2-Undecyl-4-quinolone

Details

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Internal ID 286ad03e-5d3b-4189-9adc-f11778a8a838
Taxonomy Organoheterocyclic compounds > Quinolines and derivatives > Hydroquinolines
IUPAC Name 2-undecyl-3H-quinolin-4-one
SMILES (Canonical)
SMILES (Isomeric)
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/h11-12,14-15H,2-10,13,16H2,1H3
InChI Key SUYPYUZAPYOKSO-UHFFFAOYSA-N
Popularity 12 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) 29.40 Ų
XlogP 6.50
Atomic LogP (AlogP) 6.27
H-Bond Acceptor 2
H-Bond Donor 0
Rotatable Bonds 10

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 2-Undecyl-4-quinolone

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 1.0000 100.00%
Caco-2 + 0.6914 69.14%
Blood Brain Barrier + 0.9000 90.00%
Human oral bioavailability + 0.5429 54.29%
Subcellular localzation Plasma membrane 0.4644 46.44%
OATP2B1 inhibitior - 0.8590 85.90%
OATP1B1 inhibitior + 0.9224 92.24%
OATP1B3 inhibitior + 0.9558 95.58%
MATE1 inhibitior - 0.9400 94.00%
OCT2 inhibitior + 0.6500 65.00%
BSEP inhibitior + 0.7789 77.89%
P-glycoprotein inhibitior - 0.6614 66.14%
P-glycoprotein substrate - 0.5937 59.37%
CYP3A4 substrate - 0.5076 50.76%
CYP2C9 substrate - 0.5994 59.94%
CYP2D6 substrate - 0.7794 77.94%
CYP3A4 inhibition - 0.6419 64.19%
CYP2C9 inhibition - 0.6566 65.66%
CYP2C19 inhibition - 0.5622 56.22%
CYP2D6 inhibition - 0.7928 79.28%
CYP1A2 inhibition + 0.7533 75.33%
CYP2C8 inhibition - 0.8057 80.57%
CYP inhibitory promiscuity + 0.5325 53.25%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.8900 89.00%
Carcinogenicity (trinary) Non-required 0.6872 68.72%
Eye corrosion - 0.9714 97.14%
Eye irritation + 0.5669 56.69%
Skin irritation - 0.6658 66.58%
Skin corrosion - 0.8061 80.61%
Ames mutagenesis - 0.6937 69.37%
Human Ether-a-go-go-Related Gene inhibition + 0.9047 90.47%
Micronuclear - 0.7100 71.00%
Hepatotoxicity + 0.5584 55.84%
skin sensitisation - 0.6958 69.58%
Respiratory toxicity + 0.5556 55.56%
Reproductive toxicity + 0.6503 65.03%
Mitochondrial toxicity + 0.7375 73.75%
Nephrotoxicity + 0.6138 61.38%
Acute Oral Toxicity (c) III 0.7518 75.18%
Estrogen receptor binding + 0.7228 72.28%
Androgen receptor binding - 0.7464 74.64%
Thyroid receptor binding + 0.8107 81.07%
Glucocorticoid receptor binding - 0.5539 55.39%
Aromatase binding - 0.5334 53.34%
PPAR gamma + 0.8018 80.18%
Honey bee toxicity - 0.9752 97.52%
Biodegradation - 0.5000 50.00%
Crustacea aquatic toxicity + 0.8250 82.50%
Fish aquatic toxicity + 0.7905 79.05%

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 99.15% 98.95%
CHEMBL240 Q12809 HERG 96.38% 89.76%
CHEMBL4769 O95749 Geranylgeranyl pyrophosphate synthetase 94.77% 92.08%
CHEMBL1907 P15144 Aminopeptidase N 92.05% 93.31%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 91.77% 96.09%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 91.70% 95.56%
CHEMBL2265 P23141 Acyl coenzyme A:cholesterol acyltransferase 91.36% 85.94%
CHEMBL4026 P40763 Signal transducer and activator of transcription 3 91.24% 82.69%
CHEMBL1293249 Q13887 Kruppel-like factor 5 90.96% 86.33%
CHEMBL5805 Q9NR97 Toll-like receptor 8 90.38% 96.25%
CHEMBL230 P35354 Cyclooxygenase-2 89.30% 89.63%
CHEMBL3060 Q9Y345 Glycine transporter 2 86.28% 99.17%
CHEMBL5043 Q6P179 Endoplasmic reticulum aminopeptidase 2 85.30% 91.81%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 85.19% 99.23%
CHEMBL253 P34972 Cannabinoid CB2 receptor 83.85% 97.25%
CHEMBL2693 Q9UIQ6 Cystinyl aminopeptidase 82.56% 97.64%
CHEMBL1781 P11387 DNA topoisomerase I 81.89% 97.00%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 80.37% 91.11%
CHEMBL3401 O75469 Pregnane X receptor 80.26% 94.73%

Plants that contains it

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Below are displayed all the plants proven (via scientific papers) to contain this compound!
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There are no matching plants.

Cross-Links

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PubChem 129677843
LOTUS LTS0002963
wikiData Q105261688