-
1
-
-
0032568207
-
Progress and problems in the fight against AIDS. N
-
Hirschel, B.; Francioli, P. Progress and problems in the fight against AIDS. N. Engl. J. Med., 1998, 338, 906-908.
-
(1998)
Engl. J. Med.
, vol.338
, pp. 906-908
-
-
Hirschel, B.1
Francioli, P.2
-
2
-
-
77951136077
-
Progress of Bis (heteroaryl) piperazines (BHAPs) as non-nucleoside reverse transcriptase inhibitors (NNRTIs) against human immunodeficiency virus type 1 (HIV-1)
-
Hui, Xu. Progress of Bis (heteroaryl) piperazines (BHAPs) as Non-nucleoside Reverse Transcriptase Inhibitors (NNRTIs) against Human Immunodeficiency Virus Type 1 (HIV-1). Mini. Rev. Med. Chem., 2010, 10, 62-72.
-
(2010)
Mini. Rev. Med. Chem.
, vol.10
, pp. 62-72
-
-
Hui, X.1
-
3
-
-
43049148447
-
Mechanisms of inhibition of HIV replication by non-nucleoside reverse transcriptase inhibitors
-
Sluis-Cremer, N.; Tachedjian, G. Mechanisms of inhibition of HIV replication by non-nucleoside reverse transcriptase inhibitors. Virus Res., 2008, 134, 147-156.
-
(2008)
Virus Res.
, vol.134
, pp. 147-156
-
-
Sluis-Cremer, N.1
Tachedjian, G.2
-
4
-
-
77950654271
-
Computational analysis of human immunodeficiency virus (HIV) Type-1 reverse transcriptase crystallographic models based on significant conserved residues found in Highly Active Antiretroviral Therapy (HAART)-treated patients
-
Alcaro, S.; Artese, A.; Ceccherini-Silberstein, F.; Chiarella, V.; Dimonte, S.; Ortuso, F.; Perno, C. F. Computational analysis of Human Immunodeficiency Virus (HIV) Type-1 reverse transcriptase crystallographic models based on significant conserved residues found in Highly Active Antiretroviral Therapy (HAART)-treated patients. Curr. Med. Chem., 2010, 17, 290-308.
-
(2010)
Curr. Med. Chem.
, vol.17
, pp. 290-308
-
-
Alcaro, S.1
Artese, A.2
Ceccherini-Silberstein, F.3
Chiarella, V.4
Dimonte, S.5
Ortuso, F.6
Perno, C.F.7
-
5
-
-
84871328320
-
-
http://www.fda.gov/Drugs/default.htm
-
-
-
-
6
-
-
37249019061
-
Inhibitors of HIV-1 reverse transcriptase
-
Ilina, T.; Parniak, M. A. Inhibitors of HIV-1 reverse transcriptase. Adv. Pharmacol., 2008, 56, 121-167.
-
(2008)
Adv. Pharmacol.
, vol.56
, pp. 121-167
-
-
Ilina, T.1
Parniak, M.A.2
-
7
-
-
43049106403
-
Novel HIV-1 reverse transcriptase inhibitors
-
Jochmans, D. Novel HIV-1 reverse transcriptase inhibitors. Virus Res., 2008, 134, 171-185.
-
(2008)
Virus Res.
, vol.134
, pp. 171-185
-
-
Jochmans, D.1
-
8
-
-
36749073433
-
The design of drugs for HIV and HCV
-
De Clercq, E. The design of drugs for HIV and HCV. Nat. Rev. Drug Discov., 2007, 6, 1001-1018.
-
(2007)
Nat. Rev. Drug Discov.
, vol.6
, pp. 1001-1018
-
-
De Clercq, E.1
-
9
-
-
42949177476
-
FDA approval: Etravirine
-
Sax, P. E. FDA approval: etravirine. AIDS. Clin. Care, 2008, 20, 17-18.
-
(2008)
AIDS. Clin. Care
, vol.20
, pp. 17-18
-
-
Sax, P.E.1
-
10
-
-
84871272090
-
-
Intelence (etravirine) - Important Drug Warning. 2009, Tibotec Therapeutics. http://www.fda.gov/Safety/MedWatch/SafetyInformation/ SafetyAlertsfor HumanMedicalProducts/ucm180579.htm.
-
(2009)
Tibotec Therapeutics
-
-
-
11
-
-
85014459203
-
Safety, efficacy, and pharmacokinetics of rilpivirine: Systematic review with an emphasis on resourcelimited settings
-
Ford, N.; Lee, J.; Andrieux-Meyer, I.; Calmy, A. Safety, efficacy, and pharmacokinetics of rilpivirine: systematic review with an emphasis on resourcelimited settings. HIV. AIDS., 2011, 3, 35-44.
-
(2011)
HIV. AIDS
, vol.3
, pp. 35-44
-
-
Ford, N.1
Lee, J.2
Andrieux-Meyer, I.3
Calmy, A.4
-
12
-
-
68149109726
-
Sulfanyltriazole/tetrazoles: A promising class of HIV-1 NNRTIs
-
(a) Zhan, P.; Li, Z.; Liu, X.; De Clercq, E. Sulfanyltriazole/tetrazoles: a promising class of HIV-1 NNRTIs. Mini. Rev. Med. Chem., 2009, 9, 1014-1023.
-
(2009)
Mini. Rev. Med. Chem.
, vol.9
, pp. 1014-1023
-
-
Zhan, P.1
Li, Z.2
Liu, X.3
De Clercq, E.4
-
13
-
-
79251472419
-
Recent advances in DAPYs and related analogues as HIV-1 NNRTIs
-
(b) Chen, X.; Zhan, P.; Li, D.; De Clercq, E.; Liu, X. Recent advances in DAPYs and related analogues as HIV-1 NNRTIs. Curr. Med. Chem., 2011, 18, 359-376.
-
(2011)
Curr. Med. Chem.
, vol.18
, pp. 359-376
-
-
Chen, X.1
Zhan, P.2
Li, D.3
De Clercq, E.4
Liu, X.5
-
14
-
-
84866342514
-
The development of HEPT-type HIV non-nucleoside reverse transcriptase inhibitors and its implications for DABO family
-
(c) Chen, W. M.; Zhan, P.; Wu, J. D.; Li, Z. Y.; Liu, X. Y. The development of HEPT-type HIV non-nucleoside reverse transcriptase inhibitors and its implications for DABO family. Curr. Pharm. Des., 2012, 18, 4165-4186.
-
(2012)
Curr. Pharm. Des.
, vol.18
, pp. 4165-4186
-
-
Chen, W.M.1
Zhan, P.2
Wu, J.D.3
Li, Z.Y.4
Liu, X.Y.5
-
15
-
-
84860527224
-
Recent advances in the research of 2, 3-diaryl-1, 3-thiazolidin-4-one derivatives as potent HIV-1 non-nucleoside reverse transcriptase inhibitors
-
(d) Tian, Y.; Zhan, P.; Rai, D.; Zhang, J.; De Clercq, E.; Liu, X. Recent advances in the research of 2, 3-diaryl-1, 3-thiazolidin-4-one derivatives as potent HIV-1 non-nucleoside reverse transcriptase inhibitors. Curr. Med. Chem., 2012, 19, 2026-2037.
