CAS No. 112811-59-3

Batch: Purity:99.62
Gatifloxacin Chemical Structure
Chemical Structure
Check the Gatifloxacin product page for in-depth specifications, including solubility, stock solutions, MOA, and working concentrations.

Chemical Information

IUPAC Name 1-cyclopropyl-6-fluoro-8-methoxy-7-(3-methylpiperazin-1-yl)-4-oxoquinoline-3-carboxylic acid
CAS Number 112811-59-3
Molecular Formula

C19H22FN3O4

Molecular Weight (MW) 375.39
SMILES CC1CN(CCN1)C2=C(C=C3C(=C2OC)N(C=C(C3=O)C(=O)O)C4CC4)F
InChIKey XUBOMFCQGDBHNK-UHFFFAOYSA-N

Ordering Information

Biological Activity

Gatifloxacin is a synthetic broad-spectrum antibiotic belonging to the fourth-generation fluoroquinolone class that targets bacterial DNA gyrase and topoisomerase IV. By inhibiting these essential type II topoisomerases, gatifloxacin blocks bacterial DNA replication, transcription, and repair processes. This target inhibition leads to double-strand DNA breaks and ultimately induces rapid bactericidal cell death across both Gram-positive and Gram-negative bacterial strains.

How to Prepare Stock Solution?

Concentration Volume Mass
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Solubility

Batch:
All in vitro solubility values are batch-tested experimental data (non-literature values).
Solvent Solubility & Note
DMSO 7 mg/mL (18.64 mM)
(Moisture-contaminated DMSO may reduce solubility. Use fresh, anhydrous DMSO. The recommended stock concentration is 10 mM in DMSO.)
Water Insoluble
Ethanol Insoluble
FAQ
Q: Why does a DMSO stock precipitate in media/saline?
A: It is caused by unheated aqueous media (supersaturation), local solvent shock, or incorrect mixing sequence.
How to fix it?
  • Preheat media/saline to 37°C.
  • Mix rapidly (pipette/vortex) upon addition.
  • For complex mixes, always add the aqueous phase last.
  • Re-dissolve minor precipitates with a 37°C water bath and sonication (≤30 min).

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Note: Technical data last updated: Sep 1, 2026.