-
1
-
-
0024832408
-
Highly specific inhibition of human immunodeficiency virus type 1 by a novel 6-substituted acyclouridine derivative
-
Baba, M.; Tanaka, H.; De Clercq, E.; Pauwels, R.; Balzarini, J.; Schols, D.; Nakashima, H.; Perno, C. F.; Walker, R. T.; Miyasaka, T. Highly specific inhibition of human immunodeficiency virus type 1 by a novel 6-substituted acyclouridine derivative. Biochem Biophys Res Commun. 1989, 165, 1375-1381.
-
(1989)
Biochem. Biophys. Res. Commun.
, vol.165
, pp. 1375-1381
-
-
Baba, M.1
Tanaka, H.2
De Clercq, E.3
Pauwels, R.4
Balzarini, J.5
Schols, D.6
Nakashima, H.7
Perno, C.F.8
Walker, R.T.9
Miyasaka, T.10
-
2
-
-
0025014499
-
Potent and selective inhibition of HIV-1 replication in vitro by a novel series of TIBO derivatives
-
Pauwels, R.; Andries, K.; Desmyter, J.; Schols, D.; Kukla, M. J.; Breslin, H. J.; Raeymaeckers, A.; Van Gelder, J.; Woestenborghs, R.; Heykants, J.; Schellekens, K.; Janssen, M. A. C.; De Clercq, E.; Janssen, P. A. J. Potent and selective inhibition of HIV-1 replication in vitro by a novel series of TIBO derivatives. Nature 1990, 343, 470-474.
-
(1990)
Nature
, vol.343
, pp. 470-474
-
-
Pauwels, R.1
Andries, K.2
Desmyter, J.3
Schols, D.4
Kukla, M.J.5
Breslin, H.J.6
Raeymaeckers, A.7
Van Gelder, J.8
Woestenborghs, R.9
Heykants, J.10
Schellekens, K.11
Janssen, M.A.C.12
De Clercq, E.13
Janssen, P.A.J.14
-
3
-
-
0025679303
-
Inhibition of HIV-1 replication by a nonnucleoside reverse transcriptase inhibitor
-
Merluzzi, V. J.; Hargrave, K. D.; Labadia, M.; Grozinger, K.; Skoog, M.; Wu, J. C.; Shih, C. K.; Eckner, K.; Hattox, S.; Adams, J.; Rosenthal, A. S.; Faanes, R.; Eckner, R. J.; Koup, R. A.; Sullivan, J. L. Inhibition of HIV-1 replication by a nonnucleoside reverse transcriptase inhibitor. Science 1990, 250, 1411-1413.
-
(1990)
Science
, vol.250
, pp. 1411-1413
-
-
Merluzzi, V.J.1
Hargrave, K.D.2
Labadia, M.3
Grozinger, K.4
Skoog, M.5
Wu, J.C.6
Shih, C.K.7
Eckner, K.8
Hattox, S.9
Adams, J.10
Rosenthal, A.S.11
Faanes, R.12
Eckner, R.J.13
Koup, R.A.14
Sullivan, J.L.15
-
4
-
-
12144265244
-
Nonnucleoside reverse transcriptase inhibitors (NNRTIs): Past, present, future
-
De Clercq, E. Nonnucleoside reverse transcriptase inhibitors (NNRTIs): Past, present, future. Chem. Biodiversity 2004, 1, 44-64.
-
(2004)
Chem. Biodiversity
, vol.1
, pp. 44-64
-
-
De Clercq, E.1
-
5
-
-
2942524068
-
Current status of the non-nucleoside reverse transcriptase inhibitors of human immunodeficiency virus type 1
-
Balzarini, J. Current status of the non-nucleoside reverse transcriptase inhibitors of human immunodeficiency virus type 1. Curr. Top. Med. Chem. 2004, 4, 921-944.
-
(2004)
Curr. Top. Med. Chem.
