-
1
-
-
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.; 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 F.J., Jr.1
Delaney, K.M.2
Moorman, A.C.3
Loveless, M.O.4
Fuhrer, J.5
Satten, G.A.6
Aschman, D.7
Holmberg, S.D.8
-
2
-
-
0033927489
-
Novel compounds in preclinical/early clinical development for the treatment of HIV infections
-
De Clercq, E. Novel compounds in preclinical/early clinical development for the treatment of HIV infections. Rev. Med. Virol. 2000, 10, 255-277.
-
(2000)
Rev. Med. Virol.
, vol.10
, pp. 255-277
-
-
De Clercq, E.1
-
3
-
-
0033959183
-
Antiretroviral therapy: State of the HAART
-
Vella, S.; Palmisano, L. Antiretroviral therapy: state of the HAART. Antiviral Res. 2000, 45, 1-7.
-
(2000)
Antiviral Res.
, vol.45
, pp. 1-7
-
-
Vella, S.1
Palmisano, L.2
-
4
-
-
0033587510
-
Highly active antiretroviral therapy in a large urban clinic: Risk factors for virologic failure and adverse drug reactions
-
Lucas, G. M.; Chaisson, R. E.; Moore, R. D. Highly active antiretroviral therapy in a large urban clinic: risk factors for virologic failure and adverse drug reactions. Ann. Intern. Med. 1999, 13, 81-87.
-
(1999)
Ann. Intern. Med.
, vol.13
, pp. 81-87
-
-
Lucas, G.M.1
Chaisson, R.E.2
Moore, R.D.3
-
5
-
-
0033612928
-
Transmission of antiretroviral-drug-resistant HIV-1 variants
-
Yerly, S.; Kaiser, L.; Race, E.; Bru, J. P.; Clavel, F.; Perrin, L. Transmission of antiretroviral-drug-resistant HIV-1 variants. Lancet 1999, 354, 729-733.
-
(1999)
Lancet
, vol.354
, pp. 729-733
-
-
Yerly, S.1
Kaiser, L.2
Race, E.3
Bru, J.P.4
Clavel, F.5
Perrin, L.6
-
7
-
-
0033609374
-
Persistence of HIV-1 transcription in peripheral-blood mononuclear cells in patients receiving potent antiretroviral therapy
-
Furtado, M. R.; Callaway, D. S.; Phair, J. P.; Kunstman, K. J.; Stanton, J. L.; Macken, C. A.; Perelson, A. S.; Wolinsky, S. M. Persistence of HIV-1 transcription in peripheral-blood mononuclear cells in patients receiving potent antiretroviral therapy. N. Engl. J. Med. 1999, 340, 1614-1622.
-
(1999)
N. Engl. J. Med.
, vol.340
, pp. 1614-1622
-
-
Furtado, M.R.1
Callaway, D.S.2
Phair, J.P.3
Kunstman, K.J.4
Stanton, J.L.5
Macken, C.A.6
Perelson, A.S.7
Wolinsky, S.M.8
-
8
-
-
0034304841
-
New targets for inhibitors of HIV-1 replication
-
Moore, J. P.; Stevenson, M. New targets for inhibitors of HIV-1 replication. Nat. Rev. Mol. Cell Biol. 2000, 1, 40-49.
-
(2000)
Nat. Rev. Mol. Cell Biol.
, vol.1
, pp. 40-49
-
-
Moore, J.P.1
Stevenson, M.2
-
11
-
-
0034059835
-
The HIV-1 reverse transcription (RT) process as target for RT inhibitors
-
Jonckheere, H.; Anne, J.; De Clercq, E. The HIV-1 reverse transcription (RT) process as target for RT inhibitors. Med. Res. Rev. 2000, 20, 129-154.
-
(2000)
Med. Res. Rev.
, vol.20
, pp. 129-154
-
-
Jonckheere, H.1
Anne, J.2
De Clercq, E.3
-
12
-
-
34250082672
-
Review of HIV-1 reverse transcriptase three-dimensional structure: Implication for drug design
-
Nanni, R. G.; Ding, J.; Jacobo-Molina, A.; Hughes, S. H.; Arnold, E. Review of HIV-1 reverse transcriptase three-dimensional structure: Implication for drug design. Perspect. Drug Discovery Des. 1993, 1, 129-150.
