2-Pentylquinoline

Details

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Internal ID 974e9a61-791e-4c70-ad60-6bec90f92aa3
Taxonomy Organoheterocyclic compounds > Quinolines and derivatives
IUPAC Name 2-pentylquinoline
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C14H17N/c1-2-3-4-8-13-11-10-12-7-5-6-9-14(12)15-13/h5-7,9-11H,2-4,8H2,1H3
InChI Key GMTGCIAJHZEUNB-UHFFFAOYSA-N
Popularity 21 references in papers

Physical and Chemical Properties

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Molecular Formula C14H17N
Molecular Weight 199.29 g/mol
Exact Mass 199.136099547 g/mol
Topological Polar Surface Area (TPSA) 12.90 Ų
XlogP 4.50
Atomic LogP (AlogP) 3.97
H-Bond Acceptor 1
H-Bond Donor 0
Rotatable Bonds 4

Synonyms

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Quinoline, 2-pentyl
93005-16-4
Amylchinolin
2-Pentyl-quinoline
2-N-Pentylquinoleine
SCHEMBL860157
CHEMBL170722
DTXSID50239242
GMTGCIAJHZEUNB-UHFFFAOYSA-N
AKOS006321316

2D Structure

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2D Structure of 2-Pentylquinoline

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9974 99.74%
Caco-2 + 0.9626 96.26%
Blood Brain Barrier + 0.9250 92.50%
Human oral bioavailability - 0.5286 52.86%
Subcellular localzation Lysosomes 0.3952 39.52%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9159 91.59%
OATP1B3 inhibitior + 0.9546 95.46%
MATE1 inhibitior - 0.9600 96.00%
OCT2 inhibitior - 0.5750 57.50%
BSEP inhibitior - 0.7394 73.94%
P-glycoprotein inhibitior - 0.9629 96.29%
P-glycoprotein substrate - 0.8081 80.81%
CYP3A4 substrate - 0.5901 59.01%
CYP2C9 substrate - 0.8204 82.04%
CYP2D6 substrate + 0.3709 37.09%
CYP3A4 inhibition - 0.9083 90.83%
CYP2C9 inhibition - 0.6489 64.89%
CYP2C19 inhibition + 0.6594 65.94%
CYP2D6 inhibition - 0.7485 74.85%
CYP1A2 inhibition + 0.9360 93.60%
CYP2C8 inhibition + 0.5591 55.91%
CYP inhibitory promiscuity + 0.5972 59.72%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.8400 84.00%
Carcinogenicity (trinary) Non-required 0.7090 70.90%
Eye corrosion - 0.9552 95.52%
Eye irritation + 0.8186 81.86%
Skin irritation + 0.5148 51.48%
Skin corrosion - 0.8384 83.84%
Ames mutagenesis - 0.5723 57.23%
Human Ether-a-go-go-Related Gene inhibition + 0.7723 77.23%
Micronuclear - 0.8500 85.00%
Hepatotoxicity + 0.5651 56.51%
skin sensitisation - 0.5974 59.74%
Respiratory toxicity - 0.6222 62.22%
Reproductive toxicity - 0.6327 63.27%
Mitochondrial toxicity + 0.5500 55.00%
Nephrotoxicity + 0.4726 47.26%
Acute Oral Toxicity (c) III 0.6863 68.63%
Estrogen receptor binding + 0.7435 74.35%
Androgen receptor binding - 0.5407 54.07%
Thyroid receptor binding - 0.4940 49.40%
Glucocorticoid receptor binding - 0.6108 61.08%
Aromatase binding + 0.5296 52.96%
PPAR gamma + 0.7145 71.45%
Honey bee toxicity - 0.9836 98.36%
Biodegradation - 0.7250 72.50%
Crustacea aquatic toxicity + 0.8200 82.00%
Fish aquatic toxicity + 0.9196 91.96%

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
CHEMBL240 Q12809 HERG 97.34% 89.76%
CHEMBL2581 P07339 Cathepsin D 96.33% 98.95%
CHEMBL4769 O95749 Geranylgeranyl pyrophosphate synthetase 92.65% 92.08%
CHEMBL230 P35354 Cyclooxygenase-2 92.53% 89.63%
CHEMBL1293249 Q13887 Kruppel-like factor 5 92.40% 86.33%
CHEMBL2885 P07451 Carbonic anhydrase III 89.95% 87.45%
CHEMBL3401 O75469 Pregnane X receptor 89.60% 94.73%
CHEMBL5805 Q9NR97 Toll-like receptor 8 88.93% 96.25%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 84.51% 91.11%
CHEMBL1907 P15144 Aminopeptidase N 83.61% 93.31%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 82.49% 96.09%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 82.32% 96.00%
CHEMBL3060 Q9Y345 Glycine transporter 2 81.27% 99.17%

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.
Angostura bracteata

Cross-Links

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PubChem 185231
LOTUS LTS0093644
wikiData Q83121578