-
(2012)
Curr. Med. Chem.
, vol.19
, pp. 2026-2037
-
-
Tian, Y.1
Zhan, P.2
Rai, D.3
Zhang, J.4
De Clercq, E.5
Liu, X.6
-
16
-
-
67349142564
-
Medicinal chemistry strategies in follow-on drug discovery
-
Zhao, H.; Guo, Z. Medicinal chemistry strategies in follow-on drug discovery. Drug Discov. Today, 2009, 14, 516-522.
-
(2009)
Drug Discov. Today
, vol.14
, pp. 516-522
-
-
Zhao, H.1
Guo, Z.2
-
17
-
-
78650811196
-
Competitiveness in follow-on drug R&D: A race or imitation?
-
DiMasi, J. A.; Faden, L. B. Competitiveness in follow-on drug R&D: a race or imitation? Nat. Rev. Drug. Discov., 2011, 10, 23-27.
-
(2011)
Nat. Rev. Drug. Discov.
, vol.10
, pp. 23-27
-
-
Di Masi, J.A.1
Faden, L.B.2
-
19
-
-
70349774254
-
Synthesis and anti-HIV activity evaluation of 2-(4-(naphthalen-2-yl)-1, 2, 3-thiadiazol-5-ylthio)-N-acetamides as novel non-nucleoside HIV-1 reverse transcriptase inhibitors
-
(a) Zhan, P.; Liu, X.; Fang, Z.; Li, Z.; Pannecouque, C.; De Clercq, E. Synthesis and anti-HIV activity evaluation of 2-(4-(naphthalen-2-yl)-1, 2, 3-thiadiazol-5-ylthio)-N-acetamides as novel non-nucleoside HIV-1 reverse transcriptase inhibitors. Eur. J. Med. Chem., 2009, 44, 4648-4653.
-
(2009)
Eur. J. Med. Chem.
, vol.44
, pp. 4648-4653
-
-
Zhan, P.1
Liu, X.2
Fang, Z.3
Li, Z.4
Pannecouque, C.5
De Clercq, E.6
-
20
-
-
68649109125
-
1, 2, 3-Selenadiazole thioacetanilides: Synthesis and anti-HIV activity evaluation
-
(b) Zhan, P.; Liu, X.; Fang, Z., Pannecouque, C.; De Clercq, E. 1, 2, 3-Selenadiazole thioacetanilides: Synthesis and anti-HIV activity evaluation. Bioorg. Med. Chem., 2009, 17, 6374-6379.
-
(2009)
Bioorg. Med. Chem.
, vol.17
, pp. 6374-6379
-
-
Zhan, P.1
Liu, X.2
Fang, Z.3
Pannecouque, C.4
De Clercq, E.5
-
21
-
-
68149145657
-
Novel 1, 2, 3-thiadiazole derivatives as HIV-1 NNRTIs with improved potency: Synthesis and preliminary SAR studies
-
(c) Zhan, P.; Liu, X.; Li, Z.; Fang, Z.; Li, Z.; Wang, D.; Pannecouque, C.; De Clercq, E. Novel 1, 2, 3-thiadiazole derivatives as HIV-1 NNRTIs with improved potency: synthesis and preliminary SAR studies. Bioorg. Med. Chem., 2009, 17, 5920-5927.
-
(2009)
Bioorg. Med. Chem.
, vol.17
, pp. 5920-5927
-
-
Zhan, P.1
Liu, X.2
Li, Z.3
Fang, Z.4
Li, Z.5
Wang, D.6
Pannecouque, C.7
De Clercq, E.8
-
22
-
-
68149089670
-
Synthesis and biological evaluation of imidazole thioacetanilides as novel non-nucleoside HIV-1 reverse transcriptase inhibitors
-
(d) Zhan, P.; Liu, X.; Zhu, J.; Fang, Z.; Li, Z.; Pannecouque, C.; De Clercq, E. Synthesis and biological evaluation of imidazole thioacetanilides as novel non-nucleoside HIV-1 reverse transcriptase inhibitors. Bioorg. Med. Chem., 2009, 17, 5775-5781.
-
(2009)
Bioorg. Med. Chem.
, vol.17
, pp. 5775-5781
-
-
Zhan, P.1
Liu, X.2
Zhu, J.3
Fang, Z.4
Li, Z.5
Pannecouque, C.6
De Clercq, E.7
-
23
-
-
53349162138
-
1, 2, 3-Thiadiazole thioacetanilides as a novel class of potent HIV-1 nonnucleoside reverse transcriptase inhibitors
-
(e) Zhan, P.; Liu, X.; Cao, Y.; Wang, Y.; Pannecouque, C.; De Clercq, E. 1, 2, 3-Thiadiazole thioacetanilides as a novel class of potent HIV-1 nonnucleoside reverse transcriptase inhibitors. Bioorg. Med. Chem. Lett., 2008, 18, 5368-5371.
-
(2008)
Bioorg. Med. Chem. Lett.
, vol.18
, pp. 5368-5371
-
-
Zhan, P.1
Liu, X.2
Cao, Y.3
Wang, Y.4
Pannecouque, C.5
De Clercq, E.6
-
24
-
-
77954695191
-
1, 2, 3-thiadiazole thioacetanilides. Part 2: Synthesis and biological evaluation of a new series of 2-{[4-(3, 4-dichlorophenyl)-1, 2, 3-thiadiazol-5-yl]sulfanyl} acetanilides as HIV-1 inhibitors
-
(e) Zhan, P.; Liu, X.; Li, Z.; Fang, Z.; Pannecouque, C.; De Clercq, E. 1, 2, 3-thiadiazole thioacetanilides. Part 2: Synthesis and biological evaluation of a new series of 2-{[4-(3, 4-dichlorophenyl)-1, 2, 3-thiadiazol-5-yl]sulfanyl} acetanilides as HIV-1 inhibitors. Chem. Biodivers., 2010, 7, 1717-1727.
-
(2010)
Chem. Biodivers.
, vol.7
, pp. 1717-1727
-
-
Zhan, P.1
Liu, X.2
Li, Z.3
Fang, Z.4
Pannecouque, C.5
De Clercq, E.6
-
25
-
-
77956478098
-
Synthesis and anti-HIV activity evaluation of novel N'-arylidene-2-[1- (naphthalen-1-yl)-1H-tetrazol-5-ylthio] acetohy drazides
-
(f) Zhan, P.; Liu, H.; Liu, X.; Wang, Y.; Pannecouque, C.; Witvrouw, M.; De Clercq, E. Synthesis and anti-HIV activity evaluation of novel N'-arylidene-2-[1-(naphthalen-1-yl)-1H-tetrazol-5-ylthio] acetohy drazides. Med. Chem. Res., 2009, 19, 652-663.
-
(2009)
Med. Chem. Res.
