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Volumn 17, Issue 19, 2009, Pages 6879-6889

Design, synthesis and biological evaluations of novel 7-[3-(1-aminocycloalkyl)pyrrolidin-1-yl]-6-desfluoro-8-methoxyquinolones with potent antibacterial activity against multi-drug resistant Gram-positive bacteria

Author keywords

6 Desfluoro quinolones; Antibacterial agents; Gram positive bacteria; Type II topoisomerases

Indexed keywords

1 (2 FLUOROCYCLOPROPAN 1 YL) 1,4 DIHYDRO 8 METHOXY 7 [3 (1 METHYLAMINOCYCLOPROPAN 1 YL)PYRROLIDIN 1 YL] 4 OXOQUINOLIN 3 CARBOXYLIC ACID; 6 FLUORO 1 (2 FLUOROCYCLOPROPAN 1 YL) 1,4 DIHYDRO 8 METHOXY 7 [3 (1 METHYLAMINOCYCLOPROPAN 1 YL)PYRROLIDIN 1 YL] 4 OXOQUINOLIN 3 CARBOXYLIC ACID; 7 [3 (1 AMINOCYCLOBUTAN 1 YL)PYRROLIDIN 1 YL] 1 (2 FLUOROCYCLOPROPAN 1 YL) 1,4 DIHYDRO 8 METHOXY 4 OXOQUINOLIN 3 CARBOXYLIC ACID; 7 [3 (1 AMINOCYCLOBUTAN 1 YL)PYRROLIDIN 1 YL] 6 FLUORO 1 (2 FLUOROCYCLOPROPAN 1 YL) 1,4 DIHYDRO 8 METHOXY 4 OXOQUINOLIN 3 CARBOXYLIC ACID; 7 [3 (1 AMINOCYCLOPROPYL) 1 PYRROLIDINYL] 1 (2 FLUOROCYCLOPROPYL) 1,4 DIHYDRO 8 METHOXY 4 OXO 3 QUINOLINECARBOXYLIC ACID; 7[3 (1 AMINOCYCLOPROPAN 1 YL)PYRROLIDIN 1 YL] 6 FLUORO 1 (2 FLUOROCYCLOPROPAN 1 YL) 1,4 DIHYDRO 8 METHOXY 4 OXOQUINOLIN 3 CARBOXYLIC ACID; CIPROFLOXACIN; DALFOPRISTIN PLUS QUINUPRISTIN; DNA TOPOISOMERASE (ATP HYDROLYSING) A; DNA TOPOISOMERASE (ATP HYDROLYSING) B; GARENOXACIN; GATIFLOXACIN; HABEKACIN; LINEZOLID; MOXIFLOXACIN; QUINOLINE DERIVED ANTIINFECTIVE AGENT; TEICOPLANIN; TROVAFLOXACIN; UNCLASSIFIED DRUG; VANCOMYCIN;

EID: 69949131276     PISSN: 09680896     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.bmc.2009.08.026     Document Type: Article
Times cited : (15)

References (45)
  • 33
    • 69949163597 scopus 로고    scopus 로고
    • The C-7 substituent moiety of compound 3 or 6 was prepared by our reported method. (Takemura, M.; Kimura, Y.; Kawakami, K.; Kimura, K.; Ohki, H.; Matsuhashi, N.; Kawato, H. PCT Int. WO9623782, 1996.) The quinolone derivatives having this isomer (isomer 11) of the C-7 substituent have been become clear that the compounds are higher activity the corresponding quinolones bearing an enantiomer of 11.
    • The C-7 substituent moiety of compound 3 or 6 was prepared by our reported method. (Takemura, M.; Kimura, Y.; Kawakami, K.; Kimura, K.; Ohki, H.; Matsuhashi, N.; Kawato, H. PCT Int. WO9623782, 1996.) The quinolone derivatives having this isomer (isomer 11) of the C-7 substituent have been become clear that the compounds are higher activity the corresponding quinolones bearing an enantiomer of 11.
  • 35
    • 69949118355 scopus 로고    scopus 로고
    • Ledoussal, B.; Almstead, J. K.; Gray, J. L.; Hu, X. E. PCT Int. WO9914214, 1999.
    • Ledoussal, B.; Almstead, J. K.; Gray, J. L.; Hu, X. E. PCT Int. WO9914214, 1999.
  • 36
    • 69949159656 scopus 로고    scopus 로고
    • The racemate of compound 9 was reported by Chu, D. T. (Chu, D. T.; Li, Q.; Cooper, C. S.; Fung, A. K. L.; Lee, C. M.; Plattner, J. J.; Ma, Z.; Wang, W.-B. PCT Int. WO9639407, 1996.).
    • The racemate of compound 9 was reported by Chu, D. T. (Chu, D. T.; Li, Q.; Cooper, C. S.; Fung, A. K. L.; Lee, C. M.; Plattner, J. J.; Ma, Z.; Wang, W.-B. PCT Int. WO9639407, 1996.).
  • 38
    • 0037435067 scopus 로고    scopus 로고
    • Compounds 21-24 were reported in our previous paper. (Inagaki, H.; Miyauchi, S.; Miyauchi, R.; Kawato, H.; Ohki, H.; Matsuhashi, N.; Kawakami, K.; Takahashi, H.; Takemura, M. J. Med. Chem. 2003, 46, 1005.).
    • Compounds 21-24 were reported in our previous paper. (Inagaki, H.; Miyauchi, S.; Miyauchi, R.; Kawato, H.; Ohki, H.; Matsuhashi, N.; Kawakami, K.; Takahashi, H.; Takemura, M. J. Med. Chem. 2003, 46, 1005.).
  • 40
    • 69949150933 scopus 로고    scopus 로고
    • Compound 7 (PEG9215875) was also reported in our previous patent, Hayakawa, I, Kimura, Y. Jpn. Kokai Tokkyo Koho JP03072476, 1991
    • Compound 7 (PEG9215875) was also reported in our previous patent. (Hayakawa, I.; Kimura, Y. Jpn. Kokai Tokkyo Koho JP03072476, 1991.).


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.