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> Main
CHEBI:134619 - leukotriene C
3
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ChEBI Name
leukotriene C
3
ChEBI ID
CHEBI:134619
ChEBI ASCII Name
leukotriene C3
Definition
A leukotriene that is (5
S
,7
E
,9
E
,11
Z
)-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.
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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 C
3
(
CHEBI:134619
)
has role
mouse metabolite (
CHEBI:75771
)
leukotriene C
3
(
CHEBI:134619
)
has role
rat metabolite (
CHEBI:86264
)
leukotriene C
3
(
CHEBI:134619
)
is a
glutathione derivative (
CHEBI:24337
)
leukotriene C
3
(
CHEBI:134619
)
is a
leukotriene (
CHEBI:25029
)
leukotriene C
3
(
CHEBI:134619
)
is a
organic sulfide (
CHEBI:16385
)
leukotriene C
3
(
CHEBI:134619
)
is conjugate acid of
leukotriene C
3
(2−) (
CHEBI:133597
)
Incoming
leukotriene C
3
(2−) (
CHEBI:133597
)
is conjugate base of
leukotriene C
3
(
CHEBI:134619
)
IUPAC Name
L
-
γ-
glutamyl-
S
-
[(4
S
,5
R
,6
E
,8
E
,10
Z
)-
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
LTC
3
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