124394-59-8

Upstream product

• 2577-46-0 L-isoleucine methyl ester 
• 42406-72-4 L-isoleucine benzyl ester 
• 3978-80-1 Boc-Tyr-OH 
• 124394-58-7 Boc-L-Tyr-L-Ile-OMe 
• 197706-58-4 (2S,3S)-2-[(S)-2-tert-Butoxycarbonylamino-3-(4-hydroxy-phenyl)-propionylamino]-3-methyl-pentanoic acid benzyl ester 
• 73-32-5 L-isoleucine 

Downstream Products

• 176685-66-8 Boc-Tyr-Ile-Asn(tri-O-acetyl-β-GlcNAc-CH2)-Ala-Ser-OMe 
• 197706-54-0 (S)-3-{(2S,3S)-2-[(S)-2-tert-Butoxycarbonylamino-3-(4-hydroxy-phenyl)-propionylamino]-3-methyl-pentanoylamino}-N-[(S)-1-((S)-2-hydroxy-1-methoxycarbonyl-ethylcarbamoyl)-ethyl]-succinamic acid benzyl ester 
• 213010-61-8 C₄₅H₆₆N₆O₂₀ 
• 176685-67-9 C₃₄H₅₄N₈O₁₃ 
• 197706-55-1 (S)-3-{(2S,3S)-2-[(S)-2-tert-Butoxycarbonylamino-3-(4-hydroxy-phenyl)-propionylamino]-3-methyl-pentanoylamino}-N-[(S)-1-((S)-2-hydroxy-1-methoxycarbonyl-ethylcarbamoyl)-ethyl]-succinamic acid 
• 197706-57-3 C₃₃H₅₂N₈O₁₃ 
• 197706-56-2 C₄₅H₆₇N₇O₁₉ 
• 124394-60-1 BOCCys(Bzl)TyrIleOH 

Relevant academic research and scientific papers

Combined chemical and enzymatic synthesis of a C-glycopeptide and its inhibitory activity toward glycoamidases

A novel chemoenzymatic approach to synthesizing high-mannose-type N-glycopeptide and its C-linked glycopeptide analog is described, The synthesis consists of two steps: a chemical synthesis of GlcNAc-containing peptides and an enzymatic glycosyl transfer

USE OF TRIMETHYLSILYL PROTECTION IN THE SYNTHESIS OF OXYTOCIN FRAGMENTS

The possibility has been studied of obtaining silyl derivatives of amino acids forming components of oxytocin and of obtaining the corresponding peptides from them by the mixed-anhydride method.

SYNTHESIS OF THE N-TERMINAL TRIPEPTIDE OF THE OXYTOCIN SEQUENCE

Two schemes for the synthesis of the hydrazide of the N-terminal tripeptide of the oxytocin sequence are considered.It is shown that the most rational is a 1 + 2 scheme.