-
1
-
-
0023268502
-
The efficacy of azidothymidine (AZT) in the treatment of patients with AIDS and AIDS-related complex. A double-blind, placebo-controlled trial
-
Fischl, M. A.; Richman, D. D.; Grieco, M. H.; Gottlieb, M. S.; Volberding, P. A.; Laskin, O. L.; Leedom, J. M.; Groopman, J. E.; Mildvan, D.; Schooley R. T.;. The efficacy of azidothymidine (AZT) in the treatment of patients with AIDS and AIDS-related complex. A double-blind, placebo-controlled trial. N. Engl. J. Med., 1987, 317(4), 185-191.
-
(1987)
N. Engl. J. Med
, vol.317
, Issue.4
, pp. 185-191
-
-
Fischl, M.A.1
Richman, D.D.2
Grieco, M.H.3
Gottlieb, M.S.4
Volberding, P.A.5
Laskin, O.L.6
Leedom, J.M.7
Groopman, J.E.8
Mildvan, D.9
Schooley, R.T.10
-
2
-
-
0023270510
-
Approval of zidovudine (AZT) for acquired immunodeficiency syndrome. A challenge to the medical and pharmaceutical communities
-
Brook, I. Approval of zidovudine (AZT) for acquired immunodeficiency syndrome. A challenge to the medical and pharmaceutical communities. JAMA, 1987, 258(11), 1517.
-
(1987)
JAMA
, vol.258
, Issue.11
, pp. 1517
-
-
Brook, I.1
-
3
-
-
0030869269
-
Treatment with Indinavir, Zidovudine, and Lamivudine in adults with human immunodeficiency virus infection and prior antiretroviral therapy
-
Gulick, R. M.; Mellors, J. W.; Havlir, D.; Eron, J. J.; Gonzalez, C.; McMahon, D.; Richman, D. D.; Valentine, F. T.; Jonas, L.; Meibohm, A.; Emini, E. A.; Chodakewitz, J. A.; Deutsch, P.; Holder, D.; Schleif, W. A.; Condra, J. H. Treatment with Indinavir, Zidovudine, and Lamivudine in adults with human immunodeficiency virus infection and prior antiretroviral therapy. N. Engl. J. Med., 1997, 337(11), 734-739.
-
(1997)
N. Engl. J. Med
, vol.337
, Issue.11
, pp. 734-739
-
-
Gulick, R.M.1
Mellors, J.W.2
Havlir, D.3
Eron, J.J.4
Gonzalez, C.5
McMahon, D.6
Richman, D.D.7
Valentine, F.T.8
Jonas, L.9
Meibohm, A.10
Emini, E.A.11
Chodakewitz, J.A.12
Deutsch, P.13
Holder, D.14
Schleif, W.A.15
Condra, J.H.16
-
4
-
-
0030952479
-
Decay characteristics of HIV-1-infected compartments during combination therapy
-
Perelson, A. S.; Essunger, P.; Cao, Y.; Vesanen, M.; Hurley, A.; Saksela, K.; Markowitz, M.; Ho, D. D. Decay characteristics of HIV-1-infected compartments during combination therapy. Nature, 1997, 387(6629), 188-191.
-
(1997)
Nature
, vol.387
, Issue.6629
, pp. 188-191
-
-
Perelson, A.S.1
Essunger, P.2
Cao, Y.3
Vesanen, M.4
Hurley, A.5
Saksela, K.6
Markowitz, M.7
Ho, D.D.8
-
6
-
-
0027179560
-
HIV-1 inhibition by a peptide
-
Jiang, S.; Lin, K.; Strick, N.; Neurath, A. R. HIV-1 inhibition by a peptide. Nature, 1993, 365(6442), 113.
-
(1993)
Nature
, vol.365
, Issue.6442
, pp. 113
-
-
Jiang, S.1
Lin, K.2
Strick, N.3
Neurath, A.R.4
-
7
-
-
0027203897
-
Inhibition of HIV-1 infection by a fusion domain binding peptide from HIV-1 envelope glycoprotein gp41
-
Jiang, S.; Lin, K.; Strick, N.; Neurath, A. R. Inhibition of HIV-1 infection by a fusion domain binding peptide from HIV-1 envelope glycoprotein gp41. Biochem. Biophys. Res. Commun., 1993, 195(2), 533-538.
-
(1993)
Biochem. Biophys. Res. Commun
, vol.195
, Issue.2
, pp. 533-538
-
-
Jiang, S.1
Lin, K.2
Strick, N.3
Neurath, A.R.4
-
9
-
-
0027692502
-
Synthetic peptide from HIV-1 gp41 is a potent inhibitor of virus-mediated cell-cell fusion
-
Wild, C.; Greenwell, T.; Matthews, T. A synthetic peptide from HIV-1 gp41 is a potent inhibitor of virus-mediated cell-cell fusion. AIDS Res. Hum. Retroviruses., 1993, 9(11), 1051-1053.
-
(1993)
AIDS Res. Hum. Retroviruses
, vol.9
, Issue.11
, pp. 1051-1053
-
-
Wild, C.1
Greenwell, T.2
Matthews, T.A.3
-
10
-
-
0027959493
-
Peptides corresponding to a predictive alphahelical domain of human immunodeficiency virus type 1 gp41 are potent inhibitors of virus infection
-
Wild, C. T.; Shugars, D. C.; Greenwell, T. K.; McDanal, C. B.; Matthews, T. J. Peptides corresponding to a predictive alphahelical domain of human immunodeficiency virus type 1 gp41 are potent inhibitors of virus infection. Proc. Natl. Acad. Sci. USA, 1994, 91(21), 9770-9774.
-
(1994)
Proc. Natl. Acad. Sci. USA
, vol.91
, Issue.21
, pp. 9770-9774
-
-
Wild, C.T.1
Shugars, D.C.2
Greenwell, T.K.3
McDanal, C.B.4
Matthews, T.J.5
-
11
-
-
0028834461
-
Trimeric structural domain of the HIV-1 transmembrane glycoprotein
-
Lu, M.; Blacklow, S. C.; Kim, P. S. A trimeric structural domain of the HIV-1 transmembrane glycoprotein. Nat. Struct. Biol., 1995, 2(12), 1075-1082.
-
(1995)
Nat. Struct. Biol
, vol.2
, Issue.12
, pp. 1075-1082
-
-
Lu, M.1
Blacklow, S.C.2
Kim, P.3
-
12
-
-
0031441562
-
Trimeric structural subdomain of the HIV-1 transmembrane glycoprotein
-
Lu, M.; Kim, P. S. A trimeric structural subdomain of the HIV-1 transmembrane glycoprotein. J. Biomol. Struct. Dyn., 1997, 15(3), 465-471.
-
(1997)
J. Biomol. Struct. Dyn
, vol.15
, Issue.3
, pp. 465-471
-
-
Lu, M.1
Kim, P.2
-
13
-
-
0030970693
-
Core structure of gp41 from the HIV envelope glycoprotein
-
Chan, D. C.; Fass, D.; Berger, J. M.; Kim, P. S. Core structure of gp41 from the HIV envelope glycoprotein. Cell, 1997, 89(2), 263-273.
-
(1997)
Cell
, vol.89
, Issue.2
, pp. 263-273
-
-
Chan, D.C.1
Fass, D.2
Berger, J.M.3
Kim, P.S.4
-
14
-
-
0028864218
-
A synthetic peptide corresponding to a conserved heptad repeat domain is a potent inhibitor of Sendai virus-cell fusion: An emerging similarity with functional domains of other viruses
-
Rapaport, D.; Ovadia, M.; Shai, Y. A synthetic peptide corresponding to a conserved heptad repeat domain is a potent inhibitor of Sendai virus-cell fusion: an emerging similarity with functional domains of other viruses. EMBO J., 1995, 14(22), 5524-5531.
-
(1995)
EMBO J
, vol.14
, Issue.22
, pp. 5524-5531
-
-
Rapaport, D.1
Ovadia, M.2
Shai, Y.3
-
15
-
-
9044234408
-
Peptides from conserved regions of paramyxovirus fusion (F) proteins are potent inhibitors of viral fusion
-
Lambert, D. M.; Barney, S.; Lambert, A. L.; Guthrie, K.; Medinas, R.; Davis, D. E.; Bucy, T.; Erickson, J.; Merutka, G.; Petteway, S. R. Peptides from conserved regions of paramyxovirus fusion (F) proteins are potent inhibitors of viral fusion. Proc. Natl. Acad. Sci. USA., 1996, 93(5), 2186-2191.
-
(1996)
Proc. Natl. Acad. Sci. USA
, vol.93
, Issue.5
, pp. 2186-2191
-
-
Lambert, D.M.1
Barney, S.2
Lambert, A.L.3
Guthrie, K.4
Medinas, R.5
Davis, D.E.6
Bucy, T.7
Erickson, J.8
Merutka, G.9
Petteway, S.R.10
-
16
-
-
0345701489
-
Both heptad repeats of human respiratory syncytial virus fusion protein are potent inhibitors of viral fusion
-
Wang, E.; Sun, X.; Qian, Y.; Zhao, L.; Tien, P.; Gao, G. F. Both heptad repeats of human respiratory syncytial virus fusion protein are potent inhibitors of viral fusion. Biochem. Biophys. Res. Commun., 2003, 302(3), 469-475.
-
(2003)
Biochem. Biophys. Res. Commun
, vol.302
, Issue.3
, pp. 469-475
-
-
Wang, E.1
Sun, X.2
Qian, Y.3
Zhao, L.4
Tien, P.5
Gao, G.F.6
-
17
-
-
0038111976
-
Design and analysis of post-fusion 6-helix bundle of heptad repeat regions from Newcastle disease virus F protein
-
Zhu, J.; Li, P.; Wu, T.; Gao, F.; Ding, Y.; Zhang, C. W.; Rao, Z.; Gao, G. F.; Tien, P. Design and analysis of post-fusion 6-helix bundle of heptad repeat regions from Newcastle disease virus F protein. Protein Eng., 2003, 16(5), 373-379.
-
(2003)
Protein Eng
, vol.16
, Issue.5
, pp. 373-379
-
-
Zhu, J.1
Li, P.2
Wu, T.3
Gao, F.4
Ding, Y.5
Zhang, C.W.6
Rao, Z.7
Gao, G.F.8
Tien, P.9
-
18
-
-
0038268418
-
Biochemical and biophysical analysis of heptad repeat regions from the fusion protein of Menangle virus, a newly emergent paramyxovirus
-
Zhu, J. Q.; Zhang, C. W.; Rao, Z.; Tien, P.; Gao, G. F. Biochemical and biophysical analysis of heptad repeat regions from the fusion protein of Menangle virus, a newly emergent paramyxovirus. Arch. Virol., 2003, 148(7), 1301-1316.
-
(2003)
Arch. Virol
, vol.148
, Issue.7
, pp. 1301-1316
-
-
Zhu, J.Q.1
Zhang, C.W.2
Rao, Z.3
Tien, P.4
Gao, G.F.5
-
19
-
-
0346848907
-
Six-helix bundle assembly and analysis of the central core of mumps virus fusion protein
-
Liu, Y.; Zhu, J.; Feng, M. G.; Tien, P.; Gao, G. F. Six-helix bundle assembly and analysis of the central core of mumps virus fusion protein. Arch. Biochem. Biophys., 2004, 421(1), 143-148.
-
(2004)
Arch. Biochem. Biophys
, vol.421
, Issue.1
, pp. 143-148
-
-
Liu, Y.1
Zhu, J.2
Feng, M.G.3
Tien, P.4
Gao, G.F.5
-
20
-
-
0028864614
-
A trimeric subdomain of the simian immunodeificiency virous envelope glycoprotein
-
Blacklow, S. C.; Lu, M.; Kim, P. S. A trimeric subdomain of the simian immunodeificiency virous envelope glycoprotein. Biochemistry, 1995, 34(46), 114955-114962.
-
(1995)
Biochemistry
, vol.34
, Issue.46
, pp. 114955-114962
-
-
Blacklow, S.C.1
Lu, M.2
Kim, P.S.3
-
21
-
-
0029952575
-
Inhibition of feline immunodeficiency virus infection in vitro by envelope glycoprotein synthetic peptides
-
Lombardi, S.; Massi, C.; Indino, E.; La Rosa, C.; Mazzetti, P.; Falcone, M. L.; Rovero, P.; Fissi, A.; Pieroni, O.; Bandecchi, P.; Esposito, F.; Tozzini, F.; Bendinelli, M.; Garzelli, C. Inhibition of feline immunodeficiency virus infection in vitro by envelope glycoprotein synthetic peptides. Virology, 1996, 220(2), 274-284.
-
(1996)
Virology
, vol.220
, Issue.2
, pp. 274-284
-
-
Lombardi, S.1
Massi, C.2
Indino, E.3
La Rosa, C.4
Mazzetti, P.5
Falcone, M.L.6
Rovero, P.7
Fissi, A.8
Pieroni, O.9
Bandecchi, P.10
Esposito, F.11
Tozzini, F.12
Bendinelli, M.13
Garzelli, C.14
-
22
-
-
82755163036
-
Capturing a Fusion Intermediate of Influenza Hemagglutinin with a Cholesterol-conjugated Peptide, a New Antiviral Strategy for Influenza Virus
-
Lee, K. K.; Pessi, A.; Gui, L.; Santoprete, A.; Talekar, A.; Moscona, A.; Porotto, M. Capturing a Fusion Intermediate of Influenza Hemagglutinin with a Cholesterol-conjugated Peptide, a New Antiviral Strategy for Influenza Virus. J. Biol. Chem., 2011, 286(49), 42141-42149.
