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Volumn 25, Issue 1, 2017, Pages 327-337

Discovery of novel multi-target indole-based derivatives as potent and selective inhibitors of chikungunya virus replication

Author keywords

Arbidol; Chikungunya; Replication; Virus

Indexed keywords

ARBIDOL; INDOLE DERIVATIVE; TERT BUTYL 2 [(2,6 DICHLOROPHENYLSULFINYL)METHYL] 4 [(DIMETHYLAMINO)METHYL] 5 HYDROXY 1 METHYL 1H INDOLE 3 CARBOXYLATE; TERT BUTYL 2 [(2,6 DICHLOROPHENYLTHIO)METHYL] 6 BROMO 4 [(DIMETHYLAMINO)METHYL] 5 HYDROXY 1 METHYL 1H INDOLE 3 CARBOXYLATE; TERT BUTYL 2 [[2 (TRIFLUOROMETHYL)PHENYLSULFINYL]METHYL] 4 [(DIMETHYLAMINO)METHYL] 5 HYDROXY 1 METHYL 1H INDOLE 3 CARBOXYLATE; TERT BUTYL 2 [[2 (TRIFLUOROMETHYL)PHENYLSULFINYL]METHYL] 6 BROMO 4 [(DIMETHYLAMINO)METHYL] 5 HYDROXY 1 METHYL 1H INDOLE 3 CARBOXYLATE; TERT BUTYL 5 HYDROXY 1 METHYL 2 [(2 TRIFLUOROMETHYLPHENYLTHIO)METHYL]INDOLE 3 CARBOXYLATE; TERT BUTYL 5 HYDROXY 1 METHYL 2 [(2 TRIFLUOROMETHYLSULFYNYL)METHYL]INDOLE 3 CARBOXYLATE; TERT BUTYL 5 HYDROXY 1 METHYL 2 [(2,6 DICHLOROPHENYLSULFYNYL)METHYL]INDOLE 3 CARBOXYLATE; TERT BUTYL 5 HYDROXY 1 METHYL 2 [(2,6 DICHLOROPHENYLTHIO)METHYL]INDOLE 3 CARBOXYLATE; TERT BUTYL 5 HYDROXY 1 METHYL 2 [(4 CHLOROPHENYLSULFYNYL)METHYL]INDOLE 3 CARBOXYLATE; TERT BUTYL 5 HYDROXY 1 METHYL 2 [(4 CHLOROPHENYLTHIO)METHYL]INDOLE 3 CARBOXYLATE; TERT BUTYL 5 HYDROXY 1 METHYL 2 [(4 FLUOROPHENYLSULFYNYL)METHYL]INDOLE 3 CARBOXYLATE; TERT BUTYL 5 HYDROXY 1 METHYL 2 [(4 FLUOROPHENYLTHIO)METHYL]INDOLE 3 CARBOXYLATE; TERT BUTYL 5 HYDROXY 1 METHYL 2 [(4 TRIFLUOROMETHYLPHENYLTHIO)METHYL]INDOLE 3 CARBOXYLATE; TERT BUTYL 5 HYDROXY 1 METHYL 2 [(4 TRIFLUOROMETHYLSULFYNYL)METHYL]INDOLE 3 CARBOXYLATE; TERT BUTYL 6 BROMO 5 HYDROXY 1 METHYL 2 [(2 TRIFLUOROMETHYLPHENYLTHIO)METHYL]INDOLE 3 CARBOXYLATE; TERT BUTYL 6 BROMO 5 HYDROXY 1 METHYL 2 [(2 TRIFLUOROMETHYLSULFYNYL)METHYL]INDOLE 3 CARBOXYLATE; TERT BUTYL 6 BROMO 5 HYDROXY 1 METHYL 2 [(2,6 DICHLOROPHENYLTHIO)METHYL]INDOLE 3 CARBOXYLATE; UNCLASSIFIED DRUG; ANTIVIRUS AGENT; GLYCOPROTEIN; SULFOXIDE; TERT-BUTYL 5-HYDROXY-1-METHYL-2-(2-TRIFLUOROMETHYSULFYNYL)METHYL)INDOLE-3-CARBOXYLATE; VIRUS ENVELOPE PROTEIN;

EID: 85006489409     PISSN: 09680896     EISSN: 14643391     Source Type: Journal    
DOI: 10.1016/j.bmc.2016.10.037     Document Type: Article
Times cited : (37)