, vol.19
, pp. 652-663
-
-
Zhan, P.1
Liu, H.2
Liu, X.3
Wang, Y.4
Pannecouque, C.5
Witvrouw, M.6
De Clercq, E.7
-
26
-
-
80053197763
-
Arylazolylthioacetanilide. Part 8: Design, synthesis and biological evaluation of novel 2-(2-(2, 4-Dichlorophenyl)-2H-1, 2, 4-triazol-3-ylthio)-N- arylacetamides as potent HIV-1 inhibitors
-
(g) Zhan, P.; Chen, X.; Li, X.; Li, D.; Tian, Y.; Chen, W.; Pannecouque, C.; De Clercq, E.; Liu, X. Arylazolylthioacetanilide. Part 8: Design, synthesis and biological evaluation of novel 2-(2-(2, 4-Dichlorophenyl)-2H-1, 2, 4-triazol-3-ylthio)-N-arylacetamides as potent HIV-1 inhibitors. Eur. J. Med. Chem., 2011, 46, 5039-5045.
-
(2011)
Eur. J. Med. Chem.
, vol.46
, pp. 5039-5045
-
-
Zhan, P.1
Chen, X.2
Li, X.3
Li, D.4
Tian, Y.5
Chen, W.6
Pannecouque, C.7
De Clercq, E.8
Liu, X.9
-
27
-
-
84864940620
-
Arylazolyl (azinyl) thioacetanilide. Part 9: Synthesis and biological investigation of thiazolylthioacetamides derivatives as a novel class of potential antiviral agents
-
(h) Zhan, P.; Wang, L.; Liu, H.; Chen, X.; Li, X.; Jiang, X.; Zhang, Q.; Liu, X.; Pannecouque, C.; Naesens, L.; De Clercq, E.; Liu A.; Du, G. Arylazolyl (azinyl) thioacetanilide. Part 9: Synthesis and biological investigation of thiazolylthioacetamides derivatives as a novel class of potential antiviral agents. Arch. Pharm. Res., 2012, 35, 1037-1048.
-
(2012)
Arch. Pharm. Res.
, vol.35
, pp. 1037-1048
-
-
Zhan, P.1
Wang, L.2
Liu, H.3
Chen, X.4
Li, X.5
Jiang, X.6
Zhang, Q.7
Liu, X.8
Pannecouque, C.9
Naesens, L.10
De Clercq, E.11
Liu, A.12
Du, G.13
-
29
-
-
78751543528
-
Functional roles of azoles motif in anti-HIV agents
-
Zhan, P.; Li, D.; Chen, X.; Liu, X.; De Clercq, E. Functional roles of azoles motif in anti-HIV agents. Curr. Med. Chem., 2011, 18, 29-46.
-
(2011)
Curr. Med. Chem.
, vol.18
, pp. 29-46
-
-
Zhan, P.1
Li, D.2
Chen, X.3
Liu, X.4
De Clercq, E.5
-
30
-
-
0031805095
-
S-1153 inhibits replication of known drug-resistant strains of human immunodeficiency virus type 1
-
Fujiwara, T.; Sato, A.; El-Farrash, M.; Miki, S.; Abe, K.; Isaka, Y.; Kodama, M.; Wu, Y.; Chen, L. B.; Harada, H.; Sugimoto, H.; Hatanaka, M.; Hinuma, Y. S-1153 inhibits replication of known drug-resistant strains of human immunodeficiency virus type 1. Antimicrob. Agents Chemother., 1998, 42, 1340-1345.
-
(1998)
Antimicrob. Agents Chemother.
, vol.42
, pp. 1340-1345
-
-
Fujiwara, T.1
Sato, A.2
El-Farrash, M.3
Miki, S.4
Abe, K.5
Isaka, Y.6
Kodama, M.7
Wu, Y.8
Chen, L.B.9
Harada, H.10
Sugimoto, H.11
Hatanaka, M.12
Hinuma, Y.13
-
31
-
-
33646036726
-
In vitro selection of mutations in human immunodeficiency virus type 1 reverse transcriptase that confer resistance to capravirine, a novel nonnucleoside reverse transcriptase inhibitor
-
Sato, A.; Hammond, J.; Alexander, T. N.; Graham, J. P.; Binford, S.; Sugita, K.; Sugimoto, H.; Fujiwara, T.; Patick, A. K. In vitro selection of mutations in human immunodeficiency virus type 1 reverse transcriptase that confer resistance to capravirine, a novel nonnucleoside reverse transcriptase inhibitor. Antiviral Res., 2006, 70, 66-74.
-
(2006)
Antiviral Res.
, vol.70
, pp. 66-74
-
-
Sato, A.1
Hammond, J.2
Alexander, T.N.3
Graham, J.P.4
Binford, S.5
Sugita, K.6
Sugimoto, H.7
Fujiwara, T.8
Patick, A.K.9
-
32
-
-
69949092805
-
Pyrazole NNRTIs 1: Design and initial optimisation of a novel template
-
Mowbray, C. E.; Burt, C.; Corbau, R.; Perros, M.; Tran, I.; Stupple, P. A.; Webster, R.; Wood, A. Pyrazole NNRTIs 1: design and initial optimisation of a novel template. Bioorg. Med. Chem. Lett., 2009, 19, 5599-5602.
-
(2009)
Bioorg. Med. Chem. Lett.
, vol.19
, pp. 5599-5602
-
-
Mowbray, C.E.1
Burt, C.2
Corbau, R.3
Perros, M.4
Tran, I.5
Stupple, P.A.6
Webster, R.7
Wood, A.8
-
33
-
-
70450184400
-
Design strategies of novel NNRTIs to overcome drug resistance
-
Zhan, P.; Liu, X.; Li, Z.; Pannecouque, C.; De Clercq, E. Design strategies of novel NNRTIs to overcome drug resistance. Curr. Med. Chem., 2009, 16, 3903-3917.
-
(2009)
Curr. Med. Chem.
, vol.16
, pp. 3903-3917
-
-
Zhan, P.1
Liu, X.2
Li, Z.3
Pannecouque, C.4
De Clercq, E.5
-
34
-
-
3042554700
-
Metabolism and excretion of capravirine, a new non-nucleoside reverse transcriptase inhibitor, alone and in combination with ritonavir in healthy volunteers
-
Bu, H. Z.; Pool, W. F.; Wu, E. Y.; Raber, S. R.; Amantea, M. A.; Shetty, B. V. Metabolism and excretion of capravirine, a new non-nucleoside reverse transcriptase inhibitor, alone and in combination with ritonavir in healthy volunteers. Drug Metab. Dispos., 2004, 32, 689-698.
-
(2004)
Drug Metab. Dispos.
, vol.32
, pp. 689-698
-
-
Bu, H.Z.1
Pool, W.F.2
Wu, E.Y.3
Raber, S.R.4
Amantea, M.A.5
Shetty, B.V.6
-
35
-
-
0034640387
-
Binding of the second generation non-nucleoside inhibitor S-1153 to HIV-1 reverse transcriptase involves extensive main chain hydrogen bonding
-
Ren, J.; Nichols, C.; Bird, L. E.; Fujiwara, T.; Sugimoto, H.; Stuart, D. I.; Stammers, D. K. Binding of the second generation non-nucleoside inhibitor S-1153 to HIV-1 reverse transcriptase involves extensive main chain hydrogen bonding. J. Biol. Chem., 2000, 275, 14316-14320.
