The chemical substance known as (S)-2-((S)-2-((S)-2-Amino-4-phenylbutanamido)-4-methylpentanamido)-3-phenylpropanoic acid hydrochloride is a complex amino acid derivative characterized by its multiple chiral centers, which contribute to its stereochemistry and biological activity. This compound features a phenyl group, which is indicative of its potential interactions in biological systems, particularly in protein synthesis or as a pharmaceutical agent. The presence of amide linkages suggests it may exhibit stability under physiological conditions, while the hydrochloride form indicates it is a salt, enhancing its solubility in aqueous environments. The compound's structure implies potential applications in medicinal chemistry, particularly in the development of therapeutics targeting specific biological pathways. Its intricate design may also allow for selective binding to receptors or enzymes, making it a candidate for further research in drug development. Overall, the characteristics of this substance highlight its significance in the field of biochemistry and pharmacology.

(S)-2-((S)-2-((S)-2-Amino-4-phenylbutanamido)-4-methylpentanamido)-3-phenylpropanoic acid hydrochloride

1545468-80-1: The chemical substance known as (S)-2-((S)-2-((S)-2-Amino-4-phenylbutanamido)-4-methylpentanamido)-3-phenylpropanoic acid hydrochloride is a complex amino acid derivative characterized by its multiple chiral centers, which contribute to its stereochemistry and biological activity. This compound features a phenyl group, which is indicative of its potential interactions in biological systems, particularly in protein synthesis or as a pharmaceutical agent. The presence of amide linkages suggests it may exhibit stability under physiological conditions, while the hydrochloride form indicates it is a salt, enhancing its solubility in aqueous environments. The compound's structure implies potential applications in medicinal chemistry, particularly in the development of therapeutics targeting specific biological pathways. Its intricate design may also allow for selective binding to receptors or enzymes, making it a candidate for further research in drug development. Overall, the characteristics of this substance highlight its significance in the field of biochemistry and pharmacology.

CAS 1545468-80-1

(S)-2-((S)-2-((S)-2-Amino-4-phenylbutanamido)-4-methylpentanamido)-3-phenylpropanoic acid hydrochloride

Carfilzomib Impurity 40

Ref: 4Z-C-121043

Carfilzomib Impurity 61

Ref: ST-EA-CP-C153052