-
(2011)
J. Biol. Chem
, vol.286
, Issue.49
, pp. 42141-42149
-
-
Lee, K.K.1
Pessi, A.2
Gui, L.3
Santoprete, A.4
Talekar, A.5
Moscona, A.6
Porotto, M.7
-
23
-
-
84873849253
-
Structure of a dengue virus envelope protein late-stage fusion intermediate
-
Klein, D. E.; Choi, J. L.; Harrison, S. C. Structure of a dengue virus envelope protein late-stage fusion intermediate. J. Virol., 2013, 87(4), 2287-2293.
-
(2013)
J. Virol
, vol.87
, Issue.4
, pp. 2287-2293
-
-
Klein, D.E.1
Choi, J.L.2
Harrison, S.C.3
-
24
-
-
0032214714
-
Crystal structure of the Ebola virus membrane fusion subunit, GP2, from the envelope glycoprotein ectodomain
-
Weissenhorn, W.; Carfi, A.; Lee, K. H.; Skehel, J. J.; Wiley, D. C. Crystal structure of the Ebola virus membrane fusion subunit, GP2, from the envelope glycoprotein ectodomain. Mol. Cell, 1998, 2(5), 605-616.
-
(1998)
Mol. Cell
, vol.2
, Issue.5
, pp. 605-616
-
-
Weissenhorn, W.1
Carfi, A.2
Lee, K.H.3
Skehel, J.J.4
Wiley, D.C.5
-
25
-
-
79955542545
-
Inhibition of Ebola Virus Entry by a C-peptide Targeted to Endosomes
-
Miller, E. H.; Harrison, J. S.; Radoshitzky, S. R.; Higgins, C. D.; Chi, X.; Dong, L.; Kuhn, J. H.; Bavari, S.; Lai, J. R.; Chandran, K. Inhibition of Ebola Virus Entry by a C-peptide Targeted to Endosomes. J. Biol. Chem., 2011, 286(18), 15854-15861.
-
(2011)
J. Biol. Chem
, vol.286
, Issue.18
, pp. 15854-15861
-
-
Miller, E.H.1
Harrison, J.S.2
Radoshitzky, S.R.3
Higgins, C.D.4
Chi, X.5
Dong, L.6
Kuhn, J.H.7
Bavari, S.8
Lai, J.R.9
Chandran, K.10
-
26
-
-
1242340426
-
Basis for fusion inhibition by peptides: Analysis of the heptad repeat regions of the fusion proteins from Nipah and Hendra viruses, newly emergent zoonotic paramyxoviruses
-
Xu, Y.; Gao, S.; Cole, D. K.; Zhu, J.; Su, N.; Wang, H.; Gao, G. F.; Rao, Z. Basis for fusion inhibition by peptides: analysis of the heptad repeat regions of the fusion proteins from Nipah and Hendra viruses, newly emergent zoonotic paramyxoviruses. Biochem. Biophys. Res. Commun., 2004, 315(3), 664-670.
-
(2004)
Biochem. Biophys. Res. Commun
, vol.315
, Issue.3
, pp. 664-670
-
-
Xu, Y.1
Gao, S.2
Cole, D.K.3
Zhu, J.4
Su, N.5
Wang, H.6
Gao, G.F.7
Rao, Z.8
-
27
-
-
33748948794
-
Inhibition of hendra virus fusion
-
Porotto, M.; Doctor, L.; Carta, P.; Fornabaio, M.; Greengard, O.; Kellogg, G. E.; Moscona, A. Inhibition of hendra virus fusion. J. Virol., 2006, 80(19), 9837-9849.
-
(2006)
J. Virol
, vol.80
, Issue.19
, pp. 9837-9849
-
-
Porotto, M.1
Doctor, L.2
Carta, P.3
Fornabaio, M.4
Greengard, O.5
Kellogg, G.E.6
Moscona, A.7
-
28
-
-
12144287276
-
Interaction between heptad repeat 1 and 2 regions in spike protein of SARS-associated coronavirus: Implications for virus fusogenic mechanism and identification of fusion inhibitors
-
Liu, S.; Xiao, G.; Chen, Y.; He, Y.; Niu, J.; Escalante, C. R.; Xiong, H.; Farmar, J.; Debnath, A. K.; Tien, P.; Jiang, S. Interaction between heptad repeat 1 and 2 regions in spike protein of SARS-associated coronavirus: implications for virus fusogenic mechanism and identification of fusion inhibitors. Lancet, 2004, 363(9413), 938-947.
-
(2004)
Lancet
, vol.363
, Issue.9413
, pp. 938-947
-
-
Liu, S.1
Xiao, G.2
Chen, Y.3
He, Y.4
Niu, J.5
Escalante, C.R.6
Xiong, H.7
Farmar, J.8
Debnath, A.K.9
Tien, P.10
Jiang, S.11
-
29
-
-
2442698802
-
Structural characterization of the SARScoronavirus spike S fusion protein core
-
Tripet, B.; Howard, M. W.; Jobling, M.; Holmes, R. K.; Holmes, K. V.; Hodges, R. S. Structural characterization of the SARScoronavirus spike S fusion protein core. J. Biol. Chem., 2004, 279(20), 20836-20849.
-
(2004)
J. Biol. Chem
, vol.279
, Issue.20
, pp. 20836-20849
-
-
Tripet, B.1
Howard, M.W.2
Jobling, M.3
Holmes, R.K.4
Holmes, K.V.5
Hodges, R.S.6
-
30
-
-
10344234242
-
Crystal structure of severe acute respiratory syndrome coronavirus spike protein fusion core
-
Xu, Y.; Lou, Z.; Liu, Y.; Pang, H.; Tien, P.; Gao, G. F.; Rao, Z. Crystal structure of severe acute respiratory syndrome coronavirus spike protein fusion core. J. Biol. Chem., 2004, 279(47), 49414-49419.
-
(2004)
J. Biol. Chem
, vol.279
, Issue.47
, pp. 49414-49419
-
-
Xu, Y.1
Lou, Z.2
Liu, Y.3
Pang, H.4
Tien, P.5
Gao, G.F.6
Rao, Z.7
-
31
-
-
2442705099
-
Following the rule: Formation of the 6-helix bundle of the fusion core from severe acute respiratory syndrome coronavirus spike protein and identification of potent peptide inhibitors. Biochem. Biophys. Res
-
Zhu, J.; Xiao, G.; Xu, Y.; Yuan, F.; Zheng, C.; Liu, Y.; Yan, H.; Cole, D. K.; Bell, J. I.; Rao, Z.; Tien, P.; Gao, G. F. Following the rule: formation of the 6-helix bundle of the fusion core from severe acute respiratory syndrome coronavirus spike protein and identification of potent peptide inhibitors. Biochem. Biophys. Res. Commun., 2004, 319(1), 283-288.
-
(2004)
Commun
, vol.319
, Issue.1
, pp. 283-288
-
-
Zhu, J.1
Xiao, G.2
Xu, Y.3
Yuan, F.4
Zheng, C.5
Liu, Y.6
Yan, H.7
Cole, D.K.8
Bell, J.I.9
Rao, Z.10
Tien, P.11
Gao, G.F.12
-
32
-
-
2942525214
-
Structural characterization of the fusion-active complex of severe acute respiratory syndrome (SARS) coronavirus
-
Ingallinella, P.; Bianchi, E.; Finotto, M.; Cantoni, G.; Eckert, D. M.; Supekar, V. M.; Bruckmann, C.; Carfi, A.; Pessi, A. Structural characterization of the fusion-active complex of severe acute respiratory syndrome (SARS) coronavirus. Proc. Natl. Acad. Sci. U. S. A., 2004, 101(23), 8709-8714.
-
(2004)
Proc. Natl. Acad. Sci. U. S. A
, vol.101
, Issue.23
, pp. 8709-8714
-
-
Ingallinella, P.1
Bianchi, E.2
Finotto, M.3
Cantoni, G.4
Eckert, D.M.5
Supekar, V.M.6
Bruckmann, C.7
Carfi, A.8
Pessi, A.9
-
33
-
-
0037849954
-
Efficacy of enfuvirtide in patients infected with drug-resistant HIV-1 in Europe and Australia
-
Lazzarin, A.; Clotet, B.; Cooper, D.; Reynes, J.; Arasteh, K.; Nelson, M.; Katlama, C.; Stellbrink, H. J.; Delfraissy, J. F.; Lange, J.; Huson, L.; DeMasi, R.; Wat, C.; Delehanty, J.; Drobnes, C.; Salgo, M. Efficacy of enfuvirtide in patients infected with drug-resistant HIV-1 in Europe and Australia. N. Engl. J. Med., 2003, 348(22), 2186-2195.
-
(2003)
N. Engl. J. Med
, vol.348
, Issue.22
, pp. 2186-2195
-
-
Lazzarin, A.1
Clotet, B.2
Cooper, D.3
Reynes, J.4
Arasteh, K.5
Nelson, M.6
Katlama, C.7
Stellbrink, H.J.8
Delfraissy, J.F.9
Lange, J.10
Huson, L.11
Demasi, R.12
Wat, C.13
Delehanty, J.14
Drobnes, C.15
Salgo, M.16
-
34
-
-
0038576281
-
Enfuvirtide, an HIV-1 fusion inhibitor, for drug-resistant HIV infection in north and south America
-
Lalezari, J. P.; Henry, K.; O'Hearn, M.; Montaner, J. S.; Piliero, P. J.; Trottier, B.; Walmsley, S.; Cohen, C.; Kuritzkes, D. R.; Eron, J. J., Jr.; Chung, J.; DeMasi, R.; Donatacci, L.; Drobnes, C.; Delehanty, J.; Salgo, M. Enfuvirtide, an HIV-1 fusion inhibitor, for drug-resistant HIV infection in north and south America. N. Engl. J. Med., 2003, 348(22), 2175-2185.
-
(2003)
N. Engl. J. Med
, vol.348
, Issue.22
, pp. 2175-2185
-
-
Lalezari, J.P.1
Henry, K.2
O'hearn, M.3
Montaner, J.S.4
Piliero, P.J.5
Trottier, B.6
Walmsley, S.7
Cohen, C.8
Kuritzkes, D.R.9
Eron, J.J.10
Chung, J.11
Demasi, R.12
Donatacci, L.13
Drobnes, C.14
Delehanty, J.15
Salgo, M.16
-
35
-
-
77950363206
-
-
FDA. FDA approves Fuzeon. http://www.fda.gov/ForConsumers/ByAudience/ForPatientAdvocates/HIVandAIDSActivities/ucm125 088.htm. 2003.
-
(2003)
FDA Approves Fuzeon
-
-
-
36
-
-
84877942415
-
Entry inhibitors directed towards glycoprotein gp120: An overview on a promising target for HIV-1 therapy
-
Flores, A.; Quesada, E. Entry inhibitors directed towards glycoprotein gp120: an overview on a promising target for HIV-1 therapy. Curr. Med. Chem., 2012, 20(6), 751-771.
-
(2012)
Curr. Med. Chem
, vol.20
, Issue.6
, pp. 751-771
-
-
Flores, A.1
Quesada, E.2
-
37
-
-
33846605763
-
Recent advances of CCR5 antagonists
-
Baba, M. Recent advances of CCR5 antagonists. Curr. Opin. HIV. AIDS, 2006, 1(5), 367-372.
-
(2006)
. Curr. Opin. HIV. AIDS
, vol.1
, Issue.5
, pp. 367-372
-
-
Baba, M.1
-
38
-
-
77951157311
-
CCR5 antagonists: Host-targeted antiviral agents for the treatment of HIV infection, 4 years on
-
Westby, M.; van der, R. E. CCR5 antagonists: host-targeted antiviral agents for the treatment of HIV infection, 4 years on. Antivir. Chem. Chemother., 2010, 20(5), 179-192.
-
(2010)
Antivir. Chem. Chemother
, vol.20
, Issue.5
, pp. 179-192
-
-
Westby, M.1
Van Der, R.E.2
-
39
-
-
84862910447
-
Recent progress in small molecule CCR5 antagonists as potential HIV-1 entry inhibitors
-
Chen, W.; Zhan, P.; De, C. E.; Liu, X. Recent progress in small molecule CCR5 antagonists as potential HIV-1 entry inhibitors. Curr. Pharm. Des., 2012, 18(1), 100-112.
-
(2012)
Curr. Pharm. Des
, vol.18
, Issue.1
, pp. 100-112
-
-
Chen, W.1
Zhan, P.2
De, C.E.3
Liu, X.4
-
40
-
-
0020596551
-
Isolation of a T-lymphotropic retrovirus from a patient at risk for acquired immune deficiency syndrome (AIDS)
-
Barre-Sinoussi, F.; Chermann, J. C.; Rey, F.; Nugeyre, M. T.; Chamaret, S.; Gruest, J.; Dauguet, C.; Axler-Blin, C.; Vezinet- Brun, F.; Rouzioux, C.; Rozenbaum, W.; Montagnier, L. Isolation of a T-lymphotropic retrovirus from a patient at risk for acquired immune deficiency syndrome (AIDS). Science, 1983, 220(4599), 868-871.
-
(1983)
Science
, vol.220
, Issue.4599
, pp. 868-871
-
-
Barre-Sinoussi, F.1
Chermann, J.C.2
Rey, F.3
Nugeyre, M.T.4
Chamaret, S.5
Gruest, J.6
Dauguet, C.7
Axler-Blin, C.8
Vezinet- Brun, F.9
Rouzioux, C.10
Rozenbaum, W.11
Montagnier, L.12
-
41
-
-
0021261510
-
Frequent detection and isolation of cytopathic retroviruses (HTLV-III) from patients with AIDS and at risk for AIDS
-
Gallo, R. C.; Salahuddin, S. Z.; Popovic, M.; Shearer, G. M.; Kaplan, M.; Haynes, B. F.; Palker, T. J.; Redfield, R.; Oleske, J.; Safai, B. Frequent detection and isolation of cytopathic retroviruses (HTLV-III) from patients with AIDS and at risk for AIDS. Science, 1984, 224(4648), 500-503.
