2,7-Dihydroxy-3,4-dimethoxydibenzofuran

Details

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Internal ID 801b1836-6420-459d-8b47-35a24d97f619
Taxonomy Organoheterocyclic compounds > Benzofurans > Dibenzofurans
IUPAC Name 3,4-dimethoxydibenzofuran-2,7-diol
SMILES (Canonical) COC1=C(C=C2C3=C(C=C(C=C3)O)OC2=C1OC)O
SMILES (Isomeric) COC1=C(C=C2C3=C(C=C(C=C3)O)OC2=C1OC)O
InChI InChI=1S/C14H12O5/c1-17-13-10(16)6-9-8-4-3-7(15)5-11(8)19-12(9)14(13)18-2/h3-6,15-16H,1-2H3
InChI Key XDODOEVDIQGYQT-UHFFFAOYSA-N
Popularity 3 references in papers

Physical and Chemical Properties

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Molecular Formula C14H12O5
Molecular Weight 260.24 g/mol
Exact Mass 260.06847348 g/mol
Topological Polar Surface Area (TPSA) 72.10 Ų
XlogP 2.90
Atomic LogP (AlogP) 3.01
H-Bond Acceptor 5
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 2,7-Dihydroxy-3,4-dimethoxydibenzofuran

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9850 98.50%
Caco-2 + 0.5892 58.92%
Blood Brain Barrier - 0.5250 52.50%
Human oral bioavailability + 0.5429 54.29%
Subcellular localzation Mitochondria 0.6866 68.66%
OATP2B1 inhibitior - 0.7268 72.68%
OATP1B1 inhibitior + 0.9004 90.04%
OATP1B3 inhibitior + 0.9549 95.49%
MATE1 inhibitior - 0.8800 88.00%
OCT2 inhibitior - 0.9250 92.50%
BSEP inhibitior - 0.6492 64.92%
P-glycoprotein inhibitior - 0.7627 76.27%
P-glycoprotein substrate - 0.8049 80.49%
CYP3A4 substrate - 0.5671 56.71%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate + 0.4038 40.38%
CYP3A4 inhibition - 0.6784 67.84%
CYP2C9 inhibition + 0.6577 65.77%
CYP2C19 inhibition + 0.8685 86.85%
CYP2D6 inhibition + 0.5000 50.00%
CYP1A2 inhibition + 0.9616 96.16%
CYP2C8 inhibition + 0.6200 62.00%
CYP inhibitory promiscuity + 0.8999 89.99%
UGT catelyzed - 0.6000 60.00%
Carcinogenicity (binary) - 0.8708 87.08%
Carcinogenicity (trinary) Warning 0.3716 37.16%
Eye corrosion - 0.9822 98.22%
Eye irritation + 0.8307 83.07%
Skin irritation - 0.7039 70.39%
Skin corrosion - 0.9556 95.56%
Ames mutagenesis - 0.5900 59.00%
Human Ether-a-go-go-Related Gene inhibition - 0.5451 54.51%
Micronuclear + 0.8000 80.00%
Hepatotoxicity - 0.5750 57.50%
skin sensitisation - 0.7940 79.40%
Respiratory toxicity - 0.6667 66.67%
Reproductive toxicity + 0.7667 76.67%
Mitochondrial toxicity + 0.6125 61.25%
Nephrotoxicity - 0.8506 85.06%
Acute Oral Toxicity (c) III 0.5056 50.56%
Estrogen receptor binding + 0.8291 82.91%
Androgen receptor binding + 0.7987 79.87%
Thyroid receptor binding + 0.6671 66.71%
Glucocorticoid receptor binding + 0.7568 75.68%
Aromatase binding + 0.6800 68.00%
PPAR gamma + 0.5181 51.81%
Honey bee toxicity - 0.9191 91.91%
Biodegradation - 0.7000 70.00%
Crustacea aquatic toxicity - 0.5100 51.00%
Fish aquatic toxicity + 0.9228 92.28%

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 98.86% 91.11%
CHEMBL242 Q92731 Estrogen receptor beta 96.48% 98.35%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 91.46% 94.45%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 90.65% 94.00%
CHEMBL2535 P11166 Glucose transporter 86.52% 98.75%
CHEMBL3194 P02766 Transthyretin 85.90% 90.71%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 85.09% 95.56%
CHEMBL1806 P11388 DNA topoisomerase II alpha 84.98% 89.00%
CHEMBL1860 P10827 Thyroid hormone receptor alpha 84.84% 99.15%
CHEMBL2581 P07339 Cathepsin D 83.60% 98.95%
CHEMBL1293249 Q13887 Kruppel-like factor 5 82.42% 86.33%
CHEMBL3060 Q9Y345 Glycine transporter 2 81.55% 99.17%
CHEMBL3401 O75469 Pregnane X receptor 80.35% 94.73%
CHEMBL1163101 O75460 Serine/threonine-protein kinase/endoribonuclease IRE1 80.21% 98.11%

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.
Croptilon divaricatum
Sorbus domestica

Cross-Links

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PubChem 11777364
LOTUS LTS0103064
wikiData Q104403253