-
(1993)
Perspect. Drug Discovery Des.
, vol.1
, pp. 129-150
-
-
Nanni, R.G.1
Ding, J.2
Jacobo-Molina, A.3
Hughes, S.H.4
Arnold, E.5
-
13
-
-
0028924567
-
Mechanism of inhibition of HIV-1 reverse transcriptase by non-nucleoside inhibitors
-
Esnouf, R.; Ren, J.; Ross, C.; Jones, Y.; Stammers, D.; Stuart, D. Mechanism of inhibition of HIV-1 reverse transcriptase by non-nucleoside 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
-
14
-
-
0026318387
-
Human immunodeficiency virus type 1 mutants resistant to nonnucleoside inhibitors of reverse transcriptase arise in tissue culture
-
Richman, D.; Smith, C. K.; Lowy, I.; Rose, J.; Prodanovich, P.; Goff. S.; Griffin, J. Human Immunodeficiency Virus Type 1 Mutants Resistant to Nonnucleoside Inhibitors of Reverse Transcriptase Arise in Tissue Culture. Proc. Natl. Acad. Sci. U.S.A. 1991, 88, 11241-11245.
-
(1991)
Proc. Natl. Acad. Sci. U.S.A.
, vol.88
, pp. 11241-11245
-
-
Richman, D.1
Smith, C.K.2
Lowy, I.3
Rose, J.4
Prodanovich, P.5
Goff, S.6
Griffin, J.7
-
15
-
-
0027957791
-
Nevirapine resistance mutations of human immunodeficiency virus type 1 selected during therapy
-
Richman, D.; D.; Havlir, D.; Corbeil, J.; Looney, D.; Ignacio, C.; Spector, S. A.; Sullivan, J.; Cheeseman, S.; Barringer, K.; Pauletti, D. Nevirapine resistance mutations of human immunodeficiency virus type 1 selected during therapy J. Virol. 1994, 68, 1660-1666.
-
(1994)
J. Virol.
, vol.68
, pp. 1660-1666
-
-
Richman, D.D.1
Havlir, D.2
Corbeil, J.3
Looney, D.4
Ignacio, C.5
Spector, S.A.6
Sullivan, J.7
Cheeseman, S.8
Barringer, K.9
Pauletti, D.10
-
16
-
-
0028271687
-
Structure of the binding site for nonnucleoside inhibitors of the reverse transcriptase of human immunodeficiency virus type 1
-
Smerdon, S. J.; Jager, 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.
-
(1994)
Proc. Natl. Acad. Sci. U.S.A.
, vol.91
, 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
-
17
-
-
0028172345
-
Locations of anti-AIDS drug binding sites and resistance mutations in the three-dimensional structure of HIV-1 reverse transcriptase. Implications for mechanisms of drug inhibition and resistance
-
Tantillo, C.; Ding, J.; Jacobo-Molina, A.; Nanni, R. G.; Boyer, P. L.; Hughes, S. H.; Pauwels, R.; Andries, K.; Janssen, P. A.; Arnold, E. Locations of anti-AIDS drug binding sites and resistance mutations in the three-dimensional structure of HIV-1 reverse transcriptase. Implications for mechanisms of drug inhibition and resistance. J. Mol. Biol. 1994, 243, 369-387.
-
(1994)
J. Mol. Biol.
, vol.243
, pp. 369-387
-
-
Tantillo, C.1
Ding, J.2
Jacobo-Molina, A.3
Nanni, R.G.4
Boyer, P.L.5
Hughes, S.H.6
Pauwels, R.7
Andries, K.8
Janssen, P.A.9
Arnold, E.10
-
18
-
-
0034085298
-
The flourishing synthesis of nonnucleotide reverse transcriptase inhibitors
-
Pedersen, O. S., Pedersen, E. B. The flourishing synthesis of nonnucleotide reverse transcriptase inhibitors. Synthesis 2000, 4, 479-495.
-
(2000)
Synthesis
, vol.4
, pp. 479-495
-
-
Pedersen, O.S.1
Pedersen, E.B.2
-
19
-
-
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, J. M. Jr.; 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 J.M., Jr.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..
