EC Number |
Inhibitors |
Structure |
---|
3.4.24.21 | 1,10-o-phenanthroline |
1 mM, isoform LAST, 10% residual activity, isoform LAST_MAM, 12% residual activity |
|
3.4.24.21 | 1,10-phenanthroline |
r; reactivation of apoenzyme by Zn2+ (100%), Cu2+ (70%) or Co2+ (50%); strong, kinetics |
|
3.4.24.21 | 1,10-phenanthroline |
r; strong, kinetics |
|
3.4.24.21 | 1,10-phenanthroline |
- |
|
3.4.24.21 | 1,7-phenanthroline |
weak |
|
3.4.24.21 | 1,7-phenanthroline |
not reversible by addition of Zn2+ |
|
3.4.24.21 | 2,2'-dipyridyl |
r |
|
3.4.24.21 | 3-[3-(1-aminoethenyl)-1,2,4-oxadiazol-5-yl]-6-cyclohexyl-N-hydroxyhexanamide |
- |
|
3.4.24.21 | 4-Mercaptoaniline |
weak |
|
3.4.24.21 | 6-cyclohexyl-3-[3-(2,6-dioxo-1,2,3,6-tetrahydropyrimidin-4-yl)-1,2,4-oxadiazol-5-yl]-N-hydroxyhexanamide |
- |
|