新型硒氰酸菊素的合成及抗增殖活性评价

IF 1.8 3区 化学 Q3 CHEMISTRY, ORGANIC
Zhiping Liu , Lijie Che , Yunlong Ban , Maixia Liu , Xiyan Tang , Yanmin Huang , Jianguo Cui , Chunfang Gan
{"title":"新型硒氰酸菊素的合成及抗增殖活性评价","authors":"Zhiping Liu ,&nbsp;Lijie Che ,&nbsp;Yunlong Ban ,&nbsp;Maixia Liu ,&nbsp;Xiyan Tang ,&nbsp;Yanmin Huang ,&nbsp;Jianguo Cui ,&nbsp;Chunfang Gan","doi":"10.1080/00397911.2024.2445860","DOIUrl":null,"url":null,"abstract":"<div><div>Selenocyano fragments with distinct structural characteristics were successfully incorporated into the 5- and 7-positions of chrysin via etherification and esterification of its hydroxyl groups. Eleven novel chrysin selenocyanates were synthesized, and their structures characterized by NMR and HRMS. The activities of all compounds were evaluated against human cervical cancer cell lines HeLa, ovarian cancer cell lines SKOV-3, and breast carcinoma cell lines MCF-7 using MTT assays. Results indicated that esterified chrysin derivatives significantly inhibited HeLa cells, while alkylated chrysin ethers showed notable activity against SKOV-3 and MCF-7 cells. Compounds <strong>5c</strong> and <strong>5e</strong> exhibited the strongest inhibitory effects on SKOV-3 cells, with IC<sub>50</sub> values of 2.27 ± 0.19 μM and 2.51 ± 0.33 μM, respectively. The introduction of diselenocyanate at both the 5- and 7-positions demonstrated superior inhibitory activity compared to a single selenocyanate at the 7-position alone. The findings may aid in designing novel chemotherapeutic drugs.</div></div>","PeriodicalId":22119,"journal":{"name":"Synthetic Communications","volume":"55 3","pages":"Pages 259-269"},"PeriodicalIF":1.8000,"publicationDate":"2025-02-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Synthesis and antiproliferative evaluation of novel chrysin selenocyanates\",\"authors\":\"Zhiping Liu ,&nbsp;Lijie Che ,&nbsp;Yunlong Ban ,&nbsp;Maixia Liu ,&nbsp;Xiyan Tang ,&nbsp;Yanmin Huang ,&nbsp;Jianguo Cui ,&nbsp;Chunfang Gan\",\"doi\":\"10.1080/00397911.2024.2445860\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><div>Selenocyano fragments with distinct structural characteristics were successfully incorporated into the 5- and 7-positions of chrysin via etherification and esterification of its hydroxyl groups. Eleven novel chrysin selenocyanates were synthesized, and their structures characterized by NMR and HRMS. The activities of all compounds were evaluated against human cervical cancer cell lines HeLa, ovarian cancer cell lines SKOV-3, and breast carcinoma cell lines MCF-7 using MTT assays. Results indicated that esterified chrysin derivatives significantly inhibited HeLa cells, while alkylated chrysin ethers showed notable activity against SKOV-3 and MCF-7 cells. Compounds <strong>5c</strong> and <strong>5e</strong> exhibited the strongest inhibitory effects on SKOV-3 cells, with IC<sub>50</sub> values of 2.27 ± 0.19 μM and 2.51 ± 0.33 μM, respectively. The introduction of diselenocyanate at both the 5- and 7-positions demonstrated superior inhibitory activity compared to a single selenocyanate at the 7-position alone. The findings may aid in designing novel chemotherapeutic drugs.</div></div>\",\"PeriodicalId\":22119,\"journal\":{\"name\":\"Synthetic Communications\",\"volume\":\"55 3\",\"pages\":\"Pages 259-269\"},\"PeriodicalIF\":1.8000,\"publicationDate\":\"2025-02-01\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Synthetic Communications\",\"FirstCategoryId\":\"92\",\"ListUrlMain\":\"https://www.sciencedirect.com/org/science/article/pii/S0039791124001498\",\"RegionNum\":3,\"RegionCategory\":\"化学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q3\",\"JCRName\":\"CHEMISTRY, ORGANIC\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Synthetic Communications","FirstCategoryId":"92","ListUrlMain":"https://www.sciencedirect.com/org/science/article/pii/S0039791124001498","RegionNum":3,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q3","JCRName":"CHEMISTRY, ORGANIC","Score":null,"Total":0}
引用次数: 0

摘要

具有明显结构特征的硒基氰酸酯片段通过其羟基的醚化和酯化作用成功地结合到菊花素的5位和7位上。合成了11种新型的菊花素硒氰酸酯,并通过NMR和HRMS对其结构进行了表征。采用MTT法测定了各化合物对人宫颈癌细胞株HeLa、卵巢癌细胞株SKOV-3和乳腺癌细胞株MCF-7的活性。结果表明,酯化的菊花素衍生物对HeLa细胞有明显的抑制作用,而烷基化的菊花素醚对SKOV-3和MCF-7细胞有明显的抑制作用。化合物5c和5e对SKOV-3细胞的抑制作用最强,IC50值分别为2.27±0.19 μM和2.51±0.33 μM。在5位和7位引入二硒氰酸酯比在7位单独引入硒氰酸酯表现出更好的抑制活性。这一发现可能有助于设计新的化疗药物。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Synthesis and antiproliferative evaluation of novel chrysin selenocyanates
Selenocyano fragments with distinct structural characteristics were successfully incorporated into the 5- and 7-positions of chrysin via etherification and esterification of its hydroxyl groups. Eleven novel chrysin selenocyanates were synthesized, and their structures characterized by NMR and HRMS. The activities of all compounds were evaluated against human cervical cancer cell lines HeLa, ovarian cancer cell lines SKOV-3, and breast carcinoma cell lines MCF-7 using MTT assays. Results indicated that esterified chrysin derivatives significantly inhibited HeLa cells, while alkylated chrysin ethers showed notable activity against SKOV-3 and MCF-7 cells. Compounds 5c and 5e exhibited the strongest inhibitory effects on SKOV-3 cells, with IC50 values of 2.27 ± 0.19 μM and 2.51 ± 0.33 μM, respectively. The introduction of diselenocyanate at both the 5- and 7-positions demonstrated superior inhibitory activity compared to a single selenocyanate at the 7-position alone. The findings may aid in designing novel chemotherapeutic drugs.
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
Synthetic Communications
Synthetic Communications 化学-有机化学
CiteScore
4.40
自引率
4.80%
发文量
156
审稿时长
4.3 months
期刊介绍: Synthetic Communications presents communications describing new methods, reagents, and other synthetic work pertaining to organic chemistry with sufficient experimental detail to permit reported reactions to be repeated by a chemist reasonably skilled in the art. In addition, the Journal features short, focused review articles discussing topics within its remit of synthetic organic chemistry.
×
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