Sodium 2-(pyridazin-4-yl)acetate
Names and Identifiers of Sodium 2-(pyridazin-4-yl)acetate
CAS Number |
1523571-92-7 |
|---|---|
MDL Number |
MFCD28369438 |
IUPAC Name |
sodium;2-pyridazin-4-ylacetate |
InChI |
InChI=1S/C6H6N2O2.Na/c9-6(10)3-5-1-2-7-8-4-5;/h1-2,4H,3H2,(H,9,10);/q;+1/p-1 |
InChIKey |
HUFSTXGKNYDRMS-UHFFFAOYSA-M |
Canonical SMILES |
C1=CN=NC=C1CC(=O)[O-].[Na+] |
UNSPSC Code |
12352100 |
Physical and chemical properties of Sodium 2-(pyridazin-4-yl)acetate
Exact Mass |
160.024872 |
|---|---|
Molecular Formula |
C6H5N2NaO2 |
Molecular Weight |
160.106 |
Safety Information of Sodium 2-(pyridazin-4-yl)acetate
Applications of Sodium 2-(pyridazin-4-yl)acetate
Sodium 2-(pyridazin-4-yl)acetate has potential applications in various fields:
- Pharmaceuticals: Due to its biological activity, it may serve as a lead compound for developing new drugs targeting cardiovascular diseases.
- Chemical Synthesis: It can be utilized as an intermediate in synthesizing other organic compounds, particularly those involving heterocyclic chemistry.
Interaction Studies of Sodium 2-(pyridazin-4-yl)acetate
Studies on Sodium 2-(pyridazin-4-yl)acetate's interactions reveal its potential to modulate biological pathways relevant to platelet function. Investigations into structure-activity relationships have provided insights into how modifications at different positions on the pyridazine ring affect its biological efficacy.
Biological Activity of Sodium 2-(pyridazin-4-yl)acetate
Research indicates that compounds related to pyridazine derivatives exhibit various biological activities, including antiplatelet and anti-inflammatory properties. The structural modifications in the pyridazine ring influence their pharmacological effects. For instance, some derivatives have been studied for their potential as antiplatelet agents, showing promising results in inhibiting platelet aggregation.