N-[(-)-JASMONOYL]-(S)-ISOLEUCINE (JaIle) Chemical Properties

Boiling point:

527.5±30.0 °C(Predicted)

Density 

1.064±0.06 g/cm3(Predicted)

solubility 

DMF: 25 mg/ml
DMSO: 16 mg/ml
Ethanol: 30 mg/mlPBS (pH 7.2): 3 mg/ml

form 

Solid

pka

3.61±0.10(Predicted)

color 

White to off-white

N-[(-)-JASMONOYL]-(S)-ISOLEUCINE (JaIle) Usage And Synthesis

Uses

N-Jasmonyl-L-Isoleucine-d3 (Mixture of Diastereomers) is the labeled analogue of N-Jasmonyl-L-Isoleucine (Mixture of Diastereomers) (J210550), a plant horomone.

Definition

ChEBI: (-)-Jasmonoyl-L-isoleucine is a N-acyl-amino acid and a secondary carboxamide.

IC 50

Human Endogenous Metabolite

References

[1] LERON KATSIR. Jasmonate signaling: a conserved mechanism of hormone sensing[J]. Current opinion in plant biology, 2008, 11 4: Pages 428-435. DOI: 10.1016/j.pbi.2008.05.004
[2] JONAS GOOSSENS. Jasmonates: signal transduction components and their roles in environmental stress responses.[J]. Plant Molecular Biology, 2016, 91 6: 673-689. DOI: 10.1007/s11103-016-0480-9
[3] JIN-HO KANG. Silencing threonine deaminase and JAR4 in Nicotiana attenuata impairs jasmonic acid-isoleucine-mediated defenses against Manduca sexta.[J]. ACS Central Science, 2006: 3303-3320. DOI: 10.1105/tpc.106.041103
[4] KOO A J. Metabolism of the plant hormone jasmonate: a sentinel for tissue damage and master regulator of stress response[J]. Phytochemistry Reviews, 2017, 17 1: 51-80. DOI: 10.1007/s11101-017-9510-8
[5] ROBERT KRAMELL. Amino acid conjugates of jasmonic acid induce jasmonate-responsive gene expression in barley (Hordeum vulgare L.) leaves[J]. FEBS Letters, 1997, 414 2: Pages 197-202. DOI: 10.1016/s0014-5793(97)01005-3

N-[(-)-JASMONOYL]-(S)-ISOLEUCINE (JaIle)(120330-93-0)Related Product Information

• (+)-trans-Jasmonic Acid
• (±)-JASMONICACID
• 3-oxo-2-pentylcyclopentaneacetic acid
• (-)-JASMONIC ACID
• Jasmonic Acid-d5 (Mixture of Diastereomers, (-)-trans major)
• Methyl Jasmonate
• (±)-JASMONIC ACID METHYL ESTER (MeJA)
• METHYL JASMONATE
• Methyl JasMonate (Mixture of isoMers)
• L-Isoleucine, N-[2-[(1R,2S)-3-oxo-2-(2Z)-2-penten-1-ylcyclopentyl]acetyl]-