-
20
-
-
0028850110
-
PETT compounds, a new class of HIV- 1 reverse transcriptase inhibitors. 1. Synthesis and basic structure-activity relationship studies of PETT analogues
-
Bell, F. W.; Cantrell, A. S.; Hogberg, M.; Jaskunas, S. R.; Johansson, N. G.; Jordan, C. L.; Kinnick, M. D.; Lind, P.; Morin, J. M. Jr.; Noreen, R.; Oberg, B.; Palkowitz, J. A.; Parrish, C. A.; Pranc, P.; Sahlberg, C.; Ternansky, R. J.; Vasileff; R. T.; Vrang, L.; West, S. J.; Zhang, H.; Zhou, X.-X.PETT compounds, a new class of HIV- 1 reverse transcriptase inhibitors. 1. Synthesis and basic structure-activity relationship studies of PETT analogues. J. Med. Chem. 1995, 38, 4929-36.
-
(1995)
J. Med. Chem.
, vol.38
, pp. 4929-4936
-
-
Bell, F.W.1
Cantrell, A.S.2
Hogberg, M.3
Jaskunas, S.R.4
Johansson, N.G.5
Jordan, C.L.6
Kinnick, M.D.7
Lind, P.8
Morin J.M., Jr.9
Noreen, R.10
Oberg, B.11
Palkowitz, J.A.12
Parrish, C.A.13
Pranc, P.14
Sahlberg, C.15
Ternansky, R.J.16
Vasileff, R.T.17
Vrang, L.18
West, S.J.19
Zhang, H.20
Zhou, X.-X.21
more..
-
21
-
-
10244222420
-
Phenethylthiazolylthiourea (PETT) compounds as a new class of HIV-1 reverse transcriptase inhibitors. 2. Synthesis and further structure-activity relationship studies of PETT analogues
-
Cantrell, A. S.; Engelhardt, P.; Hogberg, M.; Jaskunas, S. R.; Johansson, N. G.; Jordan, C. L.; Kangasmetsa, J.; Kinnick, M. D.; Lind, P.; Morin, J. M. Jr.; Muesing, M. A.; Noreen, R.; Oberg, B.; Pranc, P.; Sahlberg, C.; Ternansky, R. J.; Vasileff, R. T.; Vrang, L.; West, S. J.; Zhang, H. Phenethylthiazolylthiourea (PETT) compounds as a new class of HIV-1 reverse transcriptase inhibitors. 2. Synthesis and further structure-activity relationship studies of PETT analogues. J. Med. Chem. 1996, 39, 4261-4274.
-
(1996)
J. Med. Chem.
, vol.39
, pp. 4261-4274
-
-
Cantrell, A.S.1
Engelhardt, P.2
Hogberg, M.3
Jaskunas, S.R.4
Johansson, N.G.5
Jordan, C.L.6
Kangasmetsa, J.7
Kinnick, M.D.8
Lind, P.9
Morin J.M., Jr.10
Muesing, M.A.11
Noreen, R.12
Oberg, B.13
Pranc, P.14
Sahlberg, C.15
Ternansky, R.J.16
Vasileff, R.T.17
Vrang, L.18
West, S.J.19
Zhang, H.20
more..
-
22
-
-
0026693137
-
Crystal structure at 3.5 A 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 A resolution of HIV-1 reverse transcriptase complexed with an inhibitor. Science 1992, 256, 1783-90.
-
(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
-
23
-
-
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
-
24
-
-
0027528503
-
Nonnucleoside inhibitors of HIV-1 reverse transcriptase: Molecular modeling and X-ray structure investigations
-
Schafer, W.; Friebe, W. G.; Leinert, H.; Mertens, A.; Poll, T.; von der Saal, W.; Zilch, H.; Nuber, B.; Ziegler, M. L. Nonnucleoside inhibitors of HIV-1 reverse transcriptase: molecular modeling and X-ray structure investigations. J. Med. Chem. 1993, 36, 726-732.