-
(2000)
J. Biol. Chem.
, vol.275
, pp. 14316-14320
-
-
Ren, J.1
Nichols, C.2
Bird, L.E.3
Fujiwara, T.4
Sugimoto, H.5
Stuart, D.I.6
Stammers, D.K.7
-
36
-
-
0034094041
-
Mutational analysis of trp-229 of human immunodeficiency virus type 1 reverse transcriptase (RT) identifies this amino acid residue as a prime target for the rational design of new non-nucleoside RT inhibitors
-
(a) Pelemans, H.; Esnouf, R.; De Clercq, E.; Balzarini, J. Mutational analysis of trp-229 of human immunodeficiency virus type 1 reverse transcriptase (RT) identifies this amino acid residue as a prime target for the rational design of new non-nucleoside RT inhibitors. Mol. Pharmacol., 2000, 57, 954-960.
-
(2000)
Mol. Pharmacol.
, vol.57
, pp. 954-960
-
-
Pelemans, H.1
Esnouf, R.2
De Clercq, E.3
Balzarini, J.4
-
37
-
-
28544440834
-
Specific targeting highly conserved residues in the HIV-1 reverse transcriptase primer grip region. Design, synthesis, and biological evaluation of novel, potent, and broad spectrum NNRTIs with antiviral activity
-
(b) Fattorusso, C.; Gemma, S.; Butini, S.; Huleatt, P.; Catalanotti, B.; Persico, M.; De Angelis, M.; Fiorini, I.; Nacci, V.; Ramunno, A.; Rodriquez, M.; Greco, G.; Novellino, E.; Bergamini, A.; Marini, S.; Coletta, M.; Maga, G.; Spadari, S.; Campiani, G. Specific targeting highly conserved residues in the HIV-1 reverse transcriptase primer grip region. Design, synthesis, and biological evaluation of novel, potent, and broad spectrum NNRTIs with antiviral activity. J. Med. Chem., 2005, 48, 7153-7165.
-
(2005)
J. Med. Chem.
, vol.48
, pp. 7153-7165
-
-
Fattorusso, C.1
Gemma, S.2
Butini, S.3
Huleatt, P.4
Catalanotti, B.5
Persico, M.6
De Angelis, M.7
Fiorini, I.8
Nacci, V.9
Ramunno, A.10
Rodriquez, M.11
Greco, G.12
Novellino, E.13
Bergamini, A.14
Marini, S.15
Coletta, M.16
Maga, G.17
Spadari, S.18
Campiani, G.19
-
38
-
-
64349092076
-
Specific targeting of highly conserved residues in the HIV-1 reverse transcriptase primer grip region. 2. Stereoselective interaction to overcome the effects of drug resistant mutations
-
(c) Butini, S.; Brindisi, M.; Cosconati, S.; Marinelli, L.; Borrelli, G.; Coccone, S. S.; Ramunno, A.; Campiani, G.; Novellino, E.; Zanoli, S.; Samuele, A.; Giorgi, G.; Bergamini, A.; Di Mattia, M.; Lalli, S.; Galletti, B.; Gemma, S.; Maga, G. Specific targeting of highly conserved residues in the HIV-1 reverse transcriptase primer grip region. 2. Stereoselective interaction to overcome the effects of drug resistant mutations. J. Med. Chem., 2009, 52, 1224-1228.
-
(2009)
J. Med. Chem.
, vol.52
, pp. 1224-1228
-
-
Butini, S.1
Brindisi, M.2
Cosconati, S.3
Marinelli, L.4
Borrelli, G.5
Coccone, S.S.6
Ramunno, A.7
Campiani, G.8
Novellino, E.9
Zanoli, S.10
Samuele, A.11
Giorgi, G.12
Bergamini, A.13
Di Mattia, M.14
Lalli, S.15
Galletti, B.16
Gemma, S.17
Maga, G.18
-
39
-
-
9444225975
-
Capravirine, a nonnucleoside reverse-transcriptase inhibitor in patients infected with HIV-1: A phase 1 study
-
Gewurz, B. E.; Jacobs, M.; Proper, J. A.; Dahl, T. A.; Fujiwara, T.; Dezube, B. J. Capravirine, a nonnucleoside reverse-transcriptase inhibitor in patients infected with HIV-1: a phase 1 study. J Infect Dis., 2004, 190, 1957-1961.
-
(2004)
J Infect Dis.
, vol.190
, pp. 1957-1961
-
-
Gewurz, B.E.1
Jacobs, M.2
Proper, J.A.3
Dahl, T.A.4
Fujiwara, T.5
Dezube, B.J.6
-
41
-
-
79955117649
-
-
WO2005100322
-
(b) Jones, L. H.; Mohammed, S.; Mowbray, C. E. Newman, S. D.; Selby, M. D.; Stupple, P. A.; Swain, N. A. Sulfur-linked imidazole compounds for the treatment of HIV. WO2005100322 A1, 2005.
-
(2005)
Sulfur-linked Imidazole Compounds for the Treatment of HIV
-
-
Jones, L.H.1
Mohammed, S.2
Mowbray, C.E.3
Newman, S.D.4
Selby, M.D.5
Stupple, P.A.6
Swain, N.A.7
-
45
-
-
84871321137
-
-
EP 552060
-
Sugimoto, H.; Ogata, M.; Matsumoto, H.; Sugita, K.; Sato, A.; Fujiwara, T. Imidazole derivatives having anti-HIV activity. EP 552060 A1, 1993.
-
(1993)
Imidazole Derivatives Having Anti-HIV Activity
-
-
Sugimoto, H.1
Ogata, M.2
Matsumoto, H.3
Sugita, K.4
Sato, A.5
Fujiwara, T.6
-
47
-
-
84871293694
-
-
WO02068395
-
De Clercq, E.; Van Aerschot, A.; Herdewijn, P.; Lagoja, I.; Pannecoucque, Christophe. Preparation and use of N-aminoimidazole derivatives as HIV inhibitors. WO02068395 A1, 2002.
-
(2002)
Pannecoucque, Christophe. Preparation and use of N-aminoimidazole Derivatives as HIV Inhibitors
-
-
De Clercq, E.1
Van Aerschot, A.2
Herdewijn, P.3
Lagoja, I.4
-
49
-
-
84871272110
-
-
WO02085860
-
Jones, L. H.; Mowbray, C. E.; Price, D. A.; Selby, M. D.; Stupple, P. A. Pyrazole Derivatives for Treating HIV. WO02085860 A1, 2002.
-
(2002)
Pyrazole Derivatives for Treating HIV
-
-
Jones, L.H.1
Mowbray, C.E.2
Price, D.A.3
Selby, M.D.4
Stupple, P.A.5
-
52
-
-
3042840833
-
-
WO0204424
-
Corbau, R. G.; Mowbray, C. E.; Perros, M.; Stupple, P. A.; Wood, A. Pyrazole Derivatives. WO0204424 A1, 2001.
