Killing of Staphylococcus aureus by C-8-methoxy fluoroquinolones.

Abstract:

:C-8-methoxy fluoroquinolones were more lethal than C-8-bromine, C-8-ethoxy, and C-8-H derivatives for Staphylococcus aureus, especially when topoisomerase IV was resistant. The methoxy group also increased lethality against wild-type cells when protein synthesis was inhibited. These properties encourage refinement of C-8-methoxy fluoroquinolones to kill staphylococci.

authors

Zhao X,Wang JY,Xu C,Dong Y,Zhou J,Domagala J,Drlica K

doi

10.1128/AAC.42.4.956

subject

Has Abstract

pub_date

1998-04-01 00:00:00

pages

956-8

issue

4

eissn

0066-4804

issn

1098-6596

journal_volume

42

pub_type

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