-
(1993)
J. Med. Chem.
, vol.36
, 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
-
25
-
-
0029645409
-
The structure of HIV-1 reverse transcriptase complexed with 9-chloro-TIBO: Lessons for inhibitor design
-
Ren, J.; Esnouf, R.; Hopkins, A.; Ross, C.; Jones, Y.; Stammers, D.; Stuart, D. The structure of HIV-1 reverse transcriptase complexed with 9-chloro-TIBO: lessons for inhibitor design. Structure 1995, 3, 915-926.
-
(1995)
Structure
, vol.3
, pp. 915-926
-
-
Ren, J.1
Esnouf, R.2
Hopkins, A.3
Ross, C.4
Jones, Y.5
Stammers, D.6
Stuart, D.7
-
26
-
-
0029644484
-
Structure of HIV-1 reverse transcriptase in a complex with the non-nucleoside inhibitor alpha-APA R 95845 at 2.8 Å resolution
-
Ding, J.; Das, K.; Tantillo, C.; Zhang, W.; Clark, A. D. J.; Jessen, S.; Lu, V.; Hsiou, Y.; Jacobo-Molina, A.; Andries, K.; Pauwels, R.; Moereels, H.; Koymans, L.; Janssen, P. A. J.; Smith, R. H. J.; Kroeger Koepke, M.; Michejda, C. J.; Hughes, S. H.; Arnold, E. Structure of HIV-1 reverse transcriptase in a complex with the non-nucleoside inhibitor alpha-APA R 95845 at 2.8 Å resolution. Structure 1995, 3, 365-379.
-
(1995)
Structure
, vol.3
, pp. 365-379
-
-
Ding, J.1
Das, K.2
Tantillo, C.3
Zhang, W.4
Clark, A.D.J.5
Jessen, S.6
Lu, V.7
Hsiou, Y.8
Jacobo-Molina, A.9
Andries, K.10
Pauwels, R.11
Moereels, H.12
Koymans, L.13
Janssen, P.A.J.14
Smith, R.H.J.15
Kroeger Koepke, M.16
Michejda, C.J.17
Hughes, S.H.18
Arnold, E.19
-
27
-
-
0029976422
-
Complexes of HIV-1 reverse transcriptase with inhibitors of the HEPT series reveal conformational changes relevant to the design of potent nonnucleoside inhibitors
-
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 nonnucleoside inhibitors. J. Med. Chem. 1996, 39, 1589-1600.
-
(1996)
J. Med. Chem.
, vol.39
, 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
-
28
-
-
0032514718
-
Crystal structures of HIV-1 reverse transcriptase in complex with carboxanilide derivatives
-
Ren, J.; Esnouf, R. M.; Hopkins, A. L.; Warren, J.; Balzarini, J.; Stuart, D. I.; Stammers, D. K. Crystal structures of HIV-1 reverse transcriptase in complex with carboxanilide derivatives. Biochemistry. 1998, 37, 14394-14403.
-
(1998)
Biochemistry
, vol.37
, pp. 14394-14403
-
-
Ren, J.1
Esnouf, R.M.2
Hopkins, A.L.3
Warren, J.4
Balzarini, J.5
Stuart, D.I.6
Stammers, D.K.7
-
29
-
-
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
-
30
-
-
0033598368
-
Crystallographic analysis of the binding modes of thiazoloisoindolinone nonnucleoside inhibitors to HIV-1 reverse transcriptase and comparison with modeling studies
-
Ren, J.; Esnouf, R. M.; Hopkins, A. L.; Stuart, D. I.; Stammers, D. K. Crystallographic analysis of the binding modes of thiazoloisoindolinone nonnucleoside inhibitors to HIV-1 reverse transcriptase and comparison with modeling studies. J. Med. Chem. 1999, 42, 3845-3851.
-
(1999)
J. Med. Chem.
, vol.42
, pp. 3845-3851
-
-
Ren, J.1
Esnouf, R.M.2
Hopkins, A.L.3
Stuart, D.I.4
Stammers, D.K.5
-
31
-
-
0034053131
-
Phenylethylthiazolylthiourea (PETT) nonnucleoside inhibitors of HIV-1 and HIV-2 reverse transcriptases. Structural and biochemical analyses
-
Ren, J.; Diprose, J.; Warren, J.; Esnouf, R. M.; Bird, L. E.; Ikemizu, S.; Slater, M.; Milton, J.; Balzarini, J.; Stuart, D. I.; Stammers, D. K. Phenylethylthiazolylthiourea (PETT) nonnucleoside inhibitors of HIV-1 and HIV-2 reverse transcriptases. Structural and biochemical analyses. J. Biol. Chem. 2000, 275, 5633-5639.
