-
1
-
-
2342595186
-
Nonnucleoside inhibitors of HIV-1 reverse transcriptase: From the biology of reverse transcription to molecular design
-
Tronchet, J.M.; Seman, M. Nonnucleoside inhibitors of HIV-1 reverse transcriptase: from the biology of reverse transcription to molecular design. Curr. Top Med. Chem., 2003, 3, 1496-1511
-
(2003)
Curr. Top Med. Chem.
, vol.3
, pp. 1496-1511
-
-
Tronchet, J.M.1
Seman, M.2
-
2
-
-
48949117560
-
The current status of the NNRTI family of antiretrovirals used in the HAART regime against HIV infection
-
Martins, S.; Ramos, M.J.; Fernandes, P.A. The current status of the NNRTI family of antiretrovirals used in the HAART regime against HIV infection. Curr. Med. Chem., 2008, 15, 1083-1095
-
(2008)
Curr. Med. Chem.
, vol.15
, pp. 1083-1095
-
-
Martins, S.1
Ramos, M.J.2
Fernandes, P.A.3
-
3
-
-
33845462923
-
HIV-1 RT nonnucleoside inhibitors and their interaction with RT for antiviral drug development
-
Zhou, Z.; Lin, X.; Madura, J.D. HIV-1 RT nonnucleoside inhibitors and their interaction with RT for antiviral drug development. Infect. Disord. Drug Targets, 2006, 6, 391-413. (Pubitemid 44890632)
-
(2006)
Infectious Disorders - Drug Targets
, vol.6
, Issue.4
, pp. 391-413
-
-
Zhou, Z.1
Lin, X.2
Madura, J.D.3
-
4
-
-
54449084056
-
Etravirine for the treatment of HIV infection
-
Seminari, E.; Castagna, A.; Lazzarin, A. Etravirine for the treatment of HIV infection. Expert Rev. Anti Infect. Ther., 2008, 6, 427-433
-
(2008)
Expert Rev. Anti Infect. Ther.
, vol.6
, pp. 427-433
-
-
Seminari, E.1
Castagna, A.2
Lazzarin, A.3
-
5
-
-
55449092395
-
Emerging resistance profiles of newly approved antiretroviral drugs
-
Daar, E.S. Emerging resistance profiles of newly approved antiretroviral drugs. Top HIV Med., 2008, 16, 110-116
-
(2008)
Top HIV Med.
, vol.16
, pp. 110-116
-
-
Daar, E.S.1
-
6
-
-
32544442309
-
Next-generation HIV-1 non-nucleoside reverse transcriptase inhibitors
-
Boone, L.R. Next-generation HIV-1 non-nucleoside reverse transcriptase inhibitors. Curr. Opin. Investig. Drugs, 2006, 7, 128-135 (Pubitemid 43230908)
-
(2006)
Current Opinion in Investigational Drugs
, vol.7
, Issue.2
, pp. 128-135
-
-
Boone, L.R.1
-
7
-
-
0030586090
-
Structure of unliganded HIV-1 reverse transcriptase at 2.7 Å resolution: Implications of conformational changes for polymerization and inhibition mechanisms
-
DOI 10.1016/S0969-2126(96)00091-3
-
Hsiou, Y.; Ding, J.; Das, K.; Clark, A.D.; 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 (Pubitemid 26312368)
-
(1996)
Structure
, vol.4
, Issue.7
, pp. 853-860
-
-
Hsiou, Y.1
Ding, J.2
Das, K.3
Clark Jr., A.D.4
Hughes, S.H.5
Arnold, E.6
-
8
-
-
58149133507
-
Structure and function of HIV-1 reverse transcriptase: Molecular mechanisms of polymerization and inhibition
-
Sarafianos, S.G.; Marchand, B.; Das, K.; Himmel, D.M.; Parniak, M.A.; Hughes, S.H.; Arnold, E. Structure and function of HIV-1 reverse transcriptase: molecular mechanisms of polymerization and inhibition. J. Mol. Biol., 2009, 385, 693-713.
-
(2009)
J. Mol. Biol.
, vol.385
, pp. 693-713
-
-
Sarafianos, S.G.1
Marchand, B.2
Das, K.3
Himmel, D.M.4
Parniak, M.A.5
Hughes, S.H.6
Arnold, E.7
-
9
-
-
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
-
10
-
-
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
-
11
-
-
70349395798
-
Recent advances in the discovery and development of novel NNRTI platforms: 2006-2008 update
-
in press
-
Zhan, P.; Liu, X.; Li, Z. Recent advances in the discovery and development of novel NNRTI platforms: 2006-2008 update. Curr. Med. Chem., 2009, in press.
-
(2009)
Curr. Med. Chem.
-
-
Zhan, P.1
Liu, X.2
Li, Z.3
-
12
-
-
43049144549
-
Structural basis for drug resistance mechanisms for non-nucleoside inhibitors of HIV reverse transcriptase
-
Ren, J.; Stammers, D.K. Structural basis for drug resistance mechanisms for non-nucleoside inhibitors of HIV reverse transcriptase. Virus Res., 2008, 134, 157-170
-
(2008)
Virus Res.
, vol.134
, pp. 157-170
-
-
Ren, J.1
Stammers, D.K.2
-
13
-
-
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
-
14
-
-
8744243260
-
Design of non-nucleoside inhibitors of HIV-1 reverse transcriptase with improved drug resistance properties. 1
-
DOI 10.1021/jm040071z
-
Hopkins, A.L.; Ren, J.; Milton, J.; Hazen, R.J.; Chan, J.H.; Stuart, D.I.; Stammers, D.K. Design of non-nucleoside inhibitors of HIV-1 reverse transcriptase with improved drug resistance properties. 1. J. Med. Chem., 2004, 47, 5912-5922 (Pubitemid 39517015)
-
(2004)
Journal of Medicinal Chemistry
, vol.47
, Issue.24
, pp. 5912-5922
-
-
Hopkins, A.L.1
Ren, J.2
Milton, J.3
Hazen, R.J.4
Chan, J.H.5
Stuart, D.I.6
Stammers, D.K.7
-
15
-
-
8644241710
-
Design of non-nucleoside inhibitors of HIV-1 reverse transcriptase with improved drug resistance properties. 2
-
Freeman, G.A.; Andrews, Iii CW 3rd.; Hopkins, A.L.; Lowell, G.S.; Schaller, L.T.; Cowan, J.R.; Gonzales, S.S.; Koszalka, G.W.; Hazen, R.J.; Boone, L.R.; Ferris, R.G.; Creech, K.L.; Roberts, G.B.; Short, S.A.; Weaver, K.; Reynolds, D.J.; Milton, J.; Ren, J.; Stuart, D.I.; Stammers, D.K.; Chan, J.H. Design of non-nucleoside inhibitors of HIV-1 reverse transcriptase with improved drug resistance properties. 2. J. Med. Chem., 2004, 47, 5923-5936
-
(2004)
J. Med. Chem.
, vol.47
, pp. 5923-5936
-
-
Freeman, G.A.1
Andrews III, I.C.W.2
Hopkins, A.L.3
Lowell, G.S.4
Schaller, L.T.5
Cowan, J.R.6
Gonzales, S.S.7
Koszalka, G.W.8
Hazen, R.J.9
Boone, L.R.10
Ferris, R.G.11
Creech, K.L.12
Roberts, G.B.13
Short, S.A.14
Weaver, K.15
Reynolds, D.J.16
Milton, J.17
Ren, J.18
Stuart, D.I.19
Stammers, D.K.20
Chan, J.H.21
more..
-
16
-
-
9944232661
-
Taking aim at a moving target: Designing drugs to inhibit drug-resistant HIV-1 reverse transcriptases
-
Sarafianos, S.G.; Das, K.; Hughes, S.H.; Arnold, E. Taking aim at a moving target: designing drugs to inhibit drug-resistant HIV-1 reverse transcriptases. Curr. Opin. Struct. Biol., 2004, 14, 16-30.
-
(2004)
Curr. Opin. Struct. Biol.
, vol.14
, pp. 16-30
-
-
Sarafianos, S.G.1
Das, K.2
Hughes, S.H.3
Arnold, E.4
-
17
-
-
37249079137
-
Search for non-nucleoside inhibitors of HIV-1 reverse transcriptase using chemical similarity, molecular docking, and MM-GB/SA scoring
-
DOI 10.1021/ci700271z
-
Barreiro, G.; Guimarães, C.R.; Tubert-Brohman, I.; Lyons, T.M.; Tirado-Rives, J.; Jorgensen, W.L. Search for non-nucleoside inhibitors of HIV-1 reverse transcriptase using chemical similarity, molecular docking, and MM-GB/SA scoring. J. Chem. Inf. Model, 2007, 47, 2416-2428 (Pubitemid 350275106)
-
(2007)
Journal of Chemical Information and Modeling
, vol.47
, Issue.6
, pp. 2416-2428
-
-
Barreiro, G.1
Guimaraes, C.R.W.2
Tubert-Brohman, I.3
Lyons, T.M.4
Tirado-Rives, J.5
Jorgensen, W.L.6
-
18
-
-
0027528503
-
Non-nucleoside inhibitors of HIV-1 reverse transcriptase: Molecular modeling and X-ray structure investigations
-
Schäfer, W.; Friebe, W.G.; Leinert, H.; Mertens, A.; Poll, T.; von der Saal, W.; Zilch, H.; Nuber, B.; Ziegler, M.L. Non-nucleoside inhibitors of HIV-1 reverse transcriptase: molecular modeling and X-ray structure investigations. J. Med. Chem., 1993, 36, 726-732 (Pubitemid 23105726)
-
(1993)
Journal of Medicinal Chemistry
, vol.36
, Issue.6
, pp. 726-732
-
-
Schafer, W.1
Friebe, W.-G.2
Leinert, H.3
Mertens, A.4
Poll, T.5
Von Der Saal, W.6
Zilch, H.7
Nuber, B.8
Ziegler, M.L.9
-
19
-
-
31544461829
-
Aminopyimidinimo isatin analogues: Design of novel non-nucleoside HIV-1 reverse transcriptase inhibitors with broadspectrum chemotherapeutic properties
-
Sriram, D.; Bal, T.R.; Yogeeswari, P. Aminopyrimidinimino isatin analogues: design of novel non- nucleoside HIV-1 reverse transcriptase inhibitors with broad-spectrum chemotherapeutic properties. J. Pharm. Pharm. Sci., 2005, 8, 565-577 (Pubitemid 43158124)
-
(2005)
Journal of Pharmacy and Pharmaceutical Sciences
, vol.8
, Issue.3
, pp. 565-577
-
-
Sriram, D.1
Ratan Bal, T.2
Yogeeswari, P.3
-
20
-
-
19444378215
-
Newer aminopyrimidinimino isatin analogues as non-nucleoside HIV-1 reverse transcriptase inhibitors for HIV and other opportunistic infections of AIDS: Design, synthesis and biological evaluation
-
DOI 10.1016/j.farmac.2005.03.005, PII S0014827X05000662
-
Sriram, D.; Bal, T.R.; Yogeeswari, P. Newer aminopyrimidinimino isatin analogues as non-nucleoside HIV-1 reverse transcriptase inhibitors for HIV and other opportunistic infections of AIDS: design, synthesis and biological evaluation. FARMACO, 2005, 60, 377-384 (Pubitemid 40725803)
-
(2005)
Farmaco
, vol.60
, Issue.5
, pp. 377-384
-
-
Sriram, D.1
Bal, T.R.2
Yogeeswari, P.3
-
21
-
-
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
-
22
-
-
1042279567
-
A pharmacophore docking algorithm and its application to the cross-docking of 18 HIV-NNRTI's in their binding pockets
-
Daeyaert, F.; de Jonge, M. ; Heeres, J.; Koymans, L.; Lewi, P.; Vinkers, M.H.; Janssen, P.A. 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
De Jonge, M.2
Heeres, J.3
Koymans, L.4
Lewi, P.5
Vinkers, M.H.6
Janssen, P.A.7
-
23
-
-
11144355186
-
Classification and regression trees - Studies of HIV reverse transcriptase inhibitors
-
Daszykowski, M.; 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
-
-
Daszykowski, M.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
-
24
-
-
20944432342
-
Computational strategies in discovering novel non-nucleoside inhibitors of HIV-1 RT
-
DOI 10.1021/jm049279a
-
Barreca, M.L.; Rao, A.; De Luca, L.; Zappal, M.; Monforte, A.M.; Maga, G.; Pannecouque, C.; Balzarini, J.; De Clercq, E.; Chimirri, A.; Monforte, P. Computational strategies in discovering novel non-nucleoside inhibitors of HIV-1 RT. J. Med. Chem., 2005, 48, 3433-3437 (Pubitemid 40628061)
-
(2005)
Journal of Medicinal Chemistry
, vol.48
, Issue.9
, pp. 3433-3437
-
-
Barreca, M.L.1
Rao, A.2
De Luca, L.3
Zappala, M.4
Monforte, A.-M.5
Maga, G.6
Pannecouque, C.7
Balzarini, J.8
De Clercq, E.9
Chimirri, A.10
Monforte, P.11
-
25
-
-
33847618875
-
Discovery of novel benzimidazolones as potent non-nucleoside reverse transcriptase inhibitors active against wild-type and mutant HIV-1 strains
-
DOI 10.1016/j.bmcl.2007.01.025, PII S0960894X0700073X
-
Barreca, M.L.; Rao, A.; De Luca, L.; Iraci, N.; Monforte, A.M.; Maga, G.; De Clercq, E.; Pannecouque, C.; Balzarini, J.; Chimirri, A. Discovery of novel benzimidazolones as potent non-nucleoside reverse transcriptase inhibitors active against wild-type and mutant HIV-1 strains. Bioorg. Med. Chem. Lett., 2007, 17, 1956-1960 (Pubitemid 46367661)
-
(2007)
Bioorganic and Medicinal Chemistry Letters
, vol.17
, Issue.7
, pp. 1956-1960
-
-
Barreca, M.L.1
Rao, A.2
Luca, L.D.3
Iraci, N.4
Monforte, A.-M.5
Maga, G.6
Clercq, E.D.7
Pannecouque, C.8
Balzarini, J.9
Chimirri, A.10
-
26
-
-
34247227122
-
Structure-based pharmacophore identification of new chemical scaffolds as non-nucleoside reverse transcriptase inhibitors
-
DOI 10.1021/ci600320q
-
Barreca, M.L.; De Luca, L.; Iraci, N.; Rao, A.; Ferro, S.; Maga, G.; Chimirri, A. Structure-based pharmacophore identification of new chemical scaffolds as non-nucleoside reverse transcriptase inhibitors. J. Chem. Inf. Model, 2007, 47, 557-562 (Pubitemid 46615957)
-
(2007)
Journal of Chemical Information and Modeling
, vol.47
, Issue.2
, pp. 557-562
-
-
Barreca, M.L.1
De Luca, L.2
Iraci, N.3
Rao, A.4
Ferro, S.5
Maga, G.6
Chimirri, A.7
-
27
-
-
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
-
28
-
-
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
-
DOI 10.1021/jm030558s
-
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 Béthune, 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 (Pubitemid 38580092)
-
(2004)
Journal of Medicinal Chemistry
, vol.47
, Issue.10
, 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.H.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.J.22
Arnold, E.23
more..
-
29
-
-
33747140370
-
Aspects of successful drug discovery and development
-
DOI 10.1016/j.antiviral.2006.05.007, PII S0166354206001355
-
Pauwels, R. Aspects of successful drug discovery and development. Antiviral. Res., 2006, 71, 77-89. (Pubitemid 44223771)
-
(2006)
Antiviral Research
, vol.71
, Issue.2-3 SPEC. ISSUE
, pp. 77-89
-
-
Pauwels, R.1
-
30
-
-
15444380338
-
From 4,5,6,7-tetrahydro-5-methylimidazo[4,5,1-jk](1,4)benzodiazepin-2(1H) - one (TIBO) to etravirine (TMC125): Fifteen years of research on non-nucleoside inhibitors of HIV-1 reverse transcriptase
-
De Corte, B.L. From 4,5,6,7-tetrahydro-5-methylimidazo[4,5,1-jk](1,4) benzodiazepin-2(1H)- one (TIBO) to etravirine (TMC125): fifteen years of research on non-nucleoside inhibitors of HIV-1 reverse transcriptase. J. Med. Chem., 2005, 48, 1689-1696
-
(2005)
J. Med. Chem.
, vol.48
, pp. 1689-1696
-
-
De Corte, B.L.1
-
31
-
-
20144372481
-
In search of a novel anti-HIV drug: Multidisciplinary coordination in the discovery of 4-[[4-[[4-[(1E)-2-cyanoethenyl]-2,6-dimethylphenyl]amino]-2- Pyrimidinyl]amino]benzonitrile (R278474, rilpivirine)
-
DOI 10.1021/jm040840e
-
Janssen, P.A.; Lewi, P.J.; Arnold, E.; Daeyaert, F.; de Jonge, M.; Heeres, J.; Koymans, L.; Vinkers, M.; Guillemont, J.; Pasquier, E.; Kukla, M.; Ludovici, D.; Andries, K.; de Béthune, M.P.; Pauwels, R.; Das, K.; Clark, A.D.Jr.; Frenkel, Y.V.; Hughes, S.H.; Medaer, B.; De Knaep, F.; Bohets, H.; De Clerck, F.; Lampo, A.; Williams, P.; Stoffels, P. In search of a novel anti-HIV drug: multidisciplinary coordination in the discovery of 4-[[4-[[4-[(1E)-2- cyanoethenyl]-2,6-dimethylphenyl]amino]-2- pyrimidinyl]amino] benzonitrile (R278474, rilpivirine). J. Med. Chem., 2005, 48, 1901-1909 (Pubitemid 40396320)
-
(2005)
Journal of Medicinal Chemistry
, vol.48
, Issue.6
, pp. 1901-1909
-
-
Janssen, P.A.J.1
Lewi, P.J.2
Arnold, E.3
Daeyaert, F.4
De Jonge, M.5
Heeres, J.6
Koymans, L.7
Vinkers, M.8
Guillemont, J.9
Pasquier, E.10
Kukla, M.11
Ludovici, D.12
Andries, K.13
De Bethune, M.-P.14
Pauwels, R.15
Das, K.16
Clark Jr., A.D.17
Frenkel, Y.V.18
Hughes, S.H.19
Medaer, B.20
De Knaep, F.21
Bohets, H.22
De Clerck, F.23
Lampo, A.24
Williams, P.25
Stoffels, P.26
more..
-
32
-
-
40349091258
-
High-resolution structures of HIV-1 reverse transcriptase/TMC278 complexes: Strategic flexibility explains potency against resistance mutations
-
DOI 10.1073/pnas.0711209105
-
Das, K.; Bauman, J.D.; Clark, A.D.Jr.; Frenkel, Y.V.; Lewi, P.J.; Shatkin, A.J.; Hughes, S.H.; Arnold, E. High-resolution structures of HIV-1 reverse transcriptase/TMC278 complexes: Strategic flexibility explains potency against resistance mutations. Proc. Natl. Acad. Sci. U S A, 2008, 105, 1466-1471 (Pubitemid 351346537)
-
(2008)
Proceedings of the National Academy of Sciences of the United States of America
, vol.105
, Issue.5
, pp. 1466-1471
-
-
Das, K.1
Bauman, J.D.2
Clark Jr., A.D.3
Frenkel, Y.V.4
Lewi, P.J.5
Shatkin, A.J.6
Hughes, S.H.7
Arnold, E.8
-
33
-
-
33751529192
-
Crystal Structures of Clinically Relevant Lys103Asn/Tyr181Cys Double Mutant HIV-1 Reverse Transcriptase in Complexes with ATP and Non-nucleoside Inhibitor HBY 097
-
DOI 10.1016/j.jmb.2006.08.097, PII S0022283606011090
-
Das, K.; Sarafianos, S.G.; Clark, A.D.Jr.; Boyer, P.L.; Hughes, S.H.; Arnold, E. Crystal structures of clinically relevant Lys103Asn/Tyr181Cys double mutant HIV-1 reverse transcriptase in complexes with ATP and non-nucleoside inhibitor HBY 097. J. Mol. Biol., 2007, 365, 77-89. (Pubitemid 44830031)
-
(2007)
Journal of Molecular Biology
, vol.365
, Issue.1
, pp. 77-89
-
-
Das, K.1
Sarafianos, S.G.2
Clark Jr., A.D.3
Boyer, P.L.4
Hughes, S.H.5
Arnold, E.6
-
34
-
-
13144282707
-
Structures of Tyr188Leu mutant and wild-type HIV-1 reverse transcriptase complexed with the non-nucleoside inhibitor HBY 097: Inhibitor flexibility is a useful design feature for reducing drug resistance
-
DOI 10.1006/jmbi.1998.2171
-
Hsiou, Y.; Das, K.; Ding, J.; Clark, A.D.Jr.; Kleim, J-P.; Roesner, M.; Winkler, I.; Riess, G.; Hughes, S.H.; Arnold, E. Structures of Tyr188Leu mutant and wild-type HIV-1 reverse transcriptase complexed with the non-nucleoside inhibitor HBY 097: inhibitor flexibility is a useful design feature for reducing drug resistance. J. Mol. Biol., 1998, 284, 313-323 (Pubitemid 28542456)
-
(1998)
Journal of Molecular Biology
, vol.284
, Issue.2
, pp. 313-323
-
-
Hsiou, Y.1
Das, K.2
Ding, J.3
Clark Jr., A.D.4
Kleim, J.-P.5
Rosner, M.6
Winkler, I.7
Riess, G.8
Hughes, S.H.9
Arnold, E.10
-
35
-
-
0028998825
-
The PETT series, a new class of potent nonnucleoside inhibitors of human immunodeficiency virus type 1 reverse transcriptase
-
Ahgren, C.; Backro, K.; Bell, F.W.; Cantrell, A.S.; Clemens, M.; Colacino, J.M.; Deeter, J.B.; Engelhardt, J.A.; Hogberg, M.; Jaskunas, S.R.; Johansson, N.G.; Jordan, C.L.; Kasher, J.S.; Kinnick, M.D.; Lind, P.; Lopez, C.; Morin, JR., J.M.; Muesing, M.A.; Noreen, R.; Oberg, B.; Paget, C.J.; Palkowitz, J.A.; Parrish, C.A.; Pranc, P.; Rippy, M.K.; Rydergard, C.; Sahlberg, C.; Swanson, S.; Ternansky, R.J.; Unge, T.; Vasileff, R.T.; Vrang, L.; West, S.J.; Zhang, H.; Zhou, X.-X. The PETT series, a new class of potent nonnucleoside inhibitors of human immunodeficiency virus type 1 reverse transcriptase. Antimicrob. Agents Chemother., 1995, 39, 1329-1335
-
(1995)
Antimicrob. Agents Chemother.
, vol.39
, pp. 1329-1335
-
-
Ahgren, C.1
Backro, K.2
Bell, F.W.3
Cantrell, A.S.4
Clemens, M.5
Colacino, J.M.6
Deeter, J.B.7
Engelhardt, J.A.8
Hogberg, M.9
Jaskunas, S.R.10
Johansson, N.G.11
Jordan, C.L.12
Kasher, J.S.13
Kinnick, M.D.14
Lind, P.15
Lopez, C.16
Morin Jr., J.M.17
Muesing, M.A.18
Noreen, R.19
Oberg, B.20
Paget, C.J.21
Palkowitz, J.A.22
Parrish, C.A.23
Pranc, P.24
Rippy, M.K.25
Rydergard, C.26
Sahlberg, C.27
Swanson, S.28
Ternansky, R.J.29
Unge, T.30
Vasileff, R.T.31
Vrang, L.32
West, S.J.33
Zhang, H.34
Zhou, X.-X.35
more..
-
36
-
-
0031805095
-
S-1153 inhibits replication of known drugresistant 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 drugresistant 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
-
37
-
-
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
-
38
-
-
38949203748
-
Design of HIV protease inhibitors targeting protein backbone: An effective strategy for combating drug resistance
-
Ghosh, A.K.; Chapsal, B.D.; Weber, I.T.; Mitsuya, H. Design of HIV protease inhibitors targeting protein backbone: an effective strategy for combating drug resistance. Acc. Chem. Res., 2008, 41, 78-86.
-
(2008)
Acc. Chem. Res.
, vol.41
, pp. 78-86
-
-
Ghosh, A.K.1
Chapsal, B.D.2
Weber, I.T.3
Mitsuya, H.4
-
39
-
-
0028271687
-
Structure of the binding site for nonnucleoside inhibitors of the reverse transcriptase of human immunodeficiency virus type 1
-
Smerdon, S.J.; Jäger, J.; Wang, J.; Kohlstaedt, L.A.; Chirino, A.J.; Friedman, J.M.; Rice, P.A.; Steitz, T.A. Structure of the binding site for nonnucleoside inhibitors of the reverse transcriptase of human immunodeficiency virus type 1. Proc. Natl. Acad. Sci. U.S.A., 1994, 91, 3911-3915 (Pubitemid 24139542)
-
(1994)
Proceedings of the National Academy of Sciences of the United States of America
, vol.91
, Issue.9
, pp. 3911-3915
-
-
Smerdon, S.J.1
Jager, J.2
Wang, J.3
Kohlstaedt, L.A.4
Chirino, A.J.5
Friedman, J.M.6
Rice, P.A.7
Steitz, T.A.8
-
40
-
-
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 non-nucleoside 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 non-nucleoside inhibitors. J. Mol. Biol., 2001, 312, 795-805.
-
(2001)
J. Mol. Biol.
, 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
-
41
-
-
0029809694
-
Highly favorable antiviral activity and resistance profile of the novel thiocarboxanilide pentenyloxy ether derivatives UC-781 and UC-82 as inhibitors of human immunodeficiency virus type 1 replication
-
Balzarini, J.; Pelemans, H.; Aquaro, S.; Perno, C.F.; Witvrouw, M.; Schols, D.; De Clercq, E.; Karlsson, A. Highly favorable antiviral activity and resistance profile of the novel thiocarboxanilide pentenyloxy ether derivatives UC-781 and UC-82 as inhibitors of human immunodeficiency virus type 1 replication. Mol. Pharmacol., 1996, 50, 394-401. (Pubitemid 26265145)
-
(1996)
Molecular Pharmacology
, vol.50
, Issue.2
, pp. 394-401
-
-
Balzarini, J.1
Pelemans, H.2
Aquaro, S.3
Perno, C.-F.4
Witvrouw, M.5
Schols, D.6
De Clercq, E.7
Karlsson, A.8
-
42
-
-
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
-
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 (Pubitemid 30253379)
-
(2000)
Molecular Pharmacology
, vol.57
, Issue.5
, pp. 954-960
-
-
Pelemans, H.1
Esnouf, R.2
De Clercq, E.3
Balzarini, J.4
-
43
-
-
0030011406
-
Pyrrolobenzothiazepinones and pyrrolobenzoxazepinones: Novel and specific non-nucleoside HIV-1 reverse transcriptase inhibitors with antiviral activity
-
DOI 10.1021/jm950702c
-
Campiani, G.; Nacci, V.; Fiorini, I.; De Filippis, M.P.; Garofalo, A.; Greco, G.; Novellino, E.; Altamura, S.; Di Renzo, L. Pyrrolobenzothiazepinones and pyrrolobenzoxazepinones: novel and specific non-nucleoside HIV-1 reverse transcriptase inhibitors with antiviral activity. J. Med. Chem., 1996, 39, 2672-2680 (Pubitemid 26240334)
-
(1996)
Journal of Medicinal Chemistry
, vol.39
, Issue.14
, pp. 2672-2680
-
-
Campiani, G.1
Nacci, V.2
Fiorini, I.3
De Filippis, M.P.4
Garofalo, A.5
Greco, G.6
Novellino, E.7
Altamura, S.8
Di Renzo, L.9
-
44
-
-
0032747299
-
Pyrrolobenzoxazepinone derivatives as non-nucleoside HIV-1 RT inhibitors: Further structure-activity relationship studies and identification of more potent broad-spectrum HIV-1 RT inhibitors with antiviral activity
-
DOI 10.1021/jm990150o
-
Campiani, G.; Morelli, E.; Fabbrini, M.; Nacci, V.; Greco, G.; Novellino, E.; Ramunno, A.; Maga, G.; Spadari, S.; Caliendo, G.; Bergamini, A.; Faggioli, E.; Uccella, I.; Bolacchi, F.; Marini, S.; Coletta, M.; Nacca, A.; Caccia, S. Pyrrolobenzoxazepinone derivatives as non-nucleoside HIV-1 RT inhibitors: further structure-activity relationship studies and identification of more potent broad-spectrum HIV-1 RT inhibitors with antiviral activity. J. Med. Chem., 1999, 42, 4462-4470 (Pubitemid 29504150)
-
(1999)
Journal of Medicinal Chemistry
, vol.42
, Issue.21
, pp. 4462-4470
-
-
Campiani, G.1
Morelli, E.2
Fabbrini, M.3
Nacci, V.4
Greco, G.5
Novellino, E.6
Ramunno, A.7
Maga, G.8
Spadari, S.9
Caliendo, G.10
Bergamini, A.11
Faggioli, E.12
Uccella, I.13
Bolacchi, F.14
Marini, S.15
Coletta, M.16
Nacca, A.17
Caccia, S.18
-
45
-
-
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
-
DOI 10.1021/jm050257d
-
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 (Pubitemid 41743628)
-
(2005)
Journal of Medicinal Chemistry
, vol.48
, Issue.23
, 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
-
46
-
-
45649084429
-
Selective targeting of the HIV-1 reverse transcriptase catalytic complex through interaction with the "primer grip" region by pyrrolobenzoxazepinone non-nucleoside inhibitors correlates with increased activity towards drug-resistant mutants
-
Zanoli, S.; Gemma, S.; Butini, S.; Brindisi, M.; Joshi, B.P.; Campiani, G.; Fattorusso, C.; Persico, M.; Crespan, E.; Cancio, R.; Spadari, S.; Hübscher, U.; Maga, G. Selective targeting of the HIV-1 reverse transcriptase catalytic complex through interaction with the "primer grip" region by pyrrolobenzoxazepinone non-nucleoside inhibitors correlates with increased activity towards drug-resistant mutants. Biochem. Pharmacol., 2008, 76, 156-168
-
(2008)
Biochem. Pharmacol.
, vol.76
, pp. 156-168
-
-
Zanoli, S.1
Gemma, S.2
Butini, S.3
Brindisi, M.4
Joshi, B.P.5
Campiani, G.6
Fattorusso, C.7
Persico, M.8
Crespan, E.9
Cancio, R.10
Spadari, S.11
Hübscher, U.12
Maga, G.13
-
47
-
-
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
-
Jan 26. on line
-
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.; Mattia, M.D.; 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 Jan 26. on line.
-
(2009)
J. Med. Chem.
-
-
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
Mattia, M.D.14
Lalli, S.15
Galletti, B.16
Gemma, S.17
Maga, G.18
-
48
-
-
68149109726
-
Sulfanyltriazole/tetrazoles: A promising class of HIV-1 NNRTIs
-
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
-
49
-
-
34249327726
-
Scaffold hopping in the rational design of novel HIV-1 non-nucleoside reverse transcriptase inhibitors
-
DOI 10.1016/j.bmcl.2007.03.097, PII S0960894X07004179
-
O'Meara, J.A.; Jakalian, A.; LaPlante, S.; Bonneau, P.R.; Coulombe, R.; Faucher, A.M.; Guse, I.; Landry, S.; Racine, J.; Simoneau, B.; Thavonekham, B.; Yoakim, C. Scaffold hopping in the rational design of novel HIV-1 non-nucleoside reverse transcriptase inhibitors. Bioorg. Med. Chem. Lett., 2007, 17, 3362-3366 (Pubitemid 46819032)
-
(2007)
Bioorganic and Medicinal Chemistry Letters
, vol.17
, Issue.12
, pp. 3362-3366
-
-
O'Meara, J.A.1
Jakalian, A.2
Laplante, S.3
Bonneau, P.R.4
Coulombe, R.5
Faucher, A.-M.6
Guse, I.7
Landry, S.8
Racine, J.9
Simoneau, B.10
Thavonekham, B.11
Yoakim, C.12
-
50
-
-
34447319100
-
Thiotetrazole alkynylacetanilides as potent and bioavailable non-nucleoside inhibitors of the HIV-1 wild type and K103N/Y181C double mutant reverse transcriptases
-
DOI 10.1016/j.bmcl.2007.06.012, PII S0960894X07006920
-
Gagnon, A.; Amad, M.H.; Bonneau, P.R.; Coulombe, R.; DeRoy, P.L.; Doyon, L.; Duan, J.; Garneau, M.; Guse, I.; Jakalian, A.; Jolicoeur, E.; Landry, S.; Malenfant, E.; Simoneau, B.; Yoakim, C. Thiotetrazole alkynylacetanilides as potent and bioavailable nonnucleoside inhibitors of the HIV-1 wild type and K103N/Y181C double mutant reverse transcriptases. Bioorg. Med. Chem. Lett., 2007, 17, 4437-4441 (Pubitemid 47058964)
-
(2007)
Bioorganic and Medicinal Chemistry Letters
, vol.17
, Issue.16
, pp. 4437-4441
-
-
Gagnon, A.1
Amad, M.H.2
Bonneau, P.R.3
Coulombe, R.4
Deroy, P.L.5
Doyon, L.6
Duan, J.7
Garneau, M.8
Guse, I.9
Jakalian, A.10
Jolicoeur, E.11
Landry, S.12
Malenfant, E.13
Simoneau, B.14
Yoakim, C.15
-
51
-
-
0033524008
-
Design of MKC-442 (emivirine) analogues with improved activity against drug-resistant HIV mutants
-
Hopkins, A.L.; Ren, J.; Tanaka, H.; Baba, M.; Okamato, M.; Stuart, D.I.; Stammers, D.K. Design of MKC-442 (emivirine) analogues with improved activity against drug-resistant HIV mutants. J. Med. Chem., 1999, 42, 4500-4505
-
(1999)
