TEMAFLOXACIN HYDROCHLORIDE
TEMAFLOXACIN HYDROCHLORIDE Basic information
- Product Name:
- TEMAFLOXACIN HYDROCHLORIDE
- Synonyms:
-
- TEMAFLOXACIN HYDROCHLORIDE
- 1-(2,4-difluorophenyl)-6-fluoro-1,4-dihydro-7-(3-methyl-1-piperazinyl)-4-oxo-3-Quinolinecarboxylic acid hydrochloride
- Abbott 62254
- 3-Quinolinecarboxylicacid,1-(2,4-difluorophenyl)-6-fluoro-1,4-dihydro-7-(3-methyl-1-piperazinyl)-4-oxo-,hydrochloride (1:1)
- 1-(2,4-Difluorophenyl)-6-fluoro-7-(3-methylpiperazin-1-yl)-4-oxo-1,4-dihydroquinoline-3-carboxylic acid hydrochloride
- CAS:
- 105784-61-0
- MF:
- C21H18F3N3O3.ClH
- MW:
- 453.846
- Mol File:
- 105784-61-0.mol
TEMAFLOXACIN HYDROCHLORIDE Chemical Properties
- storage temp.
- Sealed in dry,Room Temperature
- solubility
- ≤2mg/ml in DMSO;5mg/ml in dimethyl formamide
- form
- crystalline solid
TEMAFLOXACIN HYDROCHLORIDE Usage And Synthesis
Description
Temafloxacin hydrochloride is a new fluoroquinolone antibacterial structurally and mechanistically related to tosufloxacin, another microbial DNA topoisomerase inhibitor introduced in 1990. It is particularly useful against beta-lactamase producing organisms and is indicated for the treatment of respiratory and urinary tract infections as well as sexually transmitted diseases, skin and soft tissue infections. The compound has high tissue penetration and is reported to have a low propensity to cause adverse effects and drug interactions.
Originator
Abbott (U.S.A.)
Uses
Temafloxacin Hydrochloride is an antimicrobial quinolone drug.
Uses
Antibacterial (microbial DNA topoisomerase inhibitor).
brand name
Omniflox (Abbott);Temac.
in vitro
the in-vitro activities of temafloxacin, ciprofloxacin, and ofloxacin against gram-negative bacteria were compared. the 90% minimal inhibitory concentrations (mic90s) of temafloxacin for respiratory pathogens were less than or equal to 0.06 micrograms/ml. temafloxacin was also active against bacterial agents of sexually transmitted diseases, such as neisseria gonorrhoeae and chlamydia trachomatis [1].
in vivo
mixed aerobic-anaerobic infection was induced by i.p. implantation of gelatin capsules containing bacteroides fragilis, escherichia coli, and sterile rat faeces. temafloxacin was found to be highly active with a 90.9% cure rate in comparison with no treatment, and as active as a combination of clindamycin and gentamicin. temafloxacin at 12 mg/dose resulted in rise to serum concentrations exceeding the mic values of both microorganisms for at least 8 h [2].
References
[1] hardy dj. in vitro activity of temafloxacin against gram-negative bacteria: an overview. am j med. 1991 dec 30;91(6a):19s-23s.
[2] thadepalli h, hajji m, perumal vk, chuah sk, gollapudi s. evaluation of temafloxacin in a rat model of intra-abdominal abscess. j antimicrob chemother. 1992 jun;29(6):687-92.
[3] ball p. the role of temafloxacin in the community setting: an overview. j antimicrob chemother. 1991 dec;28 suppl c:121-30.
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