beta-PICOLINE

Details

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Internal ID 9c7768fc-7ba5-48ad-ac94-ebc98767514f
Taxonomy Organoheterocyclic compounds > Pyridines and derivatives > Methylpyridines
IUPAC Name 3-methylpyridine
SMILES (Canonical) CC1=CN=CC=C1
SMILES (Isomeric) CC1=CN=CC=C1
InChI InChI=1S/C6H7N/c1-6-3-2-4-7-5-6/h2-5H,1H3
InChI Key ITQTTZVARXURQS-UHFFFAOYSA-N
Popularity 1,370 references in papers

Physical and Chemical Properties

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Molecular Formula C6H7N
Molecular Weight 93.13 g/mol
Exact Mass 93.057849228 g/mol
Topological Polar Surface Area (TPSA) 12.90 Ų
XlogP 1.20
Atomic LogP (AlogP) 1.39
H-Bond Acceptor 1
H-Bond Donor 0
Rotatable Bonds 0

Synonyms

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3-Picoline
108-99-6
beta-Picoline
Pyridine, 3-methyl-
m-Picoline
m-Methylpyridine
B-Picoline
beta-Methylpyridine
3-Methyl pyridine
.beta.-Picoline
There are more than 10 synonyms. If you wish to see them all click here.

2D Structure

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2D Structure of beta-PICOLINE

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9908 99.08%
Caco-2 + 0.8835 88.35%
Blood Brain Barrier + 1.0000 100.00%
Human oral bioavailability + 0.8571 85.71%
Subcellular localzation Mitochondria 0.5439 54.39%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9784 97.84%
OATP1B3 inhibitior + 0.9700 97.00%
MATE1 inhibitior - 0.9800 98.00%
OCT2 inhibitior - 0.9750 97.50%
BSEP inhibitior - 0.8298 82.98%
P-glycoprotein inhibitior - 0.9916 99.16%
P-glycoprotein substrate - 0.9830 98.30%
CYP3A4 substrate - 0.8115 81.15%
CYP2C9 substrate - 0.8000 80.00%
CYP2D6 substrate - 0.7923 79.23%
CYP3A4 inhibition - 0.8309 83.09%
CYP2C9 inhibition - 0.6235 62.35%
CYP2C19 inhibition - 0.6807 68.07%
CYP2D6 inhibition - 0.7549 75.49%
CYP1A2 inhibition + 0.5694 56.94%
CYP2C8 inhibition - 0.7811 78.11%
CYP inhibitory promiscuity - 0.8285 82.85%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.6200 62.00%
Carcinogenicity (trinary) Warning 0.5115 51.15%
Eye corrosion + 0.9836 98.36%
Eye irritation + 1.0000 100.00%
Skin irritation + 0.9698 96.98%
Skin corrosion + 0.6561 65.61%
Ames mutagenesis - 0.8900 89.00%
Human Ether-a-go-go-Related Gene inhibition - 0.7260 72.60%
Micronuclear - 0.8000 80.00%
Hepatotoxicity + 0.7875 78.75%
skin sensitisation + 0.8645 86.45%
Respiratory toxicity + 0.7111 71.11%
Reproductive toxicity - 0.8111 81.11%
Mitochondrial toxicity - 0.8625 86.25%
Nephrotoxicity + 0.5233 52.33%
Acute Oral Toxicity (c) II 0.7657 76.57%
Estrogen receptor binding - 0.9694 96.94%
Androgen receptor binding - 0.9797 97.97%
Thyroid receptor binding - 0.8758 87.58%
Glucocorticoid receptor binding - 0.8640 86.40%
Aromatase binding - 0.9153 91.53%
PPAR gamma - 0.8795 87.95%
Honey bee toxicity - 0.9590 95.90%
Biodegradation - 0.6500 65.00%
Crustacea aquatic toxicity + 0.6500 65.00%
Fish aquatic toxicity - 0.8548 85.48%

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
CHEMBL5409 Q8TDU6 G-protein coupled bile acid receptor 1 92.01% 93.65%
CHEMBL1951 P21397 Monoamine oxidase A 86.73% 91.49%
CHEMBL4224 P49759 Dual specificty protein kinase CLK1 85.66% 85.30%
CHEMBL3401 O75469 Pregnane X receptor 84.73% 94.73%
CHEMBL1868 P17948 Vascular endothelial growth factor receptor 1 83.29% 96.47%
CHEMBL3714130 P46095 G-protein coupled receptor 6 82.99% 97.36%
CHEMBL1293249 Q13887 Kruppel-like factor 5 82.84% 86.33%
CHEMBL2581 P07339 Cathepsin D 82.21% 98.95%
CHEMBL4481 P35228 Nitric oxide synthase, inducible 81.46% 94.80%

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
Coffea arabica
Mentha arvensis
Nicotiana tabacum
Santalum album

Cross-Links

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PubChem 7970
NPASS NPC76540
LOTUS LTS0131636
wikiData Q2697560