J. Med. Chem.
, vol.42
, pp. 4500-4505
-
-
Hopkins, A.L.1
Ren, J.2
Tanaka, H.3
Baba, M.4
Okamato, M.5
Stuart, D.I.6
Stammers, D.K.7
-
52
-
-
11144233697
-
HIV reverse transcriptase structures: Designing new inhibitors and understanding mechanisms of drug resistance
-
Ren, J.; Stammers, D.K. HIV reverse transcriptase structures: designing new inhibitors and understanding mechanisms of drug resistance. Trends Pharmacol. Sci., 2005, 26, 4-7.
-
(2005)
Trends Pharmacol. Sci.
, vol.26
, pp. 4-7
-
-
Ren, J.1
Stammers, D.K.2
-
53
-
-
3242657912
-
Structure of HIV-1 reverse transcriptase bound to an inhibitor active against mutant reverse transcriptases resistant to other nonnucleoside inhibitors
-
Pata, J.D.; Stirtan, W.G.; Goldstein, S.W.; Steitz, T.A. Structure of HIV-1 reverse transcriptase bound to an inhibitor active against mutant reverse transcriptases resistant to other nonnucleoside inhibitors. Proc. Natl. Acad. Sci. U.S.A., 2004, 101, 10548-10553
-
(2004)
Proc. Natl. Acad. Sci. U.S.A.
, vol.101
, pp. 10548-10553
-
-
Pata, J.D.1
Stirtan, W.G.2
Goldstein, S.W.3
Steitz, T.A.4
-
54
-
-
0035368238
-
The Lys103Asn mutation of HIV-1 RT: A novel mechanism of drug resistance
-
DOI 10.1006/jmbi.2001.4648
-
Hsiou, Y.; Ding, J.; Das, K.; Clark, A.D.; Boyer, P.L.; Lewi, P.; Janssen, P.A.; Kleim, J.P.; Rösner, M.; Hughes, S.H.; Arnold, E. The Lys103Asn mutation of HIV-1 RT: a novel mechanism of drug resistance. J. Mol. Biol., 2001, 309, 437-445 (Pubitemid 32564904)
-
(2001)
Journal of Molecular Biology
, vol.309
, Issue.2
, 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.J.7
Kleim, J.-P.8
Rosner, M.9
Hughes, S.H.10
Arnold, E.11
-
55
-
-
0036229823
-
Structural basis for the inhibitory efficacy of efavirenz (DMP-266), MSC194 and PNU142721 towards the HIV-1 RT K103N mutant
-
DOI 10.1046/j.1432-1327.2002.02811.x
-
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 (Pubitemid 34304466)
-
(2002)
European Journal of Biochemistry
, vol.269
, Issue.6
, pp. 1670-1677
-
-
Lindberg, J.1
Sigurosson, S.2
Lowgren, S.3
Andersson, H.O.4
Sahlberg, C.5
Noreen, R.6
Fridborg, K.7
Zhang, H.8
Unge, T.9
-
56
-
-
37249062449
-
HIV-1 reverse transcriptase structure with RNase H inhibitor dihydroxy benzoyl naphthyl hydrazone bound at a novel site
-
Himmel, D.M.; Sarafianos, S.G.; Dharmasena, S.; Hossain, M.M.; McCoy-Simandle, K.; Ilina, T.; Clark, A.D.Jr.; Knight, J.L.; Julias, J.G.; Clark, P.K.; Krogh-Jespersen, K.; Levy, R.M.; Hughes, S.H.; Parniak, M.A.; Arnold, E. HIV-1 reverse transcriptase structure with RNase H inhibitor dihydroxy benzoyl naphthyl hydrazone bound at a novel site. ACS Chem. Biol., 2006, 1, 702-712
-
(2006)
ACS Chem. Biol.
, vol.1
, pp. 702-712
-
-
Himmel, D.M.1
Sarafianos, S.G.2
Dharmasena, S.3
Hossain, M.M.4
McCoy-Simandle, K.5
Ilina, T.6
Clark Jr., A.D.7
Knight, J.L.8
Julias, J.G.9
Clark, P.K.10
Krogh-Jespersen, K.11
Levy, R.M.12
Hughes, S.H.13
Parniak, M.A.14
Arnold, E.15
-
57
-
-
33746883932
-
Novel nonnucleoside inhibitors that select nucleoside inhibitor resistance mutations in human immunodeficiency virus type 1 reverse transcriptase
-
DOI 10.1128/AAC.00127-06
-
Zhang, Z.; Walker, M.; Xu, W.; Shim, J.H.; Girardet, J.L.; Hamatake, R.K.; Hong, Z. Novel nonnucleoside inhibitors that select nucleoside inhibitor resistance mutations in human immunode ficiency virus type 1 reverse transcriptase. Antimicrob. Agents Chemother., 2006, 50, 2772-2781 (Pubitemid 44198700)
-
(2006)
Antimicrobial Agents and Chemotherapy
, vol.50
, Issue.8
, pp. 2772-2781
-
-
Zhang, Z.1
Walker, M.2
Xu, W.3
Shim, J.H.4
Girardet, J.-L.5
Hamatake, R.K.6
Hong, Z.7
-
58
-
-
33845410116
-
Indolopyridones inhibit human immunodeficiency virus reverse transcriptase with a novel mechanism of action
-
DOI 10.1128/JVI.00889-06
-
Jochmans, D.; Deval, J.; Kesteleyn, B.; Van Marck, H.; Bettens, E.; De Baere, I.; Dehertogh, P.; Ivens, T.; Van Ginderen, M.; Van Schoubroeck, B.; Ehteshami, M.; Wigerinck, P.; Götte, M.; Hertogs, K. Indolopyridones inhibit human immunodeficiency virus reverse transcriptase with a novel mechanism of action. J. Virol., 2006, 80, 12283-12292 (Pubitemid 44904378)
-
(2006)
Journal of Virology
, vol.80
, Issue.24
, pp. 12283-12292
-
-
Jochmans, D.1
Deval, J.2
Kesteleyn, B.3
Van Marck, H.4
Bettens, E.5
De Baere, I.6
Dehertogh, P.7
Ivens, T.8
Van Ginderen, M.9
Van Schoubroeck, B.10
Ehteshami, M.11
Wigerinck, P.12
Gotte, M.13
Hertogs, K.14
-
59
-
-
4644270641
-
Novel mechanism of inhibition of HIV-1 reverse transcriptase by a new non-nucleoside analog, KM-1
-
Wang, L.Z.; Kenyon, G.L.; Johnson, K.A. Novel mechanism of inhibition of HIV-1 reverse transcriptase by a new non-nucleoside analog, KM-1. J. Biol. Chem., 2004, 279, 38424-38432
-
(2004)
J. Biol. Chem.
, vol.279
, pp. 38424-38432
-
-
Wang, L.Z.1
Kenyon, G.L.2
Johnson, K.A.3
-
60
-
-
0036910799
-
A novel mechanism for inhibition of HIV-1 reverse transcriptase
-
DOI 10.1016/S0045-2068(02)00502-3
-
Skillman, A.G.; Maurer, K.W.; Roe, D.C.; Stauber, M.J.; Eargle, D.; Ewing, T.J.; Muscate, A.; Davioud-Charvet, E.; Medaglia, M.V.; Fisher, R.J.; Arnold, E.; Gao, H.Q.; Buckheit, R.; Boyer, P.L.; Hughes, S.H.; Kuntz, I.D.; Kenyon, G.L. A novel mechanism for inhibition of HIV-1 reverse transcriptase. Bioorg. Chem., 2002, 30, 443-458 (Pubitemid 36294220)
-
(2002)
Bioorganic Chemistry
, vol.30
, Issue.6
, pp. 443-458
-
-
Skillman, A.G.1
Maurer, K.W.2
Roe, D.C.3
Stauber, M.J.4
Eargle, D.5
Ewing, T.J.A.6
Muscate, A.7
Davioud-Charvet, E.8
Medaglia, M.V.9
Fisher, R.J.10
Arnold, E.11
Gao, H.-Q.12
Buckheit, R.13
Boyer, P.L.14
Hughes, S.H.15
Kuntz, I.D.16
Kenyon, G.L.17
-
61
-
-
33646509695
-
Developing novel nonnucleoside HIV-1 reverse transcriptase inhibitors: Beyond the butterfly
-
Basavapathruni, A.; Anderson, K.S. Developing novel nonnucleoside HIV-1 reverse transcriptase inhibitors: beyond the butterfly. Curr. Pharm. Des., 2006, 12, 1857-1865
-
(2006)
Curr. Pharm. Des.
, vol.12
, pp. 1857-1865
-
-
Basavapathruni, A.1
Anderson, K.S.2
-
62
-
-
34447574625
-
Aptamer Displacement Identifies Alternative Small-Molecule Target Sites that Escape Viral Resistance
-
DOI 10.1016/j.chembiol.2007.06.003, PII S1074552107002074
-
Yamazaki, S.; Tan, L.; Mayer, G.; Hartig, J.S.; Song, J.N.; Reuter, S.; Restle, T.; Laufer, S.D.; Grohmann, D.; Kräusslich, H.G.; Bajorath, J.; Famulok, M. Aptamer displacement identifies alternative small-molecule target sites that escape viral resistance. Chem. Biol., 2007, 14, 804-812 (Pubitemid 47081421)
-
(2007)
Chemistry and Biology
, vol.14
, Issue.7
, pp. 804-812
-
-
Yamazaki, S.1
Tan, L.2
Mayer, G.3
Hartig, J.S.4
Song, J.-N.5
Reuter, S.6
Restle, T.7
Laufer, S.D.8
Grohmann, D.9
Krausslich, H.-G.10
Bajorath, J.11
Famulok, M.12
-
63
-
-
33747116051
-
Dimerization inhibitors of HIV-1 reverse transcriptase, protease and integrase: A single mode of inhibition for the three HIV enzymes?
