6,11-Dihydroxy-2,2-dimethylpyrano(3,2-c)xanthen-7(2H)-one

Details

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Internal ID 0999c4bd-a7c5-441b-bcad-cd5ba1b535c7
Taxonomy Organoheterocyclic compounds > Benzopyrans > 1-benzopyrans > Xanthones > Pyranoxanthones
IUPAC Name 6,11-dihydroxy-2,2-dimethylpyrano[3,2-c]xanthen-7-one
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C18H14O5/c1-18(2)7-6-9-8-12(20)13-14(21)10-4-3-5-11(19)16(10)22-17(13)15(9)23-18/h3-8,19-20H,1-2H3
InChI Key FPDAJKRMMGCXCC-UHFFFAOYSA-N
Popularity 4 references in papers

Physical and Chemical Properties

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Molecular Formula C18H14O5
Molecular Weight 310.30 g/mol
Exact Mass 310.08412354 g/mol
Topological Polar Surface Area (TPSA) 76.00 Ų
XlogP 3.70
Atomic LogP (AlogP) 3.54
H-Bond Acceptor 5
H-Bond Donor 2
Rotatable Bonds 0

Synonyms

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136364-53-9
6,11-dihydroxy-2,2-dimethylpyrano[3,2-c]xanthen-7-one
DTXSID00568635
CHEBI:174963

2D Structure

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2D Structure of 6,11-Dihydroxy-2,2-dimethylpyrano(3,2-c)xanthen-7(2H)-one

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9844 98.44%
Caco-2 + 0.5634 56.34%
Blood Brain Barrier - 0.7000 70.00%
Human oral bioavailability + 0.6714 67.14%
Subcellular localzation Mitochondria 0.7893 78.93%
OATP2B1 inhibitior - 0.7048 70.48%
OATP1B1 inhibitior + 0.9140 91.40%
OATP1B3 inhibitior + 0.9791 97.91%
MATE1 inhibitior - 0.8400 84.00%
OCT2 inhibitior - 1.0000 100.00%
BSEP inhibitior - 0.4900 49.00%
P-glycoprotein inhibitior + 0.6454 64.54%
P-glycoprotein substrate - 0.6026 60.26%
CYP3A4 substrate + 0.6311 63.11%
CYP2C9 substrate - 0.6166 61.66%
CYP2D6 substrate - 0.8394 83.94%
CYP3A4 inhibition - 0.5844 58.44%
CYP2C9 inhibition + 0.5890 58.90%
CYP2C19 inhibition - 0.5000 50.00%
CYP2D6 inhibition - 0.7327 73.27%
CYP1A2 inhibition + 0.5570 55.70%
CYP2C8 inhibition + 0.5312 53.12%
CYP inhibitory promiscuity + 0.5416 54.16%
UGT catelyzed + 0.6000 60.00%
Carcinogenicity (binary) - 0.9900 99.00%
Carcinogenicity (trinary) Non-required 0.5703 57.03%
Eye corrosion - 0.9875 98.75%
Eye irritation + 0.8364 83.64%
Skin irritation - 0.6672 66.72%
Skin corrosion - 0.9381 93.81%
Ames mutagenesis + 0.7500 75.00%
Human Ether-a-go-go-Related Gene inhibition - 0.6720 67.20%
Micronuclear + 0.7200 72.00%
Hepatotoxicity + 0.6301 63.01%
skin sensitisation - 0.6617 66.17%
Respiratory toxicity + 0.6000 60.00%
Reproductive toxicity + 0.6333 63.33%
Mitochondrial toxicity + 0.5125 51.25%
Nephrotoxicity - 0.7492 74.92%
Acute Oral Toxicity (c) III 0.7361 73.61%
Estrogen receptor binding + 0.8631 86.31%
Androgen receptor binding + 0.7506 75.06%
Thyroid receptor binding + 0.7155 71.55%
Glucocorticoid receptor binding + 0.9254 92.54%
Aromatase binding + 0.7772 77.72%
PPAR gamma + 0.8687 86.87%
Honey bee toxicity - 0.8888 88.88%
Biodegradation - 0.8000 80.00%
Crustacea aquatic toxicity - 0.5000 50.00%
Fish aquatic toxicity + 0.9498 94.98%

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 99.39% 91.11%
CHEMBL1951 P21397 Monoamine oxidase A 98.00% 91.49%
CHEMBL1806 P11388 DNA topoisomerase II alpha 96.48% 89.00%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 95.33% 95.56%
CHEMBL2581 P07339 Cathepsin D 93.61% 98.95%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 93.51% 94.45%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 91.84% 85.14%
CHEMBL3192 Q9BY41 Histone deacetylase 8 91.67% 93.99%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 91.21% 94.00%
CHEMBL3401 O75469 Pregnane X receptor 90.06% 94.73%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 89.69% 99.23%
CHEMBL1937 Q92769 Histone deacetylase 2 89.20% 94.75%
CHEMBL1293249 Q13887 Kruppel-like factor 5 85.08% 86.33%
CHEMBL1860 P10827 Thyroid hormone receptor alpha 84.19% 99.15%
CHEMBL5409 Q8TDU6 G-protein coupled bile acid receptor 1 83.95% 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.
Garcinia livingstonei

Cross-Links

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PubChem 15127378
LOTUS LTS0241068
wikiData Q82454948