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Catalog Number:
28756
CAS Number:
188751-56-6
Ácido fmoc-1-amino-1-cicloheptanocarboxílico
Purity:
≥ 99 % (HPLC)
Synonym(s):
Fmoc-achc-OH
Documents
$72.31 /100 mg
Tamaño
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Información del producto

Fmoc-1-amino-1-cycloheptanecarboxylic acid is a versatile building block widely utilized in peptide synthesis and medicinal chemistry. This compound features a unique cycloheptane structure, which imparts distinctive conformational properties that can enhance the stability and bioactivity of peptides. Its Fmoc (9-fluorenylmethoxycarbonyl) protecting group allows for selective deprotection, making it an ideal choice for solid-phase peptide synthesis. Researchers appreciate its ability to facilitate the incorporation of non-standard amino acids into peptide chains, thereby expanding the scope of peptide libraries for drug discovery and development.

In addition to its applications in peptide synthesis, Fmoc-1-amino-1-cycloheptanecarboxylic acid has shown promise in the development of novel therapeutics targeting various biological pathways. Its unique structure can lead to improved binding affinities and specificities in drug design. This compound is particularly relevant for researchers focused on creating innovative peptide-based drugs, as it offers a combination of stability, versatility, and ease of use that is essential in the competitive field of pharmaceutical research.

Número CAS
188751-56-6
Fórmula molecular
C23H25NO4
Peso molecular
379.45
Número MDL
MFCD03426229
Punto de fusión
188-199 ºC
Condiciones
Conservar entre 0 y 8 °C.
Información general
Número CAS
188751-56-6
Fórmula molecular
C23H25NO4
Peso molecular
379.45
Número MDL
MFCD03426229
Punto de fusión
188-199 ºC
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

Fmoc-1-amino-1-cycloheptanecarboxylic acid is widely utilized in research focused on:

  • Peptide Synthesis: This compound serves as a protective group in solid-phase peptide synthesis, allowing for the selective modification of amino acids without affecting the rest of the peptide chain.
  • Drug Development: Its unique structure makes it valuable in the design of novel pharmaceuticals, particularly in the development of cyclic peptides that can exhibit enhanced biological activity.
  • Bioconjugation: The compound can be used to create bioconjugates, linking peptides to various biomolecules, which is essential in the development of targeted drug delivery systems.
  • Research in Neuroscience: Its derivatives are being explored for their potential applications in neuropharmacology, particularly in the study of receptor interactions and signaling pathways.
  • Material Science: The compound can be incorporated into polymeric materials to enhance their properties, such as flexibility and thermal stability, making it useful in the development of advanced materials.

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