-
(2001)
Pyrazole Derivatives
-
-
Corbau, R.G.1
Mowbray, C.E.2
Perros, M.3
Stupple, P.A.4
Wood, A.5
-
53
-
-
84871317601
-
-
WO0202524
-
Dymock, B.; Jones, P.; Merrett, J.; Parkes, K.; Parrratt, M. Pyrrole Derivatives for Treating AIDS. WO0202524 A1, 2002.
-
(2002)
Pyrrole Derivatives for Treating AIDS
-
-
Dymock, B.1
Jones, P.2
Merrett, J.3
Parkes, K.4
Parrratt, M.5
-
55
-
-
11844255399
-
Bioisosterism: A useful strategy for molecular modification and drug design
-
Lima, L. M.; Barreiro, E. J. Bioisosterism: a useful strategy for molecular modification and drug design. Curr. Med. Chem., 2005, 12, 23-49.
-
(2005)
Curr. Med. Chem.
, vol.12
, pp. 23-49
-
-
Lima, L.M.1
Barreiro, E.J.2
-
56
-
-
20344382272
-
Synthesis of 2-(aminocarbonylmethylthio)-1H-imidazoles as novel Capravirine analogues
-
Loksha, Y. M.; El-Barbary, A. A.; El-Badawi, M. A.; Nielsen, C.; Pedersen, E. B. Synthesis of 2-(aminocarbonylmethylthio)-1H-imidazoles as novel Capravirine analogues. Bioorg. Med. Chem., 2005, 13, 4209-4220.
-
(2005)
Bioorg. Med. Chem.
, vol.13
, pp. 4209-4220
-
-
Loksha, Y.M.1
El-Barbary, A.A.2
El-Badawi, M.A.3
Nielsen, C.4
Pedersen, E.B.5
-
57
-
-
70349214797
-
Pyrazole NNRTIs 4: Selection of UK-453, 061 (lersivirine) as a development candidate
-
Mowbray, C. E.; Burt, C.; Corbau, R.; Gayton, S.; Hawes, M.; Perros, M.; Tran, I.; Price, D. A.; Quinton, F. J.; Selby, M. D.; Stupple, P. A.; Webster, R.; Wood, A. Pyrazole NNRTIs 4: selection of UK-453, 061 (lersivirine) as a development candidate. Bioorg. Med. Chem. Lett., 2009, 19, 5857-5860.
-
(2009)
Bioorg. Med. Chem. Lett.
, vol.19
, pp. 5857-5860
-
-
Mowbray, C.E.1
Burt, C.2
Corbau, R.3
Gayton, S.4
Hawes, M.5
Perros, M.6
Tran, I.7
Price, D.A.8
Quinton, F.J.9
Selby, M.D.10
Stupple, P.A.11
Webster, R.12
Wood, A.13
-
58
-
-
69949108856
-
Pyrazole NNRTIs 3: Optimisation of physicochemical properties
-
(a) Mowbray, C. E.; Corbau, R.; Hawes, M.; Jones, L. H.; Mills, J. E.; Perros, M.; Selby, M. D.; Stupple, P. A.; Webster, R.; Wood, A. Pyrazole NNRTIs 3: optimisation of physicochemical properties. Bioorg. Med. Chem. Lett., 2009, 19, 5603-5606.
-
(2009)
Bioorg. Med. Chem. Lett.
, vol.19
, pp. 5603-5606
-
-
Mowbray, C.E.1
Corbau, R.2
Hawes, M.3
Jones, L.H.4
Mills, J.E.5
Perros, M.6
Selby, M.D.7
Stupple, P.A.8
Webster, R.9
Wood, A.10
-
59
-
-
77950922576
-
Activity, pharmacokinetics and safety of lersivirine (UK-453, 061), a next-generation nonnucleoside reverse transcriptase inhibitor, during 7-day monotherapy in HIV-1-infected patients
-
(b) Fätkenheuer, G.; Staszewski, S.; Plettenburg, A.; Hackman, F.; Layton, G.; McFadyen, L.; Davis, J.; Jenkins, T. M. Activity, pharmacokinetics and safety of lersivirine (UK-453, 061), a next-generation nonnucleoside reverse transcriptase inhibitor, during 7-day monotherapy in HIV-1-infected patients. AIDS., 2009, 23, 2115-2122.
-
(2009)
AIDS
, vol.23
, pp. 2115-2122
-
-
Fätkenheuer, G.1
Staszewski, S.2
Plettenburg, A.3
Hackman, F.4
Layton, G.5
McFadyen, L.6
Davis, J.7
Jenkins, T.M.8
-
60
-
-
77957370457
-
Lersivirine: A non-nucleoside reverse transcriptase inhibitor with activity against drug-resistant human immunodeficiency virus-1
-
(c) Corbau, R.; Mori, J.; Phillips, C.; Fishburn, L.; Martin, A.; Mowbray, C.; Panton, W.; Smith-Burchnell, C.; Thornberry, A.; Ringrose, H.; Knöchel, T.; Irving, S.; Westby, M.; Wood, A.; Perros, M. Lersivirine: a Non-Nucleoside Reverse Transcriptase Inhibitor with Activity against Drug-Resistant Human Immunodeficiency Virus-1. Antimicrob. Agents Chemother., 2010, 54, 4451-4463.
-
(2010)
Antimicrob. Agents Chemother.
, vol.54
, pp. 4451-4463
-
-
Corbau, R.1
Mori, J.2
Phillips, C.3
Fishburn, L.4
Martin, A.5
Mowbray, C.6
Panton, W.7
Smith-Burchnell, C.8
Thornberry, A.9
Ringrose, H.10
Knöchel, T.11
Irving, S.12
Westby, M.13
Wood, A.14
Perros, M.15
-
61
-
-
33846262498
-
Arylthiopyrrole (AThP) derivatives as non-nucleoside HIV-1 reverse transcriptaseinhibitors: Synthesis, structureactivity relationships, and docking studies (part 1)
-
(a) Di Santo, R.; Costi, R.; Artico, M.; Miele, G.; Lavecchia, A.; Novellino, E.; Bergamini, A.; Cancio, R.; Maga, G. Arylthiopyrrole (AThP) derivatives as non-nucleoside HIV-1 reverse transcriptaseinhibitors: Synthesis, structureactivity relationships, and docking studies (part 1). Chem. Med. Chem., 2006, 1, 1367-1378.
-
(2006)
Chem. Med. Chem.
