3-Vinylpyridine

Details

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Internal ID f1929167-7063-4e74-9d26-a03243860528
Taxonomy Organoheterocyclic compounds > Pyridines and derivatives
IUPAC Name 3-ethenylpyridine
SMILES (Canonical) C=CC1=CN=CC=C1
SMILES (Isomeric) C=CC1=CN=CC=C1
InChI InChI=1S/C7H7N/c1-2-7-4-3-5-8-6-7/h2-6H,1H2
InChI Key DPZYLEIWHTWHCU-UHFFFAOYSA-N
Popularity 125 references in papers

Physical and Chemical Properties

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Molecular Formula C7H7N
Molecular Weight 105.14 g/mol
Exact Mass 105.057849228 g/mol
Topological Polar Surface Area (TPSA) 12.90 Ų
XlogP 1.40
Atomic LogP (AlogP) 1.72
H-Bond Acceptor 1
H-Bond Donor 0
Rotatable Bonds 1

Synonyms

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1121-55-7
3-Ethenylpyridine
Pyridine, 3-ethenyl-
3-vinyl-pyridine
Pyridine, 3-vinyl-
CCRIS 5239
UNII-R9ZU09Z27A
AI3-18209
R9ZU09Z27A
3-Vinylpyridine (Stabilized With Tbc)
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-Vinylpyridine

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9884 98.84%
Caco-2 + 0.9576 95.76%
Blood Brain Barrier + 1.0000 100.00%
Human oral bioavailability + 0.6429 64.29%
Subcellular localzation Mitochondria 0.4324 43.24%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9631 96.31%
OATP1B3 inhibitior + 0.9632 96.32%
MATE1 inhibitior - 1.0000 100.00%
OCT2 inhibitior - 0.9500 95.00%
BSEP inhibitior - 0.9024 90.24%
P-glycoprotein inhibitior - 0.9879 98.79%
P-glycoprotein substrate - 0.9794 97.94%
CYP3A4 substrate - 0.7955 79.55%
CYP2C9 substrate - 0.8173 81.73%
CYP2D6 substrate - 0.7875 78.75%
CYP3A4 inhibition - 0.6321 63.21%
CYP2C9 inhibition + 0.6359 63.59%
CYP2C19 inhibition + 0.5807 58.07%
CYP2D6 inhibition - 0.5706 57.06%
CYP1A2 inhibition + 0.6840 68.40%
CYP2C8 inhibition - 0.6243 62.43%
CYP inhibitory promiscuity - 0.6435 64.35%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.5800 58.00%
Carcinogenicity (trinary) Warning 0.5563 55.63%
Eye corrosion + 0.9828 98.28%
Eye irritation + 1.0000 100.00%
Skin irritation + 0.9384 93.84%
Skin corrosion + 0.5880 58.80%
Ames mutagenesis - 0.9800 98.00%
Human Ether-a-go-go-Related Gene inhibition - 0.7197 71.97%
Micronuclear - 0.7900 79.00%
Hepatotoxicity + 0.8375 83.75%
skin sensitisation + 0.9477 94.77%
Respiratory toxicity + 0.6778 67.78%
Reproductive toxicity - 0.5111 51.11%
Mitochondrial toxicity - 0.8500 85.00%
Nephrotoxicity - 0.7215 72.15%
Acute Oral Toxicity (c) II 0.7443 74.43%
Estrogen receptor binding - 0.8705 87.05%
Androgen receptor binding - 0.9673 96.73%
Thyroid receptor binding - 0.8232 82.32%
Glucocorticoid receptor binding - 0.8406 84.06%
Aromatase binding - 0.8488 84.88%
PPAR gamma - 0.8063 80.63%
Honey bee toxicity - 0.8931 89.31%
Biodegradation - 0.6750 67.50%
Crustacea aquatic toxicity - 0.5100 51.00%
Fish aquatic toxicity - 0.4744 47.44%

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 93.53% 91.49%
CHEMBL4224 P49759 Dual specificty protein kinase CLK1 88.38% 85.30%
CHEMBL1293249 Q13887 Kruppel-like factor 5 85.13% 86.33%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 84.91% 94.45%
CHEMBL3902 P09211 Glutathione S-transferase Pi 82.67% 93.81%
CHEMBL1907599 P05556 Integrin alpha-4/beta-1 82.30% 92.86%
CHEMBL308 P06493 Cyclin-dependent kinase 1 82.27% 91.73%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 82.13% 96.00%
CHEMBL2035 P08912 Muscarinic acetylcholine receptor M5 81.42% 94.62%
CHEMBL3401 O75469 Pregnane X receptor 80.51% 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.
Lonicera japonica
Nicotiana tabacum

Cross-Links

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PubChem 14272
NPASS NPC229199
LOTUS LTS0218733
wikiData Q27288016