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Fluoroquinolone pharmacology

Kang, J., Wang, L., Chen, X.L., Higgle, D.J. and Rampe, D. (2001) Interactions of a series of fluoroquinolone antibacterial drugs with the human cardiac K+ channel HERG. Molecular Pharmacology, 29, 122-126. [Pg.20]

Bischoff, U., Schmidt, C., Netzer, R. and Pongs, O. (2000) Effects of fluoroquinolones on HERG currents. European Journal of Pharmacology, 406, 341-343. [Pg.80]

Pharmacology The fluoroquinolones are synthetic, broad-spectrum antibacterial agents that inhibit DNA gyrase and topoisomerase IV. DNA gyrase is an essential enzyme that is involved in the replication, transcription, and repair of bacterial DNA. Topoisomerase IV is an enzyme known to play a key role in the partitioning of the chromosomal DNA during bacterial cell division. [Pg.1570]

Among fluoroquinolones, ofloxacin, pefloxacin and sparfloxacin can be used in alternative regimen, when drugs like rifampicin can not be used. Detailed pharmacology of quinolones is discussed in chapter Sulfonamides, nitrofurans and quinolones. ... [Pg.370]

Grasela DM. Clinical pharmacology of gatifloxacin, a new fluoroquinolone. Clin Infect Dis 2000 31(Suppl 2) S51-8. [Pg.1483]

Papich MG, Riviere JE, Fluoroquinolone antimicrobial drugs, in Riviere JE, Papich MG, eds.. Veterinary Pharmacology and Therapeutics, 9th ed., Wiley-Blackwell, Iowa State Univ. Press, Ames, 2009 pp. 983-1012. [Pg.105]

See other pages where Fluoroquinolone pharmacology is mentioned: [Pg.291]    [Pg.1057]    [Pg.1027]    [Pg.238]    [Pg.158]    [Pg.1057]    [Pg.327]    [Pg.3941]    [Pg.78]    [Pg.442]    [Pg.138]    [Pg.61]    [Pg.62]   
See also in sourсe #XX -- [ Pg.194 ]



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