1,2,3-Trihydroxy-5-methoxy-9H-xanthen-9-one

Details

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Internal ID 707a78ce-6581-4031-9360-1c90cab0dec2
Taxonomy Organoheterocyclic compounds > Benzopyrans > 1-benzopyrans > Xanthones
IUPAC Name 1,2,3-trihydroxy-5-methoxyxanthen-9-one
SMILES (Canonical) COC1=CC=CC2=C1OC3=C(C2=O)C(=C(C(=C3)O)O)O
SMILES (Isomeric) COC1=CC=CC2=C1OC3=C(C2=O)C(=C(C(=C3)O)O)O
InChI InChI=1S/C14H10O6/c1-19-8-4-2-3-6-11(16)10-9(20-14(6)8)5-7(15)12(17)13(10)18/h2-5,15,17-18H,1H3
InChI Key ZKDXDGJSBPWWEM-UHFFFAOYSA-N
Popularity 5 references in papers

Physical and Chemical Properties

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Molecular Formula C14H10O6
Molecular Weight 274.22 g/mol
Exact Mass 274.04773803 g/mol
Topological Polar Surface Area (TPSA) 96.20 Ų
XlogP 2.40
Atomic LogP (AlogP) 2.07
H-Bond Acceptor 6
H-Bond Donor 3
Rotatable Bonds 1

Synonyms

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1,2,3-TRIHYDROXY-5-METHOXY-9H-XANTHEN-9-ONE
SCHEMBL22325695
DTXSID70572188
1,2,3-trihydroxy-5-methoxyxanthone

2D Structure

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2D Structure of 1,2,3-Trihydroxy-5-methoxy-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 + 0.8830 88.30%
Caco-2 - 0.7012 70.12%
Blood Brain Barrier - 0.7750 77.50%
Human oral bioavailability + 0.7571 75.71%
Subcellular localzation Mitochondria 0.5329 53.29%
OATP2B1 inhibitior - 0.5657 56.57%
OATP1B1 inhibitior + 0.9491 94.91%
OATP1B3 inhibitior + 0.9939 99.39%
MATE1 inhibitior + 0.5400 54.00%
OCT2 inhibitior - 0.9250 92.50%
BSEP inhibitior - 0.8348 83.48%
P-glycoprotein inhibitior - 0.7816 78.16%
P-glycoprotein substrate - 0.8293 82.93%
CYP3A4 substrate + 0.5724 57.24%
CYP2C9 substrate - 0.6887 68.87%
CYP2D6 substrate - 0.8370 83.70%
CYP3A4 inhibition + 0.5370 53.70%
CYP2C9 inhibition - 0.9516 95.16%
CYP2C19 inhibition - 0.7992 79.92%
CYP2D6 inhibition - 0.8274 82.74%
CYP1A2 inhibition + 0.9658 96.58%
CYP2C8 inhibition + 0.5506 55.06%
CYP inhibitory promiscuity + 0.5777 57.77%
UGT catelyzed + 0.7000 70.00%
Carcinogenicity (binary) - 0.9800 98.00%
Carcinogenicity (trinary) Non-required 0.6223 62.23%
Eye corrosion - 0.9690 96.90%
Eye irritation + 0.9019 90.19%
Skin irritation - 0.5579 55.79%
Skin corrosion - 0.9129 91.29%
Ames mutagenesis + 0.6900 69.00%
Human Ether-a-go-go-Related Gene inhibition - 0.7414 74.14%
Micronuclear + 0.9000 90.00%
Hepatotoxicity - 0.5125 51.25%
skin sensitisation - 0.8609 86.09%
Respiratory toxicity + 0.6444 64.44%
Reproductive toxicity + 0.8444 84.44%
Mitochondrial toxicity + 0.6000 60.00%
Nephrotoxicity - 0.8444 84.44%
Acute Oral Toxicity (c) III 0.7135 71.35%
Estrogen receptor binding + 0.8424 84.24%
Androgen receptor binding + 0.8133 81.33%
Thyroid receptor binding + 0.5978 59.78%
Glucocorticoid receptor binding + 0.9110 91.10%
Aromatase binding + 0.7078 70.78%
PPAR gamma + 0.8116 81.16%
Honey bee toxicity - 0.8940 89.40%
Biodegradation - 0.9000 90.00%
Crustacea aquatic toxicity + 0.5900 59.00%
Fish aquatic toxicity + 0.8178 81.78%

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 98.69% 91.11%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 96.94% 95.56%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 96.78% 94.00%
CHEMBL2581 P07339 Cathepsin D 94.39% 98.95%
CHEMBL2535 P11166 Glucose transporter 92.06% 98.75%
CHEMBL1293249 Q13887 Kruppel-like factor 5 91.97% 86.33%
CHEMBL1806 P11388 DNA topoisomerase II alpha 91.95% 89.00%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 91.14% 85.14%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 90.48% 94.45%
CHEMBL3091268 Q92753 Nuclear receptor ROR-beta 88.64% 95.50%
CHEMBL1255126 O15151 Protein Mdm4 88.34% 90.20%
CHEMBL3192 Q9BY41 Histone deacetylase 8 87.70% 93.99%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 86.33% 99.23%
CHEMBL1860 P10827 Thyroid hormone receptor alpha 85.70% 99.15%
CHEMBL5608 Q16288 NT-3 growth factor receptor 85.51% 95.89%
CHEMBL3401 O75469 Pregnane X receptor 85.10% 94.73%
CHEMBL2373 P21730 C5a anaphylatoxin chemotactic receptor 84.95% 92.62%
CHEMBL3060 Q9Y345 Glycine transporter 2 83.73% 99.17%
CHEMBL4306 P22460 Voltage-gated potassium channel subunit Kv1.5 82.77% 94.03%

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.
Centaurium erythraea
Halenia corniculata

Cross-Links

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PubChem 15379040
LOTUS LTS0108711
wikiData Q82460472