Zobrazeno 1 - 10
of 55
pro vyhledávání: '"Glenn E, Dale"'
Autor:
Hans H. Locher, Paul R. Rhomberg, Glenn E. Dale, Leonard R. Duncan, Robert K. Flamm, Helio S. Sader
Publikováno v:
Journal of Antimicrobial Chemotherapy. 75:1518-1524
Background POL7306 belongs to a new class of peptidomimetic outer-membrane-protein-targeting antibiotics with a novel mechanism of action. POL7306 is in development for the treatment of infections caused by antimicrobial-resistant Gram-negative bacte
Publikováno v:
Drug discovery today. 26(9)
Rifamycin antibiotics were discovered during the 1950s, and their main representative, rifampicin, remains a cornerstone treatment for TB. The clinical use of rifamycin is restricted to mycobacteria and Gram-positive infections because of its poor ab
Autor:
Glenn E. Dale, Michael M. Tunney, María Díez-Aguilar, Deirdre Gilpin, J. Stuart Elborn, Ad C. Fluit, Jumamurat R. Bayjanov, Francesca Bernardini, Miquel B. Ekkelenkamp, Rafael Cantón
Publikováno v:
Antimicrob Agents Chemother
The objective was to determine the in vitro antimicrobial susceptibility of Pseudomonas aeruginosa isolates cultured from cystic fibrosis (CF) patients and explore associations between strain sequence type and susceptibility. Fourteen antibiotics and
Publikováno v:
Expert Review of Anti-infective Therapy. 16:259-268
With the increase in multi-drug resistant P. aeruginosa, antimicrobials with a novel mechanism of action are needed that can target these infections. Areas covered: Intravenous murepavadin is in Phase 3 development for the treatment of HABP/VABP due
Publikováno v:
Current Opinion in Chemical Biology. 38:45-51
Fully synthetic medium-sized macrocyclic peptides mimicking the key β-hairpin and α-helical protein epitopes relevant in many protein-protein interactions have emerged as a novel class of drugs with the potential to fill an important gap between sm
Autor:
Sarah Stiegeler, Caroline Kolopp, Alessandra Vitale, Maik Müller, Anatol Luther, Sophie Hell, Nicolas Desjonquères, Annie Vermeulen, Gregory Upert, Michel Schmitt, Petra Chiquet, Leo Eberl, Elizabeth Cline, Seyed Majed Modaresi, Virginie Rithié, Parthasarathi Rath, Fabio Lo Monte, Glenn E. Dale, Francesca Bernardini, Jean-Baptiste Hartmann, Marie-Anne Westwood, Achim Wach, Alexander Lederer, Régis Jaisson, Sebastian Hiller, Karen LePoupon, Daniel Obrecht, Hans H. Locher, Shuang-Yan Wang, John A. Robinson, Bernd Wollscheid, Milon Mondal, Carolin Verbree, Emile Brabet, Timothy Sharpe, Matthias Urfer, Gabriella Pessi, Peter Zbinden, Katja Zerbe, Harsha Kocherla, Tobias Remus, Michael Zahn, Kerstin Moehle
There is an urgent need for new antibiotics against Gram-negative pathogens that are resistant to carbapenem and third-generation cephalosporins, against which antibiotics of last resort have lost most of their efficacy. Here we describe a class of s
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::59ac561055e1f885369d402e6179d3b6
https://www.zora.uzh.ch/id/eprint/184028/
https://www.zora.uzh.ch/id/eprint/184028/
Autor:
Elizabeth A Lakota, Helio S. Sader, Paul G. Ambrose, Justin C Bader, Sujata M. Bhavnani, John H. Rex, Glenn E. Dale
Publikováno v:
Antimicrobial Agents and Chemotherapy. 63
Ertapenem provides activity against many pathogens commonly associated with hospital-acquired and ventilator-associated bacterial pneumoniae (HABP and VABP, respectively), including methicillin-susceptible Staphylococcus aureus and numerous Gram-nega
Autor:
J. Teague, P. Warn, Daniel Obrecht, Glenn E. Dale, J. Hansen, Maria J. Melchers, Johan W. Mouton, Achim Wach, Francesca Bernardini
Publikováno v:
Antimicrobial Agents and Chemotherapy, 63, 3
Antimicrobial Agents & Chemotherapy, 63(3):e01699-18. American Society for Microbiology
Antimicrobial Agents and Chemotherapy, 63
Antimicrobial Agents & Chemotherapy, 63(3):e01699-18. American Society for Microbiology
Antimicrobial Agents and Chemotherapy, 63
Murepavadin (POL7080) represents the first member of a novel class of outer membrane protein-targeting antibiotics. It specifically interacts with LptD and inhibits lipopolysaccharide (LPS) transport. Murepavadin is being developed for the treatment
Publikováno v:
The Journal of antimicrobial chemotherapy. 73(9)
Background Murepavadin (POL7080) represents the first member of a novel class of outer membrane protein-targeting antibiotics. Murepavadin acts by binding to LPS transport protein D and is being developed for the treatment of hospital-acquired and ve
Publikováno v:
Antimicrobial agents and chemotherapy. 62(7)
Murepavadin (formerly POL7080), a 14-amino-acid cyclic peptide, and comparators were tested by the broth microdilution method against 1,219 Pseudomonas aeruginosa isolates from 112 medical centers. Murepavadin (MIC 50/90 , 0.12/0.12 mg/liter) was 4-