SYNTHESES AND EVALUATION OF THE ANTIMICROBIAL ACTIVITIES OF HALOGENATED IMIDAZOLES AND THEIR MN(II), NI(II), AND ZN(II) COMPLEXES

Damian Osahon Emwanta, R. Ngochindo, L. Odokuma, O. Eruteya
{"title":"SYNTHESES AND EVALUATION OF THE ANTIMICROBIAL ACTIVITIES OF HALOGENATED IMIDAZOLES AND THEIR MN(II), NI(II), AND ZN(II) COMPLEXES","authors":"Damian Osahon Emwanta, R. Ngochindo, L. Odokuma, O. Eruteya","doi":"10.53555/eijbps.v4i1.24","DOIUrl":null,"url":null,"abstract":"4, 5-Dichloroimidazole (4, 5-DCI) and 2, 4,5-Tribromoimidazole were synthesized, recrystallized from the appropriate solvents and characterized using spectroscopic methods. They were screened for their antimicrobial activities against five bacterial strains namely: Escherichia coli, Bacillus cereus strain CF7, Bacillus thuringensis strain EB151, Pseudomonas aeruginosa strain 335K55, and Pseudomonas aeruginosa strain PG1. These microorganisms were very sensitive to the compounds. Their sensitivities were increased appreciably by the Ni2+ and Mn2+ complexes of 4, 5-dichloroimidazole and reduced by its Zn2+ complex. Their sensitivities towards 2, 4, 5-tribromoimdazole were either greatly reduced or totally lost upon complexation. The differences in these sensitivities are attributed majorly to the halogens as the metal ions are common to both ligands.","PeriodicalId":257195,"journal":{"name":"EPH - International Journal of Biological & Pharmaceutical Science","volume":"15 1","pages":"0"},"PeriodicalIF":0.0000,"publicationDate":"2018-03-31","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"EPH - International Journal of Biological & Pharmaceutical Science","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.53555/eijbps.v4i1.24","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0

Abstract

4, 5-Dichloroimidazole (4, 5-DCI) and 2, 4,5-Tribromoimidazole were synthesized, recrystallized from the appropriate solvents and characterized using spectroscopic methods. They were screened for their antimicrobial activities against five bacterial strains namely: Escherichia coli, Bacillus cereus strain CF7, Bacillus thuringensis strain EB151, Pseudomonas aeruginosa strain 335K55, and Pseudomonas aeruginosa strain PG1. These microorganisms were very sensitive to the compounds. Their sensitivities were increased appreciably by the Ni2+ and Mn2+ complexes of 4, 5-dichloroimidazole and reduced by its Zn2+ complex. Their sensitivities towards 2, 4, 5-tribromoimdazole were either greatly reduced or totally lost upon complexation. The differences in these sensitivities are attributed majorly to the halogens as the metal ions are common to both ligands.
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
卤化咪唑及其mn (ii)、ni (ii)和zn (ii)配合物的合成和抗菌活性评价
合成了4,5-二氯咪唑(4,5- dci)和2,4,5 -三溴咪唑,在合适的溶剂中重结晶,并用光谱方法对其进行了表征。筛选它们对大肠杆菌、蜡样芽孢杆菌CF7、苏云金芽孢杆菌EB151、铜绿假单胞菌335K55和铜绿假单胞菌PG1 5株细菌的抑菌活性。这些微生物对这些化合物非常敏感。4,5 -二氯咪唑的Ni2+和Mn2+配合物明显提高了它们的灵敏度,而其Zn2+配合物则降低了它们的灵敏度。它们对2,4,5 -三溴咪唑的敏感性在络合后大大降低或完全丧失。这些灵敏度的差异主要归因于卤素,因为金属离子对两种配体都是共同的。
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
自引率
0.00%
发文量
0
期刊最新文献
STUDY OF VIRUSES MATERIAL RNA OR DNA BIODIVERSITY OF WILD MEDICINAL PLANTS IN SOME AREAS OF THE SOUTHERN SLOPE OF THE HISSAR RIDGE STATUS REPORT OF MYCOBACTERIUM TUBERCULOSIS IN REPUBLIC OF MALAWI, CENTRAL AFRICA (14.32’39.954’S AND 35.11’26.269’E) HYDROGEN PEROXIDE IMPEDES NK CELL AND T CELL MEDIATED CYTOTOXICITY AGAINST COLON CANCER CELL IMPACT OF THE OPERATION CIGLITAZONE ON PPAR ACTIVATION AND APOPTOSIS PROCESS IN MODELS OF GASTROINTESTINAL CANCER IN VITRO
×
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