Compound ID | 506

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E-3846

Class: Fluoroquinolone

Spectrum of activity: Gram-negative
Details of activity: Has higher Gram positive activity than ciprofloxacin, ofloxacin, enoxacin, pefloxacin, norfloxacin, and nalidixic acid, and has similar Gram negative activity as ofloxacin and pefloxacin.
Institute where first reported: Esteve, Spain
Year first mentioned: 1989
Highest developmental phase: Preclinical
Development status: Inactive
Chemical structure(s):
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Molecular weight: 312.3
Iso. SMILES: C1CC1N2C=C(C(=O)C3=CC(=C(C=C32)N4C=CC=C4)F)C(=O)O
InChI Key: ISJRMOARTUIEPA-UHFFFAOYSA-N
Can. SMILES: C1=CN(C=C1)C2=CC3=C(C=C2F)C(=O)C(=CN3C4CC4)C(=O)O
InChI: InChI=1S/C17H13FN2O3/c18-13-7-11-14(8-15(13)19-5-1-2-6-19)20(10-3-4-10)9-12(16(11)21)17(22)23/h1-2,5-10H,3-4H2,(H,22,23)
External links:
PubChem link: https://pubchem.ncbi.nlm.nih.gov/compound/129466
Citation: http://aac.asm.org/content/34/6/1262.full.pdf

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