CHEBI:134627 - leukotriene D3

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ChEBI Name leukotriene D3
ChEBI ID CHEBI:134627
ChEBI ASCII Name leukotriene D3
Definition A leukotriene that is (5S,7E,9E,11Z)-5-hydroxyicosa-7,9,11-trienoic acid in which an L-cysteinylglycinyl group is attached at position 6R via a sulfide linkage.
Stars This entity has been manually annotated by the ChEBI Team.
Supplier Information
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Formula C25H42N2O6S
Net Charge 0
Average Mass 498.678
Monoisotopic Mass 498.27636
InChI InChI=1S/C25H42N2O6S/c1-2-3-4-5-6-7-8-9-10-11-12-13-16-22(21(28)15-14-17-23(29)30)34-19-20(26)25(33)27-18-24(31)32/h9-13,16,20-22,28H,2-8,14-15,17-19,26H2,1H3,(H,27,33)(H,29,30)(H,31,32)/b10-9-,12-11+,16-13+/t20-,21-,22+/m0/s1
InChIKey SBFPHBDUKAKWJL-OGQVOSTCSA-N
SMILES C(\C=C/C=C/C=C/[C@H]([C@@H](O)CCCC(=O)O)SC[C@H](N)C(=O)NCC(=O)O)CCCCCCC
Metabolite of Species Details
Mus musculus (NCBI:txid10090) See: PubMed
Rattus norvegicus (NCBI:txid10116) See: PubMed
Roles Classification
Chemical Role(s): Bronsted base
A molecular entity capable of accepting a hydron from a donor (Bronsted acid).
(via organic amino compound )
Biological Role(s): mouse metabolite
Any mammalian metabolite produced during a metabolic reaction in a mouse (Mus musculus).
rat metabolite
Any mammalian metabolite produced during a metabolic reaction in rat (Rattus norvegicus).
xenobiotic metabolite
Any metabolite produced by metabolism of a xenobiotic compound.
View more via ChEBI Ontology
ChEBI Ontology
Outgoing leukotriene D3 (CHEBI:134627) has role mouse metabolite (CHEBI:75771)
leukotriene D3 (CHEBI:134627) has role rat metabolite (CHEBI:86264)
leukotriene D3 (CHEBI:134627) has role xenobiotic metabolite (CHEBI:76206)
leukotriene D3 (CHEBI:134627) is a dipeptide (CHEBI:46761)
leukotriene D3 (CHEBI:134627) is a leukotriene (CHEBI:25029)
leukotriene D3 (CHEBI:134627) is a organic sulfide (CHEBI:16385)
IUPAC Name
S-[(4S,5R,6E,8E,10Z)-1-carboxy-4-hydroxynonadeca-6,8,10-trien-5-yl]-L-cysteinylglycine
Synonyms Sources
5-Hydroxy-6-cysteinylglycine-7,9,11-eicosatrienoic acid ChemIDplus
Leukotriene D-3 ChemIDplus
LTD3 ChEBI
Manual Xref Database
EP0106571 Patent
View more database links
Registry Numbers Types Sources
6015329 Reaxys Registry Number Reaxys
77165-74-3 CAS Registry Number ChemIDplus
Citations Waiting for Citations Types Sources
6116705 PubMed citation Europe PMC
6273168 PubMed citation Europe PMC
6780563 PubMed citation Europe PMC
Last Modified
21 February 2017