Study on the anti-cancer activity of α-phenethylamine ferrocenecarboxylic acid co-crystals

IF 2.8 4区 化学 Q2 CHEMISTRY, ANALYTICAL Chirality Pub Date : 2024-02-25 DOI:10.1002/chir.23653
Liao Youyin, Ma Yuexing, Chen Jiahao, Qian Kun, Yang Jie, Pan Rongbin, Xu Yiyong
{"title":"Study on the anti-cancer activity of α-phenethylamine ferrocenecarboxylic acid co-crystals","authors":"Liao Youyin,&nbsp;Ma Yuexing,&nbsp;Chen Jiahao,&nbsp;Qian Kun,&nbsp;Yang Jie,&nbsp;Pan Rongbin,&nbsp;Xu Yiyong","doi":"10.1002/chir.23653","DOIUrl":null,"url":null,"abstract":"<p>Ferrocene derivatives show a wide range of pharmacological activities in the medical field, especially in the anti-tumor field, and can be used as candidate drugs or lead compounds for the treatment of tumors and other diseases. And <i>α</i>-phenethylamine is an important intermediate for the preparation of fine chemical products. (<i>R</i>)-(+)-1-Phenethylamine ferrocenecarboxylic acid/(<i>S</i>)-(−)-1-phenethylamine ferrocenecarboxylic acid were prepared, named compounds <b>1</b> and <b>2</b>, respectively. Single crystal X-ray diffraction showed that compounds <b>1</b> and <b>2</b> crystallized in the orthorhombic system space group <i>P</i>2<sub>1</sub>2<sub>1</sub>2<sub>1</sub>, and the crystal structures of compounds <b>1</b> and <b>2</b> exhibited mirror symmetry. The inhibitory effect of two compounds on SW480, MDA-MB-231, and H1299 cells was tested by MTT colorimetry. The IC<sub>50</sub> values of the compounds against cancer cells were also calculated. The anti-cancer effect was more pronounced for compounds in the <i>S</i>-configuration. Compound <b>2</b> made the wild-type cancer cells undergo apoptosis, thus preventing cancer; it also had the function of helping the cell gene repair defects.</p>","PeriodicalId":10170,"journal":{"name":"Chirality","volume":"36 3","pages":""},"PeriodicalIF":2.8000,"publicationDate":"2024-02-25","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Chirality","FirstCategoryId":"92","ListUrlMain":"https://onlinelibrary.wiley.com/doi/10.1002/chir.23653","RegionNum":4,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"CHEMISTRY, ANALYTICAL","Score":null,"Total":0}
引用次数: 0

Abstract

Ferrocene derivatives show a wide range of pharmacological activities in the medical field, especially in the anti-tumor field, and can be used as candidate drugs or lead compounds for the treatment of tumors and other diseases. And α-phenethylamine is an important intermediate for the preparation of fine chemical products. (R)-(+)-1-Phenethylamine ferrocenecarboxylic acid/(S)-(−)-1-phenethylamine ferrocenecarboxylic acid were prepared, named compounds 1 and 2, respectively. Single crystal X-ray diffraction showed that compounds 1 and 2 crystallized in the orthorhombic system space group P212121, and the crystal structures of compounds 1 and 2 exhibited mirror symmetry. The inhibitory effect of two compounds on SW480, MDA-MB-231, and H1299 cells was tested by MTT colorimetry. The IC50 values of the compounds against cancer cells were also calculated. The anti-cancer effect was more pronounced for compounds in the S-configuration. Compound 2 made the wild-type cancer cells undergo apoptosis, thus preventing cancer; it also had the function of helping the cell gene repair defects.

Abstract Image

Abstract Image

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
α-苯乙胺二茂铁羧酸共晶体的抗癌活性研究
二茂铁衍生物在医学领域,特别是抗肿瘤领域显示出广泛的药理活性,可作为治疗肿瘤和其他疾病的候选药物或先导化合物。α-苯乙胺是制备精细化工产品的重要中间体。(R)-(+)-1-苯乙胺二茂铁羧酸/(S)-(-)-1-苯乙胺二茂铁羧酸分别被命名为化合物 1 和 2。单晶 X 射线衍射显示,化合物 1 和 2 结晶为正方晶系空间群 P212121,且化合物 1 和 2 的晶体结构呈镜像对称。MTT 比色法检测了两种化合物对 SW480、MDA-MB-231 和 H1299 细胞的抑制作用。同时还计算了化合物对癌细胞的 IC50 值。S构型化合物的抗癌效果更为明显。化合物 2 能使野生型癌细胞凋亡,从而预防癌症;它还具有帮助细胞修复基因缺陷的功能。
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
Chirality
Chirality 医学-分析化学
CiteScore
4.40
自引率
5.00%
发文量
124
审稿时长
1 months
期刊介绍: The main aim of the journal is to publish original contributions of scientific work on the role of chirality in chemistry and biochemistry in respect to biological, chemical, materials, pharmacological, spectroscopic and physical properties. Papers on the chemistry (physiochemical, preparative synthetic, and analytical), physics, pharmacology, clinical pharmacology, toxicology, and other biological aspects of chiral molecules will be published.
期刊最新文献
Multiwavelength Optical Rotation Detection: An Effective Approach for the Recognition of Analytical and Semi-Preparative HPLC Enantioseparation of the Chiral Pheromone Olean and Its Stereochemical Characterization Emergence of Optical Activity and Surface Morphology Changes in Racemic Amino Acid Films Under Circularly Polarized Lyman-α Light Irradiation Proceedings From 33rd Symposium on Chirality 2023, Rome, Italy Resolution and Absolute Configuration of Fargesin Enantiomers Chiroptical Sensing of Amines With Isatins
×
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