2-(6-Fluoropyridin-2-YL)acetic acid
Names and Identifiers of 2-(6-Fluoropyridin-2-YL)acetic acid
CAS Number |
1000517-25-8 |
|---|---|
MDL Number |
MFCD09925118 |
IUPAC Name |
2-(6-fluoropyridin-2-yl)acetic acid |
InChI |
InChI=1S/C7H6FNO2/c8-6-3-1-2-5(9-6)4-7(10)11/h1-3H,4H2,(H,10,11) |
InChIKey |
SYOIOTYILFXTRK-UHFFFAOYSA-N |
Canonical SMILES |
C1=CC(=NC(=C1)F)CC(=O)O |
UNSPSC Code |
12352100 |
Physical and chemical properties of 2-(6-Fluoropyridin-2-YL)acetic acid
Exact Mass |
155.03800 |
|---|---|
LogP |
0.84780 |
Molecular Formula |
C7H6FNO2 |
Molecular Weight |
155.12600 |
PSA |
50.19000 |
Storage condition |
2-8°C |
Safety Information of 2-(6-Fluoropyridin-2-YL)acetic acid
Applications of 2-(6-Fluoropyridin-2-YL)acetic acid
2-(6-Fluoropyridin-2-YL)acetic acid has several applications, particularly in medicinal chemistry:
- Pharmaceutical Development: It serves as a building block for developing new drugs targeting inflammatory diseases and other conditions.
- Chemical Research: Its unique properties make it useful in studying enzyme interactions and drug design methodologies.
- Agricultural Chemicals: Potential applications in agrochemicals have also been suggested due to its biological activity.
Interaction Studies of 2-(6-Fluoropyridin-2-YL)acetic acid
Studies on the interactions of 2-(6-Fluoropyridin-2-YL)acetic acid with various biological targets reveal its potential as a lead compound for drug development. Its interactions with specific enzymes involved in inflammatory pathways have been documented, indicating its role as a selective inhibitor. Further research into its pharmacokinetics and dynamics is ongoing to better understand its therapeutic potential.
Biological Activity of 2-(6-Fluoropyridin-2-YL)acetic acid
The biological activity of 2-(6-Fluoropyridin-2-YL)acetic acid has been explored in various studies. It has shown potential as an anti-inflammatory agent and may act as an inhibitor of certain enzymes involved in inflammatory pathways. The fluorine substitution is believed to enhance its binding affinity to biological targets, thereby increasing its pharmacological efficacy.
Physical sample testing spectrum (NMR) of 2-(6-Fluoropyridin-2-YL)acetic acid
