10a-AZALIDE COMPOUND

[PROBLEMS] To provide a compound which has a novel structure and is effective against an influenza bacterium and an erythromycin-resistant bacterium (e.g., an erythromycin-resistant pneumococcal or streptococcal bacterium), as well as a conventional erythromycin-sensitive bacterium. [MEANS FOR SOLVI...

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Main Authors KANEMOTO, KENICHI, SASAMOTO, NAOKI, MANAKA, AKIRA, KUBOTA, DAI, OGITA, HARUHISA, KASHIMURA, MASATO, OZAWA, TOMOHIRO, KAWAMURA, MADOKA, KUROSAKA, JUN, SUGIMOTO, TOMOHIRO, YAMAMOTO, KANAKO, CHIKAUCHI, KEN, MIURA, TOMOAKI, SHITARA, EIKI
Format Patent
LanguageEnglish
French
Japanese
Published 16.08.2007
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Abstract [PROBLEMS] To provide a compound which has a novel structure and is effective against an influenza bacterium and an erythromycin-resistant bacterium (e.g., an erythromycin-resistant pneumococcal or streptococcal bacterium), as well as a conventional erythromycin-sensitive bacterium. [MEANS FOR SOLVING PROBLEMS] Disclosed is a novel 10a-azalide compound represented by the formula (I), a pharmaceutically acceptable salt or solvate thereof, or an intermediate for the production of the compound or the salt or solvate. The compound has an excellent bactericidal activity against an influenza bacterium, an erythromycin-resistant pneumococcal bacterium and the like, and therefore can be used as a therapeutic agent for an infectious disease. L'invention concerne un composé qui a une nouvelle structure et qui est efficace contre une bactérie influenza et une bactérie résistante à l'érythromycine (par exemple une bactérie pneumococcique ou streptococcique résistante à l'érythromycine) ainsi que contre une bactérie sensible à l'érythromycine classique. L'invention concerne un nouveau composé 10a-azalide représenté par la formule (I), un sel ou solvate acceptable du point de vue pharmaceutique de celui-ci ou un intermédiaire pour la production du composé ou du sel ou solvate. Le composé a une excellente activité bactéricide contre une bactérie influenza, une bactérie pneumococcique résistante à l'érythromycine et similaire et il peut par conséquent être utilisé en tant qu'agent thérapeutique pour une maladie infectieuse.
AbstractList [PROBLEMS] To provide a compound which has a novel structure and is effective against an influenza bacterium and an erythromycin-resistant bacterium (e.g., an erythromycin-resistant pneumococcal or streptococcal bacterium), as well as a conventional erythromycin-sensitive bacterium. [MEANS FOR SOLVING PROBLEMS] Disclosed is a novel 10a-azalide compound represented by the formula (I), a pharmaceutically acceptable salt or solvate thereof, or an intermediate for the production of the compound or the salt or solvate. The compound has an excellent bactericidal activity against an influenza bacterium, an erythromycin-resistant pneumococcal bacterium and the like, and therefore can be used as a therapeutic agent for an infectious disease. L'invention concerne un composé qui a une nouvelle structure et qui est efficace contre une bactérie influenza et une bactérie résistante à l'érythromycine (par exemple une bactérie pneumococcique ou streptococcique résistante à l'érythromycine) ainsi que contre une bactérie sensible à l'érythromycine classique. L'invention concerne un nouveau composé 10a-azalide représenté par la formule (I), un sel ou solvate acceptable du point de vue pharmaceutique de celui-ci ou un intermédiaire pour la production du composé ou du sel ou solvate. Le composé a une excellente activité bactéricide contre une bactérie influenza, une bactérie pneumococcique résistante à l'érythromycine et similaire et il peut par conséquent être utilisé en tant qu'agent thérapeutique pour une maladie infectieuse.
Author KUBOTA, DAI
KUROSAKA, JUN
SUGIMOTO, TOMOHIRO
MANAKA, AKIRA
SASAMOTO, NAOKI
SHITARA, EIKI
KASHIMURA, MASATO
KAWAMURA, MADOKA
OZAWA, TOMOHIRO
YAMAMOTO, KANAKO
KANEMOTO, KENICHI
OGITA, HARUHISA
MIURA, TOMOAKI
CHIKAUCHI, KEN
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– fullname: KASHIMURA, MASATO
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– fullname: KAWAMURA, MADOKA
– fullname: KUROSAKA, JUN
– fullname: SUGIMOTO, TOMOHIRO
– fullname: YAMAMOTO, KANAKO
– fullname: CHIKAUCHI, KEN
– fullname: MIURA, TOMOAKI
– fullname: SHITARA, EIKI
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TAISHO PHARMACEUTICAL CO., LTD
KUROSAKA, JUN
MEIJI SEIKA KAISHA, LTD
SUGIMOTO, TOMOHIRO
MANAKA, AKIRA
SASAMOTO, NAOKI
SHITARA, EIKI
KASHIMURA, MASATO
KAWAMURA, MADOKA
OZAWA, TOMOHIRO
YAMAMOTO, KANAKO
KANEMOTO, KENICHI
OGITA, HARUHISA
MIURA, TOMOAKI
CHIKAUCHI, KEN
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Snippet [PROBLEMS] To provide a compound which has a novel structure and is effective against an influenza bacterium and an erythromycin-resistant bacterium (e.g., an...
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SubjectTerms CHEMISTRY
DERIVATIVES THEREOF
HUMAN NECESSITIES
HYGIENE
MEDICAL OR VETERINARY SCIENCE
METALLURGY
NUCLEIC ACIDS
NUCLEOSIDES
NUCLEOTIDES
ORGANIC CHEMISTRY
PREPARATIONS FOR MEDICAL, DENTAL, OR TOILET PURPOSES
SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS ORMEDICINAL PREPARATIONS
SUGARS
Title 10a-AZALIDE COMPOUND
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