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> Main
CHEBI:45996 - ribothymidine
Main
ChEBI Ontology
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ChEBI Name
ribothymidine
ChEBI ID
CHEBI:45996
Definition
A methyluridine having a single methyl substituent at the 5-position on the uracil ring.
Stars
This entity has been manually annotated by the ChEBI Team.
Secondary ChEBI IDs
CHEBI:45995, CHEBI:45975, CHEBI:30821
Supplier Information
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Formulae
C10H14N2O6
C10H14N2O6
Net Charge
0
Average Mass
258.22804
Monoisotopic Mass
258.08519
InChI
InChI=1S/C10H14N2O6/c1-
4-
2-
12(10(17)
11-
8(4)
16)
9-
7(15)
6(14)
5(3-
13)
18-
9/h2,5-
7,9,13-
15H,3H2,1H3,(H,11,16,17)
/t5-
,6-
,7-
,9-
/m1/s1
InChIKey
DWRXFEITVBNRMK-JXOAFFINSA-N
SMILES
Cc1cn([C@@H]2O[C@H](CO)[C@@H](O)[C@H]2O)c(=O)[nH]c1=O
Metabolite of Species
Details
Escherichia coli
(NCBI:txid562)
of strain K-12 See:
PubMed
Homo sapiens
(NCBI:txid9606)
See:
PubMed
Roles Classification
Biological Role
(s):
human metabolite
Any mammalian metabolite produced during a metabolic reaction in humans (
Homo sapiens
).
Escherichia coli metabolite
Any bacterial metabolite produced during a metabolic reaction in
Escherichia coli
.
antigen
Any substance that stimulates an immune response in the body, such as through antibody production or by presentation to a T-cell receptor after binding to a major histocompability complex (MHC).
View more via ChEBI Ontology
ChEBI Ontology
Outgoing
ribothymidine (
CHEBI:45996
)
has role
Escherichia coli
metabolite (
CHEBI:76971
)
ribothymidine (
CHEBI:45996
)
has role
antigen (
CHEBI:59132
)
ribothymidine (
CHEBI:45996
)
has role
human metabolite (
CHEBI:77746
)
ribothymidine (
CHEBI:45996
)
is a
methyluridine (
CHEBI:25347
)
Incoming
TDP (
CHEBI:61377
)
has functional parent
ribothymidine (
CHEBI:45996
)
TMP (
CHEBI:45394
)
has functional parent
ribothymidine (
CHEBI:45996
)
IUPAC Name
5-methyluridine
Synonyms
Sources
1-(β-
D
-ribofuranosyl)thymine
ChEBI
ribosylthymidine
ChEBI
t
ChEBI
Thymine riboside
ChemIDplus
Manual Xrefs
Databases
5-methyluridine
Wikipedia
CPD-15123
MetaCyc
ECMDB21389
ECMDB
HMDB0000884
HMDB
View more database links
Registry Numbers
Types
Sources
1463-10-1
CAS Registry Number
ChemIDplus
90164
Reaxys Registry Number
Reaxys
Citations
Types
Sources
1100617
PubMed citation
Europe PMC
22325947
PubMed citation
Europe PMC
22806868
PubMed citation
Europe PMC
6725946
PubMed citation
Europe PMC
Last Modified
23 October 2015