-
DOI 10.1016/j.antiviral.2006.05.021, PII S0166354206001689
-
Camarasa, M.J.; Velázquez, S.; San-Félix, A.; Pérez-Pérez, M.J.; Gago, F. Dimerization inhibitors of HIV-1 reverse transcriptase, protease and integrase: a single mode of inhibition for the three HIV enzymes? Antiviral. Res., 2006, 71, 260-267 (Pubitemid 44223776)
-
(2006)
Antiviral Research
, vol.71
, Issue.2-3 SPEC. ISSUE
, pp. 260-267
-
-
Camarasa, M.-J.1
Velazquez, S.2
San-Felix, A.3
Perez-Perez, M.-J.4
Gago, F.5
-
64
-
-
33646506098
-
TSAO derivatives, inhibitors of HIV-1 reverse transcriptase dimerization: Recent progress
-
Camarasa, M.J.; Velázquez, S.; San-Félix, A.; Pérez-Pérez, M.J.; Bonache, M.C.; De Castro, S. TSAO derivatives, inhibitors of HIV-1 reverse transcriptase dimerization: recent progress. Curr. Pharm. Des., 2006, 12, 1895-1907
-
(2006)
Curr. Pharm. Des.
, vol.12
, pp. 1895-1907
-
-
Camarasa, M.J.1
Velázquez, S.2
San-Félix, A.3
Pérez-Pérez, M.J.4
Bonache, M.C.5
De Castro, S.6
-
65
-
-
27244439063
-
TSAO derivatives the first non-peptide inhibitors of HIV-1 RT dimerization
-
Camarasa, M.J.; Velázquez, S.; San-Félix, A.; Pérez-Pérez, M.J. TSAO derivatives the first non-peptide inhibitors of HIV-1 RT dimerization. Antivir. Chem. Chemother., 2005, 16, 147-153
-
(2005)
Antivir. Chem. Chemother.
, vol.16
, pp. 147-153
-
-
Camarasa, M.J.1
Velázquez, S.2
San-Félix, A.3
Pérez-Pérez, M.J.4
-
66
-
-
2942525968
-
TSAO compounds: The comprehensive story of a unique family of HIV-1 specific inhibitors of reverse transcriptase
-
DOI 10.2174/1568026043388600
-
Camarasa, M.J.; San-Félix, A.; Velázquez, S.; Pérez-Pérez, M.J.; Gago, F.; Balzarini, J. TSAO compounds: the comprehensive story of a unique family of HIV-1 specific inhibitors of reverse transcriptase. Curr. Top Med. Chem., 2004, 4, 945-963 (Pubitemid 38864692)
-
(2004)
Current Topics in Medicinal Chemistry
, vol.4
, Issue.9
, pp. 945-963
-
-
Camarasa, M.-J.1
San-Felix, A.2
Velazquez, S.3
Perez-Perez, M.-J.4
Gago, F.5
Balzarini, J.6
-
67
-
-
42049097738
-
Novel N-3 substituted TSAO-T derivatives: Synthesis and anti- HIV-evaluation
-
Bonache, M.C.; Quesada, E.; Sheen, C.W.; Balzarini, J.; Sluis- Cremer, N.; Pérez-Pérez, M.J.; Camarasa, M.J.; San-Félix, A. Novel N-3 substituted TSAO-T derivatives: synthesis and anti- HIV-evaluation. Nucleosides Nucleotides Nucleic Acids, 2008, 27, 351-367
-
(2008)
Nucleosides Nucleotides Nucleic Acids
, vol.27
, pp. 351-367
-
-
Bonache, M.C.1
Quesada, E.2
Sheen, C.W.3
Balzarini, J.4
Sluis- Cremer, N.5
Pérez-Pérez, M.J.6
Camarasa, M.J.7
San-Félix, A.8
-
68
-
-
41149136849
-
Anti-HIV-1 activity, and modeling studies of N-3 Boc TSAO compound
-
Tomassi, C.; Nguyen, V.N.; Marco-Contelles, J.; Balzarini, J.; Pannecouque, C.; De Clercq, E.; Soriano, E.; Postel, D. Synthesis, anti-HIV-1 activity, and modeling studies of N-3 Boc TSAO compound. Bioorg. Med. Chem. Lett., 2008, 18, 2277-2281
-
(2008)
Bioorg. Med. Chem. Lett.
, vol.18
, pp. 2277-2281
-
-
Tomassi, C.1
Nguyen, V.N.2
Marco-Contelles, J.3
Balzarini, J.4
Pannecouque, C.5
De Clercq, E.6
Soriano, E.7
Synthesis, P.D.8
-
69
-
-
42149114258
-
Synthesis and anti-HIV1 biological activity of novel 5″-ATSAO compounds
-
DOI 10.1016/j.bmc.2008.02.026, PII S0968089608001363
-
Tomassi, C.; Nguyen Van Nhien, A.; Marco-Contelles, J.; Balzarini, J.; Pannecouque, C.; De Clercq, E.; Postel, D. Synthesis and anti-HIV1 biological activity of novel 5″-ATSAO compounds. Bioorg. Med. Chem., 2008, 16, 4733-4741 (Pubitemid 351539016)
-
(2008)
Bioorganic and Medicinal Chemistry
, vol.16
, Issue.8
, pp. 4733-4741
-
-
Tomassi, C.1
Nguyen Van Nhien, A.2
Marco-Contelles, J.3
Balzarini, J.4
Pannecouque, C.5
De Clercq, E.6
Postel, D.7
-
70
-
-
36949009853
-
Novel non-nucleoside human cytomegalovirus inhibitors based upon TSAO nucleoside derivatives: Structure-activity relationships
-
DOI 10.1080/15257770701490431, PII 788145970
-
de Castro, S.; Andrei, G.; Snoeck, R.; Balzarini, J.; Camarasa, M.J.; Velázquez, S. Novel non-nucleoside human cytomegalovirus inhibitors based upon TSAO nucleoside derivatives: structureactivity relationships. Nucleosides Nucleotides Nucleic Acids, 2007, 26, 625-628 (Pubitemid 350239245)
-
(2007)
Nucleosides, Nucleotides and Nucleic Acids
, vol.26
, Issue.6-7
, pp. 625-628
-
-
De Castro, S.1
Andrei, G.2
Snoeck, R.3
Balzarini, J.4
Camarasa, M.-J.5
Velazquez, S.6
-
71
-
-
33746948397
-
Structure-activity relationships of [2′,5′-bis-O-(tert- Butyldimethylsilyl)-beta-D-ribofuranosyl]-3′-spiro-5″-(4′- amino-1″,2″-oxathiole-2″,2″-dioxide)thymine derivatives as inhibitors of HIV-1 reverse transcriptase dimerization
-
DOI 10.1021/jm0604575
-
Sluis-Cremer, N.; Hamamouch, N.; San Félix, A.; Velazquez, S.; Balzarini, J.; Camarasa, M.J. Structure-activity relationships of [2′,5′-bis-O-(tert-butyldimethylsilyl)-beta-D-ribofuranosyl] -3′-spiro -5″-(4″-amino-1″,2″-oxathiole-2″, 2″-dioxide)thymine derivatives as inhibitors of HIV-1 reverse transcriptase dimerization. J. Med. Chem., 2006, 49, 4834-4841 (Pubitemid 44202171)
-
(2006)
Journal of Medicinal Chemistry
, vol.49
, Issue.16
, pp. 4834-4841
-
-
Sluis-Cremer, N.1
Hamamouch, N.2
San Felix, A.3
Velazquez, S.4
Balzarini, J.5
Camarasa, M.-J.6
-
72
-
-
33746926347
-
Computational analysis of aza analogues of 2′,5′-bis-O-(tert- Butyldimethylsilyl)-beta-D-ribofuranosel-3′-spiro-5″(4″- amino-1″,2″-oxathiole-2″,2″-dioxide) (TSAO) as HIV-1 reverse transcriptase inhibitors: Relevance of conformational properties on the inhibitory activity
-
DOI 10.1021/ci0600410
-
Soriano, E.; Marco-Contelles, J.; Tomassi, C.; Nguyen Van Nhien, A.; Postel, D. Computational analysis of aza analogues of [2′,5′-bis- O-(tert-butyldimethylsilyl)-beta-D- ribofuranose]-3′-spiro-5″- (4″- amino-1″,2″-oxathiole-2″,2″-dioxide) (TSAO) as HIV-1 reverse transcriptase inhibitors: relevance of conformational properties on the inhibitory activity. J. Chem. Inf. Model, 2006, 46, 1666-1677 (Pubitemid 44185693)
-
(2006)
Journal of Chemical Information and Modeling
, vol.46
, Issue.4
, pp. 1666-1677
-
-
Soriano, E.1
Marco-Contelles, J.2
Tomassi, C.3
Van Nhien, A.N.4
Postel, D.5
-
73
-
-
33746974786
-
Discovery of TSAO derivatives with an unusual HIV-1 activity/resistance profile
-
DOI 10.1016/j.antiviral.2006.02.009, PII S0166354206000672
-
de Castro, S.; García-Aparicio, C.; Van Laethem, K.; Gago, F.; Lobatón, E.; De Clercq, E.; Balzarini, J.; Camarasa, M.J.; Velázquez, S. Discovery of TSAO derivatives with an unusual HIV-1 activity/ resistance profile. Antiviral. Res., 2006, 71, 15-23. (Pubitemid 44202207)
-
(2006)
Antiviral Research
, vol.71
, Issue.1
, pp. 15-23
-
-
De Castro, S.1
Garcia-Aparicio, C.2
Van Laethem, K.3
Gago, F.4
Lobaton, E.5
De Clercq, E.6
Balzarini, J.7
Camarasa, M.-J.8
Velazquez, S.9
-
74
-
-
27144449950
-
Improving the antiviral efficacy and selectivity of HIV-1 reverse transcriptase inhibitor TSAO-T by the introduction of functional groups at the N-3 position
-
DOI 10.1021/jm050437n
-
Bonache, M.C.; Chamorro, C.; Velázquez, S.; De Clercq, E.; Balzarini, J.; Barrios, F.R.; Gago, F.; Camarasa, M.J.; San-Félix, A. Improving the antiviral efficacy and selectivity of HIV-1 reverse transcriptase inhibitor TSAO-T by the introduction of functional groups at the N-3 position. J. Med. Chem., 2005, 48, 6653-6660 (Pubitemid 41509181)
-
(2005)
Journal of Medicinal Chemistry
, vol.48
, Issue.21
, pp. 6653-6660
-
-
Bonache, M.-C.1
Chamorro, C.2
Velazquez, S.3
De Clercq, E.4
Balzarini, J.5
Barrios, F.R.6
Gago, F.7
Camarasa, M.-J.8
San-Felix, A.9
-
75
-
-
21244499836
-
First synthesis and evaluation of the inhibitory effects of Aza analogues of TSAO on HIV-1 replication
-
DOI 10.1021/jm050091g
-
Nguyen Van Nhien, A.; Tomassi, C.; Len, C.; Marco-Contelles, J.L.; Balzarini, J.; Pannecouque, C.; De Clercq, E.; Postel, D. First synthesis and evaluation of the inhibitory effects of aza analogues of TSAO on HIV-1 replication. J. Med. Chem., 2005, 48, 4276-4284 (Pubitemid 40884931)
-
(2005)
Journal of Medicinal Chemistry
, vol.48
, Issue.13
, pp. 4276-4284
-
-
Van Nhien, A.N.1
Tomassi, C.2
Len, C.3
Marco-Contelles, J.L.4
Balzarini, J.5
Pannecouque, C.6
De Clercq, E.7
Postel, D.8
-
76
-
-
0141485341
-
N-3 substituted TSAO derivatives as a probe to explore the dimeric interface of HIV-1 reverse transcriptase
-
DOI 10.1081/NCN-120022692
-
Bonache, M.C.; Chamorro, C.; Velázquez, S.; De Clercq, E.; Balzarini, J.; Camarasa, M.J.; San-Félix, A. N-3 substituted TSAO derivatives as a probe to explore the dimeric interface of HIV-1 reverse transcriptase. Nucleosides Nucleotides Nucleic Acids, 2003, 22, 947-949 (Pubitemid 37139297)
-
(2003)
Nucleosides, Nucleotides and Nucleic Acids
, vol.22
, Issue.5-8
, pp. 947-949
-
-
Bonache, M.-C.1
Chamorro, C.2
Velazquez, S.3
De Clercq, E.4
Balzarini, J.5
Camarasa, M.-J.6
San-Felix, A.7
-
77
-
-
0035821586
-
Identification of a putative binding site for [2′,5′-Bis-O- (tert-butyldimethylsilyl) -beta-D-ribofuranosyl]-3′-spiro-5″- (4″-amino-1″,2″-oxathiole-2″,2″-dioxide)thymine (TSAO) derivatives at the p51-p66 interface of HIV-1 reverse transcriptase
-
DOI 10.1021/jm001095i
-
Rodríguez-Barrios, F.; Pérez, C.; Lobatón, E.; Velázquez, S.; Chamorro, C.; San-Félix, A.; Pérez- Pérez, M.J.; Camarasa, M.J.; Pelemans, H.; Balzarini, J.; Gago, F. Identification of a putative binding site for [2′,5′-bis-O-(tert- butyldimethylsilyl)-beta-Dribofuranosyl]- 3′-spiro-5″-(4″- amino-1″,2″-oxathiole-2″,2″-dioxide) thymine (TSAO) derivatives at the p51-p66 interface of HIV-1 reverse transcriptase. J. Med. Chem., 2001, 44, 1853-1865 (Pubitemid 32888185)
-
(2001)
Journal of Medicinal Chemistry
, vol.44
, Issue.12
, pp. 1853-1865
-
-
Rodriguez-Barrios, F.1
Perez, C.2
Lobaton, E.3
Velazquez, S.4
Chamorro, C.5
San-Felix, A.6
Perez-Perez, M.-J.7
Camarasa, M.-J.8
Pelemans, H.9
Balzarini, J.10
Gago, F.11
-
78
-
-
0036076157
-
Destabilization of the HIV-1 reverse transcriptase dimer upon interaction with N-acyl hydrazone inhibitors
-
Sluis-Cremer, N.; Arion, D.; Parniak, M.A. Destabilization of the HIV-1 reverse transcriptase dimer upon interaction with N-acyl hydrazone inhibitors. Mol. Pharmacol., 2002, 62, 398-405.
