-
1
-
-
0026649557
-
Identification of conserved amino acid residues critical for human immunodeficiency virus type 1 integrase function in vitro
-
Engelman A, Craigie R. Identification of conserved amino acid residues critical for human immunodeficiency virus type 1 integrase function in vitro. J Virol 1992; 66:6361-6369.
-
(1992)
J Virol
, vol.66
, pp. 6361-6369
-
-
Engelman, A.1
Craigie, R.2
-
2
-
-
0027179694
-
Identification of discrete functional domains of HIV-1 integrase and their organization within an active multimeric complex
-
Engelman A, Bushman FD, Craigie R. Identification of discrete functional domains of HIV-1 integrase and their organization within an active multimeric complex. EMBO J 1993; 12:3269-3275.
-
(1993)
EMBO J
, vol.12
, pp. 3269-3275
-
-
Engelman, A.1
Bushman, F.D.2
Craigie, R.3
-
3
-
-
0027246609
-
Complementation between HIV integrase proteins mutated in different domains
-
van Gent DC, Vink C, Groeneger AA, Plasterk RH. Complementation between HIV integrase proteins mutated in different domains. EMBO J 1993; 12:3261-3267.
-
(1993)
EMBO J
, vol.12
, pp. 3261-3267
-
-
van Gent, D.C.1
Vink, C.2
Groeneger, A.A.3
Plasterk, R.H.4
-
4
-
-
79959695256
-
The role of unintegrated DNA in HIV infection
-
Sloan RD, Wainberg MA. The role of unintegrated DNA in HIV infection. Retrovirology 2011; 8:52.
-
(2011)
Retrovirology
, vol.8
, pp. 52
-
-
Sloan, R.D.1
Wainberg, M.A.2
-
5
-
-
0028584269
-
Crystal structure of the catalytic domain of HIV-1 integrase: Similarity to other polynucleotidyl transferases
-
Dyda F, Hickman AB, Jenkins TM, Engelman A, Craigie R, Davies DR. Crystal structure of the catalytic domain of HIV-1 integrase: similarity to other polynucleotidyl transferases. Science 1994; 266:1981-1986.
-
(1994)
Science
, vol.266
, pp. 1981-1986
-
-
Dyda, F.1
Hickman, A.B.2
Jenkins, T.M.3
Engelman, A.4
Craigie, R.5
Davies, D.R.6
-
6
-
-
0032483022
-
Three new structures of the core domain of HIV-1 integrase: An active site that binds magnesium
-
U S A
-
Goldgur Y, Dyda F, Hickman AB, Jenkins TM, Craigie R, Davies DR. Three new structures of the core domain of HIV-1 integrase: an active site that binds magnesium. Proc Natl Acad Sci U S A 1998; 95:9150-9154.
-
(1998)
Proc Natl Acad Sci
, vol.95
, pp. 9150-9154
-
-
Goldgur, Y.1
Dyda, F.2
Hickman, A.B.3
Jenkins, T.M.4
Craigie, R.5
Davies, D.R.6
-
7
-
-
0034682511
-
Crystal structure of the HIV-1 integrase catalytic core and C-terminal domains: A model for viral DNA binding
-
U S A
-
Chen JC, Krucinski J, Miercke LJ, et al. Crystal structure of the HIV-1 integrase catalytic core and C-terminal domains: a model for viral DNA binding. Proc Natl Acad Sci U S A 2000; 97:8233-8238.
-
(2000)
Proc Natl Acad Sci
, vol.97
, pp. 8233-8238
-
-
Chen, J.C.1
Krucinski, J.2
Miercke, L.J.3
-
8
-
-
0033551443
-
The mobility of an HIV-1 integrase active site loop is correlated with catalytic activity
-
Greenwald J, Le V, Butler SL, Bushman FD, Choe S. The mobility of an HIV-1 integrase active site loop is correlated with catalytic activity. Biochemistry 1999; 38:8892-8898.
-
(1999)
Biochemistry
, vol.38
, pp. 8892-8898
-
-
Greenwald, J.1
Le, V.2
Butler, S.L.3
Bushman, F.D.4
Choe, S.5
-
9
-
-
0032544311
-
Crystal structures of the catalytic domain of HIV-1 integrase free and complexed with its metal cofactor: High level of similarity of the active site with other viral integrases
-
Maignan S, Guilloteau J P, Zhou-Liu Q, Clement-Mella C, Mikol V. Crystal structures of the catalytic domain of HIV-1 integrase free and complexed with its metal cofactor: high level of similarity of the active site with other viral integrases. J Mol Biol 1998; 282:359-368.
