메뉴 건너뛰기




Volumn 2, Issue 7, 2010, Pages 1161-1180

6-desfluoroquinolones as HIV-1 Tat-mediated transcription inhibitors

Author keywords

[No Author keywords available]

Indexed keywords

2 PHENYLQUINOLONE DERIVATIVE; 26 C; 26 I; 6 AMINO 1,4 DIHYDRO 1 METHYL 7 [4 (2 PYRIDYL) 1 PIPERAZINYL] 4 OXO 3 QUINOLINECARBOXYLIC ACID; 6 AMINOQUINOLONE; 6 DESFLUOROQUINOLONE DERIVATIVE; AMINOGLYCOSIDE; ANTI HUMAN IMMUNODEFICIENCY VIRUS AGENT; ANTIVIRUS AGENT; CIPROFLOXACIN; CYCLIN DEPENDENT KINASE INHIBITOR; ELVITEGRAVIR; FLAVOPIRIDOL; HM 12; HM 13; HM 13 N; JTK 101; NAPHTHALENE DERIVATIVE; NEOMYCIN; PROCHLORPERAZINE; PROMAZINE; QUINOLONE DERIVATIVE; RITONAVIR; ROSCOVITINE; RUFLOXACIN; TRANSACTIVATOR PROTEIN; UNCLASSIFIED DRUG; UNINDEXED DRUG; WM 14; WM 16; ZIDOVUDINE;

EID: 77954688186     PISSN: 17568919     EISSN: None     Source Type: Journal    
DOI: 10.4155/fmc.10.208     Document Type: Review
Times cited : (30)

References (111)
  • 1
    • 46049096099 scopus 로고    scopus 로고
    • Viral reservoirs, residual viremia, and the potential of highly active antiretroviral therapy to eradicate HIV infection
    • Shen L, Siliciano RF. Viral reservoirs, residual viremia, and the potential of highly active antiretroviral therapy to eradicate HIV infection. J. Allergy Clin. Immunol. 122(1), 22-28 (2008).
    • (2008) J. Allergy Clin. Immunol. , vol.122 , Issue.1 , pp. 22-28
    • Shen, L.1    Siliciano, R.F.2
  • 2
    • 53849134844 scopus 로고    scopus 로고
    • Cellular reservoirs of HIV-1 and their role in viral persistence
    • Alexaki A, Liu Y, Wigdahl B. Cellular reservoirs of HIV-1 and their role in viral persistence. Curr. HIV Res. 6(5), 388-400 (2008).
    • (2008) Curr. HIV Res. , vol.6 , Issue.5 , pp. 388-400
    • Alexaki, A.1    Liu, Y.2    Wigdahl, B.3
  • 3
    • 57649193118 scopus 로고    scopus 로고
    • Eradication of HIV: Current challenges and new directions
    • Marsden MD, Zack JA. Eradication of HIV: current challenges and new directions. Antimicrob. Chemother. 63(1), 7-10 (2009).
    • (2009) Antimicrob. Chemother. , vol.63 , Issue.1 , pp. 7-10
    • Marsden, M.D.1    Zack, J.A.2
  • 5
    • 3042719556 scopus 로고    scopus 로고
    • Can HIV be cured? Mechanisms of HIV persistence and strategies to combat it
    • Hamer DH. Can HIV be cured? Mechanisms of HIV persistence and strategies to combat it. Curr. HIVRes. 2(2), 99-111 (2004).
    • (2004) Curr. HIV Res. , vol.2 , Issue.2 , pp. 99-111
    • Hamer, D.H.1
  • 6
    • 73249136755 scopus 로고    scopus 로고
    • Molecular control of HIV-1 postintegration latency: Implications for the development of new therapeutic strategies
    • DOI: 10.1186/1742-4690-6-111 Epub ahead of print
    • Colin L, Van Lint C. Molecular control of HIV-1 postintegration latency: implications for the development of new therapeutic strategies. Retrovirology 6:111. DOI: 10.1186/1742-4690-6-111 (2009) (Epub ahead of print).
    • (2009) Retrovirology , vol.6 , Issue.111
    • Colin, L.1    Van Lint, C.2
  • 7
    • 4143089463 scopus 로고    scopus 로고
    • Administration of HDAC inhibitors to reactivate HIV-1 expression in latent cellular reservoirs: Implications for the development of therapeutic strategies
    • Demonte D, Quivy V, Colette Y, Van Lint C. Administration of HDAC inhibitors to reactivate HIV-1 expression in latent cellular reservoirs: implications for the development of therapeutic strategies. Biochem. Pharmacol. 68(6), 1231-1238 (2004).
    • (2004) Biochem. Pharmacol. , vol.68 , Issue.6 , pp. 1231-1238
    • Demonte, D.1    Quivy, V.2    Colette, Y.3    Van Lint, C.4
  • 8
    • 67650550767 scopus 로고    scopus 로고
    • Synergistic activation of HIV-1 expression by deacetylase inhibitors and prostratin: Implications for treatment of latent infection
    • Reuse S, Calao M, Kabeya K et al. Synergistic activation of HIV-1 expression by deacetylase inhibitors and prostratin: implications for treatment of latent infection. PLoS ONE 4(6), e6093 (2009).
    • (2009) PLoS ONE , vol.4 , Issue.6
    • Reuse, S.1    Calao, M.2    Kabeya, K.3
  • 9
    • 67649259174 scopus 로고    scopus 로고
    • 'Shock and kill' effects of class I-selective histone deacetylase inhibitors in combination with the glutathione synthesis inhibitor buthionine sulfoximine in cell line models for HIV-1 quiescence
    • DOI: 10.1186/1742-4690-6-52 Epub ahead of print
    • Savarino A, Mai A, Norelli S et al. 'Shock and kill' effects of class I-selective histone deacetylase inhibitors in combination with the glutathione synthesis inhibitor buthionine sulfoximine in cell line models for HIV-1 quiescence. Retrovirology 6(52). DOI: 10.1186/1742-4690-6-52 (2009) (Epub ahead of print).
    • (2009) Retrovirology , vol.6 , Issue.52
    • Savarino, A.1    Mai, A.2    Norelli, S.3
  • 10
    • 0032401752 scopus 로고    scopus 로고
    • Recruitment of a protein complex containing Tat and cyclin T1 to TAR governs the species specificity of HIV-1 Tat
    • Bieniasz PD, Grdina TA, Bogerd HP, Cullen BR. Recruitment of a protein complex containing Tat and cyclin T1 to TAR governs the species specificity of HIV-1 Tat. EMBO J. 17(23), 7056-7065 (1998).
    • (1998) EMBO J. , vol.17 , Issue.23 , pp. 7056-7065
    • Bieniasz, P.D.1    Grdina, T.A.2    Bogerd, H.P.3    Cullen, B.R.4
  • 12
    • 0034864504 scopus 로고    scopus 로고
    • Multiple modes of transcriptional regulation by the HIV-1 Tat transactivator
    • Marcello A, Zoppe M, Giacca M. Multiple modes of transcriptional regulation by the HIV-1 Tat transactivator. IUBMB Life 51(3), 175-181 (2001).