, vol.4
, pp. 921-944
-
-
Balzarini, J.1
-
6
-
-
0034899570
-
Non-nucleoside reverse transcriptase inhibitors: Perspectives on novel therapeutic compounds and strategies for the treatment of HIV infection
-
Buckheit, R. W. Non-nucleoside reverse transcriptase inhibitors: perspectives on novel therapeutic compounds and strategies for the treatment of HIV infection. Expert Opin. Investig. Drugs 2001, 10, 1423-1442.
-
(2001)
Expert Opin. Investig. Drugs
, vol.10
, pp. 1423-1442
-
-
Buckheit, R.W.1
-
7
-
-
15444370583
-
New non-nucleoside reverse transcriptase inhibitors (NNRTIs) in development for the treatment of HIV infections
-
Pauwels, R. New non-nucleoside reverse transcriptase inhibitors (NNRTIs) in development for the treatment of HIV infections. Curr. Opin. Pharmacol. 2004, 4, 437-446.
-
(2004)
Curr. Opin. Pharmacol.
, vol.4
, pp. 437-446
-
-
Pauwels, R.1
-
8
-
-
0028924567
-
Mechanism of inhibition of HIV-1 reverse transcriptase by nonnucleoside inhibitors
-
Esnouf, R.; Ren, J.; Ross, C.; Jones, Y.; Stammers, D.; Stuart, D. Mechanism of inhibition of HIV-1 reverse transcriptase by nonnucleoside inhibitors. Nat. Struct. Biol. 1995, 2, 303-308.
-
(1995)
Nat. Struct. Biol.
, vol.2
, pp. 303-308
-
-
Esnouf, R.1
Ren, J.2
Ross, C.3
Jones, Y.4
Stammers, D.5
Stuart, D.6
-
9
-
-
0028842293
-
The structure of unliganded reverse transcriptase from the human immunodeficiency virus type 1
-
Rodgers, D. W.; Gamblin, S. J.; Harris, B. A.; Ray, S.; Culp, J. S.; Hellmig, B.; Woolf, D. J.; Debouck, C.; Harrison, S. C. The structure of unliganded reverse transcriptase from the human immunodeficiency virus type 1. Proc. Natl. Acad. Sci. U.S.A. 1995, 92, 1222-1226.
-
(1995)
Proc. Natl. Acad. Sci. U.S.A.
, vol.92
, pp. 1222-1226
-
-
Rodgers, D.W.1
Gamblin, S.J.2
Harris, B.A.3
Ray, S.4
Culp, J.S.5
Hellmig, B.6
Woolf, D.J.7
Debouck, C.8
Harrison, S.C.9
-
10
-
-
0030586090
-
Structure of unliganded HIV-1 reverse transcriptase at 2.7 Å resolution: Implications of conformational changes for polymerization and inhibition mechanisms
-
Hsiou, Y.; Ding J.; Das K.; Clark, A. D., Jr.; Hughes, S. H.; Arnold, E. Structure of unliganded HIV-1 reverse transcriptase at 2.7 Å resolution: implications of conformational changes for polymerization and inhibition mechanisms. Structure 1996, 4, 853-860.
-
(1996)
Structure
, vol.4
, pp. 853-860
-
-
Hsiou, Y.1
Ding, J.2
Das, K.3
Clark Jr., A.D.4
Hughes, S.H.5
Arnold, E.6
-
11
-
-
0026693137
-
Crystal structure at 3.5 Å resolution of HIV-1 reverse transcriptase complexed with an inhibitor
-
Kohlstaedt, L. A.; Wang, J.; Friedman, J. M.; Rice, P. A.; Steitz, T. A. Crystal structure at 3.5 Å resolution of HIV-1 reverse transcriptase complexed with an inhibitor. Science 1992, 256, 1783-1790.
-
(1992)
Science
, vol.256
, pp. 1783-1790
-
-
Kohlstaedt, L.A.1
Wang, J.2
Friedman, J.M.3
Rice, P.A.4
Steitz, T.A.5
-
12
-
-
0028947588
-
High-resolution structures of HIV-1 RT from four RT-inhibitor complexes
-
Ren, J.; Esnouf, R.; Garman, E.; Somers, D.; Ross, C.; Kirby, I.; Keeling, J.; Darby, G.; Jones, Y.; Stuart, D.; Stammers, D. High-resolution structures of HIV-1 RT from four RT-inhibitor complexes. Nat. Struct. Biol. 1995, 2, 293-302.
