EC Number   |
Inhibitors |
Structure |
|---|
    1.3.8.7 | (methylenecyclopropyl)acetyl-CoA |
0.01 mM, 95% inhibition |
   |
| 1.3.8.7 | (methylenecyclopropyl)acetyl-CoA |
biphasic inhibition of medium-chain acyl-CoA dehydrogenase, rapid initial inactivation for 2 min, half-life: 1.3 min, followed by a slower decline, 95% activity lost after 30 min, no inhibition of long-chain acyl-CoA dehydrogenase |
|
| 1.3.8.7 | (R)-(-)-(methylenecyclopropyl)acetyl-CoA |
- |
|
| 1.3.8.7 | (R)-(-)-(methylenecyclopropyl)acetyl-CoA |
0.0155 mM, almost complete inactivation after 5 min, stereospecific inactivation, faster inhibition with (R)-isomer than with (S)-isomer |
|
| 1.3.8.7 | (R)-(-)-(methylenecyclopropyl)acetyl-CoA |
both (R)- and (S)-stereoisomers are potent inhibitors, inactivation is nonstereospecific |
|
| 1.3.8.7 | (S)-(+)-(Methylenecyclopropyl)acetyl-CoA |
stereospecific inactivation, faster inhibition with (R)-isomer than with (S)-isomer |
|
| 1.3.8.7 | 1-ethyl-3(3-dimethylaminopropyl)-carbodiimide |
90-96% inhibition of activity with electron transfer flavoprotein, not with phenazine methosulfate |
|
| 1.3.8.7 | 2,3-octadienoyl-CoA |
- |
|
| 1.3.8.7 | 2-decenoyl-CoA |
medium- and long-chain acyl-CoA dehydrogenase |
|
| 1.3.8.7 | 2-hexadecenoyl-CoA |
competitive, long-chain acyl-CoA dehdrogenase |
|
