N-methylhippuric acid (CHEBI:141362)

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ChEBI Name	N-methylhippuric acid

ChEBI ID	CHEBI:141362

ChEBI ASCII Name	N-methylhippuric acid

Definition	An N-acylglycine that is N-methylglycine in which the hydrogen of the amino group is substituted by a benzoyl group.

Stars	This entity has been manually annotated by the ChEBI Team.

Submitter	Mark Williams

Supplier Information

Download	Molfile XML SDF

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Formula

C10H11NO3

Net Charge

Average Mass

193.202

Monoisotopic Mass

193.07389

InChI

InChI=1S/C10H11NO3/c1-11(7-9(12)13)10(14)8-5-3-2-4-6-8/h2-6H,7H2,1H3,(H,12,13)

InChIKey

PKCSYDDSNIJRIX-UHFFFAOYSA-N

SMILES

CN(CC(O)=O)C(=O)C1=CC=CC=C1

Roles Classification
Chemical Role(s):	Bronsted acid A molecular entity capable of donating a hydron to an acceptor (Bronsted base). (via oxoacid )

Biological Role(s):	EC 1.1.1.21 (aldehyde reductase) inhibitor An EC 1.1.1.* (oxidoreductase acting on donor CH-OH group, NAD+ or NADP+ acceptor) inhibitor that interferes with the action of aldehyde reductase (EC 1.1.1.21).

ChEBI Ontology
Outgoing	N-methylhippuric acid (CHEBI:141362) has role EC 1.1.1.21 (aldehyde reductase) inhibitor (CHEBI:48550) N-methylhippuric acid (CHEBI:141362) is a N-acylglycine (CHEBI:16180) N-methylhippuric acid (CHEBI:141362) is a monocarboxylic acid (CHEBI:25384)

IUPAC Name

N-benzoyl-N-methylglycine

Synonyms	Sources
(N-methyl-1-phenylformamido)acetic acid	ChEBI
2-(N-methyl-1-phenylformamido)acetic acid	ChEBI
[benzoyl(methyl)amino]acetic acid	ChEBI
[N-benzoyl-N-methylamino]acetic acid	ChEBI
N-benzoyl-N-methylglycine	ChemIDplus
N-benzoylsarcosine	ChemIDplus

Registry Number	Type	Source
2568-34-5	CAS Registry Number	ChemIDplus

Last Modified

06 August 2020