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Catalog Number:
06131
CAS Number:
172422-76-3
N ε -Boc-L-lisina 4-nitroanilida
Purity:
≥ 99 % (HPLC)
Synonym(s):
L-Lis(Boc)-pNA
Documents
$100.05 /1G
Tamaño
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Información del producto

Ne-Boc-L-lysine 4-nitroanilide is a versatile compound widely utilized in peptide synthesis and bioconjugation applications. This protected amino acid derivative features a tert-butoxycarbonyl (Boc) group, which enhances its stability and solubility, making it an excellent choice for researchers in the fields of medicinal chemistry and biochemistry. The presence of the 4-nitroanilide moiety allows for selective reactions, facilitating the development of complex biomolecules and therapeutic agents.

This compound is particularly valuable in the synthesis of peptide-based drugs and can be employed in the preparation of various bioactive peptides. Its unique structure not only aids in the formation of peptide bonds but also provides functional groups that can be further modified for specific applications. Researchers appreciate its ability to streamline the synthesis process while maintaining high yields and purity, making Ne-Boc-L-lysine 4-nitroanilide a preferred choice for those looking to innovate in drug development and protein engineering.

Número CAS
172422-76-3
Fórmula molecular
C17H26N4O5
Peso molecular
366.38
Número MDL
MFCD00237144
Punto de fusión
91-97 °C
Rotación óptica
[α] D 20 = +30,0 ± 2º (C=0,76 en MeOH)
Condiciones
Conservar entre 0 y 8 °C.
Información general
Número CAS
172422-76-3
Fórmula molecular
C17H26N4O5
Peso molecular
366.38
Número MDL
MFCD00237144
Punto de fusión
91-97 °C
Rotación óptica
[α] D 20 = +30,0 ± 2º (C=0,76 en MeOH)
Condiciones
Conservar entre 0 y 8 °C.
Propiedades
¡Pronto habrá más información sobre la propiedad!
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Seguridad y normativas
Materiales peligrosos
-
Antibiótico
-
Regulado por la DEA
No
Advertencias
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Aplicaciones

Ne-Boc-L-lysine 4-nitroanilide is widely utilized in research focused on:

  • Peptide Synthesis: This compound serves as a key building block in the synthesis of peptides, particularly for creating modified peptides with specific functional groups, enhancing the versatility of peptide-based drugs.
  • Bioconjugation: It is employed in bioconjugation techniques, allowing researchers to attach biomolecules to surfaces or other molecules, which is crucial in developing targeted drug delivery systems.
  • Fluorescent Probes: The compound can be used to create fluorescent probes for imaging applications, helping scientists visualize biological processes in real-time.
  • Enzyme Inhibition Studies: It acts as a substrate or inhibitor in enzyme assays, aiding in the study of enzyme kinetics and the development of enzyme inhibitors for therapeutic purposes.
  • Drug Development: Its unique structure allows for modifications that can lead to the development of new pharmaceuticals, particularly in the fields of oncology and infectious diseases.

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