Synthesis of antimicrobial agents. V: In vivo metabolism of 7-(4-hydroxypiperazin-1-yl)quinolones
- Author
- UNO, T; OKUNO, T; KAWAKAMI, K; SAKAMOTO, F; TSUKAMOTO, G
Kanebo Ltd, pharmaceuticals res. cent., Miyakojima-ku, Osaka 534, Japan - Source
Journal of medicinal chemistry (Print). 1993, Vol 36, Num 19, pp 2711-2715 ; ref : 10 ref
- CODEN
- JMCMAR
- ISSN
- 0022-2623
- Scientific domain
- Pharmacology drugs
- Publisher
- American Chemical Society, Washington, DC
- Publication country
- United States
- Document type
- Article
- Language
- English
- Keyword (fr)
- Activité biologique Animal Antibactérien Fluoroquinolone dérivé In vitro In vivo Microscopie électronique transmission Pharmacocinétique Quinolone dérivé Rat Souris Synthèse chimique Sérum Voie orale Mammalia Rodentia Vertebrata
- Keyword (en)
- Biological activity Animal Antibacterial agent Fluoroquinolone derivative In vitro In vivo Transmission electron microscopy Pharmacokinetics Quinolone derivative Rat Mouse Chemical synthesis Serum Oral administration Mammalia Rodentia Vertebrata
- Keyword (es)
- Actividad biológica Animal Antibacteriano Fluoroquinolone derivado In vitro In vivo Microscopía electrónica transmisión Farmacocinética Quinolone derivado Rata Ratón Síntesis química Suero Vía oral Mammalia 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
- 3757043
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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DOI
10.1021/jm00071a001 
https://dx.doi.org/10.1021/jm00071a001
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