-
(1998)
J Mol Biol
, vol.282
, pp. 359-368
-
-
Maignan, S.1
Guilloteau, J.P.2
Zhou-Liu, Q.3
Clement-Mella, C.4
Mikol, V.5
-
10
-
-
0026668776
-
Mutational analysis of the integrase protein of human immunodeficiency virus type 2
-
van Gent DC, Groeneger AA, Plasterk RH. Mutational analysis of the integrase protein of human immunodeficiency virus type 2. Proc Natl Acad Sci U S A 1992; 89:9598-9602.
-
(1992)
Proc Natl Acad Sci U S A
, vol.89
, pp. 9598-9602
-
-
van Gent, D.C.1
Groeneger, A.A.2
Plasterk, R.H.3
-
11
-
-
0000893081
-
Minireview: HIV integrase
-
Freemont PS, Friedman JM, Beese LS, Sanderson MR, Haniford SD. Minireview: HIV integrase. Proc Natl Acad Sci U S A 1988; 85:8924-8928.
-
(1988)
Proc Natl Acad Sci U S A
, vol.85
, pp. 8924-8928
-
-
Freemont, P.S.1
Friedman, J.M.2
Beese, L.S.3
Sanderson, M.R.4
Haniford, S.D.5
-
12
-
-
0030478950
-
Zinc folds the N-terminal domain of HIV-1 integrase, promotes multimerization, and enhances catalytic activity
-
Zheng R, Jenkins TM, Craigie R. Zinc folds the N-terminal domain of HIV-1 integrase, promotes multimerization, and enhances catalytic activity. Proc Natl Acad Sci U S A 1996; 93:13659-13664.
-
(1996)
Proc Natl Acad Sci U S A
, vol.93
, pp. 13659-13664
-
-
Zheng, R.1
Jenkins, T.M.2
Craigie, R.3
-
13
-
-
0029116747
-
Solution structure of the DNA binding domain of HIV-1 integrase
-
Lodi PJ, Ernst JA, Kuszewski J, et al. Solution structure of the DNA binding domain of HIV-1 integrase. Biochemistry 1995; 34:9826-9833.
-
(1995)
Biochemistry
, vol.34
, pp. 9826-9833
-
-
Lodi, P.J.1
Ernst, J.A.2
Kuszewski, J.3
-
14
-
-
0029145047
-
The DNA-binding domain of HIV-1 integrase has an SH3-like fold
-
Eijkelenboom AP, Lutzke RA, Boelens R, Plasterk RH, Kaptein R, Hard K. The DNA-binding domain of HIV-1 integrase has an SH3-like fold. Nat Struct Biol 1995; 2:807-810.
-
(1995)
Nat Struct Biol
, vol.2
, pp. 807-810
-
-
Eijkelenboom, A.P.1
Lutzke, R.A.2
Boelens, R.3
Plasterk, R.H.4
Kaptein, R.5
Hard, K.6
-
15
-
-
0029148615
-
Mapping domains of retroviral integrase responsible for viral DNA specificity and target site selection by analysis of chimeras between human immunodefciency virus type 1 and visna virus integrases
-
Katzman M, Sudol M. Mapping domains of retroviral integrase responsible for viral DNA specificity and target site selection by analysis of chimeras between human immunodefciency virus type 1 and visna virus integrases. J Virol 1995; 69:5687-5696.
-
(1995)
J Virol
, vol.69
, pp. 5687-5696
-
-
Katzman, M.1
Sudol, M.2
-
16
-
-
0030932575
-
Central core domain of retroviral integrase is responsible for target site selection
-
Shibagaki Y, Chow SA. Central core domain of retroviral integrase is responsible for target site selection. J Biol Chem 1997; 272:8361-8369.
-
(1997)
J Biol Chem
, vol.272
, pp. 8361-8369
-
-
Shibagaki, Y.1
Chow, S.A.2
-
17
-
-
0032189652
-
Sequence specificity of viral end DNA binding by HIV-1 integrase reveals critical regions for protein-DNA interaction
-
Esposito D, Craigie R. Sequence specificity of viral end DNA binding by HIV-1 integrase reveals critical regions for protein-DNA interaction. EMBO J 1998; 17:5832-5843.
