3-(4-Hydroxy-2,3-dimethoxyphenyl)-1-benzofuran-6-ol

Details

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Internal ID 6668e1ec-21a2-4807-8477-61e306d90393
Taxonomy Organoheterocyclic compounds > Benzofurans > Phenylbenzofurans
IUPAC Name 3-(4-hydroxy-2,3-dimethoxyphenyl)-1-benzofuran-6-ol
SMILES (Canonical) COC1=C(C=CC(=C1OC)O)C2=COC3=C2C=CC(=C3)O
SMILES (Isomeric) COC1=C(C=CC(=C1OC)O)C2=COC3=C2C=CC(=C3)O
InChI InChI=1S/C16H14O5/c1-19-15-11(5-6-13(18)16(15)20-2)12-8-21-14-7-9(17)3-4-10(12)14/h3-8,17-18H,1-2H3
InChI Key FZZZVWQKWYCAEI-UHFFFAOYSA-N
Popularity 1 reference in papers

Physical and Chemical Properties

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Molecular Formula C16H14O5
Molecular Weight 286.28 g/mol
Exact Mass 286.08412354 g/mol
Topological Polar Surface Area (TPSA) 72.10 Ų
XlogP 3.20
Atomic LogP (AlogP) 3.53
H-Bond Acceptor 5
H-Bond Donor 2
Rotatable Bonds 3

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 3-(4-Hydroxy-2,3-dimethoxyphenyl)-1-benzofuran-6-ol

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9881 98.81%
Caco-2 + 0.6913 69.13%
Blood Brain Barrier - 0.5500 55.00%
Human oral bioavailability - 0.6143 61.43%
Subcellular localzation Mitochondria 0.7499 74.99%
OATP2B1 inhibitior - 0.5797 57.97%
OATP1B1 inhibitior + 0.9189 91.89%
OATP1B3 inhibitior + 0.9378 93.78%
MATE1 inhibitior - 0.8800 88.00%
OCT2 inhibitior - 0.9000 90.00%
BSEP inhibitior - 0.5484 54.84%
P-glycoprotein inhibitior - 0.7754 77.54%
P-glycoprotein substrate - 0.7721 77.21%
CYP3A4 substrate + 0.5104 51.04%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate + 0.4038 40.38%
CYP3A4 inhibition - 0.5808 58.08%
CYP2C9 inhibition + 0.8944 89.44%
CYP2C19 inhibition + 0.9181 91.81%
CYP2D6 inhibition - 0.5954 59.54%
CYP1A2 inhibition + 0.8881 88.81%
CYP2C8 inhibition + 0.6452 64.52%
CYP inhibitory promiscuity + 0.9368 93.68%
UGT catelyzed + 0.8000 80.00%
Carcinogenicity (binary) - 0.8708 87.08%
Carcinogenicity (trinary) Warning 0.3621 36.21%
Eye corrosion - 0.9874 98.74%
Eye irritation + 0.7407 74.07%
Skin irritation - 0.7313 73.13%
Skin corrosion - 0.9530 95.30%
Ames mutagenesis + 0.5400 54.00%
Human Ether-a-go-go-Related Gene inhibition - 0.4678 46.78%
Micronuclear + 0.8300 83.00%
Hepatotoxicity + 0.5375 53.75%
skin sensitisation - 0.8658 86.58%
Respiratory toxicity - 0.6111 61.11%
Reproductive toxicity + 0.7333 73.33%
Mitochondrial toxicity + 0.5500 55.00%
Nephrotoxicity - 0.7007 70.07%
Acute Oral Toxicity (c) III 0.5903 59.03%
Estrogen receptor binding + 0.8639 86.39%
Androgen receptor binding + 0.8377 83.77%
Thyroid receptor binding + 0.8203 82.03%
Glucocorticoid receptor binding + 0.8548 85.48%
Aromatase binding + 0.8914 89.14%
PPAR gamma + 0.6804 68.04%
Honey bee toxicity - 0.9195 91.95%
Biodegradation - 0.8750 87.50%
Crustacea aquatic toxicity + 0.5600 56.00%
Fish aquatic toxicity + 0.9408 94.08%

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 99.22% 91.11%
CHEMBL242 Q92731 Estrogen receptor beta 98.56% 98.35%
CHEMBL1860 P10827 Thyroid hormone receptor alpha 91.49% 99.15%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 88.46% 95.56%
CHEMBL2581 P07339 Cathepsin D 88.23% 98.95%
CHEMBL1806 P11388 DNA topoisomerase II alpha 87.32% 89.00%
CHEMBL3194 P02766 Transthyretin 87.14% 90.71%
CHEMBL1293249 Q13887 Kruppel-like factor 5 86.67% 86.33%
CHEMBL2085 P14174 Macrophage migration inhibitory factor 86.65% 80.78%
CHEMBL2535 P11166 Glucose transporter 84.85% 98.75%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 84.48% 94.00%
CHEMBL3060 Q9Y345 Glycine transporter 2 83.22% 99.17%
CHEMBL225 P28335 Serotonin 2c (5-HT2c) receptor 83.03% 89.62%
CHEMBL4208 P20618 Proteasome component C5 82.72% 90.00%

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.
Hippocrepis emerus subsp. emerus

Cross-Links

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PubChem 162914443
LOTUS LTS0255369
wikiData Q105005285