Synthesis, characterization, and biological evaluation of a β-amino carbonyl and its metal complexes using guanine hydrochloride catalyst

IF 1.7 4区 化学 Q3 CHEMISTRY, MULTIDISCIPLINARY
Mohit Panwar, Shweta Chand Thakuri, Vijay Kumar Juyal, Virendra Kasana, Viveka Nand
{"title":"Synthesis, characterization, and biological evaluation of a β-amino carbonyl and its metal complexes using guanine hydrochloride catalyst","authors":"Mohit Panwar,&nbsp;Shweta Chand Thakuri,&nbsp;Vijay Kumar Juyal,&nbsp;Virendra Kasana,&nbsp;Viveka Nand","doi":"10.1007/s12039-024-02342-x","DOIUrl":null,"url":null,"abstract":"<div><p>In this study, we synthesized 3-(4-chlorophenyl amino)-1,3-diphenyl propane-1-one and its Cu(II), Zn(II), and Ni(II) metal complexes using the novel catalyst, guanine hydrochloride. The synthesized compounds were characterized using UV–Vis, FT-IR, HRMS, elemental analysis, <sup>1</sup>HNMR, and <sup>13</sup>CNMR techniques. Subsequently, the antioxidant and antibacterial potential (biological activity) of the compounds were evaluated. Antioxidant activity was assessed using DPPH radical scavenging, H<sub>2</sub>O<sub>2</sub> hydroxyl scavenging, and FRAP assay methods, while antibacterial activity was determined via disc-diffusion method against gram-positive (<i>Bacillus subtilis</i> and <i>Staphylococcus aureus</i>) and gram-negative (<i>Erwinia amylovora</i> and <i>Escherichia coli</i>) bacteria. Ligand–protein interactions were examined using molecular docking studies. Guanine hydrochloride, the catalyst used, improved reaction time and operated under room temperature, and was easily removed. The ligand exhibited superior antioxidant potential (IC<sub>50</sub> = 470.916 ± 0.30 ppm) compared to its metal complexes in all three assays. Among the tested compounds, the Cu(II) metal complex showed the largest zone of inhibition (4–9.9 mm) against all bacteria. The metal complexes displayed better binding energy than the ligand, proving the compounds’ candidacy for future therapeutic applications.</p><h3>Graphical abstract</h3><p>Benzaldehyde, <i>p</i>-chloroanilines and acetophenone were allowed to react in this multi-component reaction to form <i>b</i>-amino carbonyl. Metal salts of Cu(II), Zn(II) and Ni(II) were mixed with the ligand to form metal-ligand complexes. The formed products were tested for their anti-oxidant and antibacterial activity, which showed appreciable results.\n</p><div><figure><div><div><picture><source><img></source></picture></div></div></figure></div></div>","PeriodicalId":616,"journal":{"name":"Journal of Chemical Sciences","volume":"137 2","pages":""},"PeriodicalIF":1.7000,"publicationDate":"2025-03-14","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of Chemical Sciences","FirstCategoryId":"92","ListUrlMain":"https://link.springer.com/article/10.1007/s12039-024-02342-x","RegionNum":4,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q3","JCRName":"CHEMISTRY, MULTIDISCIPLINARY","Score":null,"Total":0}
引用次数: 0

Abstract

In this study, we synthesized 3-(4-chlorophenyl amino)-1,3-diphenyl propane-1-one and its Cu(II), Zn(II), and Ni(II) metal complexes using the novel catalyst, guanine hydrochloride. The synthesized compounds were characterized using UV–Vis, FT-IR, HRMS, elemental analysis, 1HNMR, and 13CNMR techniques. Subsequently, the antioxidant and antibacterial potential (biological activity) of the compounds were evaluated. Antioxidant activity was assessed using DPPH radical scavenging, H2O2 hydroxyl scavenging, and FRAP assay methods, while antibacterial activity was determined via disc-diffusion method against gram-positive (Bacillus subtilis and Staphylococcus aureus) and gram-negative (Erwinia amylovora and Escherichia coli) bacteria. Ligand–protein interactions were examined using molecular docking studies. Guanine hydrochloride, the catalyst used, improved reaction time and operated under room temperature, and was easily removed. The ligand exhibited superior antioxidant potential (IC50 = 470.916 ± 0.30 ppm) compared to its metal complexes in all three assays. Among the tested compounds, the Cu(II) metal complex showed the largest zone of inhibition (4–9.9 mm) against all bacteria. The metal complexes displayed better binding energy than the ligand, proving the compounds’ candidacy for future therapeutic applications.

Graphical abstract

Benzaldehyde, p-chloroanilines and acetophenone were allowed to react in this multi-component reaction to form b-amino carbonyl. Metal salts of Cu(II), Zn(II) and Ni(II) were mixed with the ligand to form metal-ligand complexes. The formed products were tested for their anti-oxidant and antibacterial activity, which showed appreciable results.

Abstract Image

求助全文
约1分钟内获得全文 求助全文
来源期刊
Journal of Chemical Sciences
Journal of Chemical Sciences CHEMISTRY, MULTIDISCIPLINARY-
CiteScore
3.10
自引率
5.90%
发文量
107
审稿时长
1 months
期刊介绍: Journal of Chemical Sciences is a monthly journal published by the Indian Academy of Sciences. It formed part of the original Proceedings of the Indian Academy of Sciences – Part A, started by the Nobel Laureate Prof C V Raman in 1934, that was split in 1978 into three separate journals. It was renamed as Journal of Chemical Sciences in 2004. The journal publishes original research articles and rapid communications, covering all areas of chemical sciences. A significant feature of the journal is its special issues, brought out from time to time, devoted to conference symposia/proceedings in frontier areas of the subject, held not only in India but also in other countries.
×
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