒎烯、sabinene、柠檬烯、芳樟醇、松油烯-4-醇、α-松油醇和germacrene D是单组分混合物。关键词:异茶树色谱质谱对映体β-环糊精厄瓜多尔披露声明作者未报告潜在利益冲突。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
The essential oil from leaves of Mauria heterophylla Kunth (Anacardiaceae): chemical and enantioselective analyses
ABSTRACTThe first chemical and enantioselective analyses of the essential oil from the leaves of Mauria heterophylla Kunth were carried out. The dry plant materialproduced an essential oil with a 0.09 ± 0.05% yield by weight. The volatile fraction was submitted to GC-MS (qualitative) and GC-FID (quantitative) analyses, on two different stationary phases. A total of forty-four constituents were detected and quantified with at least one column, corresponding to about 85.5% of the whole oil mass. Limonene (15.2%), (E)-β-caryophyllene (11.1%), α-phellandrene (10.9%), germacrene D (6.6%), α-pinene (6.4%), myrcene (3.9%), β-phellandrene (2.8%), bicyclogermacrene (2.8%), (E)-β-farnesene (2.2%) and δ-cadinene (1.2%) were major components. Furthermore, the study was complemented with the enantioselective analysis of eleven common chiral terpenes, carried out on two β-cyclodextrin-based chiral selectors. Among the chiral metabolites, (1R,4S)-(+)-camphene, (1R,5R)-(+)-β-pinene, (S)-(+)-α-phellandrene and (S)-(+)-β-phellandrene were enantiomerically pure, whereas α-pinene, sabinene, limonene, linalool, terpinen-4-ol, α-terpineol and germacrene D were present as scalemic mixtures.KEYWORDS: Mauria heterophyllagas chromatographymass spectrometryenantiomersβ-cyclodextrinEcuador Disclosure statementNo potential conflict of interest was reported by the author(s).
求助全文
通过发布文献求助,成功后即可免费获取论文全文。 去求助
来源期刊
Journal of Essential Oil Research
Journal of Essential Oil Research 工程技术-食品科技
CiteScore
6.00
自引率
3.30%
发文量
52
审稿时长
18-36 weeks
期刊介绍: Journal of Essential Oil Research ( JEOR) is the major forum for the publication of essential oil research and analysis. Each issue includes studies performed on the chemical composition of some of the 20,000 aromatic plants known in the plant kingdom. JEOR is devoted entirely to all phases of research from every corner of the world by the experts in their field. JEOR''s main areas of focus include: -Analytical chemistry- Biological activity- Biotechnology- Chemical composition- Chemical synthesis- Chemosystematics- Microbiological activity- Plant biochemistry/biosynthesis- Toxicology. Published six times per year, JEOR provides articles on the aromatic principles of a plant or its isolates and are directed toward furthering our readers'' knowledge of the aromatic plant and animal kingdoms.
×
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
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
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 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术官方微信