A topoisomerase IV and DNA gyrase inhibitor
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Trovafloxacin (mesylate)

Item No. 9000303

Technical Information
Formal Name
7-[(1α,5α,6α)-6-amino-3-azabicyclo[3.1.0]hex-3-yl]-1-(2,4-difluorophenyl)-6-fluoro-1,4-dihydro-4-oxo-1,8-naphthyridine-3-carboxylic acid, monomethanesulfonate
CAS Number
147059-75-4
Synonyms
  • CP 99,219
Molecular Formula
C20H15F3N4O3 • CH4SO3
Formula Weight
Purity
≥98%
A crystalline solid
DMSO: 25 mg/mlWater: 20 mg/ml
λmax
269, 342 nm
SMILES
O=C1C(C(O)=O)=CN(C2=CC=C(F)C=C2F)C3=NC(N4C[C@H]([C@]5(N)[H])[C@H]5C4)=C(F)C=C31.CS(=O)(O)=O
InChi Code
InChI=1S/C20H15F3N4O3.CH4O3S/c21-8-1-2-15(13(22)3-8)27-7-12(20(29)30)17(28)9-4-14(23)19(25-18(9)27)26-5-10-11(6-26)16(10)24;1-5(2,3)4/h1-4,7,10-11,16H,5-6,24H2,(H,29,30);1H3,(H,2,3,4)/t10-,11+,16+;
InChi Key
DYNZICQDCVYXFW-AHZSKCOESA-N
Shipping & Storage Information
Storage
-20°C
Shipping
Room temperature in continental US; may vary elsewhere
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    Product Description

    Trovafloxacin is a broad spectrum antibiotic that inhibits the uncoiling of supercoiled DNA in bacteria by blocking the activity of topoisomerase IV (IC50 = 3.02 µg/ml) and DNA gyrase (IC50 = 7.13 µg/ml).1

    WARNING This product is not for human or veterinary use.

    References & Product Citations
    Product Description References

    1. Takei, M., Fukuda, H., Kishii, R., et alTarget preference of 15 quinolones against Staphylococcus aureus, based on antibacterial activities and target inhibition. Antimicrob. Agents Chemother. 45(12), 3544-3547 (2001).