Compound ID | 561

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Y-688

Class: Fluoroquinolone

Spectrum of activity: Gram-positive  &  Gram-negative
Details of activity: Against Gram positves resistant to quinolones (including MRSA and S. epidermidis), Y-688 is more active than ofloxacin, ciprofloxacin, tosufloxacin and sparfloxacin
Description: Yokoyama Y, Morimoto M, Iwao E, et al. Y-688, a new fluoroquinolone with high activity against quinolone resistant Gram positive bacteria. 35th-Intersci-Conf-Antimicrobial-Agents-Chemother 1995; 146
Institute where first reported: Yoshitomi Pharmaceuticals (Mitsubishi Pharma Corp., Japan)
Year first mentioned: 1995
Highest developmental phase: Preclinical
Development status: Inactive
Chemical structure(s):
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Molecular weight: 407.41
Iso. SMILES: COC1=C2C(=CC(=C1N3CC[C@@](C3)(CN)CF)F)C(=O)C(=CN2C4CC4)C(=O)O
InChI Key: AGRJUZPPATWGHI-FQEVSTJZSA-N
Can. SMILES: COC1=C(C(=CC2=C1N(C=C(C2=O)C(=O)O)C3CC3)F)N4CC[C@](CF)(CN)C4
InChI: InChI=1S/C20H23F2N3O4/c1-29-18-15-12(17(26)13(19(27)28)7-25(15)11-2-3-11)6-14(22)16(18)24-5-4-20(8-21,9-23)10-24/h6-7,11H,2-5,8-10,23H2,1H3,(H,27,28)/t20-/m0/s1
External links:
PubChem link: https://pubchem.ncbi.nlm.nih.gov/compound/9887640
Citations:
  • https://www.ncbi.nlm.nih.gov/pmc/articles/PMC105705/#B26
  • https://journals.asm.org/doi/10.1128/aac.42.8.1889

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