CHEBI:20553 - 5-bromouridine

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ChEBI Name 5-bromouridine
ChEBI ID CHEBI:20553
Definition A uridine having a bromo substituent at the 5-position.
Stars This entity has been manually annotated by the ChEBI Team.
Supplier Information ChemicalBook:CB9388222, eMolecules:492637, eMolecules:26753504, ZINC000006072466
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Formula C9H11BrN2O6
Net Charge 0
Average Mass 323.09752
Monoisotopic Mass 321.98005
InChI InChI=1S/C9H11BrN2O6/c10-3-1-12(9(17)11-7(3)16)8-6(15)5(14)4(2-13)18-8/h1,4-6,8,13-15H,2H2,(H,11,16,17)/t4-,5-,6-,8-/m1/s1
InChIKey AGFIRQJZCNVMCW-UAKXSSHOSA-N
SMILES OC[C@H]1O[C@H]([C@H](O)[C@@H]1O)n1cc(Br)c(=O)[nH]c1=O
Roles Classification
Biological Role(s): mutagen
An agent that increases the frequency of mutations above the normal background level, usually by interacting directly with DNA and causing it damage, including base substitution.
View more via ChEBI Ontology
ChEBI Ontology
Outgoing 5-bromouridine (CHEBI:20553) has role mutagen (CHEBI:25435)
5-bromouridine (CHEBI:20553) is a uridines (CHEBI:27242)
IUPAC Name
5-bromouridine
Synonyms Sources
1-β-ribofuranosyl-5-bromo-uracil ChemIDplus
5-bromo-1-β-D-ribofuranosylpyrimidine-2,4(1H,3H)-dione ChEBI
5-bromouridine ChEBI
5-bromouridine UniProt
BrU ChEBI
Registry Numbers Types Sources
33664 Beilstein Registry Number Beilstein
723432 Gmelin Registry Number Gmelin
957-75-5 CAS Registry Number ChemIDplus
Citation Type Source
3950402 PubMed citation Europe PMC
Last Modified
03 April 2020