Structure and anti-M.leprae activity relationships of new quinolones
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- GIDOH Masaichi
- Department of Bioregulation, Leprosy Research Center, National Institute of Infectious Diseases
Bibliographic Information
- Other Title
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- ニューキノロン系抗菌薬の構造式と抗らい菌活性の相関
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Description
Due to the emergence of drug resistant M.leprae , there is a need to look for new drugs for the treatment of leprosy. We evaluated the effectiveness of new quinolones in vitro as well as in vivo. The in vitro and in vivo results suggested that a cyclopropyl group at the 1-position, COOH at the 3-position, OH at the 4-position, NH2 or OH-substitutions at the 5-position, F at the 6-position, 5- and 6-membered rings at the 7-position, halogen (F or Cl) or OCH3 at the 8-position of the quinolone core structure, remarkably enhance ant-M.leprae activities of the drug.
Journal
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- JAPANESE JOURNAL OF LEPROSY
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JAPANESE JOURNAL OF LEPROSY 78 (1), 17-23, 2009
Japanese Leprosy Association
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Keywords
Details 詳細情報について
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- CRID
- 1390282681298654080
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- NII Article ID
- 10024786430
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- NII Book ID
- AN10559906
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- COI
- 1:STN:280:DC%2BD1M7lsV2msw%3D%3D
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- ISSN
- 1884314X
- 13423681
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- PubMed
- 19227145
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- Text Lang
- ja
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- Data Source
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- JaLC
- Crossref
- CiNii Articles
- OpenAIRE
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- Abstract License Flag
- Disallowed