1,3,5-Trimethoxyxanthone

Details

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Internal ID 6087ddac-09c7-41be-b592-a94aaaf0eeef
Taxonomy Organoheterocyclic compounds > Benzopyrans > 1-benzopyrans > Xanthones
IUPAC Name 1,3,5-trimethoxyxanthen-9-one
SMILES (Canonical) COC1=CC=CC2=C1OC3=C(C2=O)C(=CC(=C3)OC)OC
SMILES (Isomeric) COC1=CC=CC2=C1OC3=C(C2=O)C(=CC(=C3)OC)OC
InChI InChI=1S/C16H14O5/c1-18-9-7-12(20-3)14-13(8-9)21-16-10(15(14)17)5-4-6-11(16)19-2/h4-8H,1-3H3
InChI Key RZTTWIXYIUTQIT-UHFFFAOYSA-N
Popularity 4 references in papers

Physical and Chemical Properties

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Molecular Formula C16H14O5
Molecular Weight 286.28 g/mol
Exact Mass 286.08412354 g/mol
Topological Polar Surface Area (TPSA) 54.00 Ų
XlogP 2.90
Atomic LogP (AlogP) 2.97
H-Bond Acceptor 5
H-Bond Donor 0
Rotatable Bonds 3

Synonyms

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CHEMBL186416
1,3,5-trimethoxyxanthen-9-one
6563-50-4
SCHEMBL8484364
DTXSID80474588
RZTTWIXYIUTQIT-UHFFFAOYSA-N
1,3,5-Trimethoxy-xanthen-9-one
BDBM50155432

2D Structure

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2D Structure of 1,3,5-Trimethoxyxanthone

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9873 98.73%
Caco-2 + 0.7974 79.74%
Blood Brain Barrier - 0.6000 60.00%
Human oral bioavailability + 0.7429 74.29%
Subcellular localzation Mitochondria 0.5667 56.67%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9620 96.20%
OATP1B3 inhibitior + 0.9791 97.91%
MATE1 inhibitior - 0.9600 96.00%
OCT2 inhibitior - 0.9750 97.50%
BSEP inhibitior + 0.6133 61.33%
P-glycoprotein inhibitior + 0.7428 74.28%
P-glycoprotein substrate - 0.8522 85.22%
CYP3A4 substrate + 0.5470 54.70%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.7654 76.54%
CYP3A4 inhibition + 0.6462 64.62%
CYP2C9 inhibition - 0.9486 94.86%
CYP2C19 inhibition + 0.5978 59.78%
CYP2D6 inhibition - 0.8123 81.23%
CYP1A2 inhibition + 0.9723 97.23%
CYP2C8 inhibition - 0.6993 69.93%
CYP inhibitory promiscuity + 0.5998 59.98%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.9600 96.00%
Carcinogenicity (trinary) Non-required 0.5404 54.04%
Eye corrosion - 0.9027 90.27%
Eye irritation + 0.8198 81.98%
Skin irritation - 0.7224 72.24%
Skin corrosion - 0.9904 99.04%
Ames mutagenesis + 0.7700 77.00%
Human Ether-a-go-go-Related Gene inhibition - 0.3912 39.12%
Micronuclear + 0.7700 77.00%
Hepatotoxicity - 0.6375 63.75%
skin sensitisation - 0.9228 92.28%
Respiratory toxicity - 0.5333 53.33%
Reproductive toxicity + 0.7000 70.00%
Mitochondrial toxicity - 0.6000 60.00%
Nephrotoxicity - 0.6209 62.09%
Acute Oral Toxicity (c) II 0.6438 64.38%
Estrogen receptor binding + 0.8561 85.61%
Androgen receptor binding + 0.8148 81.48%
Thyroid receptor binding + 0.6546 65.46%
Glucocorticoid receptor binding + 0.8512 85.12%
Aromatase binding + 0.8576 85.76%
PPAR gamma + 0.7224 72.24%
Honey bee toxicity - 0.8811 88.11%
Biodegradation - 0.8500 85.00%
Crustacea aquatic toxicity + 0.6900 69.00%
Fish aquatic toxicity + 0.7747 77.47%

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
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 97.52% 95.56%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 95.02% 91.11%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 94.58% 94.00%
CHEMBL3192 Q9BY41 Histone deacetylase 8 94.39% 93.99%
CHEMBL2535 P11166 Glucose transporter 92.46% 98.75%
CHEMBL1907 P15144 Aminopeptidase N 91.02% 93.31%
CHEMBL2581 P07339 Cathepsin D 90.39% 98.95%
CHEMBL1293249 Q13887 Kruppel-like factor 5 89.86% 86.33%
CHEMBL1806 P11388 DNA topoisomerase II alpha 88.80% 89.00%
CHEMBL4306 P22460 Voltage-gated potassium channel subunit Kv1.5 88.60% 94.03%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 87.33% 99.23%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 85.85% 85.14%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 85.63% 96.00%
CHEMBL3091268 Q92753 Nuclear receptor ROR-beta 85.49% 95.50%
CHEMBL2373 P21730 C5a anaphylatoxin chemotactic receptor 84.91% 92.62%
CHEMBL3401 O75469 Pregnane X receptor 84.23% 94.73%
CHEMBL4478 Q00975 Voltage-gated N-type calcium channel alpha-1B subunit 83.75% 97.14%
CHEMBL2146302 O94925 Glutaminase kidney isoform, mitochondrial 83.66% 100.00%
CHEMBL5608 Q16288 NT-3 growth factor receptor 80.78% 95.89%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 80.69% 94.45%

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.
Haploclathra paniculata

Cross-Links

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PubChem 11953368
LOTUS LTS0199462
wikiData Q82304691