The Sesquiterpenoids from Aglaia cucullata Peel Fruit and Their Cytotoxic Activities Against B16-F10 and HeLa Cancer Cell Lines

Q3 Chemistry Molekul Pub Date : 2023-11-20 DOI:10.20884/1.jm.2023.18.3.7900
U. Supratman, Intan Hawina Anjari, D. Harneti, Al Arofatus Naini, K. Farabi, R. Anwar
{"title":"The Sesquiterpenoids from Aglaia cucullata Peel Fruit and Their Cytotoxic Activities Against B16-F10 and HeLa Cancer Cell Lines","authors":"U. Supratman, Intan Hawina Anjari, D. Harneti, Al Arofatus Naini, K. Farabi, R. Anwar","doi":"10.20884/1.jm.2023.18.3.7900","DOIUrl":null,"url":null,"abstract":"Sesquiterpenoids are terpenoid derivative compounds that have a diverse chemical structure and pharmacological effects. Sesquiterpenoids can be found in many plants of Aglaia which is the large source of natural compounds in the Meliaceae family. This research was aimed to elucidate the structure of sesquiterpenoids from the peel fruit of Aglaia cucullata and their cytotoxic activities against two human cancer cell lines. The n-hexane extract was separated and further purified by various chromatographic methods to yiled three sesquiterpenoids. The structure of these sesquiterpenoids were identified by spectroscopy analysis including MS, IR, 1H-NMR, 13C-NMR and DEPT as well as compared with spectral data which reported previously. The sesquiterpenoid compounds 1-3 were identified as spathulenol (1), alismol (2), and 10-oxo-isodauc-3-en-15-al (3). The cytotoxic activity of three sesquiterpenoid compounds were tested against HeLa cervical cancer cell and B16-F10 skin cancer cell using the PrestoBlue method. Compound 2 exhibited the highest activity against both HeLa and B16-F10 cancer cell lines with IC50 48.11 μg/mL and 57.05 μg/mL, respectively.","PeriodicalId":18773,"journal":{"name":"Molekul","volume":"21 5-6","pages":""},"PeriodicalIF":0.0000,"publicationDate":"2023-11-20","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Molekul","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.20884/1.jm.2023.18.3.7900","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q3","JCRName":"Chemistry","Score":null,"Total":0}
引用次数: 0

Abstract

Sesquiterpenoids are terpenoid derivative compounds that have a diverse chemical structure and pharmacological effects. Sesquiterpenoids can be found in many plants of Aglaia which is the large source of natural compounds in the Meliaceae family. This research was aimed to elucidate the structure of sesquiterpenoids from the peel fruit of Aglaia cucullata and their cytotoxic activities against two human cancer cell lines. The n-hexane extract was separated and further purified by various chromatographic methods to yiled three sesquiterpenoids. The structure of these sesquiterpenoids were identified by spectroscopy analysis including MS, IR, 1H-NMR, 13C-NMR and DEPT as well as compared with spectral data which reported previously. The sesquiterpenoid compounds 1-3 were identified as spathulenol (1), alismol (2), and 10-oxo-isodauc-3-en-15-al (3). The cytotoxic activity of three sesquiterpenoid compounds were tested against HeLa cervical cancer cell and B16-F10 skin cancer cell using the PrestoBlue method. Compound 2 exhibited the highest activity against both HeLa and B16-F10 cancer cell lines with IC50 48.11 μg/mL and 57.05 μg/mL, respectively.
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
葫芦巴果皮中的倍半萜及其对 B16-F10 和 HeLa 癌细胞株的细胞毒活性
倍半萜是萜类衍生物化合物,具有多种化学结构和药理作用。茜草科植物是天然化合物的主要来源,在茜草科的许多植物中都能发现倍半萜类化合物。本研究旨在阐明葫芦科植物果皮中的倍半萜类化合物的结构及其对两种人类癌细胞株的细胞毒活性。正己烷提取物经多种色谱法分离和进一步纯化后,分离出三种倍半萜类化合物。通过质谱、红外光谱、1H-NMR、13C-NMR 和 DEPT 等光谱分析确定了这些倍半萜化合物的结构,并与之前报道的光谱数据进行了比较。经鉴定,倍半萜化合物 1-3 分别为 spathulenol(1)、alismol(2)和 10-oxo-isodauc-3-en-15-al (3)。采用 PrestoBlue 法测试了三种倍半萜化合物对 HeLa 宫颈癌细胞和 B16-F10 皮肤癌细胞的细胞毒活性。化合物 2 对 HeLa 和 B16-F10 癌细胞株的活性最高,IC50 分别为 48.11 μg/mL 和 57.05 μg/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
Molekul
Molekul Chemistry-Chemistry (all)
CiteScore
1.30
自引率
0.00%
发文量
31
审稿时长
4 weeks
期刊最新文献
The Exploration of Bioactive Peptides that Docked to SARS-CoV-2 Spike Protein from Goats’ Milk Beta-Casein by In Silico Synthesis and Characterization of Anethole-lauryl Methacrylate Copolymer via Cationic Polymerization Glycine-modulated Zirconium Perylene-based Metal-Organic Framework for Rhodamin B Photocatalytic Degradation Production, Characterization, and Toxicity Test of L-asparaginase from Vibrio alginolyticus Bacterial Symbiont of Green Algae Caulerpa lentillifera Screening The Anticancer Activity for New Schiff Bases of Natural Steroids
×
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