393548-71-5

Upstream product

• 393548-69-1 (S)-3-(3,4-Dichloro-benzyl)-2-oxo-imidazolidine-1,5-dicarboxylic acid dibenzyl ester 
• 18880-04-1 3,4-dichlorobenzyl bromide 
• 89384-29-2 benzyl (4S)-3-(benzyloxycarbonyl)-2-oxoimidazolidine-4-carboxylate 
• 3392-12-9 Boc-Val-ONSu 
• 811803-58-4 (S)-1-(3,4-Dichloro-benzyl)-2-oxo-imidazolidine-4-carboxylic acid benzyl ester 

Downstream Products

• 811803-62-0 C₅₂H₇₈Cl₂N₈O₁₅ 
• 393547-23-4 C₅₂H₇₆Cl₂N₈O₁₅ 
• 811803-61-9 (3-{[(S)-3-((S)-2-tert-Butoxycarbonylamino-3-methyl-butyryl)-1-(3,4-dichloro-benzyl)-2-oxo-imidazolidine-4-carbonyl]-amino}-2-hydroxy-hexanoylamino)-acetic acid allyl ester 
• 811803-59-5 (S)-3-((S)-2-tert-Butoxycarbonylamino-3-methyl-butyryl)-1-(3,4-dichloro-benzyl)-2-oxo-imidazolidine-4-carboxylic acid 

Relevant academic research and scientific papers

Novel 2-oxoimidazolidine-4-carboxylic acid derivatives as Hepatitis C virus NS3-4A serine protease inhibitors: Synthesis, activity, and X-ray crystal structure of an enzyme inhibitor complex

Synthesis and HCV NS3 serine protease inhibitory activity of some novel 2-oxoimidazolidine-4-carboxylic acid derivatives are reported. X-ray structure of an inhibitor, 15c bound to the protease is presented. Synthesis and HCV NS3 serine protease inhibitor