EC Number   |
Inhibitors |
Structure |
|---|
   1.14.13.168 | 2-chlorophenylboronic acid |
moderate inhibition of enzyme activity and primary root elongation. Probably unspecific inhibition |
   |
| 1.14.13.168 | 3,5-dibromophenylboronic acid |
probably unspecific inhibition, inhibits root hair formation in wild-type Arabidopsis thaliana seedlings |
|
| 1.14.13.168 | 3,5-dichlorophenylboronic acid |
probably unspecific inhibition, inhibits root hair formation in wild-type Arabidopsis thaliana seedlings |
|
| 1.14.13.168 | 3-chlorophenylboronic acid |
probably unspecific inhibition, strongly inhibits root hair formation in wild-type Arabidopsis thaliana seedlings |
|
| 1.14.13.168 | 4-biphenylboronic acid |
BBo, competitive, inhibits the activity of recombinant YUC in vitro, reduces endogenous indole-3-acetic acid content, and strongly inhibits primary root elongation and lateral root formation in wild-type Arabidopsis thaliana seedlings |
|
| 1.14.13.168 | 4-chlorophenylboronic acid |
probably unspecific inhibition, strongly inhibits root hair formation in wild-type Arabidopsis thaliana seedlings |
|
| 1.14.13.168 | 4-methyl-4-biphenylboronic acid |
weak inhibition of enzyme activity, but strong inhibition of primary root elongation |
|
| 1.14.13.168 | 4-phenoxyphenylboronic acid |
PPBo, competitive, inhibits the activity of recombinant YUC in vitro, reduces endogenous indole-3-acetic acid content, and strongly inhibits primary root elongation and lateral root formation in wild-type Arabidopsis thaliana seedlings. The compound does not interfere with the auxin response of auxin-marker genes when it was co-treated with indole acetic acid, suggesting that PPBo is not an inhibitor of auxin sensing or signaling |
|
| 1.14.13.168 | more |
FAD and boronic acid is not the main reason for inhibition of enzyme activity by boronic acid derivatives. Poor inhibition by 2,6-dichlorophenylboronic acid |
|
| 1.14.13.168 | phenethylboronic acid |
moderate inhibition of enzyme activity and primary root elongation |
|
