| Literature DB >> 25462242 |
Giuseppe Chiodini1, Marco Pallavicini1, Carlo Zanotto2, Massimiliano Bissa3, Antonia Radaelli4, Valentina Straniero1, Cristiano Bolchi1, Laura Fumagalli1, Paola Ruggeri1, Carlo De Giuli Morghen5, Ermanno Valoti6.
Abstract
A SAR study was performed on 3-substituted 2,6-difluorobenzamides, known inhibitors of the essential bacterial cell division protein FtsZ, through a series of modifications first of 2,6-difluoro-3-nonyloxybenzamide and then of its 3-pyridothiazolylmethoxy analogue PC190723. The study led to the identification of chiral 2,6-difluorobenzamides bearing 1,4-benzodioxane-2-methyl residue at the 3-position as potent antistaphylococcal compounds.Entities:
Keywords: 2,6-Difluorobenzamide; Antibacterial activity; Benzodioxane; FtsZ; Staphylococcus aureus
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Year: 2014 PMID: 25462242 DOI: 10.1016/j.ejmech.2014.09.100
Source DB: PubMed Journal: Eur J Med Chem ISSN: 0223-5234 Impact factor: 6.514