41445-69-6

Upstream product

• 49706-31-2 Nα-benzyloxycarbonyl-L-histidine hydrazide 

Downstream Products

• 111798-43-7 N-(N^α-benzyloxycarbonyl-L-histidyl)-β-alanin-ethyl ester 
• 110366-83-1 N-(N^α-benzyloxycarbonyl-L-histidyl)-L-alanin-ethyl ester 
• 66320-09-0 N-(N^α-benzyloxycarbonyl-histidyl)-serine methyl ester 
• 106172-66-1 N-(N^α-benzyloxycarbonyl-L-histidyl)-Ξ-valine 
• 30033-84-2 N-(N^α-benzyloxycarbonyl-histidyl)-leucine methyl ester 
• 4491-15-0 Z-His-Phe-OMe 
• 16706-41-5 Cbz-L-His-NH₂ 
• 82101-60-8 Boc-Glu(OBzl)-His-Phe-Arg(Mts)-Trp-Gly-OH 
• 38972-90-6 N-(N^α-benzyloxycarbonyl-histidyl)-leucine 
• 13056-38-7 N-(N^α-benzyloxycarbonyl-L-histidyl)-L-alanine 
• 7763-65-7 (S)-2-[(S)-2-Amino-3-(1H-imidazol-4-yl)-propionylamino]-4-methyl-pentanoic acid 
• 16874-75-2 His-Ala 
• 122524-39-4 N^α-benzyloxycarbonyl-L-histidyl=>Ξ-leucyl=>Ξ-valine 
• 119851-94-4 N^α-benzyloxycarbonyl-L-histidyl=>Ξ-valyl=>L-leucine 

Relevant academic research and scientific papers

Complexation properties of histydyl-glycyl containing peptides. Part 1. Synthesis of cyclo(L-His-Gly)4

The synthesis of the peptide and of its linear precursors, as useful tools to mimic the coordination sites of some enzymes, was planned.Cyclo(L-His-Gly)4 was prepared by solution-phase peptide synthesis following two different pathways.The most convenient

Synthesis of PHI (Peptide Histidine Isoleucine) and Related Peptides and Immunochemical Confirmation of Amino Acid Residue in Position 24 of PHI with use of the Synthetic Peptides

An immunochemical approach, using synthetic peptides, was employed to establish the nature of residue 24 in the amino acid sequence of PHI (peptide histidine isoleucine).PHI(20-27) and 24>-PHI(20-27) were synthesized by conventional solutio