Cis-Resveratrol

Representations & DB's id
ChEBI:	CHEBI:36002
ChEMBL:	CHEMBL87333
PubChem:	1548910
IUPAC:	5-[(Z)-2-(4-hydroxyphenyl)ethenyl]benzene-1,3-diol
Standard InChI:	InChI=1S/C14H12O3/c15-12-5-3-10(4-6-12)1-2-11-7-13(16)9-14(17)8-11/h1-9,15-17H/b2-1-
Standard InChI Key:	LUKBXSAWLPMMSZ-UPHRSURJSA-N
SMILES:	Oc1ccc(cc1)/C=Cc1cc(O)cc(c1)O

Molecular propeties
AlogP:	2.97
Hydrogen bonds acceptors:	3
Hydrogen bonds donors:	3
Rotatable bonds:	2
Number of rings:	2
Molecular Weight:	228.08
Topological polar surface area:	60.7
Number of aromatic rings:	2
Fsp3:	0
Number of carbons:	14

Plant sources

Part of plant	Plant name	Ref.
Fruit	Vitis vinifera
Fruit	Vitis vinifera
Fruit	Vitis vinifera
Sprout Seedling	Arachis hypogaea
Plant	Lavandula vera
Sprout Seedling	Arachis hypogaea
Plant	Rheum palmatum
Plant	Humulus lupulus
Plant	Veratrum album
Plant	Veratrum album

In vitro data

Activity Type	Activity Value	Target Name	UniProt ID
Potency	4466.8 nM	Prelamin-A/C	P02545
Potency	25118.9 nM	Endoplasmic reticulum-associated amyloid beta-peptide-binding protein	Q99714
Potency	12589.3 nM	Endoplasmic reticulum-associated amyloid beta-peptide-binding protein	Q99714
Potency	12589.3 nM	Lysine-specific demethylase 4D-like	B2RXH2
Potency	28183.8 nM	Lysine-specific demethylase 4D-like	B2RXH2
Potency	14125.4 nM	Survival motor neuron protein	Q16637
Potency	1 nM	Tyrosyl-DNA phosphodiesterase 1	Q9NUW8
Potency	31622.8 nM	Cytochrome P450 2C19	P33261
Potency	2.5 nM	Cytochrome P450 2C19	P33261
Potency	14125.4 nM	Microtubule-associated protein tau	P10636
Potency	12589.3 nM	Hypoxia-inducible factor 1 alpha	Q16665
Potency	3162.3 nM	Hypoxia-inducible factor 1 alpha	Q16665
Potency	39810.7 nM	Aldehyde dehydrogenase 1A1	P00352
Potency	8912.5 nM	Aldehyde dehydrogenase 1A1	P00352
Potency	3162.3 nM	Pyruvate kinase isozymes M1/M2	P14618
Potency	19952.6 nM	Arachidonate 15-lipoxygenase	P16050
Potency	12589.3 nM	Hypoxia-inducible factor 1 alpha	Q16665
Potency	3162.3 nM	Hypoxia-inducible factor 1 alpha	Q16665
Potency	3162.3 nM	Pyruvate kinase isozymes M1/M2	P14618
Potency	10000 nM	Ubiquitin carboxyl-terminal hydrolase 2	O75604
Potency	35481.3 nM	15-hydroxyprostaglandin dehydrogenase [NAD+]	P15428
Potency	15848.9 nM	15-hydroxyprostaglandin dehydrogenase [NAD+]	P15428
Potency	12589.3 nM	Thrombopoietin	P40225
Potency	12589.3 nM	Endoplasmic reticulum-associated amyloid beta-peptide-binding protein	Q99714
Potency	10000 nM	Endoplasmic reticulum-associated amyloid beta-peptide-binding protein	Q99714
Potency	7943.3 nM	Cellular tumor antigen p53	P04637
Potency	7943.3 nM	Cellular tumor antigen p53	P04637
Potency	12589.3 nM	Endoplasmic reticulum-associated amyloid beta-peptide-binding protein	Q99714
Potency	12589.3 nM	Endoplasmic reticulum-associated amyloid beta-peptide-binding protein	Q99714
Potency	7943.3 nM	Cellular tumor antigen p53	P04637
Potency	3981.1 nM	Cellular tumor antigen p53	P04637
Potency	3162.3 nM	Cytochrome P450 3A4	P08684
Potency	2511.9 nM	Cytochrome P450 3A4	P08684
Potency	39810.7 nM	Cytochrome P450 2D6	P10635
Potency	10000 nM	Cytochrome P450 2D6	P10635
Potency	3162.3 nM	Cytochrome P450 3A4	P08684
Potency	2511.9 nM	Cytochrome P450 3A4	P08684
Potency	31622.8 nM	Cytochrome P450 2C9	P11712
Potency	25118.9 nM	Cytochrome P450 2C9	P11712
Potency	12589.3 nM	Thrombopoietin	P40225
Potency	10000 nM	Cytochrome P450 2C9	P11712
Potency	79.4 nM	Histone acetyltransferase GCN5	Q92830
IC50	50000 nM	Cytochrome P450 19A1	P11511

Cis-Resveratrol

Representations & DB's id

Molecular propeties

Plant sources

In vitro data