9H-Xanthen-9-one, 1,5-dihydroxy-2,3-dimethoxy-

Details

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Internal ID 545dca32-81b6-4bb8-aaf2-91989dc42e27
Taxonomy Organoheterocyclic compounds > Benzopyrans > 1-benzopyrans > Xanthones
IUPAC Name 1,5-dihydroxy-2,3-dimethoxyxanthen-9-one
SMILES (Canonical) COC1=C(C(=C2C(=C1)OC3=C(C2=O)C=CC=C3O)O)OC
SMILES (Isomeric) COC1=C(C(=C2C(=C1)OC3=C(C2=O)C=CC=C3O)O)OC
InChI InChI=1S/C15H12O6/c1-19-10-6-9-11(13(18)15(10)20-2)12(17)7-4-3-5-8(16)14(7)21-9/h3-6,16,18H,1-2H3
InChI Key APPOIVIWJAIHBI-UHFFFAOYSA-N
Popularity 6 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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55386-63-5
SCHEMBL16244513
DTXSID00468924

2D Structure

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2D Structure of 9H-Xanthen-9-one, 1,5-dihydroxy-2,3-dimethoxy-

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 + 0.7410 74.10%
Blood Brain Barrier - 0.7750 77.50%
Human oral bioavailability + 0.7286 72.86%
Subcellular localzation Mitochondria 0.7364 73.64%
OATP2B1 inhibitior - 0.7032 70.32%
OATP1B1 inhibitior + 0.9495 94.95%
OATP1B3 inhibitior + 0.9851 98.51%
MATE1 inhibitior + 0.5400 54.00%
OCT2 inhibitior - 0.9500 95.00%
BSEP inhibitior - 0.7473 74.73%
P-glycoprotein inhibitior - 0.4771 47.71%
P-glycoprotein substrate - 0.7579 75.79%
CYP3A4 substrate + 0.5715 57.15%
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 + 0.6131 61.31%
CYP inhibitory promiscuity + 0.6446 64.46%
UGT catelyzed - 0.6000 60.00%
Carcinogenicity (binary) - 0.9900 99.00%
Carcinogenicity (trinary) Non-required 0.6331 63.31%
Eye corrosion - 0.9655 96.55%
Eye irritation + 0.8627 86.27%
Skin irritation - 0.6099 60.99%
Skin corrosion - 0.9698 96.98%
Ames mutagenesis + 0.6400 64.00%
Human Ether-a-go-go-Related Gene inhibition - 0.7251 72.51%
Micronuclear + 0.9100 91.00%
Hepatotoxicity - 0.5750 57.50%
skin sensitisation - 0.9149 91.49%
Respiratory toxicity + 0.5667 56.67%
Reproductive toxicity + 0.8556 85.56%
Mitochondrial toxicity + 0.6125 61.25%
Nephrotoxicity - 0.9095 90.95%
Acute Oral Toxicity (c) III 0.5708 57.08%
Estrogen receptor binding + 0.7054 70.54%
Androgen receptor binding + 0.6191 61.91%
Thyroid receptor binding + 0.6500 65.00%
Glucocorticoid receptor binding + 0.8565 85.65%
Aromatase binding + 0.7905 79.05%
PPAR gamma + 0.8225 82.25%
Honey bee toxicity - 0.9069 90.69%
Biodegradation - 0.8000 80.00%
Crustacea aquatic toxicity - 0.5149 51.49%
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 98.63% 91.11%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 96.39% 95.56%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 96.32% 94.00%
CHEMBL1806 P11388 DNA topoisomerase II alpha 94.70% 89.00%
CHEMBL3192 Q9BY41 Histone deacetylase 8 93.71% 93.99%
CHEMBL2535 P11166 Glucose transporter 91.69% 98.75%
CHEMBL2581 P07339 Cathepsin D 91.24% 98.95%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 91.15% 99.23%
CHEMBL1293249 Q13887 Kruppel-like factor 5 90.80% 86.33%
CHEMBL3401 O75469 Pregnane X receptor 88.78% 94.73%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 88.72% 85.14%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 88.26% 94.45%
CHEMBL3060 Q9Y345 Glycine transporter 2 87.30% 99.17%
CHEMBL1860 P10827 Thyroid hormone receptor alpha 85.93% 99.15%
CHEMBL4306 P22460 Voltage-gated potassium channel subunit Kv1.5 83.58% 94.03%
CHEMBL1937 Q92769 Histone deacetylase 2 82.34% 94.75%
CHEMBL3091268 Q92753 Nuclear receptor ROR-beta 80.64% 95.50%
CHEMBL1255126 O15151 Protein Mdm4 80.02% 90.20%

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.
Halenia elliptica
Monnina sylvatica

Cross-Links

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PubChem 11580116
LOTUS LTS0089894
wikiData Q82296426