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Structure of 2044709-90-0
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Fmoc-N-Me-D-Trp(Boc)-OH is a stereochemically defined, bench-stable building block for peptide synthesis featuring a protected indole side chain. The N-methylated D-tryptophan moiety enhances conformational rigidity and metabolic stability, while the Fmoc group enables efficient C-terminal coupling under standard conditions. This derivative supports the incorporation of D-Trp residues with enhanced resistance to enzymatic degradation in bioactive peptide sequences.
Fmoc-N-Me-D-Trp(Boc)-OH serves as a key building block for the synthesis of D-amino acid-containing peptides, particularly in solid-phase peptide synthesis. The Fmoc group enables efficient orthogonal deprotection under mild basic conditions, while the N-methyl and Boc-protected indole side chain provide enhanced metabolic stability and reduced backbone hydrogen bonding. Its bench-stable nature and compatibility with standard coupling protocols facilitate reliable incorporation into complex peptide sequences.
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Lot numbers can be found on the outside label of a product: