EC Number   |
Inhibitors |
Structure |
|---|
    6.1.1.1 | 3-(4-hydroxyphenyl)-4-(2-morpholinoethoxy)furan-2(5H)-one |
replacement of the morpholine-ring in the side chain of the compound with a substituent containing more hydrophilic groups is probably more suitable for further modification. Most potent agent against Staphylococcus aureus ATCC 25923 with MIC50 value of 0.00023 mg/ml |
   |
| 6.1.1.1 | 3-(4-methoxyphenyl)-4-(2-morpholinoethoxy)furan-2(5H)-one |
- |
|
| 6.1.1.1 | 3-phenyl-4-(2-(piperidin-1-yl)ethoxy)furan-2(5H)-one |
- |
|
| 6.1.1.1 | 3-phenyl-4-(2-(propylamino)ethoxy)furan-2(5H)-one |
- |
|
| 6.1.1.1 | 3-phenyl-4-(2-(pyrrolidin-1-yl)ethoxy)furan-2(5H)-one |
- |
|
| 6.1.1.1 | 3-phenyl-4-(phenylamino)furan-2(5H)-one |
- |
|
| 6.1.1.1 | 4-(2-(2,4-dichlorophenylformyloxy)ethoxy)-3-phenylfuran-2(5H)-one |
- |
|
| 6.1.1.1 | 4-(2-(2,4-dihydroxyphenylformyloxy)ethoxy)-3-phenylfuran-2(5H)-one |
- |
|
| 6.1.1.1 | 4-(2-(2,5-dichlorophenylformyloxy)ethoxy)-3-phenylfuran-2(5H)-one |
- |
|
| 6.1.1.1 | 4-(2-(2-(4-nitrophenyl)hydrazinyl)ethoxy)-3-phenylfuran-2(5H)-one |
- |
|
