CHEBI:15650 - leukotriene E4

Main ChEBI Ontology Automatic Xrefs Reactions Pathways Models
ChEBI Name leukotriene E4
ChEBI ID CHEBI:15650
ChEBI ASCII Name leukotriene E4
Definition A leukotriene that is (7E,9E,11Z,14Z)-icosa-7,9,11,14-tetraenoic acid substituted by a hydroxy group at position 5 (5S) and an L-cystein-S-yl group at position 6 (6R).
Stars This entity has been manually annotated by the ChEBI Team.
Secondary ChEBI IDs CHEBI:10936, CHEBI:27921, CHEBI:261, CHEBI:18612, CHEBI:6424, CHEBI:25027
Supplier Information
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Formula C23H37NO5S
Net Charge 0
Average Mass 439.60900
Monoisotopic Mass 439.239
InChI InChI=1S/C23H37NO5S/c1-2-3-4-5-6-7-8-9-10-11-12-13-16-21(30-18-19(24)23(28)29)20(25)15-14-17-22(26)27/h6-7,9-13,16,19-21,25H,2-5,8,14-15,17-18,24H2,1H3,(H,26,27)(H,28,29)/b7-6-,10-9-,12-11+,16-13+/t19-,20-,21+/m0/s1
InChIKey OTZRAYGBFWZKMX-FRFVZSDQSA-N
SMILES CCCCC\C=C/C\C=C/C=C/C=C/[C@@H](SC[C@H](N)C(O)=O)[C@@H](O)CCCC(O)=O
Roles Classification
Chemical Role(s): Bronsted acid
A molecular entity capable of donating a hydron to an acceptor (Bronsted base).
(via oxoacid )
Biological Role(s): mouse metabolite
Any mammalian metabolite produced during a metabolic reaction in a mouse (Mus musculus).
(via L-alpha-amino acid )
View more via ChEBI Ontology
ChEBI Ontology
Outgoing leukotriene E4 (CHEBI:15650) has functional parent icosa-7,9,11,14-tetraenoic acid (CHEBI:36038)
leukotriene E4 (CHEBI:15650) is a L-cysteine thioether (CHEBI:27532)
leukotriene E4 (CHEBI:15650) is a amino dicarboxylic acid (CHEBI:36164)
leukotriene E4 (CHEBI:15650) is a leukotriene (CHEBI:25029)
leukotriene E4 (CHEBI:15650) is a non-proteinogenic L-α-amino acid (CHEBI:83822)
leukotriene E4 (CHEBI:15650) is a secondary alcohol (CHEBI:35681)
leukotriene E4 (CHEBI:15650) is conjugate acid of leukotriene E4(1−) (CHEBI:57462)
Incoming 16-carboxy-Δ13-17,18,19,20-tetranor-leukotriene E4 (CHEBI:74016) has functional parent leukotriene E4 (CHEBI:15650)
16-carboxy-17,18,19,20-tetranor-leukotriene E3 (CHEBI:74014) has functional parent leukotriene E4 (CHEBI:15650)
18-carboxy-19,20-dinor-leukotriene E4 (CHEBI:74017) has functional parent leukotriene E4 (CHEBI:15650)
20-carboxyleukotriene E4 (CHEBI:134517) has functional parent leukotriene E4 (CHEBI:15650)
20-hydroxy-leukotriene E4 (CHEBI:28700) has functional parent leukotriene E4 (CHEBI:15650)
20-oxoleukotriene E4 (CHEBI:134513) has functional parent leukotriene E4 (CHEBI:15650)
N-acetylleukotriene E4 (CHEBI:7210) has functional parent leukotriene E4 (CHEBI:15650)
leukotriene E4 methyl ester (CHEBI:138126) has functional parent leukotriene E4 (CHEBI:15650)
leukotriene E4(1−) (CHEBI:57462) is conjugate base of leukotriene E4 (CHEBI:15650)
IUPAC Names
(5S,6R,7E,9E,11Z,14Z)-6-(L-cystein-S-yl)-5-hydroxyicosa-7,9,11,14-tetraenoic acid
S-{(1R,2E,4E,6Z,9Z)-1-[(1S)-4-carboxy-1-hydroxybutyl]pentadeca-2,4,6,9-tetraen-1-yl}-L-cysteine
Synonyms Sources
(5S-(5R*,6S*(S*),7E,9E,11Z,14Z))-6-((2-Amino-2-carboxyethyl)thio)-5-hydroxy-7,9,11,14-eicosatetraenoic acid ChemIDplus
(7E,9E,11Z,14Z)-(5S,6R)-6-(Cystein-S-yl)-5-hydroxyeicosa-7,9,11,14-tetraenoate KEGG COMPOUND
(7E,9E,11Z,14Z)-(5S,6R)-6-(Cystein-S-yl)-5-hydroxyicosa-7,9,11,14-tetraenoate KEGG COMPOUND
5S-hydroxy,6R-(S-cysteinyl),7E,9E,11Z,14Z-eicosatetraenoic acid LIPID MAPS
Leukotriene E4 KEGG COMPOUND
LTE4 KEGG COMPOUND
Database Links Databases
C05952 KEGG COMPOUND
LMFA03020002 LIPID MAPS
View more database links
Registry Number Type Source
75715-89-8 CAS Registry Number ChemIDplus
Citation Waiting for Citations Type Source
19291727 PubMed citation Europe PMC
Last Modified
09 August 2017