1,6-Dihydroxy-7-methoxyxanthone

Details

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Internal ID 6edcd650-8e66-4965-9b17-d5ccae2662c2
Taxonomy Organoheterocyclic compounds > Benzopyrans > 1-benzopyrans > Xanthones
IUPAC Name 1,6-dihydroxy-7-methoxyxanthen-9-one
SMILES (Canonical) COC1=C(C=C2C(=C1)C(=O)C3=C(C=CC=C3O2)O)O
SMILES (Isomeric) COC1=C(C=C2C(=C1)C(=O)C3=C(C=CC=C3O2)O)O
InChI InChI=1S/C14H10O5/c1-18-12-5-7-11(6-9(12)16)19-10-4-2-3-8(15)13(10)14(7)17/h2-6,15-16H,1H3
InChI Key ZPHCTBYBIZXYGV-UHFFFAOYSA-N
Popularity 3 references in papers

Physical and Chemical Properties

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Molecular Formula C14H10O5
Molecular Weight 258.23 g/mol
Exact Mass 258.05282342 g/mol
Topological Polar Surface Area (TPSA) 76.00 Ų
XlogP 2.80
Atomic LogP (AlogP) 2.37
H-Bond Acceptor 5
H-Bond Donor 2
Rotatable Bonds 1

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 1,6-Dihydroxy-7-methoxyxanthone

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9711 97.11%
Caco-2 + 0.7245 72.45%
Blood Brain Barrier - 0.8000 80.00%
Human oral bioavailability + 0.8143 81.43%
Subcellular localzation Mitochondria 0.7377 73.77%
OATP2B1 inhibitior - 0.7060 70.60%
OATP1B1 inhibitior + 0.9449 94.49%
OATP1B3 inhibitior + 0.9934 99.34%
MATE1 inhibitior + 0.5400 54.00%
OCT2 inhibitior - 0.9000 90.00%
BSEP inhibitior - 0.8214 82.14%
P-glycoprotein inhibitior - 0.6650 66.50%
P-glycoprotein substrate - 0.8304 83.04%
CYP3A4 substrate + 0.5118 51.18%
CYP2C9 substrate - 0.6401 64.01%
CYP2D6 substrate - 0.8296 82.96%
CYP3A4 inhibition - 0.7181 71.81%
CYP2C9 inhibition - 0.5805 58.05%
CYP2C19 inhibition + 0.7909 79.09%
CYP2D6 inhibition - 0.7438 74.38%
CYP1A2 inhibition + 0.9811 98.11%
CYP2C8 inhibition - 0.5861 58.61%
CYP inhibitory promiscuity + 0.6572 65.72%
UGT catelyzed - 0.5000 50.00%
Carcinogenicity (binary) - 0.9900 99.00%
Carcinogenicity (trinary) Non-required 0.5675 56.75%
Eye corrosion - 0.9577 95.77%
Eye irritation + 0.9214 92.14%
Skin irritation - 0.5200 52.00%
Skin corrosion - 0.9642 96.42%
Ames mutagenesis + 0.6800 68.00%
Human Ether-a-go-go-Related Gene inhibition - 0.7299 72.99%
Micronuclear + 0.9200 92.00%
Hepatotoxicity - 0.6000 60.00%
skin sensitisation - 0.9205 92.05%
Respiratory toxicity + 0.5778 57.78%
Reproductive toxicity + 0.8444 84.44%
Mitochondrial toxicity + 0.5750 57.50%
Nephrotoxicity - 0.6698 66.98%
Acute Oral Toxicity (c) III 0.8197 81.97%
Estrogen receptor binding + 0.9179 91.79%
Androgen receptor binding + 0.7267 72.67%
Thyroid receptor binding + 0.7038 70.38%
Glucocorticoid receptor binding + 0.9673 96.73%
Aromatase binding + 0.7947 79.47%
PPAR gamma + 0.7945 79.45%
Honey bee toxicity - 0.9243 92.43%
Biodegradation - 0.9000 90.00%
Crustacea aquatic toxicity - 0.5949 59.49%
Fish aquatic toxicity + 0.8258 82.58%

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 96.62% 95.56%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 96.44% 91.11%
CHEMBL3192 Q9BY41 Histone deacetylase 8 94.86% 93.99%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 93.99% 94.00%
CHEMBL2581 P07339 Cathepsin D 93.97% 98.95%
CHEMBL1806 P11388 DNA topoisomerase II alpha 92.50% 89.00%
CHEMBL2535 P11166 Glucose transporter 91.14% 98.75%
CHEMBL1293249 Q13887 Kruppel-like factor 5 90.53% 86.33%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 87.74% 94.45%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 86.89% 99.23%
CHEMBL3401 O75469 Pregnane X receptor 84.44% 94.73%
CHEMBL241 Q14432 Phosphodiesterase 3A 84.42% 92.94%
CHEMBL1907 P15144 Aminopeptidase N 84.40% 93.31%
CHEMBL4306 P22460 Voltage-gated potassium channel subunit Kv1.5 84.06% 94.03%
CHEMBL5409 Q8TDU6 G-protein coupled bile acid receptor 1 82.11% 93.65%
CHEMBL1255126 O15151 Protein Mdm4 81.96% 90.20%
CHEMBL3060 Q9Y345 Glycine transporter 2 80.25% 99.17%

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.
Agasthiyamalaia pauciflora
Garcinia linii

Cross-Links

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PubChem 85728427
LOTUS LTS0042376
wikiData Q105380900