68802-67-5

Upstream product

• 40332-33-0 cyclo(triglycyltri(N⁵-acetyl-N⁵-(benzyloxy)-L-ornithyl)) 
• 117652-75-2 N-(tert-butoxycarbonyl)diglycyltri(N⁵-acetyl-N⁵-(benzyloxy)-L-ornithyl)glycine methyl ester 
• 117652-85-4 [(S)-5-(Acetyl-benzyloxy-amino)-2-((S)-5-(acetyl-benzyloxy-amino)-2-{(S)-5-(acetyl-benzyloxy-amino)-2-[2-(2-tert-butoxycarbonylamino-acetylamino)-acetylamino]-pentanoylamino}-pentanoylamino)-pentanoylamino]-acetic acid 
• 117652-87-6 C₅₇H₇₆N₁₀O₁₇ 
• 31972-52-8 Boc-Gly-Gly-OH 

Relevant academic research and scientific papers

Synthesis and application of an Nδ-acetyl-N δ-hydroxyornithine analog: Identification of novel metal complexes of deferriferrichrysin

Synthesis of Fmoc-protected Nδ-acetyl-N δ-(tert-butoxy)-l-ornithine has revealed it to be a metal-chelating amino-acid precursor. This protected amino acid was compatible with the preparation of ferrichrome peptides by standard Fmoc-

N-Hydroxy Amides. 7. Synthesis and Properties of Linear and Cyclic Hexapeptides Containing Three N5-Acetyl-N5-hydroxy-L-ornithine Residues as Models for Ferrichrome

As sequence-modified analogues of desferriferrichrome (1), linear and cyclic peptides have been prepared.They are (OrnAH-Gly)3 (2), Ac-Gly2-OrnAH3-Gly-OMe (3), Ac-(OrnAH-Gly)3-OMe (4), and Ac-Gly-OrnAH-(OrnAH-Gly)2-OMe (5), where OrnAH stands for an Nsup