    • (2001) IUBMB Life , vol.51 , Issue.3 , pp. 175-181
    • Marcello, A.1    Zoppe, M.2    Giacca, M.3
  • 13
    • 33747162419 scopus 로고    scopus 로고
    • The regulation of HIV-1 transcription: Molecular targets for chemotherapeutic intervention
    • Stevens M, De Clercq E, Balzarini J. The regulation of HIV-1 transcription: molecular targets for chemotherapeutic intervention. J. Med. Res. Rev. 26(5), 595-625 (2006).
    • (2006) J. Med. Res. Rev. , vol.26 , Issue.5 , pp. 595-625
    • Stevens, M.1    De Clercq, E.2    Balzarini, J.3
  • 14
    • 33746403681 scopus 로고    scopus 로고
    • Controlling the elongation phase of transcription with P-TEFb
    • Peterlin PM, Price DH. Controlling the elongation phase of transcription with P-TEFb. Mol. Cell23(3), 297-305 (2006).
    • (2006) Mol. Cell , vol.23 , Issue.3 , pp. 297-305
    • Peterlin, P.M.1    Price, D.H.2
  • 15
    • 0031777857 scopus 로고    scopus 로고
    • Treatment and prophylaxis of disseminated Mycobacterium avium complex in HIV-infected individuals
    • Faris MA, Raasch RH, Hopfer RL, Butts JD. Treatment and prophylaxis of disseminated Mycobacterium avium complex in HIV-infected individuals. Ann. Pharmacother. 32(5), 564-573 (1998).
    • (1998) Ann. Pharmacother. , vol.32 , Issue.5 , pp. 564-573
    • Faris, M.A.1    Raasch, R.H.2    Hopfer, R.L.3    Butts, J.D.4
  • 16
    • 0023130703 scopus 로고
    • Quinolonecarboxylic acids. 2. Synthesis and antibacterial evaluation of 7-oxo-2,3-dihydro-7H-pyrido[1,2,3-de][1,4] benzothiazine-6-carboxylic acids
    • Cecchetti V, Fravolini A, Fringuelli R et al. Quinolonecarboxylic acids. 2. Synthesis and antibacterial evaluation of 7-oxo-2,3-dihydro-7H-pyrido[1,2,3- de][1,4] benzothiazine-6-carboxylic acids. J. Med. Chem. 30(3), 465-473 (1987).
    • (1987) J. Med. Chem. , vol.30 , Issue.3 , pp. 465-473
    • Cecchetti, V.1    Fravolini, A.2    Fringuelli, R.3
  • 17
    • 0028965598 scopus 로고
    • 6-aminoquinolones: A new class of quinolones antibacterials?
    • Cecchetti V, Clementi S, Cruciani G et al. 6-aminoquinolones: a new class of quinolones antibacterials? J. Med. Chem. 38(6), 973-982 (1995).
    • (1995) J. Med. Chem. , vol.38 , Issue.6 , pp. 973-982
    • Cecchetti, V.1    Clementi, S.2    Cruciani, G.3
  • 18
    • 0030061794 scopus 로고    scopus 로고
    • Studies on 6-aminoquinolones: Synthesis and antibacterial evaluation of 6-amino-8-methylquinolones
    • Cecchetti V, Fravolini A, Lorenzini MC, Tabarrini O, Terni P, Xin T. Studies on 6-aminoquinolones: synthesis and antibacterial evaluation of 6-amino-8-methylquinolones. J. Med. Chem. 39(2), 436-445 (1996).
    • (1996) J. Med. Chem. , vol.39 , Issue.2 , pp. 436-445
    • Cecchetti, V.1    Fravolini, A.2    Lorenzini, M.C.3    Tabarrini, O.4    Terni, P.5    Xin, T.6
  • 19
    • 0029731375 scopus 로고    scopus 로고
    • Potent 6-desfluoro-8-methylquinolones as new lead compounds in antibacterial chemotherapy
    • Cecchetti V, Fravolini A, Palumbo M et al. Potent 6-desfluoro-8- methylquinolones as new lead compounds in antibacterial chemotherapy. J. Med. Chem. 39(25), 4952-4957 (1996).
    • (1996) J. Med. Chem. , vol.39 , Issue.25 , pp. 4952-4957
    • Cecchetti, V.1    Fravolini, A.2    Palumbo, M.3
  • 20
    • 0029093220 scopus 로고
    • In vitro activity of MF 5137, a new potent 6-aminoquinolone
    • Wise R, Pagella PG, Cecchetti V, Fravolini A, Tabarrini O. In vitro activity of MF 5137, a new potent 6-aminoquinolone. Drugs 49(2), 272-273 (1995).
    • (1995) Drugs , vol.49 , Issue.2 , pp. 272-273
    • Wise, R.1    Pagella, P.G.2    Cecchetti, V.3    Fravolini, A.4    Tabarrini, O.5
  • 21
    • 0025665238 scopus 로고
    • Fluoroquinolones protect the human lymphocyte CEM line from HIV-1 mediated cytotoxicity
    • Nozaki-Renard J, Iino T, Sato Y, Maremoto Y, Ohta G, Furusawa M. Fluoroquinolones protect the human lymphocyte CEM line from HIV-1 mediated cytotoxicity. Cell Struct. Funct. 15(5), 295-299 (1990).
    • (1990) Cell Struct. Funct. , vol.15 , Issue.5 , pp. 295-299
    • Nozaki-Renard, J.1    Iino, T.2    Sato, Y.3    Maremoto, Y.4    Ohta, G.5    Furusawa, M.6
  • 22
    • 0025637564 scopus 로고
    • A fluoroquinolone (DR3355) protects human lymphocyte cell lines from HIV-1 induced cytotoxicity
    • Nozaki-Renard J, Iino T, Sato Y, Maremoto Y, Ohta G, Furusawa M. A fluoroquinolone (DR3355) protects human lymphocyte cell lines from HIV-1 induced cytotoxicity. AIDS 4(12), 1283-1286 (1990).
    • (1990) AIDS , vol.4 , Issue.12 , pp. 1283-1286
    • Nozaki-Renard, J.1    Iino, T.2    Sato, Y.3    Maremoto, Y.4    Ohta, G.5    Furusawa, M.6
  • 23
    • 0032502654 scopus 로고    scopus 로고
    • Ciprofloxacin inhibits activation of latent human immunodeficiency virus type 1 in chronically infected promonocytic U1 cells
    • Gollapudi S, Kim CH, Roshanravan B, Gupta S. Ciprofloxacin inhibits activation of latent human immunodeficiency virus type 1 in chronically infected promonocytic U1 cells. AIDS Res. Human Retrovirus 14(6), 499-504 (1998).
