Descubra el nuevo Chem-Impex: donde la innovación comienza con un vínculo.

Catalog Number:
04817
CAS Number:
109425-51-6
Fmoc-L-histidina (resina de 2-clorotritilo)amida
Synonym(s):
Fmoc-L-His(resina de tritilo)-NH2
Documents
$127.79 /1G
Tamaño
Request Bulk Quote
Información del producto

Fmoc-L-histidine(2-chlorotrityl resin)amide is a highly versatile compound widely utilized in peptide synthesis and drug development. This protected amino acid derivative features a fluorenylmethoxycarbonyl (Fmoc) group, which provides stability during the synthesis process while allowing for easy removal under mild conditions. Its unique structure, which includes a trityl-imidazole moiety, enhances its reactivity and compatibility with various coupling agents, making it an ideal choice for researchers focused on developing complex peptides and proteins.

This compound is particularly beneficial in the pharmaceutical industry, where it serves as a building block for the synthesis of bioactive peptides, including those used in therapeutic applications. Its ability to facilitate the formation of peptide bonds while maintaining the integrity of sensitive functional groups makes it a preferred choice among chemists. Additionally, Fmoc-L-histidine(2-chlorotrityl resin)amide's compatibility with automated synthesizers streamlines the peptide synthesis process, improving efficiency and yield.

Número CAS
109425-51-6
Peso molecular
0
Número MDL
MFCD00043332
Sustitución
0,2-0,6 meq/g
Tamaño de malla
Malla 200-400
Condiciones
Conservar entre 0 y 8 °C.
Información general
Número CAS
109425-51-6
Peso molecular
0
Número MDL
MFCD00043332
Sustitución
0,2-0,6 meq/g
Tamaño de malla
Malla 200-400
Condiciones
Conservar entre 0 y 8 °C.
Propiedades
¡Pronto habrá más información sobre la propiedad!
-
Seguridad y normativas
Materiales peligrosos
-
Antibiótico
-
Regulado por la DEA
No
Advertencias
-
Aplicaciones

Fmoc-L-histidine(2-chlorotrityl resin)amide is widely utilized in research focused on:

  • Peptide Synthesis: This compound serves as a key building block in solid-phase peptide synthesis, allowing researchers to create complex peptides efficiently. Its protective Fmoc group facilitates easy deprotection, making it ideal for sequential synthesis.
  • Drug Development: In pharmaceutical research, it is used to develop peptide-based drugs. Its unique structure can enhance the stability and bioavailability of therapeutic peptides, which is crucial for effective treatment.
  • Bioconjugation: The resin can be used in bioconjugation processes, where it helps attach peptides to other molecules, such as antibodies or drugs, improving targeted delivery systems in cancer therapy.
  • Protein Engineering: Researchers utilize this compound to modify histidine residues in proteins, enabling the study of protein interactions and functions, which is essential in understanding biological processes.
  • Analytical Chemistry: It plays a role in the development of analytical methods for detecting and quantifying peptides, aiding in quality control and research applications in various industries.

Citas