2,3-Lutidine

Details

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Internal ID 74ca7d8d-6cb5-44ef-a4ca-254494af2a13
Taxonomy Organoheterocyclic compounds > Pyridines and derivatives > Methylpyridines
IUPAC Name 2,3-dimethylpyridine
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C7H9N/c1-6-4-3-5-8-7(6)2/h3-5H,1-2H3
InChI Key HPYNZHMRTTWQTB-UHFFFAOYSA-N
Popularity 959 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 1.60
Atomic LogP (AlogP) 1.70
H-Bond Acceptor 1
H-Bond Donor 0
Rotatable Bonds 0

Synonyms

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2,3-DIMETHYLPYRIDINE
583-61-9
DIMETHYLPYRIDINE
Pyridine, 2,3-dimethyl-
2,3-dimethyl-pyridine
27175-64-0
5Q0F649H6G
NSC-2157
Pyridine, dimethyl-
350818-65-4
There are more than 10 synonyms. If you wish to see them all click here.

2D Structure

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2D Structure of 2,3-Lutidine

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9931 99.31%
Caco-2 + 0.7735 77.35%
Blood Brain Barrier + 1.0000 100.00%
Human oral bioavailability + 0.9000 90.00%
Subcellular localzation Mitochondria 0.6198 61.98%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9823 98.23%
OATP1B3 inhibitior + 0.9663 96.63%
MATE1 inhibitior - 0.9800 98.00%
OCT2 inhibitior - 0.9500 95.00%
BSEP inhibitior - 0.8629 86.29%
P-glycoprotein inhibitior - 0.9911 99.11%
P-glycoprotein substrate - 0.9732 97.32%
CYP3A4 substrate - 0.7478 74.78%
CYP2C9 substrate - 0.8000 80.00%
CYP2D6 substrate - 0.7923 79.23%
CYP3A4 inhibition - 0.9069 90.69%
CYP2C9 inhibition - 0.7546 75.46%
CYP2C19 inhibition + 0.6633 66.33%
CYP2D6 inhibition - 0.6730 67.30%
CYP1A2 inhibition + 0.5693 56.93%
CYP2C8 inhibition - 0.9573 95.73%
CYP inhibitory promiscuity - 0.8378 83.78%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.6600 66.00%
Carcinogenicity (trinary) Non-required 0.5966 59.66%
Eye corrosion + 0.7540 75.40%
Eye irritation + 0.9954 99.54%
Skin irritation + 0.9138 91.38%
Skin corrosion - 0.8684 86.84%
Ames mutagenesis - 0.7100 71.00%
Human Ether-a-go-go-Related Gene inhibition - 0.6434 64.34%
Micronuclear - 0.7100 71.00%
Hepatotoxicity + 0.8069 80.69%
skin sensitisation + 0.7555 75.55%
Respiratory toxicity - 0.7778 77.78%
Reproductive toxicity - 0.6556 65.56%
Mitochondrial toxicity - 0.7750 77.50%
Nephrotoxicity - 0.6519 65.19%
Acute Oral Toxicity (c) III 0.8950 89.50%
Estrogen receptor binding - 0.9636 96.36%
Androgen receptor binding - 0.9226 92.26%
Thyroid receptor binding - 0.8358 83.58%
Glucocorticoid receptor binding - 0.8444 84.44%
Aromatase binding - 0.9013 90.13%
PPAR gamma - 0.8903 89.03%
Honey bee toxicity - 0.9883 98.83%
Biodegradation + 0.5500 55.00%
Crustacea aquatic toxicity + 0.6100 61.00%
Fish aquatic toxicity - 0.6722 67.22%

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
CHEMBL3401 O75469 Pregnane X receptor 91.84% 94.73%
CHEMBL5409 Q8TDU6 G-protein coupled bile acid receptor 1 88.11% 93.65%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 87.48% 95.56%
CHEMBL2107 P61073 C-X-C chemokine receptor type 4 85.19% 93.10%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 82.83% 96.00%
CHEMBL3524 P56524 Histone deacetylase 4 82.72% 92.97%
CHEMBL2335 P42785 Lysosomal Pro-X carboxypeptidase 82.30% 100.00%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 80.84% 94.00%

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.
Nicotiana tabacum

Cross-Links

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PubChem 11420
LOTUS LTS0099261
wikiData Q27262718