N-(alpha-L-aspartyl)-2-naphthylamine (CHEBI:90425)

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ChEBI Name	N-(α-L-aspartyl)-2-naphthylamine

ChEBI ID	CHEBI:90425

ChEBI ASCII Name	N-(alpha-L-aspartyl)-2-naphthylamine

Definition	An L-aspartic acid derivative that is the amide obtained by formal condensation of the α-carboxy group of L-aspartic acid with the amino group of 2-naphthylamine.

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

Supplier Information

Download	Molfile XML SDF

Formula

C14H14N2O3

Net Charge

Average Mass

258.273

Monoisotopic Mass

258.10044

InChI

InChI=1S/C14H14N2O3/c15-12(8-13(17)18)14(19)16-11-6-5-9-3-1-2-4-10(9)7-11/h1-7,12H,8,15H2,(H,16,19)(H,17,18)/t12-/m0/s1

InChIKey

YRMVHTZHFWHHIU-LBPRGKRZSA-N

SMILES

C(=O)([C@@H](N)CC(O)=O)NC=1C=CC2=C(C1)C=CC=C2

Roles Classification
Application(s):	chromogenic compound Colourless, endogenous or exogenous pigment precursors that may be transformed by biological mechanisms into coloured compounds. They are used in biochemical assays and in diagnosis as indicators, particularly in the form of enzyme substrates.

ChEBI Ontology
Outgoing	N-(α-L-aspartyl)-2-naphthylamine (CHEBI:90425) has role chromogenic compound (CHEBI:75050) N-(α-L-aspartyl)-2-naphthylamine (CHEBI:90425) is a N-(2-naphthyl)carboxamide (CHEBI:88330) N-(α-L-aspartyl)-2-naphthylamine (CHEBI:90425) is a L-aspartic acid derivative (CHEBI:83978) N-(α-L-aspartyl)-2-naphthylamine (CHEBI:90425) is a amino acid amide (CHEBI:22475) N-(α-L-aspartyl)-2-naphthylamine (CHEBI:90425) is conjugate acid of N-(α-L-aspartyl)-2-naphthylamine(1−) (CHEBI:90424)

Incoming	N-(α-L-aspartyl)-2-naphthylamine(1−) (CHEBI:90424) is conjugate base of N-(α-L-aspartyl)-2-naphthylamine (CHEBI:90425)

IUPAC Name

N-naphthalen-2-yl-L-α-asparagine

Synonyms	Sources
(S)-3-Amino-4-(2-naphthylamino)-4-oxobutyric acid	ChemIDplus
Aspartic acid beta-naphthylamide	ChemIDplus
L-aspartic acid 1-(2-naphthylamide)	ChEBI
L-aspartic acid 2-naphthylamide	ChEBI
L-aspartic acid α-(2-naphthylamide)	ChEBI
L-aspartic acid β-naphthylamide	ChEBI

Last Modified

18 November 2015