Pyridine, 5-phenyl-2-propyl

Details

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Internal ID 5ffa3058-1f7e-42ad-9f89-8692f8ecfbc9
Taxonomy Organoheterocyclic compounds > Pyridines and derivatives > Phenylpyridines
IUPAC Name 5-phenyl-2-propylpyridine
SMILES (Canonical) CCCC1=NC=C(C=C1)C2=CC=CC=C2
SMILES (Isomeric) CCCC1=NC=C(C=C1)C2=CC=CC=C2
InChI InChI=1S/C14H15N/c1-2-6-14-10-9-13(11-15-14)12-7-4-3-5-8-12/h3-5,7-11H,2,6H2,1H3
InChI Key BVDPEOPUDQPYDO-UHFFFAOYSA-N
Popularity 1 reference 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 3.70
Atomic LogP (AlogP) 3.70
H-Bond Acceptor 1
H-Bond Donor 0
Rotatable Bonds 3

Synonyms

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Pyridine, 5-phenyl-2-propyl
SCHEMBL18876359
BVDPEOPUDQPYDO-UHFFFAOYSA-N
EN300-24542341
6,6-Dimethyl-4-oxo-4,5,6,7-tetrahydro-2-benzothiophene-1,3-dicarbonitrile
81879-87-0

2D Structure

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2D Structure of Pyridine, 5-phenyl-2-propyl

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9969 99.69%
Caco-2 + 0.9548 95.48%
Blood Brain Barrier + 0.7500 75.00%
Human oral bioavailability + 0.8000 80.00%
Subcellular localzation Mitochondria 0.5893 58.93%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9490 94.90%
OATP1B3 inhibitior + 0.9498 94.98%
MATE1 inhibitior - 1.0000 100.00%
OCT2 inhibitior - 0.5750 57.50%
BSEP inhibitior - 0.7030 70.30%
P-glycoprotein inhibitior - 0.9714 97.14%
P-glycoprotein substrate - 0.8712 87.12%
CYP3A4 substrate - 0.6581 65.81%
CYP2C9 substrate - 0.6057 60.57%
CYP2D6 substrate - 0.7086 70.86%
CYP3A4 inhibition - 0.9331 93.31%
CYP2C9 inhibition - 0.6774 67.74%
CYP2C19 inhibition + 0.5416 54.16%
CYP2D6 inhibition - 0.6681 66.81%
CYP1A2 inhibition + 0.9267 92.67%
CYP2C8 inhibition + 0.8121 81.21%
CYP inhibitory promiscuity + 0.7249 72.49%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.6900 69.00%
Carcinogenicity (trinary) Non-required 0.6652 66.52%
Eye corrosion - 0.9205 92.05%
Eye irritation - 0.5062 50.62%
Skin irritation + 0.5000 50.00%
Skin corrosion - 0.8843 88.43%
Ames mutagenesis - 0.6200 62.00%
Human Ether-a-go-go-Related Gene inhibition + 0.7802 78.02%
Micronuclear - 0.7200 72.00%
Hepatotoxicity + 0.7750 77.50%
skin sensitisation - 0.6163 61.63%
Respiratory toxicity + 0.5889 58.89%
Reproductive toxicity - 0.6701 67.01%
Mitochondrial toxicity - 0.6125 61.25%
Nephrotoxicity - 0.6091 60.91%
Acute Oral Toxicity (c) III 0.6267 62.67%
Estrogen receptor binding + 0.6561 65.61%
Androgen receptor binding - 0.6912 69.12%
Thyroid receptor binding + 0.5297 52.97%
Glucocorticoid receptor binding - 0.6146 61.46%
Aromatase binding + 0.7528 75.28%
PPAR gamma - 0.4869 48.69%
Honey bee toxicity - 0.9523 95.23%
Biodegradation - 0.8000 80.00%
Crustacea aquatic toxicity + 0.7000 70.00%
Fish aquatic toxicity - 0.3772 37.72%

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 96.53% 98.95%
CHEMBL221 P23219 Cyclooxygenase-1 94.96% 90.17%
CHEMBL1293249 Q13887 Kruppel-like factor 5 93.59% 86.33%
CHEMBL1907 P15144 Aminopeptidase N 91.19% 93.31%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 90.32% 96.09%
CHEMBL2035 P08912 Muscarinic acetylcholine receptor M5 88.41% 94.62%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 83.57% 96.00%
CHEMBL4769 O95749 Geranylgeranyl pyrophosphate synthetase 82.47% 92.08%
CHEMBL3091268 Q92753 Nuclear receptor ROR-beta 81.35% 95.50%
CHEMBL1944 P08473 Neprilysin 81.18% 92.63%

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.
Mentha × piperita
Mentha arvensis

Cross-Links

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PubChem 529355
LOTUS LTS0007243
wikiData Q104946466