9'-O-Methylvisanol

Details

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Internal ID c36c4a80-3d7c-43bd-b515-641bf5f06677
Taxonomy Phenylpropanoids and polyketides > 2-arylbenzofuran flavonoids
IUPAC Name 2-(4-hydroxy-3-methoxyphenyl)-5-[(E)-3-hydroxyprop-1-enyl]-3-(methoxymethyl)-1-benzofuran-7-ol
SMILES (Canonical) COCC1=C(OC2=C1C=C(C=C2O)C=CCO)C3=CC(=C(C=C3)O)OC
SMILES (Isomeric) COCC1=C(OC2=C1C=C(C=C2O)/C=C/CO)C3=CC(=C(C=C3)O)OC
InChI InChI=1S/C20H20O6/c1-24-11-15-14-8-12(4-3-7-21)9-17(23)20(14)26-19(15)13-5-6-16(22)18(10-13)25-2/h3-6,8-10,21-23H,7,11H2,1-2H3/b4-3+
InChI Key VSJXKWCBZNUAQF-ONEGZZNKSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C20H20O6
Molecular Weight 356.40 g/mol
Exact Mass 356.12598835 g/mol
Topological Polar Surface Area (TPSA) 92.30 Ų
XlogP 2.70
Atomic LogP (AlogP) 3.67
H-Bond Acceptor 6
H-Bond Donor 3
Rotatable Bonds 6

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 9'-O-Methylvisanol

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9864 98.64%
Caco-2 + 0.5883 58.83%
Blood Brain Barrier + 0.5250 52.50%
Human oral bioavailability - 0.5286 52.86%
Subcellular localzation Mitochondria 0.6319 63.19%
OATP2B1 inhibitior - 0.7172 71.72%
OATP1B1 inhibitior + 0.8491 84.91%
OATP1B3 inhibitior + 0.9394 93.94%
MATE1 inhibitior - 0.9400 94.00%
OCT2 inhibitior - 0.9500 95.00%
BSEP inhibitior + 0.8859 88.59%
P-glycoprotein inhibitior + 0.7124 71.24%
P-glycoprotein substrate - 0.7886 78.86%
CYP3A4 substrate + 0.5690 56.90%
CYP2C9 substrate + 0.6077 60.77%
CYP2D6 substrate - 0.7262 72.62%
CYP3A4 inhibition + 0.5172 51.72%
CYP2C9 inhibition + 0.7370 73.70%
CYP2C19 inhibition + 0.7589 75.89%
CYP2D6 inhibition - 0.7155 71.55%
CYP1A2 inhibition - 0.5735 57.35%
CYP2C8 inhibition + 0.8684 86.84%
CYP inhibitory promiscuity + 0.9237 92.37%
UGT catelyzed - 0.6000 60.00%
Carcinogenicity (binary) - 0.9108 91.08%
Carcinogenicity (trinary) Non-required 0.4814 48.14%
Eye corrosion - 0.9879 98.79%
Eye irritation - 0.6653 66.53%
Skin irritation - 0.8161 81.61%
Skin corrosion - 0.9503 95.03%
Ames mutagenesis + 0.5100 51.00%
Human Ether-a-go-go-Related Gene inhibition + 0.6758 67.58%
Micronuclear + 0.6800 68.00%
Hepatotoxicity - 0.5601 56.01%
skin sensitisation - 0.7019 70.19%
Respiratory toxicity - 0.7333 73.33%
Reproductive toxicity + 0.6667 66.67%
Mitochondrial toxicity + 0.5500 55.00%
Nephrotoxicity - 0.7468 74.68%
Acute Oral Toxicity (c) III 0.5619 56.19%
Estrogen receptor binding + 0.9111 91.11%
Androgen receptor binding + 0.7654 76.54%
Thyroid receptor binding + 0.7649 76.49%
Glucocorticoid receptor binding + 0.9306 93.06%
Aromatase binding + 0.7871 78.71%
PPAR gamma + 0.8890 88.90%
Honey bee toxicity - 0.8076 80.76%
Biodegradation - 0.8000 80.00%
Crustacea aquatic toxicity - 0.5200 52.00%
Fish aquatic toxicity + 0.9532 95.32%

Targets

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Proven Targets:

CHEMBL ID UniProt ID Name Min activity Assay type Source
No proven targets yet!

Predicted Targets (via Super-PRED):

CHEMBL ID UniProt ID Name Probability Model accuracy
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 98.31% 91.11%
CHEMBL1293249 Q13887 Kruppel-like factor 5 94.28% 86.33%
CHEMBL242 Q92731 Estrogen receptor beta 94.22% 98.35%
CHEMBL2288 Q13526 Peptidyl-prolyl cis-trans isomerase NIMA-interacting 1 93.89% 91.71%
CHEMBL3060 Q9Y345 Glycine transporter 2 93.24% 99.17%
CHEMBL1806 P11388 DNA topoisomerase II alpha 92.35% 89.00%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 91.73% 96.00%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 91.06% 95.56%
CHEMBL1860 P10827 Thyroid hormone receptor alpha 90.99% 99.15%
CHEMBL4016 P42262 Glutamate receptor ionotropic, AMPA 2 90.28% 86.92%
CHEMBL3194 P02766 Transthyretin 90.15% 90.71%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 88.16% 94.45%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 84.54% 94.00%
CHEMBL1163101 O75460 Serine/threonine-protein kinase/endoribonuclease IRE1 81.66% 98.11%
CHEMBL3401 O75469 Pregnane X receptor 80.50% 94.73%

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.
Berberis japonica
Isodon nervosus
Isodon xerophilus
Lonicera macrantha

Cross-Links

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PubChem 10498464
NPASS NPC275821