    • (1998) AIDS Res. Human Retrovirus , vol.14 , Issue.6 , pp. 499-504
    • Gollapudi, S.1    Kim, C.H.2    Roshanravan, B.3    Gupta, S.4
  • 25
    • 0034609799 scopus 로고    scopus 로고
    • 6-aminoquinolones as new potential anti-HIV agents
    • Cecchetti V, Parolin C, Moro S et al. 6-aminoquinolones as new potential anti-HIV agents. J. Med. Chem. 43(20), 3799-3802 (2000).
    • (2000) J. Med. Chem. , vol.43 , Issue.20 , pp. 3799-3802
    • Cecchetti, V.1    Parolin, C.2    Moro, S.3
  • 26
    • 0037416975 scopus 로고    scopus 로고
    • New anti-human immunodeficiency type 1 6-aminoquinolones: Mechanism of action
    • Parolin C, Gatto B, Del Vecchio C et al. New anti-human immunodeficiency type 1 6-aminoquinolones: mechanism of action. Antimicrob. Agents Chemother. 47(3), 889-895 (2003).
    • (2003) Antimicrob. Agents Chemother. , vol.47 , Issue.3 , pp. 889-895
    • Parolin, C.1    Gatto, B.2    Del Vecchio, C.3
  • 27
    • 43149103943 scopus 로고    scopus 로고
    • Targeting RNA with small molecules
    • Thomas JR, Hergenrother PJ. Targeting RNA with small molecules. Chem Rev. 108(4), 1171-1224 (2008).
    • (2008) Chem Rev. , vol.108 , Issue.4 , pp. 1171-1224
    • Thomas, J.R.1    Hergenrother, P.J.2
  • 28
    • 77953440212 scopus 로고    scopus 로고
    • Strategies for the design of RNA-binding small molecules
    • Aboul-Ela F. Strategies for the design of RNA-binding small molecules. Future Med. Chem. 2(1), 93-119 (2010).
    • (2010) Future Med. Chem. , vol.2 , Issue.1 , pp. 93-119
    • Aboul-Ela, F.1
  • 29
    • 2142753038 scopus 로고    scopus 로고
    • Inhibition of human immunodeficiency virus type 1 Tat-trans-activation- responsive region interaction by an antiviral quinolone derivative
    • Richter S, Parolin C, Gatto B et al. Inhibition of human immunodeficiency virus type 1 Tat-trans-activation-responsive region interaction by an antiviral quinolone derivative. Antimicrob. Agents Chemother. 48(5), 1895-1899 (2004).
    • (2004) Antimicrob. Agents Chemother. , vol.48 , Issue.5 , pp. 1895-1899
    • Richter, S.1    Parolin, C.2    Gatto, B.3
  • 30
    • 58549111785 scopus 로고    scopus 로고
    • Synthesis and biological evaluation of 2-phenylquinolones targeted as Tat/TAR recognition
    • Manfroni G, Gatto B, Tabarrini O et al. Synthesis and biological evaluation of 2-phenylquinolones targeted as Tat/TAR recognition. Bioorg. Med. Chem. 19(3), 714-717 (2009).
    • (2009) Bioorg. Med. Chem. , vol.19 , Issue.3 , pp. 714-717
    • Manfroni, G.1    Gatto, B.2    Tabarrini, O.3
  • 31
    • 6044239447 scopus 로고    scopus 로고
    • Structure modification of 6-aminoquinolones with potent anti-HIV activity
    • Tabarrini O, Stevens M, Checchetti V et al. Structure modification of 6-aminoquinolones with potent anti-HIV activity. J. Med. Chem. 47(22), 5567-5578 (2004).
    • (2004) J. Med. Chem. , vol.47 , Issue.22 , pp. 5567-5578
    • Tabarrini, O.1    Stevens, M.2    Checchetti, V.3
  • 32
    • 51849133134 scopus 로고    scopus 로고
    • Structure-activity relationship study on anti-HIV 6-desfluoroquinolones
    • Tabarrini O, Massari S, Daelemans D et al. Structure-activity relationship study on anti-HIV 6-desfluoroquinolones. J. Med. Chem. 51(17), 5454-5458 (2008).
    • (2008) J. Med. Chem. , vol.51 , Issue.17 , pp. 5454-5458
    • Tabarrini, O.1    Massari, S.2    Daelemans, D.3
  • 33
    • 58549093913 scopus 로고    scopus 로고
    • Studies on anti-HIV quinolones: New insights on the C-6 position
    • Massari S, Daelemans D, Manfroni G et al. Studies on anti-HIV quinolones: new insights on the C-6 position. Bioorg. Med. Chem. 17(2), 667-674 (2009).
    • (2009) Bioorg. Med. Chem. , vol.17 , Issue.2 , pp. 667-674
    • Massari, S.1    Daelemans, D.2    Manfroni, G.3
  • 34
    • 77249177585 scopus 로고    scopus 로고
    • A 1,8-naphthyridone derivative targets the HIV-1 Tat-mediated transcription and potently inhibits the HIV-1 replication
    • Massari S, Daelemans D, Barreca ML et al. A 1,8-naphthyridone derivative targets the HIV-1 Tat-mediated transcription and potently inhibits the HIV-1 replication. J. Med. Chem. 53(2), 641-648 (2010).
    • (2010) J. Med. Chem. , vol.53 , Issue.2 , pp. 641-648
    • Massari, S.1    Daelemans, D.2    Barreca, M.L.3
  • 37
    • 34247140849 scopus 로고    scopus 로고
    • A novel in vivo model for the study of HIV-1 transcription inhibitors: Evaluation of new 6-desfluoroquinolones derivatives (6-DFQs)
    • Stevens M, Pollicita M, Pannecouque C et al. A novel in vivo model for the study of HIV-1 transcription inhibitors: evaluation of new 6-desfluoroquinolones derivatives (6-DFQs). Antimicrob. Agents Chemother. 5(4), 1407-1413 (2007).
    • (2007) Antimicrob. Agents Chemother. , vol.5 , Issue.4 , pp. 1407-1413
    • Stevens, M.1    Pollicita, M.2    Pannecouque, C.3
  • 38
    • 0002200781 scopus 로고    scopus 로고
    • Structure-activity relationships in Quinolone Antimicrobial Agents (2nd Edition)
    • Hooper DC, Wolfson JS (Eds.) Washington DC, USA
    • Mitscher LA, Devasthale P, Zavod R. Structure-activity relationships. In Quinolone Antimicrobial Agents (2nd Edition). Hooper DC, Wolfson JS (Eds.). American Society for Microbiology. Washington DC, USA, 3-51 (1998).
