1,3-Dihydroxy-4,5-dimethoxyxanthone

Details

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Internal ID 0cc47a24-ad46-4504-bda7-1a362e92d8c7
Taxonomy Organoheterocyclic compounds > Benzopyrans > 1-benzopyrans > Xanthones
IUPAC Name 1,3-dihydroxy-4,5-dimethoxyxanthen-9-one
SMILES (Canonical) COC1=CC=CC2=C1OC3=C(C2=O)C(=CC(=C3OC)O)O
SMILES (Isomeric) COC1=CC=CC2=C1OC3=C(C2=O)C(=CC(=C3OC)O)O
InChI InChI=1S/C15H12O6/c1-19-10-5-3-4-7-12(18)11-8(16)6-9(17)14(20-2)15(11)21-13(7)10/h3-6,16-17H,1-2H3
InChI Key OKHSSWSJVGEHDK-UHFFFAOYSA-N
Popularity 4 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 1,3-Dihydroxy-4,5-dimethoxyxanthone

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9261 92.61%
Caco-2 + 0.8405 84.05%
Blood Brain Barrier - 0.7750 77.50%
Human oral bioavailability + 0.7286 72.86%
Subcellular localzation Mitochondria 0.5592 55.92%
OATP2B1 inhibitior - 0.7124 71.24%
OATP1B1 inhibitior + 0.9512 95.12%
OATP1B3 inhibitior + 0.9627 96.27%
MATE1 inhibitior + 0.5400 54.00%
OCT2 inhibitior - 0.9750 97.50%
BSEP inhibitior - 0.6620 66.20%
P-glycoprotein inhibitior - 0.5892 58.92%
P-glycoprotein substrate - 0.8007 80.07%
CYP3A4 substrate + 0.5472 54.72%
CYP2C9 substrate - 0.6401 64.01%
CYP2D6 substrate - 0.8296 82.96%
CYP3A4 inhibition + 0.6908 69.08%
CYP2C9 inhibition - 0.7416 74.16%
CYP2C19 inhibition + 0.6596 65.96%
CYP2D6 inhibition - 0.5311 53.11%
CYP1A2 inhibition + 0.9466 94.66%
CYP2C8 inhibition - 0.6338 63.38%
CYP inhibitory promiscuity + 0.7479 74.79%
UGT catelyzed + 0.7000 70.00%
Carcinogenicity (binary) - 0.9900 99.00%
Carcinogenicity (trinary) Non-required 0.6775 67.75%
Eye corrosion - 0.9667 96.67%
Eye irritation + 0.9384 93.84%
Skin irritation - 0.6148 61.48%
Skin corrosion - 0.9417 94.17%
Ames mutagenesis + 0.7000 70.00%
Human Ether-a-go-go-Related Gene inhibition - 0.5651 56.51%
Micronuclear + 0.9100 91.00%
Hepatotoxicity + 0.5625 56.25%
skin sensitisation - 0.8849 88.49%
Respiratory toxicity + 0.5333 53.33%
Reproductive toxicity + 0.8556 85.56%
Mitochondrial toxicity + 0.6375 63.75%
Nephrotoxicity - 0.6831 68.31%
Acute Oral Toxicity (c) III 0.6228 62.28%
Estrogen receptor binding + 0.8864 88.64%
Androgen receptor binding + 0.6853 68.53%
Thyroid receptor binding + 0.7026 70.26%
Glucocorticoid receptor binding + 0.9279 92.79%
Aromatase binding + 0.7456 74.56%
PPAR gamma + 0.7804 78.04%
Honey bee toxicity - 0.9009 90.09%
Biodegradation - 0.8250 82.50%
Crustacea aquatic toxicity + 0.5200 52.00%
Fish aquatic toxicity + 0.8268 82.68%

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 97.86% 91.11%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 96.45% 95.56%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 94.24% 94.00%
CHEMBL3192 Q9BY41 Histone deacetylase 8 93.28% 93.99%
CHEMBL1806 P11388 DNA topoisomerase II alpha 92.76% 89.00%
CHEMBL2535 P11166 Glucose transporter 92.76% 98.75%
CHEMBL2581 P07339 Cathepsin D 90.98% 98.95%
CHEMBL1293249 Q13887 Kruppel-like factor 5 90.52% 86.33%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 88.47% 99.23%
CHEMBL1860 P10827 Thyroid hormone receptor alpha 86.20% 99.15%
CHEMBL4306 P22460 Voltage-gated potassium channel subunit Kv1.5 83.84% 94.03%
CHEMBL5409 Q8TDU6 G-protein coupled bile acid receptor 1 83.04% 93.65%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 82.92% 94.45%
CHEMBL3401 O75469 Pregnane X receptor 82.21% 94.73%
CHEMBL3091268 Q92753 Nuclear receptor ROR-beta 81.91% 95.50%
CHEMBL3060 Q9Y345 Glycine transporter 2 81.53% 99.17%
CHEMBL2094127 P06493 Cyclin-dependent kinase 1/cyclin B 81.50% 96.00%
CHEMBL1255126 O15151 Protein Mdm4 81.10% 90.20%
CHEMBL2373 P21730 C5a anaphylatoxin chemotactic receptor 80.53% 92.62%

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.
Frasera speciosa
Polygala tenuifolia
Swertia pseudochinensis

Cross-Links

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PubChem 5316765
NPASS NPC276164
LOTUS LTS0198479
wikiData Q105193550