-
1
-
-
13044256383
-
A small-molecule, nonpeptide CCR5 antagonist with highly potent and selective anti-HIV-1 activity
-
Baba, M., O. Nishimura, N. Kanzaki, M. Okamoto, H. Sawada, Y. Iizawa, M. Shiraishi, Y. Aramaki, K. Okonogi, Y. Ogawa, K. Meguro, and M. Fujino. 1999. A small-molecule, nonpeptide CCR5 antagonist with highly potent and selective anti-HIV-1 activity. Proc. Natl. Acad. Sci. USA 96:5698-5703.
-
(1999)
Proc. Natl. Acad. Sci. USA
, vol.96
, pp. 5698-5703
-
-
Baba, M.1
Nishimura, O.2
Kanzaki, N.3
Okamoto, M.4
Sawada, H.5
Iizawa, Y.6
Shiraishi, M.7
Aramaki, Y.8
Okonogi, K.9
Ogawa, Y.10
Meguro, K.11
Fujino, M.12
-
2
-
-
0033012398
-
Chemokine receptors as HIV-1 coreceptors: Roles in viral entry, tropism, and disease
-
Berger, E. A., P. M. Murphy, and J. M. Farber. 1999. Chemokine receptors as HIV-1 coreceptors: roles in viral entry, tropism, and disease. Annu. Rev. Immunol. 17:657-700.
-
(1999)
Annu. Rev. Immunol.
, vol.17
, pp. 657-700
-
-
Berger, E.A.1
Murphy, P.M.2
Farber, J.M.3
-
4
-
-
0035000023
-
Mapping the determinants of the CCR5 amino-terminal sulfopeptide interaction with soluble human immunodeficiency virus type 1 gp120-CD4 complexes
-
Cormier, E. G., D. N. Tran, L. Yukhayeva, W. C. Olson, and T. Dragic. 2001. Mapping the determinants of the CCR5 amino-terminal sulfopeptide interaction with soluble human immunodeficiency virus type 1 gp120-CD4 complexes. J. Virol. 75:5541-5549.
-
(2001)
J. Virol.
, vol.75
, pp. 5541-5549
-
-
Cormier, E.G.1
Tran, D.N.2
Yukhayeva, L.3
Olson, W.C.4
Dragic, T.5
-
5
-
-
0032499791
-
Crystal structure of chemically synthesized [N33A] stromal cell-derived factor 1α, a potent ligand for the HIV-1 "fusin" coreceptor
-
Dealwis, C., E. J. Fernandez, D. A. Thompson, R. J. Simon, M. A. Siani, and E. Lolis. 1998. Crystal structure of chemically synthesized [N33A] stromal cell-derived factor 1α, a potent ligand for the HIV-1 "fusin" coreceptor. Proc. Natl. Acad. Sci. USA 95:6941-6946.
-
(1998)
Proc. Natl. Acad. Sci. USA
, vol.95
, pp. 6941-6946
-
-
Dealwis, C.1
Fernandez, E.J.2
Thompson, D.A.3
Simon, R.J.4
Siani, M.A.5
Lolis, E.6
-
6
-
-
0001633495
-
Genetic restriction of HIV-1 infection and progression to AIDS by a deletion allele of the CKR5 structural gene. Hemophilia Growth and Development Study, Multicenter AIDS Cohort Study, Multicenter Hemophilia Cohort Study, San Francisco City Cohort, ALIVE Study
-
Erratum, 274:1069
-
Dean, M., M. Carrington, C. Winkler, G. A. Huttley, M. W. Smith, R. Allikmets, J. J. Goedert, S. P. Buchbinder, E. Vittinghoff, E. Gomperts, S. Donfield, D. Vlahov, R. Kaslow, A. Saah, C. Rinaldo, R. Detels, and S. J. O'Brien. 1996. Genetic restriction of HIV-1 infection and progression to AIDS by a deletion allele of the CKR5 structural gene. Hemophilia Growth and Development Study, Multicenter AIDS Cohort Study, Multicenter Hemophilia Cohort Study, San Francisco City Cohort, ALIVE Study. Science 273:1856-1862. (Erratum, 274:1069.)