-
(1998)
EMBO J
, vol.17
, pp. 5832-5843
-
-
Esposito, D.1
Craigie, R.2
-
18
-
-
73249134612
-
DNA double strand break repair enzymes function at multiple steps in retroviral infection
-
Sakurai Y, Komatsu K, Agematsu K, Matsuoka M. DNA double strand break repair enzymes function at multiple steps in retroviral infection. Retrovirology 2009; 6:114.
-
(2009)
Retrovirology
, vol.6
, pp. 114
-
-
Sakurai, Y.1
Komatsu, K.2
Agematsu, K.3
Matsuoka, M.4
-
19
-
-
13044295993
-
Structure of the HIV-1 integrase catalytic domain complexed with an inhibitor: A platform for antiviral drug design
-
Goldgur Y, Craigie R, Cohen GH, Fugiwara T, Yoshinaga T, Fujishita T. Structure of the HIV-1 integrase catalytic domain complexed with an inhibitor: a platform for antiviral drug design. Proc Natl Acad Sci U S A 1999; 96:13040-13043.
-
(1999)
Proc Natl Acad Sci U S A
, vol.96
, pp. 13040-13043
-
-
Goldgur, Y.1
Craigie, R.2
Cohen, G.H.3
Fugiwara, T.4
Yoshinaga, T.5
Fujishita, T.6
-
20
-
-
0034723439
-
Inhibitors of strand transfer that prevent integration and inhibit HIV-1 replication in cells
-
Hazuda DJ, Felock P, Witmer M, et al. Inhibitors of strand transfer that prevent integration and inhibit HIV-1 replication in cells. Science 2000; 287:646-650.
-
(2000)
Science
, vol.287
, pp. 646-650
-
-
Hazuda, D.J.1
Felock, P.2
Witmer, M.3
-
21
-
-
33644989711
-
Conformationally restrained carbazolone-containing a,B-diketo acids as inhibitors of HIV integrase
-
Li X, Vince R. Conformationally restrained carbazolone-containing a,B-diketo acids as inhibitors of HIV integrase. Bioorg Med Chem 2006; 14:2942-2955.
-
(2006)
Bioorg Med Chem
, vol.14
, pp. 2942-2955
-
-
Li, X.1
Vince, R.2
-
22
-
-
0037317788
-
HIV-1 integrase inhibitors that block HIV-1 replication in infected cells. Planning synthetic derivatives from natural products
-
Di Santo R, Costi R, Artico M, Tramontano E, Colla PL, Pani A. HIV-1 integrase inhibitors that block HIV-1 replication in infected cells. Planning synthetic derivatives from natural products. Pure Appl Chem 2003; 75:195-206.
-
(2003)
Pure Appl Chem
, vol.75
, pp. 195-206
-
-
Di Santo, R.1
Costi, R.2
Artico, M.3
Tramontano, E.4
Colla, P.L.5
Pani, A.6
-
23
-
-
0034727864
-
4-Aryl-2,4-dioxobutanoic acid inhibitors of HIV-1 integrase and viral replication in cells
-
Wai JS, Egberston MS, Payne LS, et al. 4-Aryl-2,4-dioxobutanoic acid inhibitors of HIV-1 integrase and viral replication in cells. J Med Chem 2000; 43:4923-4926.
-
(2000)
J Med Chem
, vol.43
, pp. 4923-4926
-
-
Wai, J.S.1
Egberston, M.S.2
Payne, L.S.3
-
24
-
-
17144362894
-
Design of novel bioisosteres of beta-diketo acid inhibitors of HIV-1 integrase
-
Sechi M, Sannia L, Carta F, et al. Design of novel bioisosteres of beta-diketo acid inhibitors of HIV-1 integrase. Antivir Chem Chemother 2005; 16:41-61.
-
(2005)
Antivir Chem Chemother
, vol.16
, pp. 41-61
-
-
Sechi, M.1
Sannia, L.2
Carta, F.3
-
25
-
-
33845934513
-
Synthesis and biological evaluation of novel 5(H)-phenanthridin-6-ones, 5(H)-phenanthridin-6-one diketo acid, and polycyclic aromatic diketo acid analogs as new HIV-1 integrase inhibitors
-
Patil S, Kamath S, Sanchez T, Neamati N, Schinazic RF, Buolamwinia JK. Synthesis and biological evaluation of novel 5(H)-phenanthridin-6-ones, 5(H)-phenanthridin-6-one diketo acid, and polycyclic aromatic diketo acid analogs as new HIV-1 integrase inhibitors. Bioorg Med Chem 2007; 15:1212-1228.