-
(1984)
Science
, vol.224
, Issue.4648
, pp. 500-503
-
-
Gallo, R.C.1
Salahuddin, S.Z.2
Popovic, M.3
Shearer, G.M.4
Kaplan, M.5
Haynes, B.F.6
Palker, T.J.7
Redfield, R.8
Oleske, J.9
Safai, B.10
-
42
-
-
0021746228
-
Molecular cloning of AIDS-associated retrovirus
-
Luciw, P. A.; Potter, S. J.; Steimer, K.; Dina, D.; Levy, J. A. Molecular cloning of AIDS-associated retrovirus. Nature, 1984, 312(5996), 760-763.
-
(1984)
Nature
, vol.312
, Issue.5996
, pp. 760-763
-
-
Luciw, P.A.1
Potter, S.J.2
Steimer, K.3
Dina, D.4
Levy, J.A.5
-
43
-
-
0022459886
-
Identification and characterization of conserved and variable regions in the envelope gene of HTLV-III/LAV, the retrovirus of AIDS
-
Starcich, B. R.; Hahn, B. H.; Shaw, G. M.; McNeely, P. D.; Modrow, S.; Wolf, H.; Parks, E. S.; Parks, W. P.; Josephs, S. F.; Gallo, R. C.;. Identification and characterization of conserved and variable regions in the envelope gene of HTLV-III/LAV, the retrovirus of AIDS. Cell, 1986, 45(5), 637-648.
-
(1986)
Cell
, vol.45
, Issue.5
, pp. 637-648
-
-
Starcich, B.R.1
Hahn, B.H.2
Shaw, G.M.3
McNeely, P.D.4
Modrow, S.5
Wolf, H.6
Parks, E.S.7
Parks, W.P.8
Josephs, S.F.9
Gallo, R.C.10
-
44
-
-
84859561617
-
Unliganded HIV-1 gp120 core structures assume the CD4-bound conformation with regulation by quaternary interactions and variable loops
-
Kwon, Y. D.; Finzi, A.; Wu, X.; Dogo-Isonagie, C.; Lee, L. K.; Moore, L. R.; Schmidt, S. D.; Stuckey, J.; Yang, Y.; Zhou, T.; Zhu, J.; Vicic, D. A.; Debnath, A. K.; Shapiro, L.; Bewley, C. A.; Mas cola, J. R.; Sodroski, J. G.; Kwong, P. D. Unliganded HIV-1 gp120 core structures assume the CD4-bound conformation with regulation by quaternary interactions and variable loops. Proc. Natl. Acad. Sci. U. S. A., 2012, 109(15), 5663-5668.
-
(2012)
Proc. Natl. Acad. Sci. U. S. A
, vol.109
, Issue.15
, pp. 5663-5668
-
-
Kwon, Y.D.1
Finzi, A.2
Wu, X.3
Dogo-Isonagie, C.4
Lee, L.K.5
Moore, L.R.6
Schmidt, S.D.7
Stuckey, J.8
Yang, Y.9
Zhou, T.10
Zhu, J.11
Vicic, D.A.12
Debnath, A.K.13
Shapiro, L.14
Bewley, C.A.15
Mas Cola, J.R.16
Sodroski, J.G.17
Kwong, P.D.18
-
45
-
-
27744597054
-
Structure of a V3-containing HIV-1 gp120 core
-
Huang, C. C.; Tang, M.; Zhang, M. Y.; Majeed, S.; Montabana, E.; Stanfield, R. L.; Dimitrov, D. S.; Korber, B.; Sodroski, J.; Wilson, I. A.; Wyatt, R.; Kwong, P. D. Structure of a V3-containing HIV-1 gp120 core. Science, 2005, 310(5750), 1025-1028.
-
(2005)
Science
, vol.310
, Issue.5750
, pp. 1025-1028
-
-
Huang, C.C.1
Tang, M.2
Zhang, M.Y.3
Majeed, S.4
Montabana, E.5
Stanfield, R.L.6
Dimitrov, D.S.7
Korber, B.8
Sodroski, J.9
Wilson, I.A.10
Wyatt, R.11
Kwong, P.D.12
-
46
-
-
75749133275
-
Structure of HIV-1 gp120 with gp41-interactive region reveals layered envelope architecture and basis of conformational mobility
-
Pancera, M.; Majeed, S.; Ban, Y. E. A.; Chen, L.; Huang, C. c.; Kong, L.; Kwon, Y. D.; Stuckey, J.; Zhou, T.; Robinson, J. E.; Schief, W. R.; Sodroski, J.; Wyatt, R.; Kwong, P. D. Structure of HIV-1 gp120 with gp41-interactive region reveals layered envelope architecture and basis of conformational mobility. Proc. Natl. Acad. Sci., 2010, 107(3), 1166-1171.
-
(2010)
Proc. Natl. Acad. Sci
, vol.107
, Issue.3
, pp. 1166-1171
-
-
Pancera, M.1
Majeed, S.2
Ban, Y.E.A.3
Chen, L.4
Huang, C.C.5
Kong, L.6
Kwon, Y.D.7
Stuckey, J.8
Zhou, T.9
Robinson, J.E.10
Schief, W.R.11
Sodroski, J.12
Wyatt, R.13
Kwong, P.D.14
-
47
-
-
0030962291
-
Atomic Structure of the Ectodomain from HIV-1 gp41
-
Weissenhorn, W.; Dessen, A.; Harrison, S. C.; Skehel, J. J.; Wiley, D. C. Atomic Structure of the Ectodomain from HIV-1 gp41. Nature, 1997, 387(6631), 426-428.
-
(1997)
Nature
, vol.387
, Issue.6631
, pp. 426-428
-
-
Weissenhorn, W.1
Dessen, A.2
Harrison, S.C.3
Skehel, J.J.4
Wiley, D.C.5
-
48
-
-
0030780614
-
Atomic structure of a thermostable subdomain of HIV-1 gp41
-
Tan, K.; Liu, J.; Wang, J.; Shen, S.; Liu, M. Atomic structure of a thermostable subdomain of HIV-1 gp41. Proc. Natl. Acad. Sci. U.S.A., 1997, 94(23), 12303-12308.
-
(1997)
Proc. Natl. Acad. Sci. U.S.A
, vol.94
, Issue.23
, pp. 12303-12308
-
-
Tan, K.1
Liu, J.2
Wang, J.3
Shen, S.4
Liu, M.5
-
49
-
-
0032850583
-
Inhibition of HIV-1 infectivity by the gp41 core: Role of a conserved hydrophobic cavity in membrane fusion
-
Ji, H.; Shu, W.; Burling, T.; Jiang, S.; Lu, M. Inhibition of HIV-1 infectivity by the gp41 core: role of a conserved hydrophobic cavity in membrane fusion. J. Virol., 1999, 73(10), 8578-8586.
-
(1999)
J. Virol
, vol.73
, Issue.10
, pp. 8578-8586
-
-
Ji, H.1
Shu, W.2
Burling, T.3
Jiang, S.4
Lu, M.5
-
50
-
-
0032433685
-
Evidence that a prominent cavity in the coiled coil of HIV type 1 gp41 is an attractive drug target
-
Chan, D. C.; Chutkowski, C. T.; Kim, P. S. Evidence that a prominent cavity in the coiled coil of HIV type 1 gp41 is an attractive drug target. Proc. Natl. Acad. Sci. U.S.A., 1998, 95(26), 15613-15617.
-
(1998)
Proc. Natl. Acad. Sci. U.S.A
, vol.95
, Issue.26
, pp. 15613-15617
-
-
Chan, D.C.1
Chutkowski, C.T.2
Kim, P.S.3
-
51
-
-
0038671938
-
The hydrophobic pocket contributes to the structural stability of the N-terminal coiled coil of HIV gp41 but is not required for six-helix bundle formation
-
Dwyer, J. J.; Hasan, A.; Wilson, K. L.; White, J. M.; Matthews, T. J.; Delmedico, M. K. The hydrophobic pocket contributes to the structural stability of the N-terminal coiled coil of HIV gp41 but is not required for six-helix bundle formation. Biochemistry, 2003, 42(17), 4945-4953.
-
(2003)
Biochemistry
, vol.42
, Issue.17
, pp. 4945-4953
-
-
Dwyer, J.J.1
Hasan, A.2
Wilson, K.L.3
White, J.M.4
Matthews, T.J.5
Delmedico, M.K.6
-
52
-
-
0141856289
-
Biochemical and genetic characterizations of a novel human immunodeficiency virus type 1 inhibitor that blocks gp120-CD4 interactions
-
Guo, Q.; Ho, H. T.; Dicker, I.; Fan, L.; Zhou, N.; Friborg, J.; Wang, T.; McAuliffe, B. V.; Wang, H. G.; Rose, R. E.; Fang, H.; Scarnati, H. T.; Langley, D. R.; Meanwell, N. A.; Abraham, R.; Colonno, R. J.; Lin, P. F. Biochemical and genetic characterizations of a novel human immunodeficiency virus type 1 inhibitor that blocks gp120-CD4 interactions. J. Virol., 2003, 77(19), 10528-10536.
-
(2003)
J. Virol
, vol.77
, Issue.19
, pp. 10528-10536
-
-
Guo, Q.1
Ho, H.T.2
Dicker, I.3
Fan, L.4
Zhou, N.5
Friborg, J.6
Wang, T.7
McAuliffe, B.V.8
Wang, H.G.9
Rose, R.E.10
Fang, H.11
Scarnati, H.T.12
Langley, D.R.13
Meanwell, N.A.14
Abraham, R.15
Colonno, R.J.16
Lin, P.F.17
-
53
-
-
0141703204
-
A small molecule HIV-1 inhibitor that targets the HIV-1 envelope and inhibits CD4 receptor binding
-
Lin, P. F.; Blair, W.; Wang, T.; Spicer, T.; Guo, Q.; Zhou, N.; Gong, Y. F.; Wang, H. G.; Rose, R.; Yamanaka, G.; Robinson, B.; Li, C. B.; Fridell, R.; Deminie, C.; Demers, G.; Yang, Z.; Zadjura, L.; Meanwell, N.; Colonno, R. A small molecule HIV-1 inhibitor that targets the HIV-1 envelope and inhibits CD4 receptor binding. Proc. Natl. Acad. Sci. U. S. A., 2003, 100(19), 11013-11018.
-
(2003)
Proc. Natl. Acad. Sci. U. S. A
, vol.100
, Issue.19
, pp. 11013-11018
-
-
Lin, P.F.1
Blair, W.2
Wang, T.3
Spicer, T.4
Guo, Q.5
Zhou, N.6
Gong, Y.F.7
Wang, H.G.8
Rose, R.9
Yamanaka, G.10
Robinson, B.11
Li, C.B.12
Fridell, R.13
Deminie, C.14
Demers, G.15
Yang, Z.16
Zadjura, L.17
Meanwell, N.18
Colonno, R.19
-
54
-
-
13844302894
-
Structure of an unliganded simian immunodeficiency virus gp120 core
-
Chen, B.; Vogan, E. M.; Gong, H.; Skehel, J. J.; Wiley, D. C.; Harrison, S. C. Structure of an unliganded simian immunodeficiency virus gp120 core. Nature, 2005, 433(7028), 834-841.
-
(2005)
Nature
, vol.433
, Issue.7028
, pp. 834-841
-
-
Chen, B.1
Vogan, E.M.2
Gong, H.3
Skehel, J.J.4
Wiley, D.C.5
Harrison, S.C.6
-
55
-
-
11144358392
-
Small-molecule inhibitors of HIV-1 entry block receptor-induced conformational changes in the viral envelope glycoproteins
-
Si, Z.; Madani, N.; Cox, J. M.; Chruma, J. J.; Klein, J. C.; Schon, A.; Phan, N.; Wang, L.; Biorn, A. C.; Cocklin, S.; Chaiken, I.; Freire, E.; Smith, A. B.; Sodroski, J. G. Small-molecule inhibitors of HIV-1 entry block receptor-induced conformational changes in the viral envelope glycoproteins. Proc. Natl. Acad. Sci. U. S. A., 2004, 101(14), 5036-5041.
-
(2004)
Proc. Natl. Acad. Sci. U. S. A
, vol.101
, Issue.14
, pp. 5036-5041
-
-
Si, Z.1
Madani, N.2
Cox, J.M.3
Chruma, J.J.4
Klein, J.C.5
Schon, A.6
Phan, N.7
Wang, L.8
Biorn, A.C.9
Cocklin, S.10
Chaiken, I.11
Freire, E.12
Smith, A.B.13
Sodroski, J.G.14
-
56
-
-
33645766774
-
Envelope conformational changes induced by human immunodeficiency virus type 1 attachment inhibitors prevent CD4 binding and downstream entry events
-
Ho, H. T.; Fan, L.; Nowicka-Sans, B.; McAuliffe, B.; Li, C. B.; Yamanaka, G.; Zhou, N.; Fang, H.; Dicker, I.; Dalterio, R.; Gong, Y. F.; Wang, T.; Yin, Z.; Ueda, Y.; Matiskella, J.; Kadow, J.; Clapham, P.; Robinson, J.; Colonno, R.; Lin, P. F. Envelope conformational changes induced by human immunodeficiency virus type 1 attachment inhibitors prevent CD4 binding and downstream entry events. J. Virol., 2006, 80(8), 4017-4025.
