Eoxin E4

CAT: 0804-HY-115356Size: 1 EachDry Ice: NoHazardous: No
CAT#:0804-HY-115356Size:1 Each
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AVAILABILITY: InStock
24/48H Stock Items & 2 to 6 Weeks non Stock Items.
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Description
Eoxin E4 (14,15-LTE4) is the metabolite of 14,15-LTC4 and 14,15-LTD4. Eoxin E4 increases vascular permeability of human endothelial cell monolayers with about 10-fold less potency than LTC4, but approximately 100-fold greater potency than histamine[1][2].
CAS Number
[1000852-57-2]
Product Name Alternative
14,15-LTE4; EoxE4
UNSPSC
12352211
Hazard Statement
H225-H301+H311+H331-H370
Target
Drug Metabolite
Type
Reference compound
Related Pathways
Metabolic Enzyme/Protease
Field of Research
Cardiovascular Disease
Assay Protocol
https://www.medchemexpress.com/eoxin-e4.html
Smiles
CCCCC[C@@H]([C@@H](/C=C/C=C/C=C\C/C=C\CCCC(O)=O)SC[C@@H](C(O)=O)N)O
Molecular Formula
C23H37NO5S
Molecular Weight
439.61
Precautions
P210-P233-P240-P241-P242-P243-P260-P261-P264-P270-P271-P280-P302+P352-P303+P361+P353-P304+P340-P308+P311-P330-P361+P364-P370+P378-P403+P233-P403+P235-P405-P501
References & Citations
[1]Bryant RW, et al. Leukotriene formation by a purified reticulocyte lipoxygenase enzyme. Conversion of arachidonic acid and 15-hydroperoxyeicosatetraenoic acid to 14, 15-leukotriene A4. J Biol Chem. 1985 Mar 25;260 (6) :3548-55. |[2]Luo M, et al. Leukotriene synthesis by epithelial cells. Histol Histopathol. 2003 Apr;18 (2) :587-95.
Shipping Conditions
Room temperature
Scientific Category
Reference compound1
Clinical Information
No Development Reported

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