CHEBI:46319 - 6-azauridine 5'-monophosphate

ChEBI IDCHEBI:46319
ChEBI Name6-azauridine 5'-monophosphate
Stars
DefinitionA N-glycosyl-1,2,4-triazine that is the 6-aza analogue of uridine 5'-monophosphate.
Last Modified17 April 2020
DownloadsMolfile
FormulaC8H12N3O9P
Net Charge0
Average Mass325.170
Monoisotopic Mass325.03112
SMILESO=c1cnn([C@@H]2O[C@H](COP(=O)(O)O)[C@@H](O)[C@H]2O)c(=O)n1
InChIInChI=1S/C8H12N3O9P/c12-4-1-9-11(8(15)10-4)7-6(14)5(13)3(20-7)2-19-21(16,17)18/h1,3,5-7,13-14H,2H2,(H,10,12,15)(H2,16,17,18)/t3-,5-,6-,7-/m1/s1
InChIKeyLRVZOSYMNMNQFR-SHUUEZRQSA-N
Roles Classification
Biological Role:
EC 4.1.1.23 (orotidine-5'-phosphate decarboxylase) inhibitor  Any EC 4.1.1.* (carboxy-lyase) inhibitor that interferes with the action of orotidine-5'-phosphate decarboxylase (EC 4.1.1.23).
Application:
antineoplastic agent  A substance that inhibits or prevents the proliferation of neoplasms.
ChEBI Ontology
Outgoing Relation(s)
6-azauridine 5'-monophosphate (CHEBI:46319) has functional parent 6-azauridine (CHEBI:35668)
6-azauridine 5'-monophosphate (CHEBI:46319) has role antineoplastic agent (CHEBI:35610)
6-azauridine 5'-monophosphate (CHEBI:46319) has role EC 4.1.1.23 (orotidine-5'-phosphate decarboxylase) inhibitor (CHEBI:90285)
6-azauridine 5'-monophosphate (CHEBI:46319) is a N-glycosyl-1,2,4-triazine (CHEBI:48018)
6-azauridine 5'-monophosphate (CHEBI:46319) is a nucleoside monophosphate analogue (CHEBI:48208)
6-azauridine 5'-monophosphate (CHEBI:46319) is conjugate acid of 6-azauridine 5'-monophosphate(2−) (CHEBI:147401)
Incoming Relation(s)
6-azauridine 5'-monophosphate(2−) (CHEBI:147401) is conjugate base of 6-azauridine 5'-monophosphate (CHEBI:46319)
IUPAC Name 
2-(5-O-phosphono-β-D-ribofuranosyl)-1,2,4-triazine-3,5(2H,4H)-dione
Synonyms  Source
6-aza uridine 5'-monophosphateDrugBank
6-azauridine 5'-monophosphateChEBI
6-aza-UMPDrugBank
6-aza-uridine monophosphateDrugBank
6-azauridine-5'-monophosphateDrugBank
6-azauridine 5'-phosphoric acidChEBI
Manual XrefsDatabases
UP6PDBeChem
DB03718DrugBank
Registry NumbersSources
CAS:2018-19-1ChemIDplus
Citations