Services
Research
Training
Industry
About us
ChEBI
Examples:
iron*
,
InChI=1S/CH4O/c1-2/h2H,1H3
,
caffeine
Advanced
Home
Advanced Search
Browse
Documentation
Download
Tools
About ChEBI
Submit
Contact us
DiNA
Statistics
Entity of the Month
Periodic Table
Ontology
Train online
User Manual
Annotation Manual
Developer Manual
FAQ's
BiNChE
libChEBI
Web Services
ChEBI
> Main
CHEBI:90478 -
L
-lysine 2-naphthylamide
Main
ChEBI Ontology
Automatic Xrefs
Reactions
Pathways
Models
ChEBI Name
L
-lysine 2-naphthylamide
ChEBI ID
CHEBI:90478
ChEBI ASCII Name
L-lysine 2-naphthylamide
Definition
An
L
-lysine derivative that is the amide obtained by formal condensation of the carboxy group of
L
-lysine with the amino group of 2-naphthylamine.
Stars
This entity has been manually annotated by the ChEBI Team.
Supplier Information
Download
Molfile
XML
SDF
Find compounds which contain this structure
Find compounds which resemble this structure
Take structure to the Advanced Search
Formula
C16H21N3O
Net Charge
0
Average Mass
271.358
Monoisotopic Mass
271.16846
InChI
InChI=1S/C16H21N3O/c17-
10-
4-
3-
7-
15(18)
16(20)
19-
14-
9-
8-
12-
5-
1-
2-
6-
13(12)
11-
14/h1-
2,5-
6,8-
9,11,15H,3-
4,7,10,17-
18H2,(H,19,20)
/t15-
/m0/s1
InChIKey
QXMBQGUYVQPOCP-HNNXBMFYSA-N
SMILES
N(C([C@H](CCCCN)N)=O)C=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.
View more via ChEBI Ontology
ChEBI Ontology
Outgoing
L
-lysine 2-naphthylamide (
CHEBI:90478
)
has role
chromogenic compound (
CHEBI:75050
)
L
-lysine 2-naphthylamide (
CHEBI:90478
)
is a
N
-(2-naphthyl)carboxamide (
CHEBI:88330
)
L
-lysine 2-naphthylamide (
CHEBI:90478
)
is a
L
-lysine derivative (
CHEBI:25095
)
L
-lysine 2-naphthylamide (
CHEBI:90478
)
is a
amino acid amide (
CHEBI:22475
)
IUPAC Name
N
-naphthalen-2-yl-
L
-lysinamide
Synonyms
Sources
L
-lysine β-naphthylamide
ChEBI
Lys-2-naphthylamide
ChemIDplus
Lysine-2-naphthylamide
ChemIDplus
N
-(2-naphthyl)-
L
-lysinamide
ChEBI
N
-(β-naphthyl)-
L
-lysinamide
ChEBI
N
-lysyl-2-aminonaphthalene
ChEBI
Registry Numbers
Types
Sources
2381059
Reaxys Registry Number
Reaxys
4420-88-6
CAS Registry Number
ChemIDplus
Last Modified
19 November 2015