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Catalog Number:
16941
CAS Number:
1185841-84-2
N α -Fmoc- N ω , N ω -dimetil- N ω -(2,2,4,6,7-pentametildihidrobenzofuran-5-sulfonil)-L-arginina
Purity:
≥ 99 % (HPLC quiral)
Synonym(s):
Fmoc-L-ADMA(Pbf)-OH
Documents
$100.00 /25 mg
Tamaño
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Información del producto

Na-Fmoc-Nw, Nw-dimethyl-Nw'-(2,2,4,6,7-pentamethyldihydrobenzofuran-5-sulfonyl)-L-arginine is a sophisticated amino acid derivative that plays a crucial role in peptide synthesis and drug development. This compound features a unique sulfonyl group, which enhances its reactivity and solubility, making it an excellent choice for researchers focused on developing novel therapeutics. Its Fmoc (9-fluorenylmethoxycarbonyl) protecting group allows for easy incorporation into peptide chains, facilitating the synthesis of complex peptides with precision.

This compound is particularly valuable in the field of medicinal chemistry, where it can be utilized to create targeted peptide-based drugs. Its distinctive structure not only improves the stability of the resulting peptides but also enhances their biological activity. Researchers can leverage Na-Fmoc-Nw, Nw-dimethyl-Nw'-(2,2,4,6,7-pentamethyldihydrobenzofuran-5-sulfonyl)-L-arginine for applications in drug discovery, particularly in the development of peptides that target specific biological pathways, offering a promising avenue for innovative therapeutic solutions.

Número CAS
1185841-84-2
Fórmula molecular
C36H44N4O7S
Peso molecular
676.8
Número MDL
MFCD08064313
Condiciones
Conservar entre 0 y 8 °C.
Información general
Número CAS
1185841-84-2
Fórmula molecular
C36H44N4O7S
Peso molecular
676.8
Número MDL
MFCD08064313
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

Na-Fmoc-Nw, Nw-dimethyl-Nw'-(2,2,4,6,7-pentamethyldihydrobenzofuran-5-sulfonyl)-L-arginine is widely utilized in research focused on:

  • Peptide Synthesis: This compound serves as a protective group in peptide synthesis, allowing for the selective modification of amino acids. It enhances the efficiency of creating complex peptides used in drug development.
  • Drug Development: Its unique structure aids in the design of novel therapeutic agents, particularly in targeting specific biological pathways, making it valuable in pharmaceutical research.
  • Bioconjugation: The sulfonyl group facilitates bioconjugation processes, enabling the attachment of biomolecules to surfaces or other compounds, which is crucial in creating targeted drug delivery systems.
  • Research in Neuroscience: The compound's ability to cross the blood-brain barrier makes it a candidate for studies related to neurological disorders, potentially leading to new treatments.
  • Protein Engineering: It is used in the modification of proteins to enhance their stability and functionality, which is essential in various biotechnological applications.

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