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Volumn 45, Issue 6, 2010, Pages 2214-2222

Design, synthesis and determination of antifungal activity of 5(6)-substituted benzotriazoles

Author keywords

Antifungal activity; Benzotriazole; Docking; Regioisomer; X ray crystallography

Indexed keywords

2 (2,4 DIFLUOROPHENYL) 1 (1H BENZO[D][1,2,3]TRIAZOL 1 YL) 3 (1H 1,2,4 TRIAZOL 1 YL)PROPAN 2 OL; 2 (2,4 DIFLUOROPHENYL) 1 (3H [1,2,3]TRIAZOLO[4,5 B]PYRIDIN 3 YL) 3 (1H 1,2,4 TRIAZOL 1 YL)PROPAN 2 OL; 2 (2,4 DIFLUOROPHENYL) 1 (5 CHLORO 1H BENZO[D][1,2,3]TRIAZOL 1 YL) 3 (1H 1,2,4 TRIAZOL 1 YL)PROPAN 2 OL; 2 (2,4 DIFLUOROPHENYL) 1 (5 FLUORO 1H BENZO[D][1,2,3]TRIAZOL 1 YL) 3 (1H 1,2,4 TRIAZOL 1 YL)PROPAN 2 OL; 2 (2,4 DIFLUOROPHENYL) 1 (5 METHOXY 1H BENZO[D][1,2,3]TRIAZOL 1 YL) 3 (1H 1,2,4 TRIAZOL 1 YL)PROPAN 2 OL; 2 (2,4 DIFLUOROPHENYL) 1 (5 METHYL 1H BENZO[D][1,2,3]TRIAZOL 1 YL) 3 (1H 1,2,4 TRIAZOL 1 YL)PROPAN 2 OL; 2 (2,4 DIFLUOROPHENYL) 1 (5 NITRO 1H BENZO[D][1,2,3]TRIAZOL 1 YL) 3 (1H 1,2,4 TRIAZOL 1 YL)PROPAN 2 OL; 2 (2,4 DIFLUOROPHENYL) 1 (5,6 DIMETHYL 1H BENZO[D][1,2,3] TRIAZOL 1 YL) 3 (1H 1,2,4 TRIAZOL 1 YL)PROPAN 2 OL; 2 (2,4 DIFLUOROPHENYL) 1 (5,6 DIMETHYL 2H BENZO[D][1,2,3] TRIAZOL 2 YL) 3 (1H 1,2,4 TRIAZOL 1 YL)PROPAN 2 OL; 2 (2,4 DIFLUOROPHENYL) 1 (6 CHLORO 1H BENZO[D][1,2,3]TRIAZOL 1 YL) 3 (1H 1,2,4 TRIAZOL 1 YL)PROPAN 2 OL; 2 (2,4 DIFLUOROPHENYL) 1 (6 FLUORO 1H BENZO[D][1,2,3]TRIAZOL 1 YL) 3 (1H 1,2,4 TRIAZOL 1 YL)PROPAN 2 OL; 2 (2,4 DIFLUOROPHENYL) 1 (6 METHYL 1H BENZO[D][1,2,3]TRIAZOL 1 YL) 3 (1H 1,2,4 TRIAZOL 1 YL)PROPAN 2 OL; 2 (2,4 DIFLUOROPHENYL) 1 (6 NITRO 1H BENZO[D][1,2,3]TRIAZOL 1 YL) 3 (1H 1,2,4-TRIAZOL 1 YL)PROPAN 2 OL; ANTIFUNGAL AGENT; BENZOTRIAZOLE DERIVATIVE; UNCLASSIFIED DRUG;

EID: 77950861936     PISSN: 02235234     EISSN: 17683254     Source Type: Journal    
DOI: 10.1016/j.ejmech.2010.01.062     Document Type: Article
Times cited : (23)

References (35)
  • 27
    • 77950862912 scopus 로고    scopus 로고
    • Crystal structures were determined using X-ray data collected at 90K, for 3c using MoKα radiation (λ = 0.71073 Å), on a Nonius KappaCCD diffractometer and for 3c′ using Cu Kα radiation (λ = 1.54178 Å) on a Bruker Kappa Apex-II diffractometer. The CIFs have been deposited at the Cambridge Crystallographic Data Centre, CCDC711857 and 711858.
    • Crystal structures were determined using X-ray data collected at 90K, for 3c using MoKα radiation (λ = 0.71073 Å), on a Nonius KappaCCD diffractometer and for 3c′ using Cu Kα radiation (λ = 1.54178 Å) on a Bruker Kappa Apex-II diffractometer. The CIFs have been deposited at the Cambridge Crystallographic Data Centre, CCDC711857 and 711858.
  • 28
    • 70350566491 scopus 로고    scopus 로고
    • Susceptibility Test methods: Yeasts and Filamentous Fungi
    • Murray P.R., Baron E.J., Jorgensen J.H., Pfaller M.A., and Yolken R.H. (Eds), ASM Press, Washington, D.C.
    • Espinell-Ingroff A.V., and Pfaller M.A. Susceptibility Test methods: Yeasts and Filamentous Fungi. In: Murray P.R., Baron E.J., Jorgensen J.H., Pfaller M.A., and Yolken R.H. (Eds). Manual of Clinical Microbiology. eighth ed. vol. 2 (2005), ASM Press, Washington, D.C. 1880-1893
    • (2005) Manual of Clinical Microbiology. eighth ed. , vol.2 , pp. 1880-1893
    • Espinell-Ingroff, A.V.1    Pfaller, M.A.2


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.