3-Ethylpyridine

Details

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Internal ID 431d997e-6772-4e23-adf8-b274d1e0265e
Taxonomy Organoheterocyclic compounds > Pyridines and derivatives
IUPAC Name 3-ethylpyridine
SMILES (Canonical) CCC1=CN=CC=C1
SMILES (Isomeric) CCC1=CN=CC=C1
InChI InChI=1S/C7H9N/c1-2-7-4-3-5-8-6-7/h3-6H,2H2,1H3
InChI Key MFEIKQPHQINPRI-UHFFFAOYSA-N
Popularity 120 references in papers

Physical and Chemical Properties

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Molecular Formula C7H9N
Molecular Weight 107.15 g/mol
Exact Mass 107.073499291 g/mol
Topological Polar Surface Area (TPSA) 12.90 Ų
XlogP 1.70
Atomic LogP (AlogP) 1.64
H-Bond Acceptor 1
H-Bond Donor 0
Rotatable Bonds 1

Synonyms

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536-78-7
Pyridine, 3-ethyl-
3-Ethyl pyridine
beta-Ethylpyridine
3-Ethyl-pyridine
beta-Lutidine
5-Ethylpyridine
Lutidine, beta-
FEMA No. 3394
UNII-A25I3EZ88V
There are more than 10 synonyms. If you wish to see them all click here.

2D Structure

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2D Structure of 3-Ethylpyridine

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9924 99.24%
Caco-2 + 0.9369 93.69%
Blood Brain Barrier + 1.0000 100.00%
Human oral bioavailability + 0.7286 72.86%
Subcellular localzation Mitochondria 0.5453 54.53%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9578 95.78%
OATP1B3 inhibitior + 0.9616 96.16%
MATE1 inhibitior - 1.0000 100.00%
OCT2 inhibitior - 0.9250 92.50%
BSEP inhibitior - 0.8569 85.69%
P-glycoprotein inhibitior - 0.9934 99.34%
P-glycoprotein substrate - 0.9267 92.67%
CYP3A4 substrate - 0.7881 78.81%
CYP2C9 substrate - 0.6057 60.57%
CYP2D6 substrate - 0.7086 70.86%
CYP3A4 inhibition - 0.8037 80.37%
CYP2C9 inhibition - 0.5824 58.24%
CYP2C19 inhibition - 0.6567 65.67%
CYP2D6 inhibition - 0.6734 67.34%
CYP1A2 inhibition + 0.7639 76.39%
CYP2C8 inhibition - 0.6886 68.86%
CYP inhibitory promiscuity - 0.6432 64.32%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) + 0.5100 51.00%
Carcinogenicity (trinary) Warning 0.5290 52.90%
Eye corrosion + 0.9183 91.83%
Eye irritation + 0.9920 99.20%
Skin irritation + 0.9256 92.56%
Skin corrosion + 0.5513 55.13%
Ames mutagenesis - 0.8400 84.00%
Human Ether-a-go-go-Related Gene inhibition - 0.6038 60.38%
Micronuclear - 0.7800 78.00%
Hepatotoxicity - 0.5375 53.75%
skin sensitisation + 0.8989 89.89%
Respiratory toxicity + 0.8333 83.33%
Reproductive toxicity - 0.9333 93.33%
Mitochondrial toxicity - 0.8500 85.00%
Nephrotoxicity - 0.7891 78.91%
Acute Oral Toxicity (c) III 0.7064 70.64%
Estrogen receptor binding - 0.9502 95.02%
Androgen receptor binding - 0.9610 96.10%
Thyroid receptor binding - 0.8540 85.40%
Glucocorticoid receptor binding - 0.8498 84.98%
Aromatase binding - 0.8551 85.51%
PPAR gamma - 0.9196 91.96%
Honey bee toxicity - 0.9568 95.68%
Biodegradation - 0.6500 65.00%
Crustacea aquatic toxicity + 0.5700 57.00%
Fish aquatic toxicity - 0.8009 80.09%

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 93.43% 98.95%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 92.65% 96.09%
CHEMBL221 P23219 Cyclooxygenase-1 91.31% 90.17%
CHEMBL4224 P49759 Dual specificty protein kinase CLK1 89.45% 85.30%
CHEMBL5409 Q8TDU6 G-protein coupled bile acid receptor 1 88.97% 93.65%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 88.41% 94.45%
CHEMBL255 P29275 Adenosine A2b receptor 87.53% 98.59%
CHEMBL1293249 Q13887 Kruppel-like factor 5 85.88% 86.33%
CHEMBL3401 O75469 Pregnane X receptor 85.75% 94.73%

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.
Camellia sinensis
Lonicera japonica
Nicotiana tabacum

Cross-Links

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PubChem 10823
NPASS NPC27802
LOTUS LTS0162629
wikiData Q27273525