(2-Isobutylpyridin-3-yl)methanol
Names and Identifiers of (2-Isobutylpyridin-3-yl)methanol
CAS Number |
1030829-24-3 |
|---|---|
MDL Number |
MFCD18802823 |
IUPAC Name |
[2-(2-methylpropyl)pyridin-3-yl]methanol |
InChI |
InChI=1S/C10H15NO/c1-8(2)6-10-9(7-12)4-3-5-11-10/h3-5,8,12H,6-7H2,1-2H3 |
InChIKey |
HIEINLRZXMTSEU-UHFFFAOYSA-N |
Canonical SMILES |
CC(C)CC1=C(C=CC=N1)CO |
UNSPSC Code |
12352100 |
Physical and chemical properties of (2-Isobutylpyridin-3-yl)methanol
Molecular Formula |
C10H15NO |
|---|---|
Molecular Weight |
165.23 |
Safety Information of (2-Isobutylpyridin-3-yl)methanol
Applications of (2-Isobutylpyridin-3-yl)methanol
(2-Isobutylpyridin-3-yl)methanol has potential applications in various fields:
- Pharmaceuticals: Its anti-inflammatory properties make it a candidate for drug development targeting inflammatory diseases.
- Agrochemicals: Similar compounds are often explored for their herbicidal or fungicidal activities.
- Materials Science: The compound may serve as a building block in creating novel materials with specific electronic or optical properties.
Interaction Studies of (2-Isobutylpyridin-3-yl)methanol
Interaction studies involving (2-Isobutylpyridin-3-yl)methanol focus on its binding affinity to various biological targets. For instance, studies have indicated its potential as a ligand for certain receptors or enzymes, which could lead to therapeutic applications. Investigations into its pharmacokinetics reveal that it is likely to penetrate biological membranes effectively, suggesting good bioavailability .
Biological Activity of (2-Isobutylpyridin-3-yl)methanol
Research indicates that (2-Isobutylpyridin-3-yl)methanol exhibits notable biological activities, particularly in anti-inflammatory and analgesic domains. The compound's structure suggests potential interactions with biological targets such as enzymes involved in inflammatory pathways. Preliminary studies have shown that derivatives of pyridine compounds can inhibit cyclooxygenase enzymes (COX-1 and COX-2), which are key players in inflammation and pain responses .