-
(1996)
Science
, vol.273
, pp. 1856-1862
-
-
Dean, M.1
Carrington, M.2
Winkler, C.3
Huttley, G.A.4
Smith, M.W.5
Allikmets, R.6
Goedert, J.J.7
Buchbinder, S.P.8
Vittinghoff, E.9
Gomperts, E.10
Donfield, S.11
Vlahov, D.12
Kaslow, R.13
Saah, A.14
Rinaldo, C.15
Detels, R.16
O'Brien, S.J.17
-
7
-
-
0035160478
-
New developments in anti-HIV chemotherapy
-
De Clercq, E. 2001. New developments in anti-HIV chemotherapy. Curr. Med. Chem. 8:1543-1572.
-
(2001)
Curr. Med. Chem.
, vol.8
, pp. 1543-1572
-
-
De Clercq, E.1
-
8
-
-
0001914545
-
Chemokine receptors and HIV entry
-
Doms, R. W. 2001. Chemokine receptors and HIV entry. AIDS 15(Suppl. 1):S34-S35.
-
(2001)
AIDS
, vol.15
, Issue.SUPPL. 1
-
-
Doms, R.W.1
-
9
-
-
0031891516
-
AMD3100, a small molecule inhibitor of HIV-1 entry via the CXCR4 co-receptor
-
Donzella, G. A., D. Schols, S. W. Lin, J. A. Este, K. A. Nagashima, P. J. Maddon, G. P. Allaway, T. P. Sakmar, G. Henson, E. De Clercq, and J. P. Moore. 1998. AMD3100, a small molecule inhibitor of HIV-1 entry via the CXCR4 co-receptor. Nat. Med. 4:72-77.
-
(1998)
Nat. Med.
, vol.4
, pp. 72-77
-
-
Donzella, G.A.1
Schols, D.2
Lin, S.W.3
Este, J.A.4
Nagashima, K.A.5
Maddon, P.J.6
Allaway, G.P.7
Sakmar, T.P.8
Henson, G.9
De Clercq, E.10
Moore, J.P.11
-
10
-
-
0034906440
-
An overview of the determinants of CCR5 and CXCR4 co-receptor function
-
Dragic, T. 2001. An overview of the determinants of CCR5 and CXCR4 co-receptor function. J. Gen. Virol. 82:1807-1814.
-
(2001)
J. Gen. Virol.
, vol.82
, pp. 1807-1814
-
-
Dragic, T.1
-
11
-
-
0031984539
-
Amino-terminal substitutions in the CCR5 coreceptor impair gp120 binding and human immunodeficiency virus type 1 entry
-
Dragic, T., A. Trkola, S. W. Lin, K. A. Nagashima, F. Kajumo, L. Zhao, W. C. Olson, L. Wu, C. R. Mackay, G. P. Allaway, T. P. Sakmar, J. P. Moore, and P. J. Maddon. 1998. Amino-terminal substitutions in the CCR5 coreceptor impair gp120 binding and human immunodeficiency virus type 1 entry. J. Virol. 72:279-285.
-
(1998)
J. Virol.
, vol.72
, pp. 279-285
-
-
Dragic, T.1
Trkola, A.2
Lin, S.W.3
Nagashima, K.A.4
Kajumo, F.5
Zhao, L.6
Olson, W.C.7
Wu, L.8
Mackay, C.R.9
Allaway, G.P.10
Sakmar, T.P.11
Moore, J.P.12
Maddon, P.J.13
-
12
-
-
0034625144
-
A binding pocket for a small molecule inhibitor of HIV-1 entry within the transmembrane helices of CCR5
-
Dragic, T., A. Trkola, D. A. Thompson, E. G. Cormier, F. A. Kajumo, E. Maxwell, S. W. Lin, W. Ying, S. O. Smith, T. P. Sakmar, and J. P. Moore. 2000. A binding pocket for a small molecule inhibitor of HIV-1 entry within the transmembrane helices of CCR5. Proc. Natl. Acad. Sci. USA 97:5639-5644.
