4-Methoxy-1-methyl-8-(2'-oxo-3'-methylbutoxy)-2-quinolone

Details

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Internal ID a75e0a15-b811-4f4f-a705-32a5d90acdfd
Taxonomy Organoheterocyclic compounds > Quinolines and derivatives > Quinolones and derivatives > Hydroquinolones
IUPAC Name 4-methoxy-1-methyl-8-(3-methyl-2-oxobutoxy)quinolin-2-one
SMILES (Canonical) CC(C)C(=O)COC1=CC=CC2=C1N(C(=O)C=C2OC)C
SMILES (Isomeric) CC(C)C(=O)COC1=CC=CC2=C1N(C(=O)C=C2OC)C
InChI InChI=1S/C16H19NO4/c1-10(2)12(18)9-21-13-7-5-6-11-14(20-4)8-15(19)17(3)16(11)13/h5-8,10H,9H2,1-4H3
InChI Key KQBPHAMPXSFIPO-UHFFFAOYSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C16H19NO4
Molecular Weight 289.33 g/mol
Exact Mass 289.13140809 g/mol
Topological Polar Surface Area (TPSA) 55.80 Ų
XlogP 2.00
Atomic LogP (AlogP) 2.15
H-Bond Acceptor 5
H-Bond Donor 0
Rotatable Bonds 5

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 4-Methoxy-1-methyl-8-(2'-oxo-3'-methylbutoxy)-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 + 0.9375 93.75%
Caco-2 + 0.8460 84.60%
Blood Brain Barrier + 0.6500 65.00%
Human oral bioavailability + 0.6857 68.57%
Subcellular localzation Mitochondria 0.5818 58.18%
OATP2B1 inhibitior - 0.8602 86.02%
OATP1B1 inhibitior + 0.9559 95.59%
OATP1B3 inhibitior + 0.9344 93.44%
MATE1 inhibitior - 0.8600 86.00%
OCT2 inhibitior - 0.9250 92.50%
BSEP inhibitior + 0.6388 63.88%
P-glycoprotein inhibitior - 0.7481 74.81%
P-glycoprotein substrate - 0.5250 52.50%
CYP3A4 substrate + 0.5849 58.49%
CYP2C9 substrate - 0.8027 80.27%
CYP2D6 substrate - 0.8624 86.24%
CYP3A4 inhibition - 0.5651 56.51%
CYP2C9 inhibition - 0.7640 76.40%
CYP2C19 inhibition - 0.6888 68.88%
CYP2D6 inhibition - 0.9510 95.10%
CYP1A2 inhibition + 0.7562 75.62%
CYP2C8 inhibition - 0.7905 79.05%
CYP inhibitory promiscuity + 0.5000 50.00%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.9600 96.00%
Carcinogenicity (trinary) Non-required 0.6043 60.43%
Eye corrosion - 0.9917 99.17%
Eye irritation - 0.9242 92.42%
Skin irritation - 0.8606 86.06%
Skin corrosion - 0.9616 96.16%
Ames mutagenesis - 0.6400 64.00%
Human Ether-a-go-go-Related Gene inhibition + 0.7330 73.30%
Micronuclear + 0.6700 67.00%
Hepatotoxicity + 0.5679 56.79%
skin sensitisation - 0.9194 91.94%
Respiratory toxicity + 0.6556 65.56%
Reproductive toxicity + 0.7889 78.89%
Mitochondrial toxicity + 0.6375 63.75%
Nephrotoxicity - 0.7464 74.64%
Acute Oral Toxicity (c) III 0.7477 74.77%
Estrogen receptor binding + 0.7266 72.66%
Androgen receptor binding + 0.6790 67.90%
Thyroid receptor binding - 0.4904 49.04%
Glucocorticoid receptor binding + 0.5864 58.64%
Aromatase binding + 0.5703 57.03%
PPAR gamma + 0.5436 54.36%
Honey bee toxicity - 0.9208 92.08%
Biodegradation - 0.8250 82.50%
Crustacea aquatic toxicity - 0.6300 63.00%
Fish aquatic toxicity - 0.3856 38.56%

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
CHEMBL2581 P07339 Cathepsin D 98.54% 98.95%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 98.52% 96.09%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 96.02% 95.56%
CHEMBL2535 P11166 Glucose transporter 95.71% 98.75%
CHEMBL1293249 Q13887 Kruppel-like factor 5 92.10% 86.33%
CHEMBL4208 P20618 Proteasome component C5 91.66% 90.00%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 91.49% 91.11%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 91.47% 96.00%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 90.99% 94.00%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 90.66% 85.14%
CHEMBL3060 Q9Y345 Glycine transporter 2 89.16% 99.17%
CHEMBL225 P28335 Serotonin 2c (5-HT2c) receptor 88.31% 89.62%
CHEMBL1806 P11388 DNA topoisomerase II alpha 88.16% 89.00%
CHEMBL1860 P10827 Thyroid hormone receptor alpha 85.09% 99.15%
CHEMBL2373 P21730 C5a anaphylatoxin chemotactic receptor 81.51% 92.62%
CHEMBL1907 P15144 Aminopeptidase N 80.98% 93.31%

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.
Haplophyllum griffithianum

Cross-Links

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PubChem 14167659
LOTUS LTS0160993
wikiData Q105144462