메뉴 건너뛰기




Volumn 10, Issue 8, 2000, Pages 839-841

Synthesis and antifungal activity of a ferrocene-fluconazole analogue

Author keywords

[No Author keywords available]

Indexed keywords

FERROCENE DERIVATIVE; FERROCENE FLUCONAZOLE; UNCLASSIFIED DRUG;

EID: 0342313480     PISSN: 0960894X     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0960-894X(00)00120-7     Document Type: Article
Times cited : (136)

References (23)
  • 3
    • 33646952828 scopus 로고    scopus 로고
    • For a review about metal complexes for therapy and diagnosis of drug resistance, see:
    • For a review about metal complexes for therapy and diagnosis of drug resistance, see: Sharma, V.; Piwnica-Worms, D. Chem. Rev. 1999, 99, 2545.
    • (1999) Chem. Rev. , vol.99 , pp. 2545
    • Sharma, V.1    Piwnica-Worms, D.2
  • 7
    • 0001115199 scopus 로고    scopus 로고
    • Brevet International PCT/FR 96/00721, 1996
    • Brocard, J.; Lebibi, J.; Maciejewski, L. Brevet International PCT/FR 96/00721, 1996; Chem. Abs. 1997, 126, 60137E.
    • (1997) Chem. Abs. , vol.126
    • Brocard, J.1    Lebibi, J.2    MacIejewski, L.3
  • 10
    • 0032895608 scopus 로고    scopus 로고
    • For a review about the azoles as antifungal agents, see:
    • For a review about the azoles as antifungal agents, see: Terrell, C. L. Maya Clin. Proc. 1999, 74, 78.
    • (1999) Maya Clin. Proc. , vol.74 , pp. 78
    • Terrell, C.L.1
  • 18
    • 0342924572 scopus 로고    scopus 로고
    • U.S. Patent 4,404,216, 1983.
    • Richardson, K. U.S. Patent 4,404,216, 1983.
    • Richardson, K.1
  • 19
    • 0342924569 scopus 로고    scopus 로고
    • Note
    • 6OFe:C, 59.97; H, 4.76; N, 22.22; found:C, 60.01; H, 4.93; N, 22.51.
  • 20
    • 0342924570 scopus 로고    scopus 로고
    • Note
    • 3OClFe: C, 52.10; H, 4.63; N, 12.16; found: C, 52.32; H, 4.44; N, 12.30.
  • 22
    • 0025949720 scopus 로고
    • The antifungal activity was determined by liquid-phase turbidimetry using Titertek Multiskan apparatus operating at 620 nm.
    • The antifungal activity was determined by liquid-phase turbidimetry using Titertek Multiskan apparatus operating at 620 nm. Dei Cas, E.; Duardin, L.; Ribeiro Pinto, M. E.; Ajana, F.; Fruit, J.; Poulain, D.; Camus, D.; Vernes, A. Mycoses 1991, 34, 167.
    • (1991) Mycoses , vol.34 , pp. 167
    • Dei Cas, E.1    Duardin, L.2    Ribeiro Pinto, M.E.3    Ajana, F.4    Fruit, J.5    Poulain, D.6    Camus, D.7    Vernes, A.8
  • 23
    • 0342924564 scopus 로고    scopus 로고
    • Ten Candida isolates were used in this study according to their MIC, which was defined as the FCZ concentration leading to 80% growth inhibition. Three C. albicans strains (MIC <1.5 μg/mL), two C. glabrata strains (MIC >48 μg/mL), two C. parapsilosis strains (MIC <12 μg/mL) and three C. krusei strains (MIC >48 μg/mL).
    • Ten Candida isolates were used in this study according to their MIC, which was defined as the FCZ concentration leading to 80% growth inhibition. Three C. albicans strains (MIC <1.5 μg/mL), two C. glabrata strains (MIC >48 μg/mL), two C. parapsilosis strains (MIC <12 μg/mL) and three C. krusei strains (MIC >48 μg/mL).


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.