-
(2002)
Mol. Pharmacol.
, vol.62
, pp. 398-405
-
-
Sluis-Cremer, N.1
Arion, D.2
Parniak, M.A.3
-
79
-
-
44049097439
-
Small molecule inhibitors targeting HIV-1 reverse transcriptase dimerization
-
Grohmann, D.; Corradi, V.; Elbasyouny, M.; Baude, A.; Horenkamp, F.; Laufer, S.D.; Manetti, F.; Botta, M.; Restle, T. Small molecule inhibitors targeting HIV-1 reverse transcriptase dimerization. Chembiochem, 2008, 9, 916-922
-
(2008)
Chembiochem
, vol.9
, pp. 916-922
-
-
Grohmann, D.1
Corradi, V.2
Elbasyouny, M.3
Baude, A.4
Horenkamp, F.5
Laufer, S.D.6
Manetti, F.7
Botta, M.8
Restle, T.9
-
80
-
-
22444443468
-
The amino acid Asn136 in HIV-1 reverse transcriptase (RT) maintains efficient association of both RT subunits and enables the rational design of novel RT inhibitors
-
DOI 10.1124/mol.105.012435
-
Balzarini, J.; Auwerx, J.; Rodríguez-Barrios, F.; Chedad, A.; Farkas, V.; Ceccherini-Silberstein, F.; García-Aparicio, C.; Velázquez, S.; De Clercq, E.; Perno, C.F.; Camarasa, M.J.; Gago, F. The amino acid Asn136 in HIV-1 reverse transcriptase (RT) maintains efficient association of both RT subunits and enables the rational design of novel RT inhibitors. Mol. Pharmacol., 2005, 68, 49-60. (Pubitemid 41007052)
-
(2005)
Molecular Pharmacology
, vol.68
, Issue.1
, pp. 49-60
-
-
Balzarini, J.1
Auwerx, J.2
Rodriguez-Barrios, F.3
Chedad, A.4
Farkas, V.5
Ceccherini-Silberstein, F.6
Garcia-Aparicio, C.7
Velazquez, S.8
De Clercq, E.9
Perno, C.-F.10
Camarasa, M.-J.11
Gago, F.12
-
81
-
-
33846069355
-
Analysis of Amino Acids in the β7-β8 Loop of Human Immunodeficiency Virus Type 1 Reverse Transcriptase for their Role in Virus Replication
-
DOI 10.1016/j.jmb.2006.10.089, PII S0022283606015178
-
Mulky, A.; Vu, B.C.; Conway, J.A.; Hughes, S.H.; Kappes, J.C. Analysis of amino acids in the β7-β8 loop of human immunodeficiency virus type 1 reverse transcriptase for their role in virus replication. J. Mol. Biol., 2007, 365, 1368-1378 (Pubitemid 46061425)
-
(2007)
Journal of Molecular Biology
, vol.365
, Issue.5
, pp. 1368-1378
-
-
Mulky, A.1
Vu, B.C.2
Conway, J.A.3
Hughes, S.H.4
Kappes, J.C.5
-
82
-
-
29144436035
-
Effect of a bound non-nucleoside RT inhibitor on the dynamics of wild-type and mutant HIV-1 reverse transcriptase
-
Zhou, Z.; Madrid, M.; Evanseck, J.D.; Madura, J.D. Effect of a bound non-nucleoside RT inhibitor on the dynamics of wild-type and mutant HIV-1 reverse transcriptase. J. Am. Chem. Soc., 2005, 127, 17253-17260
-
(2005)
J. Am. Chem. Soc.
, vol.127
, pp. 17253-17260
-
-
Zhou, Z.1
Madrid, M.2
Evanseck, J.D.3
Madura, J.D.4
-
83
-
-
0026607918
-
Nonnucleoside inhibitors of HIV-1 reverse transcriptase: Nevirapine as a prototype drug
-
Grob, P.M.; Wu, J.C.; Cohen, K.A.; Ingraham, R.H.; Shih, C.K.; Hargrave, K.D.; McTague, T.L.; Merluzzi, V.J. Nonnucleoside inhibitors of HIV-1 reverse transcriptase: nevirapine as a prototype drug. AIDS Res. Hum. Retroviruses, 1992, 8, 145-152
-
(1992)
AIDS Res. Hum. Retroviruses
, vol.8
, pp. 145-152
-
-
Grob, P.M.1
Wu, J.C.2
Cohen, K.A.3
Ingraham, R.H.4
Shih, C.K.5
Hargrave, K.D.6
McTague, T.L.7
Merluzzi, V.J.8
-
84
-
-
14444278761
-
Novel nonnucleoside inhibitors of HIV-1 reverse transcriptase. 7. 8-Arylethyldipyridodiazepinones as potent broadspectrum inhibitors of wild-type and mutant enzymes
-
Klunder, J.M.; Hoermann, M.; Cywin, C.L.; David, E.; Brickwood, J.R.; Schwartz, R.; Barringer, K.J.; Pauletti, D.; Shih, C.K.; Erickson, D.A.; Sorge C.L.; Joseph, D.P.; Hattox, S.E.; Adams, J.; Grob, P.M. Novel nonnucleoside inhibitors of HIV-1 reverse transcriptase. 7. 8-Arylethyldipyridodiazepinones as potent broadspectrum inhibitors of wild-type and mutant enzymes. J. Med. Chem., 1998, 41, 2960-2971
-
(1998)
