1,4-Dimethoxy-2-quinolone

Details

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Internal ID 6e9f710d-fc88-497c-a0df-a2d0dd28cd30
Taxonomy Organoheterocyclic compounds > Quinolines and derivatives > Quinolones and derivatives > Hydroquinolones
IUPAC Name 1,4-dimethoxyquinolin-2-one
SMILES (Canonical) COC1=CC(=O)N(C2=CC=CC=C21)OC
SMILES (Isomeric) COC1=CC(=O)N(C2=CC=CC=C21)OC
InChI InChI=1S/C11H11NO3/c1-14-10-7-11(13)12(15-2)9-6-4-3-5-8(9)10/h3-7H,1-2H3
InChI Key FVVMQXAIHDUZMW-UHFFFAOYSA-N
Popularity 1 reference in papers

Physical and Chemical Properties

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Molecular Formula C11H11NO3
Molecular Weight 205.21 g/mol
Exact Mass 205.07389321 g/mol
Topological Polar Surface Area (TPSA) 38.80 Ų
XlogP 1.30
Atomic LogP (AlogP) 1.07
H-Bond Acceptor 4
H-Bond Donor 0
Rotatable Bonds 2

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 1,4-Dimethoxy-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 + 0.9921 99.21%
Caco-2 + 0.9146 91.46%
Blood Brain Barrier + 0.7250 72.50%
Human oral bioavailability + 0.8429 84.29%
Subcellular localzation Mitochondria 0.6786 67.86%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9485 94.85%
OATP1B3 inhibitior + 0.9571 95.71%
MATE1 inhibitior - 0.9200 92.00%
OCT2 inhibitior - 0.9750 97.50%
BSEP inhibitior - 0.8159 81.59%
P-glycoprotein inhibitior - 0.9446 94.46%
P-glycoprotein substrate - 0.8761 87.61%
CYP3A4 substrate - 0.5154 51.54%
CYP2C9 substrate - 0.7985 79.85%
CYP2D6 substrate - 0.8325 83.25%
CYP3A4 inhibition - 0.9145 91.45%
CYP2C9 inhibition - 0.8353 83.53%
CYP2C19 inhibition - 0.5100 51.00%
CYP2D6 inhibition - 0.9251 92.51%
CYP1A2 inhibition + 0.7424 74.24%
CYP2C8 inhibition - 0.8472 84.72%
CYP inhibitory promiscuity + 0.5356 53.56%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.8500 85.00%
Carcinogenicity (trinary) Non-required 0.4786 47.86%
Eye corrosion - 0.9837 98.37%
Eye irritation + 0.9644 96.44%
Skin irritation - 0.8399 83.99%
Skin corrosion - 0.9602 96.02%
Ames mutagenesis + 0.6900 69.00%
Human Ether-a-go-go-Related Gene inhibition - 0.5754 57.54%
Micronuclear + 0.7659 76.59%
Hepatotoxicity + 0.6679 66.79%
skin sensitisation - 0.8836 88.36%
Respiratory toxicity - 0.5111 51.11%
Reproductive toxicity + 0.6667 66.67%
Mitochondrial toxicity + 0.6125 61.25%
Nephrotoxicity + 0.4601 46.01%
Acute Oral Toxicity (c) III 0.6073 60.73%
Estrogen receptor binding - 0.5296 52.96%
Androgen receptor binding - 0.4938 49.38%
Thyroid receptor binding - 0.6325 63.25%
Glucocorticoid receptor binding - 0.8709 87.09%
Aromatase binding - 0.5681 56.81%
PPAR gamma - 0.7461 74.61%
Honey bee toxicity - 0.8741 87.41%
Biodegradation - 0.7750 77.50%
Crustacea aquatic toxicity + 0.6600 66.00%
Fish aquatic toxicity - 0.3918 39.18%

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 97.53% 95.56%
CHEMBL2581 P07339 Cathepsin D 94.34% 98.95%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 93.96% 85.14%
CHEMBL3192 Q9BY41 Histone deacetylase 8 91.58% 93.99%
CHEMBL1293249 Q13887 Kruppel-like factor 5 91.57% 86.33%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 90.59% 96.09%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 88.96% 91.11%
CHEMBL2535 P11166 Glucose transporter 87.29% 98.75%
CHEMBL1907 P15144 Aminopeptidase N 83.36% 93.31%
CHEMBL4478 Q00975 Voltage-gated N-type calcium channel alpha-1B subunit 83.22% 97.14%
CHEMBL1806 P11388 DNA topoisomerase II alpha 82.51% 89.00%
CHEMBL2095172 P14867 GABA-A receptor; alpha-1/beta-2/gamma-2 80.20% 92.67%

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.
Conchocarpus heterophyllus
Haplophyllum obtusifolium

Cross-Links

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PubChem 21770010
LOTUS LTS0096397
wikiData Q104166826