-
(2007)
Bioorg Med Chem
, vol.15
, pp. 1212-1228
-
-
Patil, S.1
Kamath, S.2
Sanchez, T.3
Neamati, N.4
Schinazic, R.F.5
Buolamwinia, J.K.6
-
26
-
-
1842457823
-
Azido-containing diketo acid derivatives inhibit human immunodeficiency virus type 1 integrase in vivo and influence the frequency of deletions at two-long-terminal-repeat-circle junctions
-
Svarovskaia ES, Barr R, Zhang X, et al. Azido-containing diketo acid derivatives inhibit human immunodeficiency virus type 1 integrase in vivo and influence the frequency of deletions at two-long-terminal-repeat-circle junctions. J Virol 2004; 78:3210-3222.
-
(2004)
J Virol
, vol.78
, pp. 3210-3222
-
-
Svarovskaia, E.S.1
Barr, R.2
Zhang, X.3
-
27
-
-
0026659014
-
Inhibition of HIV-1 integration protein by aurintricarboxylic acid monomers, monomer analogs, and polymer fractions
-
Cushman M, Sherman P. Inhibition of HIV-1 integration protein by aurintricarboxylic acid monomers, monomer analogs, and polymer fractions. Biochem Biophys Res Commun 1992; 185:85-90.
-
(1992)
Biochem Biophys Res Commun
, vol.185
, pp. 85-90
-
-
Cushman, M.1
Sherman, P.2
-
28
-
-
0028798026
-
Inhibition of human immunodeficiency virus integrase by bis-catechols
-
LaFemina RL, Graham PL, Legrow K, et al. Inhibition of human immunodeficiency virus integrase by bis-catechols. Antimicrob Agents Chemother 1995; 39:320-324.
-
(1995)
Antimicrob Agents Chemother
, vol.39
, pp. 320-324
-
-
Lafemina, R.L.1
Graham, P.L.2
Legrow, K.3
-
29
-
-
15844424316
-
Antiretroviral agents as inhibitors of both human immunodeficiency virus type 1 integrase and protease
-
Mazumder A, Wang S, Neamati N, et al. Antiretroviral agents as inhibitors of both human immunodefciency virus type 1 integrase and protease. J Med Chem 1996; 39:2472-2481.
-
(1996)
J Med Chem
, vol.39
, pp. 2472-2481
-
-
Mazumder, A.1
Wang, S.2
Neamati, N.3
-
30
-
-
0028070994
-
Inhibition of HIV-1 integrase by favones, caffeic acid phenethyl ester (CAPE) and related compounds
-
Fesen MR, Pommier Y, Leteurtre F, Hirogouchi S, Yung J, Kohn KW. Inhibition of HIV-1 integrase by favones, caffeic acid phenethyl ester (CAPE) and related compounds. Biochem Pharmacol 1994; 48:595-608.
-
(1994)
Biochem Pharmacol
, vol.48
, pp. 595-608
-
-
Fesen, M.R.1
Pommier, Y.2
Leteurtre, F.3
Hirogouchi, S.4
Yung, J.5
Kohn, K.W.6
-
31
-
-
0028928463
-
Inhibition of human immunodeficiency virus type-1 integrase by curcumin
-
Mazumder A, Raghavan K, Weinstein K, Kohn KW, Pommier Y. Inhibition of human immunodeficiency virus type-1 integrase by curcumin. Biochem Pharmacol 1995; 49:1165-1170.
-
(1995)
Biochem Pharmacol
, vol.49
, pp. 1165-1170
-
-
Mazumder, A.1
Raghavan, K.2
Weinstein, K.3
Kohn, K.W.4
Pommier, Y.5
-
32
-
-
0030805998
-
Curcumin analogs with altered potencies against HIV-1 integrase as probes for biochemical mechanisms of drug action
-
Mazumder A, Neamati N, Sunder S, et al. Curcumin analogs with altered potencies against HIV-1 integrase as probes for biochemical mechanisms of drug action. J Med Chem 1997; 40:3057-3063.
