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Catalog Number:
04023
CAS Number:
3392-11-8
Éster de N -hidroxisuccinimida de N α - Boc-L-triptófano
Purity:
≥ 97 % (HPLC)
Synonym(s):
Boc-L-Trp-OSu
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Información del producto

Na-Boc-L-tryptophan N-hydroxysuccinimide ester is a versatile compound widely utilized in peptide synthesis and bioconjugation applications. This compound features a unique structure that enhances its reactivity, making it an ideal choice for researchers looking to develop novel peptides and protein conjugates. Its N-hydroxysuccinimide ester functionality allows for efficient coupling reactions with amines, facilitating the formation of stable amide bonds. This property is particularly beneficial in the pharmaceutical industry, where the development of peptide-based therapeutics is on the rise.

In addition to its applications in drug development, Na-Boc-L-tryptophan N-hydroxysuccinimide ester is also valuable in the field of biochemistry for studying protein interactions and modifications. Its ability to selectively modify amino acids in proteins opens up new avenues for research in proteomics and biomolecular studies. Researchers appreciate its ease of use and the high yields it provides in synthetic processes, making it a preferred choice for both academic and industrial laboratories.

Número CAS
3392-11-8
Fórmula molecular
C20H23N3O6
Peso molecular
401.42
Número MDL
MFCD00022756
Punto de fusión
141-146 ºC
Rotación óptica
-24,0±1° (c= 1% dioxano)
Condiciones
Conservar entre 0 y 8 °C.
Información general
Número CAS
3392-11-8
Fórmula molecular
C20H23N3O6
Peso molecular
401.42
Número MDL
MFCD00022756
Punto de fusión
141-146 ºC
Rotación óptica
-24,0±1° (c= 1% dioxano)
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

Na-Boc-L-tryptophan N-hydroxysuccinimide ester is widely utilized in research focused on:

  • Peptide Synthesis: This compound serves as a key building block in the synthesis of peptides, particularly those involving tryptophan, enhancing the efficiency of the coupling reactions.
  • Drug Development: It plays a role in the development of pharmaceuticals, especially in creating compounds that target serotonin receptors, which are crucial for mood regulation.
  • Bioconjugation: The N-hydroxysuccinimide ester functionality allows for easy conjugation with various biomolecules, making it valuable in creating targeted drug delivery systems.
  • Research in Neuroscience: Its applications extend to neuroscience research, where it is used to study the effects of tryptophan derivatives on neurotransmitter pathways.
  • Protein Labeling: The compound can be used for labeling proteins, aiding in the visualization and tracking of protein interactions in biological studies.

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