-
(2000)
J. Biol. Chem.
, vol.275
, pp. 5633-5639
-
-
Ren, J.1
Diprose, J.2
Warren, J.3
Esnouf, R.M.4
Bird, L.E.5
Ikemizu, S.6
Slater, M.7
Milton, J.8
Balzarini, J.9
Stuart, D.I.10
Stammers, D.K.11
-
32
-
-
0013441516
-
-
Ferrara, Italy, August. Poster 115
-
A preliminar account of this synthetic methodology was presented at the II Italian-Spanish joint meeting of Medicinal Chemistry, Ferrara, Italy, August 1995. Poster 115.
-
(1995)
II Italian-Spanish Joint Meeting of Medicinal Chemistry
-
-
-
33
-
-
0013401814
-
-
Taormina, Italy, September. Poster 50
-
A preliminar account of anti-HIV activity of O-(2-phenoxyethyl-N-acyl-N-phenylthiocarbamates was presented at the Italian-Hungarian-Polish joint meeting on Medicinal Chemistry Taormina, Italy, September 1999. Poster 50.
-
(1999)
Italian-Hungarian-Polish Joint Meeting on Medicinal Chemistry
-
-
-
34
-
-
0031407305
-
Anti-HIV activity of N-1-adamantyl-4-aminophthalimide
-
Van Derpoorten, K.; Balzarini, J.; De Clercq, E.; Poupaert, J. H. Anti-HIV activity of N-1-adamantyl-4-aminophthalimide. Biomed. Pharmacother. 1997, 51, 464-468.
-
(1997)
Biomed. Pharmacother.
, vol.51
, pp. 464-468
-
-
Van Derpoorten, K.1
Balzarini, J.2
De Clercq, E.3
Poupaert, J.H.4
-
35
-
-
0032476159
-
Anticonvulsant phenytoinergic pharmacophores and anti-HIV activity-preliminary evidence for the dual requirement of the 4-aminophthalimide platform and the N-(1-adamantyl) substitution for antiviral properties
-
Vamecq, J.; Van derpoorten, K.; Poupaert, J. H.; Balzarini, J.; De Clercq, E.; Stables, J. P. Anticonvulsant phenytoinergic pharmacophores and anti-HIV activity-preliminary evidence for the dual requirement of the 4-aminophthalimide platform and the N-(1-adamantyl) substitution for antiviral properties. Life Sci. 1998, 63, 267-274.
-
(1998)
Life Sci.
, vol.63
, pp. 267-274
-
-
Vamecq, J.1
Van derpoorten, K.2
Poupaert, J.H.3
Balzarini, J.4
De Clercq, E.5
Stables, J.P.6
-
36
-
-
0028129705
-
Synthesis and antiviral activity evaluation of some aminoadamantane derivatives
-
Kolocouris, N.; Foscolos, G. B.; Kolocouris, A.; Marakos, P.; Pouli, N.; Fytas, G.; Ikeda, S.; De Clercq, E. Synthesis and antiviral activity evaluation of some aminoadamantane derivatives. J. Med. Chem. 1994, 37, 2896-2902.
-
(1994)
J. Med. Chem.
, vol.37
, pp. 2896-2902
-
-
Kolocouris, N.1
Foscolos, G.B.2
Kolocouris, A.3
Marakos, P.4
Pouli, N.5
Fytas, G.6
Ikeda, S.7
De Clercq, E.8
-
37
-
-
0013449908
-
Discovery and Development of 2-Pyridinone HIV-1 Reverse Transcriptase
-
Adams, J., Merluzzi, V. J., Eds.; Birkhäuser: Boston
-
Goldman, M. E. Discovery and Development of 2-Pyridinone HIV-1 Reverse Transcriptase in The Search for antiviral Drugs. Case Histories from Concept to Clinic; Adams, J., Merluzzi, V. J., Eds.; Birkhäuser: Boston, 1993; p 105.
