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Catalog Number:
05972
CAS Number:
27 de febrero de 2009
Clorhidrato de éster metílico de N- im -tritil-D-histidina
Purity:
≥ 99 % (TLC)
Synonym(s):
D-His(Trt)-OMe·HCl
Documents
$93.14 /250 mg
Tamaño
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Información del producto

Nim-Trityl-D-histidine methyl ester hydrochloride is a specialized amino acid derivative that plays a crucial role in peptide synthesis and drug development. This compound is particularly valued for its ability to enhance the stability and bioavailability of therapeutic peptides, making it an essential tool for researchers in pharmaceutical and biotechnological applications. Its unique trityl group provides protection against degradation, allowing for more efficient synthesis and purification processes.

In addition to its use in peptide synthesis, Nim-Trityl-D-histidine methyl ester hydrochloride has shown potential in the development of targeted drug delivery systems, where its structural properties can be leveraged to improve the efficacy of drug formulations. Researchers can utilize this compound in various applications, including the design of novel therapeutics and the exploration of new biochemical pathways. Its versatility and effectiveness make it a valuable asset in both academic and industrial settings, particularly for those focused on innovative drug development and peptide research.

Número CAS
27 de febrero de 2009
Fórmula molecular
C26H25N3O2 · HCl
Peso molecular
448.0
Número MDL
MFCD00237101
Condiciones
Conservar entre 0 y 8 °C.
Información general
Número CAS
27 de febrero de 2009
Fórmula molecular
C26H25N3O2 · HCl
Peso molecular
448.0
Número MDL
MFCD00237101
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
-
Aplicaciones

Nim-Trityl-D-histidine methyl ester hydrochloride is widely utilized in research focused on:

  • Peptide Synthesis: This compound serves as a key building block in the synthesis of peptides, particularly in the development of therapeutic agents. Its unique structure allows for the introduction of trityl protection, enhancing stability during chemical reactions.
  • Drug Development: It plays a significant role in pharmaceutical research, especially in creating novel drugs targeting specific biological pathways. The compound's ability to mimic natural amino acids makes it valuable in designing more effective medications.
  • Bioconjugation: Researchers use this chemical for bioconjugation processes, linking biomolecules to drugs or imaging agents. This application is crucial in developing targeted therapies and diagnostic tools in medicine.
  • Protein Engineering: In the field of biotechnology, it is employed to modify proteins for enhanced functionality. This modification can lead to improved enzyme activity or stability, benefiting various industrial applications.
  • Research in Cancer Therapy: The compound is being explored for its potential in cancer treatment, particularly in designing inhibitors that can selectively target cancer cells, offering a promising approach compared to traditional therapies.

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