-
(1995)
Nat. Struct. Biol.
, vol.2
, pp. 293-302
-
-
Ren, J.1
Esnouf, R.2
Garman, E.3
Somers, D.4
Ross, C.5
Kirby, I.6
Keeling, J.7
Darby, G.8
Jones, Y.9
Stuart, D.10
Stammers, D.11
-
13
-
-
0028925773
-
Mechanism of inhibition of HIV-1 reverse transcriptase by nonnucleoside inhibitors
-
Spence, R. A.; Kati, W. M.; Anderson, K. S.; Johnson, K. A. Mechanism of inhibition of HIV-1 reverse transcriptase by nonnucleoside inhibitors. Science 1995, 267, 988-993.
-
(1995)
Science
, vol.267
, pp. 988-993
-
-
Spence, R.A.1
Kati, W.M.2
Anderson, K.S.3
Johnson, K.A.4
-
14
-
-
2642709177
-
Declining morbidity and mortality among patients with advanced human immunodeficiency virus infection
-
HIV Outpatient Study Investigators
-
Palella, F. J., Jr.; Delaney, K. M.; Moorman, A. C.; Loveless, M. O.; Fuhrer, J.; Satten, G. A.; Aschman, D. J.; Holmberg, S. D. Declining morbidity and mortality among patients with advanced human immunodeficiency virus infection. HIV Outpatient Study Investigators. N. Engl. J. Med. 1998, 338, 853-860.
-
(1998)
N. Engl. J. Med.
, vol.338
, pp. 853-860
-
-
Palella Jr., F.J.1
Delaney, K.M.2
Moorman, A.C.3
Loveless, M.O.4
Fuhrer, J.5
Satten, G.A.6
Aschman, D.J.7
Holmberg, S.D.8
-
15
-
-
0032576426
-
Changing patterns of mortality across Europe in patients infected with HIV-1
-
EuroSIDA Study Group
-
Mocroft, A.; Vella, S.; Benfield, T. L.; Chiesi, A.; Miller, V.; Gargalianos, P.; d'Arminio Monforte, A.; Yust, I.; Bruun, J. N.; Phillips, A. N.; Lundgren, J. D. Changing patterns of mortality across Europe in patients infected with HIV-1. EuroSIDA Study Group. Lancet 1998, 352, 1725-1730.
-
(1998)
Lancet
, vol.352
, pp. 1725-1730
-
-
Mocroft, A.1
Vella, S.2
Benfield, T.L.3
Chiesi, A.4
Miller, V.5
Gargalianos, P.6
D'Arminio Monforte, A.7
Yust, I.8
Bruun, J.N.9
Phillips, A.N.10
Lundgren, J.D.11
-
16
-
-
0034083833
-
Mutations in retroviral genes associated with drug resistance
-
Schinazi, R. F.; Larder, B. A.; Mellors, J. W. Mutations in retroviral genes associated with drug resistance. Int. Antivir. News 2000, 8, 65-91.
-
(2000)
Int. Antivir. News
, vol.8
, pp. 65-91
-
-
Schinazi, R.F.1
Larder, B.A.2
Mellors, J.W.3
-
17
-
-
0032918170
-
Perspectives of non-nucleoside reverse transcriptase inhibitors (NNRTIs) in the therapy of HIV-1 infection
-
De Clercq, E. Perspectives of non-nucleoside reverse transcriptase inhibitors (NNRTIs) in the therapy of HIV-1 infection. Il Farmaco 1999, 54, 26-45.
-
(1999)
Il Farmaco
, vol.54
, pp. 26-45
-
-
De Clercq, E.1
-
18
-
-
0033840455
-
Human immunodeficiency virus type 1 mutations selected in patients failing efavirenz combination therapy
-
Bacheler, L. T.; Anton, E. D.; Kudish, P.; Baker, D.; Bunville, J.; Krakowski, K.; Boiling, L.; Aujay, M.; Wang, X. V.; Ellis, D.; Becker, M. F.; Lasut, A. L.; George, H. J.; Spalding, D. R.; Hollis, G.; Abremski, K. Human immunodeficiency virus type 1 mutations selected in patients failing efavirenz combination therapy. Antimicrob. Agents Chemother. 2000, 44, 2475-2484.