-
(1993)
The Search for Antiviral Drugs. Case Histories from Concept to Clinic
, pp. 105
-
-
Goldman, M.E.1
-
38
-
-
17144438394
-
Non-nucleoside HIV-1 reverse transcriptase inhibitors: Synthesis and biological evaluation of novel quinoxalinylethylpyridylthioureas as potent antiviral agents
-
Campiani, G.; Fabbrini, M.; Morelli, E.; Nacci, V.; Greco, G.; Novellino, E.; Maga, G.; Spadari, S.; Bergamini, A.; Faggioli, E.; Uccella, I.; Bolacchi, F.; Marini, S.; Coletta, M.; Fracasso, C.; Caccia, S. Non-nucleoside HIV-1 reverse transcriptase inhibitors: synthesis and biological evaluation of novel quinoxalinylethylpyridylthioureas as potent antiviral agents. Antivir. Chem. Chemother. 2000, 11, 141-155.
-
(2000)
Antivir. Chem. Chemother.
, vol.11
, pp. 141-155
-
-
Campiani, G.1
Fabbrini, M.2
Morelli, E.3
Nacci, V.4
Greco, G.5
Novellino, E.6
Maga, G.7
Spadari, S.8
Bergamini, A.9
Faggioli, E.10
Uccella, I.11
Bolacchi, F.12
Marini, S.13
Coletta, M.14
Fracasso, C.15
Caccia, S.16
-
39
-
-
84981805785
-
Syntheses of thiocarbamates
-
Walter, W.; Bode, K. D. Syntheses of thiocarbamates. Angew. Chem., Internat. Edit. 1967, 6, 281-384.
-
(1967)
Angew. Chem., Internat. Edit.
, vol.6
, pp. 281-384
-
-
Walter, W.1
Bode, K.D.2
-
41
-
-
0345114077
-
Hard and soft acids and bases
-
Pearson, R. G. Hard and soft acids and bases. J. Am. Chem. Soc. 1963, 85, 3533-3539.
-
(1963)
J. Am. Chem. Soc.
, vol.85
, pp. 3533-3539
-
-
Pearson, R.G.1
-
42
-
-
33845279338
-
Chemical hardness and bond dissociation energies
-
Pearson, R. G. Chemical hardness and bond dissociation energies. J. Am. Chem. Soc. 1988, 110, 7684-7690.
-
(1988)
J. Am. Chem. Soc.
, vol.110
, pp. 7684-7690
-
-
Pearson, R.G.1
-
43
-
-
0027946480
-
5-Substituted 2,3-dihydro-6-mercapto-1,3-diphenyl-2-thioxo-4(3H)-pyrimidinones and their 6-(acylthio) derivatives with platelet antiaggregating, antiinflammatory, antiarrhythmic, antihyperlipidemic and other activities
-
Ranise, A.; Bruno, O.; Bondavalli, F.; Schenone, S.; D'Amico, M.; Falciani, M.; Filippelli, W.; Rossi, F. 5-Substituted 2,3-dihydro-6-mercapto-1,3-diphenyl-2-thioxo-4(3H)-pyrimidinones and their 6-(acylthio) derivatives with platelet antiaggregating, antiinflammatory, antiarrhythmic, antihyperlipidemic and other activities. Farmaco 1994, 49, 551-558.
-
(1994)
Farmaco
, vol.49
, pp. 551-558
-
-
Ranise, A.1
Bruno, O.2
Bondavalli, F.3
Schenone, S.4
D'Amico, M.5
Falciani, M.6
Filippelli, W.7
Rossi, F.8
-
44
-
-
0026086958
-
3,3-Disubstituted 1-acyl-l-phenylthioureas with platelet antiaggregating and other activities
-
Ranise, A.; Bondavalli, F.; Bruno, O.; Schenone, S.; Losasso, C.; Costantino, M.; Cenicola, M. L.; Donnoli, D.; Marmo, E. 3,3-disubstituted 1-acyl-l-phenylthioureas with platelet antiaggregating and other activities. Farmaco 1991, 46, 317-338.
