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

Details

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Internal ID e274b669-2741-4bcf-a16f-6df5b30cd64a
Taxonomy Organoheterocyclic compounds > Benzopyrans > 1-benzopyrans > Xanthones
IUPAC Name 3,8-dihydroxy-1,2,4-trimethoxyxanthen-9-one
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C16H14O7/c1-20-13-10-11(18)9-7(17)5-4-6-8(9)23-14(10)16(22-3)12(19)15(13)21-2/h4-6,17,19H,1-3H3
InChI Key URTSJLZSLJCTDJ-UHFFFAOYSA-N
Popularity 4 references in papers

Physical and Chemical Properties

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Molecular Formula C16H14O7
Molecular Weight 318.28 g/mol
Exact Mass 318.07395278 g/mol
Topological Polar Surface Area (TPSA) 94.50 Ų
XlogP 2.70
Atomic LogP (AlogP) 2.38
H-Bond Acceptor 7
H-Bond Donor 2
Rotatable Bonds 3

Synonyms

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110187-38-7
DTXSID90149159

2D Structure

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

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9617 96.17%
Caco-2 + 0.7394 73.94%
Blood Brain Barrier - 0.7750 77.50%
Human oral bioavailability + 0.6714 67.14%
Subcellular localzation Mitochondria 0.7093 70.93%
OATP2B1 inhibitior - 0.7101 71.01%
OATP1B1 inhibitior + 0.8883 88.83%
OATP1B3 inhibitior + 0.9698 96.98%
MATE1 inhibitior + 0.5400 54.00%
OCT2 inhibitior - 0.9500 95.00%
BSEP inhibitior - 0.6279 62.79%
P-glycoprotein inhibitior - 0.5065 50.65%
P-glycoprotein substrate - 0.8977 89.77%
CYP3A4 substrate - 0.5000 50.00%
CYP2C9 substrate - 0.6401 64.01%
CYP2D6 substrate - 0.8296 82.96%
CYP3A4 inhibition - 0.7782 77.82%
CYP2C9 inhibition - 0.9325 93.25%
CYP2C19 inhibition - 0.5514 55.14%
CYP2D6 inhibition - 0.7363 73.63%
CYP1A2 inhibition + 0.9561 95.61%
CYP2C8 inhibition - 0.6152 61.52%
CYP inhibitory promiscuity + 0.5753 57.53%
UGT catelyzed - 0.6000 60.00%
Carcinogenicity (binary) - 0.9900 99.00%
Carcinogenicity (trinary) Non-required 0.6097 60.97%
Eye corrosion - 0.9746 97.46%
Eye irritation + 0.8131 81.31%
Skin irritation - 0.6975 69.75%
Skin corrosion - 0.9788 97.88%
Ames mutagenesis + 0.6400 64.00%
Human Ether-a-go-go-Related Gene inhibition - 0.7441 74.41%
Micronuclear + 0.8500 85.00%
Hepatotoxicity + 0.6250 62.50%
skin sensitisation - 0.9328 93.28%
Respiratory toxicity + 0.5333 53.33%
Reproductive toxicity + 0.8111 81.11%
Mitochondrial toxicity + 0.5750 57.50%
Nephrotoxicity - 0.6887 68.87%
Acute Oral Toxicity (c) II 0.4834 48.34%
Estrogen receptor binding + 0.7584 75.84%
Androgen receptor binding + 0.5327 53.27%
Thyroid receptor binding + 0.6417 64.17%
Glucocorticoid receptor binding + 0.8307 83.07%
Aromatase binding + 0.5224 52.24%
PPAR gamma + 0.7371 73.71%
Honey bee toxicity - 0.9499 94.99%
Biodegradation - 0.6500 65.00%
Crustacea aquatic toxicity - 0.6400 64.00%
Fish aquatic toxicity + 0.8676 86.76%

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 97.21% 91.11%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 94.45% 95.56%
CHEMBL2581 P07339 Cathepsin D 93.49% 98.95%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 93.10% 94.00%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 92.03% 99.23%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 91.52% 94.45%
CHEMBL3192 Q9BY41 Histone deacetylase 8 91.08% 93.99%
CHEMBL1806 P11388 DNA topoisomerase II alpha 88.41% 89.00%
CHEMBL1293249 Q13887 Kruppel-like factor 5 87.68% 86.33%
CHEMBL1163101 O75460 Serine/threonine-protein kinase/endoribonuclease IRE1 85.86% 98.11%
CHEMBL3401 O75469 Pregnane X receptor 83.83% 94.73%
CHEMBL1937 Q92769 Histone deacetylase 2 80.79% 94.75%
CHEMBL2535 P11166 Glucose transporter 80.55% 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.
Calophyllum teysmannii

Cross-Links

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PubChem 5491745
LOTUS LTS0240595
wikiData Q83014849