19 articles for thisTarget
The following articles (labelled with PubMed ID or TBD) are for your review
PMID
Data
Article Title
Organization
Identification of methionine aminopeptidase 2 as a molecular target of the organoselenium drug ebselen and its derivatives/analogues: Synthesis, inhibitory activity and molecular modeling study.
Wroclaw University of Technology
Discovery of potent and selective inhibitors of human aminopeptidases ERAP1 and ERAP2 by screening libraries of phosphorus-containing amino acid and dipeptide analogues.
Wroclaw University of Technology
A structural insight into the P1S1 binding mode of diaminoethylphosphonic and phosphinic acids, selective inhibitors of alanine aminopeptidases.
Wroclaw University of Technology
Peptide-based inhibitors of protein-protein interactions.
Wroclaw University of Technology
Synthesis and biological activity of diisothiocyanate-derived mercapturic acids.
Wroclaw University of Technology
Phosphonic analogues of glutamic acid as irreversible inhibitors of Staphylococcus aureus endoproteinase GluC: an efficient synthesis and inhibition of the human IgG degradation.
Wroclaw University of Technology
The development of first Staphylococcus aureus SplB protease inhibitors: phosphonic analogues of glutamine.
Wroclaw University of Technology
Remarkable potential of thea-aminophosphonate/phosphinate structural motif in medicinal chemistry.
Wroclaw University of Technology
Design, synthesis, and activity of analogues of phosphinothricin as inhibitors of glutamine synthetase.
Wroclaw University of Technology
The most potent organophosphorus inhibitors of leucine aminopeptidase. Structure-based design, chemistry, and activity.
Wroclaw University of Technology
Synthesis and activity of phosphinic tripeptide inhibitors of cathepsin C.
Wroclaw University of Technology
New aromatic monoesters of alpha-aminoaralkylphosphonic acids as inhibitors of aminopeptidase N/CD13.
Wroclaw University of Technology
First synthesis of alpha-aminoalkyl-(N-substituted)thiocarbamoyl-phosphinates: inhibitors of aminopeptidase N (APN/CD13) with the new zinc-binding group.
Wroclaw University of Technology
Individual stereoisomers of phosphinic dipeptide inhibitor of leucine aminopeptidase.
Wroclaw University of Technology
Novel hydroxamic acid-related phosphinates: inhibition of neutral aminopeptidase N (APN).
Wroclaw University of Technology
Inhibition of trypsin and urokinase by Cbz-amino(4-guanidinophenyl)methanephosphonate aromatic ester derivatives: the influence of the ester group on their biological activity.
Wroclaw University of Technology
1,2-Benzisoselenazol-3(2H)-one Derivatives As a New Class of Bacterial Urease Inhibitors.
Wroclaw University of Technology
Recent developments in the synthesis and applications of phosphinic peptide analogs.
Wroclaw University of Technology
