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Substance Name: Balofloxacin dihydrate
RN: 151060-21-8
UNII: SH1AVB6TVK
InChIKey: WEGNYJXOCPJAPS-UHFFFAOYSA-N

Note

  • Showed potent bactericidal activity & inhibited the supercoiling activity of DNA gyrase of S. aureus, E. coli, & P aeruginosa.

Molecular Weight

  • 425.4542
 

Classification Codes

  • Anti-Bacterial Agents
  • Anti-Infective Agents
  • Enzyme Inhibitors
  • Topoisomerase II Inhibitors
  • Topoisomerase Inhibitors
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Names and Synonyms

Name of Substance

  • Balofloxacin dihydrate

Synonyms

  • (+/-)-1-Cyclopropyl-6-fluoro-1,4-dihydro-8-methoxy-7-(3-(methylamino)piperidino)-4-oxo-3-quinolinecarboxylic acid, dihydrate
  • 3-Quinolinecarboxylic acid, 1-cyclopropyl-6-fluoro-1,4-dihydro-8-methoxy-7-(3-(methylamino)-1-piperidinyl)-4-oxo-, (+/-), dihydrate
  • 3-Quinolinecarboxylic acid, 1-cyclopropyl-6-fluoro-1,4-dihydro-8-methoxy-7-(3-(methylamino)-1-piperidinyl)-4-oxo-, dihydrate
  • 3-Quinolinecarboxylic acid, 1-cyclopropyl-6-fluoro-1,4-dihydro-8-methoxy-7-(3-(methylamino)-1-piperidinyl)-4-oxo-, dihydrate, (+/-)-
  • Balofloxacin dihydrate
  • Balofloxacin hydrate
  • Balofloxacin hydrate [JAN]
  • UNII-SH1AVB6TVK

Registry Numbers

CAS Registry Number

  • 151060-21-8

FDA UNII

  • SH1AVB6TVK

System Generated Number

  • 0151060218

Structure Descriptors

InChI

InChI=1S/C20H24FN3O4.2H2O/c1-22-11-4-3-7-23(9-11)17-15(21)8-13-16(19(17)28-2)24(12-5-6-12)10-14(18(13)25)20(26)27;;/h8,10-12,22H,3-7,9H2,1-2H3,(H,26,27);2*1H2

InChIKey

WEGNYJXOCPJAPS-UHFFFAOYSA-N

Smiles

O.O.CNC1CCCN(C1)c2c(F)cc3C(=O)C(=CN(C4CC4)c3c2OC)C(=O)O