-
(1991)
Farmaco
, vol.46
, pp. 317-338
-
-
Ranise, A.1
Bondavalli, F.2
Bruno, O.3
Schenone, S.4
Losasso, C.5
Costantino, M.6
Cenicola, M.L.7
Donnoli, D.8
Marmo, E.9
-
45
-
-
0000830161
-
1H NMR spectra of acylated ureas and thioureas
-
1H NMR spectra of acylated ureas and thioureas. Coll. Czech. Chem. Commun. 1987, 52, 2474-2481.
-
(1987)
Coll. Czech. Chem. Commun.
, vol.52
, pp. 2474-2481
-
-
Jirman, J.1
Lycka, A.2
-
46
-
-
0027376921
-
Viral resistance to the thiazolo-iso-indolinones, a new class of nonnucleoside inhibitors of human immunodeficiency virus type 1 reverse transcriptase
-
Maass, G.; Immendoerfer, U.; Koenig, B.; Leser, U.; Mueller, B.; Goody, R.; Pfaff, E. Viral resistance to the thiazolo-iso-indolinones, a new class of nonnucleoside inhibitors of human immunodeficiency virus type 1 reverse transcriptase. Antimicrob. Agents Chemother. 1993, 37, 2612-2617.
-
(1993)
Antimicrob. Agents Chemother.
, vol.37
, pp. 2612-2617
-
-
Maass, G.1
Immendoerfer, U.2
Koenig, B.3
Leser, U.4
Mueller, B.5
Goody, R.6
Pfaff, E.7
-
47
-
-
0036095739
-
A tight-binding mode of inhibition essential for anti-human immunodeficiency virus type 1 virucidal activity of nonnucleoside reverse transcriptase inhibitors
-
Motakis, D.; Parniak, M. A. A Tight-Binding Mode of Inhibition Essential for Anti-Human Immunodeficiency Virus Type 1 Virucidal Activity of Nonnucleoside Reverse Transcriptase Inhibitors. Antimicrobial Agents Chemother. 2002, 46, 1851-1856.
-
(2002)
Antimicrobial Agents Chemother.
, vol.46
, pp. 1851-1856
-
-
Motakis, D.1
Parniak, M.A.2
-
48
-
-
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. J.; Moereels, H.; Koymans, L.; Andries, K.; Pauwels, R.; Janssen, P. A.; Boyer, P. L.; Clark, P.; Smith, R. H. J.; 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, 1085-100.
-
(1996)
J. Mol. Biol.
, vol.264
, pp. 1085-1100
-
-
Das, K.1
Ding, J.2
Hsiou, Y.3
Clark, A.D.J.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, R.H.J.12
Kroeger Smith, M.B.13
Michejda, C.J.14
Hughes, S.H.15
Arnold, E.16
-
49
-
-
0032744956
-
Novel modifications in the alkenyldiarylmethane (ADAM) series of non-nucleoside reverse transcriptase inhibitors
-
Casimiro-Garcia, A.; Micklatcher, M.; Turpin, J. A.; Stup, T. L.; Watson, K.; Buckheit, R. W.; Cushman, M. Novel modifications in the alkenyldiarylmethane (ADAM) series of non-nucleoside reverse transcriptase inhibitors. J. Med. Chem. 1999, 42, 4861-4874.
-
(1999)
J. Med. Chem.
, vol.42
, pp. 4861-4874
-
-
Casimiro-Garcia, A.1
Micklatcher, M.2
Turpin, J.A.3
Stup, T.L.4
Watson, K.5
Buckheit, R.W.6
Cushman, M.7
-
50
-
-
0003501442
-
-
Columbia University, New York
-
MacroModel Version 5.5, Columbia University, New York, 1996.
-
(1996)
MacroModel Version 5.5
-
-
-
51
-
-
0004318778
-
-
Quantum Chemistry Program Exchange, Indiana University, Bloomington, IN
-
AM1-MOPAC: QCPE-Program No 455, Version 6.0, Quantum Chemistry Program Exchange, Indiana University, Bloomington, IN.
-
AM1-MOPAC: QCPE-Program No 455, Version 6.0
-
-
-
52
-
-
0026730489
-
Structure-based strategies for drug design and discovery
-
Kuntz, I. D. Structure-based strategies for drug design and discovery. Science 1992, 257, 1078-1082.