-
(2006)
J. Virol
, vol.80
, Issue.8
, pp. 4017-4025
-
-
Ho, H.T.1
Fan, L.2
Nowicka-Sans, B.3
McAuliffe, B.4
Li, C.B.5
Yamanaka, G.6
Zhou, N.7
Fang, H.8
Dicker, I.9
Dalterio, R.10
Gong, Y.F.11
Wang, T.12
Yin, Z.13
Ueda, Y.14
Matiskella, J.15
Kadow, J.16
Clapham, P.17
Robinson, J.18
Colonno, R.19
Lin, P.F.20
more..
-
57
-
-
77953025786
-
Increased sensitivity of HIV variants selected by attachment inhibitors to broadly neutralizing antibodies
-
Zhou, N.; Fan, L.; Ho, H. T.; Nowicka-Sans, B.; Sun, Y.; Zhu, Y.; Hu, Y.; McAuliffe, B.; Rose, B.; Fang, H.; Wang, T.; Kadow, J.; Krystal, M.; Alexander, L.; Colonno, R.; Lin, P. F. Increased sensitivity of HIV variants selected by attachment inhibitors to broadly neutralizing antibodies. Virology, 2010, 402(2), 256-261.
-
(2010)
Virology
, vol.402
, Issue.2
, pp. 256-261
-
-
Zhou, N.1
Fan, L.2
Ho, H.T.3
Nowicka-Sans, B.4
Sun, Y.5
Zhu, Y.6
Hu, Y.7
McAuliffe, B.8
Rose, B.9
Fang, H.10
Wang, T.11
Kadow, J.12
Krystal, M.13
Alexander, L.14
Colonno, R.15
Lin, P.F.16
-
58
-
-
72249103816
-
Inhibitors of human immunodeficiency virus type 1 (HIV-1) attachment. 5. An evolution from indole to azaindoles leading to the discovery of 1-(4-benzoylpiperazin-1-yl)-2-(4,7- dimethoxy-1H-pyrrolo[2,3-c]pyridin-3-yl)ethane -1,2-dione (BMS- 488043), a drug candidate that demonstrates antiviral activity in HIV-1-infected subjects
-
Wang, T.; Yin, Z.; Zhang, Z.; Bender, J. A.; Yang, Z.; Johnson, G.; Yang, Z.; Zadjura, L. M.; D'Arienzo, C. J.; DiGiugno, P. D.; Gesenberg, C.; Yamanaka, G. A.; Gong, Y. F.; Ho, H. T.; Fang, H.; Zhou, N.; McAuliffe, B. V.; Eggers, B. J.; Fan, L.; Nowicka-Sans, B.; Dicker, I. B.; Gao, Q.; Colonno, R. J.; Lin, P. F.; Meanwell, N. A.; Kadow, J. F. Inhibitors of human immunodeficiency virus type 1 (HIV-1) attachment. 5. An evolution from indole to azaindoles leading to the discovery of 1-(4-benzoylpiperazin-1-yl)-2-(4,7- dimethoxy-1H-pyrrolo[2,3-c]pyridin-3-yl)ethane -1,2-dione (BMS- 488043), a drug candidate that demonstrates antiviral activity in HIV-1-infected subjects. J. Med. Chem., 2009, 52(23), 7778-7787.
-
(2009)
J. Med. Chem
, vol.52
, Issue.23
, pp. 7778-7787
-
-
Wang, T.1
Yin, Z.2
Zhang, Z.3
Bender, J.A.4
Yang, Z.5
Johnson, G.6
Yang, Z.7
Zadjura, L.M.8
D'arienzo, C.J.9
Digiugno, P.D.10
Gesenberg, C.11
Yamanaka, G.A.12
Gong, Y.F.13
Ho, H.T.14
Fang, H.15
Zhou, N.16
McAuliffe, B.V.17
Eggers, B.J.18
Fan, L.19
Nowicka-Sans, B.20
Dicker, I.B.21
Gao, Q.22
Colonno, R.J.23
Lin, P.F.24
Meanwell, N.A.25
Kadow, J.F.26
more..
-
59
-
-
84862569941
-
In vitro antiviral characteristics of HIV-1 attachment inhibitor BMS-626529, the active component of the prodrug BMS-663068. Antimicrob
-
Nowicka-Sans, B.; Gong, Y. F.; McAuliffe, B.; Dicker, I.; Ho, H. T.; Zhou, N.; Eggers, B.; Lin, P. F.; Ray, N.; Wind-Rotolo, M.; Zhu, L.; Majumdar, A.; Stock, D.; Lataillade, M.; Hanna, G. J.; Matiskella, J. D.; Ueda, Y.; Wang, T.; Kadow, J. F.; Meanwell, N. A.; Krystal, M. In vitro antiviral characteristics of HIV-1 attachment inhibitor BMS-626529, the active component of the prodrug BMS-663068. Antimicrob. Agents Chemother., 2012, 56(7), 3498-3507.
-
(2012)
Agents Chemother
, vol.56
, Issue.7
, pp. 3498-3507
-
-
Nowicka-Sans, B.1
Gong, Y.F.2
McAuliffe, B.3
Dicker, I.4
Ho, H.T.5
Zhou, N.6
Eggers, B.7
Lin, P.F.8
Ray, N.9
Wind-Rotolo, M.10
Zhu, L.11
Majumdar, A.12
Stock, D.13
Lataillade, M.14
Hanna, G.J.15
Matiskella, J.D.16
Ueda, Y.17
Wang, T.18
Kadow, J.F.19
Meanwell, N.A.20
Krystal, M.21
more..
-
60
-
-
84882297831
-
Activity of the HIV-1 attachment inhibitor BMS- 626529, the active component of the prodrug BMS-663068, against CD4-independent viruses and HIV-1 envelopes resistant to other entry inhibitors. Antimicrob
-
Li, Z.; Zhou, N.; Sun, Y.; Ray, N.; Lataillade, M.; Hanna, G. J.; Krystal, M. Activity of the HIV-1 attachment inhibitor BMS- 626529, the active component of the prodrug BMS-663068, against CD4-independent viruses and HIV-1 envelopes resistant to other entry inhibitors. Antimicrob. Agents Chemother., 2013, 57(9), 4172-4180.
-
(2013)
Agents Chemother
, vol.57
, Issue.9
, pp. 4172-4180
-
-
Li, Z.1
Zhou, N.2
Sun, Y.3
Ray, N.4
Lataillade, M.5
Hanna, G.J.6
Krystal, M.7
-
61
-
-
84863229866
-
Inhibitors of human immunodeficiency virus type 1 (HIV-1) attachment 6. Preclinical and human pharmacokinetic profiling of BMS-663749, a phosphonooxymethyl prodrug of the HIV-1 attachment inhibitor 2-(4-benzoyl-1- piperazinyl)-1-(4,7-dimethoxy-1H-pyrrolo[2,3-c]pyridin-3-yl)-2- oxo ethanone (BMS-488043)
-
Kadow, J. F.; Ueda, Y.; Meanwell, N. A.; Connolly, T. P.; Wang, T.; Chen, C. P.; Yeung, K. S.; Zhu, J.; Bender, J. A.; Yang, Z.; Parker, D.; Lin, P. F.; Colonno, R. J.; Mathew, M.; Morgan, D.; Zheng, M.; Chien, C.; Grasela, D. Inhibitors of human immunodeficiency virus type 1 (HIV-1) attachment 6. Preclinical and human pharmacokinetic profiling of BMS-663749, a phosphonooxymethyl prodrug of the HIV-1 attachment inhibitor 2-(4-benzoyl-1- piperazinyl)-1-(4,7-dimethoxy-1H-pyrrolo[2,3-c]pyridin-3-yl)-2- oxo ethanone (BMS-488043). J. Med. Chem., 2012, 55(5), 2048-2056.
-
(2012)
J. Med. Chem
, vol.55
, Issue.5
, pp. 2048-2056
-
-
Kadow, J.F.1
Ueda, Y.2
Meanwell, N.A.3
Connolly, T.P.4
Wang, T.5
Chen, C.P.6
Yeung, K.S.7
Zhu, J.8
Bender, J.A.9
Yang, Z.10
Parker, D.11
Lin, P.F.12
Colonno, R.J.13
Mathew, M.14
Morgan, D.15
Zheng, M.16
Chien, C.17
Grasela, D.18
-
63
-
-
84962506565
-
Antiviral activity of a new small molecule HIV-1 attachment inhibitor, BMS-626529, the parent of BMS663068 (Abstract 518)
-
2012 February 27-March 3; Boston, MA
-
Nowicka-Sans, B.; Gong, Y.F.; Ho, H.T. Antiviral activity of a new small molecule HIV-1 attachment inhibitor, BMS-626529, the parent of BMS663068 (Abstract 518). Poster session presented at: 18th Conference on Retroviruses and Opportunistic Infections; 2012 February 27-March 3; Boston, MA. 2015.
-
(2015)
Poster Session Presented At: 18Th Conference on Retroviruses and Opportunistic Infections
-
-
Nowicka-Sans, B.1
Gong, Y.F.2
Ho, H.T.3
-
64
-
-
84861127415
-
Prevalence of subtype-related polymorphisms associated with in vitro resistance to attachment inhibitor BMS-626529 in HIV-1 'non-B'-infected patients
-
Charpentier, C.; Larrouy, L.; Visseaux, B.; Landman, R.; Levittas, M.; Storto, A.; Damond, F.; Yazdanpanah, Y.; Yeni, P.; Brun- Vezinet, F.; Descamps, D. Prevalence of subtype-related polymorphisms associated with in vitro resistance to attachment inhibitor BMS-626529 in HIV-1 'non-B'-infected patients. J. Antimicrob. Chemother. 2012, 67(6), 1459-1461.
-
(2012)
J. Antimicrob. Chemother
, vol.67
, Issue.6
, pp. 1459-1461
-
-
Charpentier, C.1
Larrouy, L.2
Visseaux, B.3
Landman, R.4
Levittas, M.5
Storto, A.6
Damond, F.7
Yazdanpanah, Y.8
Yeni, P.9
Brun- Vezinet, F.10
Descamps, D.11
-
65
-
-
23844440296
-
Identification of N-phenyl-N'- (2,2,6,6-tetramethyl-piperidin-4-yl)-oxalamides as a new class of HIV-1 entry inhibitors that prevent gp120 binding to CD4
-
Zhao, Q.; Ma, L.; Jiang, S.; Lu, H.; Liu, S.; He, Y.; Strick, N.; Neamati, N.; Debnath, A. K. Identification of N-phenyl-N'- (2,2,6,6-tetramethyl-piperidin-4-yl)-oxalamides as a new class of HIV-1 entry inhibitors that prevent gp120 binding to CD4. Virology, 2005, 339(2), 213-225.
-
(2005)
Virology
, vol.339
, Issue.2
, pp. 213-225
-
-
Zhao, Q.1
Ma, L.2
Jiang, S.3
Lu, H.4
Liu, S.5
He, Y.6
Strick, N.7
Neamati, N.8
Debnath, A.K.9
-
66
-
-
33748491260
-
Thermodynamics of binding of a low-molecular-weight CD4 mimetic to HIV-1 gp120
-
Schon, A.; Madani, N.; Klein, J. C.; Hubicki, A.; Ng, D.; Yang, X.; Smith, A. B., III; Sodroski, J.; Freire, E. Thermodynamics of binding of a low-molecular-weight CD4 mimetic to HIV-1 gp120. Biochemistry, 2006, 45(36), 10973-10980.
-
(2006)
Biochemistry
, vol.45
, Issue.36
, pp. 10973-10980
-
-
Schon, A.1
Madani, N.2
Klein, J.C.3
Hubicki, A.4
Ng, D.5
Yang, X.6
Smith, A.B.7
Sodroski, J.8
Freire, E.9
-
67
-
-
55249083812
-
Small-Molecule CD4 Mimics Interact with a Highly Conserved Pocket on HIV-1 gp120
-
Madani, N.; Schn, A.; Princiotto, A. M.; LaLonde, J. M.; Courter, J. R.; Soeta, T.; Ng, D.; Wang, L.; Brower, E. T.; Xiang, S. H.; Do Kwon, Y.; Huang, C. C.; Wyatt, R.; Kwong, P. D.; Freire, E.; Smith A. B.; Sodroski, J. Small-Molecule CD4 Mimics Interact with a Highly Conserved Pocket on HIV-1 gp120. Structure, 2008, 16(11), 1689-1701.
-
(2008)
Structure
, vol.16
, Issue.11
, pp. 1689-1701
-
-
Madani, N.1
Schn, A.2
Princiotto, A.M.3
Lalonde, J.M.4
Courter, J.R.5
Soeta, T.6
Ng, D.7
Wang, L.8
Brower, E.T.9
Xiang, S.H.10
Do Kwon, Y.11
Huang, C.C.12
Wyatt, R.13
Kwong, P.D.14
Freire, E.15
Smith, A.B.16
Sodroski, J.17
-
68
-
-
79955808312
-
Enhanced dynamics of HIV gp120 glycoprotein by small molecule binding
-
Shrivastava, I.; LaLonde, J. M. Enhanced dynamics of HIV gp120 glycoprotein by small molecule binding. Biochemistry, 2011, 50(19), 4173-4183.
-
(2011)
Biochemistry
, vol.50
, Issue.19
, pp. 4173-4183
-
-
Shrivastava, I.1
Lalonde, J.M.2
-
69
-
-
77954525340
-
Enhanced exposure of human immunodeficiency virus type 1 primary isolate neutralization epitopes through binding of CD4 mimetic compounds
-
Yoshimura, K.; Harada, S.; Shibata, J.; Hatada, M.; Yamada, Y.; Ochiai, C.; Tamamura, H.; Matsushita, S. Enhanced exposure of human immunodeficiency virus type 1 primary isolate neutralization epitopes through binding of CD4 mimetic compounds. J. Virol., 2010, 84(15), 7558-7568.