-
(2000)
Antimicrob. Agents Chemother.
, vol.44
, pp. 2475-2484
-
-
Bacheler, L.T.1
Anton, E.D.2
Kudish, P.3
Baker, D.4
Bunville, J.5
Krakowski, K.6
Boiling, L.7
Aujay, M.8
Wang, X.V.9
Ellis, D.10
Becker, M.F.11
Lasut, A.L.12
George, H.J.13
Spalding, D.R.14
Hollis, G.15
Abremski, K.16
-
19
-
-
0030596068
-
Crystal structures of 8-Cl and 9-Cl TIBO complexed with wild-type HIV-1 RT and 8-Cl TIBO complexed with the Tyr181Cys HIV-1 RT drug-resistant mutant
-
Das, K.; Ding, J.; Hsiou, Y.; Clark, A. D., Jr.; Moereels, H.; Koymans, L.; Andries, K.; Pauwels, R.; Janssen, P. A.; Boyer, P. L.; Clark, P.; Smith, R. H., Jr.; Kroeger Smith, M. B.; Michejda, C. J.; Hughes, S. H.; Arnold, E. Crystal structures of 8-Cl and 9-Cl TIBO complexed with wild-type HIV-1 RT and 8-Cl TIBO complexed with the Tyr181Cys HIV-1 RT drug-resistant mutant. J. Mol Biol. 1996, 264, 1085-1100.
-
(1996)
J. Mol. Biol.
, vol.264
, pp. 1085-1100
-
-
Das, K.1
Ding, J.2
Hsiou, Y.3
Clark Jr., A.D.4
Moereels, H.5
Koymans, L.6
Andries, K.7
Pauwels, R.8
Janssen, P.A.9
Boyer, P.L.10
Clark, P.11
Smith Jr., R.H.12
Kroeger Smith, M.B.13
Michejda, C.J.14
Hughes, S.H.15
Arnold, E.16
-
20
-
-
0035965124
-
Structural mechanisms of drug resistance for mutations at codons 181 and 188 in HIV-1 reverse transcriptase and the improved resilience of second generation nonnucleoside inhibitors
-
Ren, J.; Nichols, C.; Bird, L.; Chamberlain, P.; Weaver, K.; Short, S.; Stuart, D. I.; Stammers, D. K. Structural mechanisms of drug resistance for mutations at codons 181 and 188 in HIV-1 reverse transcriptase and the improved resilience of second generation nonnucleoside inhibitors. J. Mol. Blol. 2001, 312, 795-805.
-
(2001)
J. Mol. Blol.
, vol.312
, pp. 795-805
-
-
Ren, J.1
Nichols, C.2
Bird, L.3
Chamberlain, P.4
Weaver, K.5
Short, S.6
Stuart, D.I.7
Stammers, D.K.8
-
21
-
-
0035368238
-
The Lys103Asn mutation of HIV-1 RT: A novel mechanism of drug resistance
-
Hsiou, Y.; Ding, J.; Das, K.; Clark, A. D., Jr.; Boyer, P. L.; Lewi, P.; Janssen, P. A.; Kleim, J. P.; Rosner, M.; Hughes, S. H.; Arnold, E. The Lys103Asn mutation of HIV-1 RT: a novel mechanism of drug resistance. J. Mol. Biol. 2001, 509, 437-445.
