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A novel series of parenteral cephalosporins exhibiting potent activities against both Pseudomonas aeruginosa and other Gram-negative pathogens. Part 2: Synthesis and structure-activity relationships

Author
YAMAWAKI, Kenji1 2 ; NOMURA, Takashi1 ; YASUKATA, Tatsuro1 ; TANIMOTO, Norihiko1 ; UOTANI, Koichi1 ; MIWA, Hideaki1 ; YAMANO, Yoshinori1 ; TAKEDA, Kei2 ; NISHITANI, Yasuhiro1
[1] Discovery Research Laboratories, Shionogi & Co., Ltd., 12-4, Sagisu 5-chome, Fukushima-ku, Osaka 553-0002, Japan
[2] Department of Synthetic Organic Chemistry, Graduate School of Medical Sciences, Hiroshima University, 1-2-3 Kasumi, Minami-ku, Hiroshima 734-8553, Japan
Source

Bioorganic & medicinal chemistry. 2008, Vol 16, Num 4, pp 1632-1647, 16 p ; ref : 15 ref

ISSN
0968-0896
Scientific domain
Biochemistry, molecular biology, biophysics; Pharmacology drugs
Publisher
Elsevier Science, Oxford
Publication country
United Kingdom
Document type
Article
Language
English
Author keyword
Cephalosporin Extended spectrum β-lactamase Gram-negative bacterium Pseudomonas aeruginosa Resistant β-Lactamase
Keyword (fr)
Animal Antibactérien Bactérie Gram négatif Chlore Composé organique Dérivé de la céphalosporine Dérivé du thiazole In vitro In vivo Isolat clinique Oxime Pathogène Pseudomonas aeruginosa Relation structure activité Résistance Souris Synthèse chimique Voie parentérale β-Lactamase à spectre étendu 5-Thia-1-azabicyclo[4.2.0]oct-2-ène dérivé Imidazo[4,5-b]pyridinium composé Imidazopyridinium Pyrrolo[3,2-b]pyridine dérivé Pyrrolopyridine Bactérie Mammalia Pseudomonadaceae Pseudomonadales Rodentia Vertebrata
Keyword (en)
Animal Antibacterial agent Gram negative bacteria Chlorine Organic compounds Cephalosporin derivatives Thiazole derivatives In vitro In vivo Clinical isolate Oxime Pathogenic Pseudomonas aeruginosa Structure activity relation Resistance Mouse Chemical synthesis Parenteral administration Extended-spectrum β-lactamase Bacteria Mammalia Pseudomonadaceae Pseudomonadales Rodentia Vertebrata
Keyword (es)
Animal Antibacteriano Bacteria Gram negativa Cloro Compuesto orgánico Cefalosporina derivado Tiazol derivado In vitro In vivo Aislado clinico Oxima Patógeno Pseudomonas aeruginosa Relación estructura actividad Resistencia Ratón Síntesis química Vía parenteral β-lactamasa de espectro extendido Bacteria Mammalia Pseudomonadaceae Pseudomonadales Rodentia Vertebrata
Classification
Pascal
002 Biological and medical sciences / 002B Medical sciences / 002B02 Pharmacology. Drug treatments / 002B02S Antibiotics. Antiinfectious agents. Antiparasitic agents / 002B02S02 Antibacterial agents

Discipline
Pharmacological treatments
Origin
Inist-CNRS
Database
PASCAL
INIST identifier
20140896

Sauf mention contraire ci-dessus, le contenu de cette notice bibliographique peut être utilisé dans le cadre d’une licence CC BY 4.0 Inist-CNRS / Unless otherwise stated above, the content of this bibliographic record may be used under a CC BY 4.0 licence by Inist-CNRS / A menos que se haya señalado antes, el contenido de este registro bibliográfico puede ser utilizado al amparo de una licencia CC BY 4.0 Inist-CNRS

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