{"title":"二氨基二苯基硫化物桥接的双核Zn(II)-亚甲基配合物的抗菌性能","authors":"Aziza Sarwar, Bibi Sherino, M. Ellahi, Nusrat Nabi, Bushra Naureen, Hamida Panezai","doi":"10.32350/sir.64.04","DOIUrl":null,"url":null,"abstract":"Antimicrobial resistance of microbes against treatment that once could cure, has inspired an urgent need for new drugs development. Accordingly, three binuclear Zn(II)-Schiff bases complexes ZnLa - ZnLc were prepared by direct reaction of the ligands La-Lc with Zn(II) ions in equimolar ratios bearing salicyldehydes with OH, NO2 and Cl functional groups. The synthesized compounds ZnLa - ZnLc were evaulated against Gram positive (Enterococcus faecalis NCIMB 13280, Streptococcus mutant ATCC 25175™ and Staphylococcus aureus ATCC 6538™) and gram negative (Escheria coli NCTC 12900, Salmonella typhi and Pseudomonas aeruginosa ATCC 15442) bacterial strains, respectively, by agar well diffusion and broth microdilution techniques. The minimum inhibitory concentration (MIC90) values were calculated by microplate reader at 550 nm to optimum result. It was found that all the synthesized compounds showed promising antibacterial activity against the genus Streptococcus mutant followed Staphylococcus aureus and Escheria coli. Binuclear Zn(II) complexes had a superior antibacterial activity compared to their parent Schiff base ligands. In general, 3,4-dihydroxy derived Schiff bases alongwith their relevant complexes exhibited magnificent antibacterial activity and hence merits to be established as promising keystone for subsequent antimicrobial drug advancement.","PeriodicalId":137307,"journal":{"name":"Scientific Inquiry and Review","volume":null,"pages":null},"PeriodicalIF":0.0000,"publicationDate":"2022-12-07","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"1","resultStr":"{\"title\":\"Antibacterial properties of binuclear Zn(II)-azomethine complexes derived from diaminodiphenylsulphide bridged spacer\",\"authors\":\"Aziza Sarwar, Bibi Sherino, M. Ellahi, Nusrat Nabi, Bushra Naureen, Hamida Panezai\",\"doi\":\"10.32350/sir.64.04\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"Antimicrobial resistance of microbes against treatment that once could cure, has inspired an urgent need for new drugs development. Accordingly, three binuclear Zn(II)-Schiff bases complexes ZnLa - ZnLc were prepared by direct reaction of the ligands La-Lc with Zn(II) ions in equimolar ratios bearing salicyldehydes with OH, NO2 and Cl functional groups. The synthesized compounds ZnLa - ZnLc were evaulated against Gram positive (Enterococcus faecalis NCIMB 13280, Streptococcus mutant ATCC 25175™ and Staphylococcus aureus ATCC 6538™) and gram negative (Escheria coli NCTC 12900, Salmonella typhi and Pseudomonas aeruginosa ATCC 15442) bacterial strains, respectively, by agar well diffusion and broth microdilution techniques. The minimum inhibitory concentration (MIC90) values were calculated by microplate reader at 550 nm to optimum result. It was found that all the synthesized compounds showed promising antibacterial activity against the genus Streptococcus mutant followed Staphylococcus aureus and Escheria coli. Binuclear Zn(II) complexes had a superior antibacterial activity compared to their parent Schiff base ligands. In general, 3,4-dihydroxy derived Schiff bases alongwith their relevant complexes exhibited magnificent antibacterial activity and hence merits to be established as promising keystone for subsequent antimicrobial drug advancement.\",\"PeriodicalId\":137307,\"journal\":{\"name\":\"Scientific Inquiry and Review\",\"volume\":null,\"pages\":null},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2022-12-07\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"1\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Scientific Inquiry and Review\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.32350/sir.64.04\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Scientific Inquiry and Review","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.32350/sir.64.04","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
Antibacterial properties of binuclear Zn(II)-azomethine complexes derived from diaminodiphenylsulphide bridged spacer
Antimicrobial resistance of microbes against treatment that once could cure, has inspired an urgent need for new drugs development. Accordingly, three binuclear Zn(II)-Schiff bases complexes ZnLa - ZnLc were prepared by direct reaction of the ligands La-Lc with Zn(II) ions in equimolar ratios bearing salicyldehydes with OH, NO2 and Cl functional groups. The synthesized compounds ZnLa - ZnLc were evaulated against Gram positive (Enterococcus faecalis NCIMB 13280, Streptococcus mutant ATCC 25175™ and Staphylococcus aureus ATCC 6538™) and gram negative (Escheria coli NCTC 12900, Salmonella typhi and Pseudomonas aeruginosa ATCC 15442) bacterial strains, respectively, by agar well diffusion and broth microdilution techniques. The minimum inhibitory concentration (MIC90) values were calculated by microplate reader at 550 nm to optimum result. It was found that all the synthesized compounds showed promising antibacterial activity against the genus Streptococcus mutant followed Staphylococcus aureus and Escheria coli. Binuclear Zn(II) complexes had a superior antibacterial activity compared to their parent Schiff base ligands. In general, 3,4-dihydroxy derived Schiff bases alongwith their relevant complexes exhibited magnificent antibacterial activity and hence merits to be established as promising keystone for subsequent antimicrobial drug advancement.