CHEBI:17013 - dTMP

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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 ChemicalBook:CB2185552, ZINC000008215481
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Wikipedia License
Guanosine diphosphate, abbreviated GDP, is a nucleoside diphosphate. It is an ester of pyrophosphoric acid with the nucleoside guanosine. GDP consists of a pyrophosphate group, a pentose sugar ribose, and the nucleobase guanine. GDP is the product of GTP dephosphorylation by GTPases, e.g., the G-proteins that are involved in signal transduction. GDP is converted into GTP with the help of pyruvate kinase and phosphoenolpyruvate.
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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.
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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