EC Number |
Inhibitors |
Structure |
---|
3.5.2.3 | (1-methyl-1H-indol-4-yl)methanol |
- |
|
3.5.2.3 | (S)-1,2,3,6-tetrahydro-6-oxopyridine-2-carboxylic acid |
competitive inhibitor versus dihydroorotate and thio-dihydroorotate |
|
3.5.2.3 | 1,10-phenanthroline |
- |
|
3.5.2.3 | 1-(5-methoxy-1H-indol-2-yl)methanamine |
- |
|
3.5.2.3 | 1-(8-methoxy-1,3,4,5-tetrahydro-2H-pyrido[4,3-b]indol-2-yl)ethan-1-one |
- |
|
3.5.2.3 | 1-ethyl-1,2,3,4-tetrahydropyrrolo[1,2-a]pyrazine |
- |
|
3.5.2.3 | 2-oxo-1,2,3,6-tetrahydropyrimidine-4,6-dicarboxylate |
- |
|
3.5.2.3 | 2-oxo-1,2,3,6-tetrahydropyrimidine-4,6-dicarboxylic acid |
at 37°C or 60°c the enzyme binds 2-oxo-1,2,3,6-tetrahydropyrimidine-4,6-dicarboxylic acid only slightly more strongly than DHO; competitive inhibitor |
|
3.5.2.3 | 2-oxo-1,2,3,6-tetrahydropyrimidine-4,6-dicarboxylic acid |
at 37°C or 60°C the enzyme binds 2-oxo-1,2,3,6-tetrahydropyrimidine-4,6-dicarboxylic acid more tightly than DHO |
|
3.5.2.3 | 2-oxo-1,2,3,6-tetrahydropyrimidine-4,6-dicarboxylic acid |
competitive inhibitor |
|