EC Number   |
Inhibitors |
Structure |
|---|
   1.1.5.5 | 2,6-dichloro-4-dicyanovinylphenol |
i.e. PC-16, competitive quinone reduction inhibition mode, the inhibitor binds to the low affinity quinone binding site(S) QN and/or QL of quinone-bound ADH, overview |
   |
| 1.1.5.5 | antimycin A |
inhibits Q2H2 oxidation and Q reduction |
|
| 1.1.5.5 | antimycin A |
powerful inhibitor of the purified ADH complex, most likely acting at the ubiquinone acceptor site in subunit II |
|
| 1.1.5.5 | Myxothiazol |
powerful inhibitor of the purified ADH complex, most likely acting at the ubiquinone acceptor site in subunit II |
|
| 1.1.5.5 | Triton X-100 |
- |
|
| 1.1.5.5 | Zinc acetate |
7% residual activity at 20 mM |
|