-
(2010)
J. Virol
, vol.84
, Issue.15
, pp. 7558-7568
-
-
Yoshimura, K.1
Harada, S.2
Shibata, J.3
Hatada, M.4
Yamada, Y.5
Ochiai, C.6
Tamamura, H.7
Matsushita, S.8
-
70
-
-
78650721466
-
Synthesis and biological evaluation of small molecule inhibitors of CD4-gp120 binding based on virtual screening
-
LaLonde, J. M.; Elban, M. A.; Courter, J. R.; Sugawara, A.; Soeta, T.; Madani, N.; Princiotto, A. M.; Kwon, Y. D.; Kwong, P. D.; Schon, A.; Freire, E.; Sodroski, J.; Smith, A. B., III. Design, synthesis and biological evaluation of small molecule inhibitors of CD4-gp120 binding based on virtual screening. Bioorg. Med. Chem., 2011, 19(1), 91-101.
-
(2011)
Bioorg. Med. Chem
, vol.19
, Issue.1
, pp. 91-101
-
-
Lalonde, J.M.1
Elban, M.A.2
Courter, J.R.3
Sugawara, A.4
Soeta, T.5
Madani, N.6
Princiotto, A.M.7
Kwon, Y.D.8
Kwong, P.D.9
Schon, A.10
Freire, E.11
Sodroski, J.12
Smith, A.B.13
Design, I.I.14
-
71
-
-
84861048825
-
III. Structure-based design, synthesis, and characterization of dual hotspot small-molecule HIV-1 entry inhibitors
-
LaLonde, J. M.; Kwon, Y. D.; Jones, D. M.; Sun, A. W.; Courter, J. R.; Soeta, T.; Kobayashi, T.; Princiotto, A. M.; Wu, X.; Schon, A.; Freire, E.; Kwong, P. D.; Mascola, J. R.; Sodroski, J.; Madani, N.; Smith, A. B., III. Structure-based design, synthesis, and characterization of dual hotspot small-molecule HIV-1 entry inhibitors. J. Med. Chem., 2012, 55(9), 4382-4396.
-
(2012)
J. Med. Chem
, vol.55
, Issue.9
, pp. 4382-4396
-
-
Lalonde, J.M.1
Kwon, Y.D.2
Jones, D.M.3
Sun, A.W.4
Courter, J.R.5
Soeta, T.6
Kobayashi, T.7
Princiotto, A.M.8
Wu, X.9
Schon, A.10
Freire, E.11
Kwong, P.D.12
Mascola, J.R.13
Sodroski, J.14
Madani, N.15
Smith, A.B.16
-
72
-
-
84875155171
-
Structure-Based Design and Synthesis of an HIV-1 Entry Inhibitor Exploiting X-Ray and Thermodynamic Characterization
-
LaLonde, J. M.; Le-Khac, M.; Jones, D. M.; Courter, J. R.; Park, J.; Schon, A.; Princiotto, A. M.; Wu, X.; Mascola, J. R.; Freire, E.; Sodroski, J.; Madani, N.; Hendrickson, W. A.; Smith, A. B.. Structure-Based Design and Synthesis of an HIV-1 Entry Inhibitor Exploiting X-Ray and Thermodynamic Characterization. ACS Med. Chem. Lett., 2013, 4(3), 338-343.
-
(2013)
ACS Med. Chem. Lett
, vol.4
, Issue.3
, pp. 338-343
-
-
Lalonde, J.M.1
Le-Khac, M.2
Jones, D.M.3
Courter, J.R.4
Park, J.5
Schon, A.6
Princiotto, A.M.7
Wu, X.8
Mascola, J.R.9
Freire, E.10
Sodroski, J.11
Madani, N.12
Hendrickson, W.A.13
Smith, A.B.14
-
73
-
-
84900319832
-
Crystal structures of HIV-1 gp120 envelope glycoprotein in complex with NBD analogues that target the CD4- binding site
-
Kwon, Y. D.; LaLonde, J. M.; Yang, Y.; Elban, M. A.; Sugawara, A.; Courter, J. R.; Jones, D. M.; Smith, A. B.,; Debnath, A. K.; Kwong, P. D. Crystal structures of HIV-1 gp120 envelope glycoprotein in complex with NBD analogues that target the CD4- binding site. PLoS ONE, 2014, 9(1), e85940.
-
(2014)
Plos ONE
, vol.9
, Issue.1
-
-
Kwon, Y.D.1
Lalonde, J.M.2
Yang, Y.3
Elban, M.A.4
Sugawara, A.5
Courter, J.R.6
Jones, D.M.7
Smith, A.B.8
Debnath, A.K.9
Kwong, P.D.10
-
74
-
-
84906074757
-
Binding mode characterization of NBD series CD4-mimetic HIV-1 entry inhibitors by X-ray structure and resistance study
-
Curreli, F.; Kwon, Y. D.; Zhang, H.; Yang, Y.; Scacalossi, D.; Kwong, P. D.; Debnath, A. K. Binding mode characterization of NBD series CD4-mimetic HIV-1 entry inhibitors by X-ray structure and resistance study. Antimicrob. Agents Chemother., 2014, 58(9), 5478-5491.
-
(2014)
Antimicrob. Agents Chemother
, vol.58
, Issue.9
, pp. 5478-5491
-
-
Curreli, F.1
Kwon, Y.D.2
Zhang, H.3
Yang, Y.4
Scacalossi, D.5
Kwong, P.D.6
Debnath, A.K.7
-
75
-
-
84861496877
-
Design, synthesis and antiviral activity of entry inhibitors that target the CD4-binding site of HIV-1
-
Curreli, F.; Choudhury, S.; Pyatkin, I.; Zagorodnikov, V. P.; Bulay, A. K.; Altieri, A.; Kwon, Y. D.; Kwong, P. D.; Debnath, A. K. Design, synthesis and antiviral activity of entry inhibitors that target the CD4-binding site of HIV-1. J. Med. Chem., 2012, 55(10), 4764-4775.
-
(2012)
J. Med. Chem
, vol.55
, Issue.10
, pp. 4764-4775
-
-
Curreli, F.1
Choudhury, S.2
Pyatkin, I.3
Zagorodnikov, V.P.4
Bulay, A.K.5
Altieri, A.6
Kwon, Y.D.7
Kwong, P.D.8
Debnath, A.K.9
-
76
-
-
84922062993
-
A broad HIV-1 inhibitor blocks envelope glycoprotein transitions critical for entry
-
Herschhorn, A.; Gu, C.; Espy, N.; Richard, J.; Finzi, A. S.; Sodroski, J. G. A broad HIV-1 inhibitor blocks envelope glycoprotein transitions critical for entry. Nat. Chem. Biol., 2014, 10(10), 845-852.
-
(2014)
Nat. Chem. Biol
, vol.10
, Issue.10
, pp. 845-852
-
-
Herschhorn, A.1
Gu, C.2
Espy, N.3
Richard, J.4
Finzi, A.S.5
Sodroski, J.G.6
-
77
-
-
84890858459
-
Crystal structure of a soluble cleaved HIV-1 envelope trimer
-
Oct 31.[Epub ahead of print]
-
Julien, J. P.; Cupo, A.; Sok, D.; Stanfield, R. L.; Lyumkis, D.; Deller, M. C.; Klasse, P. J.; Burton, D. R.; Sanders, R. W.; Moore, J. P.; Ward, A. B.; Wilson, I. A. Crystal structure of a soluble cleaved HIV-1 envelope trimer. Science, 2013, Oct 31.[Epub ahead of print]
-
(2013)
Science
-
-
Julien, J.P.1
Cupo, A.2
Sok, D.3
Stanfield, R.L.4
Lyumkis, D.5
Deller, M.C.6
Klasse, P.J.7
Burton, D.R.8
Sanders, R.W.9
Moore, J.P.10
Ward, A.B.11
Wilson, I.A.12
-
78
-
-
0031743949
-
A conformation-specific monoclonal antibody reacting with fusion-active gp41 from the HIV-1 envelope glycoprotein
-
Jiang, S.; Lin, K.; Lu, M. A conformation-specific monoclonal antibody reacting with fusion-active gp41 from the HIV-1 envelope glycoprotein. J. Virol., 1998, 72(12), 10213-10217.
-
(1998)
J. Virol
, vol.72
, Issue.12
, pp. 10213-10217
-
-
Jiang, S.1
Lin, K.2
Lu, M.3
-
79
-
-
0033041322
-
Screening assay for antiviral compounds targeted to the HIV-1 gp41 core structure using a conformation-specific monoclonal antibody
-
Jiang, S.; Lin, K.; Zhang, L.; Debnath, A. K. A screening assay for antiviral compounds targeted to the HIV-1 gp41 core structure using a conformation-specific monoclonal antibody. J. Virol. Methods, 1999, 80(1), 85-96.
-
(1999)
J. Virol. Methods
, vol.80
, Issue.1
, pp. 85-96
-
-
Jiang, S.1
Lin, K.2
Zhang, L.3
Debnath, A.4
-
80
-
-
0033607028
-
Structure-based identification of small molecule antiviral compounds targeted to the gp41 core structure of the human immunodecifiency virus type 1
-
Debnath, A. K.; Radigan, L.; Jiang, S. Structure-based identification of small molecule antiviral compounds targeted to the gp41 core structure of the human immunodecifiency virus type 1. J. Med. Chem., 1999, 42(17), 3203-3209.
-
(1999)
J. Med. Chem
, vol.42
, Issue.17
, pp. 3203-3209
-
-
Debnath, A.K.1
Radigan, L.2
Jiang, S.3
-
81
-
-
71249111434
-
ADS-J1 inhibits HIV- 1 entry by interacting with the gp41 pocket region and blocking the fusion-active gp41 core formation
-
Wang, H.; Qi, Z.; Guo, A.; Mao, Q.; Lu, H.; An, X.; Xia, C.; Li, X.; Debnath, A. K.; Wu, S.; Liu, S.; Jiang, S. ADS-J1 inhibits HIV- 1 entry by interacting with the gp41 pocket region and blocking the fusion-active gp41 core formation. Antimicrob. Agents Chemother., 2009, 53(12), 4987-4998.
-
(2009)
Antimicrob. Agents Chemother
, vol.53
, Issue.12
, pp. 4987-4998
-
-
Wang, H.1
Qi, Z.2
Guo, A.3
Mao, Q.4
Lu, H.5
An, X.6
Xia, C.7
Li, X.8
Debnath, A.K.9
Wu, S.10
Liu, S.11
Jiang, S.12
-
82
-
-
27644505400
-
The anti-HIV activity of ADS-J1 targets the HIV-1 gp120
-
Armand-Ugon, M.; Clotet-Codina, I.; Tintori, C.; Manetti, F.; Clotet, B.; Botta, M.; Este, J. A. The anti-HIV activity of ADS-J1 targets the HIV-1 gp120. Virology, 2005, 343(1), 141-149.
-
(2005)
Virology
, vol.343
, Issue.1
, pp. 141-149
-
-
Armand-Ugon, M.1
Clotet-Codina, I.2
Tintori, C.3
Manetti, F.4
Clotet, B.5
Botta, M.6
Este, J.A.7
-
83
-
-
77957350309
-
ADS-J1 inhibits HIV-1 entry by interacting with gp120 and does not block fusion-active gp41 core formation. Antimicrob
-
Gonzalez-Ortega, E.; Mena, M. P.; Permanyer, M.; Ballana, E.; Clotet, B.; Este, J. A. ADS-J1 inhibits HIV-1 entry by interacting with gp120 and does not block fusion-active gp41 core formation. Antimicrob. Agents Chemother., 2010, 54(10), 4487-4492.
-
(2010)
Agents Chemother
, vol.54
, Issue.10
, pp. 4487-4492
-
-
Gonzalez-Ortega, E.1
Mena, M.P.2
Permanyer, M.3
Ballana, E.4
Clotet, B.5
Este, J.A.6
-
84
-
-
65249151382
-
Resistance to CCR5 inhibitors caused by sequence changes in the fusion peptide of HIV-1 gp41
-
Anastassopoulou, C. G.; Ketas, T. J.; Klasse, P. J.; Moore, J. P. Resistance to CCR5 inhibitors caused by sequence changes in the fusion peptide of HIV-1 gp41. Proc. Natl. Acad. Sci. U.S.A., 2009, 106(13), 5318-5323.
-
(2009)
Proc. Natl. Acad. Sci. U.S.A
, vol.106
, Issue.13
, pp. 5318-5323
-
-
Anastassopoulou, C.G.1
Ketas, T.J.2
Klasse, P.J.3
Moore, J.P.4
-
85
-
-
79953086675
-
Resistance of a human immunodeficiency virus type 1 isolate to a small molecule CCR5 inhibitor can involve sequence changes in both gp120 and gp41
-
Anastassopoulou, C. G.; Ketas, T. J.; Depetris, R. S.; Thomas, A. M.; Klasse, P. J.; Moore, J. P. Resistance of a human immunodeficiency virus type 1 isolate to a small molecule CCR5 inhibitor can involve sequence changes in both gp120 and gp41. Virology, 2011, 413(1), 47-59.