-
(1997)
J Med Chem
, vol.40
, pp. 3057-3063
-
-
Mazumder, A.1
Neamati, N.2
Sunder, S.3
-
33
-
-
0028820595
-
Effects of tyrphostins, protein kinase inhibitors, on human immunodefciency virus type 1 integrase
-
Mazumder A, Gazit A, Levitzki A, et al. Effects of tyrphostins, protein kinase inhibitors, on human immunodeficiency virus type 1 integrase. Biochemistry 1995; 34:15111-15122.
-
(1995)
Biochemistry
, vol.34
, pp. 15111-15122
-
-
Mazumder, A.1
Gazit, A.2
Levitzki, A.3
-
34
-
-
0030041593
-
(-)-Arctigenin as a lead structure for inhibitors of human immunodeficiency virus type-1 integrase
-
Eich E, Pertz H, Kaloga M, et al. (-)-Arctigenin as a lead structure for inhibitors of human immunodeficiency virus type-1 integrase. J Med Chem 1996; 39:86-95.
-
(1996)
J Med Chem
, vol.39
, pp. 86-95
-
-
Eich, E.1
Pertz, H.2
Kaloga, M.3
-
35
-
-
0031013534
-
Coumarin-based inhibitors of HIV integrase
-
Zhao H, Neamati N, Hong H, et al. Coumarin-based inhibitors of HIV integrase. J Med Chem 1997; 40:242-249.
-
(1997)
J Med Chem
, vol.40
, pp. 242-249
-
-
Zhao, H.1
Neamati, N.2
Hong, H.3
-
36
-
-
0029065930
-
Cosalane analogs with enhanced potencies as inhibitors of HIV-1 protease and integrase
-
Cushman M, Golebiewsky WM, Pommier Y, et al. Cosalane analogs with enhanced potencies as inhibitors of HIV-1 protease and integrase. J Med Chem 1995; 38:443-452.
-
(1995)
J Med Chem
, vol.38
, pp. 443-452
-
-
Cushman, M.1
Golebiewsky, W.M.2
Pommier, Y.3
-
37
-
-
0030891930
-
Depsides and depsidones as inhibitors of HIV-1 integrase: Discovery of novel inhibitors through 3D database searching
-
Neamati N, Hong H, Mazumder A, et al. Depsides and depsidones as inhibitors of HIV-1 integrase: discovery of novel inhibitors through 3D database searching. J Med Chem 1997; 40:942-951.
-
(1997)
J Med Chem
, vol.40
, pp. 942-951
-
-
Neamati, N.1
Hong, H.2
Mazumder, A.3
-
38
-
-
0033519708
-
Lamellarin α 20-sulfate, an inhibitor of HIV-1 integrase active against HIV-1 virus in cell culture
-
Reddy MVR, Rao MR, Rhodes D, et al. Lamellarin α 20-sulfate, an inhibitor of HIV-1 integrase active against HIV-1 virus in cell culture. J Med Chem 1999; 42:1901-1907.
-
(1999)
J Med Chem
, vol.42
, pp. 1901-1907
-
-
Reddy, M.V.R.1
Rao, M.R.2
Rhodes, D.3
-
39
-
-
9244252539
-
Globoidnan A: A lignan from Eucalyptus globoidea inhibits HIV integrase
-
Ovenden SP, Simon PB, Yu J, et al. Globoidnan A: a lignan from Eucalyptus globoidea inhibits HIV integrase. Phytochemistry 2004; 65:3255-3259.
-
(2004)
Phytochemistry
, vol.65
, pp. 3255-3259
-
-
Ovenden, S.P.1
Simon, P.B.2
Yu, J.3
-
40
-
-
0347301799
-
2,6-Bis(3,4,5-trihydroxybenzylydene) derivatives of cyclohexanone: Novel potent HIV-1 integrase inhibitors that prevent HIV-1 multiplication in cell-based assays
-
Costi R, Di Santo R, Artico M, et al. 2,6-Bis(3,4,5-trihydroxybenzylydene) derivatives of cyclohexanone: novel potent HIV-1 integrase inhibitors that prevent HIV-1 multiplication in cell-based assays. Bioorg Med Chem 2004; 12:199-215.
