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> Main
CHEBI:28728 - thromboxane B
2
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ChEBI Name
thromboxane B
2
ChEBI ID
CHEBI:28728
ChEBI ASCII Name
thromboxane B2
Definition
A member of the class of thromboxanes B that is (5
Z
,13
E
)-thromboxa-5,13-dien-1-oic acid substituted by hydroxy groups at positions 9, 11 and 15.
Stars
This entity has been manually annotated by the ChEBI Team.
Secondary ChEBI IDs
CHEBI:9576, CHEBI:26994
Supplier Information
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Formula
C20H34O6
Net Charge
0
Average Mass
370.48036
Monoisotopic Mass
370.23554
InChI
InChI=1S/C20H34O6/c1-
2-
3-
6-
9-
15(21)
12-
13-
18-
16(17(22)
14-
20(25)
26-
18)
10-
7-
4-
5-
8-
11-
19(23)
24/h4,7,12-
13,15-
18,20-
22,25H,2-
3,5-
6,8-
11,14H2,1H3,(H,23,24)
/b7-
4-
,13-
12+/t15-
,16-
,17-
,18+,20?/m0/s1
InChIKey
XNRNNGPBEPRNAR-JQBLCGNGSA-N
SMILES
CCCCC[C@H](O)\C=C\[C@H]1OC(O)C[C@H](O)[C@@H]1C\C=C/CCCC(O)=O
Metabolite of Species
Details
Mus musculus
(NCBI:txid10090)
See:
MetaboLights Study
Homo sapiens
(NCBI:txid9606)
See:
DOI
Roles Classification
Biological Role
(s):
human metabolite
Any mammalian metabolite produced during a metabolic reaction in humans (
Homo sapiens
).
mouse metabolite
Any mammalian metabolite produced during a metabolic reaction in a mouse (
Mus musculus
).
View more via ChEBI Ontology
ChEBI Ontology
Outgoing
thromboxane B
2
(
CHEBI:28728
)
has role
human metabolite (
CHEBI:77746
)
thromboxane B
2
(
CHEBI:28728
)
has role
mouse metabolite (
CHEBI:75771
)
thromboxane B
2
(
CHEBI:28728
)
is a
thromboxanes B (
CHEBI:26996
)
thromboxane B
2
(
CHEBI:28728
)
is conjugate acid of
thromboxane B
2
(1−) (
CHEBI:90696
)
Incoming
11-dehydro-thromboxane B
2
(
CHEBI:28667
)
has functional parent
thromboxane B
2
(
CHEBI:28728
)
thromboxane B
2
(1−) (
CHEBI:90696
)
is conjugate base of
thromboxane B
2
(
CHEBI:28728
)
IUPAC Name
(5
Z
,13
E
,15
S
)-9α,11,15-trihydroxythromboxa-5,13-dien-1-oic acid
Synonyms
Sources
Thromboxane B2
KEGG COMPOUND
TXB2
KEGG COMPOUND
TXB2
LIPID MAPS
TXB
2
ChEBI
Manual Xrefs
Databases
C05963
KEGG COMPOUND
HMDB0003252
HMDB
LMFA03030002
LIPID MAPS
Thromboxane_B2
Wikipedia
View more database links
Registry Numbers
Types
Sources
1399489
Reaxys Registry Number
Reaxys
54397-85-2
CAS Registry Number
ChemIDplus
Citations
Types
Sources
24433337
PubMed citation
Europe PMC
24786190
PubMed citation
Europe PMC
7847191
PubMed citation
Europe PMC
Last Modified
18 January 2016