, vol.1
, pp. 1367-1378
-
-
Di Santo, R.1
Costi, R.2
Artico, M.3
Miele, G.4
Lavecchia, A.5
Novellino, E.6
Bergamini, A.7
Cancio, R.8
Maga, G.9
-
62
-
-
33846214344
-
Arylthiopyrrole (AThP) derivatives as non-nucleoside HIV-1reverse transcriptase inhibitors: Synthesis, structure-activity relationships, and docking studies (part 2)
-
(b) Lavecchia, A.; Costi, R.; Artico, M.; Miele, G.; Novellino, E.; Bergamini, A.; Crespan, E.; Maga, G.; Di Santo, R. Arylthiopyrrole (AThP) derivatives as non-nucleoside HIV-1reverse transcriptase inhibitors: Synthesis, structure-activity relationships, and docking studies (part 2). Chem. Med. Chem., 2006, 1, 1379-1390
-
(2006)
Chem. Med. Chem.
, vol.1
, pp. 1379-1390
-
-
Lavecchia, A.1
Costi, R.2
Artico, M.3
Miele, G.4
Novellino, E.5
Bergamini, A.6
Crespan, E.7
Maga, G.8
Di Santo, R.9
-
63
-
-
38749122085
-
Triazole derivatives as non-nucleoside inhibitors of HIV-1 reverse transcriptase-structure activity relationships and crystallographic analysis
-
Kirschberg, T. A.; Balakrishnan, M.; Huang, W.; Hluhanich, R.; Kutty, N.; Liclican, A. C.; McColl, D. J.; Squires, N. H.; Lansdon, E. B. Triazole derivatives as non-nucleoside inhibitors of HIV-1 reverse transcriptase- structure activity relationships and crystallographic analysis. Bioorg. Med. Chem. Lett., 2008, 18, 1131-1134.
-
(2008)
Bioorg. Med. Chem. Lett.
, vol.18
, pp. 1131-1134
-
-
Kirschberg, T.A.1
Balakrishnan, M.2
Huang, W.3
Hluhanich, R.4
Kutty, N.5
Liclican, A.C.6
McColl, D.J.7
Squires, N.H.8
Lansdon, E.B.9
-
64
-
-
34547484265
-
Molecular hybridization: A useful tool in the design of new drug prototypes
-
Viegas-Junior, C.; Danuello, A.; Da Silva Bolzani, V.; Barreiro, E. J.; Fraga, C. A. Molecular hybridization: A useful tool in the design of new drug prototypes. Curr. Med. Chem., 2007, 14, 1829-1852.
-
(2007)
Curr. Med. Chem.
, vol.14
, pp. 1829-1852
-
-
Viegas Jr., C.1
Danuello, A.2
Da Silva Bolzani, V.3
Barreiro, E.J.4
Fraga, C.A.5
-
65
-
-
0347129832
-
A highly potent nonnucleoside adenosine deaminase inhibitor: Efficient drug discovery by intentional lead hybridization
-
Terasaka, T.; Kinoshita, T.; Kuno, M.; Nakanishi, I. A highly potent nonnucleoside adenosine deaminase inhibitor: Efficient drug discovery by intentional lead hybridization. J. Am. Chem. Soc., 2004, 126, 34-35.
-
(2004)
J. Am. Chem. Soc.
, vol.126
, pp. 34-35
-
-
Terasaka, T.1
Kinoshita, T.2
Kuno, M.3
Nakanishi, I.4
-
66
-
-
79955455754
-
Diarylpyrimidinedihydrobenzyloxopyrimidine hybrids: New, wide-spectrum anti-HIV-1 agents active at (sub)-nanomolar level
-
Rotili, D.; Tarantino, D.; Artico, M.; Nawrozkij, M. B.; Gonzalez-Ortega, E.; Clotet, B.; Samuele, A.; Este, J. A.; Maga, G.; Mai, A. Diarylpyrimidinedihydrobenzyloxopyrimidine hybrids: new, wide-spectrum anti-HIV-1 agents active at (sub)-nanomolar level. J. Med. Chem., 2011, 54, 3091-3096.
-
(2011)
J. Med. Chem.
, vol.54
, pp. 3091-3096
-
-
Rotili, D.1
Tarantino, D.2
Artico, M.3
Nawrozkij, M.B.4
Gonzalez-Ortega, E.5
Clotet, B.6
Samuele, A.7
Este, J.A.8
Maga, G.9
Mai, A.10
-
67
-
-
64349086788
-
Novel indazole nonnucleoside reverse transcriptase inhibitors using molecular hybridization based on crystallographic overlays
-
Jones, L. H.; Allan, G.; Barba, O.; Burt, C.; Corbau, R.; Dupont, T.; Knöchel, T.; Irving, S.; Middleton, D. S.; Mowbray, C. E.; Perros, M.; Ringrose, H.; Swain, N. A.; Webster, R.; Westby, M.; Phillips, C. Novel indazole nonnucleoside reverse transcriptase inhibitors using molecular hybridization based on crystallographic overlays. J. Med. Chem., 2009, 52, 1219-1223.
-
(2009)
J. Med. Chem.
, vol.52
, pp. 1219-1223
-
-
Jones, L.H.1
Allan, G.2
Barba, O.3
Burt, C.4
Corbau, R.5
Dupont, T.6
Knöchel, T.7
Irving, S.8
Middleton, D.S.9
Mowbray, C.E.10
Perros, M.11
Ringrose, H.12
Swain, N.A.13
Webster, R.14
Westby, M.15
Phillips, C.16
-
68
-
-
24944473828
-
Synthesis, anti-HIV activity, and metabolic stability of new alkenyldiarylmethane HIV-1 non-nucleoside reverse transcriptase inhibitors
-
Deng, B. L.; Hartman, T. L.; Buckheit, R. W.; Jr Pannecouque, C.; De Clercq, E.; Fanwick, P. E.; Cushman, M. Synthesis, anti-HIV activity, and metabolic stability of new alkenyldiarylmethane HIV-1 non-nucleoside reverse transcriptase inhibitors. J. Med. Chem., 2005, 48, 6140-6155.
-
(2005)
J. Med. Chem.
, vol.48
, pp. 6140-6155
-
-
Deng, B.L.1
Hartman, T.L.2
Buckheit Jr., R.W.3
Pannecouque, C.4
De Clercq, E.5
Fanwick, P.E.6
Cushman, M.7
-
69
-
-
33747593758
-
Replacement of the metabolically labile methyl esters in the alkenyldiarylmethane series of nonnucleosidereverse transcriptase inhibitors with isoxazolone, isoxazole, oxazolone, or cyano substituents
-
Deng B. L.; Hartman, T. L.; Buckheit, R. W.; Jr Pannecouque, C.; De Clercq, E.; Cushman, M. Replacement of the metabolically labile methyl esters in the alkenyldiarylmethane series of nonnucleosidereverse transcriptase inhibitors with isoxazolone, isoxazole, oxazolone, or cyano substituents. J. Med. Chem., 2006, 49, 5316-5323.
-
(2006)
J. Med. Chem.
, vol.49
, pp. 5316-5323
-
-
Deng, B.L.1
Hartman, T.L.2
Buckheit Jr., R.W.3
Pannecouque, C.4
De Clercq, E.5
Cushman, M.6
-
70
-
-
55949106137
-
Optimization of 5-aryloxyimidazole nonnucleoside reverse transcriptase inhibitors
-
Jones, L. H.; Allan, G.; Corbau, R.; Hay, D.; Middleton, D. S.; Mowbray, C. E.; Newman, S. D.; Perros, M.; Randall, A.; Vuong, H.; Webster, R.; Westby, M.; Williams, D. Optimization of 5-aryloxyimidazole nonnucleoside reverse transcriptase inhibitors. Chem. Med. Chem., 2008, 3, 1756-1762.
