The chemical substance known as (S)-2-((S)-2-((S)-2-Acetamido-4-phenylbutanamido)-4-methylpentanamido)-3-phenylpropanoic acid, with the CAS number 890660-08-9, is a complex amino acid derivative characterized by multiple chiral centers, which contribute to its stereochemistry and biological activity. This compound features an acetamido group, indicating the presence of an amide functional group, which is significant for its potential interactions in biological systems. The presence of phenyl groups suggests that it may exhibit hydrophobic characteristics, influencing its solubility and interaction with lipid membranes. Additionally, the structure includes multiple amide linkages, which can enhance its stability and affect its pharmacokinetic properties. Such compounds are often studied for their potential therapeutic applications, particularly in the fields of medicinal chemistry and drug design, where the stereochemistry can play a crucial role in the efficacy and specificity of the compound's action. Overall, this substance exemplifies the complexity and diversity of amino acid derivatives in biochemical research.

(S)-2-((S)-2-((S)-2-Acetamido-4-phenylbutanamido)-4-methylpentanamido)-3-phenylpropanoic acid

890660-08-9: The chemical substance known as (S)-2-((S)-2-((S)-2-Acetamido-4-phenylbutanamido)-4-methylpentanamido)-3-phenylpropanoic acid, with the CAS number 890660-08-9, is a complex amino acid derivative characterized by multiple chiral centers, which contribute to its stereochemistry and biological activity. This compound features an acetamido group, indicating the presence of an amide functional group, which is significant for its potential interactions in biological systems. The presence of phenyl groups suggests that it may exhibit hydrophobic characteristics, influencing its solubility and interaction with lipid membranes. Additionally, the structure includes multiple amide linkages, which can enhance its stability and affect its pharmacokinetic properties. Such compounds are often studied for their potential therapeutic applications, particularly in the fields of medicinal chemistry and drug design, where the stereochemistry can play a crucial role in the efficacy and specificity of the compound's action. Overall, this substance exemplifies the complexity and diversity of amino acid derivatives in biochemical research.

CAS 890660-08-9

(S)-2-((S)-2-((S)-2-Acetamido-4-phenylbutanamido)-4-methylpentanamido)-3-phenylpropanoic acid

Carfilzomib Impurity 87

Ref: ST-EA-CP-C153067