2-Undecyl-4(1H)-quinolinone

Details

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Internal ID 86060526-06fc-431d-95ec-7540b1b0a4cd
Taxonomy Organoheterocyclic compounds > Quinolines and derivatives > Quinolones and derivatives > Hydroquinolones
IUPAC Name 2-undecyl-1H-quinolin-4-one
SMILES (Canonical) CCCCCCCCCCCC1=CC(=O)C2=CC=CC=C2N1
SMILES (Isomeric) CCCCCCCCCCCC1=CC(=O)C2=CC=CC=C2N1
InChI InChI=1S/C20H29NO/c1-2-3-4-5-6-7-8-9-10-13-17-16-20(22)18-14-11-12-15-19(18)21-17/h11-12,14-16H,2-10,13H2,1H3,(H,21,22)
InChI Key KKSIGOUTTVXAKQ-UHFFFAOYSA-N
Popularity 9 references in papers

Physical and Chemical Properties

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Molecular Formula C20H29NO
Molecular Weight 299.40 g/mol
Exact Mass 299.224914549 g/mol
Topological Polar Surface Area (TPSA) 29.10 Ų
XlogP 7.10

Synonyms

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2-undecyl-4(1h)-quinolone
2-undecyl-1H-quinolin-4-one
56183-46-1
CHEMBL2042447
2-undecyl-1,4-dihydroquinolin-4-one
2-Undecyl-4-quinolinol
4-Quinolinol, 2-undecyl-
Z2S75NSY7P
2-undecyl-4-hydroxyquinoline
4-Hydroxy-2-undecylquinoline
There are more than 10 synonyms. If you wish to see them all click here.

2D Structure

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2D Structure of 2-Undecyl-4(1H)-quinolinone

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
No predicted properties yet!

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 98.91% 98.95%
CHEMBL4769 O95749 Geranylgeranyl pyrophosphate synthetase 97.45% 92.08%
CHEMBL240 Q12809 HERG 97.34% 89.76%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 96.24% 91.11%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 94.77% 95.56%
CHEMBL3192 Q9BY41 Histone deacetylase 8 94.61% 93.99%
CHEMBL2288 Q13526 Peptidyl-prolyl cis-trans isomerase NIMA-interacting 1 93.95% 91.71%
CHEMBL255 P29275 Adenosine A2b receptor 93.52% 98.59%
CHEMBL230 P35354 Cyclooxygenase-2 91.81% 89.63%
CHEMBL1907 P15144 Aminopeptidase N 91.15% 93.31%
CHEMBL5043 Q6P179 Endoplasmic reticulum aminopeptidase 2 89.31% 91.81%
CHEMBL1781 P11387 DNA topoisomerase I 88.44% 97.00%
CHEMBL3401 O75469 Pregnane X receptor 88.12% 94.73%
CHEMBL2885 P07451 Carbonic anhydrase III 87.95% 87.45%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 85.29% 96.09%
CHEMBL2535 P11166 Glucose transporter 85.28% 98.75%
CHEMBL2717 Q9HCR9 Phosphodiesterase 11A 84.94% 85.00%
CHEMBL3060 Q9Y345 Glycine transporter 2 84.79% 99.17%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 83.84% 94.45%
CHEMBL1293249 Q13887 Kruppel-like factor 5 83.78% 86.33%
CHEMBL1951 P21397 Monoamine oxidase A 82.93% 91.49%
CHEMBL1806 P11388 DNA topoisomerase II alpha 82.38% 89.00%
CHEMBL2265 P23141 Acyl coenzyme A:cholesterol acyltransferase 81.10% 85.94%

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.
Ptelea trifoliata
Ruta graveolens

Cross-Links

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PubChem 10063343
LOTUS LTS0086806
wikiData Q105142342