-
(2011)
Virology
, vol.413
, Issue.1
, pp. 47-59
-
-
Anastassopoulou, C.G.1
Ketas, T.J.2
Depetris, R.S.3
Thomas, A.M.4
Klasse, P.J.5
Moore, J.P.6
-
86
-
-
34547854349
-
Design of helical, oligomeric HIV-1 fusion inhibitor peptides with potent activity against enfuvirtideresistant virus
-
Dwyer, J. J.; Wilson, K. L.; Davison, D. K.; Freel, S. A.; Seedorff, J. E.; Wring, S. A.; Tvermoes, N. A.; Matthews, T. J.; Greenberg, M. L.; Delmedico, M. K. Design of helical, oligomeric HIV-1 fusion inhibitor peptides with potent activity against enfuvirtideresistant virus. Proc. Natl. Acad. Sci. U.S.A., 2007, 104(31), 12772-12777.
-
(2007)
Proc. Natl. Acad. Sci. U.S.A
, vol.104
, Issue.31
, pp. 12772-12777
-
-
Dwyer, J.J.1
Wilson, K.L.2
Davison, D.K.3
Freel, S.A.4
Seedorff, J.E.5
Wring, S.A.6
Tvermoes, N.A.7
Matthews, T.J.8
Greenberg, M.L.9
Delmedico, M.K.10
-
87
-
-
80055013474
-
Resistance of human immunodeficiency virus type 1 to a thirdgeneration fusion inhibitor requires multiple mutations in gp41 and is accompanied by a dramatic loss of gp41 function
-
Eggink, D.; Bontjer, I.; Langedijk, J. P.; Berkhout, B.; Sanders, R. W. Resistance of human immunodeficiency virus type 1 to a thirdgeneration fusion inhibitor requires multiple mutations in gp41 and is accompanied by a dramatic loss of gp41 function. J. Virol., 2011, 85(20), 10785-10797.
-
(2011)
J. Virol
, vol.85
, Issue.20
, pp. 10785-10797
-
-
Eggink, D.1
Bontjer, I.2
Langedijk, J.P.3
Berkhout, B.4
Sanders, R.W.5
-
88
-
-
84894601292
-
ADS-J1 inhibits HIV-1 infection and membrane fusion by targeting the highly conserved pocket in the gp41 NHR-trimer
-
Yu, F.; Lu, L.; Liu, Q.; Yu, X.; Wang, L.; He, E.; Zou, P.; Du, L.; Sanders, R. W.; Liu, S.; Jiang, S. ADS-J1 inhibits HIV-1 infection and membrane fusion by targeting the highly conserved pocket in the gp41 NHR-trimer. Biochim. Biophys. Acta, 2014, 1838(5), 1296-1305.
-
(2014)
Biochim. Biophys. Acta
, vol.1838
, Issue.5
, pp. 1296-1305
-
-
Yu, F.1
Lu, L.2
Liu, Q.3
Yu, X.4
Wang, L.5
He, E.6
Zou, P.7
Du, L.8
Sanders, R.W.9
Liu, S.10
Jiang, S.11
-
89
-
-
84862927851
-
Mutations of Gln64 in the HIV-1 gp41 N-terminal heptad repeat render viruses resistant to peptide HIV fusion inhibitors targeting gp41 pocket
-
Yu, X.; Lu, L.; Cai, L.; Tong, P.; Tan, S.; Zou, P.; Meng, F.; Chen, Y. H.; Jiang, S. Mutations of Gln64 in the HIV-1 gp41 N-terminal heptad repeat render viruses resistant to peptide HIV fusion inhibitors targeting gp41 pocket. J. Virol., 2012, 86(1), 589-593.
-
(2012)
J. Virol
, vol.86
, Issue.1
, pp. 589-593
-
-
Yu, X.1
Lu, L.2
Cai, L.3
Tong, P.4
Tan, S.5
Zou, P.6
Meng, F.7
Chen, Y.H.8
Jiang, S.9
-
90
-
-
84865335285
-
HIV-1 variants with a single-point mutation in the gp41 pocket region exhibiting different susceptibility to HIV fusion inhibitors with pocket- or membrane-binding domain
-
Lu, L.; Tong, P.; Yu, X.; Pan, C.; Zou, P.; Chen, Y. H.; Jiang, S. HIV-1 variants with a single-point mutation in the gp41 pocket region exhibiting different susceptibility to HIV fusion inhibitors with pocket- or membrane-binding domain. Biochim. Biophys. Acta, 2012, 1818(12), 2950-2957.
-
(2012)
Biochim. Biophys. Acta
, vol.1818
, Issue.12
, pp. 2950-2957
-
-
Lu, L.1
Tong, P.2
Yu, X.3
Pan, C.4
Zou, P.5
Chen, Y.H.6
Jiang, S.7
-
91
-
-
77955275844
-
Novel recombinant engineered gp41 N-terminal heptad repeat trimers and their potential as anti-HIV-1 therapeutics or microbicides
-
Chen, X.; Lu, L.; Qi, Z.; Lu, H.; Wang, J.; Yu, X.; Chen, Y.; Jiang, S. Novel recombinant engineered gp41 N-terminal heptad repeat trimers and their potential as anti-HIV-1 therapeutics or microbicides. J. Biol. Chem., 2010, 285(33), 25506-25515.
-
(2010)
J. Biol. Chem
, vol.285
, Issue.33
, pp. 25506-25515
-
-
Chen, X.1
Lu, L.2
Qi, Z.3
Lu, H.4
Wang, J.5
Yu, X.6
Chen, Y.7
Jiang, S.8
-
92
-
-
0347689876
-
Rapid and automated fluorescence-linked immunosorbent assay for high throughput screening of HIV-1 fusion inhibitors targeting gp41
-
Liu, S.; Boyer-Chatenet, L.; Lu, H.; Jiang, S. Rapid and automated fluorescence-linked immunosorbent assay for high throughput screening of HIV-1 fusion inhibitors targeting gp41. J. Biomol. Screening, 2003, 8(6), 685-693.
-
(2003)
J. Biomol. Screening
, vol.8
, Issue.6
, pp. 685-693
-
-
Liu, S.1
Boyer-Chatenet, L.2
Lu, H.3
Jiang, S.4
-
93
-
-
7244253012
-
Nsubstituted pyrrole derivatives as novel human immunodeficiency virus type 1 entry inhibitors that interfere with the gp41 six-helix bundle formation and block virus fusion
-
Jiang, S.; Lu, H.; Liu, S.; Zhao, Q.; He, Y.; Debnath, A. K. Nsubstituted pyrrole derivatives as novel human immunodeficiency virus type 1 entry inhibitors that interfere with the gp41 six-helix bundle formation and block virus fusion. Antimicrob. Agents Chemother., 2004, 48(11), 4349-4359.
-
(2004)
Antimicrob. Agents Chemother
, vol.48
, Issue.11
, pp. 4349-4359
-
-
Jiang, S.1
Lu, H.2
Liu, S.3
Zhao, Q.4
He, Y.5
Debnath, A.K.6
-
94
-
-
58149090406
-
Design, synthesis, and biological evaluation of N-carboxyphenylpyrrole derivatives as potent HIV fusion inhibitors targeting gp41
-
Liu, K.; Lu, H.; Hou, L.; Qi, Z.; Teixeira, C.; Barbault, F.; Fan, B. T.; Liu, S.; Jiang, S.; Xie, L. Design, synthesis, and biological evaluation of N-carboxyphenylpyrrole derivatives as potent HIV fusion inhibitors targeting gp41. J. Med. Chem., 2008, 51(24), 7843-7854.
-
(2008)
J. Med. Chem
, vol.51
, Issue.24
, pp. 7843-7854
-
-
Liu, K.1
Lu, H.2
Hou, L.3
Qi, Z.4
Teixeira, C.5
Barbault, F.6
Fan, B.T.7
Liu, S.8
Jiang, S.9
Xie, L.10
-
95
-
-
72049084473
-
Structure-based design, synthesis and biological evaluation of new Ncarboxyphenylpyrrole derivatives as HIV fusion inhibitors targeting gp41
-
Wang, Y.; Lu, H.; Zhu, Q.; Jiang, S.; Liao, Y. Structure-based design, synthesis and biological evaluation of new Ncarboxyphenylpyrrole derivatives as HIV fusion inhibitors targeting gp41. Bioorg. Med. Chem. Lett., 2010, 20(1), 189-192.
-
(2010)
Bioorg. Med. Chem. Lett
, vol.20
, Issue.1
, pp. 189-192
-
-
Wang, Y.1
Lu, H.2
Zhu, Q.3
Jiang, S.4
Liao, Y.5
-
96
-
-
72249122328
-
Design, synthesis, and structure-activity relationship of a novel series of 2- Aryl 5-(4-oxo-3-phenethyl-2-thioxothiazolidin-ylidenemethyl) furans as HIV-1 entry inhibitors
-
Katritzky, A. R.; Tala, S. R.; Lu, H.; Vakulenko, A. V.; Chen, Q. Y.; Sivapackiam, J.; Pandya, K.; Jiang, S.; Debnath, A. K. Design, synthesis, and structure-activity relationship of a novel series of 2- Aryl 5-(4-oxo-3-phenethyl-2-thioxothiazolidin-ylidenemethyl) furans as HIV-1 entry inhibitors. J. Med. Chem., 2009, 52(23), 7631-7639.
-
(2009)
J. Med. Chem
, vol.52
, Issue.23
, pp. 7631-7639
-
-
Katritzky, A.R.1
Tala, S.R.2
Lu, H.3
Vakulenko, A.V.4
Chen, Q.Y.5
Sivapackiam, J.6
Pandya, K.7
Jiang, S.8
Debnath, A.K.9
-
97
-
-
78751657690
-
Design, synthesis, and biological activity of novel 5-((arylfuran/1H-pyrrol-2-yl)methylene)-2- thioxo-3-(3-(trifluoromethyl)phenyl)thi azolidin-4-ones as HIV-1 fusion inhibitors targeting gp41
-
Jiang, S.; Tala, S. R.; Lu, H.; bo-Dya, N. E.; Avan, I.; Gyanda, K.; Lu, L.; Katritzky, A. R.; Debnath, A. K. Design, synthesis, and biological activity of novel 5-((arylfuran/1H-pyrrol-2-yl)methylene)-2- thioxo-3-(3-(trifluoromethyl)phenyl)thi azolidin-4-ones as HIV-1 fusion inhibitors targeting gp41. J. Med. Chem., 2011, 54(2), 572-579.
-
(2011)
J. Med. Chem
, vol.54
, Issue.2
, pp. 572-579
-
-
Jiang, S.1
Tala, S.R.2
Lu, H.3
Bo-Dya, N.E.4
Avan, I.5
Gyanda, K.6
Lu, L.7
Katritzky, A.R.8
Debnath, A.K.9
-
98
-
-
78349299437
-
Development of peptide and small-molecule HIV- 1 fusion inhibitors that target gp41
-
Cai, L.; Jiang, S. Development of peptide and small-molecule HIV- 1 fusion inhibitors that target gp41. ChemMedChem, 2010, 5(11), 1813-1824.
-
(2010)
Chemmedchem
, vol.5
, Issue.11
, pp. 1813-1824
-
-
Cai, L.1
Jiang, S.2
-
99
-
-
84855252915
-
Biochemistry and biophysics of HIV-1 gp41 - membrane interactions and implications for HIV-1 envelope protein mediated viral-cell fusion and fusion inhibitor design
-
Cai, L.; Gochin, M.; Liu, K. Biochemistry and biophysics of HIV-1 gp41 - membrane interactions and implications for HIV-1 envelope protein mediated viral-cell fusion and fusion inhibitor design. Curr. Top. Med. Chem., 2011, 11(24), 2959-2984.
-
(2011)
Curr. Top. Med. Chem
, vol.11
, Issue.24
, pp. 2959-2984
-
-
Cai, L.1
Gochin, M.2
Liu, K.3
-
100
-
-
0035793406
-
Protein design of an HIV-1 entry inhibitor
-
Root, M. J.; Kay, M. S.; Kim, P. S. Protein design of an HIV-1 entry inhibitor. Science, 2001, 291(5505), 884-888.
-
(2001)
Science
, vol.291
, Issue.5505
, pp. 884-888
-
-
Root, M.J.1
Kay, M.S.2
Kim, P.S.3
-
101
-
-
0030987357
-
Assembly of a rod-shaped chimera of a trimeric GCN4 zipper and the HIV-1 gp41 ectodomain expressed in Escherichia coli
-
Weissenhorn, W.; Calder, L. J.; Dessen, A.; Laue, T.; Skehel, J. J.; Wiley, D. C. Assembly of a rod-shaped chimera of a trimeric GCN4 zipper and the HIV-1 gp41 ectodomain expressed in Escherichia coli. Proc. Natl. Acad. Sci. U. S. A., 1997, 94(12), 6065-6069.
-
(1997)
"');">
, vol.94
, Issue.12
, pp. 6065-6069
-
-
Weissenhorn, W.1
Calder, L.J.2
Dessen, A.3
Laue, T.4
Skehel, J.J.5
Wiley, D.C.6
-
102
-
-
0032509096
-
Crystal structure of GCN4-pIQI, a trimeric coiled coil with buried polar residues
-
Eckert, D. M.; Malashkevich, V. N.; Kim, P. S. Crystal structure of GCN4-pIQI, a trimeric coiled coil with buried polar residues. J. Mol. Biol., 1998, 284(4), 859-865.
-
(1998)
J. Mol. Biol
, vol.284
, Issue.4
, pp. 859-865
-
-
Eckert, D.M.1
Malashkevich, V.N.2
Kim, P.S.3
-
103
-
-
0037490139
-
Covalent trimers of the internal N-terminal trimeric coiled-coil of gp41 and antibodies directed against them are potent inhibitors of HIV envelope-mediated cell fusion
-
Louis, J. M.; Nesheiwat, I.; Chang, L.; Clore, G. M.; Bewley, C. A. Covalent trimers of the internal N-terminal trimeric coiled-coil of gp41 and antibodies directed against them are potent inhibitors of HIV envelope-mediated cell fusion. J. Biol. Chem., 2003, 278(22), 20278-20285.
