메뉴 건너뛰기




Volumn 16, Issue 4, 2005, Pages 267-276

Synthesis and anti-rhinovirus properties of fluoro-substituted flavonoids

Author keywords

2 styrylchromones; Anti rhinovirus activity; Flavonoids; X ray crystal structure determination

Indexed keywords

4',6 DICHLOROFLAVAN; 6 FLUORO 3 HYDROXY 2 STYRYLCHROMONE; 6 FLUORO 3 HYDROXYFLAVONE; 6 FLUORO 3 METHOXY 2 STYRYLCHROMONE; 6 FLUORO 3 METHOXYFLAVONE; 6 FLUOROFLAVANONE; 6 FLUOROFLAVONE; 6 FLURO 2 STYRYLCHROMONE; FLAVONE DERIVATIVE; FLAVONOID; UNCLASSIFIED DRUG;

EID: 23744516313     PISSN: 09563202     EISSN: None     Source Type: Journal    
DOI: 10.1177/095632020501600406     Document Type: Article
Times cited : (44)

References (34)
  • 2
    • 0025217342 scopus 로고
    • Two groups of rhinoviruses revealed by a panel of antiviral compounds present sequence divergence and differential pathogenicity
    • Andries K, Dewindt B, Snoeks J, Wouters L, Moereels H, Lewi PJ & Janssen PAJ (1990) Two groups of rhinoviruses revealed by a panel of antiviral compounds present sequence divergence and differential pathogenicity. Journal of Virology 64:1117-1123.
    • (1990) Journal of Virology , vol.64 , pp. 1117-1123
    • Andries, K.1    Dewindt, B.2    Snoeks, J.3    Wouters, L.4    Moereels, H.5    Lewi, P.J.6    Janssen, P.A.J.7
  • 3
    • 0026072328 scopus 로고
    • A comparative test of fifteen compounds against all known rhinovirus serotypes as a basis for a more rational screening program
    • Andries K, Dewindt B, Snoeks J, Willebrords R, Stokbroekx R & Lewi, PJ (1991) A comparative test of fifteen compounds against all known rhinovirus serotypes as a basis for a more rational screening program. Antiviral Research 16:213-225.
    • (1991) Antiviral Research , vol.16 , pp. 213-225
    • Andries, K.1    Dewindt, B.2    Snoeks, J.3    Willebrords, R.4    Stokbroekx, R.5    Lewi, P.J.6
  • 13
    • 0142011520 scopus 로고    scopus 로고
    • Synthesis and evaluation of antirhinovirus activity of 3-hydroxy and 3-methoxy 2-styrylchromones
    • Desideri N, Mastromarino P & Conti C (2003) Synthesis and evaluation of antirhinovirus activity of 3-hydroxy and 3-methoxy 2-styrylchromones. Antiviral Chemistry & Chemotherapy 14:195-203.
    • (2003) Antiviral Chemistry & Chemotherapy , vol.14 , pp. 195-203
    • Desideri, N.1    Mastromarino, P.2    Conti, C.3
  • 16
    • 84903185610 scopus 로고
    • Graph-set analysis of hydrogen-bond patterns in organic crystals
    • Etter MC, MacDonald JC & Bernstein J (1990) Graph-set analysis of hydrogen-bond patterns in organic crystals. Acta Crystallographica B46:256-262.
    • (1990) Acta Crystallographica , vol.B46 , pp. 256-262
    • Etter, M.C.1    MacDonald, J.C.2    Bernstein, J.3
  • 17
    • 33646767009 scopus 로고    scopus 로고
    • ORTEP-3 for windows - A version of ORTEP-III with a graphical user interface (GUI)
    • Farrugia LJ (1997) ORTEP-3 for windows - a version of ORTEP-III with a graphical user interface (GUI). Journal of Applied Crystallography 30:565.
    • (1997) Journal of Applied Crystallography , vol.30 , pp. 565
    • Farrugia, L.J.1
  • 18
    • 0013991984 scopus 로고
    • Enhancement of rhinovirus plaque formation in human heteroploid cell cultures by magnesium and calcium
    • Fiala M & Kenny GE (1966) Enhancement of rhinovirus plaque formation in human heteroploid cell cultures by magnesium and calcium. Journal of Bacteriology 92:1710-1715.
    • (1966) Journal of Bacteriology , vol.92 , pp. 1710-1715
    • Fiala, M.1    Kenny, G.E.2
  • 19
    • 0037429119 scopus 로고    scopus 로고
    • Respiratory consequences of rhinovirus infection
    • Greenberg SB (2003) Respiratory consequences of rhinovirus infection. Archives of Internal Medicine 163:278-284.
    • (2003) Archives of Internal Medicine , vol.163 , pp. 278-284
    • Greenberg, S.B.1
  • 20
