新型含硒氰酸酯的硒酚酰胺衍生物的设计、合成及抗增殖活性研究

IF 2 3区 化学 Q2 CHEMISTRY, ORGANIC
Zhiping Liu, Lijie Che, Jie Pang, Xiyan Tang, Chunfang Gan, Jianguo Cui, Yanmin Huang
{"title":"新型含硒氰酸酯的硒酚酰胺衍生物的设计、合成及抗增殖活性研究","authors":"Zhiping Liu,&nbsp;Lijie Che,&nbsp;Jie Pang,&nbsp;Xiyan Tang,&nbsp;Chunfang Gan,&nbsp;Jianguo Cui,&nbsp;Yanmin Huang","doi":"10.1002/jhet.70009","DOIUrl":null,"url":null,"abstract":"<div>\n \n <p>Twelve novel amide-linked selenophenol selenocyanates were synthesized by integrating selenocyanates into selenophenol rings via amide bonds with diversified alkyl chain lengths. Their structures were confirmed by <sup>1</sup>H/<sup>13</sup>C NMR and HR-MS. The antiproliferation activities of these compounds was assessed using the MTT assay against multiple cancer cell lines. Notably, compound <b>6h</b> exhibited potent inhibitory effects against SKOV-3 cells (IC<sub>50</sub> = 1.96 μM), while compound <b>6l</b> demonstrated significant activity against MCF-7 (IC<sub>50</sub> = 7.29 μM) and HepG-2 cells (IC<sub>50</sub> = 6.71 μM). These results suggest that these selenophenol selenocyanate derivatives represent a promising class of small-molecule selenium-based therapeutics, warranting further investigations for potential medicinal applications.</p>\n </div>","PeriodicalId":194,"journal":{"name":"Journal of Heterocyclic Chemistry","volume":"62 9","pages":"720-729"},"PeriodicalIF":2.0000,"publicationDate":"2025-07-17","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Design, Synthesis, and Antiproliferative Activity of New Selenocyanate-Containing Selenophenol Amide Derivatives\",\"authors\":\"Zhiping Liu,&nbsp;Lijie Che,&nbsp;Jie Pang,&nbsp;Xiyan Tang,&nbsp;Chunfang Gan,&nbsp;Jianguo Cui,&nbsp;Yanmin Huang\",\"doi\":\"10.1002/jhet.70009\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div>\\n \\n <p>Twelve novel amide-linked selenophenol selenocyanates were synthesized by integrating selenocyanates into selenophenol rings via amide bonds with diversified alkyl chain lengths. Their structures were confirmed by <sup>1</sup>H/<sup>13</sup>C NMR and HR-MS. The antiproliferation activities of these compounds was assessed using the MTT assay against multiple cancer cell lines. Notably, compound <b>6h</b> exhibited potent inhibitory effects against SKOV-3 cells (IC<sub>50</sub> = 1.96 μM), while compound <b>6l</b> demonstrated significant activity against MCF-7 (IC<sub>50</sub> = 7.29 μM) and HepG-2 cells (IC<sub>50</sub> = 6.71 μM). These results suggest that these selenophenol selenocyanate derivatives represent a promising class of small-molecule selenium-based therapeutics, warranting further investigations for potential medicinal applications.</p>\\n </div>\",\"PeriodicalId\":194,\"journal\":{\"name\":\"Journal of Heterocyclic Chemistry\",\"volume\":\"62 9\",\"pages\":\"720-729\"},\"PeriodicalIF\":2.0000,\"publicationDate\":\"2025-07-17\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Journal of Heterocyclic Chemistry\",\"FirstCategoryId\":\"92\",\"ListUrlMain\":\"https://onlinelibrary.wiley.com/doi/10.1002/jhet.70009\",\"RegionNum\":3,\"RegionCategory\":\"化学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q2\",\"JCRName\":\"CHEMISTRY, ORGANIC\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of Heterocyclic Chemistry","FirstCategoryId":"92","ListUrlMain":"https://onlinelibrary.wiley.com/doi/10.1002/jhet.70009","RegionNum":3,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"CHEMISTRY, ORGANIC","Score":null,"Total":0}
引用次数: 0

摘要

通过不同烷基链长度的酰胺键,将硒氰酸酯整合到硒酚环上,合成了12种新型的酰胺链硒酚酸酯。它们的结构经1H/13C NMR和HR-MS证实。用MTT法测定了这些化合物对多种癌细胞的抗增殖活性。值得注意的是,化合物6h对SKOV-3细胞具有较强的抑制作用(IC50 = 1.96 μM),而化合物6l对MCF-7细胞(IC50 = 7.29 μM)和HepG-2细胞(IC50 = 6.71 μM)具有较强的抑制作用。这些结果表明,这些硒酚硒氰酸酯衍生物代表了一类有前途的小分子硒基治疗药物,值得进一步研究潜在的医学应用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Design, Synthesis, and Antiproliferative Activity of New Selenocyanate-Containing Selenophenol Amide Derivatives

Twelve novel amide-linked selenophenol selenocyanates were synthesized by integrating selenocyanates into selenophenol rings via amide bonds with diversified alkyl chain lengths. Their structures were confirmed by 1H/13C NMR and HR-MS. The antiproliferation activities of these compounds was assessed using the MTT assay against multiple cancer cell lines. Notably, compound 6h exhibited potent inhibitory effects against SKOV-3 cells (IC50 = 1.96 μM), while compound 6l demonstrated significant activity against MCF-7 (IC50 = 7.29 μM) and HepG-2 cells (IC50 = 6.71 μM). These results suggest that these selenophenol selenocyanate derivatives represent a promising class of small-molecule selenium-based therapeutics, warranting further investigations for potential medicinal applications.

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 Heterocyclic Chemistry
Journal of Heterocyclic Chemistry 化学-有机化学
CiteScore
5.20
自引率
4.20%
发文量
177
审稿时长
3.9 months
期刊介绍: The Journal of Heterocyclic Chemistry is interested in publishing research on all aspects of heterocyclic chemistry, especially development and application of efficient synthetic methodologies and strategies for the synthesis of various heterocyclic compounds. In addition, Journal of Heterocyclic Chemistry promotes research in other areas that contribute to heterocyclic synthesis/application, such as synthesis design, reaction techniques, flow chemistry and continuous processing, multiphase catalysis, green chemistry, catalyst immobilization and recycling.
×
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