Zobrazeno 1 - 5
of 5
pro vyhledávání: '"Bérangère Gaucher"'
Autor:
Klaus Gebhardt, Clothilde Dantier, Malcolm G. P. Page, Anne Schmitt-Hoffmann, Bérangère Gaucher, Eric Desarbre
Publikováno v:
Antimicrobial Agents and Chemotherapy. 55:1510-1519
BAL30376 is a triple combination comprising a siderophore monobactam, BAL19764 ; a novel bridged monobactam, BAL29880 , which specifically inhibits class C β-lactamases; and clavulanic acid, which inhibits many class A and some class D β-lactamases
Autor:
Laure Thenoz, Sibylle Siegrist, Patrick Caspers, Stuart Shapiro, Heinrich Urwyler, Luc Bury, Anne Schmitt-Hoffmann, Bérangère Gaucher, Jutta Heim
Publikováno v:
Antimicrobial agents and chemotherapy. 53(9)
Racemic 2,4-diaminopyrimidine dihydrophthalazine derivatives BAL0030543, BAL0030544, and BAL0030545 exhibited low in vitro MICs toward small, selected panels of Enterococcus faecalis , Enterococcus faecium , Streptococcus pneumoniae , Moraxella catar
Antistaphylococcal activity of dihydrophthalazine antifolates, a family of novel antibacterial drugs
Autor:
Klaudia Kosowska-Shick, Linda Beachel, Bérangère Gaucher, Kathy Smith, Lois M. Ednie, Bonifacio Dewasse, Pamela McGhee, Patrick Caspers, Catherine Clark, Peter C. Appelbaum, Gengrong Lin, Stuart Shapiro, Gürkan Mert
Publikováno v:
Antimicrobial agents and chemotherapy. 53(4)
For a panel of 153 Staphylococcus aureus clinical isolates (including 13 vancomycin-intermediate or heterogeneous vancomycin-intermediate and 4 vancomycin-resistant strains), MIC 50 s and MIC 90 s of three novel dihydrophthalazine antifolates, BAL003
Autor:
Marielle, Rouquayrol, Bérangère, Gaucher, Dominique, Roche, Jacques, Greiner, Pierre, Vierling
Publikováno v:
Pharmaceutical research. 19(11)
[corrected] This study is dedicated to the permeation of various amino acid-, D-glucose-, and PEG-conjugates of indinavir, saquinavir, and nelfinavir across monolayers of Caco-2 cells as models of the intestinal barrier. This screening is aimed at de
Publikováno v:
CHIMIA, Vol 57, Iss 5 (2003)
Heterocyclic compounds are an attractive source of screening library structures because they possess varied structural diversity and can exhibit potent biological activity. In this context, we present some of our new and versatile approaches to rapid
Externí odkaz:
https://doaj.org/article/c30efec8a9234b228e2d301c2dad100a