1,3,8-Trihydroxy-2,6-dimethoxy-9H-xanthen-9-one

Details

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Internal ID 7bdab521-f960-463f-9918-0788551dde81
Taxonomy Organoheterocyclic compounds > Benzopyrans > 1-benzopyrans > Xanthones
IUPAC Name 1,3,8-trihydroxy-2,6-dimethoxyxanthen-9-one
SMILES (Canonical) COC1=CC(=C2C(=C1)OC3=C(C2=O)C(=C(C(=C3)O)OC)O)O
SMILES (Isomeric) COC1=CC(=C2C(=C1)OC3=C(C2=O)C(=C(C(=C3)O)OC)O)O
InChI InChI=1S/C15H12O7/c1-20-6-3-7(16)11-9(4-6)22-10-5-8(17)15(21-2)14(19)12(10)13(11)18/h3-5,16-17,19H,1-2H3
InChI Key WWLABYIROBORPO-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C15H12O7
Molecular Weight 304.25 g/mol
Exact Mass 304.05830272 g/mol
Topological Polar Surface Area (TPSA) 105.00 Ų
XlogP 2.40
Atomic LogP (AlogP) 2.08
H-Bond Acceptor 7
H-Bond Donor 3
Rotatable Bonds 2

Synonyms

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1,3,8-TRIHYDROXY-2,6-DIMETHOXY-9H-XANTHEN-9-ONE
DTXSID50766568

2D Structure

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2D Structure of 1,3,8-Trihydroxy-2,6-dimethoxy-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 + 0.9261 92.61%
Caco-2 + 0.8251 82.51%
Blood Brain Barrier - 0.7750 77.50%
Human oral bioavailability - 0.5571 55.71%
Subcellular localzation Mitochondria 0.5592 55.92%
OATP2B1 inhibitior - 0.6986 69.86%
OATP1B1 inhibitior + 0.8896 88.96%
OATP1B3 inhibitior + 0.9627 96.27%
MATE1 inhibitior + 0.5400 54.00%
OCT2 inhibitior - 0.9750 97.50%
BSEP inhibitior - 0.8836 88.36%
P-glycoprotein inhibitior - 0.6175 61.75%
P-glycoprotein substrate - 0.9304 93.04%
CYP3A4 substrate - 0.5000 50.00%
CYP2C9 substrate - 0.6401 64.01%
CYP2D6 substrate - 0.8296 82.96%
CYP3A4 inhibition + 0.6908 69.08%
CYP2C9 inhibition - 0.7416 74.16%
CYP2C19 inhibition + 0.6596 65.96%
CYP2D6 inhibition - 0.5311 53.11%
CYP1A2 inhibition + 0.9466 94.66%
CYP2C8 inhibition - 0.5751 57.51%
CYP inhibitory promiscuity + 0.7479 74.79%
UGT catelyzed + 0.6000 60.00%
Carcinogenicity (binary) - 0.9900 99.00%
Carcinogenicity (trinary) Non-required 0.6775 67.75%
Eye corrosion - 0.9667 96.67%
Eye irritation + 0.8329 83.29%
Skin irritation - 0.6148 61.48%
Skin corrosion - 0.9417 94.17%
Ames mutagenesis + 0.5800 58.00%
Human Ether-a-go-go-Related Gene inhibition - 0.6553 65.53%
Micronuclear + 0.9100 91.00%
Hepatotoxicity + 0.5500 55.00%
skin sensitisation - 0.8849 88.49%
Respiratory toxicity + 0.5556 55.56%
Reproductive toxicity + 0.8556 85.56%
Mitochondrial toxicity + 0.6375 63.75%
Nephrotoxicity - 0.7830 78.30%
Acute Oral Toxicity (c) III 0.6228 62.28%
Estrogen receptor binding + 0.8041 80.41%
Androgen receptor binding + 0.6668 66.68%
Thyroid receptor binding + 0.6245 62.45%
Glucocorticoid receptor binding + 0.8906 89.06%
Aromatase binding + 0.7637 76.37%
PPAR gamma + 0.7355 73.55%
Honey bee toxicity - 0.9008 90.08%
Biodegradation - 0.8250 82.50%
Crustacea aquatic toxicity - 0.5800 58.00%
Fish aquatic toxicity + 0.8268 82.68%

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 97.86% 91.11%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 93.81% 94.00%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 91.91% 85.14%
CHEMBL1860 P10827 Thyroid hormone receptor alpha 91.79% 99.15%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 89.84% 95.56%
CHEMBL1806 P11388 DNA topoisomerase II alpha 88.56% 89.00%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 86.78% 94.45%
CHEMBL3060 Q9Y345 Glycine transporter 2 86.75% 99.17%
CHEMBL3194 P02766 Transthyretin 86.24% 90.71%
CHEMBL2581 P07339 Cathepsin D 86.01% 98.95%
CHEMBL4208 P20618 Proteasome component C5 85.88% 90.00%
CHEMBL1293249 Q13887 Kruppel-like factor 5 85.59% 86.33%
CHEMBL3192 Q9BY41 Histone deacetylase 8 84.19% 93.99%
CHEMBL3401 O75469 Pregnane X receptor 83.54% 94.73%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 82.18% 99.23%
CHEMBL3864 Q06124 Protein-tyrosine phosphatase 2C 82.01% 94.42%
CHEMBL5409 Q8TDU6 G-protein coupled bile acid receptor 1 81.52% 93.65%

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.
Ixanthus viscosus

Cross-Links

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PubChem 71339074
LOTUS LTS0169094
wikiData Q82724077