-
(2001)
J. Mol. Biol.
, vol.509
, pp. 437-445
-
-
Hsiou, Y.1
Ding, J.2
Das, K.3
Clark Jr., A.D.4
Boyer, P.L.5
Lewi, P.6
Janssen, P.A.7
Kleim, J.P.8
Rosner, M.9
Hughes, S.H.10
Arnold, E.11
-
22
-
-
0031578901
-
Resistance to nevirapine of HIV-1 reverse transcriptase mutants: Loss of stabilizing interactions and thermodynamic or steric barriers are induced by different single amino acid substitutions
-
Maga, G.; Amacker, M.; Ruel, N.; Hubscher, U.; Spadafi, S. Resistance to nevirapine of HIV-1 reverse transcriptase mutants: loss of stabilizing interactions and thermodynamic or steric barriers are induced by different single amino acid substitutions. J. Mol. Biol. 1997, 274, 738-747.
-
(1997)
J. Mol. Biol.
, vol.274
, pp. 738-747
-
-
Maga, G.1
Amacker, M.2
Ruel, N.3
Hubscher, U.4
Spadafi, S.5
-
23
-
-
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
-
24
-
-
9644291579
-
TMC125, a novel next-generation nonnucleoside reverse transcriptase inhibitor active against nonnucleoside reverse transcriptase inhibitor-resistant human immunodeficiency virus type 1
-
Andries, K.; Azijn, H.; Thielemans, T.; Ludovici, D.; Kukla, M.; Heeres, J.; Janssen, P.; De Corte, B.; Vingerhoets, J.; Pauwels, R.; de Bethune, M. P. TMC125, a novel next-generation nonnucleoside reverse transcriptase inhibitor active against nonnucleoside reverse transcriptase inhibitor-resistant human immunodeficiency virus type 1. Antimicrob. Agents Chemother. 2004, 48, 4680-4686.
-
(2004)
Antimicrob. Agents Chemother.
, vol.48
, pp. 4680-4686
-
-
Andries, K.1
Azijn, H.2
Thielemans, T.3
Ludovici, D.4
Kukla, M.5
Heeres, J.6
Janssen, P.7
De Corte, B.8
Vingerhoets, J.9
Pauwels, R.10
De Bethune, M.P.11
-
25
-
-
33646103676
-
Biosensor-based kinetic characterization of the interaction between HIV-1 reverse transcriptase and non-nucleoside inhibitors
-
Geitmann, M.; Unge, T.; Danielson, U. H. Biosensor-based kinetic characterization of the interaction between HIV-1 reverse transcriptase and non-nucleoside inhibitors. J. Med. Chem. 2006, 49, 2367-2374.
-
(2006)
J. Med. Chem.
, vol.49
, pp. 2367-2374
-
-
Geitmann, M.1
Unge, T.2
Danielson, U.H.3
-
26
-
-
0036782103
-
Inhibitor binding alters the directions of domain motions in HIV-1 reverse transcriptase
-
Temiz, N. A.; Bahar, I. Inhibitor binding alters the directions of domain motions in HIV-1 reverse transcriptase. Proteins 2002, 49, 61-70.
-
(2002)
Proteins
, vol.49
, pp. 61-70
-
-
Temiz, N.A.1
Bahar, I.2
-
27
-
-
33644683832
-
Effects of efavirenz binding on the subunit equilibria of HIV-1 reverse transcriptase
-
Venezia, C. F.; Howard, K. J.; Ignatov, M. E.; Holladay, L. A.; Barkley, M. D. Effects of Efavirenz Binding on the Subunit Equilibria of HIV-1 Reverse Transcriptase. Biochemistry 2006 45, 2779-2789.
-
(2006)
Biochemistry
, vol.45
, pp. 2779-2789
-
-
Venezia, C.F.1
Howard, K.J.2
Ignatov, M.E.3
Holladay, L.A.4
Barkley, M.D.5
-
28
-
-
0036229823
-
Structural basis for the inhibitory efficacy of efavirenz (DMP-266), MSC194 and PNU142721 towards the HIV-1 RT K103N mutant
-
Lindberg, J.; Sigurdsson, S.; Löwgren, S.; Andersson, H. O.; Sahlberg, C.; Noréen, R.; Fridborg, K.; Zhang, H.; Unge, T. Structural basis for the inhibitory efficacy of efavirenz (DMP-266), MSC194 and PNU142721 towards the HIV-1 RT K103N mutant. Eur. J. Biochem. 2002, 269, 1670-1677.
-
(2002)
Eur. J. Biochem.
