EC Number |
Inhibitors |
Structure |
---|
2.7.11.15 | (6R)-6-([[(1S)-1-(5-fluoro-2-methoxyphenyl)ethyl]amino]methyl)-4,5,6,7-tetrahydropyrazolo[1,5-a]pyrimidine-3-carboxamide |
- |
|
2.7.11.15 | 1-[(3R)-1-benzylpyrrolidin-3-yl]-3-[(3,5-dimethyl-1,2-oxazol-4-yl)methyl]urea |
- |
|
2.7.11.15 | 2,3-diphosphoglycerate |
weak |
|
2.7.11.15 | 2,3-diphosphoglycerate |
inhibits in the millimolar range, IC50: 1.1 mM with rhodopsin as substrate; weak |
|
2.7.11.15 | 2-(3-methoxybenzyl)-7-(1H-pyrazol-4-yl)phthalazin-1(2H)-one |
- |
|
2.7.11.15 | 2-[(2-amino-2-oxoethyl)(propan-2-yl)amino]-N-[(1S)-1-(naphthalen-2-yl)ethyl]acetamide |
- |
|
2.7.11.15 | 2-[(3S)-3-[(phenylsulfanyl)methyl]pyrrolidin-1-yl]-N-(pyridin-3-ylmethyl)acetamide |
- |
|
2.7.11.15 | 3-(3-fluoro-4-methoxybenzyl)-6-(1H-pyrazol-4-yl)quinazolin-4(3H)-one |
- |
|
2.7.11.15 | 3-(3-methoxybenzyl)-6-(1H-pyrazol-4-yl)quinazolin-4(3H)-one |
- |
|
2.7.11.15 | 3-(4-fluoro-3-methoxybenzyl)-6-(1H-pyrazol-4-yl)quinazolin-4(3H)-one |
- |
|