2-(4-Hydroxy-2,5-dimethoxyphenyl)-1-benzofuran-6-ol

Details

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Internal ID 5d1dd4e9-86fd-4c6a-9dc5-7628025dfdac
Taxonomy Phenylpropanoids and polyketides > 2-arylbenzofuran flavonoids
IUPAC Name 2-(4-hydroxy-2,5-dimethoxyphenyl)-1-benzofuran-6-ol
SMILES (Canonical) COC1=CC(=C(C=C1C2=CC3=C(O2)C=C(C=C3)O)OC)O
SMILES (Isomeric) COC1=CC(=C(C=C1C2=CC3=C(O2)C=C(C=C3)O)OC)O
InChI InChI=1S/C16H14O5/c1-19-14-8-12(18)16(20-2)7-11(14)15-5-9-3-4-10(17)6-13(9)21-15/h3-8,17-18H,1-2H3
InChI Key ZXVCAYAYUZVPPH-UHFFFAOYSA-N
Popularity 0 references 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 2-(4-Hydroxy-2,5-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 + 0.7886 78.86%
Blood Brain Barrier - 0.5500 55.00%
Human oral bioavailability - 0.5286 52.86%
Subcellular localzation Mitochondria 0.7499 74.99%
OATP2B1 inhibitior - 0.5803 58.03%
OATP1B1 inhibitior + 0.8154 81.54%
OATP1B3 inhibitior + 0.9378 93.78%
MATE1 inhibitior - 0.8800 88.00%
OCT2 inhibitior - 0.9000 90.00%
BSEP inhibitior - 0.4624 46.24%
P-glycoprotein inhibitior - 0.5486 54.86%
P-glycoprotein substrate - 0.5979 59.79%
CYP3A4 substrate - 0.5000 50.00%
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 + 0.7558 75.58%
CYP inhibitory promiscuity + 0.9368 93.68%
UGT catelyzed - 0.5000 50.00%
Carcinogenicity (binary) - 0.8708 87.08%
Carcinogenicity (trinary) Warning 0.3621 36.21%
Eye corrosion - 0.9874 98.74%
Eye irritation + 0.7692 76.92%
Skin irritation - 0.7313 73.13%
Skin corrosion - 0.9530 95.30%
Ames mutagenesis - 0.5500 55.00%
Human Ether-a-go-go-Related Gene inhibition - 0.5105 51.05%
Micronuclear + 0.8300 83.00%
Hepatotoxicity - 0.7500 75.00%
skin sensitisation - 0.8658 86.58%
Respiratory toxicity - 0.7111 71.11%
Reproductive toxicity + 0.7333 73.33%
Mitochondrial toxicity + 0.5500 55.00%
Nephrotoxicity - 0.6904 69.04%
Acute Oral Toxicity (c) III 0.5903 59.03%
Estrogen receptor binding + 0.8990 89.90%
Androgen receptor binding + 0.8425 84.25%
Thyroid receptor binding + 0.7365 73.65%
Glucocorticoid receptor binding + 0.8993 89.93%
Aromatase binding + 0.8586 85.86%
PPAR gamma + 0.7879 78.79%
Honey bee toxicity - 0.9078 90.78%
Biodegradation - 0.8750 87.50%
Crustacea aquatic toxicity + 0.5351 53.51%
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 94.71% 91.11%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 93.77% 94.00%
CHEMBL1293249 Q13887 Kruppel-like factor 5 90.31% 86.33%
CHEMBL3194 P02766 Transthyretin 89.89% 90.71%
CHEMBL3060 Q9Y345 Glycine transporter 2 87.40% 99.17%
CHEMBL225 P28335 Serotonin 2c (5-HT2c) receptor 87.22% 89.62%
CHEMBL2581 P07339 Cathepsin D 86.00% 98.95%
CHEMBL1860 P10827 Thyroid hormone receptor alpha 85.44% 99.15%
CHEMBL242 Q92731 Estrogen receptor beta 84.60% 98.35%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 84.42% 96.09%
CHEMBL4208 P20618 Proteasome component C5 84.35% 90.00%
CHEMBL4793 Q86TI2 Dipeptidyl peptidase IX 84.19% 96.95%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 82.11% 95.56%
CHEMBL2535 P11166 Glucose transporter 81.97% 98.75%

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.
Erythrina abyssinica
Erythrina herbacea
Erythrina variegata

Cross-Links

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PubChem 11471684
LOTUS LTS0206225
wikiData Q105385807