Synthesis and biological evaluation of novel pleuromutilin derivatives with nitrogen-containing heterocycles as antibacterial agents / 药学学报
Yao Xue Xue Bao
; (12): 1297-1304, 2015.
Article
en Zh
| WPRIM
| ID: wpr-320086
Biblioteca responsable:
WPRO
ABSTRACT
A series of new pleuromutilins derivatives were designed and synthesized through coupling 2-aminothiazole ring of WL001 with different nitrogen-containing substituted heterocycles in the side chain. Their biological activities were evaluated against both Gram-positive and Gram-negative clinical bacteria in vitro Most new compounds displayed specificity to certain strain of bacteria. Particularly, compounds with saturated nitrogen-containing heterocycles exhibited significant antibacterial activities (0.062 5-8 µg · mL(-1)) superior or similar to those of amoxicillin, tiamulin and levofloxcin. Furthermore, treatment with 15a and 15b having piperidine or morpholine residues also could effectively inhibit Gram-negative bacteria. Therefore, our novel findings may provide a new insight into the design of novel pleuromutilin derivatives and lay the basis for further studies on the treatment of drug-resistance of pathogenic bacteria.
Texto completo:
1
Base de datos:
WPRIM
Asunto principal:
Relación Estructura-Actividad
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Pruebas de Sensibilidad Microbiana
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Química
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Diterpenos
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Levofloxacino
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Bacterias Gramnegativas
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Amoxicilina
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Antibacterianos
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Nitrógeno
Idioma:
Zh
Revista:
Yao Xue Xue Bao
Año:
2015
Tipo del documento:
Article