CHEBI:91058 - N-benzoyl-L-phenylalanine 2-naphthylamide

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ChEBI Name N-benzoyl-L-phenylalanine 2-naphthylamide
ChEBI ID CHEBI:91058
ChEBI ASCII Name N-benzoyl-L-phenylalanine 2-naphthylamide
Definition An N-{1-[(naphthalen-2-yl)amino]-1-oxo-3-phenylpropan-2-yl}benzamide that is the amide obtained by formal condensation of the carboxy group of N-benzoyl-L-phenylalanine with the amino group of 2-aminonaphthalene.
Stars This entity has been manually annotated by the ChEBI Team.
Supplier Information
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Formula C26H22N2O2
Net Charge 0
Average Mass 394.466
Monoisotopic Mass 394.16813
InChI InChI=1S/C26H22N2O2/c29-25(21-12-5-2-6-13-21)28-24(17-19-9-3-1-4-10-19)26(30)27-23-16-15-20-11-7-8-14-22(20)18-23/h1-16,18,24H,17H2,(H,27,30)(H,28,29)/t24-/m0/s1
InChIKey UYXGHMPRWWMUID-DEOSSOPVSA-N
SMILES C=1(C[C@@H](C(NC=2C=CC3=C(C2)C=CC=C3)=O)NC(=O)C=4C=CC=CC4)C=CC=CC1
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.
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ChEBI Ontology
Outgoing N-benzoyl-L-phenylalanine 2-naphthylamide (CHEBI:91058) has role chromogenic compound (CHEBI:75050)
N-benzoyl-L-phenylalanine 2-naphthylamide (CHEBI:91058) is a N-{1-[(naphthalen-2-yl)amino]-1-oxo-3-phenylpropan-2-yl}benzamide (CHEBI:91057)
N-benzoyl-L-phenylalanine 2-naphthylamide (CHEBI:91058) is a L-phenylalanine derivative (CHEBI:84144)
N-benzoyl-L-phenylalanine 2-naphthylamide (CHEBI:91058) is enantiomer of N-benzoyl-D-phenylalanine 2-naphthylamide (CHEBI:91059)
Incoming N-benzoyl-DL-phenylalanine 2-naphthylamide (CHEBI:91056) has part N-benzoyl-L-phenylalanine 2-naphthylamide (CHEBI:91058)
N-benzoyl-D-phenylalanine 2-naphthylamide (CHEBI:91059) is enantiomer of N-benzoyl-L-phenylalanine 2-naphthylamide (CHEBI:91058)
IUPAC Name
Nα-benzoyl-N-naphthalen-2-yl-L-phenylalaninamide
Synonym Source
N-benzoyl-L-phenylalanine β-naphthylamide ChEBI
Last Modified
03 February 2016