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Catalog Number:
11637
CAS Number:
148515-78-0
Fmoc- N -(2-hidroxi-4-metoxi-bencil)-Gly-OH
Purity:
≥ 98 % (HPLC)
Synonym(s):
Fmoc-(HMB)Gly-OH
Documents
$106.96 /100 mg
Tamaño
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Información del producto

Fmoc-N-(2-hydroxy-4-methoxy-benzyl)-Gly-OH is a versatile compound widely utilized in peptide synthesis and drug development. This amino acid derivative features a fluorenylmethoxycarbonyl (Fmoc) protecting group, which is essential for the selective protection of amino groups during solid-phase peptide synthesis. Its unique structure, characterized by the presence of a 2-hydroxy-4-methoxy-benzyl moiety, enhances its reactivity and solubility, making it an ideal choice for researchers focused on developing complex peptides and biologically active compounds.

In addition to its role in peptide synthesis, this compound has shown potential in medicinal chemistry, particularly in the design of novel therapeutics targeting various biological pathways. Its favorable properties allow for easier purification and characterization of peptides, which is crucial in pharmaceutical research. Researchers can leverage Fmoc-N-(2-hydroxy-4-methoxy-benzyl)-Gly-OH to streamline their workflows and improve the efficiency of their synthesis processes, ultimately leading to faster development of new drugs and therapies.

Número CAS
148515-78-0
Fórmula molecular
C25H23NO6
Peso molecular
433.46
Número MDL
MFCD06796005
Punto de fusión
161 - 168 °C
Condiciones
Conservar a ≤ -4 °C
Información general
Número CAS
148515-78-0
Fórmula molecular
C25H23NO6
Peso molecular
433.46
Número MDL
MFCD06796005
Punto de fusión
161 - 168 °C
Condiciones
Conservar a ≤ -4 °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

Fmoc-N-(2-hydroxy-4-methoxy-benzyl)-Gly-OH is widely utilized in research focused on:

  • Peptide Synthesis: This compound serves as a protecting group in solid-phase peptide synthesis, allowing for the selective modification of amino acids without interfering with other functional groups.
  • Drug Development: It plays a crucial role in the development of peptide-based therapeutics, particularly in enhancing the stability and bioavailability of drug candidates.
  • Bioconjugation: The compound is used in bioconjugation techniques to attach peptides to various biomolecules, aiding in the creation of targeted drug delivery systems.
  • Research in Cancer Therapy: Its application in designing peptide inhibitors can contribute to advancements in cancer treatment by targeting specific pathways involved in tumor growth.
  • Material Science: The compound is also explored in the development of smart materials that respond to biological stimuli, which can be beneficial in various biomedical applications.

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