N-Phenylnaphthalen-2-Amine

Representations & DB's id
ChEBI:	CHEBI:34877
ChEMBL:	CHEMBL1543632
PubChem:	8679
IUPAC:	N-phenylnaphthalen-2-amine
Standard InChI:	InChI=1S/C16H13N/c1-2-8-15(9-3-1)17-16-11-10-13-6-4-5-7-14(13)12-16/h1-12,17H
Standard InChI Key:	KEQFTVQCIQJIQW-UHFFFAOYSA-N
SMILES:	c1ccc(cc1)Nc1ccc2c(c1)cccc2

Molecular propeties
AlogP:	4.58
Hydrogen bonds acceptors:	1
Hydrogen bonds donors:	1
Rotatable bonds:	2
Number of rings:	3
Molecular Weight:	219.1
Topological polar surface area:	12
Number of aromatic rings:	3
Fsp3:	0
Number of carbons:	16

Plant sources

Part of plant	Plant name	Ref.
Plant	Aconitum karakolicum
Plant	Aconitum karakolicum

In vitro data

Activity Type	Activity Value	Target Name	UniProt ID	Ref.
Potency	31622.8 nM	Endoplasmic reticulum-associated amyloid beta-peptide-binding protein	Q99714
Potency	31622.8 nM	Aldehyde dehydrogenase 1A1	P00352
Potency	12589.3 nM	15-hydroxyprostaglandin dehydrogenase [NAD+]	P15428
Potency	39810.7 nM	Endoplasmic reticulum-associated amyloid beta-peptide-binding protein	Q99714
Potency	25118.9 nM	Cytochrome P450 3A4	P08684
Potency	25118.9 nM	Cytochrome P450 3A4	P08684
Potency	20596.2 nM	Nuclear factor erythroid 2-related factor 2	Q16236
Potency	50118.7 nM	Aryl hydrocarbon receptor	P35869
Potency	44668.4 nM	Aryl hydrocarbon receptor	P35869
Potency	54482.7 nM	Nuclear factor erythroid 2-related factor 2	Q16236
Potency	42163.2 nM	Nuclear factor erythroid 2-related factor 2	Q16236
Potency	15848.9 nM	Breast cancer type 1 susceptibility protein	P38398
Potency	2984.9 nM	Nuclear receptor ROR-gamma	P51449