N-[(1,1-Dimethylethoxy)Carbonyl]-2-Methylalanyl-L-Tryptophan

98%

Reagent Code: #220050
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CAS Number 210481-85-9

science Other reagents with same CAS 210481-85-9

blur_circular Chemical Specifications

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Weight 389.45 g/mol
Formula C₂₀H₂₇N₃O₅
inventory_2 Storage & Handling
Storage Room temperature

description Product Description

Used in peptide synthesis as a protected intermediate, particularly in the preparation of complex bioactive peptides. The tert-butoxycarbonyl (Boc) group provides amine protection, while the 2-methylalanyl moiety introduces structural constraint that can enhance metabolic stability and influence conformational folding. Commonly applied in pharmaceutical research for developing enzyme inhibitors and receptor ligands, especially in studies targeting neurological pathways due to the presence of the tryptophan residue. Its modified backbone supports improved selectivity and binding affinity in peptidomimetic drug design.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿15,210.00
N-[(1,1-Dimethylethoxy)Carbonyl]-2-Methylalanyl-L-Tryptophan
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Used in peptide synthesis as a protected intermediate, particularly in the preparation of complex bioactive peptides. The tert-butoxycarbonyl (Boc) group provides amine protection, while the 2-methylalanyl moiety introduces structural constraint that can enhance metabolic stability and influence conformational folding. Commonly applied in pharmaceutical research for developing enzyme inhibitors and receptor ligands, especially in studies targeting neurological pathways due to the presence of the tryptoph

Used in peptide synthesis as a protected intermediate, particularly in the preparation of complex bioactive peptides. The tert-butoxycarbonyl (Boc) group provides amine protection, while the 2-methylalanyl moiety introduces structural constraint that can enhance metabolic stability and influence conformational folding. Commonly applied in pharmaceutical research for developing enzyme inhibitors and receptor ligands, especially in studies targeting neurological pathways due to the presence of the tryptophan residue. Its modified backbone supports improved selectivity and binding affinity in peptidomimetic drug design.

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