1,5-Dihydroxy-3-(2-oxopropyl)-6-methoxycarbonylxanthone

Details

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Internal ID fdd72014-0668-4901-a40a-dea2a101a797
Taxonomy Organoheterocyclic compounds > Benzopyrans > 1-benzopyrans > Xanthones
IUPAC Name methyl 4,8-dihydroxy-9-oxo-6-(2-oxopropyl)xanthene-3-carboxylate
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C18H14O7/c1-8(19)5-9-6-12(20)14-13(7-9)25-17-10(15(14)21)3-4-11(16(17)22)18(23)24-2/h3-4,6-7,20,22H,5H2,1-2H3
InChI Key KIJTTYRRBNSKMV-UHFFFAOYSA-N
Popularity 3 references in papers

Physical and Chemical Properties

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Molecular Formula C18H14O7
Molecular Weight 342.30 g/mol
Exact Mass 342.07395278 g/mol
Topological Polar Surface Area (TPSA) 110.00 Ų
XlogP 2.80
Atomic LogP (AlogP) 2.28
H-Bond Acceptor 7
H-Bond Donor 2
Rotatable Bonds 3

Synonyms

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RefChem:73479
CHEBI:203066
methyl 4,8-dihydroxy-9-oxo-6-(2-oxopropyl)xanthene-3-carboxylate

2D Structure

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2D Structure of 1,5-Dihydroxy-3-(2-oxopropyl)-6-methoxycarbonylxanthone

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.7617 76.17%
Caco-2 - 0.6500 65.00%
Blood Brain Barrier - 0.8250 82.50%
Human oral bioavailability - 0.5286 52.86%
Subcellular localzation Mitochondria 0.6942 69.42%
OATP2B1 inhibitior - 0.7034 70.34%
OATP1B1 inhibitior + 0.8537 85.37%
OATP1B3 inhibitior + 0.9294 92.94%
MATE1 inhibitior - 0.9200 92.00%
OCT2 inhibitior - 0.9250 92.50%
BSEP inhibitior - 0.6212 62.12%
P-glycoprotein inhibitior - 0.6828 68.28%
P-glycoprotein substrate - 0.5202 52.02%
CYP3A4 substrate + 0.5837 58.37%
CYP2C9 substrate + 0.6558 65.58%
CYP2D6 substrate - 0.8669 86.69%
CYP3A4 inhibition - 0.8742 87.42%
CYP2C9 inhibition + 0.5489 54.89%
CYP2C19 inhibition - 0.7751 77.51%
CYP2D6 inhibition - 0.6948 69.48%
CYP1A2 inhibition + 0.5487 54.87%
CYP2C8 inhibition + 0.5988 59.88%
CYP inhibitory promiscuity - 0.7257 72.57%
UGT catelyzed + 0.6000 60.00%
Carcinogenicity (binary) - 1.0000 100.00%
Carcinogenicity (trinary) Non-required 0.6372 63.72%
Eye corrosion - 0.9854 98.54%
Eye irritation + 0.5518 55.18%
Skin irritation - 0.8113 81.13%
Skin corrosion - 0.9582 95.82%
Ames mutagenesis + 0.6936 69.36%
Human Ether-a-go-go-Related Gene inhibition - 0.5580 55.80%
Micronuclear + 0.7100 71.00%
Hepatotoxicity + 0.6296 62.96%
skin sensitisation - 0.9308 93.08%
Respiratory toxicity + 0.6667 66.67%
Reproductive toxicity + 0.9778 97.78%
Mitochondrial toxicity + 0.8250 82.50%
Nephrotoxicity - 0.7700 77.00%
Acute Oral Toxicity (c) I 0.4685 46.85%
Estrogen receptor binding + 0.8078 80.78%
Androgen receptor binding + 0.7629 76.29%
Thyroid receptor binding - 0.7569 75.69%
Glucocorticoid receptor binding + 0.8210 82.10%
Aromatase binding - 0.6180 61.80%
PPAR gamma + 0.8258 82.58%
Honey bee toxicity - 0.8725 87.25%
Biodegradation - 0.8000 80.00%
Crustacea aquatic toxicity - 0.6600 66.00%
Fish aquatic toxicity + 0.9468 94.68%

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 99.41% 91.11%
CHEMBL2581 P07339 Cathepsin D 98.20% 98.95%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 98.02% 94.45%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 95.27% 94.00%
CHEMBL1951 P21397 Monoamine oxidase A 94.37% 91.49%
CHEMBL3401 O75469 Pregnane X receptor 91.69% 94.73%
CHEMBL3864 Q06124 Protein-tyrosine phosphatase 2C 87.82% 94.42%
CHEMBL1293249 Q13887 Kruppel-like factor 5 87.76% 86.33%
CHEMBL1293267 Q9HC97 G-protein coupled receptor 35 87.39% 89.34%
CHEMBL3060 Q9Y345 Glycine transporter 2 86.90% 99.17%
CHEMBL1806 P11388 DNA topoisomerase II alpha 85.52% 89.00%
CHEMBL3091268 Q92753 Nuclear receptor ROR-beta 85.43% 95.50%
CHEMBL2535 P11166 Glucose transporter 84.98% 98.75%
CHEMBL5409 Q8TDU6 G-protein coupled bile acid receptor 1 81.61% 93.65%
CHEMBL5608 Q16288 NT-3 growth factor receptor 81.60% 95.89%

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 72710899
LOTUS LTS0074350
wikiData Q77375143