5,6-Dihydroxy-1,3-dimethoxy-9H-xanthen-9-one

Details

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Internal ID db6b2e65-a079-45b6-8862-6cfd6706fcd2
Taxonomy Organoheterocyclic compounds > Benzopyrans > 1-benzopyrans > Xanthones
IUPAC Name 5,6-dihydroxy-1,3-dimethoxyxanthen-9-one
SMILES (Canonical) COC1=CC2=C(C(=C1)OC)C(=O)C3=C(O2)C(=C(C=C3)O)O
SMILES (Isomeric) COC1=CC2=C(C(=C1)OC)C(=O)C3=C(O2)C(=C(C=C3)O)O
InChI InChI=1S/C15H12O6/c1-19-7-5-10(20-2)12-11(6-7)21-15-8(13(12)17)3-4-9(16)14(15)18/h3-6,16,18H,1-2H3
InChI Key UWYJVMLBMYBZSD-UHFFFAOYSA-N
Popularity 3 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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94936-03-5
CHEMBL3093481
DTXSID60701682
1,3-dimethoxy-5,6-dihydroxyxanthone

2D Structure

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2D Structure of 5,6-Dihydroxy-1,3-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 + 0.9336 93.36%
Caco-2 - 0.5695 56.95%
Blood Brain Barrier - 0.8000 80.00%
Human oral bioavailability - 0.5429 54.29%
Subcellular localzation Mitochondria 0.7175 71.75%
OATP2B1 inhibitior - 0.5712 57.12%
OATP1B1 inhibitior + 0.9459 94.59%
OATP1B3 inhibitior + 0.9936 99.36%
MATE1 inhibitior - 0.7600 76.00%
OCT2 inhibitior - 0.9500 95.00%
BSEP inhibitior - 0.7336 73.36%
P-glycoprotein inhibitior - 0.6053 60.53%
P-glycoprotein substrate - 0.8332 83.32%
CYP3A4 substrate + 0.5000 50.00%
CYP2C9 substrate - 0.8397 83.97%
CYP2D6 substrate - 0.7876 78.76%
CYP3A4 inhibition - 0.6979 69.79%
CYP2C9 inhibition - 0.9200 92.00%
CYP2C19 inhibition - 0.6079 60.79%
CYP2D6 inhibition - 0.7756 77.56%
CYP1A2 inhibition + 0.9559 95.59%
CYP2C8 inhibition + 0.4528 45.28%
CYP inhibitory promiscuity - 0.5584 55.84%
UGT catelyzed - 0.5000 50.00%
Carcinogenicity (binary) - 0.9900 99.00%
Carcinogenicity (trinary) Non-required 0.6247 62.47%
Eye corrosion - 0.9696 96.96%
Eye irritation + 0.8582 85.82%
Skin irritation - 0.6228 62.28%
Skin corrosion - 0.9539 95.39%
Ames mutagenesis + 0.7300 73.00%
Human Ether-a-go-go-Related Gene inhibition - 0.8338 83.38%
Micronuclear + 0.9000 90.00%
Hepatotoxicity - 0.6375 63.75%
skin sensitisation - 0.8959 89.59%
Respiratory toxicity + 0.5222 52.22%
Reproductive toxicity + 0.8556 85.56%
Mitochondrial toxicity + 0.6375 63.75%
Nephrotoxicity - 0.7935 79.35%
Acute Oral Toxicity (c) III 0.5393 53.93%
Estrogen receptor binding + 0.8872 88.72%
Androgen receptor binding + 0.8308 83.08%
Thyroid receptor binding + 0.6480 64.80%
Glucocorticoid receptor binding + 0.9071 90.71%
Aromatase binding + 0.8260 82.60%
PPAR gamma + 0.8417 84.17%
Honey bee toxicity - 0.9101 91.01%
Biodegradation - 0.7750 77.50%
Crustacea aquatic toxicity + 0.5151 51.51%
Fish aquatic toxicity + 0.8793 87.93%

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%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 96.47% 94.00%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 95.84% 95.56%
CHEMBL1860 P10827 Thyroid hormone receptor alpha 94.43% 99.15%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 93.13% 94.45%
CHEMBL1806 P11388 DNA topoisomerase II alpha 92.30% 89.00%
CHEMBL3192 Q9BY41 Histone deacetylase 8 92.04% 93.99%
CHEMBL3194 P02766 Transthyretin 88.28% 90.71%
CHEMBL2581 P07339 Cathepsin D 86.13% 98.95%
CHEMBL2535 P11166 Glucose transporter 85.96% 98.75%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 85.82% 99.23%
CHEMBL1293249 Q13887 Kruppel-like factor 5 85.03% 86.33%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 82.96% 85.14%
CHEMBL1163101 O75460 Serine/threonine-protein kinase/endoribonuclease IRE1 82.46% 98.11%
CHEMBL3864 Q06124 Protein-tyrosine phosphatase 2C 82.12% 94.42%
CHEMBL1951 P21397 Monoamine oxidase A 81.54% 91.49%
CHEMBL2373 P21730 C5a anaphylatoxin chemotactic receptor 81.31% 92.62%
CHEMBL4208 P20618 Proteasome component C5 81.28% 90.00%
CHEMBL5608 Q16288 NT-3 growth factor receptor 81.17% 95.89%
CHEMBL2085 P14174 Macrophage migration inhibitory factor 81.12% 80.78%
CHEMBL3401 O75469 Pregnane X receptor 80.99% 94.73%
CHEMBL5409 Q8TDU6 G-protein coupled bile acid receptor 1 80.94% 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.
Haploclathra leiantha
Mesua ferrea

Cross-Links

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PubChem 53439039
LOTUS LTS0068916
wikiData Q82633439