109772-32-9

Upstream product

• 112142-71-9 N-benzyloxycarbonyl-L-alanyl-N¹,N¹,2-trimethylalanin-amid 
• 1142-20-7 N-Cbz-Ala 
• 112142-82-2 N-benzyloxycarbonyl-L-alanyl-2-aminoisobutyric acid methyl ester 
• 1113-49-1 2-methylalanine ethyl ester 
• 49760-60-3 N-benzyloxycarbonyl-L-alanyl chloride 

Downstream Products

• 160457-40-9 Z-Ala-Aib-Ala-Aib-Aib-OMe 
• 82427-27-8 methyl N-4-chlorobenzoyl-L-prolyl-2-methylalanyl-L-alanyl-2-methylalanyl-L-alaninate 
• 105590-91-8 methyl N-4-chlorobenzoyl-D-alanyl-2-methylalanyl-L-alaninate 
• 105590-86-1 methyl N-4-chlorobenzoyl-L-alanyl-2-methylalanyl-L-alaninate 
• 105590-92-9 (S)-2-(1-{(S)-1-[1-((S)-1-Methoxycarbonyl-ethylcarbamoyl)-1-methyl-ethylcarbamoyl]-ethylcarbamoyl}-1-methyl-ethylcarbamoyl)-pyrrolidine-1-carboxylic acid benzyl ester 
• 112142-82-2 N-benzyloxycarbonyl-L-alanyl-2-aminoisobutyric acid methyl ester 

Relevant academic research and scientific papers

Fungal metabolites. XVII. Synthesis and NMR study of ion channel-forming peptides, trichosporin B-VIa and its derivative

A membrane-modifying peptide antibiotic, trichosporin B-VIa, having catecholamine secretion-inducing activity on bovine adrenal chromaffin cells has been synthesized. Aib14-Trichosporin B-Vla, in which Pro14 was replaced by Aib, has

Selective Amide Cleavage in Peptides Containing α,α-Disubstituted α-Amino Acids

A new synthesis of dipeptides with terminal α,α-disubstituted α-amino acids, using 2,2-disubstituted 3-amino-2H-azirines 1 as amino-acid equivalents, is demonstrated.The reaction of 1 with N-protected amino acids leads to the corresponding dipeptide amide