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Description: Flumequine (formerly R-802; R 802; R802) is a synthetic quinolone, 1st generation and broad-spectrum chemotherapeutic antibiotic that was once used to treat bacterial infections but has been removed from market. It acts by inhibiting topoisomerase II with an IC50 of 15 uM. Flumequine inhibits eukaryotic topoisomerase II, which is responsible for the double-strand DNA breakage reaction as well as bacterial gyrase, inhibitory effects of FL on topoisomerase II are high relative to the influence on bacterial gyrase. Flumequine has minimum inhibitory concentration (MIC) ranging from 0.06 ug/mL to 32 ug/mL in 12 clinical A. salmonicida isolates.
References: Toxicol Sci. 2002 Oct; 69(2):317-21; Antimicrob Agents Chemother. 1995 May; 39(5):1059-64.
Chemical Name: 7-Fluoro-12-methyl-4-oxo-1-azatricyclo[7.3.1.05, 13]trideca-2, 5, 7, 9(13)-tetraene-3-carboxylic acid
InChi Key: DPSPPJIUMHPXMA-UHFFFAOYSA-N
InChi Code: InChI=1S/C14H12FNO3/c1-7-2-3-8-4-9(15)5-10-12(8)16(7)6-11(13(10)17)14(18)19/h4-7H, 2-3H2, 1H3, (H, 18, 19)
SMILES Code: O=C(C(C1=O)=CN2C(C)CCC3=C2C1=CC(F)=C3)O
Note: The presented information and documents (Manual, Product Datasheet, Safety Datasheet and Certificate of Analysis) correspond to our latest update and should serve for orientational purpose only. We do not guarantee the topicality. We would kindly ask you to make a request for specific requirements, if necessary.
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