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100490-36-6

100490-36-6 Structure

100490-36-6 Structure
IdentificationMore
[Name]

TOSUFLOXACIN TOSILATE
[CAS]

100490-36-6
[Synonyms]

TOSUFLOXACIN
TOSUFLOXACIN TOSILATE
TOSUFLOXACIN TOSYLATE
1,8-naphthyridine-3-carboxylicacid,1,4-dihydro-7-(3-amino-1-pyrrolidinyl)-1-(
4-difluorophenyl)-6-fluoro-4-oxo-
a61827
a67107
abbott61827
1-(2,4-Difluorophenyl)-6-fluoro-1,4-dihydro-7-(3-aminopyrrolidin-1-yl)-4-oxo-1,8-naphthyridine-3-carboxylic acid
1,8-Naphthyridine-3-carboxylic acid, 7-(3-amino-1-pyrrolidinyl)-1-(2,4-difluorophenyl)-6-fluoro-1,4-dihydro-4-oxo-(9CI)
(+)-7-(3-Amino-1-pyrrolidinyl)-6-fluoro-1-(2,4-difluo-rophenyl)-1,4-dihydrcr-4-oxo-1,8-naphthyridine-3-carboxyli cacid
A-60969
Ozex
Toskisasin
7-(3-Aminopyrrolidin-1-yl)-1-(2,4-difluorophenyl)-6-fluoro-4-oxo-1,4-dihydro-1,8-naphthyridine-3-carboxylic acid
7-(3-Aminopyrrolizino)-1-(2,4-difluorophenyl)-6-fluoro-1,4-dihydro-4-oxo-1,8-naphthyridine-3-carboxylic acid
TFLX
[Molecular Formula]

C26H23F3N4O6S
[MDL Number]

MFCD01711971
[Molecular Weight]

576.54
[MOL File]

100490-36-6.mol
Chemical PropertiesBack Directory
[Boiling point ]

614.4±55.0 °C(Predicted)
[density ]

1.558±0.06 g/cm3(Predicted)
[pka]

5.79±0.70(Predicted)
[InChI]

InChI=1S/C19H15F3N4O3/c20-9-1-2-15(13(21)5-9)26-8-12(19(28)29)16(27)11-6-14(22)18(24-17(11)26)25-4-3-10(23)7-25/h1-2,5-6,8,10H,3-4,7,23H2,(H,28,29)
[InChIKey]

WUWFMDMBOJLQIV-UHFFFAOYSA-N
[SMILES]

N1(C2=CC=C(F)C=C2F)C2C(=CC(F)=C(N3CCC(N)C3)N=2)C(=O)C(C(O)=O)=C1
[CAS DataBase Reference]

100490-36-6(CAS DataBase Reference)
Raw materials And Preparation ProductsBack Directory
[Raw materials]

p-Toluenesulfonic acid-->Glycine-->Pyrrolidine-->2,4-Difluoroaniline-->2-Chloropyridine-N-oxide-->Ethyl fluoroacetate-->3-Aminopyrrolidine-->Tosufloxacin
Hazard InformationBack Directory
[Uses]

Tosufloxacin Tosilate (CAS# 100490-36-6) was identified in a Haemophilus influenza clone ST422.
[Definition]

ChEBI: 7-(3-aminopyrrolidin-1-yl)-1-(2,4-difluorophenyl)-6-fluoro-4-oxo-1,4-dihydro-1,8-naphthyridine-3-carboxylic acid is a 1,8-naphthyridine derivative that is 4-oxo-1,4-dihydro-1,8-naphthyridine-3-carboxylic acid bearing additional 2,4-difluorophenyl, fluoro and 3-aminopyrrolidin-1-yl substituents at positions 1, 6 and 7 respectively. It is a 1,8-naphthyridine derivative, an amino acid, a monocarboxylic acid, an organofluorine compound, an aminopyrrolidine, a tertiary amino compound, a primary amino compound and a quinolone antibiotic. It is a conjugate base of a 1-[6-carboxy-8-(2,4-difluorophenyl)-3-fluoro-5-oxo-5,8-dihydro-1,8-naphthyridin-2-yl]pyrrolidin-3-aminium.
[in vivo]

Tosufloxacin tosylate hydrate (T-3262) (oral gavage; 0.16-13.39 mg/kg; once) treatment shows antibacterial activity against S. aureus, E. coli, and P. aeruginosa in vivo[2].

Animal Model:Male Slc:ICR mice infected with S. aureus[2]
Dosage:1.27-2.15 mg/kg
Administration:Oral gavage; 1.27-2.15 mg/kg; once
Result:Showed 50% effective dose (ED50) of 1.62 mg/kg (body weight) at 7 days after infection.
Showed MIC value of 0.0125 μg/mL.
Animal Model:Male Slc:ICR mice infected with E. coli[2]
Dosage:0.16-0.30 mg/kg
Administration:Oral gavage; 0.16-0.30 mg/kg; once
Result:Showed 50% effective dose (ED50) of 0.22 mg/kg (body weight) at 7 days after infection.
Showed MIC value of 0.0125 μg/mL.
Animal Model:Male Slc:ICR mice infected with P. aeruginosa[2]
Dosage:7.66-13.39 mg/kg
Administration:Oral gavage; 7.66-13.39 mg/kg; once
Result:Showed 50% effective dose (ED50) of 10.13 mg/kg (body weight) at 7 days after infection.
Showed MIC value of 0.78 μg/mL.
[IC 50]

Quinolone
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