-
(2004)
Bioorg Med Chem
, vol.12
, pp. 199-215
-
-
Costi, R.1
Di Santo, R.2
Artico, M.3
-
41
-
-
2642685126
-
Inhibitors of HIV-1 replication that inhibit HIV integrase
-
Robinson WE, Reinecke MG, Abdel MS, Jia Q, Chow SA. Inhibitors of HIV-1 replication that inhibit HIV integrase. Proc Natl Acad Sci U S A 1996; 93:6326-6331.
-
(1996)
Proc Natl Acad Sci U S A
, vol.93
, pp. 6326-6331
-
-
Robinson, W.E.1
Reinecke, M.G.2
Abdel, M.S.3
Jia, Q.4
Chow, S.A.5
-
42
-
-
0031469396
-
Potent inhibitors of human immunodefciency virus type 1 integrase: Identifcation of a novel four-point pharmacophore and tetracyclines as novel inhibitors
-
Neamati N, Hong HX, Sunder S, Milne GWA, Pommier Y. Potent inhibitors of human immunodefciency virus type 1 integrase: identifcation of a novel four-point pharmacophore and tetracyclines as novel inhibitors. Mol Pharmacol 1997; 52:1041-1055.
-
(1997)
Mol Pharmacol
, vol.52
, pp. 1041-1055
-
-
Neamati, N.1
Hong, H.X.2
Sunder, S.3
Milne, G.W.A.4
Pommier, Y.5
-
43
-
-
11144356237
-
Linker-modifed quinoline derivatives targeting HIV-1 integrase: Synthesis and biological activity
-
Bénard C, Zouhiri F, Normand-Bayle M, et al. Linker-modifed quinoline derivatives targeting HIV-1 integrase: synthesis and biological activity. Bioorg Med Chem Lett 2004; 14:2473-2476.
-
(2004)
Bioorg Med Chem Lett
, vol.14
, pp. 2473-2476
-
-
Bénard, C.1
Zouhiri, F.2
Normand-Bayle, M.3
-
44
-
-
0031875905
-
Styrylquinoline derivatives: A new class of potent HIV-1 integrase inhibitors that block HIV-1 replication in CEM cells
-
Mekouar K, Mouscadet JF, Desmaele D, et al. Styrylquinoline derivatives: a new class of potent HIV-1 integrase inhibitors that block HIV-1 replication in CEM cells. J Med Chem 1998; 41:2846-2857.
-
(1998)
J Med Chem
, vol.41
, pp. 2846-2857
-
-
Mekouar, K.1
Mouscadet, J.F.2
Desmaele, D.3
-
45
-
-
33644863638
-
Novel HIV-1 integrase inhibitors derived from quinolone antibiotics
-
Sato M, Motomura T, Aramaki H, et al. Novel HIV-1 integrase inhibitors derived from quinolone antibiotics. J Med Chem 2006; 49:1506-1508.
-
(2006)
J Med Chem
, vol.49
, pp. 1506-1508
-
-
Sato, M.1
Motomura, T.2
Aramaki, H.3
-
46
-
-
0034609799
-
6-Aminoquinolones as new potential anti-HIV agents
-
Cecchetti V, Parolin C, Moro S, et al. 6-Aminoquinolones as new potential anti-HIV agents. J Med Chem 2000; 43:3799-3802.
-
(2000)
J Med Chem
, vol.43
, pp. 3799-3802
-
-
Cecchetti, V.1
Parolin, C.2
Moro, S.3
-
47
-
-
84863107302
-
CNRS assignee. Quinoline derivatives having in particular antiviral properties, preparation and biological application thereof
-
Inventors, October 15
-
Mekouar K, D'Angelo J, Desmaele D, Mouscadet JF, Subra F, Auclair C, inventors; CNRS assignee. Quinoline derivatives having in particular antiviral properties, preparation and biological application thereof. WO9845269A1. 1998 October 15.
-
(1998)
WO9845269A1
-
-
Mekouar, K.1
D'Angelo, J.2
Desmaele, D.3
Mouscadet, J.F.4
Subra, F.5
Auclair, C.6
-
48
-
-
0034692178
-
Structure-activity relationships and binding mode of styrylquinolines as potent inhibitors of HIV-1 integrase and replication of HIV-1 in cell culture
-
Zouhiri F, Mouscadet JF, Mekouar K, et al. Structure-activity relationships and binding mode of styrylquinolines as potent inhibitors of HIV-1 integrase and replication of HIV-1 in cell culture. J Med Chem 2000; 43:1533-1540.
