Design of the first highly potent and selective aminopeptidase N (EC 3.4.11.2) inhibitor

Bioorganic and Medicinal Chemistry Letters

Volumn 9, Issue 11, 1999, Pages 1511-1516

  Chen, Huixiong ^a   Roques, Bernard P ^a   Fournié Zaluski, Marie Claude ^a  

^a CNRS   (France)

Author keywords

Enzyme inhibitors; Phosphinic acids and derivatives; Resolution

Indexed keywords

AMASTATIN; AMINOPEPTIDASE INHIBITOR; BESTATIN; MICROSOMAL AMINOPEPTIDASE; NOCICEPTIN; PHOSPHINIC ACID DERIVATIVE; UNCLASSIFIED DRUG;

ARTICLE; CANCER INVASION; DRUG DESIGN; DRUG POTENCY; ENZYME INACTIVATION; ENZYME MECHANISM; ENZYME SUBSTRATE; NONHUMAN; SWINE;

ANIMALS; ANTIGENS, CD13; DRUG DESIGN; ENZYME INHIBITORS; KIDNEY; KINETICS; SWINE;

SUS SCROFA;

EID: 0033532555     PISSN: 0960894X     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0960-894X(99)00219-X     Document Type: Article

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