2010
DOI: 10.1007/s11859-010-0113-0
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Antibacterial activity and structure-activity relationships of Schiff bases on Staphylococcus aureus by microcalorimetry

Abstract: The growth of Staphylococcus aureus under the action of six kinds of Schiff bases (A, B, C, D, E, F) was studied by means of microcalorimetry. Growth constant k and inhibition ratio I were calculated. Also, the antibacterial activity, the action characteristics and the structure-activity relationships of the compounds on S. aureus were analyzed. Results indicate that B, F show good antibacterial activity (IC 50 : 293.6 mg • L −1 and 307.8 mg • L −1 ), D, E show moderate antibacterial activity (IC 50 : 966.3 mg… Show more

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Cited by 4 publications
(2 citation statements)
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“…In disc diffusion method the diameter of the inhibition zone is related to the sensitivity of the isolate and to the diffusion rate of the drug through the agar medium [64]. Diffusion rate of chemical compounds on agar plates may be affected by other factors as: solubility, dipole moment, molecular mass and hydrophobicity [65]; Additionally, chemicals structure might influence their antibacterial activities [66], generally, the electronic nature (electron withdrawing and electron releasing) and position of substituents of the phenyl ring determines the antimicrobial activities [67], studies of structure activity relationship revealed that the presence of electron-withdrawing group Br on the para position of the phenyl rings has a positive effect on the antibacterial activity [68].…”
Section: Antibacterial Activity Evaluationmentioning
confidence: 99%
“…In disc diffusion method the diameter of the inhibition zone is related to the sensitivity of the isolate and to the diffusion rate of the drug through the agar medium [64]. Diffusion rate of chemical compounds on agar plates may be affected by other factors as: solubility, dipole moment, molecular mass and hydrophobicity [65]; Additionally, chemicals structure might influence their antibacterial activities [66], generally, the electronic nature (electron withdrawing and electron releasing) and position of substituents of the phenyl ring determines the antimicrobial activities [67], studies of structure activity relationship revealed that the presence of electron-withdrawing group Br on the para position of the phenyl rings has a positive effect on the antibacterial activity [68].…”
Section: Antibacterial Activity Evaluationmentioning
confidence: 99%
“…They also form basic units in certain dyes [1]. Schiff bases are reported to exhibit antibacterial [2][3][4][5], antifungal [6] and antitumor activity [7]. In addition, the compounds and their metal complexes exhibit interesting photophysical properties [8].…”
Section: Introductionmentioning
confidence: 99%