3,5,6-Trihydroxy-1-methoxy-9h-xanthen-9-one

Details

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Internal ID 86650b00-4931-43c4-a1a9-0d072fd77644
Taxonomy Organoheterocyclic compounds > Benzopyrans > 1-benzopyrans > Xanthones
IUPAC Name 3,5,6-trihydroxy-1-methoxyxanthen-9-one
SMILES (Canonical) COC1=CC(=CC2=C1C(=O)C3=C(O2)C(=C(C=C3)O)O)O
SMILES (Isomeric) COC1=CC(=CC2=C1C(=O)C3=C(O2)C(=C(C=C3)O)O)O
InChI InChI=1S/C14H10O6/c1-19-9-4-6(15)5-10-11(9)12(17)7-2-3-8(16)13(18)14(7)20-10/h2-5,15-16,18H,1H3
InChI Key RPWWZFGIMKOBGX-UHFFFAOYSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C14H10O6
Molecular Weight 274.22 g/mol
Exact Mass 274.04773803 g/mol
Topological Polar Surface Area (TPSA) 96.20 Ų
XlogP 1.90
Atomic LogP (AlogP) 2.07
H-Bond Acceptor 6
H-Bond Donor 3
Rotatable Bonds 1

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 3,5,6-Trihydroxy-1-methoxy-9h-xanthen-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 + 0.9448 94.48%
Caco-2 - 0.8754 87.54%
Blood Brain Barrier - 0.7750 77.50%
Human oral bioavailability - 0.6571 65.71%
Subcellular localzation Mitochondria 0.7176 71.76%
OATP2B1 inhibitior - 0.5587 55.87%
OATP1B1 inhibitior + 0.9334 93.34%
OATP1B3 inhibitior + 1.0000 100.00%
MATE1 inhibitior - 0.7600 76.00%
OCT2 inhibitior - 0.9000 90.00%
BSEP inhibitior - 0.7790 77.90%
P-glycoprotein inhibitior - 0.8323 83.23%
P-glycoprotein substrate - 0.7610 76.10%
CYP3A4 substrate + 0.5142 51.42%
CYP2C9 substrate - 0.8397 83.97%
CYP2D6 substrate - 0.7876 78.76%
CYP3A4 inhibition - 0.7681 76.81%
CYP2C9 inhibition - 0.8896 88.96%
CYP2C19 inhibition - 0.5820 58.20%
CYP2D6 inhibition - 0.8589 85.89%
CYP1A2 inhibition + 0.9796 97.96%
CYP2C8 inhibition + 0.6104 61.04%
CYP inhibitory promiscuity - 0.5398 53.98%
UGT catelyzed - 0.5000 50.00%
Carcinogenicity (binary) - 0.9800 98.00%
Carcinogenicity (trinary) Non-required 0.5599 55.99%
Eye corrosion - 0.9632 96.32%
Eye irritation + 0.8707 87.07%
Skin irritation - 0.5421 54.21%
Skin corrosion - 0.9458 94.58%
Ames mutagenesis + 0.7000 70.00%
Human Ether-a-go-go-Related Gene inhibition - 0.8311 83.11%
Micronuclear + 0.9100 91.00%
Hepatotoxicity - 0.5125 51.25%
skin sensitisation - 0.8982 89.82%
Respiratory toxicity + 0.5222 52.22%
Reproductive toxicity + 0.8444 84.44%
Mitochondrial toxicity + 0.6000 60.00%
Nephrotoxicity - 0.6948 69.48%
Acute Oral Toxicity (c) III 0.7485 74.85%
Estrogen receptor binding + 0.9093 90.93%
Androgen receptor binding + 0.8560 85.60%
Thyroid receptor binding + 0.5364 53.64%
Glucocorticoid receptor binding + 0.9241 92.41%
Aromatase binding + 0.7954 79.54%
PPAR gamma + 0.7369 73.69%
Honey bee toxicity - 0.8888 88.88%
Biodegradation - 0.7750 77.50%
Crustacea aquatic toxicity + 0.5151 51.51%
Fish aquatic toxicity + 0.8510 85.10%

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 99.32% 91.11%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 95.69% 94.00%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 94.80% 95.56%
CHEMBL1806 P11388 DNA topoisomerase II alpha 93.77% 89.00%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 93.42% 94.45%
CHEMBL3194 P02766 Transthyretin 92.66% 90.71%
CHEMBL1163101 O75460 Serine/threonine-protein kinase/endoribonuclease IRE1 91.33% 98.11%
CHEMBL1951 P21397 Monoamine oxidase A 90.89% 91.49%
CHEMBL1293249 Q13887 Kruppel-like factor 5 89.03% 86.33%
CHEMBL2581 P07339 Cathepsin D 88.72% 98.95%
CHEMBL1860 P10827 Thyroid hormone receptor alpha 88.20% 99.15%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 86.57% 99.23%
CHEMBL2535 P11166 Glucose transporter 86.07% 98.75%
CHEMBL3192 Q9BY41 Histone deacetylase 8 85.90% 93.99%
CHEMBL2085 P14174 Macrophage migration inhibitory factor 83.49% 80.78%
CHEMBL225 P28335 Serotonin 2c (5-HT2c) receptor 83.27% 89.62%
CHEMBL3864 Q06124 Protein-tyrosine phosphatase 2C 83.07% 94.42%
CHEMBL3060 Q9Y345 Glycine transporter 2 82.05% 99.17%
CHEMBL5409 Q8TDU6 G-protein coupled bile acid receptor 1 81.61% 93.65%
CHEMBL3401 O75469 Pregnane X receptor 80.43% 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.
Cratoxylum cochinchinense

Cross-Links

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PubChem 11277329
LOTUS LTS0186773
wikiData Q105243106