, vol.269
, pp. 1670-1677
-
-
Lindberg, J.1
Sigurdsson, S.2
Löwgren, S.3
Andersson, H.O.4
Sahlberg, C.5
Noréen, R.6
Fridborg, K.7
Zhang, H.8
Unge, T.9
-
29
-
-
0037764052
-
Steered molecular dynamics simulation on the binding of NNRTI to HIV-1 RT
-
Shen, L.; Shen, J.; Luo, X.; Cheng, F.; Xu, Y.; Chen, K.; Arnold, E.; Ding, J.; Jiang, H. Steered molecular dynamics simulation on the binding of NNRTI to HIV-1 RT. Biophys. J. 2003, 84, 3547-3563.
-
(2003)
Biophys. J.
, vol.84
, pp. 3547-3563
-
-
Shen, L.1
Shen, J.2
Luo, X.3
Cheng, F.4
Xu, Y.5
Chen, K.6
Arnold, E.7
Ding, J.8
Jiang, H.9
-
30
-
-
0034640387
-
Binding of the second generation nonnucleoside 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 nonnucleoside 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
-
31
-
-
2342620790
-
Roles of conformational and positional adaptability in structure-based design of TMC125-R165335 (etravirine) and related non-nucleoside reverse transcriptase inhibitors that are highly potent and effective against wild-type and drug-resistant HIV-1 variants
-
Das, K.; Clark, A. D., Jr.; Lewi, P. J.; Heeres, J.; De Jonge, M. R. Koymans, L. M.; Vinkers, H. M.; Daeyaert, F.; Ludovici, D. W. Kukla, M. J.; De Corte, B.; Kavash, R. W.; Ho, C. Y.; Ye, H. Lichtenstein, M. A.; Andries, K.; Pauwels, R.; De Bethune, M. P. Boyer, P. L.; Clark, P.; Hughes, S. H.; Janssen, P. A.; Arnold, E. Roles of conformational and positional adaptability in structure-based design of TMC125-R165335 (etravirine) and related non-nucleoside reverse transcriptase inhibitors that are highly potent and effective against wild-type and drug-resistant HIV-1 variants. J. Med. Chem. 2004, 47, 2550-2560.
-
(2004)
J. Med. Chem.
, vol.47
, pp. 2550-2560
-
-
Das, K.1
Clark Jr., A.D.2
Lewi, P.J.3
Heeres, J.4
De Jonge, M.R.5
Koymans, L.M.6
Vinkers, H.M.7
Daeyaert, F.8
Ludovici, D.W.9
Kukla, M.J.10
De Corte, B.11
Kavash, R.W.12
Ho, C.Y.13
Ye, H.14
Lichtenstein, M.A.15
Andries, K.16
Pauwels, R.17
De Bethune, M.P.18
Boyer, P.L.19
Clark, P.20
Hughes, S.H.21
Janssen, P.A.22
Arnold, E.23
more..
-
32
-
-
9744258219
-
Crystallography and the design of anti-AIDS drugs: Conformational flexibility and positional adaptability are important in the design of non-nucleoside HIV-1 reverse transcriptase inhibitors
-
Das, K.; Lewi, P. J.; Hughes, S. H.; Arnold, E. Crystallography and the design of anti-AIDS drugs: conformational flexibility and positional adaptability are important in the design of non-nucleoside HIV-1 reverse transcriptase inhibitors. Prog. Biophys. Mol. Biol. 2005, 88, 209-231.
-
(2005)
Prog. Biophys. Mol. Biol.
, vol.88
, pp. 209-231
-
-
Das, K.1
Lewi, P.J.2
Hughes, S.H.3
Arnold, E.4
-
33
-
-
0035821597
-
K.2-Amino-6-arylsulfonylbenzonitriles as non-nucleoside reverse transcriptase inhibitors of HIV-1
-
Chan, J. H.; Hong, J. S.; Hunter, R. N., 3rd; Orr, G. F.; Cowan, J. R.; Sherman, D. B.; Sparks, S. M.; Reitter, B. E.; Andrews, C. W., 3rd; Hazen, R. J.; St. Clair, M.; Boone, L. R.; Ferris, R. G.; Creech, K. L.; Roberts, G. B.; Short, S. A.; Weaver, K.; Ott, R. J.; Ren, J.; Hopkins, A.; Stuart, D. I.; Stammers, D. K.2-Amino-6-arylsulfonylbenzonitriles as non-nucleoside reverse transcriptase inhibitors of HIV-1. J. Med. Chem. 2001, 44, 1866-1882.
