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

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ChEBI Name 4-amino-5-hydroxymethyl-2-methylpyrimidine
Definition An aminopyrimidine that is pyrimidine in which the hydrogens at positions 2, 4, and 5 are replaced by methyl, amino, and hydroxymethyl substituents, respectively.
Stars This entity has been manually annotated by the ChEBI Team.
Secondary ChEBI IDs CHEBI:1781, CHEBI:43206, CHEBI:11957, CHEBI:20312
Supplier Information
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Formula C6H9N3O
Net Charge 0
Average Mass 139.15520
Monoisotopic Mass 139.07456
InChI InChI=1S/C6H9N3O/c1-4-8-2-5(3-10)6(7)9-4/h2,10H,3H2,1H3,(H2,7,8,9)
SMILES Cc1ncc(CO)c(N)n1
Metabolite of Species Details
Saccharomyces cerevisiae (NCBI:txid4932) Source: See: PubMed
Escherichia coli (NCBI:txid562) See: PubMed
Roles Classification
Chemical Role(s): Bronsted base
A molecular entity capable of accepting a hydron from a donor (Bronsted acid).
(via organic amino compound )
Biological Role(s): 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 ).
View more via ChEBI Ontology
ChEBI Ontology
Outgoing 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)
Synonyms Sources
2-methyl-4-amino-5-hydroxymethylpyrimidine ChemIDplus
4-amino-2-methyl-5-hydroxymethylpyrimidine ChEBI
4-amino-2-methyl-5-pyrimidinemethanol ChEBI
4-Amino-2-methyl-5-pyrimidinemethanol KEGG COMPOUND
4-Amino-5-hydroxymethyl-2-methylpyrimidine KEGG COMPOUND
4-amino-5-hydroxymethyl-2-methylpyrimidine UniProt
Atoxopyrimidine ChemIDplus
Pyramin ChemIDplus
Pyramine ChemIDplus
Toxopyrimidine KEGG COMPOUND
Manual Xrefs Databases
C00007494 KNApSAcK
DB02022 DrugBank
HMP MetaCyc
View more database links
Registry Numbers Types Sources
126858 Reaxys Registry Number Reaxys
73-67-6 CAS Registry Number KEGG COMPOUND
73-67-6 CAS Registry Number ChemIDplus
Citation Waiting for Citations Type Source
16497163 PubMed citation Europe PMC
Last Modified
25 January 2016