118741-05-2

Upstream product

• 118741-09-6 (3RS,4S)-4-benzyloxycarbonyl-amino-5-cyclohexyl-3-hydroxy-1-pentene 
• 131116-20-6 (4S,5R)-3-benzyloxycarbonyl-4-cyclohexylmethyl-5-formyl-2,2-dimethyloxazolidine 
• 118741-29-0 N-benzyloxycarbonyl-L-cyclohexylalanine 3,5-dimethyl-pyrazolide 
• 118741-11-0 (4S,5RS)-3-benzyloxycarbonyl-L-cyclohexylmethyl-5-ethenyl-2,2-dimethyloxazolidine 
• 105852-47-9 2-<(benzyloxycarbonyl)amino>-3-cyclohexyl-(2S)-propionaldehyde 
• 118741-13-2 (4S,5S)-3-benzyloxycarbonyl-4-cyclohexylmethyl-5-(2-ethoxycarbonyl-1-butenyl)-2,2-dimethyloxazolidine 

Downstream Products

• 141738-66-1 (2RS,4S,5S)-N-isobutyl-5--L-norleucyl>amino-6-cyclohexyl-2-ethyl-4-hydroxyhexanamide 
• 141713-98-6 {(S)-1-[(S)-1-((1S,2S)-1-Cyclohexylmethyl-2-hydroxy-4-isobutylcarbamoyl-hexylcarbamoyl)-pentylcarbamoyl]-2-phenyl-ethyl}-carbamic acid benzyl ester 
• 118741-10-9 (Z)-(4S,5S)-3-benzyloxycarbonyl-4-cyclohexylmethyl-5-<2-(isobutylcarbamoyl)-1-butenyl>-2,2-dimethyloxazolidine 
• 118741-14-3 (E)-(4S,5S)-3-benzyloxycarbonyl-4-cyclohexylmethyl-5-<2-(isobutylcarbamoyl)-1-butenyl>-2,2-dimethyloxazolidine 

Relevant academic research and scientific papers

Renin inhibitors. I. Synthesis and structure-activity relationship of transition-state inhibitors containing homostatine analogues at the scissile bond

The synthesis and structure-activity relationships of transition-state renin inhibitors containing the homostatine analogues at the scissile bond are described. These inhibitors incorporate the amino acid side chains corresponding to positions 7-12 (Psub