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Novel inhibitors of bacterial two-component systems with gram positive antibacterial activity: pharmacophore identification based on the screening hit closantel.
Hlasta, D J; Demers, J P; Foleno, B D; Fraga-Spano, S A; Guan, J; Hilliard, J J; Macielag, M J; Ohemeng, K A; Sheppard, C M; Sui, Z; Webb, G C; Weidner-Wells, M A; Werblood, H; Barrett, J F.
Afiliación
  • Hlasta DJ; R.W. Johnson Pharmaceutical Research Institute, Raritan, NJ 08869, USA.
Bioorg Med Chem Lett ; 8(14): 1923-8, 1998 Jul 21.
Article en En | MEDLINE | ID: mdl-9873460
This SAR study has shown that the salicylanilide is the pharmacophore for inhibition of the bacterial two-component system. Hydrophobic substituents improve the potency of inhibitors in this series; however, hydrophobicity is not the sole determinant for inhibition; structural and electronic requirements also exist. Closantel (1) was found to inhibit a two-component system and to have antibacterial activity against drug resistant S. aureus and E. faecium.
Asunto(s)
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Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Salicilanilidas / Bacterias Grampositivas / Antibacterianos Tipo de estudio: Diagnostic_studies / Screening_studies Idioma: En Revista: Bioorg Med Chem Lett Asunto de la revista: BIOQUIMICA / QUIMICA Año: 1998 Tipo del documento: Article País de afiliación: Estados Unidos Pais de publicación: Reino Unido
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Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Salicilanilidas / Bacterias Grampositivas / Antibacterianos Tipo de estudio: Diagnostic_studies / Screening_studies Idioma: En Revista: Bioorg Med Chem Lett Asunto de la revista: BIOQUIMICA / QUIMICA Año: 1998 Tipo del documento: Article País de afiliación: Estados Unidos Pais de publicación: Reino Unido