Basic information Safety Supplier Related

(-)-LEUKOTRIENE A4 METHYL ESTER

Basic information Safety Supplier Related

(-)-LEUKOTRIENE A4 METHYL ESTER Basic information

Product Name:
(-)-LEUKOTRIENE A4 METHYL ESTER
Synonyms:
  • (-)-LEUKOTRIENE A4 METHYL ESTER
  • LEUKOTRIENE A4 METHYL ESTER
  • (-)-leukotriene A4
  • LEUKOTRIENE A4-METHYLESTER SOLUTION (100UG/ML HEXANE/1% TRIETHYLAMINE)
  • LTA4 (Leukotriene A4 methyl ester)
  • PWXYNAKNLZUYAL-WAQVJNLQSA-N
  • 5S-TRANS-5,6-OXIDO-7E,9E,11Z,14Z-EICOSATETRAENOIC ACID, METHYL ESTER
  • 2-Oxiranebutanoic acid, 3-(1E,3E,5Z,8Z)-1,3,5,8-tetradecatetraen-1-yl-, methyl ester, (2S,3S)-
CAS:
73466-12-3
MF:
C21H32O3
MW:
332.48
Mol File:
73466-12-3.mol
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(-)-LEUKOTRIENE A4 METHYL ESTER Chemical Properties

storage temp. 
−20°C
solubility 
Acetone: >50 mg/ml; DMF: >50 mg/ml; DMSO: >50 mg/ml; Ethanol: >50 mg/ml; PBS pH 7.2: insoluble and unstable.
form 
triethylamine:hexane solution
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Safety Information

Hazard Codes 
F,Xn,N
Risk Statements 
11-36/37/38-48/20-51/53-62-65-67
Safety Statements 
9-16-29-33-36/37-61-62
RIDADR 
UN 1208 3/PG 2
WGK Germany 
2

MSDS

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(-)-LEUKOTRIENE A4 METHYL ESTER Usage And Synthesis

Description

Leukotriene A4 (LTA4) is synthesized in mast cells, eosinophils, and neutrophils from arachidonic acid by 5-lipoxygenase (5-LO), which exhibits both lipoxygenase and LTA4 synthase activities. LTA4 is rapidly metabolized by LTA4 hydrolase or LTC4 synthase to LTB4 or LTC4, respectively. LTA4, from leukocytes, is known to undergo transcellular metabolism in platelets, erythrocytes, and endothelial cells. Further metabolism of LTA4 by 15-LO leads to lipoxin biosynthesis. LTA4 as a free acid is highly unstable. The methyl ester is stable and can be readily hydrolyzed to the free acid as needed.

Uses

LTA4 (Leukotriene A4 methyl ester) is an unstable intermediate in the biosynthesis of LTB4 and LTC4.

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