1,6,7-Trihydroxy-3,5-Dimethoxyxanthen-9-one

Details

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Internal ID 8286eb3d-0f9b-4406-baf9-1b9ae587020e
Taxonomy Organoheterocyclic compounds > Benzopyrans > 1-benzopyrans > Xanthones
IUPAC Name 1,6,7-trihydroxy-3,5-dimethoxyxanthen-9-one
SMILES (Canonical) COC1=CC(=C2C(=C1)OC3=C(C(=C(C=C3C2=O)O)O)OC)O
SMILES (Isomeric) COC1=CC(=C2C(=C1)OC3=C(C(=C(C=C3C2=O)O)O)OC)O
InChI InChI=1S/C15H12O7/c1-20-6-3-8(16)11-10(4-6)22-14-7(12(11)18)5-9(17)13(19)15(14)21-2/h3-5,16-17,19H,1-2H3
InChI Key YMWRHUWNNOOQLF-UHFFFAOYSA-N
Popularity 1 reference 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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1,6,7-trihydroxy-3,5-dimethoxy-xanthen-9-one

2D Structure

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2D Structure of 1,6,7-Trihydroxy-3,5-Dimethoxyxanthen-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 + 0.9336 93.36%
Caco-2 - 0.5951 59.51%
Blood Brain Barrier - 0.8000 80.00%
Human oral bioavailability - 0.5000 50.00%
Subcellular localzation Mitochondria 0.7175 71.75%
OATP2B1 inhibitior - 0.5642 56.42%
OATP1B1 inhibitior + 0.8833 88.33%
OATP1B3 inhibitior + 0.9936 99.36%
MATE1 inhibitior + 0.5400 54.00%
OCT2 inhibitior - 0.9500 95.00%
BSEP inhibitior - 0.7144 71.44%
P-glycoprotein inhibitior - 0.6167 61.67%
P-glycoprotein substrate - 0.8852 88.52%
CYP3A4 substrate + 0.5155 51.55%
CYP2C9 substrate - 0.6887 68.87%
CYP2D6 substrate - 0.8370 83.70%
CYP3A4 inhibition - 0.6979 69.79%
CYP2C9 inhibition - 0.9200 92.00%
CYP2C19 inhibition - 0.6079 60.79%
CYP2D6 inhibition - 0.7756 77.56%
CYP1A2 inhibition + 0.9559 95.59%
CYP2C8 inhibition + 0.4574 45.74%
CYP inhibitory promiscuity - 0.5584 55.84%
UGT catelyzed + 0.6000 60.00%
Carcinogenicity (binary) - 0.9900 99.00%
Carcinogenicity (trinary) Non-required 0.6247 62.47%
Eye corrosion - 0.9696 96.96%
Eye irritation + 0.8968 89.68%
Skin irritation - 0.6228 62.28%
Skin corrosion - 0.9539 95.39%
Ames mutagenesis + 0.6500 65.00%
Human Ether-a-go-go-Related Gene inhibition - 0.6184 61.84%
Micronuclear + 0.9000 90.00%
Hepatotoxicity - 0.6250 62.50%
skin sensitisation - 0.8959 89.59%
Respiratory toxicity + 0.5889 58.89%
Reproductive toxicity + 0.8556 85.56%
Mitochondrial toxicity + 0.6375 63.75%
Nephrotoxicity - 0.8202 82.02%
Acute Oral Toxicity (c) III 0.5393 53.93%
Estrogen receptor binding + 0.8436 84.36%
Androgen receptor binding + 0.7385 73.85%
Thyroid receptor binding + 0.5855 58.55%
Glucocorticoid receptor binding + 0.9066 90.66%
Aromatase binding + 0.7472 74.72%
PPAR gamma + 0.7832 78.32%
Honey bee toxicity - 0.9118 91.18%
Biodegradation - 0.7750 77.50%
Crustacea aquatic toxicity - 0.5200 52.00%
Fish aquatic toxicity + 0.8793 87.93%

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 99.37% 91.11%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 95.68% 94.00%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 94.92% 94.45%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 94.32% 95.56%
CHEMBL1860 P10827 Thyroid hormone receptor alpha 92.07% 99.15%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 91.97% 85.14%
CHEMBL1806 P11388 DNA topoisomerase II alpha 91.15% 89.00%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 88.49% 99.23%
CHEMBL3060 Q9Y345 Glycine transporter 2 87.85% 99.17%
CHEMBL215 P09917 Arachidonate 5-lipoxygenase 86.40% 92.68%
CHEMBL1951 P21397 Monoamine oxidase A 85.52% 91.49%
CHEMBL3194 P02766 Transthyretin 85.46% 90.71%
CHEMBL2581 P07339 Cathepsin D 84.18% 98.95%
CHEMBL3192 Q9BY41 Histone deacetylase 8 83.11% 93.99%
CHEMBL1293249 Q13887 Kruppel-like factor 5 83.08% 86.33%
CHEMBL3401 O75469 Pregnane X receptor 82.52% 94.73%
CHEMBL2535 P11166 Glucose transporter 81.97% 98.75%
CHEMBL4208 P20618 Proteasome component C5 80.72% 90.00%

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.
Canscora alata

Cross-Links

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PubChem 5479777
LOTUS LTS0172271
wikiData Q105350777