Two new compounds from Pentadesma butyracea and their biological activities

IF 1.3 4区 生物学 Q4 CHEMISTRY, MEDICINAL
Yue Yang, Li Hua Gong, Fu Hua Peng, Tao Jiang, Jian Guo Hu, Hong Dong Liu, Bin Li, Yin Xia Yang, Jing Ying Peng, Xue Mei Gao
{"title":"Two new compounds from Pentadesma butyracea and their biological activities","authors":"Yue Yang,&nbsp;Li Hua Gong,&nbsp;Fu Hua Peng,&nbsp;Tao Jiang,&nbsp;Jian Guo Hu,&nbsp;Hong Dong Liu,&nbsp;Bin Li,&nbsp;Yin Xia Yang,&nbsp;Jing Ying Peng,&nbsp;Xue Mei Gao","doi":"10.1016/j.phytol.2025.02.012","DOIUrl":null,"url":null,"abstract":"<div><div>Two new compounds (<strong>1</strong>-<strong>2</strong>) and twenty-two known compounds (<strong>3</strong>-<strong>24</strong>) were isolated from the ethanol extract of the stems and leaves of <em>Pentadesma butyracea</em> Sabine (Clusiaceae). The structures of compounds <strong>1</strong>-<strong>2</strong> were elucidated by spectroscopic methods, including extensive 1D- and 2D-NMR spectroscopy and HRMS techniques. According to previous literature research and molecular docking, we tested antiproliferative and <em>α</em>-glucosidase inhibitory activities of these compounds. Compounds <strong>1</strong>, <strong>5</strong>, and <strong>6</strong> showed good <em>α</em>-glucosidase inhibitory activities with IC<sub>50</sub> values of 23.12, 3.60, and 16.83 <em>μ</em>M, respectively. Molecular docking results showed that compounds <strong>1</strong>, <strong>5</strong>, and <strong>6</strong> have strong binding affinities with <em>α</em>-glucosidase. In addition, the antiproliferative activities of compounds <strong>1</strong>, <strong>5</strong>, and <strong>6</strong> against human cancer A549 cells exhibited IC<sub>50</sub> values of 41.47, 19.46 and 45.75 <em>μ</em>M, respectively. Except for compound <strong>14</strong>, all the compounds were isolated from the genus <em>Pentadesma</em> for the first time. The findings propose that xanthones with isoprenyl groups may be effective lead compounds for the development of <em>α</em>-glucosidase inhibitors and anticancer therapies.</div></div>","PeriodicalId":20408,"journal":{"name":"Phytochemistry Letters","volume":"66 ","pages":"Pages 119-125"},"PeriodicalIF":1.3000,"publicationDate":"2025-03-03","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Phytochemistry Letters","FirstCategoryId":"99","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S1874390025010249","RegionNum":4,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q4","JCRName":"CHEMISTRY, MEDICINAL","Score":null,"Total":0}
引用次数: 0

Abstract

Two new compounds (1-2) and twenty-two known compounds (3-24) were isolated from the ethanol extract of the stems and leaves of Pentadesma butyracea Sabine (Clusiaceae). The structures of compounds 1-2 were elucidated by spectroscopic methods, including extensive 1D- and 2D-NMR spectroscopy and HRMS techniques. According to previous literature research and molecular docking, we tested antiproliferative and α-glucosidase inhibitory activities of these compounds. Compounds 1, 5, and 6 showed good α-glucosidase inhibitory activities with IC50 values of 23.12, 3.60, and 16.83 μM, respectively. Molecular docking results showed that compounds 1, 5, and 6 have strong binding affinities with α-glucosidase. In addition, the antiproliferative activities of compounds 1, 5, and 6 against human cancer A549 cells exhibited IC50 values of 41.47, 19.46 and 45.75 μM, respectively. Except for compound 14, all the compounds were isolated from the genus Pentadesma for the first time. The findings propose that xanthones with isoprenyl groups may be effective lead compounds for the development of α-glucosidase inhibitors and anticancer therapies.
丁酸戊二烯的两个新化合物及其生物活性
从丁酸Pentadesma butyracea Sabine (Clusiaceae)茎叶乙醇提取物中分离得到2个新化合物(1 ~ 2个)和22个已知化合物(3 ~ 24个)。化合物1-2的结构通过波谱方法进行了鉴定,包括广泛的一维和二维核磁共振波谱和HRMS技术。根据前期文献研究和分子对接,我们测试了这些化合物的抗增殖活性和α-葡萄糖苷酶抑制活性。化合物1、5、6具有良好的α-葡萄糖苷酶抑制活性,IC50值分别为23.12、3.60、16.83 μM。分子对接结果表明,化合物1、5、6与α-葡萄糖苷酶具有较强的结合亲和力。化合物1、5、6对人肿瘤A549细胞的IC50值分别为41.47、19.46和45.75 μM。除化合物14外,其余化合物均为首次从该属植物中分离得到。这些发现表明,含异戊二烯基的山酮可能是开发α-葡萄糖苷酶抑制剂和抗癌药物的有效先导化合物。
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 求助全文
来源期刊
Phytochemistry Letters
Phytochemistry Letters 生物-生化与分子生物学
CiteScore
3.00
自引率
11.80%
发文量
190
审稿时长
34 days
期刊介绍: Phytochemistry Letters invites rapid communications on all aspects of natural product research including: • Structural elucidation of natural products • Analytical evaluation of herbal medicines • Clinical efficacy, safety and pharmacovigilance of herbal medicines • Natural product biosynthesis • Natural product synthesis and chemical modification • Natural product metabolism • Chemical ecology • Biotechnology • Bioassay-guided isolation • Pharmacognosy • Pharmacology of natural products • Metabolomics • Ethnobotany and traditional usage • Genetics of natural products Manuscripts that detail the isolation of just one new compound are not substantial enough to be sent out of review and are out of scope. Furthermore, where pharmacology has been performed on one new compound to increase the amount of novel data, the pharmacology must be substantial and/or related to the medicinal use of the producing organism.
×
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:604180095
Book学术官方微信