Sen, NejdetKar, YakupKurbanov, SultanUyanik, Arzu2020-03-262020-03-2620080970-7077https://hdl.handle.net/20.500.12395/22208The synthesized [(2-hydroxypropyl)-n-oximino]pyridine derivatives has been tested against the pathogenic four Gram-positive bacteria Bacillus cereus (ATCC 11778), Staphylococcus aureus (ATCC 6538), Sarcina lutea (ATCC 934 1) and Streptococs mutans (UCTC 10499) and three Gram-negative bacteria Salmonella typhimurium (1,4,5,12:;: 1,2), Pseudomonas aeruginosa (ATCC 27853) and Escherichia coli (ATCC 29998). Generally, all synthesized compounds (IVa-c) showed strong activity compared to antibiotic drug (cefalexin). However, among this compounds (IVa) showed excellent activity against Bacillus cereus (ATCC 11778), Sarcina lutea (ATCC 9341), Salmonella typhimurium (1,4,5,12:;: 1,2) and Escherichia coli (ATCC 29998) compared to cefalexin.eninfo:eu-repo/semantics/closedAccesspyridinecarbaldehyde oximesantibacterial activityGram-positive bacteriaGram-negative bacteriaAntibacterial activity of new [(2-hydroxypropyl)-n-oximino]pyridinesArticle20539493953Q4WOS:000259602500081Q4