(3,6,7-Triacetyloxy-9-oxoxanthen-2-yl) acetate

Details

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Internal ID 811aa584-88c4-45d6-98e0-daf154df491d
Taxonomy Organoheterocyclic compounds > Benzopyrans > 1-benzopyrans > Xanthones
IUPAC Name (3,6,7-triacetyloxy-9-oxoxanthen-2-yl) acetate
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C21H16O10/c1-9(22)27-17-5-13-15(7-19(17)29-11(3)24)31-16-8-20(30-12(4)25)18(28-10(2)23)6-14(16)21(13)26/h5-8H,1-4H3
InChI Key GVZVCPHPBNOQLD-UHFFFAOYSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C21H16O10
Molecular Weight 428.30 g/mol
Exact Mass 428.07434670 g/mol
Topological Polar Surface Area (TPSA) 132.00 Ų
XlogP 2.00
Atomic LogP (AlogP) 2.65
H-Bond Acceptor 10
H-Bond Donor 0
Rotatable Bonds 4

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of (3,6,7-Triacetyloxy-9-oxoxanthen-2-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 + 0.9710 97.10%
Caco-2 - 0.5287 52.87%
Blood Brain Barrier - 0.6250 62.50%
Human oral bioavailability + 0.6143 61.43%
Subcellular localzation Mitochondria 0.5796 57.96%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9506 95.06%
OATP1B3 inhibitior + 0.9771 97.71%
MATE1 inhibitior - 0.9400 94.00%
OCT2 inhibitior - 0.9750 97.50%
BSEP inhibitior + 0.6184 61.84%
P-glycoprotein inhibitior + 0.8790 87.90%
P-glycoprotein substrate - 0.8550 85.50%
CYP3A4 substrate - 0.6214 62.14%
CYP2C9 substrate - 0.7948 79.48%
CYP2D6 substrate - 0.8827 88.27%
CYP3A4 inhibition - 0.8731 87.31%
CYP2C9 inhibition - 0.9475 94.75%
CYP2C19 inhibition - 0.9177 91.77%
CYP2D6 inhibition - 0.9817 98.17%
CYP1A2 inhibition + 0.9609 96.09%
CYP2C8 inhibition - 0.9250 92.50%
CYP inhibitory promiscuity - 0.6383 63.83%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 1.0000 100.00%
Carcinogenicity (trinary) Non-required 0.6036 60.36%
Eye corrosion - 0.9735 97.35%
Eye irritation - 0.6720 67.20%
Skin irritation - 0.7708 77.08%
Skin corrosion - 0.9799 97.99%
Ames mutagenesis - 0.6500 65.00%
Human Ether-a-go-go-Related Gene inhibition - 0.3679 36.79%
Micronuclear + 0.7759 77.59%
Hepatotoxicity + 0.5052 50.52%
skin sensitisation - 0.9180 91.80%
Respiratory toxicity + 0.6000 60.00%
Reproductive toxicity + 0.7556 75.56%
Mitochondrial toxicity - 0.5625 56.25%
Nephrotoxicity - 0.5694 56.94%
Acute Oral Toxicity (c) II 0.4736 47.36%
Estrogen receptor binding + 0.8018 80.18%
Androgen receptor binding + 0.7236 72.36%
Thyroid receptor binding + 0.5231 52.31%
Glucocorticoid receptor binding + 0.7129 71.29%
Aromatase binding - 0.5105 51.05%
PPAR gamma + 0.5461 54.61%
Honey bee toxicity - 0.8381 83.81%
Biodegradation - 0.8750 87.50%
Crustacea aquatic toxicity - 0.6849 68.49%
Fish aquatic toxicity + 0.9801 98.01%

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 96.11% 91.11%
CHEMBL2581 P07339 Cathepsin D 92.18% 98.95%
CHEMBL1806 P11388 DNA topoisomerase II alpha 90.91% 89.00%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 88.15% 94.00%
CHEMBL3060 Q9Y345 Glycine transporter 2 85.25% 99.17%
CHEMBL3401 O75469 Pregnane X receptor 84.18% 94.73%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 82.81% 95.56%
CHEMBL1293249 Q13887 Kruppel-like factor 5 81.30% 86.33%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 81.01% 94.45%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 80.95% 99.23%

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.
Tripterospermum lanceolatum

Cross-Links

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PubChem 10071226
LOTUS LTS0069986
wikiData Q105022069