CHEBI:134619 - leukotriene C₃

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ChEBI Name leukotriene C3 ChEBI ID CHEBI:134619 ChEBI ASCII Name leukotriene C3 Definition A leukotriene that is (5S,7E,9E,11Z)-5-hydroxyicosa-7,9,11-trienoic acid in which a glutathionyl group is attached at position 6 via a sulfide linkage. Stars This entity has been manually annotated by the ChEBI Team. Supplier Information Download Molfile XML SDF Find compounds which contain this structure Find compounds which resemble this structure Take structure to the Advanced Search Formula C30H49N3O9S Net Charge 0 Average Mass 627.792 Monoisotopic Mass 627.31895 InChI InChI=1S/C30H49N3O9S/c1-2-3-4-5-6-7-8-9-10-11-12-13-16-25(24(34)15-14-17-27(36)37)43-21-23(29(40)32-20-28(38)39)33-26(35)19-18-22(31)30(41)42/h9-13,16,22-25,34H,2-8,14-15,17-21,31H2,1H3,(H,32,40)(H,33,35)(H,36,37)(H,38,39)(H,41,42)/b10-9-,12-11+,16-13+/t22-,23-,24-,25+/m0/s1 InChIKey AIJDQMYBRDJHHT-ABAXQOPJSA-N SMILES C(\C=C/C=C/C=C/[C@H]([C@@H](O)CCCC(=O)O)SC[C@H](NC(CC[C@H](N)C(=O)O)=O)C(=O)NCC(=O)O)CCCCCCC Metabolite of Species Details Mus musculus (NCBI:txid10090) See: PubMed Rattus norvegicus (NCBI:txid10116) See: PubMed Roles Classification 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). View more via ChEBI Ontology ChEBI Ontology Outgoing leukotriene C3 (CHEBI:134619) has role mouse metabolite (CHEBI:75771) leukotriene C3 (CHEBI:134619) has role rat metabolite (CHEBI:86264) leukotriene C3 (CHEBI:134619) is a glutathione derivative (CHEBI:24337) leukotriene C3 (CHEBI:134619) is a leukotriene (CHEBI:25029) leukotriene C3 (CHEBI:134619) is a organic sulfide (CHEBI:16385) leukotriene C3 (CHEBI:134619) is conjugate acid of leukotriene C3(2−) (CHEBI:133597) Incoming leukotriene C3(2−) (CHEBI:133597) is conjugate base of leukotriene C3 (CHEBI:134619) IUPAC Name L-γ-glutamyl-S-[(4S,5R,6E,8E,10Z)-1-carboxy-4-hydroxynonadeca-6,8,10-trien-5-yl]-L-cysteinylglycine Synonyms Sources 5-Hydroxy-6-S-glutathionyl-7,9,11-eicosatrienoic acid ChemIDplus Leukotriene C-3 ChemIDplus LTC3 ChEBI Manual Xref Database EP0106571 Patent View more database links Registry Numbers Types Sources 5686053 Reaxys Registry Number Reaxys 77209-77-9 CAS Registry Number ChemIDplus Citations Types Sources 2161640 PubMed citation Europe PMC 2188748 PubMed citation Europe PMC 3343345 PubMed citation Europe PMC 3571276 PubMed citation Europe PMC 3916594 PubMed citation Europe PMC 6116705 PubMed citation Europe PMC 6122451 PubMed citation Europe PMC 6124100 PubMed citation Europe PMC 6273168 PubMed citation Europe PMC 6297932 PubMed citation Europe PMC 6307367 PubMed citation Europe PMC 6432878 PubMed citation Europe PMC 6780563 PubMed citation Europe PMC 7053383 PubMed citation Europe PMC 7306127 PubMed citation Europe PMC 8035338 PubMed citation Europe PMC Last Modified 21 February 2017