3,4,6,7-Tetrahydroxyxanthone

Details

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Internal ID 157c8260-d7e3-4497-b047-01858c9c17d0
Taxonomy Organoheterocyclic compounds > Benzopyrans > 1-benzopyrans > Xanthones
IUPAC Name 2,3,5,6-tetrahydroxyxanthen-9-one
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C13H8O6/c14-7-2-1-5-11(17)6-3-8(15)9(16)4-10(6)19-13(5)12(7)18/h1-4,14-16,18H
InChI Key ZIUFQHOTGSSKBS-UHFFFAOYSA-N
Popularity 3 references in papers

Physical and Chemical Properties

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Molecular Formula C13H8O6
Molecular Weight 260.20 g/mol
Exact Mass 260.03208797 g/mol
Topological Polar Surface Area (TPSA) 107.00 Ų
XlogP 1.50
Atomic LogP (AlogP) 1.77
H-Bond Acceptor 6
H-Bond Donor 4
Rotatable Bonds 0

Synonyms

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2,3,5,6-tetrahydroxyxanthen-9-one
RefChem:90954
3467-Tetrahydroxyxanthone
CHEMBL477740
141642-11-7
SCHEMBL7330918
DTXSID50438632
BDBM50292544

2D Structure

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2D Structure of 3,4,6,7-Tetrahydroxyxanthone

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9438 94.38%
Caco-2 - 0.8178 81.78%
Blood Brain Barrier - 0.7500 75.00%
Human oral bioavailability - 0.5571 55.71%
Subcellular localzation Mitochondria 0.7026 70.26%
OATP2B1 inhibitior - 0.6510 65.10%
OATP1B1 inhibitior + 0.9561 95.61%
OATP1B3 inhibitior + 0.9936 99.36%
MATE1 inhibitior - 0.7800 78.00%
OCT2 inhibitior - 0.9500 95.00%
BSEP inhibitior - 0.9233 92.33%
P-glycoprotein inhibitior - 0.9373 93.73%
P-glycoprotein substrate - 0.9187 91.87%
CYP3A4 substrate - 0.6140 61.40%
CYP2C9 substrate - 0.8303 83.03%
CYP2D6 substrate - 0.8155 81.55%
CYP3A4 inhibition - 0.7624 76.24%
CYP2C9 inhibition - 0.5560 55.60%
CYP2C19 inhibition - 0.8199 81.99%
CYP2D6 inhibition - 0.8877 88.77%
CYP1A2 inhibition + 0.9683 96.83%
CYP2C8 inhibition - 0.8328 83.28%
CYP inhibitory promiscuity - 0.6892 68.92%
UGT catelyzed + 0.6000 60.00%
Carcinogenicity (binary) - 1.0000 100.00%
Carcinogenicity (trinary) Non-required 0.5787 57.87%
Eye corrosion - 0.9831 98.31%
Eye irritation + 0.9571 95.71%
Skin irritation + 0.6757 67.57%
Skin corrosion - 0.9607 96.07%
Ames mutagenesis - 0.5200 52.00%
Human Ether-a-go-go-Related Gene inhibition - 0.8931 89.31%
Micronuclear + 0.9400 94.00%
Hepatotoxicity + 0.5533 55.33%
skin sensitisation - 0.6642 66.42%
Respiratory toxicity + 0.6000 60.00%
Reproductive toxicity + 0.7111 71.11%
Mitochondrial toxicity + 0.5750 57.50%
Nephrotoxicity - 0.7949 79.49%
Acute Oral Toxicity (c) II 0.5564 55.64%
Estrogen receptor binding + 0.7311 73.11%
Androgen receptor binding + 0.8644 86.44%
Thyroid receptor binding + 0.5265 52.65%
Glucocorticoid receptor binding + 0.9296 92.96%
Aromatase binding + 0.7093 70.93%
PPAR gamma + 0.7549 75.49%
Honey bee toxicity - 0.8936 89.36%
Biodegradation - 0.8500 85.00%
Crustacea aquatic toxicity - 0.6200 62.00%
Fish aquatic toxicity + 0.9101 91.01%

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 99.63% 91.11%
CHEMBL1806 P11388 DNA topoisomerase II alpha 91.99% 89.00%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 91.52% 95.56%
CHEMBL1951 P21397 Monoamine oxidase A 91.21% 91.49%
CHEMBL1860 P10827 Thyroid hormone receptor alpha 90.15% 99.15%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 88.56% 94.45%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 88.56% 94.00%
CHEMBL3194 P02766 Transthyretin 87.46% 90.71%
CHEMBL2581 P07339 Cathepsin D 86.41% 98.95%
CHEMBL1163101 O75460 Serine/threonine-protein kinase/endoribonuclease IRE1 85.84% 98.11%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 84.43% 99.23%
CHEMBL5845 P23415 Glycine receptor subunit alpha-1 82.68% 90.71%
CHEMBL3401 O75469 Pregnane X receptor 80.70% 94.73%

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.
Tripterospermum lanceolatum

Cross-Links

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PubChem 10355232
NPASS NPC248102
ChEMBL CHEMBL477740
LOTUS LTS0231103
wikiData Q82254434