structure of 2-(2-Oxo-2-pyridin-3-ylethylidene)-1,3-thiazolidin-4-one

2-(2-Oxo-2-pyridin-3-ylethylidene)-1,3-thiazolidin-4-one

CAS No.: 1000932-62-6
M. Wt: 220.25
M. Fa: C10H8N2O2S
InChI Key: LJKHRMZMBYAGQN-ONNFQVAWSA-N

Names and Identifiers of 1000932-62-6

CAS Number

1000932-62-6

IUPAC Name

(2E)-2-(2-oxo-2-pyridin-3-ylethylidene)-1,3-thiazolidin-4-one

InChI

InChI=1S/C10H8N2O2S/c13-8(7-2-1-3-11-5-7)4-10-12-9(14)6-15-10/h1-5H,6H2,(H,12,14)/b10-4+

InChIKey

LJKHRMZMBYAGQN-ONNFQVAWSA-N

Canonical SMILES

C1C(=O)NC(=CC(=O)C2=CN=CC=C2)S1

Isomeric SMILES

C1C(=O)N/C(=C\C(=O)C2=CN=CC=C2)/S1

Physical and chemical properties of 1000932-62-6

Molecular Formula

C10H8N2O2S

Molecular Weight

220.25

Safety Information of 1000932-62-6

Pictograms

Signal Word

 Warning

Safety Data Sheet
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Applications of 1000932-62-6

The applications of 2-(2-Oxo-2-(pyridin-3-yl)ethylidene)thiazolidin-4-one span various fields:

  • Pharmaceutical Development: Its antimicrobial and anti-inflammatory properties make it a candidate for drug development targeting infections and inflammatory diseases.
  • Biological Research: The compound serves as a tool in biological studies aimed at understanding disease mechanisms and developing new therapeutic strategies.

These applications underscore the relevance of this compound in both research and therapeutic contexts.

Interaction Studies of 1000932-62-6

Interaction studies involving 2-(2-Oxo-2-(pyridin-3-yl)ethylidene)thiazolidin-4-one focus on its binding affinity with biological targets:

  • Protein Binding Studies: Investigations into how this compound interacts with specific proteins can reveal insights into its mechanism of action and potential side effects.
  • Enzyme Inhibition Assays: The ability of this compound to inhibit specific enzymes involved in disease pathways is crucial for evaluating its therapeutic potential.

Such studies are essential for understanding how this compound functions at a molecular level.

Biological Activity of 1000932-62-6

Research indicates that 2-(2-Oxo-2-(pyridin-3-yl)ethylidene)thiazolidin-4-one exhibits significant biological activities, including:

  • Antimicrobial Activity: Studies have shown that this compound has effectiveness against various bacterial strains, suggesting its potential as an antibacterial agent.
  • Anti-inflammatory Properties: The thiazolidinone scaffold is known for its ability to modulate inflammatory pathways, which may contribute to its therapeutic potential.
  • Anticancer Activity: Preliminary investigations suggest that derivatives of this compound may inhibit cancer cell proliferation, warranting further exploration in cancer therapy.

These biological activities underline the importance of this compound in drug discovery and development.