Zobrazeno 1 - 10
of 13
pro vyhledávání: '"Céline Vidaillac"'
Autor:
Thu-Minh Nguyen, Thu-Hue Ngo, Anh-Quan Truong, Dinh-Hoa Vu, Dinh-Chi Le, Ngan-Binh Vu, Tuyet-Nga Can, Hoang-Anh Nguyen, Thu-Phuong Phan, Françoise Van Bambeke, Céline Vidaillac, Quy-Chau Ngo
Publikováno v:
Pharmaceutics, Vol 13, Iss 4, p 456 (2021)
Background: Ceftazidime and imipenem have been increasingly used to treat Acute Exacerbations of Chronic Obstructive Pulmonary Disease (AECOPD) due to their extended-spectrum covering Pseudomonas aeruginosa. This study aims to describe the population
Externí odkaz:
https://doaj.org/article/62f45f79a19248eca91ec406c5ebc259
Publikováno v:
Antimicrobial Agents and Chemotherapy
Antimicrobial Agents and Chemotherapy, American Society for Microbiology, 2012, 56 (9), pp.4856-4861. ⟨10.1128/AAC.05996-11⟩
Antimicrobial Agents and Chemotherapy, American Society for Microbiology, 2012, 56 (9), pp.4856-4861. ⟨10.1128/AAC.05996-11⟩
Colistin resistance, although uncommon, is increasingly being reported among Gram-negative clinical pathogens, and an understanding of its impact on the activity of antimicrobials is now evolving. We evaluated the potential for synergy of colistin pl
Autor:
Jean Guillon, Guillaume Hébert, Patrick Dallemagne, Jean-Michel Léger, Céline Vidaillac, Corinne Thé, Vincent Lisowski, Sylvain Rault, Jacques Demotes-Mainard, Christian Jarry
Publikováno v:
Journal of Enzyme Inhibition and Medicinal Chemistry. 18:147-153
The syntthesis of new N-propargyl-3-pyrrol-1-ylindanamine derivatives, analogues of rasagiline, is described in ten steps starting from the corresponding arylaldehydes via the corresponding cis-3-pyrrol-1-ylindanamines. The cis-configuration of some
Autor:
Jean Guillon, Jean-Michel Léger, Stéphane Massip, Corinne Thé, Céline Vidaillac, Jean-Pierre Monti, Christian Jarry
Publikováno v:
Synlett. :1249-1252
Diels-Alder cycloaddition of N'-oxazolyl-N,N-dimethylalkylamidines la,b with electron-poor dienophiles were performed, leading to new 2-phenoxymethyl-6-formyl-2,3-dihydro-5H-oxazolo[3,2-a]pyrimidines and 2-phenoxymethyl-6-nitro-2,3-dihydro-5H-oxazolo
Publikováno v:
Revista espanola de quimioterapia : publicacion oficial de la Sociedad Espanola de Quimioterapia. 25(1)
Medical device-associated infections represent a growing problem with limited or no therapeutic options beyond implant removal. Bacterial biofilm is the major and the final determinant of the poor prognosis of these difficult-to-treat infections. Due
Autor:
Daniel-Henri Caignard, Patrick Dallemagne, Stéphane Larrouture, Christian Jarry, Jean Guillon, Claudine Quentin, Annie Lagardère, Céline Vidaillac, Stéphane Moreau, Corinne Arpin
Publikováno v:
Journal of Enzyme Inhibition and Medicinal Chemistry
Journal of Enzyme Inhibition and Medicinal Chemistry, Informa Healthcare, 2007, 22 (5), pp.620-31
Journal of Enzyme Inhibition and Medicinal Chemistry, Informa Healthcare, 2007, 22 (5), pp.620-31
The synthesis of new 4-[2-(alkylamino)ethylthio]pyrrolo[1,2-a]quinoxaline derivatives la-1 is described in five or six steps starting from various substituted nitroanilines 2a-e. The bioisostere 5-[2-(alkylamino)ethylthio]pyrrolo[1,2- a]thieno[3,2-e]
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::56d6130443c4ca17cc728d43dcf8da91
https://hal.archives-ouvertes.fr/hal-00319134
https://hal.archives-ouvertes.fr/hal-00319134
Autor:
Daniel-Henri Caignard, Claudine Quentin, Stéphane Moreau, Corinne Arpin, Jean Guillon, Christian Jarry, Jean Grellet, Boubakar B. Ba, Isabelle Forfar-Bares, Céline Vidaillac
Publikováno v:
Antimicrobial agents and chemotherapy. 51(3)
A series of 11 pyrrolo[1,2- a ]quinoxaline derivatives, 1a to 1k, sharing structural analogies with omeprazole, a eukaryotic efflux pump inhibitor (EPI) used as an antiulcer agent, was synthesized. Their inhibitory effect was evaluated using Staphylo
Autor:
Boubakar B. Ba, Marie-Claude Saux, Claudine Quentin, Corinne Arpin, Céline Vidaillac, Arnaud Chausse
Publikováno v:
Antimicrobial agents and chemotherapy. 50(6)
Gatifloxacin (GAT) is a new 8-methoxy fluoroquinolone with enhanced activity against gram-positive cocci. Its activity was studied in an in vitro pharmacokinetic-pharmacodynamic model against five Staphylococcus aureus strains, either susceptible to
Autor:
H Rogier van Doorn, Guy E Thwaites, Evelyne Kestelyn, Quang Ngo Nguyen, Nam Vinh Nguyen, Dung Thi Phuong Nguyen, Celine Vidaillac, Phuong Thi Minh Trinh, Ha Thi Nhi Vo
Publikováno v:
BMJ Open, Vol 11, Iss 7 (2021)
Background Assessing the capacity of a healthcare institution to conduct and manage clinical research studies is challenging, especially in developing countries where resources are limited. The objective of this study was to develop a practical and t
Externí odkaz:
https://doaj.org/article/a44bb76d0e6c4f0bb684506d2cabfc4b
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