2-[6-(1,3-benzodioxol-5-yl)hexyl]-1H-quinolin-4-one

Details

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Internal ID e0460b4b-f754-43a5-8ddf-f76ab6e1367c
Taxonomy Organoheterocyclic compounds > Quinolines and derivatives > Quinolones and derivatives > Hydroquinolones
IUPAC Name 2-[6-(1,3-benzodioxol-5-yl)hexyl]-1H-quinolin-4-one
SMILES (Canonical) C1OC2=C(O1)C=C(C=C2)CCCCCCC3=CC(=O)C4=CC=CC=C4N3
SMILES (Isomeric) C1OC2=C(O1)C=C(C=C2)CCCCCCC3=CC(=O)C4=CC=CC=C4N3
InChI InChI=1S/C22H23NO3/c24-20-14-17(23-19-10-6-5-9-18(19)20)8-4-2-1-3-7-16-11-12-21-22(13-16)26-15-25-21/h5-6,9-14H,1-4,7-8,15H2,(H,23,24)
InChI Key CKZPIJIYEBHURL-UHFFFAOYSA-N
Popularity 1 reference in papers

Physical and Chemical Properties

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Molecular Formula C22H23NO3
Molecular Weight 349.40 g/mol
Exact Mass 349.16779360 g/mol
Topological Polar Surface Area (TPSA) 47.60 Ų
XlogP 5.60
Atomic LogP (AlogP) 4.60
H-Bond Acceptor 3
H-Bond Donor 1
Rotatable Bonds 7

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 2-[6-(1,3-benzodioxol-5-yl)hexyl]-1H-quinolin-4-one

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9973 99.73%
Caco-2 - 0.7115 71.15%
Blood Brain Barrier + 0.7250 72.50%
Human oral bioavailability - 0.6143 61.43%
Subcellular localzation Mitochondria 0.7660 76.60%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9068 90.68%
OATP1B3 inhibitior + 0.9415 94.15%
MATE1 inhibitior - 0.8200 82.00%
OCT2 inhibitior - 0.6500 65.00%
BSEP inhibitior + 0.9472 94.72%
P-glycoprotein inhibitior + 0.8686 86.86%
P-glycoprotein substrate - 0.8028 80.28%
CYP3A4 substrate + 0.6059 60.59%
CYP2C9 substrate + 0.6095 60.95%
CYP2D6 substrate - 0.8154 81.54%
CYP3A4 inhibition + 0.8666 86.66%
CYP2C9 inhibition - 0.5923 59.23%
CYP2C19 inhibition + 0.6444 64.44%
CYP2D6 inhibition + 0.5733 57.33%
CYP1A2 inhibition + 0.9053 90.53%
CYP2C8 inhibition - 0.7250 72.50%
CYP inhibitory promiscuity + 0.7891 78.91%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.9600 96.00%
Carcinogenicity (trinary) Non-required 0.6611 66.11%
Eye corrosion - 0.9890 98.90%
Eye irritation - 0.8345 83.45%
Skin irritation - 0.7548 75.48%
Skin corrosion - 0.9501 95.01%
Ames mutagenesis - 0.5600 56.00%
Human Ether-a-go-go-Related Gene inhibition + 0.9125 91.25%
Micronuclear + 0.5259 52.59%
Hepatotoxicity - 0.5342 53.42%
skin sensitisation - 0.8042 80.42%
Respiratory toxicity + 0.7000 70.00%
Reproductive toxicity + 0.8556 85.56%
Mitochondrial toxicity + 0.8125 81.25%
Nephrotoxicity - 0.6412 64.12%
Acute Oral Toxicity (c) III 0.6361 63.61%
Estrogen receptor binding + 0.8773 87.73%
Androgen receptor binding + 0.8045 80.45%
Thyroid receptor binding + 0.5962 59.62%
Glucocorticoid receptor binding + 0.6414 64.14%
Aromatase binding + 0.6838 68.38%
PPAR gamma + 0.5627 56.27%
Honey bee toxicity - 0.8817 88.17%
Biodegradation - 0.8250 82.50%
Crustacea aquatic toxicity + 0.5900 59.00%
Fish aquatic toxicity + 0.7717 77.17%

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
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 98.90% 91.11%
CHEMBL2581 P07339 Cathepsin D 98.24% 98.95%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 97.69% 94.45%
CHEMBL240 Q12809 HERG 97.56% 89.76%
CHEMBL3192 Q9BY41 Histone deacetylase 8 97.08% 93.99%
CHEMBL4481 P35228 Nitric oxide synthase, inducible 95.63% 94.80%
CHEMBL4303 P08238 Heat shock protein HSP 90-beta 95.31% 96.77%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 94.95% 95.56%
CHEMBL2288 Q13526 Peptidyl-prolyl cis-trans isomerase NIMA-interacting 1 92.86% 91.71%
CHEMBL5805 Q9NR97 Toll-like receptor 8 89.14% 96.25%
CHEMBL3310 Q96DB2 Histone deacetylase 11 88.80% 88.56%
CHEMBL2535 P11166 Glucose transporter 88.47% 98.75%
CHEMBL255 P29275 Adenosine A2b receptor 87.87% 98.59%
CHEMBL2373 P21730 C5a anaphylatoxin chemotactic receptor 87.73% 92.62%
CHEMBL1806 P11388 DNA topoisomerase II alpha 87.19% 89.00%
CHEMBL2717 Q9HCR9 Phosphodiesterase 11A 86.83% 85.00%
CHEMBL3401 O75469 Pregnane X receptor 86.55% 94.73%
CHEMBL4225 P49760 Dual specificity protein kinase CLK2 85.52% 80.96%
CHEMBL3004 P33527 Multidrug resistance-associated protein 1 84.42% 96.37%
CHEMBL5697 Q9GZT9 Egl nine homolog 1 84.05% 93.40%
CHEMBL1951 P21397 Monoamine oxidase A 83.95% 91.49%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 82.34% 94.00%
CHEMBL1781 P11387 DNA topoisomerase I 81.88% 97.00%
CHEMBL3060 Q9Y345 Glycine transporter 2 81.42% 99.17%
CHEMBL1293249 Q13887 Kruppel-like factor 5 80.57% 86.33%
CHEMBL1937 Q92769 Histone deacetylase 2 80.25% 94.75%
CHEMBL5103 Q969S8 Histone deacetylase 10 80.12% 90.08%

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.
Ruta chalepensis

Cross-Links

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PubChem 10450485
LOTUS LTS0211885
wikiData Q104963074