Descubra el nuevo Chem-Impex: donde la innovación comienza con un vínculo.

Catalog Number:
29465
CAS Number:
1060769-47-2
Ácido ( S )-Fmoc-2-amino-5-(N'-Pbf-N''-trifluoroetil-guanidino)-pentanoico
Purity:
≥ 95 % (HPLC)
Synonym(s):
Fmoc-L-Arg(CF3CH2)(Pbf)-OH
Documents
$70.50 /5 mg
Tamaño
Request Bulk Quote
Información del producto

(S)-Fmoc-2-amino-5-(N'-Pbf-N''-trifluoroethyl-guanidino)-pentanoic acid is a versatile compound widely utilized in peptide synthesis and drug development. This amino acid derivative features a protective Fmoc group, which facilitates the selective coupling of amino acids in solid-phase peptide synthesis, making it an essential tool for researchers in the field of medicinal chemistry. Its unique trifluoroethyl guanidino moiety enhances solubility and stability, allowing for more efficient synthesis of complex peptides and proteins.

This compound is particularly valuable in the development of therapeutics targeting various biological pathways, including those involved in cancer and metabolic disorders. Researchers appreciate its ability to improve the pharmacokinetic properties of peptide-based drugs, thereby increasing their efficacy and reducing potential side effects. With its robust performance in peptide synthesis and drug formulation, (S)-Fmoc-2-amino-5-(N'-Pbf-N''-trifluoroethyl-guanidino)-pentanoic acid stands out as a critical component for professionals aiming to innovate in the pharmaceutical industry.

Número CAS
1060769-47-2
Fórmula molecular
C36H41F3N4O7S
Peso molecular
730.8
Número MDL
MFCD18782822
Rotación óptica
[α] D 20 = -5 ± 2 º (C=1 en DMF)
Condiciones
Conservar entre 0 y 8 °C.
Información general
Número CAS
1060769-47-2
Fórmula molecular
C36H41F3N4O7S
Peso molecular
730.8
Número MDL
MFCD18782822
Rotación óptica
[α] D 20 = -5 ± 2 º (C=1 en DMF)
Condiciones
Conservar entre 0 y 8 °C.
Propiedades
¡Pronto habrá más información sobre la propiedad!
-
Seguridad y normativas
Materiales peligrosos
-
Antibiótico
-
Regulado por la DEA
No
Advertencias
-
Aplicaciones

(S)-Fmoc-2-amino-5-(N'-Pbf-N''-trifluoroethyl-guanidino)-pentanoic 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, enabling researchers to create complex peptide sequences efficiently.
  • Drug Development: It plays a crucial role in the development of novel therapeutic agents, especially in the design of peptide-based drugs that target specific biological pathways.
  • Bioconjugation: The chemical is used in bioconjugation processes, allowing for the attachment of peptides to various biomolecules, which is essential in creating targeted drug delivery systems.
  • Research in Neuroscience: This compound is valuable in neuroscience research for studying receptor interactions and signaling pathways, aiding in the understanding of neurological disorders.
  • Protein Engineering: It is utilized in protein engineering to modify proteins for enhanced stability and functionality, which is important in various biotechnological applications.

Citas