2-Methoxypyridine

Details

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Internal ID 4dcab9eb-a3e8-418f-927f-cbc1149755a5
Taxonomy Organic oxygen compounds > Organooxygen compounds > Ethers > Alkyl aryl ethers
IUPAC Name 2-methoxypyridine
SMILES (Canonical) COC1=CC=CC=N1
SMILES (Isomeric) COC1=CC=CC=N1
InChI InChI=1S/C6H7NO/c1-8-6-4-2-3-5-7-6/h2-5H,1H3
InChI Key IWTFOFMTUOBLHG-UHFFFAOYSA-N
Popularity 162 references in papers

Physical and Chemical Properties

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Molecular Formula C6H7NO
Molecular Weight 109.13 g/mol
Exact Mass 109.052763847 g/mol
Topological Polar Surface Area (TPSA) 22.10 Ų
XlogP 1.40
Atomic LogP (AlogP) 1.09
H-Bond Acceptor 2
H-Bond Donor 0
Rotatable Bonds 1

Synonyms

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1628-89-3
Pyridine, 2-methoxy-
Pyridine, methoxy-
2-methoxy-pyridine
UNII-GEB38J8108
2-Methoxy pyridine
GEB38J8108
EINECS 216-623-8
AI3-62040
methoxypyridine
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-Methoxypyridine

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9947 99.47%
Caco-2 + 0.7266 72.66%
Blood Brain Barrier + 0.8750 87.50%
Human oral bioavailability + 0.8286 82.86%
Subcellular localzation Mitochondria 0.6865 68.65%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9714 97.14%
OATP1B3 inhibitior + 0.9694 96.94%
MATE1 inhibitior - 0.9600 96.00%
OCT2 inhibitior - 0.9750 97.50%
BSEP inhibitior - 0.9154 91.54%
P-glycoprotein inhibitior - 0.9917 99.17%
P-glycoprotein substrate - 0.9563 95.63%
CYP3A4 substrate - 0.7235 72.35%
CYP2C9 substrate - 0.8191 81.91%
CYP2D6 substrate - 0.7206 72.06%
CYP3A4 inhibition - 0.9767 97.67%
CYP2C9 inhibition - 0.9617 96.17%
CYP2C19 inhibition - 0.9455 94.55%
CYP2D6 inhibition - 0.9281 92.81%
CYP1A2 inhibition - 0.6463 64.63%
CYP2C8 inhibition - 0.6545 65.45%
CYP inhibitory promiscuity - 0.9487 94.87%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.7663 76.63%
Carcinogenicity (trinary) Non-required 0.5135 51.35%
Eye corrosion - 0.8088 80.88%
Eye irritation + 1.0000 100.00%
Skin irritation + 0.6020 60.20%
Skin corrosion - 0.9078 90.78%
Ames mutagenesis - 0.7100 71.00%
Human Ether-a-go-go-Related Gene inhibition - 0.5856 58.56%
Micronuclear - 0.5900 59.00%
Hepatotoxicity + 0.6088 60.88%
skin sensitisation - 0.7236 72.36%
Respiratory toxicity - 0.7222 72.22%
Reproductive toxicity + 0.6222 62.22%
Mitochondrial toxicity - 0.7250 72.50%
Nephrotoxicity + 0.4792 47.92%
Acute Oral Toxicity (c) III 0.8168 81.68%
Estrogen receptor binding - 0.9393 93.93%
Androgen receptor binding - 0.9216 92.16%
Thyroid receptor binding - 0.8612 86.12%
Glucocorticoid receptor binding - 0.8752 87.52%
Aromatase binding - 0.9222 92.22%
PPAR gamma - 0.8781 87.81%
Honey bee toxicity - 0.9533 95.33%
Biodegradation - 0.6500 65.00%
Crustacea aquatic toxicity + 0.6400 64.00%
Fish aquatic toxicity - 0.9510 95.10%

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
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 91.31% 96.09%
CHEMBL1293249 Q13887 Kruppel-like factor 5 88.92% 86.33%
CHEMBL2535 P11166 Glucose transporter 84.65% 98.75%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 84.29% 94.00%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 84.09% 96.00%
CHEMBL2107 P61073 C-X-C chemokine receptor type 4 83.03% 93.10%
CHEMBL1821 P08173 Muscarinic acetylcholine receptor M4 81.46% 94.08%
CHEMBL3401 O75469 Pregnane X receptor 81.37% 94.73%
CHEMBL4306 P22460 Voltage-gated potassium channel subunit Kv1.5 81.29% 94.03%
CHEMBL2581 P07339 Cathepsin D 80.14% 98.95%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 80.11% 91.11%

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.
Curcuma longa

Cross-Links

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PubChem 74201
NPASS NPC79472