Methyl 4-hydroxy-6-(2-hydroxyethyl)-8-methoxy-9-oxoxanthene-1-carboxylate

Details

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Internal ID a7cb066f-b4ef-49b9-8dbd-e826410518ff
Taxonomy Organoheterocyclic compounds > Benzopyrans > 1-benzopyrans > Xanthones
IUPAC Name methyl 4-hydroxy-6-(2-hydroxyethyl)-8-methoxy-9-oxoxanthene-1-carboxylate
SMILES (Canonical) COC1=CC(=CC2=C1C(=O)C3=C(C=CC(=C3O2)O)C(=O)OC)CCO
SMILES (Isomeric) COC1=CC(=CC2=C1C(=O)C3=C(C=CC(=C3O2)O)C(=O)OC)CCO
InChI InChI=1S/C18H16O7/c1-23-12-7-9(5-6-19)8-13-15(12)16(21)14-10(18(22)24-2)3-4-11(20)17(14)25-13/h3-4,7-8,19-20H,5-6H2,1-2H3
InChI Key HPYOCWDHQYRQLJ-UHFFFAOYSA-N
Popularity 0 references 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 2.00
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 4-hydroxy-6-(2-hydroxyethyl)-8-methoxy-9-oxoxanthene-1-carboxylate

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.8901 89.01%
Caco-2 + 0.5726 57.26%
Blood Brain Barrier - 0.7750 77.50%
Human oral bioavailability + 0.5429 54.29%
Subcellular localzation Mitochondria 0.7417 74.17%
OATP2B1 inhibitior - 0.5697 56.97%
OATP1B1 inhibitior + 0.8905 89.05%
OATP1B3 inhibitior + 0.8658 86.58%
MATE1 inhibitior - 0.8400 84.00%
OCT2 inhibitior - 0.9000 90.00%
BSEP inhibitior - 0.6165 61.65%
P-glycoprotein inhibitior - 0.5690 56.90%
P-glycoprotein substrate - 0.5615 56.15%
CYP3A4 substrate + 0.5841 58.41%
CYP2C9 substrate - 0.7901 79.01%
CYP2D6 substrate - 0.7938 79.38%
CYP3A4 inhibition - 0.7443 74.43%
CYP2C9 inhibition - 0.8251 82.51%
CYP2C19 inhibition - 0.8392 83.92%
CYP2D6 inhibition - 0.8676 86.76%
CYP1A2 inhibition - 0.6868 68.68%
CYP2C8 inhibition + 0.8011 80.11%
CYP inhibitory promiscuity - 0.8363 83.63%
UGT catelyzed + 0.7000 70.00%
Carcinogenicity (binary) - 0.9300 93.00%
Carcinogenicity (trinary) Non-required 0.7190 71.90%
Eye corrosion - 0.9767 97.67%
Eye irritation - 0.5524 55.24%
Skin irritation - 0.8587 85.87%
Skin corrosion - 0.9647 96.47%
Ames mutagenesis + 0.7136 71.36%
Human Ether-a-go-go-Related Gene inhibition - 0.5181 51.81%
Micronuclear - 0.5767 57.67%
Hepatotoxicity - 0.6330 63.30%
skin sensitisation - 0.9259 92.59%
Respiratory toxicity + 0.5667 56.67%
Reproductive toxicity + 0.7333 73.33%
Mitochondrial toxicity + 0.6000 60.00%
Nephrotoxicity - 0.6188 61.88%
Acute Oral Toxicity (c) III 0.7252 72.52%
Estrogen receptor binding + 0.9248 92.48%
Androgen receptor binding + 0.7524 75.24%
Thyroid receptor binding - 0.6618 66.18%
Glucocorticoid receptor binding + 0.8324 83.24%
Aromatase binding + 0.8257 82.57%
PPAR gamma + 0.8059 80.59%
Honey bee toxicity - 0.8962 89.62%
Biodegradation - 0.6250 62.50%
Crustacea aquatic toxicity - 0.7366 73.66%
Fish aquatic toxicity - 0.6072 60.72%

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 98.81% 91.11%
CHEMBL4040 P28482 MAP kinase ERK2 95.08% 83.82%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 94.69% 94.45%
CHEMBL2581 P07339 Cathepsin D 93.47% 98.95%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 92.73% 94.00%
CHEMBL1293249 Q13887 Kruppel-like factor 5 91.68% 86.33%
CHEMBL2535 P11166 Glucose transporter 90.76% 98.75%
CHEMBL3060 Q9Y345 Glycine transporter 2 90.49% 99.17%
CHEMBL335 P18031 Protein-tyrosine phosphatase 1B 89.32% 95.17%
CHEMBL3401 O75469 Pregnane X receptor 85.98% 94.73%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 85.88% 96.09%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 85.50% 85.14%
CHEMBL2373 P21730 C5a anaphylatoxin chemotactic receptor 84.80% 92.62%
CHEMBL3864 Q06124 Protein-tyrosine phosphatase 2C 84.64% 94.42%
CHEMBL5845 P23415 Glycine receptor subunit alpha-1 81.87% 90.71%
CHEMBL3091268 Q92753 Nuclear receptor ROR-beta 81.24% 95.50%
CHEMBL1860 P10827 Thyroid hormone receptor alpha 80.77% 99.15%
CHEMBL4208 P20618 Proteasome component C5 80.09% 90.00%

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.
Ilex cornuta

Cross-Links

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PubChem 71726159
NPASS NPC171737