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*For research and further manufacturing use only, not for direct human use.
Structure of 220155-72-6
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Fmoc-α-Me-D-Trp(Boc)-OH is a D-configured, α-methylated tryptophan derivative featuring a fluorenylmethyloxycarbonyl (Fmoc) protecting group and a tert-butoxycarbonyl (Boc) group on the indole nitrogen. This configuration enhances metabolic stability and resistance to enzymatic degradation during peptide synthesis. The electron-rich indole moiety facilitates efficient incorporation into complex peptide sequences, particularly in bioactive peptidomimetics and cyclic structures where conformational rigidity is advantageous.
Fmoc-α-Me-D-Trp(Boc)-OH serves as a key building block for the synthesis of peptide libraries and bioactive oligomers, leveraging the D-configured tryptophan side chain for enhanced metabolic stability. The Fmoc group enables efficient solution-phase and solid-phase peptide coupling, while the Boc-protected indole nitrogen ensures orthogonal handling during sequential synthesis. This derivative exhibits excellent bench stability, facilitates straightforward purification, and supports diverse functionalization strategies in medicinal chemistry 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 : H260-H301-H311-H314
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Precautionary Statements : P223-P231+P232-P260-P264-P270-P280-P301+P330+P331-P302+P335+P334-P302+P352-P303+P361+P353-P304+P340-P305+P351+P338-P330-P361+P364-P363-P370+P378-P402+P404-P405-P501
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Lot numbers can be found on the outside label of a product: