methyl 4-acetyloxy-8-hydroxy-6-methyl-9-oxo-4H-xanthene-4a-carboxylate

Details

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Internal ID b48925dd-1db8-490c-8fc8-8809c4054638
Taxonomy Organoheterocyclic compounds > Benzopyrans > 1-benzopyrans > Xanthones
IUPAC Name methyl 4-acetyloxy-8-hydroxy-6-methyl-9-oxo-4H-xanthene-4a-carboxylate
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C18H16O7/c1-9-7-12(20)15-13(8-9)25-18(17(22)23-3)11(16(15)21)5-4-6-14(18)24-10(2)19/h4-8,14,20H,1-3H3
InChI Key OOXFQLGEGVNXBG-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) 99.10 Ų
XlogP 2.60
Atomic LogP (AlogP) 1.62
H-Bond Acceptor 7
H-Bond Donor 1
Rotatable Bonds 2

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of methyl 4-acetyloxy-8-hydroxy-6-methyl-9-oxo-4H-xanthene-4a-carboxylate

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9841 98.41%
Caco-2 + 0.7495 74.95%
Blood Brain Barrier - 0.6500 65.00%
Human oral bioavailability + 0.5571 55.71%
Subcellular localzation Mitochondria 0.7105 71.05%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.8874 88.74%
OATP1B3 inhibitior + 0.9539 95.39%
MATE1 inhibitior - 0.9000 90.00%
OCT2 inhibitior - 0.9000 90.00%
BSEP inhibitior + 0.7151 71.51%
P-glycoprotein inhibitior - 0.5000 50.00%
P-glycoprotein substrate - 0.7515 75.15%
CYP3A4 substrate + 0.6114 61.14%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8777 87.77%
CYP3A4 inhibition - 0.6628 66.28%
CYP2C9 inhibition - 0.8793 87.93%
CYP2C19 inhibition - 0.6637 66.37%
CYP2D6 inhibition - 0.9054 90.54%
CYP1A2 inhibition - 0.6247 62.47%
CYP2C8 inhibition + 0.5605 56.05%
CYP inhibitory promiscuity - 0.6142 61.42%
UGT catelyzed + 0.6000 60.00%
Carcinogenicity (binary) - 0.9718 97.18%
Carcinogenicity (trinary) Danger 0.5113 51.13%
Eye corrosion - 0.9813 98.13%
Eye irritation - 0.5000 50.00%
Skin irritation - 0.6291 62.91%
Skin corrosion - 0.9579 95.79%
Ames mutagenesis - 0.6200 62.00%
Human Ether-a-go-go-Related Gene inhibition - 0.6825 68.25%
Micronuclear + 0.7159 71.59%
Hepatotoxicity + 0.5242 52.42%
skin sensitisation - 0.8025 80.25%
Respiratory toxicity + 0.5556 55.56%
Reproductive toxicity + 0.8556 85.56%
Mitochondrial toxicity + 0.6250 62.50%
Nephrotoxicity + 0.6442 64.42%
Acute Oral Toxicity (c) III 0.4865 48.65%
Estrogen receptor binding + 0.8380 83.80%
Androgen receptor binding + 0.7050 70.50%
Thyroid receptor binding - 0.5000 50.00%
Glucocorticoid receptor binding + 0.7335 73.35%
Aromatase binding - 0.5917 59.17%
PPAR gamma + 0.8187 81.87%
Honey bee toxicity - 0.7055 70.55%
Biodegradation - 0.9250 92.50%
Crustacea aquatic toxicity - 0.5700 57.00%
Fish aquatic toxicity + 0.9709 97.09%

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 98.75% 91.11%
CHEMBL4685 P14902 Indoleamine 2,3-dioxygenase 96.88% 96.38%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 96.06% 94.45%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 95.69% 85.14%
CHEMBL4481 P35228 Nitric oxide synthase, inducible 93.19% 94.80%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 92.55% 95.56%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 91.56% 99.23%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 90.56% 96.09%
CHEMBL340 P08684 Cytochrome P450 3A4 89.29% 91.19%
CHEMBL2581 P07339 Cathepsin D 89.02% 98.95%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 88.97% 94.00%
CHEMBL3401 O75469 Pregnane X receptor 88.22% 94.73%
CHEMBL1806 P11388 DNA topoisomerase II alpha 87.72% 89.00%
CHEMBL205 P00918 Carbonic anhydrase II 85.41% 98.44%
CHEMBL5966 P55899 IgG receptor FcRn large subunit p51 83.80% 90.93%
CHEMBL3864 Q06124 Protein-tyrosine phosphatase 2C 82.04% 94.42%
CHEMBL1293249 Q13887 Kruppel-like factor 5 81.06% 86.33%
CHEMBL2007 P16234 Platelet-derived growth factor receptor alpha 80.44% 91.07%

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 9830916
LOTUS LTS0010829
wikiData Q105195759