For research use only. Not for therapeutic Use.
Ethylene, an important plant regulator, is synthesized from S-<wbr></wbr>adenosyl-<wbr></wbr>L-<wbr></wbr>methionine by the sequential action of 1-<wbr></wbr>amino-<wbr></wbr>cyclopropane-<wbr></wbr>carboxylate (ACC) synthases (ACSs) and ACC oxidases (ACOs). Aminoethoxyvinyl glycine is an inhibitor of ethylene biosynthesis that, at 1 µM, blocks the activity of both ACSs and ACOs. Through this action, it reduces ethylene-<wbr></wbr>mediated changes in plant growth and development. Aminoethoxyvinyl glycine also inhibits cystathionine γ-<wbr></wbr>lyase (K<sub>i</sub> = 10.5 μM) with slow-<wbr></wbr> and tight-<wbr></wbr>binding characteristics.
Catalog Number | R060777 |
CAS Number | 55720-26-8 |
Synonyms | (2S,3E)-2-Amino-4-(2-aminoethoxy)-3-butenoic Acid Monohydrochloride; [S-(E)]-2-Amino-4-(2-aminoethoxy)-3-butenoic Acid Monohydrochloride; (S)-trans-2-Amino-4-(2-aminoethoxy)-3-butenoic Acid Hydrochloride; ABG 3168 Hydrochloride; L-2-Amino-4-(2’-amin |
Molecular Formula | C6H13ClN2O3 |
Purity | ≥95% |
Storage | -20°C |
IUPAC Name | (E,2S)-2-amino-4-(2-aminoethoxy)but-3-enoic acid;hydrochloride |
InChI | InChI=1S/C6H12N2O3.ClH/c7-2-4-11-3-1-5(8)6(9)10;/h1,3,5H,2,4,7-8H2,(H,9,10);1H/b3-1+;/t5-;/m0./s1 |
InChIKey | ZDCPLYVEFATMJF-BTIOQYSDSA-N |
SMILES | C(COC=CC(C(=O)O)N)N.Cl |