(Z)-1-(2,4-Dihydroxyphenyl)-3-(4-Hydroxyphenyl)Prop-2-En-1-One

Representations & DB's id
ChEBI:	None
ChEMBL:	CHEMBL1395334
PubChem:	6603886
IUPAC:	(Z)-1-(2,4-dihydroxyphenyl)-3-(4-hydroxyphenyl)prop-2-en-1-one
Standard InChI:	InChI=1S/C15H12O4/c16-11-4-1-10(2-5-11)3-8-14(18)13-7-6-12(17)9-15(13)19/h1-9,16-17,19H/b8-3-
Standard InChI Key:	DXDRHHKMWQZJHT-BAQGIRSFSA-N
SMILES:	Oc1ccc(cc1)/C=CC(=O)c1ccc(cc1O)O

Molecular propeties
AlogP:	2.7
Hydrogen bonds acceptors:	4
Hydrogen bonds donors:	3
Rotatable bonds:	3
Number of rings:	2
Molecular Weight:	256.07
Topological polar surface area:	77.8
Number of aromatic rings:	2
Fsp3:	0
Number of carbons:	15

Plant sources

Activity Type	Activity Value	Target Name	UniProt ID
Potency	3162.3 nM	Nuclear factor NF-kappa-B p105 subunit	P19838
Potency	12589.3 nM	Cytochrome P450 2C19	P33261
Potency	15848.9 nM	Pyruvate kinase isozymes M1/M2	P14618
Potency	25118.9 nM	Arachidonate 15-lipoxygenase	P16050
Potency	251.2 nM	MAP kinase ERK2	P28482
Potency	15848.9 nM	Pyruvate kinase isozymes M1/M2	P14618
Potency	3162.3 nM	Nuclear factor NF-kappa-B p105 subunit	P19838
Potency	3162.3 nM	Thrombopoietin	P40225
Potency	31622.8 nM	Cellular tumor antigen p53	P04637
Potency	10000 nM	Endoplasmic reticulum-associated amyloid beta-peptide-binding protein	Q99714
Potency	3162.3 nM	Cytochrome P450 3A4	P08684
Potency	15848.9 nM	Cytochrome P450 2D6	P10635
Potency	3162.3 nM	Cytochrome P450 3A4	P08684
Potency	3162.3 nM	Thrombopoietin	P40225
Potency	19952.6 nM	Cytochrome P450 2C9	P11712