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Volumn 19, Issue 17, 2009, Pages 4933-4936

Synthesis and antibacterial activity of 7-(1,2,3,4-tetrahydropyrrolo[1,2-a]pyrazin-7-yl) quinolones

Author keywords

Antibacterial agent; Quinolone

Indexed keywords

7 (1,2,3,4 TETRAHYDROPYRROLO[1,2 A]PYRAZIN 7 YL)QUINOLONE DERIVATIVE; QUINOLONE DERIVATIVE; UNCLASSIFIED DRUG;

EID: 68349155541     PISSN: 0960894X     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.bmcl.2009.07.087     Document Type: Article
Times cited : (23)

References (21)
  • 2
    • 0033926264 scopus 로고    scopus 로고
    • For some recent reviews, see:
    • For some recent reviews, see:. Ball P. J. Antimicrob. Chemother. 46 (2000) 17
    • (2000) J. Antimicrob. Chemother. , vol.46 , pp. 17
    • Ball, P.1
  • 20
    • 68349150006 scopus 로고    scopus 로고
    • note
    • The minimum inhibitory concentrations (MICs) were determined by the broth microdilution method according to Clinical and Laboratory Standards Institute (CLSI, formerly NCCLS) guidelines. Methods for Dilution Antimicrobial Susceptibility Tests for Bacteria that Grow Aerobically, 5th ed.; Approved standard: NCCLS Document M7-A5, 2000.
  • 21
    • 68349136332 scopus 로고    scopus 로고
    • note
    • The in vivo efficacies of compound 1e and ciprofloxacin were tested in female Swiss-Webster mice infected ip with Staphylococcus aureus subsp. aureus ATCC13709. Mice were dosed subcutaneously and orally with test compound at 1 h following infection. Mortality was observed over a period of three days. A group of infected mice not treated with drug served as controls.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.