JA-ACC

Modify Date: 2024-01-02 18:48:22

JA-ACC Structure
JA-ACC structure
Common Name JA-ACC
CAS Number 371778-55-1 Molecular Weight 293.35800
Density N/A Boiling Point N/A
Molecular Formula C16H23NO4 Melting Point N/A
MSDS N/A Flash Point N/A

 Use of JA-ACC


JA-ACC (Jasmonyl-ACC) is a derivative of 1-aminocyclopropane-1-carboxylic acid (ACC). ACC is the direct precursor of the plant hormone ethylene. JA-ACC inhibits root growth in Arabidopsis and the inhibition is independent of jasmonic acid (JA) signaling[1].

 Names

Name 1-[[2-[(1R,2R)-3-oxo-2-[(Z)-pent-2-enyl]cyclopentyl]acetyl]amino]cyclopropane-1-carboxylic acid
Synonym More Synonyms

 JA-ACC Biological Activity

Description JA-ACC (Jasmonyl-ACC) is a derivative of 1-aminocyclopropane-1-carboxylic acid (ACC). ACC is the direct precursor of the plant hormone ethylene. JA-ACC inhibits root growth in Arabidopsis and the inhibition is independent of jasmonic acid (JA) signaling[1].
Related Catalog
In Vitro JA-ACC (Jasmonyl-ACC) serves as a pivotal molecule which can function as a modulator of the hormonal cross-talk between the ethylene and jasmonic acid pathway[1]. JA-ACC is the second most abundant JA conjugate detected in Arabidopsis leaves and is formed by JAR1, a JA-amino synthetase[2].
References

[1]. Van de Poel B, et al. 1-aminocyclopropane-1-carboxylic acid (ACC) in plants: more than just the precursor of ethylene! Front Plant Sci. 2014 Nov 11;5:640.  

[2]. Polko JK, et al. 1-Aminocyclopropane 1-Carboxylic Acid and Its Emerging Role as an Ethylene-Independent Growth Regulator. Front Plant Sci. 2019 Dec 5;10:1602.  

 Chemical & Physical Properties

Molecular Formula C16H23NO4
Molecular Weight 293.35800
Exact Mass 293.16300
PSA 86.96000
LogP 2.90180

 Synonyms

jasmonic acid / 1-amino-1-cyclopropane carboxylic acid
N-[(3R,7R)-()-Jasmonoyl]-aminocyclopropane carboxylic acid
cyclopropanecarboxylic acid,1-[[[(1R,2R)-3-oxo-2-[(2Z)-2-pentenyl]cyclopentyl]acetyl]amino]
Cyclopropanecarboxylic acid,1-[[[3-oxo-2-(2Z)-2-pentenylcyclopentyl]acetyl]amino]-(9CI)