VSE knjižnice (vzajemna bibliografsko-kataložna baza podatkov COBIB.SI)
  • Structure-based design of a new series of D-Glutamic acid-based inhibitors of bacterial UDP-N-acetylmuramoyl-L-alanine:D-glutamate ligase (MurD)
    Tomašič, Tihomir ...
    Mur ligases are bacterial enzymes involved in the cytoplasmic steps of peptidoglycan biosynthesis and are viable targets for antibacterial drug discovery. We have performed virtual screening for ... potential ATP-competitive inhibitors targeting MurC and MurD ligases, using a protocol of consecutive hierarchical filters. Selected compounds were evaluated for inhibition of MurCand MurD ligases, and weak inhibitors possessing dual inhibitory activity have been identified. These compounds represent new scaffolds for further optimisation towards multiple Mur ligase inhibitors with improved inhibitory potency.
    Vir: Journal of medicinal chemistry. - ISSN 0022-2623 (Vol. 54, no. 13, 2011, str. 4600-4610)
    Vrsta gradiva - članek, sestavni del
    Leto - 2011
    Jezik - angleški
    COBISS.SI-ID - 3019121

    Povezava(-e):

    http://pubs.acs.org/toc/jmcmar/0/ja
    http://pubs.acs.org/doi/pdf/10.1021/jm2002525
    DOI

vir: Journal of medicinal chemistry. - ISSN 0022-2623 (Vol. 54, no. 13, 2011, str. 4600-4610)
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