J. Med. Chem.
, vol.41
, pp. 2960-2971
-
-
Klunder, J.M.1
Hoermann, M.2
Cywin, C.L.3
David, E.4
Brickwood, J.R.5
Schwartz, R.6
Barringer, K.J.7
Pauletti, D.8
Shih, C.K.9
Erickson, D.A.10
Sorge, C.L.11
Joseph, D.P.12
Hattox, S.E.13
Adams, J.14
Grob, P.M.15
-
85
-
-
15144354770
-
Novel nonnucleoside inhibitors of HIV-1 reverse transcriptase. 8. 8- Aryloxymethyl- and 8-arylthiomethyldipyridodiazepinones
-
DOI 10.1021/jm9707030
-
Cywin, C.L.; Klunder, J.M.; Hoermann, M.; Brickwood, J.R.; David, E.; Grob, P.M.; Schwartz, R.; Pauletti, D.; Barringer, K.J.; Shih, C.K.; Sorge, C.L.; Erickson, D.A.; Joseph, D.P.; Hattox, S.E. Novel nonnucleoside inhibitors of HIV-1 reverse transcriptase. 8. 8-Aryloxymethyl- and 8- arylthiomethyldipyridodiazepinones. J. Med. Chem., 1998, 41, 2972-2984 (Pubitemid 28359932)
-
(1998)
Journal of Medicinal Chemistry
, vol.41
, Issue.16
, pp. 2972-2984
-
-
Cywin, C.L.1
Klunder, J.M.2
Hoermann, M.3
Brickwood, J.R.4
David, E.5
Grob, P.M.6
Schwartz, R.7
Pauletti, D.8
Barringer, K.J.9
Shih, C.-K.10
Sorge, C.L.11
Erickson, D.A.12
Joseph, D.P.13
Hattox, S.E.14
-
86
-
-
1642452639
-
Novel nevirapine-like inhibitors with improved activity against NNRTI-resistant HIV: 8-Heteroarylthiomethyldipyridodiazepinone derivatives
-
DOI 10.1016/j.bmcl.2003.11.049
-
Yoakim, C.; Bonneau, P.R.; Déziel, R.; Doyon, L.; Duan, J.; Guse, I.; Landry, S.; Malenfant, E.; Naud, J.; Ogilvie, W.W.; O'Meara, J.A.; Plante, R.; Simoneau, B.; Thavonekham, B.; Bös, M.; Cordingley, M.G. Novel nevirapine-like inhibitors with improved activity against NNRTI-resistant HIV: 8-heteroarylthiomethyldipyridodiazepinone derivatives. Bioorg. Med. Chem. Lett., 2004, 14, 739-742 (Pubitemid 38114863)
-
(2004)
Bioorganic and Medicinal Chemistry Letters
, vol.14
, Issue.3
, pp. 739-742
-
-
Yoakim, C.1
Bonneau, P.R.2
Deziel, R.3
Doyon, L.4
Duan, J.5
Guse, I.6
Landry, S.7
Malenfant, E.8
Naud, J.9
Ogilvie, W.W.10
O'Meara, J.A.11
Plante, R.12
Simoneau, B.13
Thavonekham, B.14
Bos, M.15
Cordingley, M.G.16
-
87
-
-
23944520311
-
Novel 8-substituted dipyridodiazepinone inhibitors with a broad-spectrum of activity against HIV-1 strains resistant to non-nucleoside reverse transcriptase inhibitors
-
DOI 10.1021/jm050255t
-
O'Meara, J.A.; Yoakim, C.; Bonneau, P.R.; Bös, M.; Cordingley, M.G.; Déziel, R.; Doyon, L.; Duan, J.; Garneau, M.; Guse, I.; Landry, S.; Malenfant, E.; Naud, J.; Ogilvie, W.W.; Thavonekham, B.; Simoneau, B. Novel 8-substituted dipyridodiazepinone inhibitors with a broad-spectrum of activity against HIV-1 strains resistant to non-nucleoside reverse transcriptase inhibitors. J. Med. Chem., 2005, 48, 5580-5588 (Pubitemid 41209255)
-
(2005)
Journal of Medicinal Chemistry
, vol.48
, Issue.17
, pp. 5580-5588
-
-
O'Meara, J.A.1
Yoakim, C.2
Bonneau, P.R.3
Bos, M.4
Cordingley, M.G.5
Deziel, R.6
Doyon, L.7
Duan, J.8
Garneau, M.9
Guse, I.10
Landry, S.11
Malenfant, E.12
Naud, J.13
Ogilvie, W.W.14
Thavonekham, B.15
Simoneau, B.16
-
88
-
-
32544437940
-
Crystallographic study with BILR 355 BS, A novel nonnucleoside reverse transcriptase inhibitor (NNRTI) with a broad anti HIV-1 profile
-
Rio de Janeiro-July 24-27
-
Coulombe, R.; Fink, D.; Landry, S.; Lessard, I.A.D.; McCollum, R.; Naud, J.; O'Meara, J.; Simoneau, B.; Yoakim, C.; Bonneau, P.R. Crystallographic study with BILR 355 BS, A novel nonnucleoside reverse transcriptase inhibitor (NNRTI) with a broad anti HIV-1 profile. 3rd International AIDS Society Conference on HIV Pathogenesis and Treatment. Rio de Janeiro-July 24-27, 2005.
-
(2005)
3rd International AIDS Society Conference on HIV Pathogenesis and Treatment
-
-
Coulombe, R.1
Fink, D.2
Landry, S.3
Lessard, I.A.D.4
McCollum, R.5
Naud, J.6
O'Meara, J.7
Simoneau, B.8
Yoakim, C.9
Bonneau, P.R.10
-
89
-
-
57349096037
-
Design of annulated pyrazoles as inhibitors of HIV-1 reverse transcriptase
-
Sweeney, Z.K.; Harris, S.F.; Arora, N.; Javanbakht, H.; Li, Y.; Fretland, J.; Davidson, J.P.; Billedeau, J.R.; Gleason, S.K.; Hirschfeld, D.; Kennedy-Smith, J.J.; Mirzadegan, T.; Roetz, R.; Smith, M.; Sperry, S.; Suh, J.M.; Wu, J.; Tsing, S.; Villasenor, A.G.; Paul, A.; Su, G.; Heilek, G.; Hang, J.Q.; Zhou, A.S.; Jernelius, J.A.; Zhang, F.J.; Klumpp, K. Design of annulated pyrazoles as inhibitors of HIV-1 reverse transcriptase. J. Med. Chem., 2008, 51, 7449-7458
-
(2008)
J. Med. Chem.
, vol.51
, pp. 7449-7458
-
-
Sweeney, Z.K.1
Harris, S.F.2
Arora, N.3
Javanbakht, H.4
Li, Y.5
Fretland, J.6
Davidson, J.P.7
Billedeau, J.R.8
Gleason, S.K.9
Hirschfeld, D.10
Kennedy-Smith, J.J.11
Mirzadegan, T.12
Roetz, R.13
Smith, M.14
Sperry, S.15
Suh, J.M.16
Wu, J.17
Tsing, S.18
Villasenor, A.G.19
Paul, A.20
Su, G.21
Heilek, G.22
Hang, J.Q.23
Zhou, A.S.24
Jernelius, J.A.25
Zhang, F.J.26
Klumpp, K.27
more..
-
90
-
-
0034435564
-
Structural basis for the resilience of efavirenz (DMP- 266) to drug resistance mutations in HIV-1 reverse transcriptase
-
Ren, J.; Milton, J.; Weaver, K.L.; Short, S.A.; Stuart, D.I.; Stammers, D.K. Structural basis for the resilience of efavirenz (DMP- 266) to drug resistance mutations in HIV-1 reverse transcriptase. Structure, 2000, 8, 1089-1094
-
(2000)
Structure
, vol.8
, pp. 1089-1094
-
-
Ren, J.1
Milton, J.2
Weaver, K.L.3
Short, S.A.4
Stuart, D.I.5
Stammers, D.K.6
-
91
-
-
15244339404
-
Combining structure-based drug design and pharmacophores
-
DOI 10.1016/j.jmgm.2004.12.001, PII S1093326304001226
-
Griffith, R.; Luu, T.T.; Garner, J.; Keller, P.A. Combining structure-based drug design and pharmacophores. J. Mol. Graph Model, 2005, 23, 439-446 (Pubitemid 40386873)
-
(2005)
Journal of Molecular Graphics and Modelling
, vol.23
, Issue.5
, pp. 439-446
-
-
Griffith, R.1
Luu, T.T.T.2
Garner, J.3
Keller, P.A.4
-
92
-
-
33748500440
-
Novel tight binding PETT, HEPT and DABO-based non-nucleoside inhibitors of HIV-1 reverse transcriptase
-
DOI 10.1080/14756360600774413, PII UH5216760405L724
-
D'Cruz, O.J.; Uckun, F.M. Novel tight binding PETT, HEPT and DABO-based non-nucleoside inhibitors of HIV-1 reverse transcriptase. J. Enzyme Inhib. Med. Chem., 2006, 21, 329-350 (Pubitemid 44355782)
-
(2006)
Journal of Enzyme Inhibition and Medicinal Chemistry
, vol.21
, Issue.4
, pp. 329-350
-
-
D'Cruz, O.J.1
Uckun, F.M.2
-
93
-
-
33745826310
-
Novel broad-spectrum thiourea nonnucleoside inhibitors for the prevention of mucosal HIV transmission
-
D'Cruz, O.J.; Uckun, F.M. Novel broad-spectrum thiourea nonnucleoside inhibitors for the prevention of mucosal HIV transmission. Curr. HIV Res., 2006, 4, 329-345
-
(2006)
Curr. HIV Res.
, vol.4
, pp. 329-345
-
-
D'Cruz, O.J.1
Uckun, F.M.2
-
94
-
-
0031788490
-
Rational design and synthesis of phenethyl-5-bromopyridyl thiourea derivatives as potent non-nucleoside inhibitors of HIV reverse transcriptase
-
DOI 10.1016/S0968-0896(98)00108-4, PII S0968089698001084
-
Vig, R.; Mao, C.; Venkatachalam, T.K.; Tuel-Ahlgren, L.; Sudbeck, E.A.; Uckun, F.M. Rational design and synthesis of phenethyl-5-bromopyridyl thiourea derivatives as potent nonnucleoside inhibitors of HIV reverse transcriptase. Bioorg. Med. Chem., 1998, 6, 1789-1797 (Pubitemid 28524233)
-
(1998)
Bioorganic and Medicinal Chemistry
, vol.6
, Issue.10
, pp. 1789-1797
-
-
Vig, R.1
Mao, C.2
Venkatachalam, T.K.3
Tuel-Ahlgren, L.4
Sudbeck, E.A.5
Uckun, F.M.6
-
95
-
-
0032544145
-
Structure-based design of N-[2-(1-piperidinylethyl)]-N′-[2-(5- Bromopyridyl)]-thiourea and N-[2-(1-piperazinylethyl)] -N′-[2-(5- bromopyridyl)]-thiourea as potent non-nucleoside inhibitors of HIV-1 reverse transcriptase
-
Mao, C.; Vig, R.; Venkatachalam, T.K.; Sudbeck, E.A.; Uckun, F.M. Structure-based design of N-[2-(1-piperidinylethyl)]-N′-[2-(5- bromopyridyl)]-thiourea and N-[2-(1-piperazinylethyl)] -N′-[2-(5- bromopyridyl)]-thiourea as potent non-nucleoside inhibitors of HIV-1 reverse transcriptase. Bioorg. Med. Chem. Lett., 1998, 8, 2213-2218
-
(1998)
Bioorg. Med. Chem. Lett.
, vol.8
, pp. 2213-2218
-
-
Mao, C.1
Vig, R.2
Venkatachalam, T.K.3
Sudbeck, E.A.4
Uckun, F.M.5
-
96
-
-
0031788490
-
Rational design and synthesis of phenethyl-5-bromopyridyl thiourea derivatives as potent nonnucleoside inhibitors of HIV reserve transcriptase
-
Vig, R.; Mao, C.; Venkatachalam, T.K.; Tuel-Ahlgren, L.; Sudbeck, E.A.; Uckun, F.M. Rational design and synthesis of phenethyl-5-bromopyridyl thiourea derivatives as potent nonnucleoside inhibitors of HIV reserve transcriptase. Bioorg. Med. Chem., 1998, 6, 1789-1797
-
(1998)
Bioorg. Med. Chem.
, vol.6
, pp. 1789-1797
-
-
Vig, R.1
Mao, C.2
Venkatachalam, T.K.3
Tuel-Ahlgren, L.4
Sudbeck, E.A.5
Uckun, F.M.6
-
97
-
-
0034333415
-
Structure-based drug design of non-nucleoside inhibitors for wildtype and drug-resistant HIV reverse transcriptase
-
Mao, C.; Sudbeck, E.A.; Venkatachalam, T.K.; Uckun, F.M. Structure-based drug design of non-nucleoside inhibitors for wildtype and drug-resistant HIV reverse transcriptase. Biochem. Pharmacol., 2000, 60, 1251-1265
-
(2000)
Biochem. Pharmacol.
, vol.60
, pp. 1251-1265
-
-
Mao, C.1
Sudbeck, E.A.2
Venkatachalam, T.K.3
Uckun, F.M.4
-
98
-
-
70450211515
-
Nonnucleoside inhibitors of reverse transcriptase, composite binding pocket and methods for use thereof
-
WO9947501A (1999); US6380190B (2002); US2005153995A (2005).
-
Vig, R.; Mao, C. Nonnucleoside inhibitors of reverse transcriptase, composite binding pocket and methods for use thereof. WO9947501A (1999); US6380190B (2002); US2005153995A (2005).
