3-(4-Hydroxy-2-methoxyphenyl)-1-benzofuran-6-ol

Details

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Internal ID d2b790e2-6cfe-4ab6-8dcd-be6116a70a27
Taxonomy Organoheterocyclic compounds > Benzofurans > Phenylbenzofurans
IUPAC Name 3-(4-hydroxy-2-methoxyphenyl)-1-benzofuran-6-ol
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C15H12O4/c1-18-14-6-9(16)2-4-11(14)13-8-19-15-7-10(17)3-5-12(13)15/h2-8,16-17H,1H3
InChI Key IVYVKQJIIWGEFH-UHFFFAOYSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C15H12O4
Molecular Weight 256.25 g/mol
Exact Mass 256.07355886 g/mol
Topological Polar Surface Area (TPSA) 62.80 Ų
XlogP 3.20
Atomic LogP (AlogP) 3.52
H-Bond Acceptor 4
H-Bond Donor 2
Rotatable Bonds 2

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 3-(4-Hydroxy-2-methoxyphenyl)-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 + 0.9933 99.33%
Caco-2 + 0.5224 52.24%
Blood Brain Barrier - 0.6000 60.00%
Human oral bioavailability - 0.6429 64.29%
Subcellular localzation Mitochondria 0.7624 76.24%
OATP2B1 inhibitior - 0.5891 58.91%
OATP1B1 inhibitior + 0.9076 90.76%
OATP1B3 inhibitior + 0.9773 97.73%
MATE1 inhibitior - 0.8800 88.00%
OCT2 inhibitior - 0.8500 85.00%
BSEP inhibitior - 0.5667 56.67%
P-glycoprotein inhibitior - 0.7993 79.93%
P-glycoprotein substrate - 0.6592 65.92%
CYP3A4 substrate + 0.5118 51.18%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate + 0.4038 40.38%
CYP3A4 inhibition - 0.6981 69.81%
CYP2C9 inhibition + 0.9665 96.65%
CYP2C19 inhibition + 0.9539 95.39%
CYP2D6 inhibition - 0.6998 69.98%
CYP1A2 inhibition + 0.9473 94.73%
CYP2C8 inhibition + 0.7354 73.54%
CYP inhibitory promiscuity + 0.9474 94.74%
UGT catelyzed + 0.8000 80.00%
Carcinogenicity (binary) - 0.8308 83.08%
Carcinogenicity (trinary) Warning 0.3857 38.57%
Eye corrosion - 0.9884 98.84%
Eye irritation + 0.7890 78.90%
Skin irritation - 0.6870 68.70%
Skin corrosion - 0.9524 95.24%
Ames mutagenesis - 0.6400 64.00%
Human Ether-a-go-go-Related Gene inhibition - 0.7035 70.35%
Micronuclear + 0.8400 84.00%
Hepatotoxicity - 0.5000 50.00%
skin sensitisation - 0.9248 92.48%
Respiratory toxicity - 0.7000 70.00%
Reproductive toxicity + 0.6444 64.44%
Mitochondrial toxicity + 0.5375 53.75%
Nephrotoxicity + 0.4628 46.28%
Acute Oral Toxicity (c) III 0.5765 57.65%
Estrogen receptor binding + 0.9125 91.25%
Androgen receptor binding + 0.9512 95.12%
Thyroid receptor binding + 0.8227 82.27%
Glucocorticoid receptor binding + 0.9000 90.00%
Aromatase binding + 0.9298 92.98%
PPAR gamma + 0.7886 78.86%
Honey bee toxicity - 0.9158 91.58%
Biodegradation - 0.9250 92.50%
Crustacea aquatic toxicity + 0.6251 62.51%
Fish aquatic toxicity + 0.9460 94.60%

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 97.76% 91.11%
CHEMBL242 Q92731 Estrogen receptor beta 97.09% 98.35%
CHEMBL225 P28335 Serotonin 2c (5-HT2c) receptor 90.99% 89.62%
CHEMBL2581 P07339 Cathepsin D 89.64% 98.95%
CHEMBL1293249 Q13887 Kruppel-like factor 5 89.03% 86.33%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 88.80% 95.56%
CHEMBL1806 P11388 DNA topoisomerase II alpha 87.78% 89.00%
CHEMBL3060 Q9Y345 Glycine transporter 2 86.46% 99.17%
CHEMBL2535 P11166 Glucose transporter 86.37% 98.75%
CHEMBL3194 P02766 Transthyretin 85.95% 90.71%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 85.73% 94.00%
CHEMBL2002 P12268 Inosine-5'-monophosphate dehydrogenase 2 84.86% 98.21%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 83.35% 96.09%
CHEMBL4208 P20618 Proteasome component C5 82.01% 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 163036761
LOTUS LTS0220894
wikiData Q105121400