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Leukotriene A4 methyl ester

Leukotriene A4 methyl ester (LTA4 methyl ester) 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.

Product Specifications

CAS Number

[73466-12-3]

Product Name Alternative

LTA4 methyl ester

UNSPSC

12352005

Hazard Statement

H225-H304-H315-H319-H336-H361-H373-H411

Target

Biochemical Assay Reagents

Type

Reference compound

Related Pathways

Others

Applications

COVID-19-immunoregulation

Field of Research

Inflammation/Immunology

Assay Protocol

https://www.medchemexpress.com/leukotriene-a4-methyl-ester.html

Smiles

O=C(OC)CCC[C@@H]1O[C@H]1/C=C/C=C/C=C\C/C=C\CCCCC

Molecular Formula

C21H32O3

Molecular Weight

332.48

Precautions

P210-P233-P240-P241-P242-P243-P260-P261-P264-P271-P273-P280-P302+P352-P303+P361+P353-P304+P340-P305+P351+P338-P331-P362+P364-P370+P378-P391-P403+P233-P403+P235-P405-P501

References & Citations

[1]Samuelsson, et al. Leukotrienes and lipoxins: Structures, biosynthesis, and biological effects. Science 237 (4819), 1171-1176 (1987) .

Shipping Conditions

Room temperature

Scientific Category

Reference compound1

Clinical Information

No Development Reported

Available Sizes

Curated Selection

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