1060716-77-9

Upstream product

• 1060716-76-8 methyl 3-{[N²-(tert-butoxycarbonyl)-N⁵-(phenoxycarbonyl)-L-ornithyl]amino}-3-deoxy-1,2-O-(1-methylethylidene)-α-D-xylofuranoate 

Downstream Products

• 1060716-79-1 methyl (3aR,5S,6R,6aR)-6-{[(2S)-2-[(tert-butoxycarbonyl)amino]-5-({[(3aR,5S,6R,6aR)-6-({(2S)-2-[(tert-butoxycarbonyl)amino]-5-[(phenoxycarbonyl)amino]pentanoyl}amino)-2,2-dimethyltetrahydrofuro[2,3-d][1,3]dioxol-5-yl]carbonyl}amino)pentanoyl]amino}-2,2-dimethyltetrahydrofuro[2,3-d][1,3]dioxole-5-carboxylate 

Relevant academic research and scientific papers

Synthesis and conformational studies of a hybrid cyclic peptide based on cis-β-furanoid sugar amino acid (FSAA) and ornithine

The conformational control of a 14-helix nucleating template, cis-β-furanoid sugar amino acid (FSAA), over a flexible δ-amino acid, ornithine is studied in a FSAA-ornithine cyclic tetrapeptide. Extensive NMR and MD studies reveal that the cyclic peptide adopts a three-dimentional bowl-shape cavity, which promotes six- and seven-membered intra- and inter-residue H-bonding, in polar and nonpolar solvents, respectively.