EC Number |
Inhibitors |
Structure |
---|
3.2.1.24 | Zn2+ |
55% inhibition at 10 mM |
|
3.2.1.24 | Zn2+ |
- |
|
3.2.1.24 | Zn2+ |
25% inhibition at 20 mM |
|
3.2.1.24 | Zn2+ |
inhibition at 1 mM |
|
3.2.1.24 | Zn2+ |
reversible by Ca2+ |
|
3.2.1.24 | Zn2+ |
mutant enzymes H228Q, H533E, and H533Q, are all inhibited by high Zn2+ concentrations (1 mM) |
|
3.2.1.24 | ZnCl2 |
92% inhibition by 1 mM, 56% inhibition by 0.01 mM |
|
3.2.1.24 | [6-(3-methylbutoxy)-3-oxo-3,6-dihydro-2H-pyran-2-yl]acetonitrile |
- |
|
3.2.1.24 | [6-(3-methylbutoxy)-3-oxo-3,6-dihydro-2H-pyran-2-yl]methyl 2,2-dimethylpropanoate |
- |
|
3.2.1.24 | [[(3S,4S,5R,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)piperidin-2-ylidene]amino] N-(4-chlorophenyl)carbamate |
- |
|