14 articles for thisTarget
The following articles (labelled with PubMed ID or TBD) are for your review
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Article Title
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Exploring S1 plasticity and probing S1' subsite of mammalian aminopeptidase N/CD13 with highly potent and selective aminobenzosuberone inhibitors.
Universit£
Remarkable potential of thea-aminophosphonate/phosphinate structural motif in medicinal chemistry.
Wroclaw University of Technology
Inhibitors of prolyl oligopeptidases for the therapy of human diseases: defining diseases and inhibitors.
Mcgill University
N-hydroxy-2-(naphthalene-2-ylsulfanyl)-acetamide, a novel hydroxamic acid-based inhibitor of aminopeptidase N and its anti-angiogenic activity.
Sejong University
The most potent organophosphorus inhibitors of leucine aminopeptidase. Structure-based design, chemistry, and activity.
Wroclaw University of Technology
Synthesis of sulfur-containing analogues of bestatin. Inhibition of aminopeptidases by alpha-thiolbestatin analogues.
University of Wisconsin
Inhibition of aminopeptidases by amastatin and bestatin derivatives. Effect of inhibitor structure on slow-binding processes.
TBA
New aromatic monoesters of alpha-aminoaralkylphosphonic acids as inhibitors of aminopeptidase N/CD13.
Wroclaw University of Technology
Individual stereoisomers of phosphinic dipeptide inhibitor of leucine aminopeptidase.
Wroclaw University of Technology
Potent new leucine aminopeptidase inhibitor of novel structure synthesised by a modified Wadsworth-Emmons (Horner) Wittig procedure.
The Queen'S University of Belfast
Apstatin analogue inhibitors of aminopeptidase P, a bradykinin-degrading enzyme.
Pharmacia and Upjohn
Development of selective tight-binding inhibitors of leukotriene A4 hydrolase.
Scripps Research Institute