-
1
-
-
46049096099
-
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
-
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
-
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
-
4
-
-
70350151888
-
Resistance to novel drug classes
-
Marcelin AG, Ceccherini-Silberstein F, Perno CF, Calvez V. Resistance to novel drug classes. Curr. Opin. HIV AIDS4(6), 531-537 (2009).
-
(2009)
Curr. Opin. HIV AIDS
, vol.4
, Issue.6
, pp. 531-537
-
-
Marcelin, A.G.1
Ceccherini-Silberstein, F.2
Perno, C.F.3
Calvez, V.4
-
5
-
-
3042719556
-
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
-
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
-
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
-
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
-
'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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
36
-
-
0035108610
-
3D-QSAR study of anti-HIV quinolone library
-
Filipponi E, Cruciani G, Tabarrini O, Cecchetti V, Fravolini A. 3D-QSAR study of anti-HIV quinolone library. J. Comp. Aid. Mol. Des. 15(3), 203-217 (2001).
-
(2001)
J. Comp. Aid. Mol. Des.
, vol.15
, Issue.3
, pp. 203-217
-
-
Filipponi, E.1
Cruciani, G.2
Tabarrini, O.3
Cecchetti, V.4
Fravolini, A.5
-
37
-
-
34247140849
-
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
-
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
-
39
-
-
2942720408
-
Antiviral properties of quinolone-based drugs
-
Richter S, Parolin C, Palumbo M, Palu G. Antiviral properties of quinolone-based drugs. Curr. Drug Targets Infect. Disor. 4(2), 111-116 (2004).
-
(2004)
Curr. Drug Targets Infect. Disor.
, vol.4
, Issue.2
, pp. 111-116
-
-
Richter, S.1
Parolin, C.2
Palumbo, M.3
Palu, G.4
-
40
-
-
0030995059
-
Potent and selective inhibition of human immunodeficiency virus type 1 transcription by piperazinyloxoquinoline derivatives
-
Baba M, Okamoto M, Makino M et al. Potent and selective inhibition of human immunodeficiency virus type 1 transcription by piperazinyloxoquinoline derivatives. Antimicrob. Agents Chemother. 41(6), 1250-1255 (1997). (Pubitemid 27231422)
-
(1997)
Antimicrobial Agents and Chemotherapy
, vol.41
, Issue.6
, pp. 1250-1255
-
-
Baba, M.1
Okamoto, M.2
Makino, M.3
Kimura, Y.4
Ikeuchi, T.5
Sakaguchi, T.6
Okamoto, T.7
-
41
-
-
0033231154
-
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
-
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
-
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
-
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
-
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
-
47
-
-
23944500355
-
Antiviral 6-aminoquinolones: Molecular basis for potency and selectivity
-
Richter S, Gatto B, Tabarrini O, Fravolini A, Palumbo M. Antiviral 6-aminoquinolones: molecular basis for potency and selectivity. Bioorg. Med. Chem. Lett. 15(19), 4247-4251 (2005).
-
(2005)
Bioorg. Med. Chem. Lett.
, vol.15
, Issue.19
, pp. 4247-4251
-
-
Richter, S.1
Gatto, B.2
Tabarrini, O.3
Fravolini, A.4
Palumbo, M.5
-
48
-
-
59749091271
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
68
-
-
0032515908
-
A new class of HIV-1 Tat antagonist acting through Tat-TAR inhibition
-
Hamy F, Brondani V, Florsheimer A, Stark W, Blommers MJ, Klimkait T. A new class of HIV-1 Tat antagonist acting through Tat-TAR inhibition. Biochemistry 37(15), 5086-5095 (1998).
-
(1998)
Biochemistry
, vol.37
, Issue.15
, pp. 5086-5095
-
-
Hamy, F.1
Brondani, V.2
Florsheimer, A.3
Stark, W.4
Blommers, M.J.5
Klimkait, T.6
-
69
-
-
0036008846
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
-
Bayer AG [DE]: EP-612731-A1 (1994)
-
Bayer AG [DE]: EP-612731-A1 (1994).
-
-
-
-
104
-
-
77954683929
-
-
Ube Industries: EP-572259-A1 (1993)
-
Ube Industries: EP-572259-A1 (1993).
-
-
-
-
105
-
-
77954663325
-
-
Bayer AG [DE]: EP-422485-A2 (1991)
-
Bayer AG [DE]: EP-422485-A2 (1991).
-
-
-
-
106
-
-
77954666014
-
-
Bayer AG [DE]: US5300643 (1994)
-
Bayer AG [DE]: US5300643 (1994).
-
-
-
-
107
-
-
77954682881
-
-
Bayer AG [DE]: US5300643 (1994)
-
Bayer AG [DE]: US5300643 (1994).
-
-
-
-
108
-
-
77954672022
-
-
Bayer AG [DE]: WO9602540 (1996)
-
Bayer AG [DE]: WO9602540 (1996).
-
-
-
-
109
-
-
77954683767
-
-
Bayer AG [DE]: WO9602540 (1996)
-
Bayer AG [DE]: WO9602532 (1996).
-
-
-
-
110
-
-
77954675451
-
-
Bayer AG [DE]: WO9602533 (1996)
-
Bayer AG [DE]: WO9602533 (1996).
-
-
-
-
111
-
-
77954674437
-
-
Bayer AG [DE]: WO9602511 (1996)
-
Bayer AG [DE]: WO9602511 (1996).
-
-
-
|