Tert-butyl N-({(3S)-2-[N-(7-nitro-2,1,3-benzoxadiazol-4-yl)-beta-alanyl-L-phenylalanyl]-1,2-oxazolidin-3-yl}carbonyl)glycinate, with CAS number 143199-54-6, is a complex organic compound characterized by its unique structural features, including a tert-butyl group, an oxazolidine ring, and a nitro-substituted benzoxadiazole moiety. This compound is likely to exhibit properties typical of peptide-like structures, such as potential bioactivity and solubility influenced by its polar and non-polar components. The presence of the nitro group may impart specific electronic properties, making it useful in fluorescence applications or as a probe in biochemical assays. Additionally, the oxazolidine structure suggests potential applications in medicinal chemistry, particularly in the development of antibiotics or other therapeutic agents. Its synthesis and stability would depend on the specific conditions used, including pH and temperature, which can affect the integrity of the functional groups present. Overall, this compound represents a fascinating example of the intersection between organic chemistry and pharmacology.

tert-butyl N-({(3S)-2-[N-(7-nitro-2,1,3-benzoxadiazol-4-yl)-beta-alanyl-L-phenylalanyl]-1,2-oxazolidin-3-yl}carbonyl)glycinate

143199-54-6: Tert-butyl N-({(3S)-2-[N-(7-nitro-2,1,3-benzoxadiazol-4-yl)-beta-alanyl-L-phenylalanyl]-1,2-oxazolidin-3-yl}carbonyl)glycinate, with CAS number 143199-54-6, is a complex organic compound characterized by its unique structural features, including a tert-butyl group, an oxazolidine ring, and a nitro-substituted benzoxadiazole moiety. This compound is likely to exhibit properties typical of peptide-like structures, such as potential bioactivity and solubility influenced by its polar and non-polar components. The presence of the nitro group may impart specific electronic properties, making it useful in fluorescence applications or as a probe in biochemical assays. Additionally, the oxazolidine structure suggests potential applications in medicinal chemistry, particularly in the development of antibiotics or other therapeutic agents. Its synthesis and stability would depend on the specific conditions used, including pH and temperature, which can affect the integrity of the functional groups present. Overall, this compound represents a fascinating example of the intersection between organic chemistry and pharmacology.

<p>S 4404 is a fluorescent peptide inhibitor of prolyl-4-hydroxylase.</p>

CAS 143199-54-6

tert-butyl N-({(3S)-2-[N-(7-nitro-2,1,3-benzoxadiazol-4-yl)-beta-alanyl-L-phenylalanyl]-1,2-oxazolidin-3-yl}carbonyl)glycinate

S 4404

Ref: TM-T70676