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Catalog Number:
03740
CAS Number:
130597-31-8
Acide Fmoc-(3 S ,4 S -4-amino-3-hydroxy-5-cyclohexylpentanoïque
Purity:
≥ 98 % (HPLC)
Synonym(s):
Fmoc-ACHPA-OH
Documents
$127.79 /100 mg
Taille
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Informations sur le produit

Fmoc-(3S,4S)-4-amino-3-hydroxy-5-cyclohexylpentanoic acid is a versatile building block widely utilized in peptide synthesis and drug development. This compound features a fluorenylmethoxycarbonyl (Fmoc) protecting group, which is crucial for the selective protection of amino groups during the synthesis of peptides. Its unique structure, characterized by the cyclohexyl group, enhances hydrophobic interactions, making it particularly valuable in the design of bioactive peptides and pharmaceuticals. Researchers appreciate its stability under various conditions, allowing for efficient coupling reactions and facilitating the synthesis of complex peptide sequences.

In addition to its role in peptide synthesis, this compound has shown potential in the development of therapeutic agents targeting various biological pathways. Its ability to form stable conjugates with other biomolecules opens avenues for innovative drug delivery systems and targeted therapies. With its favorable properties and practical applications, Fmoc-(3S,4S)-4-amino-3-hydroxy-5-cyclohexylpentanoic acid stands out as an essential tool for researchers and industry professionals focused on advancing peptide-based therapeutics.

Numéro CAS 
130597-31-8
Formule moléculaire
C 26 H 315
Poids moléculaire 
437.5
Informations générales
Numéro CAS 
130597-31-8
Formule moléculaire
C 26 H 315
Poids moléculaire 
437.5
Propriétés
Informations complémentaires sur la propriété à venir prochainement !
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Sécurité et réglementation
Matières dangereuses
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Antibiotique
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Réglementé par la DEA
Non
Avertissements 
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Applications

Fmoc-(3S,4S)-4-amino-3-hydroxy-5-cyclohexylpentanoic acid is widely utilized in research focused on:

  • Peptide Synthesis: This compound serves as a key building block in the synthesis of peptides, particularly in solid-phase peptide synthesis, where its protective Fmoc group allows for selective deprotection and coupling.
  • Drug Development: Researchers leverage its unique structural properties to design and develop new pharmaceuticals, especially in the field of neuroactive compounds, enhancing the efficacy and specificity of drug candidates.
  • Bioconjugation: It is used in bioconjugation processes to attach peptides to various biomolecules, facilitating the creation of targeted therapies and diagnostic agents in biotechnology.
  • Material Science: The compound finds applications in the development of novel materials, particularly in creating hydrogels that mimic biological environments for tissue engineering applications.
  • Research on Amino Acid Analogues: It is valuable in studying amino acid analogues, helping researchers understand the structure-activity relationships that influence biological functions and interactions.

Citations