-
(2000)
J Med Chem
, vol.43
, pp. 1533-1540
-
-
Zouhiri, F.1
Mouscadet, J.F.2
Mekouar, K.3
-
49
-
-
2442660260
-
Styrylquinolines, integrase inhibitors acting prior to integration: A new mechanism of action for anti-integrase agents
-
Bonnenfant S, Thomas CM, Vita C, et al. Styrylquinolines, integrase inhibitors acting prior to integration: a new mechanism of action for anti-integrase agents. J Virol 2004; 78:5728-5736.
-
(2004)
J Virol
, vol.78
, pp. 5728-5736
-
-
Bonnenfant, S.1
Thomas, C.M.2
Vita, C.3
-
51
-
-
0037434509
-
Design and synthesis of 8-hydroxy- [1,6]naphthyridines as novel inhibitors of HIV-1 integrase in vitro and in infected cells
-
Zhuang L, Wai JS, Embrey MW, et al. Design and synthesis of 8-hydroxy- [1,6]naphthyridines as novel inhibitors of HIV-1 integrase in vitro and in infected cells. J Med Chem 2003; 46:453-456.
-
(2003)
J Med Chem
, vol.46
, pp. 453-456
-
-
Zhuang, L.1
Wai, J.S.2
Embrey, M.W.3
-
52
-
-
33646037293
-
A series of 5-aminosubstituted 4-fuorobenzyl-8-hydroxy- [1,6] naphthyridine-7-carboxamide HIV-1 integrase inhibitors
-
Guare J P, Pai JS, Gomez RP, et al. A series of 5-aminosubstituted 4-fuorobenzyl-8-hydroxy- [1,6] naphthyridine-7-carboxamide HIV-1 integrase inhibitors. Bioorg Med Chem Lett 2006; 16:2900-2904.
-
(2006)
Bioorg Med Chem Lett
, vol.16
, pp. 2900-2904
-
-
Guare, J.P.1
Pai, J.S.2
Gomez, R.P.3
-
53
-
-
0037162281
-
New class of HIV integrase inhibitors that block viral replication in cell culture
-
Pannecouque C, Pluymers W, Van Maele B, et al. New class of HIV integrase inhibitors that block viral replication in cell culture. Curr Biol 2002; 12:1169-1177.
-
(2002)
Curr Biol
, vol.12
, pp. 1169-1177
-
-
Pannecouque, C.1
Pluymers, W.2
van Maele, B.3
-
54
-
-
10744226580
-
Development of resistance against diketo derivatives of human immunodefciency virus type 1 by progressive cumulation of integrase mutations
-
Fikkert V, Maele BV, Vercammen J, et al. Development of resistance against diketo derivatives of human immunodefciency virus type 1 by progressive cumulation of integrase mutations. J Virol 2003; 77:11459-11470.
-
(2003)
J Virol
, vol.77
, pp. 11459-11470
-
-
Fikkert, V.1
Maele, B.V.2
Vercammen, J.3
-
55
-
-
60849096049
-
HIV-integrase variability in non-B subtypes and positions potentially associated with resistance to integrase inhibitors
-
17-20 September, Chicago, IL, USA. Abstract H-1024
-
Garrido C, de Mendoza C, Zahonero N, et al. HIV-integrase variability in non-B subtypes and positions potentially associated with resistance to integrase inhibitors. 47th Interscience Conference on Antimicrobial Agents and Chemotherapy. 17-20 September 2007, Chicago, IL, USA. Abstract H-1024.
-
(2007)
47th Interscience Conference On Antimicrobial Agents and Chemotherapy
-
-
Garrido, C.1
de Mendoza, C.2
Zahonero, N.3
-
56
-
-
66249092459
-
Novel HIV-1 integrase mutations, found as minority quasispecies in patients naive to integrase inhibitors, are associated with decreased susceptibility to integrase inhibitors in vitro
-
3-6 February, Boston, MA, USA. Abstract 876
-
Ceccherini-Silberstein F, van Baelen K, Armenia D, et al. Novel HIV-1 integrase mutations, found as minority quasispecies in patients naive to integrase inhibitors, are associated with decreased susceptibility to integrase inhibitors in vitro. 15th Conference on Retroviruses and Opportunistic Infections. 3-6 February 2008, Boston, MA, USA. Abstract 876.