    • (1998) American Society for Microbiology , pp. 3-51
    • Mitscher, L.A.1    Devasthale, P.2    Zavod, R.3
  • 41
    • 0033231154 scopus 로고    scopus 로고
    • Synthesis and anti-HIV activity of arylpiperazinyl fluoroquinolones: A new class of anti-HIV agents
    • Hagihara M, Kashiwase H, Katsube T et al. Synthesis and anti-HIV activity of arylpiperazinyl fluoroquinolones: a new class of anti-HIV agents. Bioorg. Med. Chem. Lett. 9(21), 3063-3068 (1999).
    • (1999) Bioorg. Med. Chem. Lett. , vol.9 , Issue.21 , pp. 3063-3068
    • Hagihara, M.1    Kashiwase, H.2    Katsube, T.3
  • 42
    • 34250207355 scopus 로고    scopus 로고
    • Inhibition of human immunodeficiency virus type 1 transcription by N-aminoimidazole derivatives
    • Stevens M, Balzarini J, Lagoja IM et al. Inhibition of human immunodeficiency virus type 1 transcription by N-aminoimidazole derivatives. Virology 365(1), 220-237 (2007).
    • (2007) Virology , vol.365 , Issue.1 , pp. 220-237
    • Stevens, M.1    Balzarini, J.2    Lagoja, I.M.3
  • 43
    • 27744576773 scopus 로고    scopus 로고
    • Cell-dependent interference of a series of new 6-aminoquinolone derivatives with viral (HIV/CMV) transactivation
    • Stevens M, Balzarini J, Tabarrini O et al. Cell-dependent interference of a series of new 6-aminoquinolone derivatives with viral (HIV/CMV) transactivation. J. Antimicrob. Chemother. 56(5), 847-855 (2005).
    • (2005) J. Antimicrob. Chemother. , vol.56 , Issue.5 , pp. 847-855
    • Stevens, M.1    Balzarini, J.2    Tabarrini, O.3
  • 45
    • 34447548922 scopus 로고    scopus 로고
    • HIV integrase inhibitors as therapeutic agents in AIDS
    • Nair V, Chi G. HIV integrase inhibitors as therapeutic agents in AIDS. Rev. Med. Virol. 17(4), 277-295 (2007).
    • (2007) Rev. Med. Virol. , vol.17 , Issue.4 , pp. 277-295
    • Nair, V.1    Chi, G.2
  • 46
    • 34247092052 scopus 로고    scopus 로고
    • Characterization of a replication-competent, integrase-defective human immunodeficiency virus (HIV)/ simian virus 40 chimera as a powerful tool for the discovery and validation of HIV integrase inhibitors
    • Daelemans D, Lu R, De Clercq E, Engelman A. Characterization of a replication-competent, integrase-defective human immunodeficiency virus (HIV)/ simian virus 40 chimera as a powerful tool for the discovery and validation of HIV integrase inhibitors. J. Virol. 81(8), 4381-4385 (2007).
    • (2007) J. Virol. , vol.81 , Issue.8 , pp. 4381-4385
    • Daelemans, D.1    Lu, R.2    De Clercq, E.3    Engelman, A.4
  • 48
    • 59749091271 scopus 로고    scopus 로고
    • A 6-aminoquinolone compound, WC5, with potent and selective anti-human cytomegalovirus activity
    • Mercorelli B, Muratore G, Sinigalia E et al. A 6-aminoquinolone compound, WC5, with potent and selective anti-human cytomegalovirus activity. Antimicrob. Agents Chemother. 53(1), 312-315 (2009).
    • (2009) Antimicrob. Agents Chemother. , vol.53 , Issue.1 , pp. 312-315
    • Mercorelli, B.1    Muratore, G.2    Sinigalia, E.3
  • 49
    • 77951226066 scopus 로고    scopus 로고
    • The 6-aminoquinolone compound WC5 inhibits human cytomegalovirus replication at an early stage by interfering with the transactivating activity of viral IE2 protein
    • Loregian A, Mercorelli B, Muratore G et al. The 6-aminoquinolone compound WC5 inhibits human cytomegalovirus replication at an early stage by interfering with the transactivating activity of viral IE2 protein. J. Antimicrob. Chemother. 54(5), 1930-1940 (2010).
    • (2010) J. Antimicrob. Chemother. , vol.54 , Issue.5 , pp. 1930-1940
    • Loregian, A.1    Mercorelli, B.2    Muratore, G.3
  • 50
    • 18344373269 scopus 로고    scopus 로고
    • Broad-spectrum antiviral activity of PNU-183792, a 4-oxo- dihydroquinoline, against human and animal herpesviruses
    • Brideau RJ, Knechtel ML, Huang A et al. Broad-spectrum antiviral activity of PNU-183792, a 4-oxo-dihydroquinoline, against human and animal herpesviruses. Antiviral Res. 54(1), 19-28 (2002).
    • (2002) Antiviral Res. , vol.54 , Issue.1 , pp. 19-28
    • Brideau, R.J.1    Knechtel, M.L.2    Huang, A.3
  • 51
    • 0036167879 scopus 로고    scopus 로고
    • Broad-spectrum antiherpes activities of 4-hydroxyquinoline carboxamides, a novel class of herpesvirus polymerase inhibitors
    • Oien NL, Brideau RJ, Hopkins TA et al. Broad-spectrum antiherpes activities of 4-hydroxyquinoline carboxamides, a novel class of herpesvirus polymerase inhibitors. Antimicrob. Agents Chemother. 46(3), 724-730 (2002).
    • (2002) Antimicrob. Agents Chemother. , vol.46 , Issue.3 , pp. 724-730
    • Oien, N.L.1    Brideau, R.J.2    Hopkins, T.A.3
  • 52
    • 77249134151 scopus 로고    scopus 로고
    • Twenty-six years of anti-HIV drug discovery: Where do we stand and where do we go?
    • Mehellou Y, De Clercq E. Twenty-six years of anti-HIV drug discovery: where do we stand and where do we go? J. Med. Chem. 53 (2), 521-538 (2010).
    • (2010) J. Med. Chem. , vol.53 , Issue.2 , pp. 521-538
    • Mehellou, Y.1    De Clercq, E.2
  • 53
    • 33747140372 scopus 로고    scopus 로고
    • Recent status of HIV-1 gene expression inhibitors
    • Baba M. Recent status of HIV-1 gene expression inhibitors. Antiviral Res. 71(2-3), 301-306 (2006).
    • (2006) Antiviral Res. , vol.71 , Issue.2-3 , pp. 301-306
    • Baba, M.1
  • 54
    • 34748852513 scopus 로고    scopus 로고
    • Blocking interactions between HIV-1 integrase and cellular cofactors: An emerging anti-retroviral strategy
    • Al-Mawsawi LQ, Neamati N. Blocking interactions between HIV-1 integrase and cellular cofactors: an emerging anti-retroviral strategy. Trends Pharmacol. Sci. 28(10), 526-535 (2007).
