Details
Stereochemistry | ACHIRAL |
Molecular Formula | C17H18FN3O3S |
Molecular Weight | 363.407 |
Optical Activity | NONE |
Defined Stereocenters | 0 / 0 |
E/Z Centers | 0 |
Charge | 0 |
SHOW SMILES / InChI
SMILES
CN1CCN(CC1)C2=C(F)C=C3C(=O)C(=CN4CCSC2=C34)C(O)=O
InChI
InChIKey=NJCJBUHJQLFDSW-UHFFFAOYSA-N
InChI=1S/C17H18FN3O3S/c1-19-2-4-20(5-3-19)14-12(18)8-10-13-16(14)25-7-6-21(13)9-11(15(10)22)17(23)24/h8-9H,2-7H2,1H3,(H,23,24)
Molecular Formula | C17H18FN3O3S |
Molecular Weight | 363.407 |
Charge | 0 |
Count |
|
Stereochemistry | ACHIRAL |
Additional Stereochemistry | No |
Defined Stereocenters | 0 / 0 |
E/Z Centers | 0 |
Optical Activity | NONE |
Rufloxacin (MF-934) is a fluoroquinolone antibacterial drug. It acts as a DNA gyrase inhibitor. Rufloxacin shows in vitro antibacterial activity against E. coli, Salmonella, Klebsiella, Proteus and Staphylococcus spp. Lower in vitro activity was observed with Pseudomonas, Serratia, Enterobacter and the streptococci group D. Rufloxacin is indicated for the treatment of lower respiratory tract and urinary tract infections caused by germs sensitive to rufloxacin.
CNS Activity
Sources: https://www.ncbi.nlm.nih.gov/pubmed/3253051
Curator's Comment: Rufloxacin does not appear to enter the brain in rats and in monkeys, even after repeated administration (90 days).
Originator
Approval Year
PubMed
Title | Date | PubMed |
---|---|---|
Effects of some quinolones on imipenem-induced seizures in DBA/2 mice. | 1994 Mar |
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Anti-toxoplasma activities of 24 quinolones and fluoroquinolones in vitro: prediction of activity by molecular topology and virtual computational techniques. | 2000 Oct |
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Prediction of quinolone activity against Mycobacterium avium by molecular topology and virtual computational screening. | 2000 Oct |
Sample Use Guides
The recommended dosage is 2 Tebraxin tablets (rufloxacin hydrochloride 150 or 200 mg) taken together the first day and one tablet per day in the following days. The duration of the treatment must be adapted to the severity of the case as well as to the clinical and bacteriological course; generally, 5 to 10 days of therapy are sufficient.
Route of Administration:
Oral
Substance Class |
Chemical
Created
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admin
on
Edited
Fri Dec 15 15:59:50 GMT 2023
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Record UNII |
Y521XM2900
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Record Status |
Validated (UNII)
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Record Version |
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NCI_THESAURUS |
C795
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QJ01MA10
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J01MA10
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m9697
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DTXSID6048412
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6080
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Rufloxacin
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Y521XM2900
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C72638
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SALT/SOLVATE -> PARENT |
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ACTIVE MOIETY |