Exploring Peptide Synthesis: The Role of Fmoc-Lys(Alloc)-OH
Fmoc-Lys(Alloc)-OH is a protected derivative of L-lysine that integrates two distinct protecting groups: the base-labile Fmoc group for the alpha-amino functionality and the palladium-labile Alloc group for the epsilon-amino functionality. This orthogonal protection scheme is a cornerstone of modern Fmoc-based solid-phase peptide synthesis (SPPS). It enables chemists to meticulously control the order of reactions, allowing for selective modifications or elaborations at the lysine side chain without affecting the growing peptide backbone or other protected amino acids.
The strategic application of Fmoc-Lys(Alloc)-OH is evident in its use for creating peptides with branched structures or cyclic motifs, where the lysine side chain might be involved in secondary linkages. The ability to selectively cleave the Alloc group using palladium catalysis provides a pathway for introducing non-standard amino acids, linkers, or labels at a specific stage of the synthesis. For researchers seeking to purchase Fmoc-Lys(Alloc)-OH, engaging with a reputable manufacturer like NINGBO INNO PHARMCHEM CO.,LTD. guarantees access to a product that meets stringent purity standards. Understanding the price and value proposition of this essential reagent is key to optimizing your peptide synthesis workflows.
Perspectives & Insights
Silicon Analyst 88
“Fmoc-Lys(Alloc)-OH is a protected derivative of L-lysine that integrates two distinct protecting groups: the base-labile Fmoc group for the alpha-amino functionality and the palladium-labile Alloc group for the epsilon-amino functionality.”
Quantum Seeker Pro
“This orthogonal protection scheme is a cornerstone of modern Fmoc-based solid-phase peptide synthesis (SPPS).”
Bio Reader 7
“It enables chemists to meticulously control the order of reactions, allowing for selective modifications or elaborations at the lysine side chain without affecting the growing peptide backbone or other protected amino acids.”