187872-75-9

Upstream product

• 28920-43-6 (fluorenylmethoxy)carbonyl chloride 
• 187872-73-7 (2S,3S)-2-[(R)-7-Amino-4-(4-hydroxy-benzyl)-3-oxo-3,4-dihydro-1H-isoquinolin-2-yl]-3-methyl-pentanoic acid tert-butyl ester 
• 5544-60-5 4-(benzyloxy)benzyl bromide 
• 187872-31-7 4-(4-Benzyloxy-benzyl)-7-nitro-isochroman-3-one 
• 187872-71-5 (2S,3S)-2-[(R)-4-(4-Benzyloxy-benzyl)-7-nitro-3-oxo-3,4-dihydro-1H-isoquinolin-2-yl]-3-methyl-pentanoic acid tert-butyl ester 
• 187872-43-1 (2S,3S)-2-{2-[2-(4-Benzyloxy-phenyl)-1-ethoxycarbonyl-ethyl]-5-nitro-benzylamino}-3-methyl-pentanoic acid tert-butyl ester 
• 187872-35-1 3-(4-Benzyloxy-phenyl)-2-(2-hydroxymethyl-4-nitro-phenyl)-propionic acid ethyl ester 
• 187872-38-4 3-(4-Benzyloxy-phenyl)-2-(2-bromomethyl-4-nitro-phenyl)-propionic acid ethyl ester 
• 4385-35-7 isochroman-3-one 

Downstream Products

• 187872-77-1 (2S,3S)-2-[(R)-7-(9H-Fluoren-9-ylmethoxycarbonylamino)-4-(4-hydroxy-benzyl)-3-oxo-3,4-dihydro-1H-isoquinolin-2-yl]-3-methyl-pentanoic acid 

Relevant academic research and scientific papers

Design, synthesis, and biological activities of four angiotensin II receptor ligands with γ-turn mimetics replacing amino acid residues 3-5

Disulfide cyclization is a powerful method for reducing the conformational space of a peptide. This in turn may enable the study of its bioactive conformation. Several analogues of angiotensin II (Ang II) containing a disulfide bridge between amino acids