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> Main
CHEBI:17025 - (
S
)-dihydroorotic acid
Main
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ChEBI Name
(
S
)-dihydroorotic acid
ChEBI ID
CHEBI:17025
ChEBI ASCII Name
(S)-dihydroorotic acid
Definition
The (
S
)-enantiomer of dihydroorotic acid that is an intermediate in the metabolism of pyridine.
Stars
This entity has been manually annotated by the ChEBI Team.
Secondary ChEBI IDs
CHEBI:42132, CHEBI:417, CHEBI:18778
Supplier Information
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Formula
C5H6N2O4
Net Charge
0
Average Mass
158.11222
Monoisotopic Mass
158.03276
InChI
InChI=1S/C5H6N2O4/c8-3-1-2(4(9)10)6-5(11)7-3/h2H,1H2,(H,9,10)(H2,6,7,8,11)/t2-/m0/s1
InChIKey
UFIVEPVSAGBUSI-REOHCLBHSA-N
SMILES
OC(=O)[C@@H]1CC(=O)NC(=O)N1
Metabolite of Species
Details
Mus musculus
(NCBI:txid10090)
Source: BioModels - MODEL1507180067 See:
PubMed
Escherichia coli
(NCBI:txid562)
See:
PubMed
Roles Classification
Chemical Role
(s):
Bronsted acid
A molecular entity capable of donating a hydron to an acceptor (Br
o
nsted base).
(via
oxoacid
)
Biological Role
(s):
Escherichia coli metabolite
Any bacterial metabolite produced during a metabolic reaction in
Escherichia coli
.
mouse metabolite
Any mammalian metabolite produced during a metabolic reaction in a mouse (
Mus musculus
).
Saccharomyces cerevisiae metabolite
Any fungal metabolite produced during a metabolic reaction in Baker's yeast (
Saccharomyces cerevisiae
).
human metabolite
Any mammalian metabolite produced during a metabolic reaction in humans (
Homo sapiens
).
View more via ChEBI Ontology
ChEBI Ontology
Outgoing
(
S
)-dihydroorotic acid (
CHEBI:17025
)
has role
Escherichia coli
metabolite (
CHEBI:76971
)
(
S
)-dihydroorotic acid (
CHEBI:17025
)
has role
Saccharomyces cerevisiae
metabolite (
CHEBI:75772
)
(
S
)-dihydroorotic acid (
CHEBI:17025
)
has role
human metabolite (
CHEBI:77746
)
(
S
)-dihydroorotic acid (
CHEBI:17025
)
has role
mouse metabolite (
CHEBI:75771
)
(
S
)-dihydroorotic acid (
CHEBI:17025
)
is a
dihydroorotic acid (
CHEBI:30865
)
(
S
)-dihydroorotic acid (
CHEBI:17025
)
is conjugate acid of
(
S
)-dihydroorotate (
CHEBI:30864
)
(
S
)-dihydroorotic acid (
CHEBI:17025
)
is enantiomer of
(
R
)-dihydroorotic acid (
CHEBI:30866
)
Incoming
(
S
)-dihydroorotate (
CHEBI:30864
)
is conjugate base of
(
S
)-dihydroorotic acid (
CHEBI:17025
)
(
R
)-dihydroorotic acid (
CHEBI:30866
)
is enantiomer of
(
S
)-dihydroorotic acid (
CHEBI:17025
)
IUPAC Name
(4
S
)-2,6-dioxohexahydropyrimidine-4-carboxylic acid
Synonyms
Sources
(S)-4,5-dihydroorotic acid
ChEBI
Dihydro-L-orotic acid
KEGG COMPOUND
L-Dihydroorotic acid
KEGG COMPOUND
Manual Xrefs
Databases
C00007302
KNApSAcK
C00337
KEGG COMPOUND
DI-H-OROTATE
MetaCyc
DOR
PDBeChem
EP0933633
Patent
EP1036319
Patent
HK1033171
Patent
HMDB0003349
HMDB
RU2228932
Patent
WO9930146
Patent
View more database links
Registry Numbers
Types
Sources
1473795
Gmelin Registry Number
Gmelin
5988-19-2
CAS Registry Number
KEGG COMPOUND
83957
Reaxys Registry Number
Reaxys
Citation
Type
Source
3089167
PubMed citation
Europe PMC
Last Modified
27 January 2016