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ChEBI
> Main
CHEBI:104011 -
p
-aminohippuric acid
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ChEBI Name
p
-aminohippuric acid
ChEBI ID
CHEBI:104011
ChEBI ASCII Name
p-aminohippuric acid
Definition
An
N
-acylglycine that is the 4-amino derivative of hippuric acid; used as a diagnostic agent in the measurement of renal plasma flow.
Stars
This entity has been manually annotated by the ChEBI Team.
Submitter
Bijay
Secondary ChEBI IDs
CHEBI:59134
Supplier Information
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Formula
C9H10N2O3
Net Charge
0
Average Mass
194.18730
Monoisotopic Mass
194.06914
InChI
InChI=1S/C9H10N2O3/c10-7-3-1-6(2-4-7)9(14)11-5-8(12)13/h1-4H,5,10H2,(H,11,14)(H,12,13)
InChIKey
HSMNQINEKMPTIC-UHFFFAOYSA-N
SMILES
Nc1ccc(cc1)C(=O)NCC(O)=O
Metabolite of Species
Details
Daphnia magna
(NCBI:txid35525)
See: Mixtures of similarly acting compounds in Daphnia magna: From gene to metabolite and beyondTine Vandenbrouck, Oliver A.H. Jones, Nathalie Dom, Julian L. Griffin, Wim De CoenEnvironment International 36 (2010) 254-268
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):
Daphnia magna metabolite
A
Daphnia
metabolite produced by the species
Daphnia magna
.
View more via ChEBI Ontology
ChEBI Ontology
Outgoing
p
-aminohippuric acid (
CHEBI:104011
)
has role
Daphnia magna
metabolite (
CHEBI:83056
)
p
-aminohippuric acid (
CHEBI:104011
)
is a
N
-acylglycine (
CHEBI:16180
)
p
-aminohippuric acid (
CHEBI:104011
)
is conjugate acid of
p
-aminohippurate (
CHEBI:64703
)
Incoming
p
-aminohippurate (
CHEBI:64703
)
is conjugate base of
p
-aminohippuric acid (
CHEBI:104011
)
IUPAC Name
N
-(4-aminobenzoyl)glycine
Synonyms
Sources
4-aminohippuric acid
SUBMITTER
Aminohippuric acid
KEGG DRUG
N-(p-Aminobenzoyl)aminoacetic acid
ChemIDplus
N-(p-Aminobenzoyl)glycine
ChemIDplus
N-(para-aminobenzoyl)glycine
ChemIDplus
p-aminohippurate
SUBMITTER
PAH
SUBMITTER
Paha
HMDB
para-Aminohippuric acid
ChemIDplus
paraaminohippuric acid
HMDB
Manual Xrefs
Databases
165
DrugCentral
Aminohippuric_Acid
Wikipedia
D06890
KEGG DRUG
DB00345
DrugBank
HMDB0001867
HMDB
LSM-5739
LINCS
View more database links
Registry Numbers
Types
Sources
1213676
Reaxys Registry Number
Reaxys
1216376
Beilstein Registry Number
Beilstein
61-78-9
CAS Registry Number
ChemIDplus
61-78-9
CAS Registry Number
KEGG DRUG
848144
Gmelin Registry Number
Gmelin
Citations
Types
Sources
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ChEMBL
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Europe PMC
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Europe PMC
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PubMed citation
Europe PMC
843496
PubMed citation
Europe PMC
933268
PubMed citation
Europe PMC
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PubMed citation
Europe PMC
Last Modified
22 February 2017