-
-
-
Vig, R.1
Mao, C.2
-
99
-
-
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. U.S.A., 1997, 94, 3984-3989
-
(1997)
Proc. Natl. Acad. Sci. U.S.A.
, 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
-
100
-
-
0029976422
-
Complexes of HIV-1 reverse transcriptase with inhibitors of the HEPT series reveal conformational changes relevant to the design of potent non- Nucleoside inhibitors
-
DOI 10.1021/jm960056x
-
Hopkins, A.L.; Ren, J.; Esnouf, R.M.; Willcox, B.E.; Jones, E.Y.; Ross, C.; Miyasaka, T.; Walker, R.T.; Tanaka, H.; Stammers, D.K.; Stuart, D.I. Complexes of HIV-1 reverse transcriptase with inhibitors of the HEPT series reveal conformational changes relevant to the design of potent non-nucleoside inhibitors. J. Med. Chem., 1996, 39, 1589-1600 (Pubitemid 26124233)
-
(1996)
Journal of Medicinal Chemistry
, vol.39
, Issue.8
, pp. 1589-1600
-
-
Hopkins, A.L.1
Ren, J.2
Esnouf, R.M.3
Willcox, B.E.4
Jones, E.Y.5
Ross, C.6
Miyasaka, T.7
Walker, R.T.8
Tanaka, H.9
Stammers, D.K.10
Stuart, D.I.11
-
101
-
-
27144449695
-
Designed multiple ligands. An emerging drug discovery paradigm
-
DOI 10.1021/jm058225d
-
Morphy, R.; Rankovic, Z. Designed multiple ligands. An emerging drug discovery paradigm. J. Med. Chem., 2005, 48, 6523-6543 (Pubitemid 41504710)
-
(2005)
Journal of Medicinal Chemistry
, vol.48
, Issue.21
, pp. 6523-6543
-
-
Morphy, R.1
Rankovic, Z.2
-
102
-
-
3242794178
-
From magic bullets to designed multiple ligands
-
DOI 10.1016/S1359-6446(04)03163-0, PII S1359644604031630
-
Morphy, R.; Kay, C.; Rankovic, Z. From magic bullets to designed multiple ligands. Drug Discov. Today, 2004, 9, 641-651 (Pubitemid 38981718)
-
(2004)
Drug Discovery Today
, vol.9
, Issue.15
, pp. 641-651
-
-
Morphy, R.1
Kay, C.2
Rankovic, Z.3
-
103
-
-
33746862160
-
The physicochemical challenges of designing multiple ligands
-
DOI 10.1021/jm0603015
-
Morphy, R.; Rankovic, Z. The physicochemical challenges of designing multiple ligands. J. Med. Chem., 2006, 49, 4961-4970 (Pubitemid 44201054)
-
(2006)
Journal of Medicinal Chemistry
, vol.49
, Issue.16
, pp. 4961-4970
-
-
Morphy, R.1
Rankovic, Z.2
-
104
-
-
33846574259
-
Fragments, network biology and designing multiple ligands
-
Morphy, R.; Rankovic, Z. Fragments, network biology and designing multiple ligands. Drug Discov. Today, 2007, 12, 156-160
-
(2007)
Drug Discov. Today
, vol.12
, pp. 156-160
-
-
Morphy, R.1
Rankovic, Z.2
-
105
-
-
65549171659
-
Designing Multiple Ligands-Medicinal Chemistry Strategies and Challenges
-
Morphy, R.; Rankovic, Z. Designing Multiple Ligands-Medicinal Chemistry Strategies and Challenges. Curr. Pharm. Des., 2009, 15, 587-600.
-
(2009)
Curr. Pharm. Des.
, vol.15
, pp. 587-600
-
-
Morphy, R.1
Rankovic, Z.2
-
106
-
-
68449098788
-
Designed multiple ligands: An emerging anti-HIV drug discovery paradigm
-
Zhan, P.; Liu, X. Designed multiple ligands: an emerging anti-HIV drug discovery paradigm. Curr. Pharm. Des., 2009, 15, 1893-1917
-
(2009)
Curr. Pharm. Des.
, vol.15
, pp. 1893-1917
-
-
Zhan, P.1
Liu, X.2
-
107
-
-
34547583281
-
Rationally designed dual inhibitors of HIV reverse transcriptase and integrase
-
DOI 10.1021/jm070512p
-
Wang, Z.; Bennett, E.M.; Wilson, D.J.; Salomon, C.; Vince, R. Rationally designed dual inhibitors of HIV reverse transcriptase and integrase. J. Med. Chem., 2007, 50, 3416-3419 (Pubitemid 47195448)
-
(2007)
Journal of Medicinal Chemistry
, vol.50
, Issue.15
, pp. 3416-3419
-
-
Wang, Z.1
Bennett, E.M.2
Wilson, D.J.3
Salomon, C.4
Vince, R.5
-
108
-
-
38949192885
-
Synthesis of pyrimidine and quinolone conjugates as a scaffold for dual inhibitors of HIV reverse transcriptase and integrase
-
DOI 10.1016/j.bmcl.2008.01.025, PII S0960894X08000395
-
Wang, Z.; Vince, R. Synthesis of pyrimidine and quinolone conjugates as a scaffold for dual inhibitors of HIV reverse transcriptase and integrase. Bioorg. Med. Chem. Lett., 2008, 1118, 1293-1296 (Pubitemid 351226545)
-
(2008)
Bioorganic and Medicinal Chemistry Letters
, vol.18
, Issue.4
, pp. 1293-1296
-
-
Wang, Z.1
Vince, R.2
-
109
-
-
41649107669
-
And synthesis of dual inhibitors of HIV reverse transcriptase and integrase: Introducing a diketoacid functionality into delavirdine
-
Wang, Z.; Vince, R. Design and synthesis of dual inhibitors of HIV reverse transcriptase and integrase: introducing a diketoacid functionality into delavirdine. Bioorg. Med. Chem., 2008, 16, 3587-3595
-
(2008)
Bioorg. Med. Chem.
, vol.16
, pp. 3587-3595
-
-
Wang, Z.1
Design, V.R.2
-
110
-
-
43049147306
-
The design and synthesis of diaryl ether second generation HIV-1 non-nucleoside reverse transcriptase inhibitors (NNRTIs) with enhanced potency versus key clinical mutations
-
DOI 10.1016/j.bmcl.2008.03.064, PII S0960894X08003491
-
Tucker, T.J.; Saggar, S.; Sisko, J.T.; Tynebor, R.M.; Williams, T.M.; Felock, P.J.; Flynn, J.A.; Lai, M.T.; Liang, Y.; McGaughey, G.; Liu, M.; Miller, M.; Moyer, G.; Munshi, V.; Perlow-Poehnelt, R.; Prasad, S.; Sanchez, R.;
-
(2008)
Bioorganic and Medicinal Chemistry Letters
, vol.18
, Issue.9
, pp. 2959-2966
-
-
Tucker, T.J.1
Saggar, S.2
Sisko, J.T.3
Tynebor, R.M.4
Williams, T.M.5
Felock, P.J.6
Flynn, J.A.7
Lai, M.-T.8
Liang, Y.9
McGaughey, G.10
Liu, M.11
Miller, M.12
Moyer, G.13
Munshi, V.14
Perlow-Poehnelt, R.15
Prasad, S.16
Sanchez, R.17
Torrent, M.18
Vacca, J.P.19
Wan, B.-L.20
Yan, Y.21
more..
-
111
-
-
58549120191
-
Diphenyl ether non-nucleoside reverse transcriptase inhibitors with excellent potency against resistant mutant viruses and promising pharmacokinetic properties
-
Sweeney, Z.K.; Kennedy-Smith, J.J.; Wu, J.; Arora, N.; Billedeau, J.R.; Davidson, J.P.; Fretland, J.; Hang, J.Q.; Heilek, G.M.; Harris, S.F.; Hirschfeld, D.; Inbar, P.; Javanbakht, H.; Jernelius, J.A.; Jin, Q.; Li, Y.; Liang, W.; Roetz, R.; Sarma, K.; Smith, M.; Stefanidis, D.; Su, G.; Suh, J.M.; Villaseñor, A.G.; Welch, M.; Zhang, F.J.; Klumpp, K. Diphenyl ether non-nucleoside reverse transcriptase inhibitors with excellent potency against resistant mutant viruses and promising pharmacokinetic properties. ChemMedChem, 2008, 4, 88-99.
-
(2008)
ChemMedChem
, vol.4
, pp. 88-99
-
-
Sweeney, Z.K.1
Kennedy-Smith, J.J.2
Wu, J.3
Arora, N.4
Billedeau, J.R.5
Davidson, J.P.6
Fretland, J.7
Hang, J.Q.8
Heilek, G.M.9
Harris, S.F.10
Hirschfeld, D.11
Inbar, P.12
Javanbakht, H.13
Jernelius, J.A.14
Jin, Q.15
Li, Y.16
Liang, W.17
Roetz, R.18
Sarma, K.19
Smith, M.20
Stefanidis, D.21
Su, G.22
Suh, J.M.23
Villaseñor, A.G.24
Welch, M.25
Zhang, F.J.26
Klumpp, K.27
more..
-
112
-
-
31544435514
-
Structure-activity relationship studies of novel benzophenones leading to the discovery of a potent, next generation HIV nonnucleoside reverse transcriptase inhibitor
-
rd.; Stammers, D.K.; Hazen, R.J.; Ferris, R.G.; Short, S.A.; Chan, J.H.; Boone, L.R. Structure-activity relationship studies of novel benzophenones leading to the discovery of a potent, next generation HIV nonnucleoside reverse transcriptase inhibitor. J. Med. Chem., 2006, 49, 727-739
-
(2006)
J. Med. Chem.
, vol.49
, pp. 727-739
-
-
Romines, K.R.1
Freeman, G.A.2
Schaller, L.T.3
Cowan, J.R.4
Gonzales, S.S.5
Tidwell, J.H.6
Andrews III, C.W.7
Stammers, D.K.8
Hazen, R.J.9
Ferris, R.G.10
Short, S.A.11
Chan, J.H.12
Boone, L.R.13
-
113
-
-
50249149488
-
Structural basis for the improved drug resistance profile of new generation benzophenone non-nucleoside HIV-1 reverse transcriptase inhibitors
-
Ren, J.; Chamberlain, P.P.; Stamp, A.; Short, S.A.; Weaver, K.L.; Romines, K.R.; Hazen, R.; Freeman, A.; Ferris, R.G.; Andrews, C.W.; Boone, L.; Chan, J.H.; Stammers, D.K. Structural basis for the improved drug resistance profile of new generation benzophenone non-nucleoside HIV-1 reverse transcriptase inhibitors. J. Med. Chem., 2008, 51, 5000-5008
-
(2008)
J. Med. Chem.
, vol.51
, pp. 5000-5008
-
-
Ren, J.1
Chamberlain, P.P.2
Stamp, A.3
Short, S.A.4
Weaver, K.L.5
Romines, K.R.6
Hazen, R.7
Freeman, A.8
Ferris, R.G.9
Andrews, C.W.10
Boone, L.11
Chan, J.H.12
Stammers, D.K.13
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