872983-72-7

Upstream product

• 872984-04-8 2-amino-N¹-{1-benzylcarbamoyl-1-[2-(tert-butyl-diphenyl-silanyloxy)-ethyl]-3-methyl-butyl}-N⁴,N⁴-dimethyl-succinamide 
• 5680-86-4 N-benzyloxycarbonyl-5-O-benzyl-L-glutamic acid 
• 872983-43-2 3-amino-3-isobutyldihydrofuran-2-one 
• 872983-51-2 N-((1S)-1-{1-benzylcarbamoyl-1-[2-(tert-butyldiphenylsiloxy)ethyl]-3-methylbutylcarbamoyl}-3-dimethylamino-3-oxopropyl)carbamic acid benzyl ester 
• 872984-00-4 2-(2-benzyloxycarbonylamino-3-dimethylcarbamoyl-propionylamino)-2-[2-(tert-butyl-diphenyl-silanyloxy)-ethyl]-4-methyl-pentanoic acid 
• 872983-99-8 [(S)-2-Dimethylcarbamoyl-1-(3-isobutyl-2-oxo-tetrahydro-furan-3-ylcarbamoyl)-ethyl]-carbamic acid benzyl ester 
• 872983-39-6 2-amino-2-(2-hydroxy-ethyl)-4-methyl-pent-4-enoic acid 

Downstream Products

• 872984-16-2 (S)-4-{(S)-1-[1-Benzylcarbamoyl-1-(2-hydroxy-ethyl)-3-methyl-butylcarbamoyl]-2-dimethylcarbamoyl-ethylcarbamoyl}-4-benzyloxycarbonylamino-butyric acid benzyl ester 

Relevant academic research and scientific papers

Engineering D-amino acid containing novel protease inhibitors using catalytic site architecture

The mechanism of proteolysis by serine proteases is a reasonably well-understood process. Typically, a histidine residue acting as a general base deprotonates the catalytic serine residue and the hydrolytic water molecule. We disclose here, the use of an