Switch to
| Predicate | Object |
|---|---|
| rdf:type | |
| lifeskim:mentions | |
| pubmed:issue |
4
|
| pubmed:dateCreated |
1992-4-3
|
| pubmed:abstractText |
A series of novel 6-fluoro-7-diazabicycloalkylquinolonecarboxylic acids substituted with various C8 (H, F, Cl, N) and N1 (ethyl, cyclopropyl, vinyl, 2-fluoroethyl, 4-fluorophenyl, 2,4-difluorophenyl) substituents, as well as, 9-fluoro-10-diazabicycloalkylpyridobenzoxazinecarboxylic acids, were prepared and evaluated for antibacterial activity against a range of important veterinary pathogenic bacteria. The diazabicycloalkyl side chains investigated at the 7-position (benzoxazine 10-position) include (1S,4S)-5-methyl-2,5-diazabicyclo[2.2.1]heptane (2), (1S,4S)-2,5-diazabicyclo[2.2.1]heptane (3), (1R,4R)-5-methyl-2,5-diazabicyclo[2.2.1]heptane (4), 8-methyl-3,8-diazabicyclo[3.2.1]octane (5), 9-methyl-3,9-diazabicyclo[4.2.1]nonane (6), 1,4-diazabicyclo[3.2.2]nonane (7), 1,4-diazabicyclo[3.3.1]nonane (8), and 9-methyl-3,9-diazabicyclo[3.3.1]nonane (9). Among these side chains, in vitro potency was not highly variable; other properties therefore proved more critical to the selection of possible development candidates. However, the relative potencies observed for several of these compounds in mouse, swine, and cattle infection models correlated well with those seen in vitro. A combination of the N1 cyclopropyl group and the C7 (1S,4S)-5-methyl-2,5-diazabicyclo[2.2.1]hept-2-yl appendage conferred the best overall antibacterial, physiochemical, and pharmacodynamic properties. Hence, danofloxacin (Advocin, 2c) (originally CP-76,136, 1-cyclopropyl-6-fluoro-7-[(1S,4S)-5-methyl-2,5-diazabicyclo[2.2.1] hept-2-yl]-1,4-dihydro-4-oxo-3-quinolinecarboxylic acid) was selected as a candidate for development as a therapeutic antibacterial agent for veterinary medicine.
|
| pubmed:language |
eng
|
| pubmed:journal | |
| pubmed:citationSubset |
IM
|
| pubmed:chemical | |
| pubmed:status |
MEDLINE
|
| pubmed:month |
Feb
|
| pubmed:issn |
0022-2623
|
| pubmed:author | |
| pubmed:issnType |
Print
|
| pubmed:day |
21
|
| pubmed:volume |
35
|
| pubmed:owner |
NLM
|
| pubmed:authorsComplete |
N
|
| pubmed:pagination |
611-20
|
| pubmed:dateRevised |
2004-11-17
|
| pubmed:meshHeading |
pubmed-meshheading:1311762-Actinobacillus Infections,
pubmed-meshheading:1311762-Actinobacillus pleuropneumoniae,
pubmed-meshheading:1311762-Aerobiosis,
pubmed-meshheading:1311762-Anaerobiosis,
pubmed-meshheading:1311762-Animals,
pubmed-meshheading:1311762-Anti-Infective Agents,
pubmed-meshheading:1311762-Bacterial Infections,
pubmed-meshheading:1311762-Cattle,
pubmed-meshheading:1311762-Cattle Diseases,
pubmed-meshheading:1311762-Female,
pubmed-meshheading:1311762-Fluoroquinolones,
pubmed-meshheading:1311762-Gram-Negative Bacteria,
pubmed-meshheading:1311762-Gram-Positive Bacteria,
pubmed-meshheading:1311762-Mice,
pubmed-meshheading:1311762-Molecular Structure,
pubmed-meshheading:1311762-Pasteurella Infections,
pubmed-meshheading:1311762-Quinolones,
pubmed-meshheading:1311762-Structure-Activity Relationship,
pubmed-meshheading:1311762-Swine,
pubmed-meshheading:1311762-Swine Diseases
|
| pubmed:year |
1992
|
| pubmed:articleTitle |
Synthesis and structure-activity relationships of 7-diazabicycloalkylquinolones, including danofloxacin, a new quinolone antibacterial agent for veterinary medicine.
|
| pubmed:affiliation |
Central Research Division, Pfizer Inc., Groton, Connecticut 06340.
|
| pubmed:publicationType |
Journal Article
|