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CHEBI:16892 - 4-amino-5-hydroxymethyl-2-methylpyrimidine

ChEBI IDCHEBI:16892
ChEBI Name4-amino-5-hydroxymethyl-2-methylpyrimidine
Stars
DefinitionAn aminopyrimidine that is pyrimidine in which the hydrogens at positions 2, 4, and 5 are replaced by methyl, amino, and hydroxymethyl substituents, respectively.
Secondary ChEBI IDsCHEBI:1781, CHEBI:11957, CHEBI:20312, CHEBI:43206
Last Modified25 January 2016
DownloadsMolfile
FormulaC6H9N3O
Net Charge0
Average Mass139.158
Monoisotopic Mass139.07456
SMILESCc1ncc(CO)c(N)n1
InChIInChI=1S/C6H9N3O/c1-4-8-2-5(3-10)6(7)9-4/h2,10H,3H2,1H3,(H2,7,8,9)
InChIKeyVUTBELPREDJDDH-UHFFFAOYSA-N
Species of MetaboliteComponentSourceComments
Escherichia coli (ncbitaxon:562) - PubMed (21988831)
Saccharomyces cerevisiae (ncbitaxon:4932) - PubMed (24678285) Source: yeast.sf.net
Roles Classification
Chemical Role:
Bronsted base  A molecular entity capable of accepting a hydron from a donor (Brønsted acid).
Biological Roles:
Escherichia coli metabolite  Any bacterial metabolite produced during a metabolic reaction in Escherichia coli.
Saccharomyces cerevisiae metabolite  Any fungal metabolite produced during a metabolic reaction in Baker's yeast (Saccharomyces cerevisiae ).
ChEBI Ontology
Outgoing Relation(s)
4-amino-5-hydroxymethyl-2-methylpyrimidine (CHEBI:16892) has role Escherichia coli metabolite (CHEBI:76971)
4-amino-5-hydroxymethyl-2-methylpyrimidine (CHEBI:16892) has role Saccharomyces cerevisiae metabolite (CHEBI:75772)
4-amino-5-hydroxymethyl-2-methylpyrimidine (CHEBI:16892) is a aminopyrimidine (CHEBI:38338)
4-amino-5-hydroxymethyl-2-methylpyrimidine (CHEBI:16892) is a aromatic primary alcohol (CHEBI:33857)
IUPAC Name 
(4-amino-2-methylpyrimidin-5-yl)methanol
Synonyms  Source
2-methyl-4-amino-5-hydroxymethylpyrimidineChemIDplus
4-amino-2-methyl-5-hydroxymethylpyrimidineChEBI
4-amino-2-methyl-5-pyrimidinemethanolChEBI
4-Amino-2-methyl-5-pyrimidinemethanolKEGG COMPOUND
4-Amino-5-hydroxymethyl-2-methylpyrimidineKEGG COMPOUND
AtoxopyrimidineChemIDplus
UniProt Name  Source
4-amino-5-hydroxymethyl-2-methylpyrimidineUniProt
Manual XrefsDatabases
C00007494KNApSAcK
C01279KEGG COMPOUND
DB02022DrugBank
HMHPDBeChem
HMPMetaCyc
Registry NumbersSources
Reaxys:126858Reaxys
CAS:73-67-6KEGG COMPOUND
CAS:73-67-6ChemIDplus
Citations