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

Product Name
N-[(-)-JASMONOYL]-(S)-ISOLEUCINE (JaIle)
CAS No.
120330-93-0
Chemical Name
N-[(-)-JASMONOYL]-(S)-ISOLEUCINE (JaIle)
Synonyms
Jasmonic Acid Impurity 1;Jasmonic Acid Impurity 9;(-Jasmonic Acid-Isoleucine;N-[(-)-JASMONOYL]-(S)-ISOLEUCINE (JaIle);L-Isoleucine, N-[2-[(1R,2R)-3-oxo-2-(2Z)-2-penten-1-ylcyclopentyl]acetyl]-
CBNumber
CB72471821
Molecular Formula
C18H29NO4
Formula Weight
323.43
MOL File
120330-93-0.mol
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N-[(-)-JASMONOYL]-(S)-ISOLEUCINE (JaIle) Property

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
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Hazard and Precautionary Statements (GHS)

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N-Bromosuccinimide Price

Medical Isotopes, Inc.
Product number
51910
Product name
N-Jasmonyl-L-Isoleucine(MixtureofDiastereomers)
Packaging
10mg
Price
$650
Updated
2021/12/16
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N-[(-)-JASMONOYL]-(S)-ISOLEUCINE (JaIle) Chemical Properties,Usage,Production

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) Preparation Products And Raw materials

Raw materials

Preparation Products

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N-[(-)-JASMONOYL]-(S)-ISOLEUCINE (JaIle) Suppliers

Shanghai Macklin Biochemical Co.,Ltd.
Tel
15221275939
Fax
021-50706099
Email
shenlinxing@macklin.cn
Country
China
ProdList
15873
Advantage
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Alfa Chemistry
Tel
1-516-6625404
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1-516-927-0118
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support@alfa-chemistry.com
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United States
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021-61312847; 18021002903
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3008007409@qq.com
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ChemeGen(Shanghai) Biotechnology Co.,Ltd.
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QQ 3610331285
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sales@chemegen.com
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MedBioPharmaceutical Technology Inc
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021-69568360 18916172912
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order@med-bio.cn
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Energy Chemical
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DONBOO AMINO ACID COMPANY
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amyjetsci
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Henan Vcommend Consultrading Co., Ltd.
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120330-93-0, N-[(-)-JASMONOYL]-(S)-ISOLEUCINE (JaIle)Related Search:


  • N-[(-)-JASMONOYL]-(S)-ISOLEUCINE (JaIle)
  • (-Jasmonic Acid-Isoleucine
  • L-Isoleucine, N-[2-[(1R,2R)-3-oxo-2-(2Z)-2-penten-1-ylcyclopentyl]acetyl]-
  • Jasmonic Acid Impurity 9
  • Jasmonic Acid Impurity 1
  • 120330-93-0