5-(gamma,gamma-Dimethylallyl)-oxyresveratrol

Details

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Internal ID 643acadc-da3d-45f5-97fd-1922b8ea85fc
Taxonomy Phenylpropanoids and polyketides > Stilbenes
IUPAC Name 4-[(E)-2-(3,5-dihydroxyphenyl)ethenyl]-6-(3-methylbut-2-enyl)benzene-1,3-diol
SMILES (Canonical) CC(=CCC1=CC(=C(C=C1O)O)C=CC2=CC(=CC(=C2)O)O)C
SMILES (Isomeric) CC(=CCC1=CC(=C(C=C1O)O)/C=C/C2=CC(=CC(=C2)O)O)C
InChI InChI=1S/C19H20O4/c1-12(2)3-5-14-9-15(19(23)11-18(14)22)6-4-13-7-16(20)10-17(21)8-13/h3-4,6-11,20-23H,5H2,1-2H3/b6-4+
InChI Key KYQWCQJWDVPXKY-GQCTYLIASA-N
Popularity 1 reference in papers

Physical and Chemical Properties

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Molecular Formula C19H20O4
Molecular Weight 312.40 g/mol
Exact Mass 312.13615911 g/mol
Topological Polar Surface Area (TPSA) 80.90 Ų
XlogP 4.70
Atomic LogP (AlogP) 4.19
H-Bond Acceptor 4
H-Bond Donor 4
Rotatable Bonds 4

Synonyms

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BDBM50269599
5-(gamma,gamma-dimethylallyl)-oxyresveratrol

2D Structure

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2D Structure of 5-(gamma,gamma-Dimethylallyl)-oxyresveratrol

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9912 99.12%
Caco-2 + 0.5805 58.05%
Blood Brain Barrier - 0.5129 51.29%
Human oral bioavailability - 0.6429 64.29%
Subcellular localzation Mitochondria 0.7596 75.96%
OATP2B1 inhibitior - 0.5533 55.33%
OATP1B1 inhibitior + 0.9270 92.70%
OATP1B3 inhibitior + 0.9511 95.11%
MATE1 inhibitior - 0.9200 92.00%
OCT2 inhibitior - 0.9338 93.38%
BSEP inhibitior + 0.9069 90.69%
P-glycoprotein inhibitior - 0.6841 68.41%
P-glycoprotein substrate - 0.9088 90.88%
CYP3A4 substrate - 0.6093 60.93%
CYP2C9 substrate - 0.6075 60.75%
CYP2D6 substrate - 0.6697 66.97%
CYP3A4 inhibition + 0.5999 59.99%
CYP2C9 inhibition + 0.9401 94.01%
CYP2C19 inhibition + 0.9207 92.07%
CYP2D6 inhibition - 0.6868 68.68%
CYP1A2 inhibition + 0.9276 92.76%
CYP2C8 inhibition - 0.7367 73.67%
CYP inhibitory promiscuity + 0.9436 94.36%
UGT catelyzed + 0.8000 80.00%
Carcinogenicity (binary) - 0.7872 78.72%
Carcinogenicity (trinary) Non-required 0.7516 75.16%
Eye corrosion - 0.9825 98.25%
Eye irritation + 0.8336 83.36%
Skin irritation - 0.7774 77.74%
Skin corrosion - 0.6651 66.51%
Ames mutagenesis - 0.6200 62.00%
Human Ether-a-go-go-Related Gene inhibition - 0.4044 40.44%
Micronuclear - 0.5700 57.00%
Hepatotoxicity - 0.5551 55.51%
skin sensitisation + 0.7175 71.75%
Respiratory toxicity - 0.6222 62.22%
Reproductive toxicity + 0.7000 70.00%
Mitochondrial toxicity - 0.5875 58.75%
Nephrotoxicity + 0.5517 55.17%
Acute Oral Toxicity (c) III 0.7227 72.27%
Estrogen receptor binding + 0.9554 95.54%
Androgen receptor binding - 0.4948 49.48%
Thyroid receptor binding + 0.7949 79.49%
Glucocorticoid receptor binding + 0.9008 90.08%
Aromatase binding + 0.8439 84.39%
PPAR gamma + 0.9061 90.61%
Honey bee toxicity - 0.8746 87.46%
Biodegradation - 0.9500 95.00%
Crustacea aquatic toxicity - 0.6100 61.00%
Fish aquatic toxicity + 1.0000 100.00%

Targets

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Proven Targets:

CHEMBL ID UniProt ID Name Min activity Assay type Source
CHEMBL221 P23219 Cyclooxygenase-1 4100 nM
IC50
PMID: 11858749
CHEMBL230 P35354 Cyclooxygenase-2 36700 nM
IC50
PMID: 11858749

Predicted Targets (via Super-PRED):

CHEMBL ID UniProt ID Name Probability Model accuracy
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 98.68% 91.11%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 94.71% 96.00%
CHEMBL3401 O75469 Pregnane X receptor 92.24% 94.73%
CHEMBL3194 P02766 Transthyretin 91.93% 90.71%
CHEMBL1293249 Q13887 Kruppel-like factor 5 90.68% 86.33%
CHEMBL2581 P07339 Cathepsin D 90.18% 98.95%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 88.87% 94.45%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 88.00% 96.09%
CHEMBL1929 P47989 Xanthine dehydrogenase 87.98% 96.12%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 87.93% 95.56%
CHEMBL230 P35354 Cyclooxygenase-2 86.57% 89.63%
CHEMBL215 P09917 Arachidonate 5-lipoxygenase 85.74% 92.68%
CHEMBL1951 P21397 Monoamine oxidase A 84.48% 91.49%
CHEMBL3060 Q9Y345 Glycine transporter 2 84.01% 99.17%
CHEMBL2288 Q13526 Peptidyl-prolyl cis-trans isomerase NIMA-interacting 1 83.00% 91.71%

Plants that contains it

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Below are displayed all the plants proven (via scientific papers) to contain this compound!
To see more specific details click the taxa you are interested in.
Artocarpus lacucha
Canthium berberidifolium

Cross-Links

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PubChem 11034312
NPASS NPC43525
ChEMBL CHEMBL463126
LOTUS LTS0059690
wikiData Q105147868