1,4,7-Trimethoxydibenzofuran-3-ol

Details

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Internal ID 47a0b5ef-f95e-48d8-9eae-7fefe96eb4dd
Taxonomy Organoheterocyclic compounds > Benzofurans > Dibenzofurans
IUPAC Name 1,4,7-trimethoxydibenzofuran-3-ol
SMILES (Canonical) COC1=CC2=C(C=C1)C3=C(C=C(C(=C3O2)OC)O)OC
SMILES (Isomeric) COC1=CC2=C(C=C1)C3=C(C=C(C(=C3O2)OC)O)OC
InChI InChI=1S/C15H14O5/c1-17-8-4-5-9-11(6-8)20-15-13(9)12(18-2)7-10(16)14(15)19-3/h4-7,16H,1-3H3
InChI Key ZAALTNUGBSMZBE-UHFFFAOYSA-N
Popularity 1 reference in papers

Physical and Chemical Properties

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Molecular Formula C15H14O5
Molecular Weight 274.27 g/mol
Exact Mass 274.08412354 g/mol
Topological Polar Surface Area (TPSA) 61.10 Ų
XlogP 3.20
Atomic LogP (AlogP) 3.32
H-Bond Acceptor 5
H-Bond Donor 1
Rotatable Bonds 3

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 1,4,7-Trimethoxydibenzofuran-3-ol

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9900 99.00%
Caco-2 + 0.8310 83.10%
Blood Brain Barrier - 0.6250 62.50%
Human oral bioavailability + 0.6714 67.14%
Subcellular localzation Mitochondria 0.6304 63.04%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9345 93.45%
OATP1B3 inhibitior + 0.9646 96.46%
MATE1 inhibitior - 0.8800 88.00%
OCT2 inhibitior - 0.9000 90.00%
BSEP inhibitior - 0.5565 55.65%
P-glycoprotein inhibitior - 0.7393 73.93%
P-glycoprotein substrate - 0.8231 82.31%
CYP3A4 substrate - 0.5196 51.96%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate + 0.4038 40.38%
CYP3A4 inhibition - 0.6640 66.40%
CYP2C9 inhibition - 0.7904 79.04%
CYP2C19 inhibition + 0.6728 67.28%
CYP2D6 inhibition - 0.7457 74.57%
CYP1A2 inhibition + 0.9562 95.62%
CYP2C8 inhibition + 0.6048 60.48%
CYP inhibitory promiscuity + 0.7987 79.87%
UGT catelyzed + 0.6000 60.00%
Carcinogenicity (binary) - 0.8908 89.08%
Carcinogenicity (trinary) Warning 0.3481 34.81%
Eye corrosion - 0.9841 98.41%
Eye irritation + 0.8240 82.40%
Skin irritation - 0.7620 76.20%
Skin corrosion - 0.9801 98.01%
Ames mutagenesis + 0.5800 58.00%
Human Ether-a-go-go-Related Gene inhibition - 0.4287 42.87%
Micronuclear + 0.7259 72.59%
Hepatotoxicity - 0.7060 70.60%
skin sensitisation - 0.8285 82.85%
Respiratory toxicity - 0.8000 80.00%
Reproductive toxicity + 0.7444 74.44%
Mitochondrial toxicity + 0.5875 58.75%
Nephrotoxicity - 0.8647 86.47%
Acute Oral Toxicity (c) II 0.5356 53.56%
Estrogen receptor binding + 0.8225 82.25%
Androgen receptor binding + 0.8068 80.68%
Thyroid receptor binding + 0.6773 67.73%
Glucocorticoid receptor binding + 0.7958 79.58%
Aromatase binding + 0.8039 80.39%
PPAR gamma + 0.7300 73.00%
Honey bee toxicity - 0.9147 91.47%
Biodegradation - 0.7750 77.50%
Crustacea aquatic toxicity + 0.6251 62.51%
Fish aquatic toxicity + 0.9220 92.20%

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 99.12% 91.11%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 95.38% 94.00%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 90.50% 95.56%
CHEMBL1860 P10827 Thyroid hormone receptor alpha 90.47% 99.15%
CHEMBL2535 P11166 Glucose transporter 88.04% 98.75%
CHEMBL3060 Q9Y345 Glycine transporter 2 87.80% 99.17%
CHEMBL1806 P11388 DNA topoisomerase II alpha 86.95% 89.00%
CHEMBL4208 P20618 Proteasome component C5 86.72% 90.00%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 86.46% 94.45%
CHEMBL3194 P02766 Transthyretin 85.84% 90.71%
CHEMBL3192 Q9BY41 Histone deacetylase 8 83.76% 93.99%
CHEMBL1293249 Q13887 Kruppel-like factor 5 83.60% 86.33%
CHEMBL4306 P22460 Voltage-gated potassium channel subunit Kv1.5 83.35% 94.03%
CHEMBL2373 P21730 C5a anaphylatoxin chemotactic receptor 83.28% 92.62%
CHEMBL1907 P15144 Aminopeptidase N 82.13% 93.31%
CHEMBL3401 O75469 Pregnane X receptor 81.67% 94.73%
CHEMBL3438 Q05513 Protein kinase C zeta 80.77% 88.48%
CHEMBL225 P28335 Serotonin 2c (5-HT2c) receptor 80.50% 89.62%

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.
Hypericum revolutum

Cross-Links

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PubChem 42611453
LOTUS LTS0195948
wikiData Q105369680