Research Article

In Vitro Bactericidal Activity of 4- and 5-Chloro-2-hydroxy-N-[1-oxo-1-(phenylamino)alkan-2-yl]benzamides against MRSA

Table 2

Extent of bacterial killing exerted by 5-chloro-2-hydroxy-N-[(2S)-3-methyl-1-oxo-1-{[4-(trifluoromethyl)-phenyl]amino}butan-2-yl]benzamide (1f), N-{(2S)-1-[(4-bromophenyl)amino]-3-methyl-1-oxobutan-2-yl}-4-chloro-2-hydroxybenzamide (1g), and 4-chloro-N-{(2S)-1-[(3,4-dichlorophenyl)amino]-3-methyl-1-oxobutan-2-yl}-2-hydroxybenzamide (1h) over time against four staphylococci strains.

Drug and concentration (multiplicity of MIC) Number of strains showing the following log10 CFU/mL decreasea at the designated incubation time
4 h6 h8 h24 h
−1−2−3−1−2−3−1−2−3−1−2−3

Comp. 1f
 4× MIC211432442444
 2× MIC111111311430
 1× MIC000000000000
Comp. 1g
 4× MIC211211421442
 2× MIC110111211000
 1× MIC000000000000
Comp. 1h
 4× MIC220422432442
 2× MIC100210200100
 1× MIC000100000000

CFU: colony-forming units.
 CFU/mL) values of −1, −2, and − 3  CFU/mL correspond to 90% (bacteriostatic), 99% (bacteriostatic), and 99.9% (bactericidal) of killing, respectively.