7-Hydroxy-4-(4-hydroxy-3-methoxyphenyl)-8-methoxydibenzofuran-2-carboxylic acid

Details

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Internal ID aace538e-d24d-48dc-8cdd-dc58bd3e5abd
Taxonomy Organoheterocyclic compounds > Benzofurans > Phenylbenzofurans
IUPAC Name 7-hydroxy-4-(4-hydroxy-3-methoxyphenyl)-8-methoxydibenzofuran-2-carboxylic acid
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C21H16O7/c1-26-18-7-10(3-4-15(18)22)12-5-11(21(24)25)6-14-13-8-19(27-2)16(23)9-17(13)28-20(12)14/h3-9,22-23H,1-2H3,(H,24,25)
InChI Key DJFAUDCMYUMUNB-UHFFFAOYSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C21H16O7
Molecular Weight 380.30 g/mol
Exact Mass 380.08960285 g/mol
Topological Polar Surface Area (TPSA) 109.00 Ų
XlogP 4.00
Atomic LogP (AlogP) 4.38
H-Bond Acceptor 6
H-Bond Donor 3
Rotatable Bonds 4

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 7-Hydroxy-4-(4-hydroxy-3-methoxyphenyl)-8-methoxydibenzofuran-2-carboxylic acid

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9862 98.62%
Caco-2 + 0.4946 49.46%
Blood Brain Barrier - 0.7000 70.00%
Human oral bioavailability + 0.6286 62.86%
Subcellular localzation Mitochondria 0.7827 78.27%
OATP2B1 inhibitior + 0.5685 56.85%
OATP1B1 inhibitior + 0.9360 93.60%
OATP1B3 inhibitior - 0.2375 23.75%
MATE1 inhibitior - 0.9600 96.00%
OCT2 inhibitior - 0.9750 97.50%
BSEP inhibitior - 0.4677 46.77%
P-glycoprotein inhibitior + 0.7066 70.66%
P-glycoprotein substrate - 0.8003 80.03%
CYP3A4 substrate + 0.5062 50.62%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8464 84.64%
CYP3A4 inhibition - 0.5593 55.93%
CYP2C9 inhibition + 0.8614 86.14%
CYP2C19 inhibition + 0.7919 79.19%
CYP2D6 inhibition - 0.7516 75.16%
CYP1A2 inhibition + 0.5989 59.89%
CYP2C8 inhibition + 0.8646 86.46%
CYP inhibitory promiscuity + 0.8130 81.30%
UGT catelyzed + 0.7000 70.00%
Carcinogenicity (binary) - 0.9300 93.00%
Carcinogenicity (trinary) Non-required 0.3757 37.57%
Eye corrosion - 0.9859 98.59%
Eye irritation - 0.6782 67.82%
Skin irritation - 0.7336 73.36%
Skin corrosion - 0.9720 97.20%
Ames mutagenesis - 0.5800 58.00%
Human Ether-a-go-go-Related Gene inhibition - 0.6535 65.35%
Micronuclear + 0.9300 93.00%
Hepatotoxicity - 0.6250 62.50%
skin sensitisation - 0.9131 91.31%
Respiratory toxicity - 0.6000 60.00%
Reproductive toxicity + 0.7444 74.44%
Mitochondrial toxicity + 0.6500 65.00%
Nephrotoxicity - 0.7092 70.92%
Acute Oral Toxicity (c) II 0.4402 44.02%
Estrogen receptor binding + 0.8022 80.22%
Androgen receptor binding + 0.8467 84.67%
Thyroid receptor binding + 0.5156 51.56%
Glucocorticoid receptor binding + 0.8480 84.80%
Aromatase binding + 0.6106 61.06%
PPAR gamma + 0.7658 76.58%
Honey bee toxicity - 0.8695 86.95%
Biodegradation - 0.9000 90.00%
Crustacea aquatic toxicity - 0.8200 82.00%
Fish aquatic toxicity + 0.9766 97.66%

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
CHEMBL3194 P02766 Transthyretin 95.02% 90.71%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 94.03% 91.11%
CHEMBL1293249 Q13887 Kruppel-like factor 5 93.27% 86.33%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 92.45% 95.56%
CHEMBL2581 P07339 Cathepsin D 92.32% 98.95%
CHEMBL3060 Q9Y345 Glycine transporter 2 91.83% 99.17%
CHEMBL1293277 O15118 Niemann-Pick C1 protein 90.27% 81.11%
CHEMBL5284 Q96RR4 CaM-kinase kinase beta 90.06% 89.23%
CHEMBL1811 P34995 Prostanoid EP1 receptor 89.75% 95.71%
CHEMBL1806 P11388 DNA topoisomerase II alpha 89.68% 89.00%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 88.98% 99.23%
CHEMBL1860 P10827 Thyroid hormone receptor alpha 88.45% 99.15%
CHEMBL1255126 O15151 Protein Mdm4 87.80% 90.20%
CHEMBL1293294 P51151 Ras-related protein Rab-9A 87.77% 87.67%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 87.43% 94.00%
CHEMBL3091268 Q92753 Nuclear receptor ROR-beta 85.63% 95.50%
CHEMBL1907 P15144 Aminopeptidase N 84.48% 93.31%
CHEMBL340 P08684 Cytochrome P450 3A4 82.48% 91.19%
CHEMBL1163101 O75460 Serine/threonine-protein kinase/endoribonuclease IRE1 82.39% 98.11%
CHEMBL2535 P11166 Glucose transporter 82.11% 98.75%
CHEMBL2085 P14174 Macrophage migration inhibitory factor 81.50% 80.78%
CHEMBL241 Q14432 Phosphodiesterase 3A 81.07% 92.94%
CHEMBL3864 Q06124 Protein-tyrosine phosphatase 2C 80.72% 94.42%

Plants that contains it

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Below are displayed all the plants proven (via scientific papers) to contain this compound!
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There are no matching plants.

Cross-Links

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PubChem 24770237
LOTUS LTS0180357
wikiData Q77502163