2-Ethylpyridine

Details

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Internal ID 80ca95aa-ada4-4237-bc56-d60d7f306e77
Taxonomy Organoheterocyclic compounds > Pyridines and derivatives
IUPAC Name 2-ethylpyridine
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C7H9N/c1-2-7-5-3-4-6-8-7/h3-6H,2H2,1H3
InChI Key NRGGMCIBEHEAIL-UHFFFAOYSA-N
Popularity 348 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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100-71-0
Pyridine, 2-ethyl-
alpha-Ethylpyridine
06X1W46PYX
NSC-964
DTXSID4021844
RefChem:87008
DTXCID501844
202-881-9
Pyridine, ethyl-
There are more than 10 synonyms. If you wish to see them all click here.

2D Structure

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2D Structure of 2-Ethylpyridine

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9966 99.66%
Caco-2 + 0.8403 84.03%
Blood Brain Barrier + 1.0000 100.00%
Human oral bioavailability + 0.8571 85.71%
Subcellular localzation Mitochondria 0.4377 43.77%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9675 96.75%
OATP1B3 inhibitior + 0.9599 95.99%
MATE1 inhibitior - 1.0000 100.00%
OCT2 inhibitior - 0.8500 85.00%
BSEP inhibitior - 0.8896 88.96%
P-glycoprotein inhibitior - 0.9939 99.39%
P-glycoprotein substrate - 0.9133 91.33%
CYP3A4 substrate - 0.7625 76.25%
CYP2C9 substrate - 0.6057 60.57%
CYP2D6 substrate - 0.7086 70.86%
CYP3A4 inhibition - 0.9592 95.92%
CYP2C9 inhibition - 0.7887 78.87%
CYP2C19 inhibition - 0.7510 75.10%
CYP2D6 inhibition - 0.7199 71.99%
CYP1A2 inhibition + 0.8354 83.54%
CYP2C8 inhibition - 0.7818 78.18%
CYP inhibitory promiscuity - 0.8194 81.94%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) + 0.5300 53.00%
Carcinogenicity (trinary) Non-required 0.6417 64.17%
Eye corrosion + 0.7696 76.96%
Eye irritation + 0.9903 99.03%
Skin irritation + 0.8974 89.74%
Skin corrosion + 0.6139 61.39%
Ames mutagenesis - 0.7600 76.00%
Human Ether-a-go-go-Related Gene inhibition - 0.5888 58.88%
Micronuclear - 0.6400 64.00%
Hepatotoxicity + 0.8125 81.25%
skin sensitisation + 0.7905 79.05%
Respiratory toxicity - 0.5889 58.89%
Reproductive toxicity - 0.8111 81.11%
Mitochondrial toxicity - 0.8500 85.00%
Nephrotoxicity - 0.6229 62.29%
Acute Oral Toxicity (c) III 0.7942 79.42%
Estrogen receptor binding - 0.9533 95.33%
Androgen receptor binding - 0.8847 88.47%
Thyroid receptor binding - 0.8308 83.08%
Glucocorticoid receptor binding - 0.8581 85.81%
Aromatase binding - 0.8781 87.81%
PPAR gamma - 0.8558 85.58%
Honey bee toxicity - 0.9797 97.97%
Biodegradation - 0.5500 55.00%
Crustacea aquatic toxicity + 0.5300 53.00%
Fish aquatic toxicity - 0.8672 86.72%

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
CHEMBL2107 P61073 C-X-C chemokine receptor type 4 94.50% 93.10%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 93.55% 96.09%
CHEMBL2581 P07339 Cathepsin D 90.13% 98.95%
CHEMBL1293249 Q13887 Kruppel-like factor 5 87.97% 86.33%
CHEMBL5678 P34947 G protein-coupled receptor kinase 5 87.88% 88.00%
CHEMBL3401 O75469 Pregnane X receptor 87.19% 94.73%
CHEMBL4306 P22460 Voltage-gated potassium channel subunit Kv1.5 84.53% 94.03%
CHEMBL5409 Q8TDU6 G-protein coupled bile acid receptor 1 84.49% 93.65%
CHEMBL221 P23219 Cyclooxygenase-1 81.51% 90.17%

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.
Camellia sinensis
Mentha arvensis

Cross-Links

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PubChem 7523
LOTUS LTS0094865
wikiData Q27236227