    • (2007) Trends Pharmacol. Sci. , vol.28 , Issue.10 , pp. 526-535
    • Al-Mawsawi, L.Q.1    Neamati, N.2
  • 55
    • 70349564379 scopus 로고    scopus 로고
    • Targeting host factors: A novel rationale for the management of hepatitis C virus
    • Khattab MA. Targeting host factors: a novel rationale for the management of hepatitis C virus. World J. Gastroenterol. 15(28), 3472-3479 (2009).
    • (2009) World J. Gastroenterol. , vol.15 , Issue.28 , pp. 3472-3479
    • Khattab, M.A.1
  • 56
    • 77954669035 scopus 로고    scopus 로고
    • Targeting protein-protein interactions for HIV therapeutics
    • Rice AP, Sutton RE. Targeting protein-protein interactions for HIV therapeutics. Futur. HIV Ther. 1(3), 369-385 (2007).
    • (2007) Futur. HIV Ther. , vol.1 , Issue.3 , pp. 369-385
    • Rice, A.P.1    Sutton, R.E.2
  • 57
    • 67249156976 scopus 로고    scopus 로고
    • Targeting cell signalling pathways to fight the flu: Towards a paradigm change in anti-influenza therapy
    • Ludwig S. Targeting cell signalling pathways to fight the flu: towards a paradigm change in anti-influenza therapy. J. Antimicrob. Chemother. 64(1), 1-4 (2009).
    • (2009) J. Antimicrob. Chemother. , vol.64 , Issue.1 , pp. 1-4
    • Ludwig, S.1
  • 58
    • 67651047155 scopus 로고    scopus 로고
    • The 4-quinolone-3-carboxylic acid motif as a multivalent scaffold in medicinal chemistry
    • Mugnaini C, Pasquini S, Corelli F. The 4-quinolone-3-carboxylic acid motif as a multivalent scaffold in medicinal chemistry. Curr. Med. Chem. 16(14), 1746-1767 (2009).
    • (2009) Curr. Med. Chem. , vol.16 , Issue.14 , pp. 1746-1767
    • Mugnaini, C.1    Pasquini, S.2    Corelli, F.3
  • 59
    • 0142075333 scopus 로고    scopus 로고
    • Targeting the HIV trans-activation responsive region-approaches towards RNA-binding drugs
    • Krebs A, Ludwig V, Boden O, Gobel MW. Targeting the HIV trans-activation responsive region-approaches towards RNA-binding drugs. Chembiochem 4(10), 972-978 (2003).
    • (2003) Chembiochem , vol.4 , Issue.10 , pp. 972-978
    • Krebs, A.1    Ludwig, V.2    Boden, O.3    Gobel, M.W.4
  • 60
    • 13544264777 scopus 로고    scopus 로고
    • RNA as target for small-molecule therapeutics
    • Hermann T, Tor Y. RNA as target for small-molecule therapeutics. Expert Opin. Ther. Patents 15(1), 49-62 (2005).
    • (2005) Expert Opin. Ther. Patents , vol.15 , Issue.1 , pp. 49-62
    • Hermann, T.1    Tor, Y.2
  • 61
    • 2942615518 scopus 로고    scopus 로고
    • Inhibitors of HIV-1 gene expression and transcription
    • Baba M. Inhibitors of HIV-1 gene expression and transcription. Curr. Top. Med. Chem. 4(9), 871-882 (2004).
    • (2004) Curr. Top. Med. Chem. , vol.4 , Issue.9 , pp. 871-882
    • Baba, M.1
  • 62
    • 33646534201 scopus 로고    scopus 로고
    • Inhibitors of HIV-1 Tat-mediated transactivation
    • Richter SN, Palu G. Inhibitors of HIV-1 Tat-mediated transactivation. Curr. Med. Chem. 13(11), 1305-1315 (2006).
    • (2006) Curr. Med. Chem. , vol.13 , Issue.11 , pp. 1305-1315
    • Richter, S.N.1    Palu, G.2
  • 63
    • 29444440832 scopus 로고    scopus 로고
    • Discoveries of Tat-TAR interaction inhibitors for HIV-1
    • Yang M. Discoveries of Tat-TAR interaction inhibitors for HIV-1. Curr. Drug Targets Infect. Disord. 5(4), 433-444 (2005).
    • (2005) Curr. Drug Targets Infect. Disord. , vol.5 , Issue.4 , pp. 433-444
    • Yang, M.1
  • 64
    • 0028823853 scopus 로고
    • Inhibition of an HIV-1 Tat-derived peptide binding to TAR RNA by aminoglycoside antibiotics
    • Mei H-Y, Galan AA, Halim NS et al. Inhibition of an HIV-1 Tat-derived peptide binding to TAR RNA by aminoglycoside antibiotics. Bioorg. Med. Chem. Lett. 5(22), 2755-2760 (1995).
    • (1995) Bioorg. Med. Chem. Lett. , vol.5 , Issue.22 , pp. 2755-2760
    • Mei, H.-Y.1    Galan, A.A.2    Halim, N.S.3
  • 65
    • 0032554635 scopus 로고    scopus 로고
    • Binding of neomycin to the TAR element of HIV-1 RNA induces dissociation of Tat protein by an allosteric mechanism
    • Wang S, Huber PW, Cui M, Czarnik AW, Mei HY. Binding of neomycin to the TAR element of HIV-1 RNA induces dissociation of Tat protein by an allosteric mechanism. Biochemistry 37(16), 5549-5557 (1998).
    • (1998) Biochemistry , vol.37 , Issue.16 , pp. 5549-5557
    • Wang, S.1    Huber, P.W.2    Cui, M.3    Czarnik, A.W.4    Mei, H.Y.5
  • 66
    • 0029924327 scopus 로고    scopus 로고
    • The binding mode of drugs to the TAR RNA of HIV-1 studied by electric linear dichroism
    • Bailly C, Colson P, Houssier C, Hamy F. The binding mode of drugs to the TAR RNA of HIV-1 studied by electric linear dichroism. Nucleic Acids Res. 24(8), 1460-1464 (1996).
    • (1996) Nucleic Acids Res. , vol.24 , Issue.8 , pp. 1460-1464
    • Bailly, C.1    Colson, P.2    Houssier, C.3    Hamy, F.4
  • 67
    • 0030856838 scopus 로고    scopus 로고
    • Binding of Hoechst 33258 to the TAR RNA of HIV-1. Recognition of a pyrimidine bulge-dependent structure
    • Dassonneville L, Hamy F, Colson P, Houssier C, Bailly C. Binding of Hoechst 33258 to the TAR RNA of HIV-1. Recognition of a pyrimidine bulge-dependent structure. Nucleic Acids Res. 25(22), 4487-4492 (1997).
    • (1997) Nucleic Acids Res. , vol.25 , Issue.22 , pp. 4487-4492
    • Dassonneville, L.1    Hamy, F.2    Colson, P.3    Houssier, C.4    Bailly, C.5
  • 69
    • 0036008846 scopus 로고    scopus 로고
    • Structure-based computational database screening, in vitro assay, and NMR assessment of compounds that target TAR RNA
    • Lind KE, Du Z, Fujinaga K, Peterlin BM, James TL. Structure-based computational database screening, in vitro assay, and NMR assessment of compounds that target TAR RNA. Chem. Biol. 9(2), 185-193 (2002).
