2-(3-Ethenylpyridin-4-yl)ethanol

Details

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Internal ID 877a04b4-4763-4a5d-b038-83b26499fa56
Taxonomy Organoheterocyclic compounds > Pyridines and derivatives
IUPAC Name 2-(3-ethenylpyridin-4-yl)ethanol
SMILES (Canonical) C=CC1=C(C=CN=C1)CCO
SMILES (Isomeric) C=CC1=C(C=CN=C1)CCO
InChI InChI=1S/C9H11NO/c1-2-8-7-10-5-3-9(8)4-6-11/h2-3,5,7,11H,1,4,6H2
InChI Key NEMKMHUCTPZMSO-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C9H11NO
Molecular Weight 149.19 g/mol
Exact Mass 149.084063974 g/mol
Topological Polar Surface Area (TPSA) 33.10 Ų
XlogP 1.20
Atomic LogP (AlogP) 1.26
H-Bond Acceptor 2
H-Bond Donor 1
Rotatable Bonds 3

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 2-(3-Ethenylpyridin-4-yl)ethanol

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9887 98.87%
Caco-2 + 0.9553 95.53%
Blood Brain Barrier + 0.8500 85.00%
Human oral bioavailability + 0.5143 51.43%
Subcellular localzation Mitochondria 0.6575 65.75%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9243 92.43%
OATP1B3 inhibitior + 0.9509 95.09%
MATE1 inhibitior - 0.9200 92.00%
OCT2 inhibitior - 0.7000 70.00%
BSEP inhibitior - 0.9066 90.66%
P-glycoprotein inhibitior - 0.9794 97.94%
P-glycoprotein substrate - 0.9449 94.49%
CYP3A4 substrate - 0.7221 72.21%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8036 80.36%
CYP3A4 inhibition + 0.6709 67.09%
CYP2C9 inhibition - 0.6300 63.00%
CYP2C19 inhibition - 0.5289 52.89%
CYP2D6 inhibition - 0.7956 79.56%
CYP1A2 inhibition - 0.5499 54.99%
CYP2C8 inhibition + 0.5962 59.62%
CYP inhibitory promiscuity - 0.7073 70.73%
UGT catelyzed + 0.6000 60.00%
Carcinogenicity (binary) - 0.8028 80.28%
Carcinogenicity (trinary) Non-required 0.6877 68.77%
Eye corrosion - 0.8413 84.13%
Eye irritation + 0.9854 98.54%
Skin irritation + 0.6769 67.69%
Skin corrosion - 0.7734 77.34%
Ames mutagenesis - 0.7200 72.00%
Human Ether-a-go-go-Related Gene inhibition - 0.5566 55.66%
Micronuclear - 0.8400 84.00%
Hepatotoxicity + 0.5329 53.29%
skin sensitisation + 0.6496 64.96%
Respiratory toxicity + 0.7556 75.56%
Reproductive toxicity - 0.5111 51.11%
Mitochondrial toxicity - 0.6750 67.50%
Nephrotoxicity - 0.6311 63.11%
Acute Oral Toxicity (c) III 0.7675 76.75%
Estrogen receptor binding - 0.7129 71.29%
Androgen receptor binding - 0.8903 89.03%
Thyroid receptor binding - 0.8200 82.00%
Glucocorticoid receptor binding - 0.7987 79.87%
Aromatase binding - 0.7302 73.02%
PPAR gamma - 0.6944 69.44%
Honey bee toxicity - 0.8722 87.22%
Biodegradation + 0.5250 52.50%
Crustacea aquatic toxicity - 0.7700 77.00%
Fish aquatic toxicity - 0.9145 91.45%

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
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 95.35% 94.45%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 92.22% 91.11%
CHEMBL4224 P49759 Dual specificty protein kinase CLK1 89.21% 85.30%
CHEMBL4040 P28482 MAP kinase ERK2 88.82% 83.82%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 88.23% 96.09%
CHEMBL1907602 P06493 Cyclin-dependent kinase 1/cyclin B1 86.70% 91.24%
CHEMBL1293249 Q13887 Kruppel-like factor 5 86.08% 86.33%
CHEMBL1907605 P24864 Cyclin-dependent kinase 2/cyclin E1 85.77% 92.88%
CHEMBL4578 Q14680 Maternal embryonic leucine zipper kinase 83.90% 81.58%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 82.54% 96.00%
CHEMBL2292 Q13627 Dual-specificity tyrosine-phosphorylation regulated kinase 1A 81.66% 93.24%
CHEMBL3714130 P46095 G-protein coupled receptor 6 80.62% 97.36%

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.
Camptotheca acuminata
Gentiana acaulis
Lonicera japonica

Cross-Links

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PubChem 5317555
NPASS NPC168070