-
(2008)
Chem. Med. Chem.
, vol.3
, pp. 1756-1762
-
-
Jones, L.H.1
Allan, G.2
Corbau, R.3
Hay, D.4
Middleton, D.S.5
Mowbray, C.E.6
Newman, S.D.7
Perros, M.8
Randall, A.9
Vuong, H.10
Webster, R.11
Westby, M.12
Williams, D.13
-
71
-
-
24944549193
-
Advances in prodrug design
-
Silva, A. T.; Chung, M. C.; Castro, L. F.; Güido, R. V.; Ferreira, E. I. Advances in prodrug design. Mini. Rev. Med. Chem., 2005, 5, 893-914.
-
(2005)
Mini. Rev. Med. Chem.
, vol.5
, pp. 893-914
-
-
Silva, A.T.1
Chung, M.C.2
Castro, L.F.3
Güido, R.V.4
Ferreira, E.I.5
-
72
-
-
2342481809
-
Lessons learned from marketedand investigational prodrugs
-
Ettmayer, P.; Amidon, G. L.; Clement, B.; Testa, B. Lessons learned from marketedand investigational prodrugs. J. Med. Chem., 2004, 47, 2393-2404.
-
(2004)
J. Med. Chem.
, vol.47
, pp. 2393-2404
-
-
Ettmayer, P.1
Amidon, G.L.2
Clement, B.3
Testa, B.4
-
73
-
-
44449140547
-
-
WO 03091264
-
Chen, J. M.; Chen, X.; Kim, C. U.; Lee, W. A.; Tario, J. D.; Xu, L.; Nelson, P. H. Non-nucleoside reverse transcriptase inhibitors. WO 03091264 A1, 2003.
-
(2003)
Non-nucleoside Reverse Transcriptase Inhibitors
-
-
Chen, J.M.1
Chen, X.2
Kim, C.U.3
Lee, W.A.4
Tario, J.D.5
Xu, L.6
Nelson, P.H.7
-
74
-
-
0034681683
-
The nobel chronicles. 1988: James Whyte Black, (b 1924), Gertrude Elion (1918-99), and George H Hitchings (1905-98)
-
Raju, T. N. The Nobel chronicles. 1988: James Whyte Black, (b 1924), Gertrude Elion (1918-99), and George H Hitchings (1905-98). Lancet, 2000, 355, 1022.
-
(2000)
Lancet
, vol.355
, pp. 1022
-
-
Raju, T.N.1
-
75
-
-
84876852661
-
HIV-1 NNRTIs: Structural diversity, pharmacophore similarity, and implications for drug design
-
doi: 10.1002/med.20241
-
Zhan, P.; Chen, X.; Li, D.; Fang, Z.; De Clercq, E.; Liu, X. HIV-1 NNRTIs: Structural diversity, pharmacophore similarity, and implications for drug design. Med. Res. Rev., 2011, doi: 10.1002/med.20241.
-
(2011)
Med. Res. Rev.
-
-
Zhan, P.1
Chen, X.2
Li, D.3
Fang, Z.4
De Clercq, E.5
Liu, X.6
-
76
-
-
0036706746
-
A comparison of the pharmacophore identification programs: Catalyst, DISCO and GASP
-
Patel, Y.; Gillet, V. J.; Bravi, G.; Leach, A. R. A comparison of the pharmacophore identification programs: Catalyst, DISCO and GASP. J. Comput. Aided. Mol. Des., 2002, 16, 653-681.
-
(2002)
J. Comput. Aided. Mol. Des.
, vol.16
, pp. 653-681
-
-
Patel, Y.1
Gillet, V.J.2
Bravi, G.3
Leach, A.R.4
-
77
-
-
0032818587
-
Estimation of active conformations of drugs by a new molecular superposing procedure
-
Iwase, K.; Hirono, S. Estimation of active conformations of drugs by a new molecular superposing procedure. J. Comput. Aided Mol. Des., 1999, 13, 499-512.
-
(1999)
J. Comput. Aided Mol. Des.
, vol.13
, pp. 499-512
-
-
Iwase, K.1
Hirono, S.2
-
78
-
-
1042279567
-
A pharmacophore docking algorithm and its application to the cross-docking of 18 HIV-NNRTI's in their binding pockets
-
(a) Daeyaert, F.; Walczak, B.; Xu, Q. S.; Daeyaert, F.; De Jonge, M. R.; Heeres, J.; Koymans, L. M.; Lewi, P. J.; Vinkers, H. M.; Janssen, P. A. Massart, D. L. A pharmacophore docking algorithm and its application to the cross-docking of 18 HIV-NNRTI's in their binding pockets. Proteins, 2004, 54, 526-533
-
(2004)
Proteins
, vol.54
, pp. 526-533
-
-
Daeyaert, F.1
Walczak, B.2
Xu, Q.S.3
Daeyaert, F.4
De Jonge, M.R.5
Heeres, J.6
Koymans, L.M.7
Lewi, P.J.8
Vinkers, H.M.9
Janssen, P.A.10
Massart, D.L.11
-
79
-
-
11144355186
-
Classification and regression trees-studies of HIV reverse transcriptase inhibitors
-
(b) Daeyaert, F.; Walczak, B.; Xu, Q. S.; Daeyaert, F.; De Jonge, M. R.; Heeres, J.; Koymans, L. M.; Lewi, P. J.; Vinkers, H. M.; Janssen, P. A. Massart, D. L. Classification and regression trees-studies of HIV reverse transcriptase inhibitors. J. Chem. Inf. Comput. Sci., 2004, 44, 716-726.
-
(2004)
J. Chem. Inf. Comput. Sci.
, vol.44
, pp. 716-726
-
-
Daeyaert, F.1
Walczak, B.2
Xu, Q.S.3
Daeyaert, F.4
De Jonge, M.R.5
Heeres, J.6
Koymans, L.M.7
Lewi, P.J.8
Vinkers, H.M.9
Janssen, P.A.10
Massart, D.L.11
-
80
-
-
4544265135
-
Conformational changes in HIV-1 reverse transcriptase induced by nonnucleoside reverse transcriptase inhibitor binding
-
Sluis-Cremer, N.; Temiz, N. A.; Bahar, I. Conformational changes in HIV-1 reverse transcriptase induced by nonnucleoside reverse transcriptase inhibitor binding. Curr. HIV. Res., 2004, 2, 323-32.
-
(2004)
Curr. HIV. Res.
