SYNTHESIS AND STUDY OF BIOLOGICAL ACTIVITIES OF2,6-DIARYLPIPERIDONE –y-DERIVATIVES

Q4 Earth and Planetary Sciences Iraqi Journal of Science Pub Date : 2024-03-20 DOI:10.24996/iraqijournalofscience.v53i3.12732
K. Hamak, F. Kandil, S. Hamo
{"title":"SYNTHESIS AND STUDY OF BIOLOGICAL ACTIVITIES OF2,6-DIARYLPIPERIDONE –y-DERIVATIVES","authors":"K. Hamak, F. Kandil, S. Hamo","doi":"10.24996/iraqijournalofscience.v53i3.12732","DOIUrl":null,"url":null,"abstract":"In the present study new series of2,6-diarylpiperidones-4 derivative were synthesized and these compounds are :1-(1-oxo-2-chloro-ethyl)-3,3-dimethyl-2.6-diarylpiperidone-4(I)1-(1-oxo-2-chloro-ethyl)-3.5-dimethyl-2,6-diarylpiperidone-4(II)1-(1-oxo-2-imidazolyl-ethyl) -3,3-dimethyl-2,6-diphenyl piperidoe-4(III)1-(1-oxo-2-imidazolyl-ethyl)-3,5-dimethyl-2,6-diphenylpiperidoe-4 (IV)The prepared compounds were characterized by IR,LC-MS and 1H,13C-NMR spectra .All compounds were screened for their antibacterial activity against gram positive bacteria :Bacillus subtilis and gram negative bacteria :Escherichia coli at different concentration (1000, 500, 250, 100) ppm. These compounds show good activity against gram positive more than gram negative bacteria","PeriodicalId":14698,"journal":{"name":"Iraqi Journal of Science","volume":"38 s172","pages":""},"PeriodicalIF":0.0000,"publicationDate":"2024-03-20","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Iraqi Journal of Science","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.24996/iraqijournalofscience.v53i3.12732","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q4","JCRName":"Earth and Planetary Sciences","Score":null,"Total":0}
引用次数: 0

Abstract

In the present study new series of2,6-diarylpiperidones-4 derivative were synthesized and these compounds are :1-(1-oxo-2-chloro-ethyl)-3,3-dimethyl-2.6-diarylpiperidone-4(I)1-(1-oxo-2-chloro-ethyl)-3.5-dimethyl-2,6-diarylpiperidone-4(II)1-(1-oxo-2-imidazolyl-ethyl) -3,3-dimethyl-2,6-diphenyl piperidoe-4(III)1-(1-oxo-2-imidazolyl-ethyl)-3,5-dimethyl-2,6-diphenylpiperidoe-4 (IV)The prepared compounds were characterized by IR,LC-MS and 1H,13C-NMR spectra .All compounds were screened for their antibacterial activity against gram positive bacteria :Bacillus subtilis and gram negative bacteria :Escherichia coli at different concentration (1000, 500, 250, 100) ppm. These compounds show good activity against gram positive more than gram negative bacteria
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
2,6-二芳基哌啶酮-y-衍生物的合成及生物活性研究
本研究合成了一系列新的 2,6-二芳基哌啶酮-4 衍生物,这些化合物是:1-(1-氧代-2-氯乙基)-3,3-二甲基-2.6-二芳基哌啶酮-4(I)1-(1-氧代-2-氯乙基)-3.哌啶酮-4(II)1-(1-氧代-2-咪唑基-乙基)-3,3-二甲基-2,6-二苯基哌啶酮-4(III)1-(1-氧代-2-咪唑基-乙基)-3,5-二甲基-2,6-二苯基哌啶酮-4 (IV)制备的化合物通过 IR、LC-MS 和 1H、13C-NMR 光谱进行表征。筛选了所有化合物在不同浓度(1000、500、250、100)ppm 下对革兰氏阳性菌(枯草杆菌)和革兰氏阴性菌(大肠杆菌)的抗菌活性。这些化合物对革兰氏阳性菌的活性高于对革兰氏阴性菌的活性。
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
Iraqi Journal of Science
Iraqi Journal of Science Chemistry-Chemistry (all)
CiteScore
1.50
自引率
0.00%
发文量
241
期刊最新文献
Detection of Uropathogenic Specific Protein Gene (usp) and Multidrug Resistant Bacteria (MDR) of Pathogenic Escherichia coli Isolated from Baghdad City Applications of q-Difference Equation and q-Operator _r Φ_s (θ) in q-Polynomials Kinematic Properties of the Gaseous Stellar Dynamics Using the Tully-Fisher Relation in the Different Types of Spiral Galaxies RP-HPLC Method for Simultaneously Quantifying the Antiviral Drug Contents of Acyclovir, Amantadine, and Oseltamivir in Pharmaceutical Formulations Determination of Timewise-Source Coefficient in Time-Fractional Reaction-Diffusion Equation from First Order Heat Moment
×
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