(6-Acetyloxy-1-hydroxy-7-methoxy-9-oxoxanthen-3-yl) acetate

Details

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Internal ID ec5d8c51-7d7c-46ad-8acd-a5f6700cb89b
Taxonomy Organoheterocyclic compounds > Benzopyrans > 1-benzopyrans > Xanthones
IUPAC Name (6-acetyloxy-1-hydroxy-7-methoxy-9-oxoxanthen-3-yl) acetate
SMILES (Canonical) CC(=O)OC1=CC(=C2C(=C1)OC3=CC(=C(C=C3C2=O)OC)OC(=O)C)O
SMILES (Isomeric) CC(=O)OC1=CC(=C2C(=C1)OC3=CC(=C(C=C3C2=O)OC)OC(=O)C)O
InChI InChI=1S/C18H14O8/c1-8(19)24-10-4-12(21)17-16(5-10)26-13-7-15(25-9(2)20)14(23-3)6-11(13)18(17)22/h4-7,21H,1-3H3
InChI Key RAWBNUCTHOCPPS-UHFFFAOYSA-N
Popularity 1 reference in papers

Physical and Chemical Properties

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Molecular Formula C18H14O8
Molecular Weight 358.30 g/mol
Exact Mass 358.06886740 g/mol
Topological Polar Surface Area (TPSA) 108.00 Ų
XlogP 2.60
Atomic LogP (AlogP) 2.51
H-Bond Acceptor 8
H-Bond Donor 1
Rotatable Bonds 3

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of (6-Acetyloxy-1-hydroxy-7-methoxy-9-oxoxanthen-3-yl) acetate

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9402 94.02%
Caco-2 + 0.6296 62.96%
Blood Brain Barrier - 0.7500 75.00%
Human oral bioavailability - 0.5429 54.29%
Subcellular localzation Mitochondria 0.6634 66.34%
OATP2B1 inhibitior - 0.7166 71.66%
OATP1B1 inhibitior + 0.9223 92.23%
OATP1B3 inhibitior + 0.9524 95.24%
MATE1 inhibitior - 0.8800 88.00%
OCT2 inhibitior - 0.9750 97.50%
BSEP inhibitior - 0.6548 65.48%
P-glycoprotein inhibitior - 0.4576 45.76%
P-glycoprotein substrate - 0.6443 64.43%
CYP3A4 substrate + 0.5513 55.13%
CYP2C9 substrate + 0.6063 60.63%
CYP2D6 substrate - 0.8758 87.58%
CYP3A4 inhibition - 0.9093 90.93%
CYP2C9 inhibition - 0.9808 98.08%
CYP2C19 inhibition - 0.9780 97.80%
CYP2D6 inhibition - 0.9549 95.49%
CYP1A2 inhibition + 0.7882 78.82%
CYP2C8 inhibition + 0.4544 45.44%
CYP inhibitory promiscuity - 0.8585 85.85%
UGT catelyzed - 0.5000 50.00%
Carcinogenicity (binary) - 0.9900 99.00%
Carcinogenicity (trinary) Non-required 0.5728 57.28%
Eye corrosion - 0.9777 97.77%
Eye irritation - 0.6250 62.50%
Skin irritation - 0.7482 74.82%
Skin corrosion - 0.9804 98.04%
Ames mutagenesis + 0.6936 69.36%
Human Ether-a-go-go-Related Gene inhibition - 0.5466 54.66%
Micronuclear + 0.8359 83.59%
Hepatotoxicity - 0.6500 65.00%
skin sensitisation - 0.9484 94.84%
Respiratory toxicity + 0.6222 62.22%
Reproductive toxicity + 0.8333 83.33%
Mitochondrial toxicity + 0.5625 56.25%
Nephrotoxicity - 0.5891 58.91%
Acute Oral Toxicity (c) II 0.6878 68.78%
Estrogen receptor binding + 0.8378 83.78%
Androgen receptor binding + 0.6896 68.96%
Thyroid receptor binding + 0.5467 54.67%
Glucocorticoid receptor binding + 0.8365 83.65%
Aromatase binding + 0.6355 63.55%
PPAR gamma + 0.6935 69.35%
Honey bee toxicity - 0.7336 73.36%
Biodegradation - 0.7250 72.50%
Crustacea aquatic toxicity - 0.5849 58.49%
Fish aquatic toxicity + 0.9427 94.27%

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 98.78% 91.11%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 94.48% 94.00%
CHEMBL1806 P11388 DNA topoisomerase II alpha 93.87% 89.00%
CHEMBL3060 Q9Y345 Glycine transporter 2 92.79% 99.17%
CHEMBL2581 P07339 Cathepsin D 92.68% 98.95%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 90.56% 95.56%
CHEMBL2535 P11166 Glucose transporter 89.50% 98.75%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 88.46% 94.45%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 87.92% 85.14%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 87.86% 99.23%
CHEMBL1293249 Q13887 Kruppel-like factor 5 85.15% 86.33%
CHEMBL3401 O75469 Pregnane X receptor 82.82% 94.73%
CHEMBL340 P08684 Cytochrome P450 3A4 82.33% 91.19%
CHEMBL3194 P02766 Transthyretin 81.81% 90.71%
CHEMBL241 Q14432 Phosphodiesterase 3A 81.70% 92.94%
CHEMBL2373 P21730 C5a anaphylatoxin chemotactic receptor 81.37% 92.62%

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.
Lawsonia inermis

Cross-Links

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PubChem 69866098
LOTUS LTS0107768
wikiData Q105232909