9H-Xanthen-9-one, 1,3,8-trihydroxy-2,4,6-trimethoxy-

Details

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Internal ID ba9313ac-d127-4464-92bc-affa8fc5c3e2
Taxonomy Organoheterocyclic compounds > Benzopyrans > 1-benzopyrans > Xanthones
IUPAC Name 1,3,8-trihydroxy-2,4,6-trimethoxyxanthen-9-one
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C16H14O8/c1-21-6-4-7(17)9-8(5-6)24-14-10(11(9)18)12(19)15(22-2)13(20)16(14)23-3/h4-5,17,19-20H,1-3H3
InChI Key NQYVMORMBASBCH-UHFFFAOYSA-N
Popularity 8 references in papers

Physical and Chemical Properties

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Molecular Formula C16H14O8
Molecular Weight 334.28 g/mol
Exact Mass 334.06886740 g/mol
Topological Polar Surface Area (TPSA) 115.00 Ų
XlogP 2.40
Atomic LogP (AlogP) 2.09
H-Bond Acceptor 8
H-Bond Donor 3
Rotatable Bonds 3

Synonyms

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83016-69-7
1,6,8-Trihydroxy-3,5,7-trimethoxyxanthone
DTXSID90232131

2D Structure

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2D Structure of 9H-Xanthen-9-one, 1,3,8-trihydroxy-2,4,6-trimethoxy-

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9232 92.32%
Caco-2 + 0.6748 67.48%
Blood Brain Barrier - 0.7750 77.50%
Human oral bioavailability - 0.5571 55.71%
Subcellular localzation Mitochondria 0.5279 52.79%
OATP2B1 inhibitior - 0.7035 70.35%
OATP1B1 inhibitior + 0.8574 85.74%
OATP1B3 inhibitior + 0.9332 93.32%
MATE1 inhibitior + 0.5400 54.00%
OCT2 inhibitior - 0.9750 97.50%
BSEP inhibitior - 0.7231 72.31%
P-glycoprotein inhibitior - 0.5702 57.02%
P-glycoprotein substrate - 0.9003 90.03%
CYP3A4 substrate - 0.5000 50.00%
CYP2C9 substrate - 0.6401 64.01%
CYP2D6 substrate - 0.8296 82.96%
CYP3A4 inhibition + 0.5125 51.25%
CYP2C9 inhibition - 0.9202 92.02%
CYP2C19 inhibition - 0.6069 60.69%
CYP2D6 inhibition - 0.6399 63.99%
CYP1A2 inhibition + 0.9412 94.12%
CYP2C8 inhibition + 0.4514 45.14%
CYP inhibitory promiscuity + 0.6880 68.80%
UGT catelyzed + 0.7000 70.00%
Carcinogenicity (binary) - 0.9900 99.00%
Carcinogenicity (trinary) Non-required 0.6372 63.72%
Eye corrosion - 0.9745 97.45%
Eye irritation + 0.8424 84.24%
Skin irritation - 0.6903 69.03%
Skin corrosion - 0.9596 95.96%
Ames mutagenesis + 0.6500 65.00%
Human Ether-a-go-go-Related Gene inhibition - 0.7212 72.12%
Micronuclear + 0.8600 86.00%
Hepatotoxicity - 0.6000 60.00%
skin sensitisation - 0.9087 90.87%
Respiratory toxicity + 0.5111 51.11%
Reproductive toxicity + 0.8111 81.11%
Mitochondrial toxicity + 0.6125 61.25%
Nephrotoxicity - 0.7730 77.30%
Acute Oral Toxicity (c) III 0.5195 51.95%
Estrogen receptor binding + 0.8009 80.09%
Androgen receptor binding + 0.6265 62.65%
Thyroid receptor binding + 0.6290 62.90%
Glucocorticoid receptor binding + 0.8432 84.32%
Aromatase binding + 0.6091 60.91%
PPAR gamma + 0.7014 70.14%
Honey bee toxicity - 0.9273 92.73%
Biodegradation - 0.7500 75.00%
Crustacea aquatic toxicity - 0.6000 60.00%
Fish aquatic toxicity + 0.8379 83.79%

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 98.80% 91.11%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 94.13% 94.00%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 93.33% 94.45%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 92.55% 95.56%
CHEMBL1860 P10827 Thyroid hormone receptor alpha 91.11% 99.15%
CHEMBL1806 P11388 DNA topoisomerase II alpha 90.15% 89.00%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 86.94% 99.23%
CHEMBL2581 P07339 Cathepsin D 86.77% 98.95%
CHEMBL3060 Q9Y345 Glycine transporter 2 86.61% 99.17%
CHEMBL3194 P02766 Transthyretin 85.97% 90.71%
CHEMBL4208 P20618 Proteasome component C5 84.84% 90.00%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 83.64% 85.14%
CHEMBL1293249 Q13887 Kruppel-like factor 5 82.36% 86.33%
CHEMBL2535 P11166 Glucose transporter 80.43% 98.75%

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
Chironia krebsii

Cross-Links

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PubChem 5488734
LOTUS LTS0192445
wikiData Q83113158