1,6-Dihydroxy-5,7-dimethoxyxanthone

Details

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Internal ID 1416d268-b1a3-4104-9bb9-1d796fd525e9
Taxonomy Organoheterocyclic compounds > Benzopyrans > 1-benzopyrans > Xanthones
IUPAC Name 1,6-dihydroxy-5,7-dimethoxyxanthen-9-one
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C15H12O6/c1-19-10-6-7-12(17)11-8(16)4-3-5-9(11)21-14(7)15(20-2)13(10)18/h3-6,16,18H,1-2H3
InChI Key JNEXYTCBXFBLEK-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 2.70
Atomic LogP (AlogP) 2.37
H-Bond Acceptor 6
H-Bond Donor 2
Rotatable Bonds 2

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 1,6-Dihydroxy-5,7-dimethoxyxanthone

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9642 96.42%
Caco-2 + 0.5894 58.94%
Blood Brain Barrier - 0.7750 77.50%
Human oral bioavailability + 0.7000 70.00%
Subcellular localzation Mitochondria 0.7364 73.64%
OATP2B1 inhibitior - 0.5763 57.63%
OATP1B1 inhibitior + 0.9198 91.98%
OATP1B3 inhibitior + 0.9851 98.51%
MATE1 inhibitior + 0.5400 54.00%
OCT2 inhibitior - 0.9500 95.00%
BSEP inhibitior - 0.7362 73.62%
P-glycoprotein inhibitior - 0.5309 53.09%
P-glycoprotein substrate - 0.8315 83.15%
CYP3A4 substrate + 0.5460 54.60%
CYP2C9 substrate - 0.6401 64.01%
CYP2D6 substrate - 0.8296 82.96%
CYP3A4 inhibition - 0.6420 64.20%
CYP2C9 inhibition - 0.7071 70.71%
CYP2C19 inhibition + 0.7531 75.31%
CYP2D6 inhibition - 0.6235 62.35%
CYP1A2 inhibition + 0.9606 96.06%
CYP2C8 inhibition + 0.5345 53.45%
CYP inhibitory promiscuity + 0.6446 64.46%
UGT catelyzed - 0.6000 60.00%
Carcinogenicity (binary) - 0.9900 99.00%
Carcinogenicity (trinary) Non-required 0.6331 63.31%
Eye corrosion - 0.9655 96.55%
Eye irritation + 0.8996 89.96%
Skin irritation - 0.6099 60.99%
Skin corrosion - 0.9698 96.98%
Ames mutagenesis + 0.6700 67.00%
Human Ether-a-go-go-Related Gene inhibition - 0.8236 82.36%
Micronuclear + 0.9100 91.00%
Hepatotoxicity + 0.5250 52.50%
skin sensitisation - 0.9149 91.49%
Respiratory toxicity + 0.6222 62.22%
Reproductive toxicity + 0.8556 85.56%
Mitochondrial toxicity + 0.6125 61.25%
Nephrotoxicity - 0.8291 82.91%
Acute Oral Toxicity (c) III 0.5708 57.08%
Estrogen receptor binding + 0.8616 86.16%
Androgen receptor binding + 0.6742 67.42%
Thyroid receptor binding + 0.7200 72.00%
Glucocorticoid receptor binding + 0.8951 89.51%
Aromatase binding + 0.6364 63.64%
PPAR gamma + 0.7739 77.39%
Honey bee toxicity - 0.9230 92.30%
Biodegradation - 0.8000 80.00%
Crustacea aquatic toxicity - 0.5900 59.00%
Fish aquatic toxicity + 0.8585 85.85%

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 98.73% 91.11%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 96.44% 95.56%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 94.82% 94.00%
CHEMBL1806 P11388 DNA topoisomerase II alpha 94.24% 89.00%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 93.58% 94.45%
CHEMBL2581 P07339 Cathepsin D 93.08% 98.95%
CHEMBL1293249 Q13887 Kruppel-like factor 5 91.93% 86.33%
CHEMBL2535 P11166 Glucose transporter 91.15% 98.75%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 89.99% 99.23%
CHEMBL3192 Q9BY41 Histone deacetylase 8 89.92% 93.99%
CHEMBL1907 P15144 Aminopeptidase N 86.62% 93.31%
CHEMBL1937 Q92769 Histone deacetylase 2 85.37% 94.75%
CHEMBL4306 P22460 Voltage-gated potassium channel subunit Kv1.5 84.76% 94.03%
CHEMBL1951 P21397 Monoamine oxidase A 84.37% 91.49%
CHEMBL2373 P21730 C5a anaphylatoxin chemotactic receptor 83.91% 92.62%
CHEMBL1255126 O15151 Protein Mdm4 83.74% 90.20%
CHEMBL3060 Q9Y345 Glycine transporter 2 82.39% 99.17%
CHEMBL3401 O75469 Pregnane X receptor 82.13% 94.73%
CHEMBL1860 P10827 Thyroid hormone receptor alpha 81.99% 99.15%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 81.82% 85.14%
CHEMBL1163101 O75460 Serine/threonine-protein kinase/endoribonuclease IRE1 80.34% 98.11%

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 linii

Cross-Links

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PubChem 102412718
LOTUS LTS0138716
wikiData Q105131872