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Structure of 196808-79-4
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Fmoc-D-2-Me-Trp-OH features a D-configured tryptophan residue with a methyl group at the 2-position, enhancing metabolic stability and conformational rigidity. The Fmoc protecting group enables efficient solid-phase peptide synthesis, while the side chain retains aromaticity for π-stacking interactions. This derivative supports the incorporation of sterically hindered, non-natural amino acids in bioactive peptide design under standard coupling conditions.
Fmoc-D-2-Me-Trp-OH serves as a valuable building block in peptide synthesis, enabling the incorporation of D-configured tryptophan with a methyl group at the 2-position. The Fmoc protecting group facilitates efficient stepwise chain elongation under standard SPPS conditions. The 2-methyl substitution enhances metabolic stability and modulates conformational preferences, offering improved resistance to enzymatic degradation while maintaining favorable solubility and handling characteristics for solid-phase workflows.
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GHS Pictogram :
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GHS No : GHS07
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Signal Word : Warning
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UN#: N/A
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Class : N/A
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Packing Group : N/A
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Hazard Statements : H302-H315-H319-H335
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Precautionary Statements : P261-P264-P270-P271-P280-P302+P352-P304+P340-P330-P362+P364-P405-P501
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Lot numbers can be found on the outside label of a product: