3,5-Dihydroxy-1,2-dimethoxy-9h-xanthen-9-one

Details

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Internal ID 4c45d103-552a-40c7-8cee-fa7c07f7e343
Taxonomy Organoheterocyclic compounds > Benzopyrans > 1-benzopyrans > Xanthones
IUPAC Name 3,5-dihydroxy-1,2-dimethoxyxanthen-9-one
SMILES (Canonical) COC1=C(C2=C(C=C1O)OC3=C(C2=O)C=CC=C3O)OC
SMILES (Isomeric) COC1=C(C2=C(C=C1O)OC3=C(C2=O)C=CC=C3O)OC
InChI InChI=1S/C15H12O6/c1-19-14-9(17)6-10-11(15(14)20-2)12(18)7-4-3-5-8(16)13(7)21-10/h3-6,16-17H,1-2H3
InChI Key SBBNKQAKBWTGLF-UHFFFAOYSA-N
Popularity 0 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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DTXSID801255628
434938-92-8

2D Structure

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2D Structure of 3,5-Dihydroxy-1,2-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 + 0.5000 50.00%
Blood Brain Barrier - 0.7750 77.50%
Human oral bioavailability + 0.7429 74.29%
Subcellular localzation Mitochondria 0.7364 73.64%
OATP2B1 inhibitior - 0.5740 57.40%
OATP1B1 inhibitior + 0.9548 95.48%
OATP1B3 inhibitior + 0.9851 98.51%
MATE1 inhibitior - 0.7800 78.00%
OCT2 inhibitior - 0.9500 95.00%
BSEP inhibitior - 0.7564 75.64%
P-glycoprotein inhibitior - 0.5441 54.41%
P-glycoprotein substrate - 0.8807 88.07%
CYP3A4 substrate + 0.5408 54.08%
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 - 0.6292 62.92%
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 + 0.8792 87.92%
Skin irritation - 0.6099 60.99%
Skin corrosion - 0.9698 96.98%
Ames mutagenesis + 0.7100 71.00%
Human Ether-a-go-go-Related Gene inhibition - 0.6810 68.10%
Micronuclear + 0.9100 91.00%
Hepatotoxicity + 0.5199 51.99%
skin sensitisation - 0.9149 91.49%
Respiratory toxicity + 0.6000 60.00%
Reproductive toxicity + 0.8556 85.56%
Mitochondrial toxicity + 0.6125 61.25%
Nephrotoxicity - 0.8819 88.19%
Acute Oral Toxicity (c) III 0.5708 57.08%
Estrogen receptor binding + 0.8363 83.63%
Androgen receptor binding + 0.6335 63.35%
Thyroid receptor binding + 0.6532 65.32%
Glucocorticoid receptor binding + 0.8741 87.41%
Aromatase binding + 0.7985 79.85%
PPAR gamma + 0.7694 76.94%
Honey bee toxicity - 0.9064 90.64%
Biodegradation - 0.7500 75.00%
Crustacea aquatic toxicity + 0.5100 51.00%
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 98.36% 91.11%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 95.67% 95.56%
CHEMBL3192 Q9BY41 Histone deacetylase 8 95.29% 93.99%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 94.13% 94.00%
CHEMBL1806 P11388 DNA topoisomerase II alpha 92.39% 89.00%
CHEMBL2581 P07339 Cathepsin D 92.34% 98.95%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 91.63% 99.23%
CHEMBL2535 P11166 Glucose transporter 90.55% 98.75%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 89.92% 94.45%
CHEMBL1293249 Q13887 Kruppel-like factor 5 87.89% 86.33%
CHEMBL1860 P10827 Thyroid hormone receptor alpha 85.88% 99.15%
CHEMBL3401 O75469 Pregnane X receptor 84.90% 94.73%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 84.44% 85.14%
CHEMBL1907 P15144 Aminopeptidase N 82.67% 93.31%
CHEMBL3060 Q9Y345 Glycine transporter 2 80.61% 99.17%
CHEMBL1937 Q92769 Histone deacetylase 2 80.22% 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.
Cladogynos orientalis
Cratoxylum cochinchinense
Pelargonium reniforme
Terminalia catappa

Cross-Links

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PubChem 154926285
LOTUS LTS0042142
wikiData Q105226711