CHEBI:46823 - 1H-purine-2,6,8-triol

Main ChEBI Ontology Automatic Xrefs Reactions Pathways Models
ChEBI Name 1H-purine-2,6,8-triol
ChEBI ASCII Name 1H-purine-2,6,8-triol
Stars This entity has been manually annotated by the ChEBI Team.
Supplier Information
Download Molfile XML SDF
more structures >>
Formula C5H4N4O3
Net Charge 0
Average Mass 168.11042
Monoisotopic Mass 168.02834
InChI InChI=1S/C5H4N4O3/c10-3-1-2(7-4(11)6-1)8-5(12)9-3/h(H4,6,7,8,9,10,11,12)
SMILES Oc1nc2nc(O)[nH]c(O)c2n1
Roles Classification
Biological Role(s): human metabolite
Any mammalian metabolite produced during a metabolic reaction in humans (Homo sapiens).
(via uric acid )
View more via ChEBI Ontology
ChEBI Ontology
Outgoing 1H-purine-2,6,8-triol (CHEBI:46823) is a uric acid (CHEBI:27226)
1H-purine-2,6,8-triol (CHEBI:46823) is conjugate acid of 2,8-dihydroxy-1H-purin-6-olate (CHEBI:46822)
1H-purine-2,6,8-triol (CHEBI:46823) is tautomer of 2,6-dihydroxy-7,9-dihydro-8H-purin-8-one (CHEBI:46811)
1H-purine-2,6,8-triol (CHEBI:46823) is tautomer of 5,7-dihydro-1H-purine-2,6,8(9H)-trione (CHEBI:49051)
1H-purine-2,6,8-triol (CHEBI:46823) is tautomer of 7,9-dihydro-1H-purine-2,6,8(3H)-trione (CHEBI:17775)
1H-purine-2,6,8-triol (CHEBI:46823) is tautomer of 7H-purine-2,6,8-triol (CHEBI:46817)
1H-purine-2,6,8-triol (CHEBI:46823) is tautomer of 9H-purine-2,6,8-triol (CHEBI:46814)
Incoming 2,8-dihydroxy-1H-purin-6-olate (CHEBI:46822) is conjugate base of 1H-purine-2,6,8-triol (CHEBI:46823)
2,6-dihydroxy-7,9-dihydro-8H-purin-8-one (CHEBI:46811) is tautomer of 1H-purine-2,6,8-triol (CHEBI:46823)
5,7-dihydro-1H-purine-2,6,8(9H)-trione (CHEBI:49051) is tautomer of 1H-purine-2,6,8-triol (CHEBI:46823)
7,9-dihydro-1H-purine-2,6,8(3H)-trione (CHEBI:17775) is tautomer of 1H-purine-2,6,8-triol (CHEBI:46823)
7H-purine-2,6,8-triol (CHEBI:46817) is tautomer of 1H-purine-2,6,8-triol (CHEBI:46823)
9H-purine-2,6,8-triol (CHEBI:46814) is tautomer of 1H-purine-2,6,8-triol (CHEBI:46823)
Registry Number Type Source
8620579 Beilstein Registry Number Beilstein
Last Modified
21 April 2008