3-Methoxy-2-pentylquinoline

Details

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Internal ID 7aff9987-1296-47f7-af04-4551245705e5
Taxonomy Organoheterocyclic compounds > Quinolines and derivatives
IUPAC Name 3-methoxy-2-pentylquinoline
SMILES (Canonical) CCCCCC1=NC2=CC=CC=C2C=C1OC
SMILES (Isomeric) CCCCCC1=NC2=CC=CC=C2C=C1OC
InChI InChI=1S/C15H19NO/c1-3-4-5-10-14-15(17-2)11-12-8-6-7-9-13(12)16-14/h6-9,11H,3-5,10H2,1-2H3
InChI Key FCPDDEUTUGCTNS-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C15H19NO
Molecular Weight 229.32 g/mol
Exact Mass 229.146664230 g/mol
Topological Polar Surface Area (TPSA) 22.10 Ų
XlogP 4.40
Atomic LogP (AlogP) 3.98
H-Bond Acceptor 2
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 3-Methoxy-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 + 1.0000 100.00%
Caco-2 + 0.9267 92.67%
Blood Brain Barrier + 0.8000 80.00%
Human oral bioavailability - 0.5143 51.43%
Subcellular localzation Mitochondria 0.5557 55.57%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.8966 89.66%
OATP1B3 inhibitior + 0.9565 95.65%
MATE1 inhibitior - 0.9800 98.00%
OCT2 inhibitior - 0.5250 52.50%
BSEP inhibitior - 0.5472 54.72%
P-glycoprotein inhibitior - 0.8839 88.39%
P-glycoprotein substrate - 0.6501 65.01%
CYP3A4 substrate - 0.5000 50.00%
CYP2C9 substrate - 0.8495 84.95%
CYP2D6 substrate + 0.4356 43.56%
CYP3A4 inhibition - 0.7763 77.63%
CYP2C9 inhibition - 0.7581 75.81%
CYP2C19 inhibition + 0.5801 58.01%
CYP2D6 inhibition + 0.5171 51.71%
CYP1A2 inhibition + 0.9033 90.33%
CYP2C8 inhibition + 0.9409 94.09%
CYP inhibitory promiscuity + 0.8142 81.42%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.9200 92.00%
Carcinogenicity (trinary) Non-required 0.6822 68.22%
Eye corrosion - 0.9882 98.82%
Eye irritation - 0.7787 77.87%
Skin irritation - 0.7437 74.37%
Skin corrosion - 0.8656 86.56%
Ames mutagenesis - 0.5400 54.00%
Human Ether-a-go-go-Related Gene inhibition + 0.8205 82.05%
Micronuclear - 0.7500 75.00%
Hepatotoxicity + 0.5909 59.09%
skin sensitisation - 0.8146 81.46%
Respiratory toxicity - 0.6222 62.22%
Reproductive toxicity + 0.7503 75.03%
Mitochondrial toxicity + 0.6000 60.00%
Nephrotoxicity - 0.5618 56.18%
Acute Oral Toxicity (c) III 0.6677 66.77%
Estrogen receptor binding + 0.9296 92.96%
Androgen receptor binding - 0.6449 64.49%
Thyroid receptor binding + 0.6952 69.52%
Glucocorticoid receptor binding - 0.5296 52.96%
Aromatase binding - 0.5424 54.24%
PPAR gamma + 0.6972 69.72%
Honey bee toxicity - 0.9642 96.42%
Biodegradation - 0.8250 82.50%
Crustacea aquatic toxicity + 0.7750 77.50%
Fish aquatic toxicity + 0.8411 84.11%

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 99.54% 89.76%
CHEMBL1293249 Q13887 Kruppel-like factor 5 96.83% 86.33%
CHEMBL230 P35354 Cyclooxygenase-2 94.92% 89.63%
CHEMBL2581 P07339 Cathepsin D 94.52% 98.95%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 94.31% 96.09%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 91.55% 91.11%
CHEMBL3060 Q9Y345 Glycine transporter 2 91.22% 99.17%
CHEMBL4769 O95749 Geranylgeranyl pyrophosphate synthetase 90.80% 92.08%
CHEMBL2885 P07451 Carbonic anhydrase III 90.67% 87.45%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 90.57% 96.00%
CHEMBL1907 P15144 Aminopeptidase N 90.31% 93.31%
CHEMBL3891 P07384 Calpain 1 86.76% 93.04%
CHEMBL3401 O75469 Pregnane X receptor 85.48% 94.73%
CHEMBL2535 P11166 Glucose transporter 84.86% 98.75%
CHEMBL3091268 Q92753 Nuclear receptor ROR-beta 82.34% 95.50%
CHEMBL4306 P22460 Voltage-gated potassium channel subunit Kv1.5 82.30% 94.03%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 82.23% 94.00%
CHEMBL1255126 O15151 Protein Mdm4 82.03% 90.20%
CHEMBL2373 P21730 C5a anaphylatoxin chemotactic receptor 81.51% 92.62%
CHEMBL5043 Q6P179 Endoplasmic reticulum aminopeptidase 2 80.68% 91.81%

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 trifoliata

Cross-Links

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PubChem 140998088
LOTUS LTS0213886
wikiData Q104993265