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InChI=1S/CH4O/c1-2/h2H,1H3
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ChEBI
> Main
CHEBI:17712 - 9
H
-xanthine
Main
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ChEBI Name
9
H
-xanthine
ChEBI ID
CHEBI:17712
ChEBI ASCII Name
9H-xanthine
Definition
An oxopurine in which the purine ring is substituted by oxo groups at positions 2 and 6 and N-9 is protonated.
Stars
This entity has been manually annotated by the ChEBI Team.
Secondary ChEBI IDs
CHEBI:46377, CHEBI:10059, CHEBI:27317
Supplier Information
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Molfile
Formula
C5H4N4O2
Net Charge
0
Average Mass
152.11102
Monoisotopic Mass
152.03343
InChI
InChI=1S/C5H4N4O2/c10-4-2-3(7-1-6-2)8-5(11)9-4/h1H,(H3,6,7,8,9,10,11)
InChIKey
LRFVTYWOQMYALW-UHFFFAOYSA-N
SMILES
O=c1[nH]c2[nH]cnc2c(=O)[nH]1
Metabolite of Species
Details
Saccharomyces cerevisiae
(NCBI:txid4932)
Source: yeast.sf.net See:
PubMed
Homo sapiens
(NCBI:txid9606)
See:
DOI
Roles Classification
Biological Role
(s):
Saccharomyces cerevisiae metabolite
Any fungal metabolite produced during a metabolic reaction in Baker's yeast (
Saccharomyces cerevisiae
).
fundamental metabolite
Any metabolite produced by all living cells.
(via
xanthine
)
View more via ChEBI Ontology
ChEBI Ontology
Outgoing
9
H
-xanthine (
CHEBI:17712
)
has role
Saccharomyces cerevisiae
metabolite (
CHEBI:75772
)
9
H
-xanthine (
CHEBI:17712
)
is a
xanthine (
CHEBI:15318
)
9
H
-xanthine (
CHEBI:17712
)
is tautomer of
7
H
-xanthine (
CHEBI:48517
)
Incoming
3-isobutyl-1-methyl-9
H
-xanthine (
CHEBI:43253
)
has functional parent
9
H
-xanthine (
CHEBI:17712
)
7
H
-xanthine (
CHEBI:48517
)
is tautomer of
9
H
-xanthine (
CHEBI:17712
)
IUPAC Name
3,9-dihydro-1
H
-purine-2,6-dione
Synonyms
Sources
2,6-dihydroxypurine
NIST Chemistry WebBook
2,6-dioxo-1,2,3,6-tetrahydropurine
ChemIDplus
9
H
-purine-2,6-(1
H
,3
H
)-dione
ChemIDplus
purine-2(3
H
),6(1
H
)-dione
ChemIDplus
Xan
CBN
Xanthine
KEGG COMPOUND
XANTHINE
PDBeChem
xanthine
UniProt
Manual Xrefs
Databases
2153
BPDB
C00385
KEGG COMPOUND
HMDB0000292
HMDB
XAN
PDBeChem
View more database links
Registry Numbers
Types
Sources
609330
Reaxys Registry Number
Reaxys
69-89-6
CAS Registry Number
KEGG COMPOUND
69-89-6
CAS Registry Number
NIST Chemistry WebBook
69-89-6
CAS Registry Number
ChemIDplus
913730
Gmelin Registry Number
Gmelin
Citation
Type
Source
22770225
PubMed citation
Europe PMC
Last Modified
19 September 2018