, vol.2
, pp. 323-332
-
-
Sluis-Cremer, N.1
Temiz, N.A.2
Bahar, I.3
-
81
-
-
0030935265
-
Unique features in the structure of the complex between HIV-1 reverse transcriptase and the bis (heteroaryl) piperazine (BHAP) U-90152 explain resistance mutations for this nonnucleoside inhibitor
-
Esnouf, R. M.; Ren, J.; Hopkins, A. L.; Ross, C. K.; Jones, E. Y.; Stammers, D. K.; Stuart, D. I. Unique features in the structure of the complex between HIV-1 reverse transcriptase and the bis (heteroaryl) piperazine (BHAP) U-90152 explain resistance mutations for this nonnucleoside inhibitor. Proc. Natl. Acad. Sci. USA., 1997, 94, 3984-3989.
-
(1997)
Proc. Natl. Acad. Sci. USA
, vol.94
, pp. 3984-3989
-
-
Esnouf, R.M.1
Ren, J.2
Hopkins, A.L.3
Ross, C.K.4
Jones, E.Y.5
Stammers, D.K.6
Stuart, D.I.7
-
82
-
-
36749018204
-
Privileged structures: A useful concept for the rational design of new lead drug candidates
-
Duarte, CD.; Barreiro, E. J.; Fraga, C. A. Privileged structures: a useful concept for the rational design of new lead drug candidates. Mini. Rev. Med. Chem., 2007, 7, 1108-1119.
-
(2007)
Mini. Rev. Med. Chem.
, vol.7
, pp. 1108-1119
-
-
Duarte, C.D.1
Barreiro, E.J.2
Fraga, C.A.3
-
83
-
-
33846694819
-
Scaffold selection and scaffold hopping in lead generation: A medicinal chemistry perspective
-
Zhao, H. Scaffold selection and scaffold hopping in lead generation: a medicinal chemistry perspective. Drug Discov. Today, 2007, 12, 149-155.
-
(2007)
Drug Discov. Today
, vol.12
, pp. 149-155
-
-
Zhao, H.1
-
84
-
-
76649108538
-
N1-Heterocyclic pyrimidinediones as nonnucleoside inhibitors of HIV-1 reverse transcriptase
-
Mitchell, M. L.; Son, J. C.; Lee, I. Y.; Lee, C. K.; Kim, H. S.; Wang, J.; Hayes, J.; Wang, M.; Paul, A.; Lansdon, E. B.; Chen, J. M.; Eisenberg, G.; Geleziunas, R.; Xu, L.; Kim, C. U. N1-Heterocyclic pyrimidinediones as nonnucleoside inhibitors of HIV-1 reverse transcriptase. Bioorg. Med. Chem. Lett, 2010, 20, 1585-1588.
-
(2010)
Bioorg. Med. Chem. Lett
, vol.20
, pp. 1585-1588
-
-
Mitchell, M.L.1
Son, J.C.2
Lee, I.Y.3
Lee, C.K.4
Kim, H.S.5
Wang, J.6
Hayes, J.7
Wang, M.8
Paul, A.9
Lansdon, E.B.10
Chen, J.M.11
Eisenberg, G.12
Geleziunas, R.13
Xu, L.14
Kim, C.U.15
-
85
-
-
77953872635
-
Discovery of piperidin-4-yl-aminopyrimidines as HIV-1 reverse transcriptase inhibitors. N-Benzyl derivatives with broad potency against resistant mutant viruses
-
(a) Kertesz, D. J.; Brotherton-Pleiss, C.; Yang, M.; Wang, Z.; Lin, X.; Qiu, Z.; Hirschfeld, D. R.; Gleason, S.; Mirzadegan, T.; Dunten, P. W.; Harris, S. F.; Villaseñ, A. G.; Hang, J. Q.; Heilek, G. M.; Klumpp, K. Discovery of piperidin-4-yl-aminopyrimidines as HIV-1 reverse transcriptase inhibitors. N-Benzyl derivatives with broad potency against resistant mutant viruses. Bioorg. Med. Chem. Lett, 2010, 20, 4215-4218.
-
(2010)
Bioorg. Med. Chem. Lett
, vol.20
, pp. 4215-4218
-
-
Kertesz, D.J.1
Brotherton-Pleiss, C.2
Yang, M.3
Wang, Z.4
Lin, X.5
Qiu, Z.6
Hirschfeld, D.R.7
Gleason, S.8
Mirzadegan, T.9
Dunten, P.W.10
Harris, S.F.11
Villaseñ, A.G.12
Hang, J.Q.13
Heilek, G.M.14
Klumpp, K.15
-
86
-
-
77956908369
-
Exploration of piperidin-4-yl-aminopyrimidines as HIV-1 reverse transcriptase inhibitors. N-Phenyl derivatives with broad potency against resistant mutant viruses
-
(b) Tang, G.; Kertesz, D. J.; Yang, M.; Lin, X.; Wang, Z.; Li, W.; Qiu, Z.; Chen, J.; Mei, J.; Chen, L.; Mirzadegan, T.; Harris, S. F.; Villaseñ, A. G.; Fretland, J.; Fitch, W. L.; Hang, J. Q.; Heilek, G.; Klumpp, K. Exploration of piperidin-4-yl-aminopyrimidines as HIV-1 reverse transcriptase inhibitors. N-Phenyl derivatives with broad potency against resistant mutant viruses. Bioorg. Med. Chem. Lett. 2010, 20, 6020-6023.
-
(2010)
Bioorg. Med. Chem. Lett.
, vol.20
, pp. 6020-6023
-
-
Tang, G.1
Kertesz, D.J.2
Yang, M.3
Lin, X.4
Wang, Z.5
Li, W.6
Qiu, Z.7
Chen, J.8
Mei, J.9
Chen, L.10
Mirzadegan, T.11
Harris, S.F.12
Villaseñ, A.G.13
Fretland, J.14
Fitch, W.L.15
Hang, J.Q.16
Heilek, G.17
Klumpp, K.18
-
87
-
-
79952524156
-
Synthesis and biological activity of new pyridone diaryl ether non-nucleoside inhibitors of HIV-1 reverse transcriptase
-
Kennedy-Smith, J. J.; Arora, N.; Roland Billedeau, J.; Fretland, J.; Hang, J. Q.; Heilek, G. M.; Harris, S. F.; Hirschfeld, D.; Javanbakht, H.; Li, Y.; Liang, W.; Roetz, R.; Smith, M.; Su, G.; Suh, J. M.; Villasenor, A. G.; Wu, J.; Yasuda, D.; Klumpp, K.; Sweeney, Z. K. Synthesis and biological activity of new pyridone diaryl ether non-nucleoside inhibitors of HIV-1 reverse transcriptase. Med. Chem. Commun., 2010, 1, 79-83.
-
(2010)
Med. Chem. Commun.
, vol.1
, pp. 79-83
-
-
Kennedy-Smith, J.J.1
Arora, N.2
Roland Billedeau, J.3
Fretland, J.4
Hang, J.Q.5
Heilek, G.M.6
Harris, S.F.7
Hirschfeld, D.8
Javanbakht, H.9
Li, Y.10
Liang, W.11
Roetz, R.12
Smith, M.13
Su, G.14
Suh, J.M.15
Villasenor, A.G.16
Wu, J.17
Yasuda, D.18
Klumpp, K.19
Sweeney, Z.K.20
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