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Catalog Number:
04955
CAS Number:
268542-18-3
Acide Fmoc-(3 S ,4 S -4-amino-3-hydroxy-6-méthylthio-hexanoïque
Purity:
≥ 97 % (HPLC)
Synonym(s):
Fmoc-AHTHxA(3 S ,4 S -OH
Documents
$141.41 /25 mg
Taille
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Informations sur le produit

Fmoc-(3S,4S)-4-amino-3-hydroxy-6-methylthio-hexanoic acid is a versatile amino acid derivative widely utilized in peptide synthesis and drug development. This compound features a unique Fmoc (9-fluorenylmethoxycarbonyl) protecting group, which enhances its stability and solubility, making it an ideal choice for solid-phase peptide synthesis. Its structural characteristics, including the presence of a methylthio group, contribute to its ability to facilitate the formation of complex peptides with improved bioactivity. Researchers in pharmaceutical and biochemical fields can leverage this compound for the development of novel therapeutics, particularly in the design of peptide-based drugs and biologics.

The practical applications of Fmoc-(3S,4S)-4-amino-3-hydroxy-6-methylthio-hexanoic acid extend to various industries, including biotechnology and pharmaceuticals, where it plays a crucial role in the synthesis of bioactive peptides. Its unique properties allow for the creation of peptides with enhanced stability and specificity, making it a valuable tool for researchers aiming to develop targeted therapies. By incorporating this compound into their workflows, professionals can streamline their peptide synthesis processes, leading to more efficient and effective research outcomes.

Numéro CAS 
268542-18-3
Formule moléculaire
C 22 H 25 NON 6 S
Poids moléculaire 
415.51
Rotation optique 
[a] D 20 = -24 ± 2º (C = 1 dans DMF)
Informations générales
Numéro CAS 
268542-18-3
Formule moléculaire
C 22 H 25 NON 6 S
Poids moléculaire 
415.51
Rotation optique 
[a] D 20 = -24 ± 2º (C = 1 dans DMF)
Propriétés
Informations complémentaires sur la propriété à venir prochainement !
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Sécurité et réglementation
Matières dangereuses
-
Antibiotique
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Réglementé par la DEA
Non
Avertissements 
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Applications

Fmoc-(3S,4S)-4-amino-3-hydroxy-6-methylthio-hexanoic acid is widely utilized in research focused on:

  • Peptide Synthesis: This compound serves as a key building block in the synthesis of peptides, allowing researchers to create complex molecules for drug development and biological studies.
  • Drug Development: Its unique structure enhances the design of novel pharmaceuticals, particularly in targeting specific biological pathways, making it valuable in the pharmaceutical industry.
  • Bioconjugation: The chemical is used in bioconjugation processes, where it helps attach biomolecules to surfaces or other compounds, facilitating the development of diagnostic tools and targeted therapies.
  • Research in Neuroscience: It plays a role in the study of neuropeptides, contributing to the understanding of neurological functions and potential treatments for neurological disorders.
  • Custom Synthesis Services: Many laboratories offer custom synthesis of this compound, catering to specific research needs, which provides flexibility and efficiency in experimental design.

Citations