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5-bromouracil (CHEBI:20552)

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ChEBI Name 5-bromouracil
ChEBI ID CHEBI:20552
Definition A pyrimidine having keto groups at the 2- and 4-positions and a bromo group at the 5-position.
Stars This entity has been manually annotated by the ChEBI Team.
Supplier Information
See structure as:  Image  Applet
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Formula Source
C4H3BrN2O2 ChEBI
Net Charge 0
Average Mass 190.98300
InChI
InChI=1S/C4H3BrN2O2/c5-2-1-6-4(9)7-3(2)8/h1H,(H2,6,7,8,9)
InChIKey
LQLQRFGHAALLLE-UHFFFAOYSA-N
SMILES
Brc1c[nH]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 on the ChEBI Ontology
ChEBI Ontology
Outgoing 5-bromouracil (CHEBI:20552) has functional parent uracil (CHEBI:17568)
5-bromouracil (CHEBI:20552) has role mutagen (CHEBI:25435)
5-bromouracil (CHEBI:20552) is a nucleobase analogue (CHEBI:67142)
5-bromouracil (CHEBI:20552) is a pyrimidines (CHEBI:39447)
IUPAC Name
5-bromopyrimidine-2,4(1H,3H)-dione
Synonyms Sources
1,2,3,4-tetrahydro-5-bromo-2,4-pyrimidinedione NIST Chemistry WebBook
5-bromo-2,4(1H,3H)-pyrimidinedione NIST Chemistry WebBook
bromouracil ChemIDplus
Registry Numbers Types Sources
127176 Beilstein Registry Number Beilstein
486432 Gmelin Registry Number Gmelin
51-20-7 CAS Registry Number ChemIDplus
51-20-7 CAS Registry Number NIST Chemistry WebBook
Citation Waiting for Citations Type Source
3950402 PubMed citation CiteXplore
Last Modified
15 August 2012

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