Studies on the Development of Novel Antileprous Chemotherapeutics Using Nude Mice With Special Reference to a New Quinolone Carboxylic Acid, AT-4140
In order to develop a novel drug for antileprosy chemotherapy, the inhibitory effects of three synthesized compounds, a supplied antituberculous one and three quinolone carboxylic acids were examined on the growth of leprosy bacilli inoculated into the footpads of nude mice. Amongst them, a new quin...
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Published in | Japanese journal of leprosy Vol. 58; no. 4; pp. 250 - 258 |
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Main Authors | , |
Format | Journal Article |
Language | Japanese |
Published |
Japanese Leprosy Association
30.12.1989
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Subjects | |
Online Access | Get full text |
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Summary: | In order to develop a novel drug for antileprosy chemotherapy, the inhibitory effects of three synthesized compounds, a supplied antituberculous one and three quinolone carboxylic acids were examined on the growth of leprosy bacilli inoculated into the footpads of nude mice. Amongst them, a new quinolone carboxylic acid, AT-4140 whose chemical strurture was 5-amino-1-cyclopropyl-6, 8-difluoro-1, 4-dihydro-7-( cis-3, 5-dimethyl-1-piperazinyl )-4-oxoquinoline-3-carboxylic acid strongly inhibited the growth of leprosy bacilli at doses of 15 and 30mg/kg. Whereas, the efffct of Ofloxacin used as a positive control was limited at the same doses. |
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ISSN: | 0386-3980 2185-1360 |
DOI: | 10.5025/hansen1977.58.250 |