Tert-butyl [(1S,2S,4R)-1,4-dibenzyl-5-{[(1S)-1-{[(1S)-1-benzyl-2-morpholin-4-yl-2-oxoethyl]carbamoyl}-2-methylpropyl]amino}-2-hydroxy-5-oxopentyl]carbamate, with CAS number 150736-68-8, is a complex organic compound characterized by its intricate molecular structure, which includes multiple functional groups such as carbamates, amines, and ketones. This compound features a tert-butyl group, which contributes to its hydrophobic properties, while the presence of morpholine and benzyl groups suggests potential biological activity, possibly as a pharmaceutical agent. The stereochemistry indicated by the (1S,2S,4R) configuration implies specific spatial arrangements that can influence the compound's reactivity and interactions with biological targets. Its solubility, stability, and reactivity are likely influenced by the balance of hydrophilic and hydrophobic regions within the molecule. Such compounds are often studied for their potential applications in medicinal chemistry, particularly in drug development, due to their ability to interact with various biological pathways.

tert-butyl [(1S,2S,4R)-1,4-dibenzyl-5-{[(1S)-1-{[(1S)-1-benzyl-2-morpholin-4-yl-2-oxoethyl]carbamoyl}-2-methylpropyl]amino}-2-hydroxy-5-oxopentyl]carbamate

150736-68-8: Tert-butyl [(1S,2S,4R)-1,4-dibenzyl-5-{[(1S)-1-{[(1S)-1-benzyl-2-morpholin-4-yl-2-oxoethyl]carbamoyl}-2-methylpropyl]amino}-2-hydroxy-5-oxopentyl]carbamate, with CAS number 150736-68-8, is a complex organic compound characterized by its intricate molecular structure, which includes multiple functional groups such as carbamates, amines, and ketones. This compound features a tert-butyl group, which contributes to its hydrophobic properties, while the presence of morpholine and benzyl groups suggests potential biological activity, possibly as a pharmaceutical agent. The stereochemistry indicated by the (1S,2S,4R) configuration implies specific spatial arrangements that can influence the compound's reactivity and interactions with biological targets. Its solubility, stability, and reactivity are likely influenced by the balance of hydrophilic and hydrophobic regions within the molecule. Such compounds are often studied for their potential applications in medicinal chemistry, particularly in drug development, due to their ability to interact with various biological pathways.

<p>CGP-53437 is a novel HIV-1 protease inhibitor, also potently inhibiting major aspartyl peptidase 1 (May1), a secreted Cryptococcus neoformans protease.</p>

CAS 150736-68-8

tert-butyl [(1S,2S,4R)-1,4-dibenzyl-5-{[(1S)-1-{[(1S)-1-benzyl-2-morpholin-4-yl-2-oxoethyl]carbamoyl}-2-methylpropyl]amino}-2-hydroxy-5-oxopentyl]carbamate

CGP-53437

Ref: TM-T70518