187872-01-1

Upstream product

• 16874-08-1 L-Isoleucin-tert-butylester 
• 187871-96-1 (E)-4-(tert-Butyl-diphenyl-silanyloxymethyl)-6-(toluene-4-sulfonyloxy)-hex-3-enoic acid methyl ester 
• 69320-89-4 L-isoleucine tert-butyl ester hydrochloride 
• 160283-34-1 (E)-4-(tert-Butyl-diphenyl-silanyloxymethyl)-6-oxo-hex-3-enoic acid methyl ester 
• 187871-93-8 (E)-4-(tert-Butyl-diphenyl-silanyloxymethyl)-6-hydroxy-hex-3-enoic acid methyl ester 

Downstream Products

• 187872-17-9 (2S,3S)-2-[3-(4-Benzyloxy-benzyl)-5-(1,3-dioxo-1,3-dihydro-isoindol-2-ylmethyl)-2-oxo-2,3,6,7-tetrahydro-azepin-1-yl]-3-methyl-pentanoic acid tert-butyl ester 
• 187872-69-1 (2S,3S)-2-[5-Aminomethyl-3-(4-benzyloxy-benzyl)-2-oxo-2,3,6,7-tetrahydro-azepin-1-yl]-3-methyl-pentanoic acid tert-butyl ester 
• 187872-05-5 (2S,3S)-2-[5-(tert-Butyl-diphenyl-silanyloxymethyl)-2-oxo-2,3,6,7-tetrahydro-azepin-1-yl]-3-methyl-pentanoic acid tert-butyl ester 
• 1025973-63-0 (E)-6-((1S,2S)-1-tert-Butoxycarbonyl-2-methyl-butylamino)-4-(tert-butyl-diphenyl-silanyloxymethyl)-hex-3-enoic 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