4,7,8-trimethoxy-N-methyl-2-quinolone

Details

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Internal ID ae86a81e-4311-4cd4-8b0c-718a85a146db
Taxonomy Organoheterocyclic compounds > Quinolines and derivatives > Quinolones and derivatives > Hydroquinolones
IUPAC Name 4,7,8-trimethoxy-1-methylquinolin-2-one
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C13H15NO4/c1-14-11(15)7-10(17-3)8-5-6-9(16-2)13(18-4)12(8)14/h5-7H,1-4H3
InChI Key VPSUJSKBJXGPFW-UHFFFAOYSA-N
Popularity 6 references in papers

Physical and Chemical Properties

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Molecular Formula C13H15NO4
Molecular Weight 249.26 g/mol
Exact Mass 249.10010796 g/mol
Topological Polar Surface Area (TPSA) 48.00 Ų
XlogP 1.10
Atomic LogP (AlogP) 1.56
H-Bond Acceptor 5
H-Bond Donor 0
Rotatable Bonds 3

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 4,7,8-trimethoxy-N-methyl-2-quinolone

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9262 92.62%
Caco-2 + 0.8994 89.94%
Blood Brain Barrier + 0.7000 70.00%
Human oral bioavailability + 0.8000 80.00%
Subcellular localzation Mitochondria 0.5301 53.01%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9655 96.55%
OATP1B3 inhibitior + 0.9596 95.96%
MATE1 inhibitior - 0.9200 92.00%
OCT2 inhibitior - 0.9250 92.50%
BSEP inhibitior - 0.7737 77.37%
P-glycoprotein inhibitior - 0.8629 86.29%
P-glycoprotein substrate - 0.8302 83.02%
CYP3A4 substrate - 0.5336 53.36%
CYP2C9 substrate - 0.7985 79.85%
CYP2D6 substrate - 0.8325 83.25%
CYP3A4 inhibition + 0.5300 53.00%
CYP2C9 inhibition - 0.9498 94.98%
CYP2C19 inhibition - 0.7183 71.83%
CYP2D6 inhibition - 0.9627 96.27%
CYP1A2 inhibition + 0.6945 69.45%
CYP2C8 inhibition - 0.8766 87.66%
CYP inhibitory promiscuity + 0.5506 55.06%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.9800 98.00%
Carcinogenicity (trinary) Non-required 0.5399 53.99%
Eye corrosion - 0.9924 99.24%
Eye irritation + 0.6800 68.00%
Skin irritation - 0.8600 86.00%
Skin corrosion - 0.9717 97.17%
Ames mutagenesis - 0.5200 52.00%
Human Ether-a-go-go-Related Gene inhibition - 0.3913 39.13%
Micronuclear + 0.7559 75.59%
Hepatotoxicity + 0.5804 58.04%
skin sensitisation - 0.9427 94.27%
Respiratory toxicity - 0.6000 60.00%
Reproductive toxicity + 0.6889 68.89%
Mitochondrial toxicity + 0.6375 63.75%
Nephrotoxicity - 0.6577 65.77%
Acute Oral Toxicity (c) III 0.6379 63.79%
Estrogen receptor binding + 0.7099 70.99%
Androgen receptor binding + 0.6690 66.90%
Thyroid receptor binding - 0.5056 50.56%
Glucocorticoid receptor binding + 0.5528 55.28%
Aromatase binding + 0.5569 55.69%
PPAR gamma - 0.6110 61.10%
Honey bee toxicity - 0.9320 93.20%
Biodegradation - 0.8500 85.00%
Crustacea aquatic toxicity + 0.6300 63.00%
Fish aquatic toxicity - 0.5679 56.79%

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 94.54% 95.56%
CHEMBL2581 P07339 Cathepsin D 93.82% 98.95%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 92.43% 96.09%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 89.25% 94.00%
CHEMBL225 P28335 Serotonin 2c (5-HT2c) receptor 88.73% 89.62%
CHEMBL1293249 Q13887 Kruppel-like factor 5 88.22% 86.33%
CHEMBL4208 P20618 Proteasome component C5 87.29% 90.00%
CHEMBL2535 P11166 Glucose transporter 87.28% 98.75%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 86.72% 96.00%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 84.62% 94.45%
CHEMBL1806 P11388 DNA topoisomerase II alpha 81.20% 89.00%
CHEMBL5925 P22413 Ectonucleotide pyrophosphatase/phosphodiesterase family member 1 80.02% 92.38%

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.
Spathelia simplex

Cross-Links

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PubChem 14194291
LOTUS LTS0117792
wikiData Q105290982