-
(2003)
J. Biol. Chem
, vol.278
, Issue.22
, pp. 20278-20285
-
-
Louis, J.M.1
Nesheiwat, I.2
Chang, L.3
Clore, G.M.4
Bewley, C.A.5
-
104
-
-
0344444157
-
Metallopeptide assembly of the HIV-1 gp41 coiled coil is an ideal receptor in fluorescence detection of ligand binding
-
Gochin, M.; Kiplin, G. R.; Case, M. A. A metallopeptide assembly of the HIV-1 gp41 coiled coil is an ideal receptor in fluorescence detection of ligand binding. Angew. Chem. Int. Ed Engl., 2003, 42(43), 5325-5328.
-
(2003)
Angew. Chem. Int. Ed Engl
, vol.42
, Issue.43
, pp. 5325-5328
-
-
Gochin, M.1
Kiplin, G.R.2
Case, M.3
-
105
-
-
33645760751
-
Fluorescence assay for rapid detection of ligand binding affinity to HIV-1 gp41
-
Gochin, M.; Savage, R.; Hinckley, S.; Cai, L. A fluorescence assay for rapid detection of ligand binding affinity to HIV-1 gp41. Biol. Chem., 2006, 387(4), 477-483.
-
(2006)
Biol. Chem
, vol.387
, Issue.4
, pp. 477-483
-
-
Gochin, M.1
Savage, R.2
Hinckley, S.3
Cai, L.A.4
-
106
-
-
34447260888
-
Novel fluorescence intensity screening assay identifies new low molecular weight inhibitors of the gp41 coiled coil domain of HIV-1
-
Cai, L.; Gochin, M. A novel fluorescence intensity screening assay identifies new low molecular weight inhibitors of the gp41 coiled coil domain of HIV-1. Antimicrob. Agents Chemother., 2007, 51(7), 2388-2395.
-
(2007)
Antimicrob. Agents Chemother
, vol.51
, Issue.7
, pp. 2388-2395
-
-
Cai, L.1
Gochin, M.A.2
-
107
-
-
67049116083
-
Stable extended human immunodeficiency virus type 1 gp41 coiled coil as an effective target in an assay for high-affinity fusion inhibitors
-
Cai, L.; Balogh, E.; Gochin, M. Stable extended human immunodeficiency virus type 1 gp41 coiled coil as an effective target in an assay for high-affinity fusion inhibitors. Antimicrob. Agents Chemother., 2009, 53(6), 2444-2449.
-
(2009)
Antimicrob. Agents Chemother
, vol.53
, Issue.6
, pp. 2444-2449
-
-
Cai, L.1
Balogh, E.2
Gochin, M.3
-
108
-
-
68049108497
-
Second site screening for structure determination of ligands bound in the hydrophobic pocket of HIV-1 gp41
-
Balogh, E.; Wu, D.; Zhou, G.; Gochin, M. NMR second site screening for structure determination of ligands bound in the hydrophobic pocket of HIV-1 gp41. J. Am. Chem. Soc., 2009, 131(8), 2821-2823.
-
(2009)
J. Am. Chem. Soc
, vol.131
, Issue.8
, pp. 2821-2823
-
-
Balogh, E.1
Wu, D.2
Zhou, G.3
Gochin, M.4
-
109
-
-
76649145391
-
Design, synthesisand evaluation of indole compounds as novel inhibitors targeting gp41
-
Zhou, G.; Wu, D.; Hermel, E.; Balogh, E.; Gochin, M. Design, synthesis and evaluation of indole compounds as novel inhibitors targeting gp41. Bioorg. Med. Chem. Lett., 2010, 20(5), 1500-1503.
-
(2010)
Bioorg. Med. Chem. Lett
, vol.20
, Issue.5
, pp. 1500-1503
-
-
Zhou, G.1
Wu, D.2
Hermel, E.3
Balogh, E.4
Gochin, M.5
-
110
-
-
80054910151
-
Development of indole compounds as small molecule fusion inhibitors targeting HIV-1 glycoprotein-41
-
Zhou, G.; Wu, D.; Snyder, B.; Ptak, R. G.; Kaur, H.; Gochin, M. Development of indole compounds as small molecule fusion inhibitors targeting HIV-1 glycoprotein-41. J. Med. Chem., 2011, 54(20), 7220-7231.
-
(2011)
J. Med. Chem
, vol.54
, Issue.20
, pp. 7220-7231
-
-
Zhou, G.1
Wu, D.2
Snyder, B.3
Ptak, R.G.4
Kaur, H.5
Gochin, M.6
-
111
-
-
84903540200
-
Structure-Activity Relationship Studies of Indole-Based Compounds as Small Molecule HIV-1 Fusion Inhibitors Targeting Glycoprotein 41
-
Zhou, G.; Sofiyev, V.; Kaur, H.; Snyder, B. A.; Mankowski, M. K.; Hogan, P. A.; Ptak, R. G.; Gochin, M. Structure-Activity Relationship Studies of Indole-Based Compounds as Small Molecule HIV-1 Fusion Inhibitors Targeting Glycoprotein 41. J. Med. Chem., 2014, 57(12), 5270-5281.
-
(2014)
J. Med. Chem
, vol.57
, Issue.12
, pp. 5270-5281
-
-
Zhou, G.1
Sofiyev, V.2
Kaur, H.3
Snyder, B.A.4
Mankowski, M.K.5
Hogan, P.A.6
Ptak, R.G.7
Gochin, M.8
-
112
-
-
33749032790
-
Small molecules that bind the inner core of gp41 and inhibit HIV envelope-mediated fusion
-
Frey, G.; Rits-Volloch, S.; Zhang, X. Q.; Schooley R. T.; Chen, B.; Harrison, S. C. Small molecules that bind the inner core of gp41 and inhibit HIV envelope-mediated fusion. Proc. Natl. Acad. Sci. U. S. A., 2006, 103(38), 13938-13943.
-
(2006)
Proc. Natl. Acad. Sci. U. S. A
, vol.103
, Issue.38
, pp. 13938-13943
-
-
Frey, G.1
Rits-Volloch, S.2
Zhang, X.Q.3
Schooley, R.T.4
Chen, B.5
Harrison, S.C.6
-
113
-
-
0032876381
-
Selection of gp41-mediated HIV-1 cell entry inhibitors from biased combinatorial libraries of non-natural binding elements
-
Ferrer, M.; Kapoor, T. M.; Strassmaier, T.; Weissenhorn, W.; Skehel, J. J.; Oprian, D.; Schreiber, S. L.; Wiley, D. C.; Harrison, S. C. Selection of gp41-mediated HIV-1 cell entry inhibitors from biased combinatorial libraries of non-natural binding elements. Nat. Struct. Biol., 1999, 6(10), 953-960.
-
(1999)
Nat. Struct. Biol
, vol.6
, Issue.10
, pp. 953-960
-
-
Ferrer, M.1
Kapoor, T.M.2
Strassmaier, T.3
Weissenhorn, W.4
Skehel, J.J.5
Oprian, D.6
Schreiber, S.L.7
Wiley, D.C.8
Harrison, S.C.9
-
114
-
-
17944384967
-
The structure of an HIV-1 specific cell entry inhibitor in complex with the HIV-1 gp41 trimeric core
-
Zhou, G.; Ferrer, M.; Chopra, R.; Kapoor, T. M.; Strassmaier, T.; Weissenhorn, W.; Skehel, J. J.; Oprian, D.; Schreiber, S. L.; Harrison, S. C.; Wiley, D. C. The structure of an HIV-1 specific cell entry inhibitor in complex with the HIV-1 gp41 trimeric core. Bioorg. Med. Chem., 2000, 8(9), 2219-2227.
-
(2000)
Bioorg. Med. Chem
, vol.8
, Issue.9
, pp. 2219-2227
-
-
Zhou, G.1
Ferrer, M.2
Chopra, R.3
Kapoor, T.M.4
Strassmaier, T.5
Weissenhorn, W.6
Skehel, J.J.7
Oprian, D.8
Schreiber, S.L.9
Harrison, S.C.10
Wiley, D.C.11
-
115
-
-
0034801374
-
Toward proteomimetics: Terphenyl derivatives as structural and functional mimics of extended regions of an alpha-helix
-
Orner, B. P.; Ernst, J. T.; Hamilton, A. D. Toward proteomimetics: terphenyl derivatives as structural and functional mimics of extended regions of an alpha-helix. J. Am. Chem. Soc., 2001, 123(22), 5382-5383.
-
(2001)
J. Am. Chem. Soc
, vol.123
, Issue.22
, pp. 5382-5383
-
-
Orner, B.P.1
Ernst, J.T.2
Hamilton, A.D.3
-
116
-
-
0037126834
-
Design of a protein surface antagonist based on alphahelix mimicry: Inhibition of gp41 assembly and viral fusion
-
Ernst, J. T.; Kutzki, O.; Debnath, A. K.; Jiang, S.; Lu, H.; Hamilton, A. D. Design of a protein surface antagonist based on alphahelix mimicry: inhibition of gp41 assembly and viral fusion. Angew. Chem. Int. Ed Engl., 2002, 41(2), 278-281.
-
(2002)
Angew. Chem. Int. Ed Engl
, vol.41
, Issue.2
, pp. 278-281
-
-
Ernst, J.T.1
Kutzki, O.2
Debnath, A.K.3
Jiang, S.4
Lu, H.5
Hamilton, A.D.6
-
117
-
-
79959886414
-
Design, synthesis, and validation of a beta-turn mimetic library targeting protein-protein and peptide-receptor interactions
-
Whitby, L. R.; Ando, Y.; Setola, V.; Vogt, P. K.; Roth, B. L.; Boger, D. L. Design, synthesis, and validation of a beta-turn mimetic library targeting protein-protein and peptide-receptor interactions. J. Am. Chem. Soc., 2011, 133(26), 10184-10194.
-
(2011)
J. Am. Chem. Soc
, vol.133
, Issue.26
, pp. 10184-10194
-
-
Whitby, L.R.1
Ando, Y.2
Setola, V.3
Vogt, P.K.4
Roth, B.L.5
Boger, D.L.6
-
118
-
-
66449110287
-
DOCK 6: Combining techniques to model RNA-small molecule complexes
-
Lang, P. T.; Brozell, S. R.; Mukherjee, S.; Pettersen, E. F.; Meng, E. C.; Thomas, V.; Rizzo, R. C.; Case, D. A.; James, T. L.; Kuntz, I. D. DOCK 6: combining techniques to model RNA-small molecule complexes. RNA, 2009, 15(6), 1219-1230.
-
(2009)
RNA
, vol.15
, Issue.6
, pp. 1219-1230
-
-
Lang, P.T.1
Brozell, S.R.2
Mukherjee, S.3
Pettersen, E.F.4
Meng, E.C.5
Thomas, V.6
Rizzo, R.C.7
Case, D.A.8
James, T.L.9
Kuntz, I.D.10
-
119
-
-
84859437944
-
Footprint- based identification of viral entry inhibitors targeting HIVgp41
-
Holden, P. M.; Kaur, H.; Goyal, R.; Gochin, M.; Rizzo, R. C. Footprint- based identification of viral entry inhibitors targeting HIVgp41. Bioorg. Med. Chem. Lett., 2012, 22(8), 3011-3016.
-
(2012)
Bioorg. Med. Chem. Lett
, vol.22
, Issue.8
, pp. 3011-3016
-
-
Holden, P.M.1
Kaur, H.2
Goyal, R.3
Gochin, M.4
Rizzo, R.C.5
-
120
-
-
72249089316
-
Non-peptide entry inhibitors of HIV-1 that target the gp41 coiled-coil pocket
-
(2), 612-617
-
Stewart, K. D.; Huth, J. R.; Ng, T. I.; McDaniel, K.; Hutchinson, R. N.; Stoll, V. S.; Mendoza, R. R.; Matayoshi, E. D.; Carrick, R.; Mo, H.; Severin, J.; Walter, K.; Richardson, P. L.; Barrett, L. W.; Meadows, R.; Anderson, S.; Kohlbrenner, W.; Maring, C.; Kempf, D. J.; Molla, A.; Olejniczak, E. T. Non-peptide entry inhibitors of HIV-1 that target the gp41 coiled-coil pocket. Bioorg. Med. Chem. Lett., 2010, 20(2):612-7(2), 612-617.
-
(2010)
Bioorg. Med. Chem. Lett
, vol.20
, Issue.2
, pp. 612-617
-
-
Stewart, K.D.1
Huth, J.R.2
Ng, T.I.3
McDaniel, K.4
Hutchinson, R.N.5
Stoll, V.S.6
Mendoza, R.R.7
Matayoshi, E.D.8
Carrick, R.9
Mo, H.10
Severin, J.11
Walter, K.12
Richardson, P.L.13
Barrett, L.W.14
Meadows, R.15
Anderson, S.16
Kohlbrenner, W.17
Maring, C.18
Kempf, D.J.19
Molla, A.20
Olejniczak, E.T.21
more..
-
121
-
-
84856212593
-
Synthesis and antiviral activities of novel gossypol derivatives
-
Yang, J.; Zhang, F.; Li, J.; Chen, G.; Wu, S.; Ouyang, W.; Pan, W.; Yu, R.; Yang, J.; Tien, P. Synthesis and antiviral activities of novel gossypol derivatives. Bioorg. Med. Chem. Lett., 2012, 22(3), 1415-1420.
