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> Main
CHEBI:17013 - dTMP
Main
ChEBI Ontology
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ChEBI Name
dTMP
ChEBI ID
CHEBI:17013
Definition
The neutral species of thymidine 5'-monophosphate (2'-deoxythymidine 5'-monophosphate).
Stars
This entity has been manually annotated by the ChEBI Team.
Secondary ChEBI IDs
CHEBI:45926, CHEBI:46036, CHEBI:46013, CHEBI:47711, CHEBI:45759, CHEBI:45762, CHEBI:45772, CHEBI:10529, CHEBI:14092, CHEBI:15246, CHEBI:63549
Supplier Information
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Molfile
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Molfile
Wikipedia
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Read full article at Wikipedia
Formula
C10H15N2O8P
Net Charge
0
Average Mass
322.20850
Monoisotopic Mass
322.05660
InChI
InChI=1S/C10H15N2O8P/c1-
5-
3-
12(10(15)
11-
9(5)
14)
8-
2-
6(13)
7(20-
8)
4-
19-
21(16,17)
18/h3,6-
8,13H,2,4H2,1H3,(H,11,14,15)
(H2,16,17,18)
/t6-
,7+,8+/m0/s1
InChIKey
GYOZYWVXFNDGLU-XLPZGREQSA-N
SMILES
Cc1cn([C@H]2C[C@H](O)[C@@H](COP(O)(O)=O)O2)c(=O)[nH]c1=O
Metabolite of Species
Details
Mus musculus
(NCBI:txid10090)
Source: BioModels - MODEL1507180067 See:
PubMed
Saccharomyces cerevisiae
(NCBI:txid4932)
Source: yeast.sf.net See:
PubMed
Escherichia coli
(NCBI:txid562)
See:
PubMed
Roles Classification
Biological Role
(s):
fundamental metabolite
Any metabolite produced by all living cells.
View more via ChEBI Ontology
ChEBI Ontology
Outgoing
dTMP (
CHEBI:17013
)
has role
fundamental metabolite (
CHEBI:78675
)
dTMP (
CHEBI:17013
)
is a
thymidine 5'-monophosphate (
CHEBI:15245
)
dTMP (
CHEBI:17013
)
is conjugate acid of
dTMP
−
(
CHEBI:46960
)
dTMP (
CHEBI:17013
)
is enantiomer of
1-(2-deoxy-5-
O
-phosphono-β-
L
-ribofuranosyl)thymine (
CHEBI:42112
)
Incoming
5,6-dihydrothymidine 5'-monophosphate (
CHEBI:132172
)
has functional parent
dTMP (
CHEBI:17013
)
p
-nitrophenyl thymidine 5'-monophosphate (
CHEBI:74144
)
has functional parent
dTMP (
CHEBI:17013
)
dTMP
−
(
CHEBI:46960
)
is conjugate base of
dTMP (
CHEBI:17013
)
1-(2-deoxy-5-
O
-phosphono-β-
L
-ribofuranosyl)thymine (
CHEBI:42112
)
is enantiomer of
dTMP (
CHEBI:17013
)
dTMP 3'-end residue (
CHEBI:53118
)
is substituent group from
dTMP (
CHEBI:17013
)
dTMP 5'-end residue (
CHEBI:53102
)
is substituent group from
dTMP (
CHEBI:17013
)
thymidine 5'-monophosphate residue (
CHEBI:50300
)
is substituent group from
dTMP (
CHEBI:17013
)
IUPAC Names
2'-deoxy-5-methyluridine 5'-(dihydrogen phosphate)
5'-thymidylic acid
Synonyms
Sources
(dT)
1
ChEBI
5'-Thymidylic acid
KEGG COMPOUND
5'-TMP
ChemIDplus
5-methyl-dUMP
ChemIDplus
deoxyribosylthymine monophosphate
ChemIDplus
ribothymidine 5'-monophosphate
ChEBI
thymidine 5'-(dihydrogen phosphate)
CBN
Thymidine 5'-phosphate
KEGG COMPOUND
thymidine 5'-phosphoric acid
ChemIDplus
Thymidine monophosphate
KEGG COMPOUND
thymidine-5'-monophosphoric acid
ChemIDplus
THYMIDINE-5'-PHOSPHATE
PDBeChem
Thymidylate
KEGG COMPOUND
Thymidylic acid
KEGG COMPOUND
TMP
ChEBI
Manual Xrefs
Databases
C00019637
KNApSAcK
C00364
KEGG COMPOUND
DB01643
DrugBank
HMDB0001227
HMDB
TdF10
PDBeChem
Thymidine_monophosphate
Wikipedia
TMPdF10
PDBeChem
View more database links
Registry Numbers
Types
Sources
365-07-1
CAS Registry Number
KEGG COMPOUND
365-07-1
CAS Registry Number
ChemIDplus
47541
Reaxys Registry Number
Reaxys
47541
Beilstein Registry Number
Beilstein
Citations
Types
Sources
22512654
PubMed citation
Europe PMC
22761426
PubMed citation
Europe PMC
23149755
PubMed citation
Europe PMC
23288848
PubMed citation
Europe PMC
23362972
PubMed citation
Europe PMC
23501933
PubMed citation
Europe PMC
23518161
PubMed citation
Europe PMC
2559771
PubMed citation
Europe PMC
7110140
PubMed citation
Europe PMC
8647821
PubMed citation
Europe PMC
Last Modified
14 June 2016