9-Hydroxyeriobofuran

Details

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Internal ID bbf7846d-9fb5-41cf-94d5-2f378e9dc70f
Taxonomy Organoheterocyclic compounds > Benzofurans > Dibenzofurans
IUPAC Name 6,8-dimethoxydibenzofuran-1,7-diol
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C14H12O5/c1-17-10-6-7-11-8(15)4-3-5-9(11)19-13(7)14(18-2)12(10)16/h3-6,15-16H,1-2H3
InChI Key VQWSIJRLYROCFW-UHFFFAOYSA-N
Popularity 5 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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167278-41-3
6,8-dimethoxydibenzofuran-1,7-diol
CHEMBL1080657
HY-N9084
AKOS040761294
1,7-dihydroxy-6,8-dimethoxydibenzofuran
CS-0158670

2D Structure

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2D Structure of 9-Hydroxyeriobofuran

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 - 0.5529 55.29%
Blood Brain Barrier - 0.5250 52.50%
Human oral bioavailability + 0.6286 62.86%
Subcellular localzation Mitochondria 0.6866 68.66%
OATP2B1 inhibitior - 0.7249 72.49%
OATP1B1 inhibitior + 0.9169 91.69%
OATP1B3 inhibitior + 0.9549 95.49%
MATE1 inhibitior - 0.8800 88.00%
OCT2 inhibitior - 0.9250 92.50%
BSEP inhibitior - 0.6622 66.22%
P-glycoprotein inhibitior - 0.7149 71.49%
P-glycoprotein substrate - 0.8234 82.34%
CYP3A4 substrate + 0.5085 50.85%
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 + 0.7111 71.11%
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 + 0.8197 81.97%
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 - 0.7349 73.49%
Micronuclear + 0.8000 80.00%
Hepatotoxicity - 0.5750 57.50%
skin sensitisation - 0.7940 79.40%
Respiratory toxicity - 0.6000 60.00%
Reproductive toxicity + 0.7667 76.67%
Mitochondrial toxicity + 0.6125 61.25%
Nephrotoxicity - 0.8901 89.01%
Acute Oral Toxicity (c) III 0.5056 50.56%
Estrogen receptor binding + 0.8403 84.03%
Androgen receptor binding + 0.6779 67.79%
Thyroid receptor binding + 0.6711 67.11%
Glucocorticoid receptor binding + 0.8159 81.59%
Aromatase binding + 0.7243 72.43%
PPAR gamma + 0.7688 76.88%
Honey bee toxicity - 0.9317 93.17%
Biodegradation - 0.8000 80.00%
Crustacea aquatic toxicity + 0.5751 57.51%
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 99.20% 91.11%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 94.48% 94.00%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 92.49% 95.56%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 92.13% 94.45%
CHEMBL1806 P11388 DNA topoisomerase II alpha 90.72% 89.00%
CHEMBL2535 P11166 Glucose transporter 89.88% 98.75%
CHEMBL4306 P22460 Voltage-gated potassium channel subunit Kv1.5 88.68% 94.03%
CHEMBL1293249 Q13887 Kruppel-like factor 5 88.67% 86.33%
CHEMBL1907 P15144 Aminopeptidase N 87.77% 93.31%
CHEMBL1163101 O75460 Serine/threonine-protein kinase/endoribonuclease IRE1 85.41% 98.11%
CHEMBL2581 P07339 Cathepsin D 85.33% 98.95%
CHEMBL241 Q14432 Phosphodiesterase 3A 84.88% 92.94%
CHEMBL2373 P21730 C5a anaphylatoxin chemotactic receptor 84.42% 92.62%
CHEMBL3192 Q9BY41 Histone deacetylase 8 84.29% 93.99%
CHEMBL1860 P10827 Thyroid hormone receptor alpha 83.01% 99.15%
CHEMBL3060 Q9Y345 Glycine transporter 2 82.22% 99.17%
CHEMBL1951 P21397 Monoamine oxidase A 80.95% 91.49%

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.
Berberis koreana
Pyracantha coccinea

Cross-Links

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PubChem 46879746
LOTUS LTS0188569
wikiData Q104401145