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. 2022 May 1;15(5):563. doi: 10.3390/ph15050563

Table 3.

Antifungal activity of synthesized compounds (MIC in mg/L). Experiments were performed at least 3 times.

graphic file with name pharmaceuticals-15-00563-i001.jpg
R1 R2 C. albicans ATCC 24433
24h   48h
A. niger 37a A. fumigatus ATCC 46645 M. canis B-200 T. rubrum
2002
4a 4-Cl H >128 >128 64 >64 16 32
4b 3,4-(OBn)2 H >128 >128 >64 >64 >32 >32
4c 2,4-di-Cl H >128 >128 64 >64 64 128
4d 2-OH-5-Cl H 64 64 16 32 64 16
4e 2-OH-3,5-di-Cl H 8 32 16 32 32 16
15b 3,4-(OBn)2 H 32 >64 >64 >64 >64 >64
5a 4-Cl COOEt 8–16 16 1 4 8 8
5b 4-Cl COOi-Bu 4 8 8–16 16 4–8 8
5c 4-Cl COOAll 8 8 8 16 8 4
5d 4-Cl COOPh 16 64 32 64 4 32
5e 4-Cl COOBn >64 >64 64 >64 16 32
7a 4-Cl COPh 8 32 32 64 4 8–16
7b 3,4-(OBn)2 COPh >128 >125 32 >64 >64 >64
10a 4-Cl CH2COOt-Bu 32–64 64 >64 >64 >64 >64
10b 3,4-(OBn)2 CH2COOt-Bu >32 >64 >64 >64 >64 >64
11a 4-Cl CH2COOEt 32–64 >64 >64 >64 >64 >64
11b 3,4-(OBn)2 CH2COOEt >64 >64 >64 >64 >64 >64
12a 4-Cl CH2COOH 32 >64 64 >64 32–64 32
12b 3,4-(OBn)2 CH2COOH 64 >64 >64 >64 >64 >64
12c 2,4-Cl2 CH2COOH 32 >32 16 2 16–32 32
12d 2-OH-5-Cl CH2COOH 32 >64 4–8 16 16 16
12e 2-OH-3,5-di-Cl CH2COOH 0.125 0.5 8 16 16 16
17b 3,4-(OBn)2 CH2COOH 64 >64 >64 >64 >64 >64
17e 2-OH-3,5-di-Cl CH2COOH 8 16 8 16 2 8
Mycosidine (R1 = 4-Cl, R2 = COOMe) 16 32 4 8 4 4
Fluconazole 4 32 >64 >64 16 64