-
(2001)
J. Med. Chem.
, vol.44
, pp. 1866-1882
-
-
Chan, J.H.1
Hong, J.S.2
Hunter III, R.N.3
Orr, G.F.4
Cowan, J.R.5
Sherman, D.B.6
Sparks, S.M.7
Reitter, B.E.8
Andrews III, C.W.9
Hazen, R.J.10
St. Clair, M.11
Boone, L.R.12
Ferris, R.G.13
Creech, K.L.14
Roberts, G.B.15
Short, S.A.16
Weaver, K.17
Ott, R.J.18
Ren, J.19
Hopkins, A.20
Stuart, D.I.21
Stammers, D.22
more..
-
34
-
-
17944376896
-
Evolution of anti-HIV drug candidates. Part 1: From alpha- anilinophenylacetamide (alpha-APA) to imidoyl thiourea (ITU)
-
Ludovici, D. W.; Kukla, M. J.; Grous, P. G.; Krishnan, S.; Andries, K.; de Bethune, M. P.; Azijn, H.; Pauwels, R.; De Clercq, E.; Arnold, E.; Janssen, P. A. Evolution of anti-HIV drug candidates. Part 1: From alpha- anilinophenylacetamide (alpha-APA) to imidoyl thiourea (ITU). Bioorg. Med. Chem. Lett. 2001, 11, 2225-2228.
-
(2001)
Bioorg. Med. Chem. Lett.
, vol.11
, pp. 2225-2228
-
-
Ludovici, D.W.1
Kukla, M.J.2
Grous, P.G.3
Krishnan, S.4
Andries, K.5
De Bethune, M.P.6
Azijn, H.7
Pauwels, R.8
De Clercq, E.9
Arnold, E.10
Janssen, P.A.11
-
35
-
-
33646145006
-
-
Abstr 110
-
Jeffrey, S.; Corbett, J.; Bacheler, L. 6th Conf. Retrovir. Opportun. Infect. 1999, 6, 88 (Abstr 110).
-
(1999)
6th Conf. Retrovir. Opportun. Infect.
, vol.6
, pp. 88
-
-
Jeffrey, S.1
Corbett, J.2
Bacheler, L.3
-
36
-
-
0029922342
-
Marked inhibitory activity of non-nucleoside reverse transcriptase inhibitors against human immunodeficiency virus type 1 when combined with (-)-2′,3′-dideoxy-3′-thiacytidine
-
Balzarini, J.; Pelemans, H.; Perez-Perez, M. J.; San-Felix, A.; Camarasa, M. J.; De Clercq, E.; Karlsson, A. Marked inhibitory activity of non-nucleoside reverse transcriptase inhibitors against human immunodeficiency virus type 1 when combined with (-)-2′,3′-dideoxy-3′-thiacytidine. Mol. Pharmacol. 1996, 49, 882-890.
-
(1996)
Mol. Pharmacol.
, vol.49
, pp. 882-890
-
-
Balzarini, J.1
Pelemans, H.2
Perez-Perez, M.J.3
San-Felix, A.4
Camarasa, M.J.5
De Clercq, E.6
Karlsson, A.7
-
37
-
-
0032786364
-
Expanded-spectrum nonnucleoside reverse transcriptase inhibitors inhibit clinically relevant mutant variants of human immunodeficiency virus type 1
-
Corbett, J. W.; Ko, S. S.; Rodgers, J. D.; Jeffrey, S.; Bacheler, L. T.; Klabe, R. M.; Diamond, S.; Lai, C. M.; Rabel, S. R.; Saye, J. A.; Adams, S. P.; Trainor, G. L.; Anderson, P. S.; Erickson-Viitanen, S. K. Expanded-spectrum nonnucleoside reverse transcriptase inhibitors inhibit clinically relevant mutant variants of human immunodeficiency virus type 1. Antimicrob. Agents Chemother. 1999, 43, 2893-2897.
