The chemical substance with the name "(2S)-2-{[(1S)-1-benzyl-2-{[(1S)-2-carboxy-1-hydroxyethyl]amino}-2-oxoethyl]amino}-4-(4-hydroxyphenyl)butanoic acid" and CAS number "142621-29-2" is a complex organic compound characterized by multiple functional groups, including amino, carboxylic acid, and hydroxyl groups. This structure suggests it may exhibit both hydrophilic and hydrophobic properties, which can influence its solubility and interaction with biological systems. The presence of a benzyl group indicates potential for aromatic interactions, while the hydroxyphenyl moiety may contribute to its reactivity and ability to form hydrogen bonds. The stereochemistry, indicated by the (S) configurations, suggests specific spatial arrangements that could affect its biological activity and pharmacokinetics. Such compounds are often studied for their potential therapeutic applications, particularly in fields like medicinal chemistry, where their ability to interact with biological targets is of interest. Overall, this compound's intricate structure and functional diversity make it a candidate for further investigation in drug development and biochemical research.

(2S)-2-{[(1S)-1-benzyl-2-{[(1S)-2-carboxy-1-hydroxyethyl]amino}-2-oxoethyl]amino}-4-(4-hydroxyphenyl)butanoic acid

142621-29-2: The chemical substance with the name "(2S)-2-{[(1S)-1-benzyl-2-{[(1S)-2-carboxy-1-hydroxyethyl]amino}-2-oxoethyl]amino}-4-(4-hydroxyphenyl)butanoic acid" and CAS number "142621-29-2" is a complex organic compound characterized by multiple functional groups, including amino, carboxylic acid, and hydroxyl groups. This structure suggests it may exhibit both hydrophilic and hydrophobic properties, which can influence its solubility and interaction with biological systems. The presence of a benzyl group indicates potential for aromatic interactions, while the hydroxyphenyl moiety may contribute to its reactivity and ability to form hydrogen bonds. The stereochemistry, indicated by the (S) configurations, suggests specific spatial arrangements that could affect its biological activity and pharmacokinetics. Such compounds are often studied for their potential therapeutic applications, particularly in fields like medicinal chemistry, where their ability to interact with biological targets is of interest. Overall, this compound's intricate structure and functional diversity make it a candidate for further investigation in drug development and biochemical research.

Sch 47896 is an inhibitor of neutral metalloendopeptidase (NEP).

CAS 142621-29-2

(2S)-2-{[(1S)-1-benzyl-2-{[(1S)-2-carboxy-1-hydroxyethyl]amino}-2-oxoethyl]amino}-4-(4-hydroxyphenyl)butanoic acid

Sch 47896

Ref: TM-T28721