1,4-Dihydroxy-3,5-dimethoxy-9H-xanthen-9-one

Details

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Internal ID 4feb9f2b-f704-4f3e-b185-29f7db442602
Taxonomy Organoheterocyclic compounds > Benzopyrans > 1-benzopyrans > Xanthones
IUPAC Name 1,4-dihydroxy-3,5-dimethoxyxanthen-9-one
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C15H12O6/c1-19-9-5-3-4-7-12(17)11-8(16)6-10(20-2)13(18)15(11)21-14(7)9/h3-6,16,18H,1-2H3
InChI Key BUOWJFQCNKTARL-UHFFFAOYSA-N
Popularity 4 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 2.70
Atomic LogP (AlogP) 2.37
H-Bond Acceptor 6
H-Bond Donor 2
Rotatable Bonds 2

Synonyms

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1,4-DIHYDROXY-3,5-DIMETHOXY-9H-XANTHEN-9-ONE
DTXSID60631758
1,4-dihydroxy-3,5-dimethoxyxanthone

2D Structure

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2D Structure of 1,4-Dihydroxy-3,5-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 + 0.9642 96.42%
Caco-2 + 0.6346 63.46%
Blood Brain Barrier - 0.7750 77.50%
Human oral bioavailability + 0.6429 64.29%
Subcellular localzation Mitochondria 0.7364 73.64%
OATP2B1 inhibitior - 0.7131 71.31%
OATP1B1 inhibitior + 0.9360 93.60%
OATP1B3 inhibitior + 0.9851 98.51%
MATE1 inhibitior + 0.5400 54.00%
OCT2 inhibitior - 0.9500 95.00%
BSEP inhibitior - 0.7430 74.30%
P-glycoprotein inhibitior - 0.5361 53.61%
P-glycoprotein substrate - 0.7848 78.48%
CYP3A4 substrate + 0.5572 55.72%
CYP2C9 substrate - 0.6401 64.01%
CYP2D6 substrate - 0.8296 82.96%
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 - 0.6004 60.04%
CYP inhibitory promiscuity + 0.6446 64.46%
UGT catelyzed + 0.7000 70.00%
Carcinogenicity (binary) - 0.9900 99.00%
Carcinogenicity (trinary) Non-required 0.6331 63.31%
Eye corrosion - 0.9655 96.55%
Eye irritation + 0.8493 84.93%
Skin irritation - 0.6099 60.99%
Skin corrosion - 0.9698 96.98%
Ames mutagenesis + 0.8100 81.00%
Human Ether-a-go-go-Related Gene inhibition - 0.6163 61.63%
Micronuclear + 0.9100 91.00%
Hepatotoxicity + 0.6000 60.00%
skin sensitisation - 0.9149 91.49%
Respiratory toxicity + 0.5778 57.78%
Reproductive toxicity + 0.8556 85.56%
Mitochondrial toxicity + 0.6125 61.25%
Nephrotoxicity - 0.7209 72.09%
Acute Oral Toxicity (c) III 0.5708 57.08%
Estrogen receptor binding + 0.7107 71.07%
Androgen receptor binding + 0.6724 67.24%
Thyroid receptor binding + 0.6506 65.06%
Glucocorticoid receptor binding + 0.8974 89.74%
Aromatase binding + 0.7532 75.32%
PPAR gamma + 0.8074 80.74%
Honey bee toxicity - 0.8960 89.60%
Biodegradation - 0.8750 87.50%
Crustacea aquatic toxicity + 0.5300 53.00%
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 98.81% 91.11%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 97.18% 95.56%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 95.04% 94.00%
CHEMBL2581 P07339 Cathepsin D 93.01% 98.95%
CHEMBL3192 Q9BY41 Histone deacetylase 8 92.97% 93.99%
CHEMBL1806 P11388 DNA topoisomerase II alpha 92.49% 89.00%
CHEMBL1293249 Q13887 Kruppel-like factor 5 92.03% 86.33%
CHEMBL2535 P11166 Glucose transporter 89.47% 98.75%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 88.02% 99.23%
CHEMBL5409 Q8TDU6 G-protein coupled bile acid receptor 1 86.84% 93.65%
CHEMBL1860 P10827 Thyroid hormone receptor alpha 86.48% 99.15%
CHEMBL1163101 O75460 Serine/threonine-protein kinase/endoribonuclease IRE1 84.89% 98.11%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 84.50% 85.14%
CHEMBL2373 P21730 C5a anaphylatoxin chemotactic receptor 84.38% 92.62%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 84.08% 94.45%
CHEMBL2094127 P06493 Cyclin-dependent kinase 1/cyclin B 82.10% 96.00%
CHEMBL3401 O75469 Pregnane X receptor 82.07% 94.73%
CHEMBL4306 P22460 Voltage-gated potassium channel subunit Kv1.5 81.69% 94.03%
CHEMBL3091268 Q92753 Nuclear receptor ROR-beta 81.24% 95.50%
CHEMBL3060 Q9Y345 Glycine transporter 2 80.99% 99.17%
CHEMBL1255126 O15151 Protein Mdm4 80.24% 90.20%
CHEMBL5608 Q16288 NT-3 growth factor receptor 80.22% 95.89%
CHEMBL1937 Q92769 Histone deacetylase 2 80.09% 94.75%

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.
Centaurium erythraea

Cross-Links

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PubChem 23262985
LOTUS LTS0185384
wikiData Q82539056