1,3,5,6-Tetrahydroxy-7-methoxyxanthen-9-one

Details

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Internal ID ad4790c4-69d8-4997-8f16-da371d4cf89d
Taxonomy Organoheterocyclic compounds > Benzopyrans > 1-benzopyrans > Xanthones
IUPAC Name 1,3,5,6-tetrahydroxy-7-methoxyxanthen-9-one
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C14H10O7/c1-20-9-4-6-11(17)10-7(16)2-5(15)3-8(10)21-14(6)13(19)12(9)18/h2-4,15-16,18-19H,1H3
InChI Key LOJMAPGMVDHGEL-UHFFFAOYSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C14H10O7
Molecular Weight 290.22 g/mol
Exact Mass 290.04265265 g/mol
Topological Polar Surface Area (TPSA) 116.00 Ų
XlogP 2.10
Atomic LogP (AlogP) 1.78
H-Bond Acceptor 7
H-Bond Donor 4
Rotatable Bonds 1

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 1,3,5,6-Tetrahydroxy-7-methoxyxanthen-9-one

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.8830 88.30%
Caco-2 - 0.6861 68.61%
Blood Brain Barrier - 0.7750 77.50%
Human oral bioavailability - 0.6000 60.00%
Subcellular localzation Mitochondria 0.5329 53.29%
OATP2B1 inhibitior - 0.5420 54.20%
OATP1B1 inhibitior + 0.8672 86.72%
OATP1B3 inhibitior + 0.9939 99.39%
MATE1 inhibitior + 0.5400 54.00%
OCT2 inhibitior - 0.9250 92.50%
BSEP inhibitior - 0.7652 76.52%
P-glycoprotein inhibitior - 0.7718 77.18%
P-glycoprotein substrate - 0.7388 73.88%
CYP3A4 substrate + 0.5303 53.03%
CYP2C9 substrate - 0.6887 68.87%
CYP2D6 substrate - 0.8370 83.70%
CYP3A4 inhibition + 0.5370 53.70%
CYP2C9 inhibition - 0.9516 95.16%
CYP2C19 inhibition - 0.7992 79.92%
CYP2D6 inhibition - 0.8274 82.74%
CYP1A2 inhibition + 0.9658 96.58%
CYP2C8 inhibition + 0.6320 63.20%
CYP inhibitory promiscuity + 0.5777 57.77%
UGT catelyzed - 0.5000 50.00%
Carcinogenicity (binary) - 0.9800 98.00%
Carcinogenicity (trinary) Non-required 0.6223 62.23%
Eye corrosion - 0.9690 96.90%
Eye irritation + 0.9108 91.08%
Skin irritation - 0.5579 55.79%
Skin corrosion - 0.9129 91.29%
Ames mutagenesis + 0.7100 71.00%
Human Ether-a-go-go-Related Gene inhibition - 0.6780 67.80%
Micronuclear + 0.9000 90.00%
Hepatotoxicity - 0.5625 56.25%
skin sensitisation - 0.8609 86.09%
Respiratory toxicity + 0.6222 62.22%
Reproductive toxicity + 0.8444 84.44%
Mitochondrial toxicity + 0.6000 60.00%
Nephrotoxicity - 0.7642 76.42%
Acute Oral Toxicity (c) III 0.7135 71.35%
Estrogen receptor binding + 0.8702 87.02%
Androgen receptor binding + 0.6983 69.83%
Thyroid receptor binding + 0.5294 52.94%
Glucocorticoid receptor binding + 0.9492 94.92%
Aromatase binding + 0.7427 74.27%
PPAR gamma + 0.8160 81.60%
Honey bee toxicity - 0.8493 84.93%
Biodegradation - 0.8000 80.00%
Crustacea aquatic toxicity - 0.5000 50.00%
Fish aquatic toxicity + 0.8178 81.78%

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 98.55% 91.11%
CHEMBL1806 P11388 DNA topoisomerase II alpha 93.96% 89.00%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 93.68% 95.56%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 93.51% 94.00%
CHEMBL3194 P02766 Transthyretin 90.94% 90.71%
CHEMBL1293249 Q13887 Kruppel-like factor 5 90.02% 86.33%
CHEMBL2581 P07339 Cathepsin D 89.80% 98.95%
CHEMBL1163101 O75460 Serine/threonine-protein kinase/endoribonuclease IRE1 88.91% 98.11%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 88.85% 99.23%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 87.77% 94.45%
CHEMBL3060 Q9Y345 Glycine transporter 2 86.54% 99.17%
CHEMBL3192 Q9BY41 Histone deacetylase 8 85.51% 93.99%
CHEMBL241 Q14432 Phosphodiesterase 3A 83.69% 92.94%
CHEMBL2535 P11166 Glucose transporter 83.40% 98.75%
CHEMBL3401 O75469 Pregnane X receptor 82.39% 94.73%
CHEMBL2002 P12268 Inosine-5'-monophosphate dehydrogenase 2 81.71% 98.21%
CHEMBL3864 Q06124 Protein-tyrosine phosphatase 2C 81.55% 94.42%
CHEMBL2373 P21730 C5a anaphylatoxin chemotactic receptor 80.85% 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.
Calophyllum inophyllum

Cross-Links

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PubChem 86180520
NPASS NPC33319
LOTUS LTS0214089
wikiData Q105154753