Details
| Stereochemistry | ABSOLUTE |
| Molecular Formula | C19H21FN4O3 |
| Molecular Weight | 372.3934 |
| Optical Activity | UNSPECIFIED |
| Defined Stereocenters | 3 / 3 |
| E/Z Centers | 0 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
C[C@@]12C[C@H](N)[C@@H]1CN(C2)C3=C(F)C=C4C(=O)C(=CN(C5CC5)C4=N3)C(O)=O
InChI
InChIKey=WNVIWAUAXKEKKF-PJFSTRORSA-N
InChI=1S/C19H21FN4O3/c1-19-5-14(21)12(19)7-23(8-19)17-13(20)4-10-15(25)11(18(26)27)6-24(9-2-3-9)16(10)22-17/h4,6,9,12,14H,2-3,5,7-8,21H2,1H3,(H,26,27)/t12-,14-,19-/m0/s1
| Molecular Formula | C19H21FN4O3 |
| Molecular Weight | 372.3934 |
| Charge | 0 |
| Count |
|
| Stereochemistry | ABSOLUTE |
| Additional Stereochemistry | No |
| Defined Stereocenters | 3 / 3 |
| E/Z Centers | 0 |
| Optical Activity | UNSPECIFIED |
Ecenofloxacin (CFC-222), a fluoroquinolone, is a broad-spectrum antibacterial compound acting as a ype II DNA topoisomerase inhibitor. It exerts antibacterial activities against gram-positive, gram-negative, and anaerobic organisms. Ecenofloxacin development as an antibacterial agent has been discontinued.
Approval Year
Sample Use Guides
In Vitro Use Guide
Sources: https://www.ncbi.nlm.nih.gov/pubmed/9333049
Ecenofloxacin (CFC-222) was more active than the other fluoroquinolones tested against gram-positive bacteria. CFC-222 was particularly active against Streptococcus pneumoniae (MIC at which 90% of isolates are inhibited [MIC90], 0.2 microg/ml), Staphylococcus aureus (MIC90, 0.2 microg/ml for ciprofloxacin-susceptible strains), and Enterococcus faecalis (MIC90, 0.39 microg/ml). Against Escherichia coli and other members of the family Enterobacteriaceae, CFC-222 was slightly less active than ciprofloxacin (MIC90s for E. coli, 0.1 and 0.025 microg/ml, respectively).
| Substance Class |
Chemical
Created
by
admin
on
Edited
Mon Mar 31 18:01:29 GMT 2025
by
admin
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Mon Mar 31 18:01:29 GMT 2025
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| Record UNII |
3613ZY362L
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| Record Status |
Validated (UNII)
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NCI_THESAURUS |
C795
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C72661
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178066
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100000080486
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CHEMBL2107637
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3613ZY362L
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DTXSID70167356
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7634
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162301-05-5
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