1,3,5,8-Tetramethoxyxanthen-9-one

Details

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Internal ID 187c4bf6-aa1f-49a2-adea-5787c2447701
Taxonomy Organoheterocyclic compounds > Benzopyrans > 1-benzopyrans > Xanthones
IUPAC Name 1,3,5,8-tetramethoxyxanthen-9-one
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C17H16O6/c1-19-9-7-12(22-4)14-13(8-9)23-17-11(21-3)6-5-10(20-2)15(17)16(14)18/h5-8H,1-4H3
InChI Key YUEQENCEVQAYFU-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C17H16O6
Molecular Weight 316.30 g/mol
Exact Mass 316.09468823 g/mol
Topological Polar Surface Area (TPSA) 63.20 Ų
XlogP 2.80
Atomic LogP (AlogP) 2.98
H-Bond Acceptor 6
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 1,3,5,8-Tetramethoxyxanthen-9-one

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9873 98.73%
Caco-2 + 0.9144 91.44%
Blood Brain Barrier - 0.6000 60.00%
Human oral bioavailability + 0.7000 70.00%
Subcellular localzation Mitochondria 0.5667 56.67%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9463 94.63%
OATP1B3 inhibitior + 0.9791 97.91%
MATE1 inhibitior - 0.9600 96.00%
OCT2 inhibitior - 0.9750 97.50%
BSEP inhibitior + 0.6732 67.32%
P-glycoprotein inhibitior + 0.7643 76.43%
P-glycoprotein substrate - 0.9157 91.57%
CYP3A4 substrate - 0.5457 54.57%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.7654 76.54%
CYP3A4 inhibition + 0.6462 64.62%
CYP2C9 inhibition - 0.9486 94.86%
CYP2C19 inhibition + 0.5978 59.78%
CYP2D6 inhibition - 0.8123 81.23%
CYP1A2 inhibition + 0.9723 97.23%
CYP2C8 inhibition - 0.7094 70.94%
CYP inhibitory promiscuity + 0.5998 59.98%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.9600 96.00%
Carcinogenicity (trinary) Non-required 0.5404 54.04%
Eye corrosion - 0.9027 90.27%
Eye irritation + 0.7989 79.89%
Skin irritation - 0.7224 72.24%
Skin corrosion - 0.9904 99.04%
Ames mutagenesis + 0.7800 78.00%
Human Ether-a-go-go-Related Gene inhibition + 0.6498 64.98%
Micronuclear + 0.7700 77.00%
Hepatotoxicity - 0.6415 64.15%
skin sensitisation - 0.9228 92.28%
Respiratory toxicity - 0.6000 60.00%
Reproductive toxicity + 0.7000 70.00%
Mitochondrial toxicity - 0.6000 60.00%
Nephrotoxicity - 0.6026 60.26%
Acute Oral Toxicity (c) II 0.6438 64.38%
Estrogen receptor binding + 0.8613 86.13%
Androgen receptor binding + 0.8279 82.79%
Thyroid receptor binding + 0.6926 69.26%
Glucocorticoid receptor binding + 0.8527 85.27%
Aromatase binding + 0.8178 81.78%
PPAR gamma + 0.7390 73.90%
Honey bee toxicity - 0.8897 88.97%
Biodegradation - 0.8750 87.50%
Crustacea aquatic toxicity + 0.6200 62.00%
Fish aquatic toxicity + 0.7747 77.47%

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
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 93.84% 94.00%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 93.44% 95.56%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 89.36% 91.11%
CHEMBL1293249 Q13887 Kruppel-like factor 5 87.70% 86.33%
CHEMBL2535 P11166 Glucose transporter 86.03% 98.75%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 85.65% 96.00%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 84.67% 94.45%
CHEMBL2581 P07339 Cathepsin D 84.23% 98.95%
CHEMBL3192 Q9BY41 Histone deacetylase 8 83.14% 93.99%
CHEMBL4208 P20618 Proteasome component C5 82.69% 90.00%
CHEMBL3401 O75469 Pregnane X receptor 81.51% 94.73%
CHEMBL1806 P11388 DNA topoisomerase II alpha 81.43% 89.00%

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.
Swertia hookeri

Cross-Links

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PubChem 14157906
LOTUS LTS0166984
wikiData Q105362766