N~6~-propanoyl-L-lysine, with the CAS number 1974-17-0, is a derivative of the amino acid lysine, characterized by the addition of a propanoyl group at the nitrogen atom of the amino side chain. This modification alters its properties compared to standard lysine. The substance is typically a white to off-white solid, soluble in water due to the presence of the amino and carboxyl functional groups, which can engage in hydrogen bonding. N~6~-propanoyl-L-lysine is often studied in biochemical and pharmaceutical contexts, particularly for its potential roles in protein synthesis and as a building block in peptide synthesis. Its structural modifications can influence its biological activity, making it of interest in research related to drug development and metabolic studies. Additionally, the compound may exhibit unique interactions with enzymes and receptors, contributing to its functional applications in various biochemical pathways. As with many amino acid derivatives, its stability and reactivity can be influenced by environmental factors such as pH and temperature.

N~6~-propanoyl-L-lysine

1974-17-0: N~6~-propanoyl-L-lysine, with the CAS number 1974-17-0, is a derivative of the amino acid lysine, characterized by the addition of a propanoyl group at the nitrogen atom of the amino side chain. This modification alters its properties compared to standard lysine. The substance is typically a white to off-white solid, soluble in water due to the presence of the amino and carboxyl functional groups, which can engage in hydrogen bonding. N~6~-propanoyl-L-lysine is often studied in biochemical and pharmaceutical contexts, particularly for its potential roles in protein synthesis and as a building block in peptide synthesis. Its structural modifications can influence its biological activity, making it of interest in research related to drug development and metabolic studies. Additionally, the compound may exhibit unique interactions with enzymes and receptors, contributing to its functional applications in various biochemical pathways. As with many amino acid derivatives, its stability and reactivity can be influenced by environmental factors such as pH and temperature.

CAS 1974-17-0

N~6~-propanoyl-L-lysine

L-Lysine, N6-(1-oxopropyl)-

Ref: IN-DA002ATC

H-Lys(Propionyl)-Oh

Ref: 54-OR1013519

N6-Propionyl-L-lysine

Ref: 10-F611894