Nonivamide

Representations & DB's id
ChEBI:	CHEBI:46936
ChEMBL:	CHEMBL75124
PubChem:	2998
IUPAC:	N-[(4-hydroxy-3-methoxyphenyl)methyl]nonanamide
Standard InChI:	InChI=1S/C17H27NO3/c1-3-4-5-6-7-8-9-17(20)18-13-14-10-11-15(19)16(12-14)21-2/h10-12,19H,3-9,13H2,1-2H3,(H,18,20)
Standard InChI Key:	RGOVYLWUIBMPGK-UHFFFAOYSA-N
SMILES:	CCCCCCCCC(=NCc1ccc(c(c1)OC)O)O

Molecular propeties
AlogP:	3.77
Hydrogen bonds acceptors:	3
Hydrogen bonds donors:	2
Rotatable bonds:	10
Number of rings:	1
Molecular Weight:	293.2
Topological polar surface area:	58.6
Number of aromatic rings:	1
Fsp3:	0.588
Number of carbons:	17

Plant sources

Part of plant	Plant name	Ref.
Fructus	Capsicum annuum

In vitro data

Activity Type	Activity Value	Target Name	UniProt ID	Ref.
Potency	7943.3 nM	Cytochrome P450 2C19	P33261
Potency	25118.9 nM	Aldehyde dehydrogenase 1A1	P00352
Potency	8492.1 nM	Peripheral myelin protein 22	Q01453
Potency	25118.9 nM	Arachidonate 15-lipoxygenase	P16050
Potency	50118.7 nM	Bloom syndrome protein	P54132
Potency	22387.2 nM	15-hydroxyprostaglandin dehydrogenase [NAD+]	P15428
Potency	50118.7 nM	Bloom syndrome protein	P54132
Potency	25118.9 nM	Cytochrome P450 3A4	P08684
Potency	3981.1 nM	Cytochrome P450 3A4	P08684
Potency	25118.9 nM	Cytochrome P450 2D6	P10635
Potency	3162.3 nM	Cytochrome P450 2C9	P11712
Potency	25118.9 nM	Cytochrome P450 3A4	P08684
Potency	3981.1 nM	Cytochrome P450 3A4	P08684
Potency	89125.1 nM	Histone-lysine N-methyltransferase, H3 lysine-9 specific 3	Q96KQ7
Potency	25118.9 nM	Histone-lysine N-methyltransferase, H3 lysine-9 specific 3	Q96KQ7
Potency	10000 nM	Glutaminase kidney isoform, mitochondrial	O94925