    • (2002) Chem. Biol. , vol.9 , Issue.2 , pp. 185-193
    • Lind, K.E.1    Du, Z.2    Fujinaga, K.3    Peterlin, B.M.4    James, T.L.5
  • 70
    • 33748561836 scopus 로고    scopus 로고
    • Synthesis and testing of a focused phenothiazine library for binding to HIV-1 TAR RNA
    • Mayer M, Lang PT, Gerber S et al. Synthesis and testing of a focused phenothiazine library for binding to HIV-1 TAR RNA. Chem. Biol. 13(9), 993-1000 (2006).
    • (2006) Chem. Biol. , vol.13 , Issue.9 , pp. 993-1000
    • Mayer, M.1    Lang, P.T.2    Gerber, S.3
  • 71
    • 0141866666 scopus 로고    scopus 로고
    • Discovery of a small molecule Tat-trans-activation-responsive RNA antagonist that potently inhibits human immunodeficiency virus-1 replication
    • Hwang S, Tamilarasu N, Kibler K et al. Discovery of a small molecule Tat-trans-activation-responsive RNA antagonist that potently inhibits human immunodeficiency virus-1 replication. J. Biol. Chem. 278(40), 39092-39103 (2003).
    • (2003) J. Biol. Chem. , vol.278 , Issue.40 , pp. 39092-39103
    • Hwang, S.1    Tamilarasu, N.2    Kibler, K.3
  • 72
    • 10744222241 scopus 로고    scopus 로고
    • Structure-based drug design targeting an inactive RNA conformation: Exploiting the flexibility of HIV-1 TAR RNA
    • Murchie AI, Davis B, Isel C et al. Structure-based drug design targeting an inactive RNA conformation: exploiting the flexibility of HIV-1 TAR RNA. J. Mol. Biol. 336(3), 625-638 (2004).
    • (2004) J. Mol. Biol. , vol.336 , Issue.3 , pp. 625-638
    • Murchie, A.I.1    Davis, B.2    Isel, C.3
  • 73
    • 67049143076 scopus 로고    scopus 로고
    • 2-phenylquinolones as inhibitors of the HIV-1 Tat-TAR interaction
    • Gatto B, Tabarrini O, Massari S et al. 2-phenylquinolones as inhibitors of the HIV-1 Tat-TAR interaction. ChemMedChem 4(6), 935-938 (2009).
    • (2009) ChemMedChem , vol.4 , Issue.6 , pp. 935-938
    • Gatto, B.1    Tabarrini, O.2    Massari, S.3
  • 74
    • 33750947321 scopus 로고    scopus 로고
    • The design, synthesis and biological evaluation of novel substituted purines as HIV-1 Tat-TAR inhibitors
    • Yuan D, He M, Pang R, Lin S, Li Z, Yang M. The design, synthesis and biological evaluation of novel substituted purines as HIV-1 Tat-TAR inhibitors. Bioorg. Med. Chem. 15(1), 265-272 (2007).
    • (2007) Bioorg. Med. Chem. , vol.15 , Issue.1 , pp. 265-272
    • Yuan, D.1    He, M.2    Pang, R.3    Lin, S.4    Li, Z.5    Yang, M.6
  • 75
    • 67749088605 scopus 로고    scopus 로고
    • Simultaneous recognition of HIV-1 TAR RNA bulge and loop sequences by cyclic peptide mimics of Tat protein
    • Davidson A, Leeper TC, Athanassiou Z et al. Simultaneous recognition of HIV-1 TAR RNA bulge and loop sequences by cyclic peptide mimics of Tat protein. Proc. Natl Acad. Sci. USA 106(29), 11931-11936 (2009).
    • (2009) Proc. Natl Acad. Sci. USA , vol.106 , Issue.29 , pp. 11931-11936
    • Davidson, A.1    Leeper, T.C.2    Athanassiou, Z.3
  • 76
    • 33846021965 scopus 로고    scopus 로고
    • First demonstration of the effectiveness of inhibitors of cellular protein kinases in antiviral therapy
    • Schang LM. First demonstration of the effectiveness of inhibitors of cellular protein kinases in antiviral therapy. Expert. Rev. Anti Infect. Ther. 4(6), 953-956 (2006).
    • (2006) Expert. Rev. Anti Infect. Ther. , vol.4 , Issue.6 , pp. 953-956
    • Schang, L.M.1
  • 77
    • 35548949853 scopus 로고    scopus 로고
    • CDK9/cyclin T1: A host cellular target for antiretroviral therapy
    • Klebl BM, Choidas A. CDK9/cyclin T1: a host cellular target for antiretroviral therapy. Future Virol. 1(3), 317-330 (2006).
    • (2006) Future Virol. , vol.1 , Issue.3 , pp. 317-330
    • Klebl, B.M.1    Choidas, A.2
  • 78
    • 44549087848 scopus 로고    scopus 로고
    • Cyclin-dependent kinase 9: A key transcriptional regulator and potential drug target in oncology, virology and cardiology
    • Wang S, Fischer PM. Cyclin-dependent kinase 9: a key transcriptional regulator and potential drug target in oncology, virology and cardiology. Trends Pharmacol. Sci. 29(6), 302-313 (2008).
    • (2008) Trends Pharmacol. Sci. , vol.29 , Issue.6 , pp. 302-313
    • Wang, S.1    Fischer, P.M.2
  • 79
    • 33744736316 scopus 로고    scopus 로고
    • Potential use of pharmacological cyclin-dependent kinase inhibitors as anti-HIV therapeutics
    • Pumfery A, de la Fuente C, Berro R, Nekhai S, Kashanchi F, Chao SH. Potential use of pharmacological cyclin-dependent kinase inhibitors as anti-HIV therapeutics. Curr. Pharm. Des. 12(16), 1949-1961 (2006).
    • (2006) Curr. Pharm. Des. , vol.12 , Issue.16 , pp. 1949-1961
    • Pumfery, A.1    De La Fuente, C.2    Berro, R.3    Nekhai, S.4    Kashanchi, F.5    Chao, S.H.6
  • 80
    • 33846004815 scopus 로고    scopus 로고
    • Five years of progress on cyclin-dependent kinases and other cellular proteins as potential targets for antiviral drugs
    • Schang LM, St Vincent MR, Lacasse JJ. Five years of progress on cyclin-dependent kinases and other cellular proteins as potential targets for antiviral drugs. Antivir. Chem. Chemother. 17(6), 293-320 (2006).