-
(1992)
Science
, vol.257
, pp. 1078-1082
-
-
Kuntz, I.D.1
-
53
-
-
0023769808
-
Structure and energetics of ligand binding to proteins: Escherichia coli dihydrofolate reductase-trimethoprim, a drug-receptor system
-
Dauber-Osguthorpe, P.; Roberts, V. A.; Osguthorpe, D. J.; Wolff, J.; Genest, M.; Hagler, A. T. Structure and energetics of ligand binding to proteins: Escherichia coli dihydrofolate reductase-trimethoprim, a drug-receptor system. Proteins 1988, 4, 31-47.
-
(1988)
Proteins
, vol.4
, pp. 31-47
-
-
Dauber-Osguthorpe, P.1
Roberts, V.A.2
Osguthorpe, D.J.3
Wolff, J.4
Genest, M.5
Hagler, A.T.6
-
54
-
-
3543012707
-
Crystallography and NMR system (CNS): A new software system for macromolecular structure determination
-
Brunger, A. T.; Adams, P. D.; Clore, G. M.; Delano, W. L.; Gros, P.; Grosse-Kunstleve, R. W.; Jiangj, S.; Kuszewski, J.; Nilges, N.; Pannu, N. S.; Read, R. J.; Rice, L. M.; Simonson T.; Warren, G. L. Crystallography and NMR system (CNS): a new software system for macromolecular structure determination. Acta Crystallogr. 1998, D54, 905-921.
-
(1998)
Acta Crystallogr.
, vol.D54
, pp. 905-921
-
-
Brunger, A.T.1
Adams, P.D.2
Clore, G.M.3
Delano, W.L.4
Gros, P.5
Grosse-Kunstleve, R.W.6
Jiangj, S.7
Kuszewski, J.8
Nilges, N.9
Pannu, N.S.10
Read, R.J.11
Rice, L.M.12
Simonson, T.13
Warren, G.L.14
-
55
-
-
0023687234
-
Rapid and automated tetrazolium-based colorimetric assay for the detection of anti-HIV compounds
-
Pauwels, R.; Balzarini, J.; Baba, M.; Snoeck, R.; Schols, D.; Herdewijn, P.; Desmyter, J.; De Clercq, E. Rapid and automated tetrazolium-based colorimetric assay for the detection of anti-HIV compounds. J. Virol. Methods 1988, 20, 309-321.
-
(1988)
J. Virol. Methods
, vol.20
, pp. 309-321
-
-
Pauwels, R.1
Balzarini, J.2
Baba, M.3
Snoeck, R.4
Schols, D.5
Herdewijn, P.6
Desmyter, J.7
De Clercq, E.8
-
56
-
-
0030045677
-
2-Sulfonyl-4-chloroanilino moiety: A potent pharmacophore for the anti-human immunodeficiency virus type 1 activity of pyrrolyl aryl sulfones
-
Artico, M.; Silvestri, R.; Massa, S.; Loi, A. G.; Corrias, S.; Piras, G.; La Colla, P. 2-Sulfonyl-4-chloroanilino Moiety: A Potent Pharmacophore for the anti-Human Immunodeficiency Virus Type 1 Activity of Pyrrolyl Aryl Sulfones. J. Med. Chem. 1996, 39, 522-530.
-
(1996)
J. Med. Chem.
, vol.39
, pp. 522-530
-
-
Artico, M.1
Silvestri, R.2
Massa, S.3
Loi, A.G.4
Corrias, S.5
Piras, G.6
La Colla, P.7
-
57
-
-
0026579394
-
In vitro selection and molecular characterization of human immunodeficiency virus-1 resistant to non-nucleoside inhibitors of reverse transcriptase
-
Mellors, J. W.; Dutschman, G. E.; Im, G.-J.; Tramontano, E.; Winkler, S. R.; Cheng, Y.-C. In vitro Selection and Molecular Characterization of Human Immunodeficiency Virus-1 Resistant to Non-nucleoside Inhibitors of Reverse Transcriptase. Mol. Pharmacol. 1991, 42, 446-451.
-
(1991)
Mol. Pharmacol.
, vol.42
, pp. 446-451
-
-
Mellors, J.W.1
Dutschman, G.E.2
Im, G.-J.3
Tramontano, E.4
Winkler, S.R.5
Cheng, Y.-C.6
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