NUK - logo
E-viri
Celotno besedilo
Recenzirano
  • Potent bicyclic lactam inhi...
    St-Denis, Yves; Augelli-Szafran, Corinne E.; Bachand, Benoit; Berryman, Kent A.; DiMaio, John; Doherty, Annette M.; Edmunds, Jeremy J.; Leblond, Lorraine; Lévesque, Sophie; Narasimhan, Lakshmi S.; Penvose-Yi, Jan R.; Rubin, J.Ronald; Tarazi, Micheline; Winocour, Peter D.; Siddiqui, M.Arshad

    Bioorganic & medicinal chemistry letters, 11/1998, Letnik: 8, Številka: 22
    Journal Article

    Peptidomimetic inhibitors of general structure 1 have been prepared. Optimization of the binding affinities of these compounds through variation of the P3 hydrophobic residue is described. Selected substituted bicylic lactams displayed interesting pharmacological profiles both in vitro and in vivo. Design, synthesis, and SAR of low molecular weight peptidomimetic inhibitors of thrombin are described.