Nome Químico: (±)-1-Cyclopropyl-6-fluoro-1,4-dihydro-8-methoxy-7-(3-methyl-1-piperazinyl)-4-oxo-3-quinolinecarboxylic acid sesquihydrate ;
Sinônimo: Gatifloxacin
Sorrisos: FC1=C(N2CC(C)NCC2)C(OC)=C3C(C(C(C(O)=O)=CN3C4CC4)=O)=C1
Inchi: InChI=1S/C23H22F7N4O6P.2C7H17NO5/c1-12(14-8-15(22(25,26)27)10-16(9-14)23(28,29)30)40-20-19(13-2-4-17(24)5-3-13)33(6-7-39-20)11-18-31-21(35)34(32-18)41(36,37)38;2*1-8-2-4(10)6(12)7(13)5(11)3-9/h2-5,8-10,12,19-20H,6-7,11H2,1H3,(H,31,32,35)(H2,36,37,38);2*4-13H,2-3H2,1H3/t12-,19+,20-;2*4-,5+,6+,7+/m100/s1
A High-Throughput Impurity-Free Process for Gatifloxacin
F. Javier Villasante,* Lourdes Gude, Sara P. Ferna´ndez, Olga Alonso, Elena Garcı´a, and Antonio Cosme
Organic Process Research & Development 2008, 12, 900–903
Stability indicating RP-HPLC method for simultaneous determination of gatifloxacin and dexamethasone in binary combination
Syed Naeem Razzaq1 ,Muhammad Ashfaq2 *, Islam Ullah Khan1 *, Irfana Mariam3 , Syed Saleem Razzaq4 , Ghulam Mustafa2 , Muhammad Zubair
Braz. J. Pharm. Sci. 2017;53(1):e15177
A Validated, Specific, Stability-Indicating RP-LC Method for Analysis of Gatifloxacin in the Presence of Degradation Products and Process-Related Impurities
M. Lalitha Devi1,&, K. B. Chandrasekhar
Chromatographia 2009, 69, 985–992
Elimination of gatifloxacin from water: Treatment by electro-Fenton process and highlighting of a biological post-treatment
Mohamed Réda Arhoutane1,*, Ghizlan Kaichouh2, Muna Shueai Yahya3, Miloud El Karbane4,Hind Chakchak5, Kacem El Kacemi
Mediterranean Journal of Chemistry 2019, 8(4), 308-319