Chemical Constituents and Antimicrobial Properties of the Nonresinous Heartwood of Aquilaria sinensis

IF 0.8 4区 化学 Q4 CHEMISTRY, MEDICINAL
Xiao-Yan Duan, Dong-Bao Hu, Hataichanok Pandith, Terd Disayathanoowat, Xue Bai, Jun Yang, Ji-Feng Luo, Angkhana Inta, Yue-Hu Wang
{"title":"Chemical Constituents and Antimicrobial Properties of the Nonresinous Heartwood of Aquilaria sinensis","authors":"Xiao-Yan Duan,&nbsp;Dong-Bao Hu,&nbsp;Hataichanok Pandith,&nbsp;Terd Disayathanoowat,&nbsp;Xue Bai,&nbsp;Jun Yang,&nbsp;Ji-Feng Luo,&nbsp;Angkhana Inta,&nbsp;Yue-Hu Wang","doi":"10.1007/s10600-025-04571-z","DOIUrl":null,"url":null,"abstract":"<p>Twenty-six compounds, including one new 2-(2-phenylethyl)chromone derivative, (<i>R</i>)-2-(1-hydroxy-2- phenylethyl)chromone (<b>1</b>), and one new resorcylic acid lactone, (<i>S</i>)-de-O-methylhispidulactone A (<b>2</b>), were isolated from the nonresinous heartwood of <i>Aqualaria sinensis</i> (Lour.) Spreng. Among these compounds, (<i>S</i>)-de-<i>O</i>-methylhispidulactone A (<b>2</b>), 2-(2-phenylethyl)chromone (<b>4</b>), 2-[2-(4-hydroxyphenyl)ethyl]chromone (<b>7</b>), 6-methoxy-2-(2-phenylethyl)chromone (<b>8</b>), 6-methoxy-2-[2-(3-methoxyphenyl)ethyl]chromone (<b>9</b>), 2-[2-(3-methoxyphenyl)ethyl]chromone (<b>10</b>), 6,7-dimethoxy-2-(2-phenylethyl)chromone (<b>11</b>), 8-chloro-6- hydroxy-2-[2-(4-methoxyphenyl)ethyl]chromon-4-one (<b>13</b>), (+)-(<i>R</i>)-de-<i>O</i>-methyllasiodiplodin (<b>14</b>), lasiodiplodin (<b>15</b>), and (3<i>R</i>)-(–)-melliein (<b>20</b>) exhibited antifungal activity against <i>Epidermophyton floccosum</i>, <i>Trichophyton rubrum</i>, and <i>Microsporum gypseum</i>, with MIC values ranging from 5.8 to 51.6 μM. Furthermore, (<i>R</i>)-2-(2-hydroxy-2-phenylethyl)chromone (<b>3b</b>), <b>7</b>, <b>8</b>, <b>9</b>, <b>14, 15</b>, 5-hydroxy-7,3′,4′- trimethoxyflavone (<b>17</b>), and velutin (<b>18</b>) demonstrated antibacterial effects against <i>Staphylococcus aureus</i>, with MIC values ranging from 20.2 to 96.0 μM.</p>","PeriodicalId":514,"journal":{"name":"Chemistry of Natural Compounds","volume":"61 1","pages":"42 - 51"},"PeriodicalIF":0.8000,"publicationDate":"2025-02-08","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Chemistry of Natural Compounds","FirstCategoryId":"92","ListUrlMain":"https://link.springer.com/article/10.1007/s10600-025-04571-z","RegionNum":4,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q4","JCRName":"CHEMISTRY, MEDICINAL","Score":null,"Total":0}
引用次数: 0

Abstract

Twenty-six compounds, including one new 2-(2-phenylethyl)chromone derivative, (R)-2-(1-hydroxy-2- phenylethyl)chromone (1), and one new resorcylic acid lactone, (S)-de-O-methylhispidulactone A (2), were isolated from the nonresinous heartwood of Aqualaria sinensis (Lour.) Spreng. Among these compounds, (S)-de-O-methylhispidulactone A (2), 2-(2-phenylethyl)chromone (4), 2-[2-(4-hydroxyphenyl)ethyl]chromone (7), 6-methoxy-2-(2-phenylethyl)chromone (8), 6-methoxy-2-[2-(3-methoxyphenyl)ethyl]chromone (9), 2-[2-(3-methoxyphenyl)ethyl]chromone (10), 6,7-dimethoxy-2-(2-phenylethyl)chromone (11), 8-chloro-6- hydroxy-2-[2-(4-methoxyphenyl)ethyl]chromon-4-one (13), (+)-(R)-de-O-methyllasiodiplodin (14), lasiodiplodin (15), and (3R)-(–)-melliein (20) exhibited antifungal activity against Epidermophyton floccosum, Trichophyton rubrum, and Microsporum gypseum, with MIC values ranging from 5.8 to 51.6 μM. Furthermore, (R)-2-(2-hydroxy-2-phenylethyl)chromone (3b), 7, 8, 9, 14, 15, 5-hydroxy-7,3′,4′- trimethoxyflavone (17), and velutin (18) demonstrated antibacterial effects against Staphylococcus aureus, with MIC values ranging from 20.2 to 96.0 μM.

Abstract Image

求助全文
约1分钟内获得全文 求助全文
来源期刊
Chemistry of Natural Compounds
Chemistry of Natural Compounds 化学-有机化学
CiteScore
1.40
自引率
25.00%
发文量
265
审稿时长
7.8 months
期刊介绍: Chemistry of Natural Compounds publishes reviews and general articles about the structure of different classes of natural compounds, the chemical characteristics of botanical families, genus, and species, to establish the comparative laws and connection between physiological activity and the structure of substances.
×
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