3,6-Dihydroxy-1,7-dimethoxyxanthone

Details

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Internal ID 8bac0fef-b8c3-4f55-9c21-1db64d0a3fff
Taxonomy Organoheterocyclic compounds > Benzopyrans > 1-benzopyrans > Xanthones
IUPAC Name 3,6-dihydroxy-1,7-dimethoxyxanthen-9-one
SMILES (Canonical) COC1=CC(=CC2=C1C(=O)C3=CC(=C(C=C3O2)O)OC)O
SMILES (Isomeric) COC1=CC(=CC2=C1C(=O)C3=CC(=C(C=C3O2)O)OC)O
InChI InChI=1S/C15H12O6/c1-19-11-5-8-10(6-9(11)17)21-13-4-7(16)3-12(20-2)14(13)15(8)18/h3-6,16-17H,1-2H3
InChI Key TZVWXRWZFWCCDO-UHFFFAOYSA-N
Popularity 3 references in papers

Physical and Chemical Properties

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Molecular Formula C15H12O6
Molecular Weight 288.25 g/mol
Exact Mass 288.06338810 g/mol
Topological Polar Surface Area (TPSA) 85.20 Ų
XlogP 2.20
Atomic LogP (AlogP) 2.37
H-Bond Acceptor 6
H-Bond Donor 2
Rotatable Bonds 2

Synonyms

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262292-34-2
3,6-dihydroxy-1,7-dimethoxyxanthen-9-one
3,6-Dihydroxy-1,7-dimethoxy-9H-xanthen-9-one
starbld0014357
AKOS040761077

2D Structure

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2D Structure of 3,6-Dihydroxy-1,7-dimethoxyxanthone

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9642 96.42%
Caco-2 + 0.7438 74.38%
Blood Brain Barrier - 0.7750 77.50%
Human oral bioavailability + 0.5571 55.71%
Subcellular localzation Mitochondria 0.7364 73.64%
OATP2B1 inhibitior - 0.5784 57.84%
OATP1B1 inhibitior + 0.9388 93.88%
OATP1B3 inhibitior + 0.9851 98.51%
MATE1 inhibitior - 0.7800 78.00%
OCT2 inhibitior - 0.9500 95.00%
BSEP inhibitior - 0.8290 82.90%
P-glycoprotein inhibitior - 0.6203 62.03%
P-glycoprotein substrate - 0.8161 81.61%
CYP3A4 substrate - 0.5000 50.00%
CYP2C9 substrate - 0.8382 83.82%
CYP2D6 substrate - 0.7720 77.20%
CYP3A4 inhibition - 0.6420 64.20%
CYP2C9 inhibition - 0.7071 70.71%
CYP2C19 inhibition + 0.7531 75.31%
CYP2D6 inhibition - 0.6235 62.35%
CYP1A2 inhibition + 0.9606 96.06%
CYP2C8 inhibition + 0.4451 44.51%
CYP inhibitory promiscuity + 0.6446 64.46%
UGT catelyzed - 0.5000 50.00%
Carcinogenicity (binary) - 0.9900 99.00%
Carcinogenicity (trinary) Non-required 0.6331 63.31%
Eye corrosion - 0.9655 96.55%
Eye irritation + 0.8874 88.74%
Skin irritation - 0.6099 60.99%
Skin corrosion - 0.9698 96.98%
Ames mutagenesis + 0.5900 59.00%
Human Ether-a-go-go-Related Gene inhibition - 0.5731 57.31%
Micronuclear + 0.9100 91.00%
Hepatotoxicity - 0.7500 75.00%
skin sensitisation - 0.9149 91.49%
Respiratory toxicity + 0.6333 63.33%
Reproductive toxicity + 0.8556 85.56%
Mitochondrial toxicity + 0.6125 61.25%
Nephrotoxicity - 0.6971 69.71%
Acute Oral Toxicity (c) III 0.5708 57.08%
Estrogen receptor binding + 0.8786 87.86%
Androgen receptor binding + 0.7340 73.40%
Thyroid receptor binding + 0.6541 65.41%
Glucocorticoid receptor binding + 0.9174 91.74%
Aromatase binding + 0.8217 82.17%
PPAR gamma + 0.7350 73.50%
Honey bee toxicity - 0.8381 83.81%
Biodegradation - 0.8000 80.00%
Crustacea aquatic toxicity - 0.5249 52.49%
Fish aquatic toxicity + 0.8585 85.85%

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 97.73% 91.11%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 94.54% 94.00%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 93.99% 95.56%
CHEMBL1806 P11388 DNA topoisomerase II alpha 92.30% 89.00%
CHEMBL241 Q14432 Phosphodiesterase 3A 89.05% 92.94%
CHEMBL3194 P02766 Transthyretin 88.55% 90.71%
CHEMBL2581 P07339 Cathepsin D 87.47% 98.95%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 86.38% 94.45%
CHEMBL2535 P11166 Glucose transporter 86.29% 98.75%
CHEMBL3192 Q9BY41 Histone deacetylase 8 85.68% 93.99%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 84.05% 99.23%
CHEMBL1293249 Q13887 Kruppel-like factor 5 83.97% 86.33%
CHEMBL3060 Q9Y345 Glycine transporter 2 82.93% 99.17%
CHEMBL5409 Q8TDU6 G-protein coupled bile acid receptor 1 80.04% 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.
Hypericum ascyron
Hypericum monogynum

Cross-Links

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PubChem 101010505
NPASS NPC28514
LOTUS LTS0147590
wikiData Q105268442