Visanol

Details

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Internal ID fc3e7548-e6ed-4268-9001-d7d2af2bde5c
Taxonomy Phenylpropanoids and polyketides > 2-arylbenzofuran flavonoids
IUPAC Name 2-(4-hydroxy-3-methoxyphenyl)-3-(hydroxymethyl)-5-[(E)-3-hydroxyprop-1-enyl]-1-benzofuran-7-ol
SMILES (Canonical) COC1=C(C=CC(=C1)C2=C(C3=C(O2)C(=CC(=C3)C=CCO)O)CO)O
SMILES (Isomeric) COC1=C(C=CC(=C1)C2=C(C3=C(O2)C(=CC(=C3)/C=C/CO)O)CO)O
InChI InChI=1S/C19H18O6/c1-24-17-9-12(4-5-15(17)22)18-14(10-21)13-7-11(3-2-6-20)8-16(23)19(13)25-18/h2-5,7-9,20-23H,6,10H2,1H3/b3-2+
InChI Key KCKHQFLIKNFJMG-NSCUHMNNSA-N
Popularity 1 reference in papers

Physical and Chemical Properties

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Molecular Formula C19H18O6
Molecular Weight 342.30 g/mol
Exact Mass 342.11033829 g/mol
Topological Polar Surface Area (TPSA) 103.00 Ų
XlogP 2.10
Atomic LogP (AlogP) 3.02
H-Bond Acceptor 6
H-Bond Donor 4
Rotatable Bonds 5

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of Visanol

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9875 98.75%
Caco-2 - 0.5834 58.34%
Blood Brain Barrier + 0.5250 52.50%
Human oral bioavailability - 0.5429 54.29%
Subcellular localzation Mitochondria 0.6797 67.97%
OATP2B1 inhibitior + 0.5757 57.57%
OATP1B1 inhibitior + 0.8516 85.16%
OATP1B3 inhibitior + 0.9625 96.25%
MATE1 inhibitior - 0.9400 94.00%
OCT2 inhibitior - 0.8750 87.50%
BSEP inhibitior + 0.6994 69.94%
P-glycoprotein inhibitior - 0.5000 50.00%
P-glycoprotein substrate - 0.8000 80.00%
CYP3A4 substrate + 0.5326 53.26%
CYP2C9 substrate + 0.6085 60.85%
CYP2D6 substrate - 0.7096 70.96%
CYP3A4 inhibition - 0.5820 58.20%
CYP2C9 inhibition + 0.8691 86.91%
CYP2C19 inhibition + 0.8581 85.81%
CYP2D6 inhibition - 0.7748 77.48%
CYP1A2 inhibition + 0.6451 64.51%
CYP2C8 inhibition + 0.7743 77.43%
CYP inhibitory promiscuity + 0.9706 97.06%
UGT catelyzed - 0.6000 60.00%
Carcinogenicity (binary) - 0.9208 92.08%
Carcinogenicity (trinary) Non-required 0.4059 40.59%
Eye corrosion - 0.9885 98.85%
Eye irritation + 0.5320 53.20%
Skin irritation - 0.7717 77.17%
Skin corrosion - 0.9460 94.60%
Ames mutagenesis + 0.5100 51.00%
Human Ether-a-go-go-Related Gene inhibition - 0.4434 44.34%
Micronuclear + 0.7500 75.00%
Hepatotoxicity - 0.6476 64.76%
skin sensitisation - 0.7247 72.47%
Respiratory toxicity - 0.7222 72.22%
Reproductive toxicity + 0.6778 67.78%
Mitochondrial toxicity + 0.5375 53.75%
Nephrotoxicity - 0.8759 87.59%
Acute Oral Toxicity (c) III 0.6453 64.53%
Estrogen receptor binding + 0.9076 90.76%
Androgen receptor binding + 0.7513 75.13%
Thyroid receptor binding + 0.7701 77.01%
Glucocorticoid receptor binding + 0.9400 94.00%
Aromatase binding + 0.8072 80.72%
PPAR gamma + 0.9108 91.08%
Honey bee toxicity - 0.8277 82.77%
Biodegradation - 0.8750 87.50%
Crustacea aquatic toxicity + 0.5100 51.00%
Fish aquatic toxicity + 0.9219 92.19%

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 98.79% 91.11%
CHEMBL2288 Q13526 Peptidyl-prolyl cis-trans isomerase NIMA-interacting 1 94.17% 91.71%
CHEMBL1293249 Q13887 Kruppel-like factor 5 94.12% 86.33%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 93.41% 96.00%
CHEMBL3060 Q9Y345 Glycine transporter 2 92.86% 99.17%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 92.09% 95.56%
CHEMBL1806 P11388 DNA topoisomerase II alpha 91.68% 89.00%
CHEMBL4016 P42262 Glutamate receptor ionotropic, AMPA 2 91.64% 86.92%
CHEMBL1860 P10827 Thyroid hormone receptor alpha 90.03% 99.15%
CHEMBL3194 P02766 Transthyretin 89.69% 90.71%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 87.59% 94.45%
CHEMBL1163101 O75460 Serine/threonine-protein kinase/endoribonuclease IRE1 84.32% 98.11%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 83.71% 94.00%
CHEMBL335 P18031 Protein-tyrosine phosphatase 1B 83.55% 95.17%
CHEMBL242 Q92731 Estrogen receptor beta 80.98% 98.35%
CHEMBL1907 P15144 Aminopeptidase N 80.76% 93.31%
CHEMBL3401 O75469 Pregnane X receptor 80.52% 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 10246758
NPASS NPC96553