(3,6-Dimethoxy-8-methyl-9-oxoxanthen-1-yl) acetate

Details

Top
Internal ID 113a2128-9bb2-4d70-8eb4-7bbbdbb30e75
Taxonomy Organoheterocyclic compounds > Benzopyrans > 1-benzopyrans > Xanthones
IUPAC Name (3,6-dimethoxy-8-methyl-9-oxoxanthen-1-yl) acetate
SMILES (Canonical) CC1=CC(=CC2=C1C(=O)C3=C(O2)C=C(C=C3OC(=O)C)OC)OC
SMILES (Isomeric) CC1=CC(=CC2=C1C(=O)C3=C(O2)C=C(C=C3OC(=O)C)OC)OC
InChI InChI=1S/C18H16O6/c1-9-5-11(21-3)6-13-16(9)18(20)17-14(23-10(2)19)7-12(22-4)8-15(17)24-13/h5-8H,1-4H3
InChI Key UYQKCWXNGHXDPJ-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

Top
Molecular Formula C18H16O6
Molecular Weight 328.30 g/mol
Exact Mass 328.09468823 g/mol
Topological Polar Surface Area (TPSA) 71.10 Ų
XlogP 3.00
Atomic LogP (AlogP) 3.20
H-Bond Acceptor 6
H-Bond Donor 0
Rotatable Bonds 3

Synonyms

Top
There are no found synonyms.

2D Structure

Top
2D Structure of (3,6-Dimethoxy-8-methyl-9-oxoxanthen-1-yl) acetate

3D Structure

Top

ADMET Properties (via admetSAR 2)

Top
Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9790 97.90%
Caco-2 + 0.8327 83.27%
Blood Brain Barrier - 0.5500 55.00%
Human oral bioavailability + 0.5286 52.86%
Subcellular localzation Mitochondria 0.5549 55.49%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9486 94.86%
OATP1B3 inhibitior + 0.9720 97.20%
MATE1 inhibitior - 0.9600 96.00%
OCT2 inhibitior - 1.0000 100.00%
BSEP inhibitior - 0.4855 48.55%
P-glycoprotein inhibitior + 0.7665 76.65%
P-glycoprotein substrate - 0.8991 89.91%
CYP3A4 substrate - 0.5266 52.66%
CYP2C9 substrate - 0.6250 62.50%
CYP2D6 substrate - 0.8803 88.03%
CYP3A4 inhibition - 0.7372 73.72%
CYP2C9 inhibition - 0.9139 91.39%
CYP2C19 inhibition - 0.9125 91.25%
CYP2D6 inhibition - 0.9283 92.83%
CYP1A2 inhibition + 0.8922 89.22%
CYP2C8 inhibition - 0.7811 78.11%
CYP inhibitory promiscuity - 0.6730 67.30%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.9313 93.13%
Carcinogenicity (trinary) Non-required 0.5627 56.27%
Eye corrosion - 0.8993 89.93%
Eye irritation + 0.7455 74.55%
Skin irritation - 0.7995 79.95%
Skin corrosion - 0.9857 98.57%
Ames mutagenesis - 0.5100 51.00%
Human Ether-a-go-go-Related Gene inhibition - 0.3670 36.70%
Micronuclear + 0.7600 76.00%
Hepatotoxicity - 0.5375 53.75%
skin sensitisation - 0.9623 96.23%
Respiratory toxicity - 0.5556 55.56%
Reproductive toxicity + 0.6111 61.11%
Mitochondrial toxicity - 0.6000 60.00%
Nephrotoxicity + 0.4613 46.13%
Acute Oral Toxicity (c) III 0.4760 47.60%
Estrogen receptor binding + 0.8829 88.29%
Androgen receptor binding + 0.7874 78.74%
Thyroid receptor binding - 0.5138 51.38%
Glucocorticoid receptor binding + 0.6571 65.71%
Aromatase binding + 0.8246 82.46%
PPAR gamma + 0.6088 60.88%
Honey bee toxicity - 0.7705 77.05%
Biodegradation - 0.8750 87.50%
Crustacea aquatic toxicity - 0.5700 57.00%
Fish aquatic toxicity + 0.9292 92.92%

Targets

Top

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
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 95.49% 85.14%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 93.22% 91.11%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 92.62% 94.00%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 90.50% 95.56%
CHEMBL1293277 O15118 Niemann-Pick C1 protein 88.54% 81.11%
CHEMBL1806 P11388 DNA topoisomerase II alpha 88.29% 89.00%
CHEMBL5409 Q8TDU6 G-protein coupled bile acid receptor 1 86.64% 93.65%
CHEMBL3401 O75469 Pregnane X receptor 85.96% 94.73%
CHEMBL1293249 Q13887 Kruppel-like factor 5 84.75% 86.33%
CHEMBL2581 P07339 Cathepsin D 84.07% 98.95%
CHEMBL4793 Q86TI2 Dipeptidyl peptidase IX 83.41% 96.95%
CHEMBL4208 P20618 Proteasome component C5 82.37% 90.00%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 82.18% 99.23%
CHEMBL3091268 Q92753 Nuclear receptor ROR-beta 81.02% 95.50%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 80.98% 94.45%
CHEMBL2535 P11166 Glucose transporter 80.83% 98.75%
CHEMBL3060 Q9Y345 Glycine transporter 2 80.59% 99.17%

Plants that contains it

Top
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.
Aspidosperma formosanum

Cross-Links

Top
PubChem 86173730
LOTUS LTS0184425
wikiData Q104199082