    • 0037154405 scopus 로고    scopus 로고
    • Flavonoids - Potent and versatile biologically active compounds interacting with cytochromes P450
    • Hodek P, Trefil P & Stiborova M (2002) Flavonoids - potent and versatile biologically active compounds interacting with cytochromes P450. Chemico-Biological Interactions 139:1-21.
    • (2002) Chemico-Biological Interactions , vol.139 , pp. 1-21
    • Hodek, P.1    Trefil, P.2    Stiborova, M.3
  • 22
  • 25
    • 0034050848 scopus 로고    scopus 로고
    • A convenient synthesis of new (E)-5-hydroxy-2-styrylchromones by modifications of Baker-Venkataraman method
    • Pinto DCGA, Silva AMS & Cavaliero JAS (2000) A convenient synthesis of new (E)-5-hydroxy-2-styrylchromones by modifications of Baker-Venkataraman method. New Journal of Chemistry 24:85-92.
    • (2000) New Journal of Chemistry , vol.24 , pp. 85-92
    • Pinto, D.1    Silva, A.M.S.2    Cavaliero, J.A.S.3
  • 26
    • 0004594966 scopus 로고    scopus 로고
    • The synthesis of 8-allyl-2-styrylchromones by the modified Baker-Venkataraman transformation
    • Reddy BP & Krupadanam GLD (1996) The synthesis of 8-allyl-2-styrylchromones by the modified Baker-Venkataraman transformation. Journal of Heterocyclic Chemistry 33:1561-1565.
    • (1996) Journal of Heterocyclic Chemistry , vol.33 , pp. 1561-1565
    • Reddy, B.P.1    Krupadanam, G.L.D.2
  • 30
    • 3042613589 scopus 로고    scopus 로고
    • Selective human enterovirus and rhinovirus inhibitors: An overview of capsid-binding and protease-inhibiting molecules
    • Shih SR, Chen SJ, Hakimelahi GH, Liu HJ, Tseng CT & Shia KS (2004) Selective human enterovirus and rhinovirus inhibitors: an overview of capsid-binding and protease-inhibiting molecules. Medicinal Research Reviews 24:449-474.
    • (2004) Medicinal Research Reviews , vol.24 , pp. 449-474
    • Shih, S.R.1    Chen, S.J.2    Hakimelahi, G.H.3    Liu, H.J.4    Tseng, C.T.5    Shia, K.S.6
  • 31
    • 0001924269 scopus 로고    scopus 로고
    • Novel (E)- and (Z)-2-styrylchromones from (E,E)-2′- hydroxycinnamylidene-acetophenones - xantones from daylight photooxidative cyclization of (E)-2-styrylchromones
    • Silva AMS, Pinto DCGA, Travares HR, Cavaliero JAS, Jimeno ML & Elguero J (1998) Novel (E)- and (Z)-2-styrylchromones from (E,E)-2′- hydroxycinnamylidene-acetophenones - xantones from daylight photooxidative cyclization of (E)-2-styrylchromones. European Journal of Organic Chemistry 2031-2038.
    • (1998) European Journal of Organic Chemistry , pp. 2031-2038
    • Silva, A.M.S.1    Pinto, D.C.G.A.2    Travares, H.R.3    Cavaliero, J.A.S.4    Jimeno, M.L.5    Elguero, J.6
  • 32
    • 0036282971 scopus 로고    scopus 로고
    • An experimental NMR and semi-empirical theoretical study if the conformation of 2-styrylchromones and styryl alkyl or aryl ketones (benzylidene ketones)
    • Silva AMS, Pinto DCGA, Cavaliero JAS, Martinez A, Castro A & Elguero J (2002) An experimental NMR and semi-empirical theoretical study if the conformation of 2-styrylchromones and styryl alkyl or aryl ketones (benzylidene ketones). Journal of Chemical Research (S) 162-164.
    • (2002) Journal of Chemical Research (S) , pp. 162-164
    • Silva, A.M.S.1    Pinto, D.C.G.A.2    Cavaliero, J.A.S.3    Martinez, A.4    Castro, A.5    Elguero, J.6
  • 34
    • 0021710262 scopus 로고
    • Plant antiviral agents; V. 3-Methoxyflavones as potent inhibitors of viral-induced block of cell synthesis
    • Van Hoof L, Vanden Berghe DA, Hatfield GM & Vlietinck AJ (1984) Plant antiviral agents; V. 3-Methoxyflavones as potent inhibitors of viral-induced block of cell synthesis. Planta Medica 50:513-517.
    • (1984) Planta Medica , vol.50 , pp. 513-517
    • Van Hoof, L.1    Vanden Berghe, D.A.2    Hatfield, G.M.3    Vlietinck, A.J.4


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.