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leukotriene E4 |
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CHEBI:15650 |
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leukotriene E4 |
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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). |
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This entity has been manually annotated by the ChEBI Team.
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CHEBI:10936, CHEBI:27921, CHEBI:261, CHEBI:18612, CHEBI:6424, CHEBI:25027
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Molfile
XML
SDF
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more structures >>
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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 |
OTZRAYGBFWZKMX-FRFVZSDQSA-N |
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 |
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Bronsted base
A molecular entity capable of accepting a hydron from a donor (Bronsted acid).
(via organic amino compound )
Bronsted acid
A molecular entity capable of donating a hydron to an acceptor (Bronsted base).
(via oxoacid )
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View more via ChEBI Ontology
Outgoing
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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)
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Incoming
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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)
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(5S,6R,7E,9E,11Z,14Z)- 6- (L- cystein- S- yl)- 5- hydroxyicosa- 7,9,11,14- tetraenoic acid
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S- {(1R,2E,4E,6Z,9Z)- 1- [(1S)- 4- carboxy- 1- hydroxybutyl]pentadeca- 2,4,6,9- tetraen- 1- yl}- L- cysteine
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(5S- (5R*,6S*(S*),7E,9E,11Z,14Z))- 6- ((2- Amino- 2- carboxyethyl)thio)- 5- hydroxy- 7,9,11,14- eicosatetraenoic acid
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ChemIDplus
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(7E,9E,11Z,14Z)-(5S,6R)-6-(Cystein-S-yl)-5-hydroxyeicosa-7,9,11,14-tetraenoate
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KEGG COMPOUND
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(7E,9E,11Z,14Z)-(5S,6R)-6-(Cystein-S-yl)-5-hydroxyicosa-7,9,11,14-tetraenoate
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KEGG COMPOUND
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5S-hydroxy,6R-(S-cysteinyl),7E,9E,11Z,14Z-eicosatetraenoic acid
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LIPID MAPS
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Leukotriene E4
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KEGG COMPOUND
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LTE4
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KEGG COMPOUND
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75715-89-8
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CAS Registry Number
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ChemIDplus
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19291727
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PubMed citation
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Europe PMC
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