新型六亚甲二胺希夫碱的合成、表征及生物学评价

Kangah Niameke Jean-Baptiste, Kodjo Charles Guillaume, O. Adama, Kablan Ahmont Landry Claude, Dibi Konan Jacques, Kouamé Bosson Antoine, Ziao Nahossé
{"title":"新型六亚甲二胺希夫碱的合成、表征及生物学评价","authors":"Kangah Niameke Jean-Baptiste, Kodjo Charles Guillaume, O. Adama, Kablan Ahmont Landry Claude, Dibi Konan Jacques, Kouamé Bosson Antoine, Ziao Nahossé","doi":"10.21013/JAS.V7.N2.P3","DOIUrl":null,"url":null,"abstract":"We report herein synthesis, characterization and antimicrobial activity of four Shiff bases derived from hexamethylenediamine. Substitution of a nitro group on each aromatic ring in ortho, meta or para positions of N,N'-bis(phenylmethyl)hexane-1,6-diimineallowed to have a homogeneous series of positional isomers. These four symmetric diimine Schiff bases were characterized by conventional spectrometry methods (NMR, IR, MS), then tested against Gram-positive and Gram-negative bacterial strains. Among them, compounds 1b , 1c , 1d were found to be active against bacterial strain Staphylococcus aureus CIP with MIC value of 375 μ g/ ml, 187.5 μ g /ml and 375 μ g /ml respectively. Candida Albicans fungal strain showed resistance to all synthesized Schiff base compounds, butin the other hand, Candida glabrata has been sensitive to all compounds with MIC of 1500 μ g/ ml and one more time except 1a .","PeriodicalId":14487,"journal":{"name":"IRA-International Journal of Applied Sciences","volume":null,"pages":null},"PeriodicalIF":0.0000,"publicationDate":"2017-05-27","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"2","resultStr":"{\"title\":\"Synthesis, Characterization and Biological Evaluation of New Series of Schiff Bases Derived from Hexamethylenediamine as Potential Antibacterial and Antifungal Agents\",\"authors\":\"Kangah Niameke Jean-Baptiste, Kodjo Charles Guillaume, O. Adama, Kablan Ahmont Landry Claude, Dibi Konan Jacques, Kouamé Bosson Antoine, Ziao Nahossé\",\"doi\":\"10.21013/JAS.V7.N2.P3\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"We report herein synthesis, characterization and antimicrobial activity of four Shiff bases derived from hexamethylenediamine. Substitution of a nitro group on each aromatic ring in ortho, meta or para positions of N,N'-bis(phenylmethyl)hexane-1,6-diimineallowed to have a homogeneous series of positional isomers. These four symmetric diimine Schiff bases were characterized by conventional spectrometry methods (NMR, IR, MS), then tested against Gram-positive and Gram-negative bacterial strains. Among them, compounds 1b , 1c , 1d were found to be active against bacterial strain Staphylococcus aureus CIP with MIC value of 375 μ g/ ml, 187.5 μ g /ml and 375 μ g /ml respectively. Candida Albicans fungal strain showed resistance to all synthesized Schiff base compounds, butin the other hand, Candida glabrata has been sensitive to all compounds with MIC of 1500 μ g/ ml and one more time except 1a .\",\"PeriodicalId\":14487,\"journal\":{\"name\":\"IRA-International Journal of Applied Sciences\",\"volume\":null,\"pages\":null},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2017-05-27\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"2\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"IRA-International Journal of Applied Sciences\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.21013/JAS.V7.N2.P3\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"IRA-International Journal of Applied Sciences","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.21013/JAS.V7.N2.P3","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 2

摘要

本文报道了四种由六亚二胺衍生的Shiff碱的合成、表征和抗菌活性。在N,N'-双(苯基甲基)己烷-1,6-二亚胺的邻位、间位或对位上的每个芳香环上取代一个硝基,允许有一系列均匀的位置异构体。采用核磁共振(NMR)、红外(IR)、质谱(MS)等常规光谱方法对这4种对称二亚胺希夫碱进行了表征,并对革兰氏阳性和革兰氏阴性菌株进行了检测。其中化合物1b、1c、1d对金黄色葡萄球菌CIP有抑制作用,MIC值分别为375 μ g/ ml、187.5 μ g/ ml和375 μ g/ ml。白色念珠菌对合成的所有希夫碱化合物均有抗性,而光念珠菌对MIC为1500 μ g/ ml的所有化合物均有敏感性,除1a外均有1次敏感性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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
Synthesis, Characterization and Biological Evaluation of New Series of Schiff Bases Derived from Hexamethylenediamine as Potential Antibacterial and Antifungal Agents
We report herein synthesis, characterization and antimicrobial activity of four Shiff bases derived from hexamethylenediamine. Substitution of a nitro group on each aromatic ring in ortho, meta or para positions of N,N'-bis(phenylmethyl)hexane-1,6-diimineallowed to have a homogeneous series of positional isomers. These four symmetric diimine Schiff bases were characterized by conventional spectrometry methods (NMR, IR, MS), then tested against Gram-positive and Gram-negative bacterial strains. Among them, compounds 1b , 1c , 1d were found to be active against bacterial strain Staphylococcus aureus CIP with MIC value of 375 μ g/ ml, 187.5 μ g /ml and 375 μ g /ml respectively. Candida Albicans fungal strain showed resistance to all synthesized Schiff base compounds, butin the other hand, Candida glabrata has been sensitive to all compounds with MIC of 1500 μ g/ ml and one more time except 1a .
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
自引率
0.00%
发文量
0
期刊最新文献
Realization and Experimental Study of a Hybrid Cooker (Solar-Biomass) in a Sahelian Climate Automatic MRI Brain Tumor Segmentation Techniques: A Survey Simulation of the Injection of 25 MW Photovoltaic Energy Production: Analysis of the Impacts on the Grid of the Société Béninoise d'Energie Electrique (SBEE) Deep Learning Feature Extraction for Brain Tumor Characterization and Detection Optimal Algorithm Selection in Multimodal Medical Image Registration
×
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