Methyl 8-hydroxy-6-(2-hydroxyethyl)-4-methoxy-9-oxoxanthene-3-carboxylate

Details

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Internal ID cc4ac245-31d0-4229-8682-319ee30bcf73
Taxonomy Organoheterocyclic compounds > Benzopyrans > 1-benzopyrans > Xanthones
IUPAC Name methyl 8-hydroxy-6-(2-hydroxyethyl)-4-methoxy-9-oxoxanthene-3-carboxylate
SMILES (Canonical) COC1=C(C=CC2=C1OC3=CC(=CC(=C3C2=O)O)CCO)C(=O)OC
SMILES (Isomeric) COC1=C(C=CC2=C1OC3=CC(=CC(=C3C2=O)O)CCO)C(=O)OC
InChI InChI=1S/C18H16O7/c1-23-16-11(18(22)24-2)4-3-10-15(21)14-12(20)7-9(5-6-19)8-13(14)25-17(10)16/h3-4,7-8,19-20H,5-6H2,1-2H3
InChI Key IHQHGAQRDCZINY-UHFFFAOYSA-N
Popularity 1 reference in papers

Physical and Chemical Properties

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Molecular Formula C18H16O7
Molecular Weight 344.30 g/mol
Exact Mass 344.08960285 g/mol
Topological Polar Surface Area (TPSA) 102.00 Ų
XlogP 2.60
Atomic LogP (AlogP) 1.98
H-Bond Acceptor 7
H-Bond Donor 2
Rotatable Bonds 4

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of Methyl 8-hydroxy-6-(2-hydroxyethyl)-4-methoxy-9-oxoxanthene-3-carboxylate

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.7260 72.60%
Caco-2 - 0.5140 51.40%
Blood Brain Barrier - 0.7500 75.00%
Human oral bioavailability + 0.5857 58.57%
Subcellular localzation Mitochondria 0.7235 72.35%
OATP2B1 inhibitior - 0.5728 57.28%
OATP1B1 inhibitior + 0.8818 88.18%
OATP1B3 inhibitior + 0.9195 91.95%
MATE1 inhibitior - 0.8000 80.00%
OCT2 inhibitior - 0.8750 87.50%
BSEP inhibitior + 0.5659 56.59%
P-glycoprotein inhibitior - 0.6295 62.95%
P-glycoprotein substrate + 0.5000 50.00%
CYP3A4 substrate + 0.5848 58.48%
CYP2C9 substrate - 0.5587 55.87%
CYP2D6 substrate - 0.8330 83.30%
CYP3A4 inhibition - 0.7670 76.70%
CYP2C9 inhibition - 0.5764 57.64%
CYP2C19 inhibition - 0.8024 80.24%
CYP2D6 inhibition - 0.8685 86.85%
CYP1A2 inhibition - 0.5570 55.70%
CYP2C8 inhibition + 0.6844 68.44%
CYP inhibitory promiscuity - 0.7914 79.14%
UGT catelyzed - 0.6000 60.00%
Carcinogenicity (binary) - 0.9300 93.00%
Carcinogenicity (trinary) Non-required 0.7479 74.79%
Eye corrosion - 0.9876 98.76%
Eye irritation - 0.5931 59.31%
Skin irritation - 0.8366 83.66%
Skin corrosion - 0.9599 95.99%
Ames mutagenesis + 0.7136 71.36%
Human Ether-a-go-go-Related Gene inhibition - 0.6085 60.85%
Micronuclear - 0.5567 55.67%
Hepatotoxicity - 0.5560 55.60%
skin sensitisation - 0.9207 92.07%
Respiratory toxicity + 0.6000 60.00%
Reproductive toxicity + 0.8667 86.67%
Mitochondrial toxicity + 0.7375 73.75%
Nephrotoxicity - 0.7205 72.05%
Acute Oral Toxicity (c) III 0.6096 60.96%
Estrogen receptor binding + 0.8402 84.02%
Androgen receptor binding + 0.7671 76.71%
Thyroid receptor binding - 0.7203 72.03%
Glucocorticoid receptor binding + 0.7810 78.10%
Aromatase binding + 0.6057 60.57%
PPAR gamma + 0.8432 84.32%
Honey bee toxicity - 0.9002 90.02%
Biodegradation - 0.7000 70.00%
Crustacea aquatic toxicity - 0.7300 73.00%
Fish aquatic toxicity - 0.3785 37.85%

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 98.94% 91.11%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 97.64% 94.45%
CHEMBL2581 P07339 Cathepsin D 94.16% 98.95%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 93.60% 94.00%
CHEMBL2535 P11166 Glucose transporter 90.81% 98.75%
CHEMBL1293249 Q13887 Kruppel-like factor 5 90.81% 86.33%
CHEMBL3060 Q9Y345 Glycine transporter 2 90.34% 99.17%
CHEMBL3401 O75469 Pregnane X receptor 88.52% 94.73%
CHEMBL1951 P21397 Monoamine oxidase A 85.65% 91.49%
CHEMBL3864 Q06124 Protein-tyrosine phosphatase 2C 84.90% 94.42%
CHEMBL2373 P21730 C5a anaphylatoxin chemotactic receptor 84.68% 92.62%
CHEMBL3091268 Q92753 Nuclear receptor ROR-beta 84.19% 95.50%
CHEMBL1806 P11388 DNA topoisomerase II alpha 82.56% 89.00%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 80.59% 95.56%
CHEMBL4793 Q86TI2 Dipeptidyl peptidase IX 80.12% 96.95%
CHEMBL4016 P42262 Glutamate receptor ionotropic, AMPA 2 80.02% 86.92%

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 163192804
LOTUS LTS0143732
wikiData Q105113194