1,6-Dihydroxyxanthone

Details

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Internal ID fdde7991-8cb0-42e6-ae51-a757ece6a8d2
Taxonomy Organoheterocyclic compounds > Benzopyrans > 1-benzopyrans > Xanthones
IUPAC Name 1,6-dihydroxyxanthen-9-one
SMILES (Canonical) C1=CC(=C2C(=C1)OC3=C(C2=O)C=CC(=C3)O)O
SMILES (Isomeric) C1=CC(=C2C(=C1)OC3=C(C2=O)C=CC(=C3)O)O
InChI InChI=1S/C13H8O4/c14-7-4-5-8-11(6-7)17-10-3-1-2-9(15)12(10)13(8)16/h1-6,14-15H
InChI Key IUSXGFFUHTXSRD-UHFFFAOYSA-N
Popularity 19 references in papers

Physical and Chemical Properties

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Molecular Formula C13H8O4
Molecular Weight 228.20 g/mol
Exact Mass 228.04225873 g/mol
Topological Polar Surface Area (TPSA) 66.80 Ų
XlogP 2.80
Atomic LogP (AlogP) 2.36
H-Bond Acceptor 4
H-Bond Donor 2
Rotatable Bonds 0

Synonyms

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1,6-dihydroxyxanthen-9-one
Isoeuxanthone
5042-08-0
CHEMBL459695
SCHEMBL2316559
DTXSID60420523
IUSXGFFUHTXSRD-UHFFFAOYSA-N
1,6-Dihydroxy-9H-xanthen-9-one

2D Structure

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2D Structure of 1,6-Dihydroxyxanthone

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9810 98.10%
Caco-2 + 0.5597 55.97%
Blood Brain Barrier - 0.8250 82.50%
Human oral bioavailability + 0.6571 65.71%
Subcellular localzation Mitochondria 0.6605 66.05%
OATP2B1 inhibitior - 0.7072 70.72%
OATP1B1 inhibitior + 0.8782 87.82%
OATP1B3 inhibitior + 0.9924 99.24%
MATE1 inhibitior - 0.5200 52.00%
OCT2 inhibitior - 0.9750 97.50%
BSEP inhibitior - 0.8633 86.33%
P-glycoprotein inhibitior - 0.8945 89.45%
P-glycoprotein substrate - 0.7753 77.53%
CYP3A4 substrate - 0.5537 55.37%
CYP2C9 substrate - 0.6265 62.65%
CYP2D6 substrate - 0.8495 84.95%
CYP3A4 inhibition + 0.6912 69.12%
CYP2C9 inhibition + 0.6323 63.23%
CYP2C19 inhibition - 0.5055 50.55%
CYP2D6 inhibition - 0.9076 90.76%
CYP1A2 inhibition + 0.9559 95.59%
CYP2C8 inhibition - 0.5919 59.19%
CYP inhibitory promiscuity - 0.5777 57.77%
UGT catelyzed + 0.7000 70.00%
Carcinogenicity (binary) - 0.9313 93.13%
Carcinogenicity (trinary) Non-required 0.5084 50.84%
Eye corrosion - 0.9697 96.97%
Eye irritation + 0.9748 97.48%
Skin irritation + 0.6458 64.58%
Skin corrosion - 0.9906 99.06%
Ames mutagenesis + 0.7200 72.00%
Human Ether-a-go-go-Related Gene inhibition - 0.9036 90.36%
Micronuclear + 0.8600 86.00%
Hepatotoxicity + 0.7500 75.00%
skin sensitisation - 0.8745 87.45%
Respiratory toxicity + 0.6333 63.33%
Reproductive toxicity + 0.5889 58.89%
Mitochondrial toxicity - 0.5375 53.75%
Nephrotoxicity + 0.4795 47.95%
Acute Oral Toxicity (c) III 0.7322 73.22%
Estrogen receptor binding + 0.8450 84.50%
Androgen receptor binding + 0.8763 87.63%
Thyroid receptor binding + 0.7725 77.25%
Glucocorticoid receptor binding + 0.9368 93.68%
Aromatase binding + 0.8268 82.68%
PPAR gamma + 0.8598 85.98%
Honey bee toxicity - 0.9358 93.58%
Biodegradation - 0.8000 80.00%
Crustacea aquatic toxicity - 0.6600 66.00%
Fish aquatic toxicity + 0.8204 82.04%

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 96.82% 91.11%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 94.72% 95.56%
CHEMBL1806 P11388 DNA topoisomerase II alpha 94.60% 89.00%
CHEMBL2581 P07339 Cathepsin D 93.63% 98.95%
CHEMBL3192 Q9BY41 Histone deacetylase 8 92.63% 93.99%
CHEMBL3401 O75469 Pregnane X receptor 88.05% 94.73%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 87.69% 99.23%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 86.95% 94.45%
CHEMBL2535 P11166 Glucose transporter 85.99% 98.75%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 85.50% 94.00%
CHEMBL1293249 Q13887 Kruppel-like factor 5 85.33% 86.33%
CHEMBL1951 P21397 Monoamine oxidase A 85.30% 91.49%
CHEMBL3194 P02766 Transthyretin 83.50% 90.71%
CHEMBL1860 P10827 Thyroid hormone receptor alpha 83.12% 99.15%

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 cowa
Garcinia gardneriana
Garcinia griffithii
Garcinia vieillardii
Hypericum sampsonii
Polygala tenuifolia
Rhachidosorus mesosorus

Cross-Links

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PubChem 5493674
NPASS NPC9985
LOTUS LTS0257994
wikiData Q82231811