    • (2006) Antivir. Chem. Chemother. , vol.17 , Issue.6 , pp. 293-320
    • Schang, L.M.1    St Vincent, M.R.2    Lacasse, J.J.3
  • 81
    • 16344381710 scopus 로고    scopus 로고
    • Advances on cyclin-dependent kinases (CDKs) as novel targets for antiviral drugs
    • Schang LM. Advances on cyclin-dependent kinases (CDKs) as novel targets for antiviral drugs. Curr. Drug Targets Infect. Disord. 5(1), 29-37 (2005).
    • (2005) Curr. Drug Targets Infect. Disord. , vol.5 , Issue.1 , pp. 29-37
    • Schang, L.M.1
  • 82
    • 65349093357 scopus 로고    scopus 로고
    • Role of the HIV-1 positive elongation factor P-TEFb and inhibitors thereof
    • Wang Y, Liu XY, De Clercq E. Role of the HIV-1 positive elongation factor P-TEFb and inhibitors thereof. Mini Rev. Med. Chem. 9(3), 379-385 (2009).
    • (2009) Mini Rev. Med. Chem. , vol.9 , Issue.3 , pp. 379-385
    • Wang, Y.1    Liu, X.Y.2    De Clercq, E.3
  • 84
    • 14444281157 scopus 로고    scopus 로고
    • P-TEFb kinase is required for HIV Tat transcriptional activation in vivo and in vitro
    • Mancebo HS, Lee G, Flygare J et al. P-TEFb kinase is required for HIV Tat transcriptional activation in vivo and in vitro. Genes Dev. 11(20), 2633-2644 (1997).
    • (1997) Genes Dev. , vol.11 , Issue.20 , pp. 2633-2644
    • Mancebo, H.S.1    Lee, G.2    Flygare, J.3
  • 85
    • 0034665961 scopus 로고    scopus 로고
    • Flavopiridol inhibits P-TEFb and blocks HIV-1 replication
    • Chao SH, Fujinaga K, Marion JE et al. Flavopiridol inhibits P-TEFb and blocks HIV-1 replication. J. Biol. Chem. 275(37), 28345-28348 (2000).
    • (2000) J. Biol. Chem. , vol.275 , Issue.37 , pp. 28345-28348
    • Chao, S.H.1    Fujinaga, K.2    Marion, J.E.3
  • 86
    • 34548016988 scopus 로고    scopus 로고
    • Inhibition of HIV-1 replication by P-TEFb inhibitors DRB, seliciclib and flavopiridol correlates with release of free P-TEFb from the large, inactive form of the complex
    • Biglione S, Byers SA, Price JP et al. Inhibition of HIV-1 replication by P-TEFb inhibitors DRB, seliciclib and flavopiridol correlates with release of free P-TEFb from the large, inactive form of the complex. Retrovirology 4, 47 (2007).
    • (2007) Retrovirology , vol.4 , pp. 47
    • Biglione, S.1    Byers, S.A.2    Price, J.P.3
  • 87
    • 70349558526 scopus 로고    scopus 로고
    • Identification of flavopiridol analogues that selectively inhibit positive transcription elongation factor (P-TEFb) and block HIV-1 replication
    • Ali A, Ghosh A, Nathans RS, et al. Identification of flavopiridol analogues that selectively inhibit positive transcription elongation factor (P-TEFb) and block HIV-1 replication. Chembiochem 10(12), 2072-2080 (2009).
    • (2009) Chembiochem , vol.10 , Issue.12 , pp. 2072-2080
    • Ali, A.1    Ghosh, A.2    Nathans, R.S.3
  • 88
    • 0034910933 scopus 로고    scopus 로고
    • Inhibition of human immunodeficiency virus type 1 transcription by chemical cyclin-dependent kinase inhibitors
    • Wang D, de la Fuente C, Santiago F et al. Inhibition of human immunodeficiency virus type 1 transcription by chemical cyclin-dependent kinase inhibitors. J. Virol. 75(16), 7266-7279 (2001).
    • (2001) J. Virol. , vol.75 , Issue.16 , pp. 7266-7279
    • Wang, D.1    De La Fuente, C.2    Santiago, F.3
  • 89
    • 13244260958 scopus 로고    scopus 로고
    • Antiviral activity of CYC202 in HIV-1-infected cells
    • A gbot ta h E , de La Fuente C , Nek ha i S et al. Antiviral activity of CYC202 in HIV-1-infected cells. J. Biol. Chem. 280(4), 3029-3042 (2005).
    • (2005) J. Biol. Chem. , vol.280 , Issue.4 , pp. 3029-3042
    • Gbot Ta, H.E.A.1    De La Fuente, C.2    Nek Ha, I.S.3
  • 90
    • 27944474355 scopus 로고    scopus 로고
    • Indirubin-3'-monoxime, a derivative of a Chinese antileukemia medicine, inhibits P-TEFb function and HIV-1 replication
    • Heredia A, Davis C, Bamba D et al. Indirubin-3'-monoxime, a derivative of a Chinese antileukemia medicine, inhibits P-TEFb function and HIV-1 replication. AIDS 19(18), 2087-2095 (2005).
    • (2005) AIDS , vol.19 , Issue.18 , pp. 2087-2095
    • Heredia, A.1    Davis, C.2    Bamba, D.3
  • 91
    • 34848903905 scopus 로고    scopus 로고
    • Potent and selective inhibition of Tat-dependent HIV-1 replication in chronically infected cells by a novel naphthalene derivative JTK-101
    • Wang X, Yamataka K, Okamoto M, Ikeda S, Baba M. Potent and selective inhibition of Tat-dependent HIV-1 replication in chronically infected cells by a novel naphthalene derivative JTK-101. Antivir. Chem. Chemother. 18(4), 201-211 (2007).
    • (2007) Antivir. Chem. Chemother. , vol.18 , Issue.4 , pp. 201-211
    • Wang, X.1    Yamataka, K.2    Okamoto, M.3    Ikeda, S.4    Baba, M.5
  • 92
    • 0031866266 scopus 로고    scopus 로고
    • Inhibition of human immunodeficiency virus type 1 replication and cytokine production by fluoroquinoline derivatives
    • Baba M, Okamoto M, Kawamura M et al. Inhibition of human immunodeficiency virus type 1 replication and cytokine production by fluoroquinoline derivatives. Mol. Pharmacol. 53(6), 1097-1103 (1998).
    • (1998) Mol. Pharmacol. , vol.53 , Issue.6 , pp. 1097-1103
    • Baba, M.1    Okamoto, M.2    Kawamura, M.3
  • 93
    • 0031710730 scopus 로고    scopus 로고
    • Broad spectrum antiviral activity and mechanism of antiviral action of fluoroquinolone derivative K-12
    • Witvrouw M, Daelemans D, Pannecouque C et al. Broad spectrum antiviral activity and mechanism of antiviral action of fluoroquinolone derivative K-12. Antiviral Chem. Chemother. 9(5), 403-411 (1998).
