Synthesis and Antimicrobial Activity of Some Piperazine Dithiocarbamate Derivatives; [Bazı Piperazin Ditiyokarbamat Türevlerinin Sentezi ve Antimikrobiyal Aktiviteleri]

2 [[4 (2 methyl 4 thiazolyl)phenyl]amino] 2 oxoethyl 4 (2 hydroxyethyl)piperazine 1 carbodithioic acid; 2 [[4 (2 methyl 4 thiazolyl)phenyl]amino] 2 oxoethyl 4 (4 fluorophenyl)piperazine 1 carbodithioic acid; 2 [[4 (2 methyl 4 thiazolyl)phenyl]amino] 2 oxoethyl 4 (4 methoxyphenyl)piperazine 1 carbodithioic acid; 2 [[4 (2 methyl 4 thiazolyl)phenyl]amino] 2 oxoethyl 4 (4 methylbenzyl)piperazine 1 carbodithioic acid; 2 [[4 (2 methyl 4 thiazolyl)phenyl]amino] 2 oxoethyl 4 (4 nitrophenyl)piperazine 1 carbodithioic acid; 2 [[4 (2 methyl 4 thiazolyl)phenyl]amino] 2 oxoethyl 4 cyclohexylpiperazine 1 carbodithioic acid; 2 [[4 (2 methyl 4 thiazolyl)phenyl]amino] 2 oxoethyl 4 phenylpiperazine 1 carbodithioic acid; 2 [[4 (2 methyl 4 thiazolyl)phenyl]amino] 2 oxoethyl 4 substituted piperazine 1 carbodithioic acid; 2 [[4 (2 methyl 4 thiazolyl)phenyl]amino] 2 oxoethyl 4 [2 (n,n dimethylamino)ethyl] piperazine 1 carbodithioic acid; 2 [[4 (2 methyl 4 thiazolyl)phenyl]amino] 2 oxoethyl 4 [3 (n,n dimethylamino)propyl] piperazine 1 carbodithioic acid; chloramphenicol; dithiocarbamic acid; ketoconazole; piperazine derivative; thiazole derivative; unclassified drug; antimicrobial activity; Article; broth dilution; Candida albicans; Candida glabrata; Candida krusei; Candida parapsilosis; carbon nuclear magnetic resonance; controlled study; drug potency; drug structure; drug synthesis; Enterococcus faecalis; Escherichia coli; human; infrared spectroscopy; Klebsiella pneumoniae; mass spectrometry; proton nuclear magnetic resonance; Pseudomonas aeruginosa; Staphylococcus aureus