Structure and anti-M.leprae activity relationships of new quinolones

  • GIDOH Masaichi
    Department of Bioregulation, Leprosy Research Center, National Institute of Infectious Diseases

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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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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.

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