    • (1998) Antiviral Chem. Chemother. , vol.9 , Issue.5 , pp. 403-411
    • Witvrouw, M.1    Daelemans, D.2    Pannecouque, C.3
  • 94
    • 0033016647 scopus 로고    scopus 로고
    • Inhibition of human immunodeficiency virus type 1 replication by combination of transcription inhibitor K-12 and other antiretroviral agents in acutely and chronically infected cells
    • Okamoto M, Okamoto T, Baba M. Inhibition of human immunodeficiency virus type 1 replication by combination of transcription inhibitor K-12 and other antiretroviral agents in acutely and chronically infected cells. Antimicrob. Agents Chemother. 43(3), 492-497 (1999). (Pubitemid 29109508)
    • (1999) Antimicrobial Agents and Chemotherapy , vol.43 , Issue.3 , pp. 492-497
    • Okamoto, M.1    Okamoto, T.2    Baba, M.3
  • 95
    • 0034608946 scopus 로고    scopus 로고
    • Inhibition of the RNA-dependent transactivation and replication of the human immunodeficiency virus type 1 by a fluoroquinoline derivative K-37
    • Okamoto H, Cujec TP, Okamoto M, Peterlin MB, Baba M, Okamoto T. Inhibition of the RNA-dependent transactivation and replication of the human immunodeficiency virus type 1 by a fluoroquinoline derivative K-37. Virology 272(2), 402-408 (2000).
    • (2000) Virology , vol.272 , Issue.2 , pp. 402-408
    • Okamoto, H.1    Cujec, T.P.2    Okamoto, M.3    Peterlin, M.B.4    Baba, M.5    Okamoto, T.6
  • 96
    • 0036265349 scopus 로고    scopus 로고
    • Inhibition of the tax-dependent human T-lymphotropic virus type i replication in persistently infected cells by the fluoroquinolone derivative K-37
    • Wang X, Miyake H, Okamoto M et al. Inhibition of the tax-dependent human T-lymphotropic virus type I replication in persistently infected cells by the fluoroquinolone derivative K-37. Mol. Pharmacol. 61(6), 1359-1365 (2002).
    • (2002) Mol. Pharmacol. , vol.61 , Issue.6 , pp. 1359-1365
    • Wang, X.1    Miyake, H.2    Okamoto, M.3
  • 97
    • 0032903126 scopus 로고    scopus 로고
    • A new fluoroquinolone derivative exhibits inhibitory activity against human immunodeficiency virus type 1 replication
    • Kashiwase H, Momota K, Ohmine T et al. A new fluoroquinolone derivative exhibits inhibitory activity against human immunodeficiency virus type 1 replication. Chemotherapy 45(1), 48-55 (1999).
    • (1999) Chemotherapy , vol.45 , Issue.1 , pp. 48-55
    • Kashiwase, H.1    Momota, K.2    Ohmine, T.3
  • 98
    • 67349188417 scopus 로고    scopus 로고
    • Inhibition of porcine endogenous retrovirus (PERV) replication by HIV-1 gene expression inhibitors
    • Shi M, Wang X, Okamoto M, Takao S, Baba M. Inhibition of porcine endogenous retrovirus (PERV) replication by HIV-1 gene expression inhibitors. Antiviral Res. 83(2), 201-204 (2009).
    • (2009) Antiviral Res. , vol.83 , Issue.2 , pp. 201-204
    • Shi, M.1    Wang, X.2    Okamoto, M.3    Takao, S.4    Baba, M.5
  • 99
    • 0000859397 scopus 로고
    • Recent advances in the synthesis of antibacterial quinolones
    • Radl S, Bouzard D. Recent advances in the synthesis of antibacterial quinolones. Heterocycles 34(11), 2143-2177 (1992).
    • (1992) Heterocycles , vol.34 , Issue.11 , pp. 2143-2177
    • Radl, S.1    Bouzard, D.2
  • 100
    • 0000139329 scopus 로고
    • The synthesis of certain substituted quinolones and 5,6-benzoquinolines
    • Gould RJ, Jacobs WA. The synthesis of certain substituted quinolones and 5,6-benzoquinolines. J. Am. Chem. Soc. 61(10), 2890-2895 (1939).
    • (1939) J. Am. Chem. Soc. , vol.61 , Issue.10 , pp. 2890-2895
    • Gould, R.J.1    Jacobs, W.A.2
  • 101
    • 84985278773 scopus 로고
    • Cycloaracylation of enamines, I. Synthesis of 4-quinolone-3-carboxylic acids
    • 1987
    • Grohe K, Heitzer H. Cycloaracylation of enamines, I. Synthesis of 4-quinolone-3-carboxylic acids. Liebigs Ann. Chem. 1987(1), 29-37 (1987).
    • (1987) Liebigs Ann. Chem. , Issue.1 , pp. 29-37
    • Grohe, K.1    Heitzer, H.2
  • 102
    • 84986976919 scopus 로고
    • The omportance of the cycloaracylation process for the synthesis of modern fluoroquinolones
    • Grohe K. The omportance of the cycloaracylation process for the synthesis of modern fluoroquinolones. Prakt. Chem. 335(5), 397-409 (1993).
    • (1993) Prakt. Chem. , vol.335 , Issue.5 , pp. 397-409
    • Grohe, K.1
  • 103
    • 77954662594 scopus 로고    scopus 로고
    • Bayer AG [DE]: EP-612731-A1 (1994)
    • Bayer AG [DE]: EP-612731-A1 (1994).
  • 104
    • 77954683929 scopus 로고    scopus 로고
    • Ube Industries: EP-572259-A1 (1993)
    • Ube Industries: EP-572259-A1 (1993).
  • 105
    • 77954663325 scopus 로고    scopus 로고
    • Bayer AG [DE]: EP-422485-A2 (1991)
    • Bayer AG [DE]: EP-422485-A2 (1991).
  • 106
    • 77954666014 scopus 로고    scopus 로고
    • Bayer AG [DE]: US5300643 (1994)
    • Bayer AG [DE]: US5300643 (1994).
  • 107
    • 77954682881 scopus 로고    scopus 로고
    • Bayer AG [DE]: US5300643 (1994)
    • Bayer AG [DE]: US5300643 (1994).
  • 108
    • 77954672022 scopus 로고    scopus 로고
    • Bayer AG [DE]: WO9602540 (1996)
    • Bayer AG [DE]: WO9602540 (1996).
  • 109
    • 77954683767 scopus 로고    scopus 로고
    • Bayer AG [DE]: WO9602540 (1996)
    • Bayer AG [DE]: WO9602532 (1996).
  • 110
    • 77954675451 scopus 로고    scopus 로고
    • Bayer AG [DE]: WO9602533 (1996)
    • Bayer AG [DE]: WO9602533 (1996).
  • 111
    • 77954674437 scopus 로고    scopus 로고
    • Bayer AG [DE]: WO9602511 (1996)
    • Bayer AG [DE]: WO9602511 (1996).


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.