110582-34-8

Upstream product

• 110582-44-0 ((R)-1-Benzyloxycarbonylamino-3-methyl-butyl)-{[(S)-1-(3-methyl-butylcarbamoyl)-ethylcarbamoyl]-methyl}-phosphinic acid 
• 128948-77-6 <(1R)-1-amino>-3-methylbutyl>phosphonic acid 
• 90763-55-6 C₁₄H₂₁ClNO₄P 
• 128948-78-7 methyl hydrogen ((1R)-1-{N-[(phenylmethoxy)carbonyl]amino}-3-methylbutyl)phosphonate 
• 90763-64-7 [((R)-1-Benzyloxycarbonylamino-3-methyl-butyl)-methoxy-phosphinoyl]-acetic acid 
• 90763-58-9 [((R)-1-Benzyloxycarbonylamino-3-methyl-butyl)-methoxy-phosphinoyl]-acetic acid tert-butyl ester 
• 90763-60-3 ((R)-1-Benzyloxycarbonylamino-3-methyl-butyl)-{[(S)-1-(3-methyl-butylcarbamoyl)-ethylcarbamoyl]-methyl}-phosphinic acid methyl ester 
• 88081-77-0 L-Leucine phosphonate 
• 128948-79-8 (R)-benzyl N-[1-(dimethoxyphosphoryl)-3-methylbutyl]carbamate 
• 501-53-1 benzyl chloroformate 
• 110582-44-0 (1-Benzyloxycarbonylamino-3-methyl-butyl)-{[1-(3-methyl-butylcarbamoyl)-ethylcarbamoyl]-methyl}-phosphinic acid 

Relevant academic research and scientific papers

Potent Inhibition of Pepsin and Penicillopepsin by Phosphorus-Containing Peptide Analogues

Phosphinic and phosphonic acid peptide derivatives have been evaluated as inhibitors of the aspartic proteases pepsin and penicillopepsin.The most potent of those studied is isovaleryl-Val-Val-LeuP-(O)Phe-Ala-Ala-OMe (4) (LeuP repres

Synthesis of phosphonamides and phosphinamides related to pepstatin

Activation with diphenyl phosphoryl azide (DPPA) and displacement with ammonia constitute a general procedure for conversion of phosphonic and phosphinic acids into their amides.This procedure can be applied to oligopeptide derivatives, unless intramolecu