-
(2012)
Bioorg. Med. Chem. Lett
, vol.22
, Issue.3
, pp. 1415-1420
-
-
Yang, J.1
Zhang, F.2
Li, J.3
Chen, G.4
Wu, S.5
Ouyang, W.6
Pan, W.7
Yu, R.8
Yang, J.9
Tien, P.10
-
122
-
-
33746357565
-
Evaluation of "credit card" libraries for inhibition of HIV-1 gp41 fusogenic core formation
-
Xu, Y.; Lu, H.; Kennedy, J. P.; Yan, X.; McAllister, L. A.; Yamamoto, N.; Moss, J. A.; Boldt, G. E.; Jiang, S.; Janda, K. D. Evaluation of "credit card" libraries for inhibition of HIV-1 gp41 fusogenic core formation. J Comb. Chem., 2006, 8(4), 531-539.
-
(2006)
J Comb. Chem
, vol.8
, Issue.4
, pp. 531-539
-
-
Xu, Y.1
Lu, H.2
Kennedy, J.P.3
Yan, X.4
McAllister, L.A.5
Yamamoto, N.6
Moss, J.A.7
Boldt, G.E.8
Jiang, S.9
Janda, K.D.10
-
123
-
-
84893254396
-
Structure-based discovery of Middle East respiratory syndrome coronavirus fusion inhibitor
-
Lu, L.; Liu, Q.; Zhu, Y.; Chan, K. H.; Qin, L.; Li, Y.; Wang, Q.; Chan, J. F.; Du, L.; Yu, F.; Ma, C.; Ye, S.; Yuen, K. Y.; Zhang, R.; Jiang, S. Structure-based discovery of Middle East respiratory syndrome coronavirus fusion inhibitor. Nat. Commun., 2014, 5(3067).
-
(2014)
Nat. Commun
, vol.5
, Issue.3067
-
-
Lu, L.1
Liu, Q.2
Zhu, Y.3
Chan, K.H.4
Qin, L.5
Li, Y.6
Wang, Q.7
Chan, J.F.8
Du, L.9
Yu, F.10
Ma, C.11
Ye, S.12
Yuen, K.Y.13
Zhang, R.14
Jiang, S.15
-
124
-
-
80054723128
-
Design, synthesis, and biological activity of a novel series of 2,5- disubstituted furans/pyrroles as HIV-1 fusion inhibitors targeting gp41
-
Jiang, S.; Tala, S. R.; Lu, H.; Zou, P.; Avan, I.; Ibrahim, T. S.; bo- Dya, N. E.; Abdelmajeid, A.; Debnath, A. K.; Katritzky, A. R. Design, synthesis, and biological activity of a novel series of 2,5- disubstituted furans/pyrroles as HIV-1 fusion inhibitors targeting gp41. Bioorg. Med. Chem. Lett., 2011, 21(22), 6895-6898.
-
(2011)
Bioorg. Med. Chem. Lett
, vol.21
, Issue.22
, pp. 6895-6898
-
-
Jiang, S.1
Tala, S.R.2
Lu, H.3
Zou, P.4
Avan, I.5
Ibrahim, T.S.6
Bo- Dya, N.E.7
Abdelmajeid, A.8
Debnath, A.K.9
Katritzky, A.R.10
-
125
-
-
13344286960
-
Blocking viral entry: A complementary strategy for HIV therapy
-
Jiang, S.; Siddiqui, P.; Liu, S. Blocking viral entry: a complementary strategy for HIV therapy. Drug Discov. Today: Ther. Strateg., 2004, 1(4), 497-503.
-
(2004)
Drug Discov. Today: Ther. Strateg
, vol.1
, Issue.4
, pp. 497-503
-
-
Jiang, S.1
Siddiqui, P.2
Liu, S.3
-
126
-
-
2442511737
-
High throughput screening and characterization of HIV-1 entry inhibitors targeting gp41: Theories and techniques
-
Liu, S.; Jiang, S. High throughput screening and characterization of HIV-1 entry inhibitors targeting gp41: theories and techniques. Curr. Pharm. Des., 2004, 10(15), 1827-1843.
-
(2004)
Curr. Pharm. Des
, vol.10
, Issue.15
, pp. 1827-1843
-
-
Liu, S.1
Jiang, S.2
-
127
-
-
0037966960
-
Targeting therapeutics to an exposed and conserved binding element of the HIV-1 fusion protein
-
Root, M. J.; Hamer, D. H. Targeting therapeutics to an exposed and conserved binding element of the HIV-1 fusion protein. Proc. Natl. Acad. Sci. U. S. A., 2003, 100(9), 5016-5021.
-
(2003)
Proc. Natl. Acad. Sci. U. S. A
, vol.100
, Issue.9
, pp. 5016-5021
-
-
Root, M.J.1
Hamer, D.H.2
-
128
-
-
34248155890
-
HIV gp41 C-terminal heptad repeat contains multifunctional domains: Relation to mechanisms of action of anti-HIV peptides
-
Liu, S.; Jing, W.; Cheung, B.; Lu, H.; Sun, J.; Yan, X.; Niu, J.; Farmar, J.; Wu, S.; Jiang, S. HIV gp41 C-terminal heptad repeat contains multifunctional domains: relation to mechanisms of action of anti-HIV peptides. J. Biol. Chem., 2007, 282(13), 9612-9620.
-
(2007)
J. Biol. Chem
, vol.282
, Issue.13
, pp. 9612-9620
-
-
Liu, S.1
Jing, W.2
Cheung, B.3
Lu, H.4
Sun, J.5
Yan, X.6
Niu, J.7
Farmar, J.8
Wu, S.9
Jiang, S.10
-
129
-
-
0033214895
-
Inhibiting HIV-1 entry: Discovery of D-peptide inhibitors that target the gp41 coiled-coil pocket
-
Eckert, D. M.; Malashkevich, V. N.; Hong, L. H.; Carr, P. A.; Kim, P. S. Inhibiting HIV-1 entry: discovery of D-peptide inhibitors that target the gp41 coiled-coil pocket. Cell, 1999, 99(1), 103-115.
-
(1999)
Cell
, vol.99
, Issue.1
, pp. 103-115
-
-
Eckert, D.M.1
Malashkevich, V.N.2
Hong, L.H.3
Carr, P.A.4
Kim, P.S.5
-
130
-
-
36749087580
-
Potent D-peptide inhibitors of HIV-1 entry
-
Welch, B. D.; VanDemark, A. P.; Heroux, A.; Hill, C. P.; Kay, M. S. Potent D-peptide inhibitors of HIV-1 entry. Proc. Natl. Acad. Sci. U.S.A., 2007, 104(43), 16828-16833.
-
(2007)
Proc. Natl. Acad. Sci. U.S.A
, vol.104
, Issue.43
, pp. 16828-16833
-
-
Welch, B.D.1
Vandemark, A.P.2
Heroux, A.3
Hill, C.P.4
Kay, M.S.5
-
131
-
-
77957942154
-
Design of a potent D-peptide HIV-1 entry inhibitor with a strong barrier to resistance
-
Welch, B. D.; Francis, J. N.; Redman, J. S.; Paul, S.; Weinstock, M. T.; Reeves, J. D.; Lie, Y. S.; Whitby, F. G.; Eckert, D. M.; Hill, C. P.; Root, M. J.; Kay, M. S. Design of a potent D-peptide HIV-1 entry inhibitor with a strong barrier to resistance. J. Virol., 2010, 84(21), 11235-11244.
-
(2010)
J. Virol
, vol.84
, Issue.21
, pp. 11235-11244
-
-
Welch, B.D.1
Francis, J.N.2
Redman, J.S.3
Paul, S.4
Weinstock, M.T.5
Reeves, J.D.6
Lie, Y.S.7
Whitby, F.G.8
Eckert, D.M.9
Hill, C.P.10
Root, M.J.11
Kay, M.S.12
-
132
-
-
34147137981
-
Discovery and optimization of a natural HIV-1 entry inhibitor targeting the gp41 fusion peptide
-
Munch, J.; Standker, L.; Adermann, K.; Schulz, A.; Schindler, M.; Chinnadurai, R.; Pohlmann, S.; Chaipan, C.; Biet, T.; Peters, T.; Meyer, B.; Wilhelm, D.; Lu, H.; Jing, W.; Jiang, S.; Forssmann, W. G.; Kirchhoff, F. Discovery and optimization of a natural HIV-1 entry inhibitor targeting the gp41 fusion peptide. Cell, 2007, 129(2), 263-275.
-
(2007)
Cell
, vol.129
, Issue.2
, pp. 263-275
-
-
Munch, J.1
Standker, L.2
Adermann, K.3
Schulz, A.4
Schindler, M.5
Chinnadurai, R.6
Pohlmann, S.7
Chaipan, C.8
Biet, T.9
Peters, T.10
Meyer, B.11
Wilhelm, D.12
Lu, H.13
Jing, W.14
Jiang, S.15
Forssmann, W.G.16
Kirchhoff, F.17
-
133
-
-
9344268284
-
Restricted antigenic variability of the epitope recognized by the neutralizing gp41 antibody 2F5
-
Purtscher, M.; Trkola, A.; Grassauer, A.; Schulz, P. M.; Klima, A.; Dopper, S.; Gruber, G.; Buchacher, A.; Muster, T.; Katinger, H. Restricted antigenic variability of the epitope recognized by the neutralizing gp41 antibody 2F5. AIDS, 1996, 10(6), 587-593.
-
(1996)
AIDS
, vol.10
, Issue.6
, pp. 587-593
-
-
Purtscher, M.1
Trkola, A.2
Grassauer, A.3
Schulz, P.M.4
Klima, A.5
Dopper, S.6
Gruber, G.7
Buchacher, A.8
Muster, T.9
Katinger, H.10
-
134
-
-
11144227042
-
Anti-human immunodeficiency virus type 1 (HIV-1) antibodies 2F5 and 4E10 require surprisingly few crucial residues in the membrane-proximal external region of glycoprotein gp41 to neutralize HIV-1
-
Zwick, M. B.; Jensen, R.; Church, S.; Wang, M.; Stiegler, G.; Kunert, R.; Katinger, H.; Burton, D. R. Anti-human immunodeficiency virus type 1 (HIV-1) antibodies 2F5 and 4E10 require surprisingly few crucial residues in the membrane-proximal external region of glycoprotein gp41 to neutralize HIV-1. J. Virol., 2005, 79(2), 1252-1261.
-
(2005)
J. Virol
, vol.79
, Issue.2
, pp. 1252-1261
-
-
Zwick, M.B.1
Jensen, R.2
Church, S.3
Wang, M.4
Stiegler, G.5
Kunert, R.6
Katinger, H.7
Burton, D.R.8
-
135
-
-
84866493348
-
Broad and potent neutralization of HIV-1 by a gp41- specific human antibody
-
Huang, J.; Ofek, G.; Laub, L.; Louder, M. K.; Doria-Rose, N. A.; Longo, N. S.; Imamichi, H.; Bailer, R. T.; Chakrabarti, B.; Sharma, S. K.; Alam, S. M.; Wang, T.; Yang, Y.; Zhang, B.; Migueles, S. A.; Wyatt, R.; Haynes, B. F.; Kwong, P. D.; Mascola, J. R.; Connors, M. Broad and potent neutralization of HIV-1 by a gp41- specific human antibody. Nature, 2012, 491(7424), 406-412.
-
(2012)
Nature
, vol.491
, Issue.7424
, pp. 406-412
-
-
Huang, J.1
Ofek, G.2
Laub, L.3
Louder, M.K.4
Doria-Rose, N.A.5
Longo, N.S.6
Imamichi, H.7
Bailer, R.T.8
Chakrabarti, B.9
Sharma, S.K.10
Alam, S.M.11
Wang, T.12
Yang, Y.13
Zhang, B.14
Migueles, S.A.15
Wyatt, R.16
Haynes, B.F.17
Kwong, P.D.18
Mascola, J.R.19
Connors, M.20
more..
-
136
-
-
84921607768
-
Broad and potent HIV-1 neutralization by a human antibody that binds the gp41-gp120 interface
-
Huang, J.; Kang, B. H.; Pancera, M.; Lee, J. H.; Tong, T.; Feng, Y.; Imamichi, H.; Georgiev, I. S.; Chuang, G. Y.; Druz, A.; Doria- Rose, N. A.; Laub, L.; Sliepen, K.; van Gils, M. J.; de la Pena, A. T.; Derking, R.; Klasse, P. J.; Migueles, S. A.; Bailer, R. T.; Alam, M.; Pugach, P.; Haynes, B. F.; Wyatt, R. T.; Sanders, R. W.; Binley, J. M.; Ward, A. B.; Mascola, J. R.; Kwong, P. D.; Connors, M. Broad and potent HIV-1 neutralization by a human antibody that binds the gp41-gp120 interface. Nature, 2014, 515(7525), 138-142.
-
(2014)
Nature
, vol.515
, Issue.7525
, pp. 138-142
-
-
Huang, J.1
Kang, B.H.2
Pancera, M.3
Lee, J.H.4
Tong, T.5
Feng, Y.6
Imamichi, H.7
Georgiev, I.S.8
Chuang, G.Y.9
Druz, A.10
Doria- Rose, N.A.11
Laub, L.12
Sliepen, K.13
Van Gils, M.J.14
De La Pena, A.T.15
Derking, R.16
Klasse, P.J.17
Migueles, S.A.18
Bailer, R.T.19
Alam, M.20
Pugach, P.21
Haynes, B.F.22
Wyatt, R.T.23
Sanders, R.W.24
Binley, J.M.25
Ward, A.B.26
Mascola, J.R.27
Kwong, P.D.28
Connors, M.29
more..
|