References (30)
  • 1
    • 46849106951 scopus 로고    scopus 로고
    • An animal model for studying the pathogenesis of chikungunya virus infection
    • 1 Ziegler, S.A., Lu, L., da Rosa, A.P., Xiao, S.Y., Tesh, R.B., An animal model for studying the pathogenesis of chikungunya virus infection. Am J Trop Med Hyg 79 (2008), 133–139.
    • (2008) Am J Trop Med Hyg , vol.79 , pp. 133-139
    • Ziegler, S.A.1    Lu, L.2    da Rosa, A.P.3    Xiao, S.Y.4    Tesh, R.B.5
  • 2
    • 84880637794 scopus 로고    scopus 로고
    • Design of inhibitors of influenza virus membrane fusion: synthesis, structure-activity relationship and in vitro antiviral activity of a novel indole series
    • 2 Brancato, V., Peduto, A., Wharton, S., et al. Design of inhibitors of influenza virus membrane fusion: synthesis, structure-activity relationship and in vitro antiviral activity of a novel indole series. Antiviral Res 99 (2013), 125–135.
    • (2013) Antiviral Res , vol.99 , pp. 125-135
    • Brancato, V.1    Peduto, A.2    Wharton, S.3
  • 3
    • 44349125733 scopus 로고    scopus 로고
    • Arbidol: a broad-spectrum antiviral compound that blocks viral fusion
    • 3 Boriskin, Y.S., Leneva, I.A., Pecheur, E.I., Polyak, S.J., Arbidol: a broad-spectrum antiviral compound that blocks viral fusion. Curr Med Chem 15 (2008), 997–1005.
    • (2008) Curr Med Chem , vol.15 , pp. 997-1005
    • Boriskin, Y.S.1    Leneva, I.A.2    Pecheur, E.I.3    Polyak, S.J.4
  • 4
    • 84908317950 scopus 로고    scopus 로고
    • In vitro antiviral and immunomodulatory activity of arbidol and structurally related derivatives in herpes simplex virus type 1-infected human keratinocytes (HaCat)
    • 4 Perfetto, B., Filosa, R., De Gregorio, V., et al. In vitro antiviral and immunomodulatory activity of arbidol and structurally related derivatives in herpes simplex virus type 1-infected human keratinocytes (HaCat). J Med Microbiol 63 (2014), 1474–1483.
    • (2014) J Med Microbiol , vol.63 , pp. 1474-1483
    • Perfetto, B.1    Filosa, R.2    De Gregorio, V.3
  • 5
    • 79953805715 scopus 로고    scopus 로고
    • In vitro antiviral activity of arbidol against Chikungunya virus and characteristics of a selected resistant mutant
    • 5 Delogu, S., Pastorino, B., Baronti, C., Nougairède, A., Bonnet, E., de Lamballerie, X., In vitro antiviral activity of arbidol against Chikungunya virus and characteristics of a selected resistant mutant. Antiviral Res 90 (2011), 99–107.
    • (2011) Antiviral Res , vol.90 , pp. 99-107
    • Delogu, S.1    Pastorino, B.2    Baronti, C.3    Nougairède, A.4    Bonnet, E.5    de Lamballerie, X.6
  • 25
    • 85038408892 scopus 로고    scopus 로고
    • Molecular Operating Environment (MOE 2015.10); Chemical Computing Group, Inc.: Montreal, Quebec, Canada; URL <>; 2015.
    • 25 Molecular Operating Environment (MOE 2015.10); Chemical Computing Group, Inc.: Montreal, Quebec, Canada; URL < http://www.chemcomp.com>; 2015.
  • 26
    • 85052043802 scopus 로고    scopus 로고
    • Schrödinger Release 2015-4: LigPrep, version 3.6, New York, NY: Schrödinger, LLC; 2015.
    • 26 Schrödinger Release 2015-4: LigPrep, version 3.6, New York, NY: Schrödinger, LLC; 2015.
  • 27
    • 85052046865 scopus 로고    scopus 로고
    • Schrödinger Release 2015-4: Schrödinger Suite 2015-4 Protein Preparation Wizard; Epik version 3.4, New York, NY: Schrödinger, LLC; 2015; Impact version 6.9, New York, NY: Schrödinger, LLC; 2015; Prime version 4.2, New York, NY: Schrödinger, LLC; 2015.
    • 27 Schrödinger Release 2015-4: Schrödinger Suite 2015-4 Protein Preparation Wizard; Epik version 3.4, New York, NY: Schrödinger, LLC; 2015; Impact version 6.9, New York, NY: Schrödinger, LLC; 2015; Prime version 4.2, New York, NY: Schrödinger, LLC; 2015.
  • 28
    • 85052035152 scopus 로고    scopus 로고
    • Small-Molecule Drug Discovery Suite: Glide, version 6.9, New York, NY: Schrödinger, LLC; 2015.
    • 28 Small-Molecule Drug Discovery Suite: Glide, version 6.9, New York, NY: Schrödinger, LLC; 2015.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.