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Tosufloxacin tosilate

Basic information Safety Supplier Related

Tosufloxacin tosilate Basic information

Product Name:
Tosufloxacin tosilate
Synonyms:
  • Tosufloxacin Tosylate Monohydrate
  • TOSUFLOXACIN TOSILATE
  • Tosufloxacin tosilate###TOSUFLOXACIN TOSILATE
  • Tosufloxacin tosilate hydrate
  • 7-(3-Aminopyrrolidin-1-yl)-1-(2,4-difluorophenyl)-6-fluoro-4-oxo-1,8-naphthyridine-3-carboxylic acid 4-methylbenzenesulfonate hydrate
  • Tosufloxacin hydrate
  • Tosufloxacin monohydrate
  • Unii-6239812J7l
CAS:
107097-79-0
MF:
C19H17F3N4O4
MW:
422.36
EINECS:
1308068-626-2
Product Categories:
  • API
Mol File:
107097-79-0.mol
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Tosufloxacin tosilate Chemical Properties

Melting point:
approximate 254℃ (dec.)
InChI
InChI=1S/C19H15F3N4O3.H2O/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);1H2
InChIKey
FCHGAGZTPICOSW-UHFFFAOYSA-N
SMILES
O=C1C(=CN(C2C=CC(F)=CC=2F)C2=NC(N3CCC(N)C3)=C(F)C=C12)C(=O)O.O
CAS DataBase Reference
107097-79-0(CAS DataBase Reference)
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Tosufloxacin tosilate Usage And Synthesis

Uses

Tosufloxacin (A-61827) tosylate is an orally active fluoroquinolone antibiotic. Tosufloxacin tosylate shows a broad spectrum of antibacterial activity against gram-positive and gram-negative bacteria[1][2].

Definition

ChEBI: Tosufloxacin tosylate hydrate is a racemate comprising equimolar amounts of (R)- and (S)-tosufloxacin tosylate hydrate. It has a role as an antimicrobial agent, an antiinfective agent, a DNA synthesis inhibitor, a hepatotoxic agent and a topoisomerase IV inhibitor. It contains a (S)-tosufloxacin tosylate hydrate, a (R)-tosufloxacin tosylate hydrate and a tosufloxacin tosylate.

brand name

Tosufloxacin Tosilate is JAN.

References

[1] Chu DT, et al. Synthesis and biological properties of A-71497: a prodrug of tosufloxacin. Drugs Exp Clin Res. 1990;16(9):435-43. PMID:2100244
[2] Fujimaki K, et al. In vitro and in vivo antibacterial activities of T-3262, a new fluoroquinolone. Antimicrob Agents Chemother. 1988 Jun;32(6):827-33. DOI:10.1128/AAC.32.6.827

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