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":"65 1","pages":"69-74"},"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\":\"65 1\",\"pages\":\"69-74\"},\"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}
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 .