-
(1999)
Antimicrob. Agents Chemother.
, vol.43
, pp. 2893-2897
-
-
Corbett, J.W.1
Ko, S.S.2
Rodgers, J.D.3
Jeffrey, S.4
Bacheler, L.T.5
Klabe, R.M.6
Diamond, S.7
Lai, C.M.8
Rabel, S.R.9
Saye, J.A.10
Adams, S.P.11
Trainor, G.L.12
Anderson, P.S.13
Erickson-Viitanen, S.K.14
-
38
-
-
17944379430
-
-
Abstr 1172
-
Jeffrey, S.; Baker, D.; Corbett, J.; Logue, K.; Bacheler, L. T. 39th ICAAC Abstr. 1999, 39, 495 (Abstr 1172).
-
(1999)
39th ICAAC Abstr.
, vol.39
, pp. 495
-
-
Jeffrey, S.1
Baker, D.2
Corbett, J.3
Logue, K.4
Bacheler, L.T.5
-
39
-
-
0032030658
-
Retention of marked sensitivity to (S)-4-isopropoxycarbonyl-6-methoxy-3- (methylthiomethyl)-3,4-di hydroquin oxaline-2(IH)-thione (HBY 097) by an azidothymidine (AZT)-resistant human immunodeficiency virus type 1 (HIV-1) strain subcultured in the combined presence of quinoxaline HBY 097 and 2′,3′-dideoxy-3′-thiacytidine (lamivudine)
-
Balzarini, J.; Pelemans, H.; Riess, G.; Roesner, M.; Winkler, I.; De Clercq, E.; KIeim, J. P. Retention of marked sensitivity to (S)-4- isopropoxycarbonyl-6-methoxy-3-(methylthiomethyl)-3,4-di hydroquin oxaline-2(IH)-thione (HBY 097) by an azidothymidine (AZT)-resistant human immunodeficiency virus type 1 (HIV-1) strain subcultured in the combined presence of quinoxaline HBY 097 and 2′,3′-dideoxy-3′- thiacytidine (lamivudine). Biochem. Pharmacol. 1998, 55, 617-625.
-
(1998)
Biochem. Pharmacol.
, vol.55
, pp. 617-625
-
-
Balzarini, J.1
Pelemans, H.2
Riess, G.3
Roesner, M.4
Winkler, I.5
De Clercq, E.6
Kieim, J.P.7
-
40
-
-
33646122609
-
-
Huddinge, Sweden. Personal communication
-
Vrang, L.; Medivir, A. B., Huddinge, Sweden. Personal communication.
-
-
-
Vrang, L.1
Medivir, A.B.2
-
41
-
-
0037679871
-
Urea-PETT compounds as a new class of HIV-1 reverse transcriptase inhibitors: Synthesis and further structure-activity relationship studies of PETT analogues
-
Högberg, M.; Sahlberg, C.; Engelhardt, P.; Noréen, R.; Kangasmetsä, J.; Johansson, N. G.; Öberg, B.; Vrang, L.; Zhang, H.; Sahlberg, B.-L.; Unge, T.; Lövgren, S.; Fridborg, K.; Bäckbro, K. Urea-PETT compounds as a new class of HIV-1 reverse transcriptase inhibitors: Synthesis and further structure-activity relationship studies of PETT analogues, J. Med. Chem. 1999, 42, 4150-4160.
-
(1999)
J. Med. Chem.
, vol.42
, pp. 4150-4160
-
-
Högberg, M.1
Sahlberg, C.2
Engelhardt, P.3
Noréen, R.4
Kangasmetsä, J.5
Johansson, N.G.6
Öberg, B.7
Vrang, L.8
Zhang, H.9
Sahlberg, B.-L.10
Unge, T.11
Lövgren, S.12
Fridborg, K.13
Bäckbro, K.14
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