-
(2008)
15th Conference On Retroviruses and Opportunistic Infections
-
-
Ceccherini-Silberstein, F.1
van Baelen, K.2
Armenia, D.3
-
57
-
-
55949130714
-
New drug raltegravir: The first HIV integrase inhibitor
-
Cocohoba J, Dong BJ. New drug raltegravir: the first HIV integrase inhibitor. Clin Ther 2008; 30:1747-1765.
-
(2008)
Clin Ther
, vol.30
, pp. 1747-1765
-
-
Cocohoba, J.1
Dong, B.J.2
-
58
-
-
47949114939
-
Subgroup and resistance analyses of raltegravir for resistant HIV-1 infection
-
Cooper DA, Steigbigel RT, Gatell JM, et al. Subgroup and resistance analyses of raltegravir for resistant HIV-1 infection. N Engl J Med 2008; 359:355-365.
-
(2008)
N Engl J Med
, vol.359
, pp. 355-365
-
-
Cooper, D.A.1
Steigbigel, R.T.2
Gatell, J.M.3
-
59
-
-
62349120391
-
Dynamic patterns of human immunodeficiency virus type 1 integrase gene evolution in patients failing raltegravir-based salvage therapies
-
Canducci F, Sampaolo M, Marinozzi MC, et al. Dynamic patterns of human immunodeficiency virus type 1 integrase gene evolution in patients failing raltegravir-based salvage therapies. AIDS 2009; 23:455-460.
-
(2009)
AIDS
, vol.23
, pp. 455-460
-
-
Canducci, F.1
Sampaolo, M.2
Marinozzi, M.C.3
-
60
-
-
37849002059
-
Broad antiretroviral activity and resistance profile of the novel human immunodefciency virus integrase inhibitor elvitegravir (JTK-303/GS-9137)
-
Shimura K, Kodama E, Sakagami Y, et al. Broad antiretroviral activity and resistance profile of the novel human immunodeficiency virus integrase inhibitor elvitegravir (JTK-303/GS-9137). J Virol 2008; 82:764-774.
-
(2008)
J Virol
, vol.82
, pp. 764-774
-
-
Shimura, K.1
Kodama, E.2
Sakagami, Y.3
-
61
-
-
63549089353
-
Raltegravir, elvitegravir, and metoogravir: The birth of 'me-too' HIV-1 integrase inhibitors
-
Serrao E, Odde S, Ramkumar K, Neamati N. Raltegravir, elvitegravir, and metoogravir: the birth of 'me-too' HIV-1 integrase inhibitors. Retrovirology 2009; 6:25.
-
(2009)
Retrovirology
, vol.6
, pp. 25
-
-
Serrao, E.1
Odde, S.2
Ramkumar, K.3
Neamati, N.4
-
62
-
-
50949099460
-
Analysis of natural sequence variation and covariation in human immunodeficiency virus type 1 integrase
-
Myers RE, Pillay D. Analysis of natural sequence variation and covariation in human immunodeficiency virus type 1 integrase. J Virol 2008; 82:9228-9235.
-
(2008)
J Virol
, vol.82
, pp. 9228-9235
-
-
Myers, R.E.1
Pillay, D.2
-
63
-
-
34447263572
-
Links natural polymorphism of the HIV-1 integrase gene and mutations associated with integrase inhibitor resistance
-
Lataillade M, Chiarella J, Kozal MJ. Links natural polymorphism of the HIV-1 integrase gene and mutations associated with integrase inhibitor resistance. Antivir Ther 2007; 12:563-570.
-
(2007)
Antivir Ther
, vol.12
, pp. 563-570
-
-
Lataillade, M.1
Chiarella, J.2
Kozal, M.J.3
-
64
-
-
84863092942
-
Resistance profile of the integrase inhibitor S/GSK-364735
-
3-6 February, Boston, MA, USA. Abstract 860
-
Yoshinaga T, Nakahara K, Kobayashi M, et al. Resistance profle of the integrase inhibitor S/GSK-364735. 15th Conference on Retroviruses and Opportunistic Infections (CROI). 3-6 February 2008, Boston, MA, USA. Abstract 860.
-
(2008)
15th Conference On Retroviruses and Opportunistic Infections (CROI)
-
-
Yoshinaga, T.1
Nakahara, K.2
Kobayashi, M.3
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