将抗疟药物重新用于癌症:探索 N-肉桂酰氨基吖啶的抗增殖作用。

IF 2.5 4区 医学 Q3 CHEMISTRY, MEDICINAL
Mélanie Fonte , Catarina Rôla , Sofia Santana , Miguel Prudêncio , Joana Almeida , Ricardo Ferraz , Cristina Prudêncio , Cátia Teixeira , Paula Gomes
{"title":"将抗疟药物重新用于癌症:探索 N-肉桂酰氨基吖啶的抗增殖作用。","authors":"Mélanie Fonte ,&nbsp;Catarina Rôla ,&nbsp;Sofia Santana ,&nbsp;Miguel Prudêncio ,&nbsp;Joana Almeida ,&nbsp;Ricardo Ferraz ,&nbsp;Cristina Prudêncio ,&nbsp;Cátia Teixeira ,&nbsp;Paula Gomes","doi":"10.1016/j.bmcl.2024.129894","DOIUrl":null,"url":null,"abstract":"<div><p>Drug repurposing and rescuing have been widely explored as cost-effective approaches to expand the portfolio of chemotherapeutic agents. Based on the reported antitumor properties of both <em>trans-</em>cinnamic acids and quinacrine, an antimalarial aminoacridine, we explored the antiproliferative properties of two series of <em>N</em>-cinnamoyl-aminoacridines recently identified as multi-stage antiplasmodial leads. The compounds were evaluated <em>in vitro</em> against three cancer cell lines (MKN-28, Huh-7, and HepG2), and human primary dermal fibroblasts. One of the series displayed highly selective antiproliferative activity in the micromolar range against the three cancer cell lines tested, without any toxicity to non-carcinogenic cells.</p></div>","PeriodicalId":256,"journal":{"name":"Bioorganic & Medicinal Chemistry Letters","volume":"111 ","pages":"Article 129894"},"PeriodicalIF":2.5000,"publicationDate":"2024-07-21","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.sciencedirect.com/science/article/pii/S0960894X24002968/pdfft?md5=64b1393a93a69f30efeab293c0c1102c&pid=1-s2.0-S0960894X24002968-main.pdf","citationCount":"0","resultStr":"{\"title\":\"Repurposing antiplasmodial leads for cancer: Exploring the antiproliferative effects of N-cinnamoyl-aminoacridines\",\"authors\":\"Mélanie Fonte ,&nbsp;Catarina Rôla ,&nbsp;Sofia Santana ,&nbsp;Miguel Prudêncio ,&nbsp;Joana Almeida ,&nbsp;Ricardo Ferraz ,&nbsp;Cristina Prudêncio ,&nbsp;Cátia Teixeira ,&nbsp;Paula Gomes\",\"doi\":\"10.1016/j.bmcl.2024.129894\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><p>Drug repurposing and rescuing have been widely explored as cost-effective approaches to expand the portfolio of chemotherapeutic agents. Based on the reported antitumor properties of both <em>trans-</em>cinnamic acids and quinacrine, an antimalarial aminoacridine, we explored the antiproliferative properties of two series of <em>N</em>-cinnamoyl-aminoacridines recently identified as multi-stage antiplasmodial leads. The compounds were evaluated <em>in vitro</em> against three cancer cell lines (MKN-28, Huh-7, and HepG2), and human primary dermal fibroblasts. One of the series displayed highly selective antiproliferative activity in the micromolar range against the three cancer cell lines tested, without any toxicity to non-carcinogenic cells.</p></div>\",\"PeriodicalId\":256,\"journal\":{\"name\":\"Bioorganic & Medicinal Chemistry Letters\",\"volume\":\"111 \",\"pages\":\"Article 129894\"},\"PeriodicalIF\":2.5000,\"publicationDate\":\"2024-07-21\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"https://www.sciencedirect.com/science/article/pii/S0960894X24002968/pdfft?md5=64b1393a93a69f30efeab293c0c1102c&pid=1-s2.0-S0960894X24002968-main.pdf\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Bioorganic & Medicinal Chemistry Letters\",\"FirstCategoryId\":\"3\",\"ListUrlMain\":\"https://www.sciencedirect.com/science/article/pii/S0960894X24002968\",\"RegionNum\":4,\"RegionCategory\":\"医学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q3\",\"JCRName\":\"CHEMISTRY, MEDICINAL\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Bioorganic & Medicinal Chemistry Letters","FirstCategoryId":"3","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S0960894X24002968","RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q3","JCRName":"CHEMISTRY, MEDICINAL","Score":null,"Total":0}
引用次数: 0

摘要

作为扩大化疗药物组合的具有成本效益的方法,药物再利用和抢救已被广泛探讨。根据反式肉桂酸和抗疟氨基吖啶喹吖啶抗肿瘤特性的报道,我们探索了最近被确定为多级抗疟线索的两个系列 N-肉桂酰氨基吖啶的抗增殖特性。这些化合物针对三种癌细胞株(MKN-28、Huh-7 和 HepG2)和人类原发性真皮成纤维细胞进行了体外评估。其中一个系列的化合物在微摩尔范围内对所测试的三种癌细胞株显示出高度选择性的抗增殖活性,而对非致癌细胞没有任何毒性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Repurposing antiplasmodial leads for cancer: Exploring the antiproliferative effects of N-cinnamoyl-aminoacridines

Repurposing antiplasmodial leads for cancer: Exploring the antiproliferative effects of N-cinnamoyl-aminoacridines

Drug repurposing and rescuing have been widely explored as cost-effective approaches to expand the portfolio of chemotherapeutic agents. Based on the reported antitumor properties of both trans-cinnamic acids and quinacrine, an antimalarial aminoacridine, we explored the antiproliferative properties of two series of N-cinnamoyl-aminoacridines recently identified as multi-stage antiplasmodial leads. The compounds were evaluated in vitro against three cancer cell lines (MKN-28, Huh-7, and HepG2), and human primary dermal fibroblasts. One of the series displayed highly selective antiproliferative activity in the micromolar range against the three cancer cell lines tested, without any toxicity to non-carcinogenic cells.

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
CiteScore
5.70
自引率
3.70%
发文量
463
审稿时长
27 days
期刊介绍: Bioorganic & Medicinal Chemistry Letters presents preliminary experimental or theoretical research results of outstanding significance and timeliness on all aspects of science at the interface of chemistry and biology and on major advances in drug design and development. The journal publishes articles in the form of communications reporting experimental or theoretical results of special interest, and strives to provide maximum dissemination to a large, international audience.
×
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