149603-82-7

Upstream product

• 149603-83-8 N-[N-(tert-butoxycarbonyl)-L-norleucyl]-L-tyrosine methyl ester 

Downstream Products

• 398526-33-5 [1-((13S)-{2-[(4-acetylamino-benzenesulfonyl)-(3-methylbutyl)-amino]-(1R)-hydroxy-ethyl}-(10S)-butyl-8,11-dioxo-2-oxa-9,12-diaza-bicyclo[13.2.2]nonadeca-1⁽¹⁸⁾,15⁽¹⁹⁾,16-trien-(7S)-ylcarbamoyl)-(2S)-hydroxy-ethyl]-carbamic acid tert-butyl ester 
• 398526-30-2 ((13S)-{2-[(4-acetylamino-benzenesulfonyl)-(3-methylbutyl)-amino]-(1R)-hydroxy-ethyl}-(10S)-butyl-8,11-dioxo-2-oxa-9,12-diaza-bicyclo[13.2.2]nonadeca-1⁽¹⁸⁾,15⁽¹⁹⁾,16-trien-(7S)-yl)-carbamic acid tert-butyl ester 
• 398526-29-9 4-amino-N-[2-((7S)-amino-(10S)-butyl-8,11-dioxo-2-oxa-9,12-diaza-bicyclo[13.2.2]nonadeca-1⁽¹⁸⁾,15⁽¹⁹⁾,16-trien-(13S)-yl)-(2R)-hydroxy-ethyl]-N-(3-methyl-butyl)benzenesulfonamide 
• 398526-18-6 (2S)-[(2S)-((2S)-tert-butoxycarbonylamino-6-hydroxyhexanoylamino)hexanoylamino]-3-(4-hydroxyphenyl)propionic acid methyl ester 

Relevant academic research and scientific papers

β-strand mimicking macrocyclic amino acids: Templates for protease inhibitors with antiviral activity

New amino acids are reported in which component macrocycles are constrained to mimic tripeptides locked in a β-strand conformation. The novel amino acids involve macrocycles functionalized with both an N- and a C-terminus enabling addition of appendages a