N-[3-(2-Furyl)acryloyl]-Phe-Gly-Gly CAS:64967-39-1

Biological activity: The addition of the furan ring may modify the compound's biological activity, such as enhancing or inhibiting its interaction with specific receptors, enzymes, or biomolecules. This property can be crucial in drug discovery or therapeutic applications.

Fluorescence properties: The furan modification may confer fluorescence properties to the compound. This can be utilized in biological imaging techniques, where the compound can be used as a fluorescent probe to visualize specific molecules, cells, or biological processes.

Stability and chemical reactivity: The furan modification can improve the compound's stability against enzymatic degradation or chemical reactions, allowing for prolonged activity or enhanced resistance. This can be advantageous in drug formulation or as a tool in chemical synthesis.

Structural studies: The modified compound can be used as a reference or model compound in structural studies, such as NMR spectroscopy or X-ray crystallography. These studies can provide insights into the three-dimensional structure of the compound and its interactions with other molecules.