1-Hydroxy-5-methoxyxanthone

Details

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Internal ID 01f7e845-5d04-4c2e-a612-1f0839fbd3b6
Taxonomy Organoheterocyclic compounds > Benzopyrans > 1-benzopyrans > Xanthones
IUPAC Name 1-hydroxy-5-methoxyxanthen-9-one
SMILES (Canonical) COC1=CC=CC2=C1OC3=CC=CC(=C3C2=O)O
SMILES (Isomeric) COC1=CC=CC2=C1OC3=CC=CC(=C3C2=O)O
InChI InChI=1S/C14H10O4/c1-17-11-7-2-4-8-13(16)12-9(15)5-3-6-10(12)18-14(8)11/h2-7,15H,1H3
InChI Key NJTOSCMFMNLPNQ-UHFFFAOYSA-N
Popularity 3 references in papers

Physical and Chemical Properties

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Molecular Formula C14H10O4
Molecular Weight 242.23 g/mol
Exact Mass 242.05790880 g/mol
Topological Polar Surface Area (TPSA) 55.80 Ų
XlogP 3.10
Atomic LogP (AlogP) 2.66
H-Bond Acceptor 4
H-Bond Donor 1
Rotatable Bonds 1

Synonyms

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CHEMBL4862786

2D Structure

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2D Structure of 1-Hydroxy-5-methoxyxanthone

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9846 98.46%
Caco-2 + 0.6130 61.30%
Blood Brain Barrier - 0.7750 77.50%
Human oral bioavailability + 0.7857 78.57%
Subcellular localzation Mitochondria 0.6551 65.51%
OATP2B1 inhibitior - 0.7329 73.29%
OATP1B1 inhibitior + 0.9425 94.25%
OATP1B3 inhibitior + 0.9952 99.52%
MATE1 inhibitior + 0.5400 54.00%
OCT2 inhibitior - 0.9250 92.50%
BSEP inhibitior + 0.5577 55.77%
P-glycoprotein inhibitior - 0.6481 64.81%
P-glycoprotein substrate - 0.8634 86.34%
CYP3A4 substrate + 0.5517 55.17%
CYP2C9 substrate - 0.6401 64.01%
CYP2D6 substrate - 0.8296 82.96%
CYP3A4 inhibition + 0.5981 59.81%
CYP2C9 inhibition - 0.7716 77.16%
CYP2C19 inhibition + 0.6254 62.54%
CYP2D6 inhibition - 0.8637 86.37%
CYP1A2 inhibition + 0.9667 96.67%
CYP2C8 inhibition - 0.7259 72.59%
CYP inhibitory promiscuity - 0.5933 59.33%
UGT catelyzed + 0.6000 60.00%
Carcinogenicity (binary) - 0.9600 96.00%
Carcinogenicity (trinary) Non-required 0.4627 46.27%
Eye corrosion - 0.8980 89.80%
Eye irritation + 0.8736 87.36%
Skin irritation - 0.5327 53.27%
Skin corrosion - 0.9840 98.40%
Ames mutagenesis + 0.7400 74.00%
Human Ether-a-go-go-Related Gene inhibition - 0.6711 67.11%
Micronuclear + 0.8600 86.00%
Hepatotoxicity + 0.5750 57.50%
skin sensitisation - 0.9316 93.16%
Respiratory toxicity + 0.5333 53.33%
Reproductive toxicity + 0.7333 73.33%
Mitochondrial toxicity + 0.5250 52.50%
Nephrotoxicity + 0.5571 55.71%
Acute Oral Toxicity (c) III 0.9193 91.93%
Estrogen receptor binding + 0.9279 92.79%
Androgen receptor binding + 0.6304 63.04%
Thyroid receptor binding + 0.6221 62.21%
Glucocorticoid receptor binding + 0.8610 86.10%
Aromatase binding + 0.8045 80.45%
PPAR gamma + 0.7300 73.00%
Honey bee toxicity - 0.9244 92.44%
Biodegradation - 0.8000 80.00%
Crustacea aquatic toxicity - 0.5500 55.00%
Fish aquatic toxicity + 0.6426 64.26%

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
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 97.27% 95.56%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 95.78% 91.11%
CHEMBL3192 Q9BY41 Histone deacetylase 8 93.91% 93.99%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 93.66% 99.23%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 93.05% 94.00%
CHEMBL2581 P07339 Cathepsin D 92.63% 98.95%
CHEMBL1806 P11388 DNA topoisomerase II alpha 91.48% 89.00%
CHEMBL2535 P11166 Glucose transporter 90.42% 98.75%
CHEMBL1293249 Q13887 Kruppel-like factor 5 88.43% 86.33%
CHEMBL1255126 O15151 Protein Mdm4 85.30% 90.20%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 85.10% 94.45%
CHEMBL1937 Q92769 Histone deacetylase 2 83.47% 94.75%
CHEMBL4306 P22460 Voltage-gated potassium channel subunit Kv1.5 82.96% 94.03%
CHEMBL3091268 Q92753 Nuclear receptor ROR-beta 82.60% 95.50%
CHEMBL3401 O75469 Pregnane X receptor 81.88% 94.73%
CHEMBL5409 Q8TDU6 G-protein coupled bile acid receptor 1 80.57% 93.65%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 80.12% 85.14%

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.
Calophyllum thwaitesii
Patrinia rupestris
Pentaclethra eetveldeana

Cross-Links

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PubChem 86168207
LOTUS LTS0053150
wikiData Q104665116