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ChEBI
> Main
CHEBI:9008 - salicyluric acid
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ChEBI Ontology
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ChEBI Name
salicyluric acid
ChEBI ID
CHEBI:9008
Definition
An
N
-acylglycine in which the acyl group is specified as 2-hydroxybenzoyl.
Stars
This entity has been manually annotated by the ChEBI Team.
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Read full article at Wikipedia
Formula
C9H9NO4
Net Charge
0
Average Mass
195.17210
Monoisotopic Mass
195.05316
InChI
InChI=1S/C9H9NO4/c11-7-4-2-1-3-6(7)9(14)10-5-8(12)13/h1-4,11H,5H2,(H,10,14)(H,12,13)
InChIKey
ONJSZLXSECQROL-UHFFFAOYSA-N
SMILES
OC(=O)CNC(=O)c1ccccc1O
Roles Classification
Chemical Role
(s):
Bronsted acid
A molecular entity capable of donating a hydron to an acceptor (Br
o
nsted base).
(via
oxoacid
)
Biological Role
(s):
uremic toxin
A toxin that accumulates in patients with chronic kidney disease.
human xenobiotic metabolite
Any human metabolite produced by metabolism of a xenobiotic compound in humans.
View more via ChEBI Ontology
ChEBI Ontology
Outgoing
salicyluric acid (
CHEBI:9008
)
has functional parent
glycine (
CHEBI:15428
)
salicyluric acid (
CHEBI:9008
)
has role
human xenobiotic metabolite (
CHEBI:76967
)
salicyluric acid (
CHEBI:9008
)
has role
uremic toxin (
CHEBI:64584
)
salicyluric acid (
CHEBI:9008
)
is a
N
-acylglycine (
CHEBI:16180
)
salicyluric acid (
CHEBI:9008
)
is a
secondary carboxamide (
CHEBI:140325
)
salicyluric acid (
CHEBI:9008
)
is conjugate acid of
salicylurate (
CHEBI:132923
)
Incoming
5-aminosalicyluric acid (
CHEBI:68589
)
has functional parent
salicyluric acid (
CHEBI:9008
)
salicyluric β-
D
-glucuronide (
CHEBI:133026
)
has functional parent
salicyluric acid (
CHEBI:9008
)
salicylurate (
CHEBI:132923
)
is conjugate base of
salicyluric acid (
CHEBI:9008
)
IUPAC Names
(2-hydroxybenzamido)acetic acid
N
-(2-hydroxybenzoyl)glycine
Synonyms
Sources
N-(2-Hydroxybenzoyl)-glycine
KEGG COMPOUND
N-Salicyloylglycine
ChemIDplus
o-Hydroxyhippuric acid
ChemIDplus
Salicyloylglycine
ChemIDplus
Salicylurate
KEGG COMPOUND
Salicyluric acid
KEGG COMPOUND
Manual Xrefs
Databases
C07588
KEGG COMPOUND
HMDB0000840
HMDB
Salicyluric_acid
Wikipedia
View more database links
Registry Numbers
Types
Sources
2213833
Reaxys Registry Number
Reaxys
487-54-7
CAS Registry Number
KEGG COMPOUND
487-54-7
CAS Registry Number
ChemIDplus
Citations
Types
Sources
1686904
PubMed citation
Europe PMC
2079643
PubMed citation
Europe PMC
22770225
PubMed citation
Europe PMC
2605706
PubMed citation
Europe PMC
2630630
PubMed citation
Europe PMC
3216284
PubMed citation
Europe PMC
3385604
PubMed citation
Europe PMC
3805574
PubMed citation
Europe PMC
6101164
PubMed citation
Europe PMC
7074905
PubMed citation
Europe PMC
947617
PubMed citation
Europe PMC
Last Modified
12 March 2018