2-Pent-1-enylquinoline

Details

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Internal ID b6ea56c1-6418-48a4-94c8-e1a69f720c4f
Taxonomy Organoheterocyclic compounds > Quinolines and derivatives
IUPAC Name 2-pent-1-enylquinoline
SMILES (Canonical) CCCC=CC1=NC2=CC=CC=C2C=C1
SMILES (Isomeric) CCCC=CC1=NC2=CC=CC=C2C=C1
InChI InChI=1S/C14H15N/c1-2-3-4-8-13-11-10-12-7-5-6-9-14(12)15-13/h4-11H,2-3H2,1H3
InChI Key ZAPKXDJGBCUUKL-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C14H15N
Molecular Weight 197.27 g/mol
Exact Mass 197.120449483 g/mol
Topological Polar Surface Area (TPSA) 12.90 Ų
XlogP 4.20
Atomic LogP (AlogP) 4.05
H-Bond Acceptor 1
H-Bond Donor 0
Rotatable Bonds 3

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 2-Pent-1-enylquinoline

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9964 99.64%
Caco-2 + 0.9155 91.55%
Blood Brain Barrier + 0.9500 95.00%
Human oral bioavailability + 0.7143 71.43%
Subcellular localzation Plasma membrane 0.6512 65.12%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.8945 89.45%
OATP1B3 inhibitior + 0.9582 95.82%
MATE1 inhibitior - 0.9600 96.00%
OCT2 inhibitior - 0.6750 67.50%
BSEP inhibitior + 0.6407 64.07%
P-glycoprotein inhibitior - 0.9399 93.99%
P-glycoprotein substrate - 0.9272 92.72%
CYP3A4 substrate - 0.6055 60.55%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.7851 78.51%
CYP3A4 inhibition - 0.8179 81.79%
CYP2C9 inhibition - 0.5300 53.00%
CYP2C19 inhibition + 0.7996 79.96%
CYP2D6 inhibition - 0.6757 67.57%
CYP1A2 inhibition + 0.9414 94.14%
CYP2C8 inhibition - 0.6359 63.59%
CYP inhibitory promiscuity + 0.7627 76.27%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.8000 80.00%
Carcinogenicity (trinary) Non-required 0.6292 62.92%
Eye corrosion - 0.9346 93.46%
Eye irritation + 0.9292 92.92%
Skin irritation + 0.5562 55.62%
Skin corrosion - 0.9204 92.04%
Ames mutagenesis + 0.5200 52.00%
Human Ether-a-go-go-Related Gene inhibition + 0.7590 75.90%
Micronuclear - 0.7500 75.00%
Hepatotoxicity - 0.5197 51.97%
skin sensitisation + 0.6130 61.30%
Respiratory toxicity + 0.5556 55.56%
Reproductive toxicity - 0.6222 62.22%
Mitochondrial toxicity - 0.6375 63.75%
Nephrotoxicity - 0.6619 66.19%
Acute Oral Toxicity (c) III 0.8310 83.10%
Estrogen receptor binding + 0.9273 92.73%
Androgen receptor binding + 0.5323 53.23%
Thyroid receptor binding + 0.5402 54.02%
Glucocorticoid receptor binding + 0.5770 57.70%
Aromatase binding + 0.7796 77.96%
PPAR gamma + 0.6489 64.89%
Honey bee toxicity - 0.9658 96.58%
Biodegradation - 0.7500 75.00%
Crustacea aquatic toxicity + 0.6700 67.00%
Fish aquatic toxicity + 0.8260 82.60%

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
CHEMBL1293249 Q13887 Kruppel-like factor 5 93.67% 86.33%
CHEMBL221 P23219 Cyclooxygenase-1 90.77% 90.17%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 90.07% 96.00%
CHEMBL2581 P07339 Cathepsin D 88.17% 98.95%
CHEMBL3959 P16083 Quinone reductase 2 88.02% 89.49%
CHEMBL3401 O75469 Pregnane X receptor 87.30% 94.73%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 83.05% 91.11%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 82.93% 95.56%
CHEMBL230 P35354 Cyclooxygenase-2 81.33% 89.63%
CHEMBL3060 Q9Y345 Glycine transporter 2 80.84% 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 513388
LOTUS LTS0127615
wikiData Q104202254