2-Ethyl-4-prop-1-en-2-ylpyridine

Details

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Internal ID f744e717-873d-4f4f-ba33-ada26dae23a8
Taxonomy Organoheterocyclic compounds > Pyridines and derivatives
IUPAC Name 2-ethyl-4-prop-1-en-2-ylpyridine
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C10H13N/c1-4-10-7-9(8(2)3)5-6-11-10/h5-7H,2,4H2,1,3H3
InChI Key YWBBITMUIVBYJO-UHFFFAOYSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C10H13N
Molecular Weight 147.22 g/mol
Exact Mass 147.104799419 g/mol
Topological Polar Surface Area (TPSA) 12.90 Ų
XlogP 3.10
Atomic LogP (AlogP) 2.68
H-Bond Acceptor 1
H-Bond Donor 0
Rotatable Bonds 2

Synonyms

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142896-08-0
Pyridine, 2-ethyl-4-(1-methylethenyl)- (9CI)
Pyridine, 2-ethyl-4-(1-methylethenyl)
Pyridine, 2-ethyl-4-(1-methylethenyl)-
SCHEMBL9444923
YWBBITMUIVBYJO-UHFFFAOYSA-N
DB-289270

2D Structure

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2D Structure of 2-Ethyl-4-prop-1-en-2-ylpyridine

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9950 99.50%
Caco-2 + 0.7850 78.50%
Blood Brain Barrier + 0.9500 95.00%
Human oral bioavailability + 0.6857 68.57%
Subcellular localzation Lysosomes 0.3885 38.85%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9464 94.64%
OATP1B3 inhibitior + 0.9528 95.28%
MATE1 inhibitior - 0.9600 96.00%
OCT2 inhibitior - 0.7500 75.00%
BSEP inhibitior - 0.8504 85.04%
P-glycoprotein inhibitior - 0.9834 98.34%
P-glycoprotein substrate - 0.8185 81.85%
CYP3A4 substrate - 0.6940 69.40%
CYP2C9 substrate - 0.8151 81.51%
CYP2D6 substrate - 0.7529 75.29%
CYP3A4 inhibition - 0.7306 73.06%
CYP2C9 inhibition - 0.5769 57.69%
CYP2C19 inhibition + 0.5071 50.71%
CYP2D6 inhibition - 0.5627 56.27%
CYP1A2 inhibition + 0.7458 74.58%
CYP2C8 inhibition - 0.8934 89.34%
CYP inhibitory promiscuity - 0.5511 55.11%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) + 0.5100 51.00%
Carcinogenicity (trinary) Non-required 0.6137 61.37%
Eye corrosion - 0.5848 58.48%
Eye irritation + 0.9835 98.35%
Skin irritation + 0.6565 65.65%
Skin corrosion - 0.7810 78.10%
Ames mutagenesis - 0.7554 75.54%
Human Ether-a-go-go-Related Gene inhibition - 0.5000 50.00%
Micronuclear - 0.6100 61.00%
Hepatotoxicity + 0.6875 68.75%
skin sensitisation + 0.8075 80.75%
Respiratory toxicity - 0.5778 57.78%
Reproductive toxicity - 0.6333 63.33%
Mitochondrial toxicity - 0.7125 71.25%
Nephrotoxicity - 0.6697 66.97%
Acute Oral Toxicity (c) III 0.7954 79.54%
Estrogen receptor binding - 0.9436 94.36%
Androgen receptor binding - 0.7724 77.24%
Thyroid receptor binding - 0.7140 71.40%
Glucocorticoid receptor binding - 0.8997 89.97%
Aromatase binding - 0.8476 84.76%
PPAR gamma - 0.9293 92.93%
Honey bee toxicity - 0.9686 96.86%
Biodegradation - 0.8500 85.00%
Crustacea aquatic toxicity - 0.5800 58.00%
Fish aquatic toxicity + 0.6541 65.41%

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
CHEMBL1951 P21397 Monoamine oxidase A 95.52% 91.49%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 93.09% 96.09%
CHEMBL2107 P61073 C-X-C chemokine receptor type 4 91.67% 93.10%
CHEMBL1293249 Q13887 Kruppel-like factor 5 91.02% 86.33%
CHEMBL3401 O75469 Pregnane X receptor 86.77% 94.73%
CHEMBL4208 P20618 Proteasome component C5 86.29% 90.00%
CHEMBL2581 P07339 Cathepsin D 85.53% 98.95%
CHEMBL5409 Q8TDU6 G-protein coupled bile acid receptor 1 82.76% 93.65%
CHEMBL3060 Q9Y345 Glycine transporter 2 81.09% 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.
Mentha arvensis

Cross-Links

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PubChem 529346
LOTUS LTS0242721
wikiData Q105366399