Compound ID | 869

U-87947

Class: Quinolone

Spectrum of activity: Gram-positive  &  Gram-negative
Details of activity: More active against S. aureus, S. epidermidis, S. faecalis, S. pneumoniae, S. pyogenes, E. coli and B. fragilis than ciprofloxacin
Institute where first reported: Upjohn Company (Pfizer, USA)
Year first mentioned: 1991
Highest developmental phase: Preclinical
Development status: Inactive
Chemical structure(s):
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Molecular weight: 499.53
Iso. SMILES: C[C@H]1CN(C[C@H]1CN)C2=C(C=C3C(=C2F)N(C=C(C3=O)C(=O)O)C45CC(C4)C5)F.CS(=O)(=O)O
InChI Key: WOOTYTHCLUCBAN-BQQVRQSRSA-N
Can. SMILES: C[C@H]1CN(C[C@H]1CN)C2=C(C3=C(C=C2F)C(=O)C(=CN3C45CC(C4)C5)C(=O)O)F.CS(=O)(=O)O
InChI: InChI=1S/C21H23F2N3O3.CH4O3S/c1-10-7-25(8-12(10)6-24)18-15(22)2-13-17(16(18)23)26(21-3-11(4-21)5-21)9-14(19(13)27)20(28)29;1-5(2,3)4/h2,9-12H,3-8,24H2,1H3,(H,28,29);1H3,(H,2,3,4)/t10-,11?,12+,21?;/m0./s1

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