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. 2017 Apr 25;22(5):687. doi: 10.3390/molecules22050687

Table 1.

In-vitro antibacterial activity of 2-salicyloylbenzofuran derivatives.

Compound b Zone of Inhibition in mm (MIC in mM) a
E. coli S. faecalis MSSA MRSA
4 9.5 (>2.50) 9.5 (>2.50)
5 9 (>2.59) 10 (>2.59) 13 (>2.59)
7a 8 (>2.41) 12 (>2.41)
7b 8 (>2.35) 12 (2.35) 16 (2.35)
7c
7d 8(>1.97) 14 (>1.97)
7e 8 (>1.84) 18 (>1.84)
7f 8 (>2.12)
8f 12 (0.28) 16 (0.14) 14 (0.14)
8g 11 (0.55) 19 (0.27) 17 (0.27)
8h 15 (0.12) 17 (0.06) 15 (0.12)
14a 10 (0.86) 11 (>3.46)
14b 9 (1.65) 9 (3.30)
14c 9 (3.14) 9 (1.57) 9 (1.57)
14d 9 (3.10) 9 (>3.10) 9 (1.55) 10 (1.55)
14e 9 (2.73) 9 (1.36) 11 (1.36)
14f 11 (1.40) 9 (0.70) 11 (0.70)
Ampicillin 35 (0.006) 28 (0.006) 31 (0.0007) 15 (0.05)
Cefuroxime 33 (0.02) 31 (0.02) 25 (0.04)
Vancomycin 23 (0.0014) 30 (0.00004) 30 (0.00004) 31 (0.00004)

a E. coli: Escherichia coli ATCC 25922; S. faecalis: Streptococcus faecalis ATCC 29212; MSSA: methicillin-sensitive Staphylococcus aureus ATCC 29213; MRSA: methicillin-resistant Staphylococcus aureus ATCC 43300; b other compounds: not tested; (–): not inhibition at tested concentration.