Bachem

The chemical substance known as L-a-Asparagine, N-[(phenylmethoxy)carbonyl]-L-valyl-L-a-aspartyl-L-valyl-L-alanyl-N-[2-oxo-4-(trifluoromethyl)-2H-1-benzopyran-7-yl] (9CI) with CAS number 219138-08-6 is a complex organic compound characterized by its peptide structure, which includes multiple amino acid residues and a benzopyran moiety. This compound features a phenylmethoxycarbonyl group, which enhances its stability and solubility, making it suitable for various biochemical applications. The presence of the trifluoromethyl group contributes to its unique electronic properties, potentially influencing its reactivity and interactions with biological targets. The compound's structure suggests potential applications in medicinal chemistry, particularly in drug design and development, due to its ability to mimic natural peptides. Additionally, its specific stereochemistry and functional groups may impart selective binding properties, making it a candidate for further research in therapeutic contexts. Overall, this substance exemplifies the intricate relationship between structure and function in bioactive molecules.

L-a-Asparagine,N-[(phenylmethoxy)carbonyl]-L-valyl-L-a-aspartyl-L-valyl-L-alanyl-N-[2-oxo-4-(trifluoromethyl)-2H-1-benzopyran-7-yl]-(9CI)

219138-08-6: The chemical substance known as L-a-Asparagine, N-[(phenylmethoxy)carbonyl]-L-valyl-L-a-aspartyl-L-valyl-L-alanyl-N-[2-oxo-4-(trifluoromethyl)-2H-1-benzopyran-7-yl] (9CI) with CAS number 219138-08-6 is a complex organic compound characterized by its peptide structure, which includes multiple amino acid residues and a benzopyran moiety. This compound features a phenylmethoxycarbonyl group, which enhances its stability and solubility, making it suitable for various biochemical applications. The presence of the trifluoromethyl group contributes to its unique electronic properties, potentially influencing its reactivity and interactions with biological targets. The compound's structure suggests potential applications in medicinal chemistry, particularly in drug design and development, due to its ability to mimic natural peptides. Additionally, its specific stereochemistry and functional groups may impart selective binding properties, making it a candidate for further research in therapeutic contexts. Overall, this substance exemplifies the intricate relationship between structure and function in bioactive molecules.

Z-VDVAD-AFC, fluorogenic substrate for caspase-2 (ICH-1).

CAS 219138-08-6

L-a-Asparagine,N-[(phenylmethoxy)carbonyl]-L-valyl-L-a-aspartyl-L-valyl-L-alanyl-N-[2-oxo-4-(trifluoromethyl)-2H-1-benzopyran-7-yl]-(9CI)

Z-Val-Asp-Val-Ala-Asp-AFC

Ref: 01-4027893