EC Number   |
Inhibitors |
Structure |
|---|
   4.4.1.14 | (2E,3E)-4-(2-aminoethoxy)-2-[([3-hydroxy-2-methyl-5[(phosphonooxy)methyl]pyridin-4-yl]methyl)imino] but-3-enoic acid |
best inhibitor tested |
   |
| 4.4.1.14 | 1-aminocyclopropane-1-carboxylate |
- |
|
| 4.4.1.14 | 1-aminoethoxyvinyl glycine |
- |
|
| 4.4.1.14 | 1-methylcyclopropene |
completely inhibits the ethylene-associated transcription of isozyme ACS1 in the whole fruit; completely inhibits the ethylene-associated transcription of isozyme ACS4 in the whole fruit |
|
| 4.4.1.14 | 2-(cyclopentylamino)-7,7-dimethyl-7,8-dihydroquinazolin-5(6H)-one |
inhibition of ethylene biosynthesis at the step of converting S-adenosylmethionine to 1-aminocyclopropane-1-carboxylic acid by ACC synthase |
|
| 4.4.1.14 | 2-(cyclopentylamino)-7-(4-methylphenyl)-7,8-dihydroquinazolin-5(6H)-one |
inhibition of ethylene biosynthesis at the step of converting S-adenosylmethionine to 1-aminocyclopropane-1-carboxylic acid by ACC synthase |
|
| 4.4.1.14 | 2-amino-7-(4-methylphenyl)-7,8-dihydro-5(6H)-quinazolinone |
uncompetitive |
|
| 4.4.1.14 | 2-aminooxyisobutyric acid |
75% inhibition at 1.1 mM. The compound's action resembles aminooxyacetic acid. The inhibitor significantly increases the vase life of cut flowers by highly reducing the ethylene production through inhibition of the enzyme |
|
| 4.4.1.14 | 2-[(3-hydroxy-2-methyl-5-phosphonooxymethyl-pyridin-4-ylmethyl)-imino]-5-phosphonopent-3-enoic acid |
strong binding capacity |
|
| 4.4.1.14 | 7-(4-methoxyphenyl)-2-(phenylamino)-7,8-dihydroquinazolin-5(6H)-one |
inhibition of ethylene biosynthesis at the step of converting S-adenosylmethionine to 1-aminocyclopropane-1-carboxylic acid by ACC synthase |
|
