1,7-Dihydroxy-2,3,4-trimethoxy-9H-xanthen-9-one

Details

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Internal ID 0489e316-ee2c-4f05-8318-046959fb4f87
Taxonomy Organoheterocyclic compounds > Benzopyrans > 1-benzopyrans > Xanthones
IUPAC Name 1,7-dihydroxy-2,3,4-trimethoxyxanthen-9-one
SMILES (Canonical) COC1=C(C(=C2C(=C1O)C(=O)C3=C(O2)C=CC(=C3)O)OC)OC
SMILES (Isomeric) COC1=C(C(=C2C(=C1O)C(=O)C3=C(O2)C=CC(=C3)O)OC)OC
InChI InChI=1S/C16H14O7/c1-20-14-12(19)10-11(18)8-6-7(17)4-5-9(8)23-13(10)15(21-2)16(14)22-3/h4-6,17,19H,1-3H3
InChI Key WJNCOCOQNPOXCB-UHFFFAOYSA-N
Popularity 1 reference in papers

Physical and Chemical Properties

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Molecular Formula C16H14O7
Molecular Weight 318.28 g/mol
Exact Mass 318.07395278 g/mol
Topological Polar Surface Area (TPSA) 94.40 Ų
XlogP 2.70
Atomic LogP (AlogP) 2.38
H-Bond Acceptor 7
H-Bond Donor 2
Rotatable Bonds 3

Synonyms

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DTXSID90824015

2D Structure

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2D Structure of 1,7-Dihydroxy-2,3,4-trimethoxy-9H-xanthen-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 + 0.9617 96.17%
Caco-2 + 0.6242 62.42%
Blood Brain Barrier - 0.7750 77.50%
Human oral bioavailability + 0.5429 54.29%
Subcellular localzation Mitochondria 0.7093 70.93%
OATP2B1 inhibitior - 0.7082 70.82%
OATP1B1 inhibitior + 0.8532 85.32%
OATP1B3 inhibitior + 0.9698 96.98%
MATE1 inhibitior + 0.5400 54.00%
OCT2 inhibitior - 0.9500 95.00%
BSEP inhibitior - 0.5752 57.52%
P-glycoprotein inhibitior - 0.5148 51.48%
P-glycoprotein substrate - 0.7815 78.15%
CYP3A4 substrate - 0.5000 50.00%
CYP2C9 substrate - 0.6401 64.01%
CYP2D6 substrate - 0.8296 82.96%
CYP3A4 inhibition - 0.7782 77.82%
CYP2C9 inhibition - 0.9325 93.25%
CYP2C19 inhibition - 0.5514 55.14%
CYP2D6 inhibition - 0.7363 73.63%
CYP1A2 inhibition + 0.9561 95.61%
CYP2C8 inhibition + 0.4744 47.44%
CYP inhibitory promiscuity + 0.5753 57.53%
UGT catelyzed + 0.6000 60.00%
Carcinogenicity (binary) - 0.9900 99.00%
Carcinogenicity (trinary) Non-required 0.6097 60.97%
Eye corrosion - 0.9746 97.46%
Eye irritation + 0.8594 85.94%
Skin irritation - 0.6975 69.75%
Skin corrosion - 0.9788 97.88%
Ames mutagenesis + 0.6600 66.00%
Human Ether-a-go-go-Related Gene inhibition - 0.6451 64.51%
Micronuclear + 0.8500 85.00%
Hepatotoxicity + 0.5750 57.50%
skin sensitisation - 0.9328 93.28%
Respiratory toxicity + 0.6667 66.67%
Reproductive toxicity + 0.8111 81.11%
Mitochondrial toxicity + 0.5750 57.50%
Nephrotoxicity - 0.8615 86.15%
Acute Oral Toxicity (c) II 0.4834 48.34%
Estrogen receptor binding + 0.6913 69.13%
Androgen receptor binding + 0.7460 74.60%
Thyroid receptor binding + 0.6619 66.19%
Glucocorticoid receptor binding + 0.8537 85.37%
Aromatase binding + 0.6220 62.20%
PPAR gamma + 0.7030 70.30%
Honey bee toxicity - 0.8888 88.88%
Biodegradation - 0.6500 65.00%
Crustacea aquatic toxicity - 0.5400 54.00%
Fish aquatic toxicity + 0.8676 86.76%

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 98.76% 91.11%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 95.49% 94.45%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 93.95% 94.00%
CHEMBL2581 P07339 Cathepsin D 93.08% 98.95%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 92.34% 95.56%
CHEMBL1806 P11388 DNA topoisomerase II alpha 91.92% 89.00%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 91.34% 99.23%
CHEMBL2535 P11166 Glucose transporter 87.16% 98.75%
CHEMBL3401 O75469 Pregnane X receptor 86.13% 94.73%
CHEMBL1293249 Q13887 Kruppel-like factor 5 85.61% 86.33%
CHEMBL3192 Q9BY41 Histone deacetylase 8 85.25% 93.99%
CHEMBL3060 Q9Y345 Glycine transporter 2 83.35% 99.17%

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.
Frasera speciosa
Halenia elata
Polygala virgata

Cross-Links

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PubChem 71403088
LOTUS LTS0132884
wikiData Q82807315