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. 2017 Dec 15;13(2):142–155. doi: 10.1016/j.jtumed.2017.10.007

Table 3.

Antimicrobial activities of novel metal complexes of 2-amino-4-substituted phenylthiazole Schiff bases against different microbial strains (mean ± S.D.).

Compounds Bacterial strain
Fungal strain
E. coli (res) K. pneumoniae S. aureus (res) C. albicans C. neoformans
4e 15.83 ± 1.47 15.17 ± 2.14 16.17 ± 2.04 10.17 ± 1.84 12.5 ± 1.52
5a(Lig) 13.67 ± 2.34 12.67 ± 2.25 15.83 ± 2.79 12.17 ± 2.23 13.33 ± 1.37
5b(Lig) 15.33 ± 2.07 13.5 ± 2.43 11.5 ± 1.87 12 ± 1.27 12.33 ± 1.75
6a 16.67 ± 2.34 16.17 ± 1.94 20.83 ± 1.84 12.83 ± 2.23 13.67 ± 2.94
6b 15.83 ± 1.84 16 ± 2.37 18.33 ± 1.75 13.33 ± 2.34 12.67 ± 1.51
6c 14.67 ± 3.14 14.83 ± 1.84 11.33 ± 1.51 15.83 ± 1.84
6d 15.5 ± 3.21 16.17 ± 2.99 16.83 ± 2.71 12.67 ± 2.34 12.17 ± 2.71
6e 14.83 ± 2.56 15.83 ± 2.23 14.5 ± 1.52 11.17 ± 6.21 10.5 ± 1.52
6f 16.67 ± 1.37 15.17 ± 1.94 12.5 ± 1.52 10.33 ± 1.75
RA 12.67 ± 1.51 15.33 ± 1.97 13 ± 1.67 19.33 ± 4.68 24.17 ± 1.94
RA1 15.09 ± 1.13

Results expressed in Mean ± S.D. (n = 6), The data were analysed by One Way ANOVA followed by Dunnett's Post Hoc test, (statistical significance at *p < 0.05 in comparison to reference antibiotic (RA): amoxicillin (antibacterial), fluconazole (antifungal) and RA1: ampicillin (antibacterial); -, no zone of inhibition.