Fmoc-3-methoxy-L-homophenylalanine

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Reagent Code: #38045
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CAS Number 1260610-23-8

science Other reagents with same CAS 1260610-23-8

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Weight 431.4804 g/mol
Formula C₂₆H₂₅NO₅
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description Product Description

Fmoc-3-methoxy-L-homophenylalanine is widely used in peptide synthesis, particularly in solid-phase peptide synthesis (SPPS) methods. It serves as a protected amino acid derivative, where the Fmoc (fluorenylmethyloxycarbonyl) group acts as a temporary protecting group for the amino functionality. This allows for the sequential assembly of peptides with high precision and efficiency. The 3-methoxy group on the homophenylalanine side chain can influence the peptide's conformation and binding properties, making it valuable in designing peptides with specific biological activities. It is commonly employed in the development of peptide-based drugs, enzyme inhibitors, and research tools for studying protein-protein interactions. Its stability and compatibility with standard SPPS protocols make it a reliable choice for synthesizing complex peptides in both academic and industrial settings.

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inventory 25mg
10-20 days ฿7,551.00

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Fmoc-3-methoxy-L-homophenylalanine
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Fmoc-3-methoxy-L-homophenylalanine is widely used in peptide synthesis, particularly in solid-phase peptide synthesis (SPPS) methods. It serves as a protected amino acid derivative, where the Fmoc (fluorenylmethyloxycarbonyl) group acts as a temporary protecting group for the amino functionality. This allows for the sequential assembly of peptides with high precision and efficiency. The 3-methoxy group on the homophenylalanine side chain can influence the peptide's conformation and binding properties, ma

Fmoc-3-methoxy-L-homophenylalanine is widely used in peptide synthesis, particularly in solid-phase peptide synthesis (SPPS) methods. It serves as a protected amino acid derivative, where the Fmoc (fluorenylmethyloxycarbonyl) group acts as a temporary protecting group for the amino functionality. This allows for the sequential assembly of peptides with high precision and efficiency. The 3-methoxy group on the homophenylalanine side chain can influence the peptide's conformation and binding properties, making it valuable in designing peptides with specific biological activities. It is commonly employed in the development of peptide-based drugs, enzyme inhibitors, and research tools for studying protein-protein interactions. Its stability and compatibility with standard SPPS protocols make it a reliable choice for synthesizing complex peptides in both academic and industrial settings.

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