-
(2000)
Proc. Natl. Acad. Sci. USA
, vol.97
, pp. 5639-5644
-
-
Dragic, T.1
Trkola, A.2
Thompson, D.A.3
Cormier, E.G.4
Kajumo, F.A.5
Maxwell, E.6
Lin, S.W.7
Ying, W.8
Smith, S.O.9
Sakmar, T.P.10
Moore, J.P.11
-
13
-
-
0032959316
-
CCR5-mediated human immunodeficiency virus entry depends on an amino-terminal gp120-binding site and on the conformational integrity of all four extracellular domains
-
Genoud, S., F. Kajumo, Y. Guo, D. Thompson, and T. Dragic. 1999. CCR5-mediated human immunodeficiency virus entry depends on an amino-terminal gp120-binding site and on the conformational integrity of all four extracellular domains. J. Virol. 73:1645-1648.
-
(1999)
J. Virol.
, vol.73
, pp. 1645-1648
-
-
Genoud, S.1
Kajumo, F.2
Guo, Y.3
Thompson, D.4
Dragic, T.5
-
14
-
-
19244384846
-
Global survey of genetic variation in CCR5, RANTES, and MIP-1α: Impact on the epidemiology of the HIV-1 pandemic
-
Gonzalez, E., R. Dhanda, M. Bamshad, S. Mummidi, R. Geevarghese, G. Catano, S. A. Anderson, E. A. Walter, K. T. Stephan, M. F. Hammer, A. Mangano, L. Sen, R. A. Clark, S. S. Ahuja, M. J. Dolan, and S. K. Ahuja. 2001. Global survey of genetic variation in CCR5, RANTES, and MIP-1α: impact on the epidemiology of the HIV-1 pandemic. Proc. Natl. Acad. Sci. USA 98:5199-5204.
-
(2001)
Proc. Natl. Acad. Sci. USA
, vol.98
, pp. 5199-5204
-
-
Gonzalez, E.1
Dhanda, R.2
Bamshad, M.3
Mummidi, S.4
Geevarghese, R.5
Catano, G.6
Anderson, S.A.7
Walter, E.A.8
Stephan, K.T.9
Hammer, M.F.10
Mangano, A.11
Sen, L.12
Clark, R.A.13
Ahuja, S.S.14
Dolan, M.J.15
Ahuja, S.K.16
-
15
-
-
0034120373
-
Pharmacokinetics and safety of AMD-3100, a novel antagonist of the CXCR-4 chemokine receptor, in human volunteers
-
Hendrix, C. W., C. Flexner, R. T. MacFarland, C. Giandomenico, E. J. Fuchs, E. Redpath, G. Bridger, and G. W. Henson. 2000. Pharmacokinetics and safety of AMD-3100, a novel antagonist of the CXCR-4 chemokine receptor, in human volunteers. Antimicrob. Agents Chemother. 44:1667-1673.
-
(2000)
Antimicrob. Agents Chemother
, vol.44
, pp. 1667-1673
-
-
Hendrix, C.W.1
Flexner, C.2
MacFarland, R.T.3
Giandomenico, C.4
Fuchs, E.J.5
Redpath, E.6
Bridger, G.7
Henson, G.W.8
-
16
-
-
0032168915
-
The amino terminus ofhuman CCR5 is required for its function as a receptor for diverse human and simian immunodeficiency virus envelope glycoproteins
-
Hill, C. M., D. Kwon, M. Jones, C. B. Davis, S. Marmon, B. L. Daugherty, J. A. DeMartino, M. S. Springer, D. Unutmaz, and D. R. Littman. 1998. The amino terminus ofhuman CCR5 is required for its function as a receptor for diverse human and simian immunodeficiency virus envelope glycoproteins. Virology 248:357-371.
-
(1998)
Virology
, vol.248
, pp. 357-371
-
-
Hill, C.M.1
Kwon, D.2
Jones, M.3
Davis, C.B.4
Marmon, S.5
Daugherty, B.L.6
DeMartino, J.A.7
Springer, M.S.8
Unutmaz, D.9
Littman, D.R.10
-
17
-
-
0033515588
-
Epitope mapping of CCR5 reveals multiple conformational states and distinct but overlapping structures involved in chemokine and coreceptor function
-
Lee, B., M. Sharron, C. Blanpain, B. J. Doranz, J. Vakili, P. Setoh, E. Berg, G. Liu, H. R. Guy, S. R. Durell, M. Parmentier, C. N. Chang, K. Price, M. Tsang, and R. W. Doms. 1999. Epitope mapping of CCR5 reveals multiple conformational states and distinct but overlapping structures involved in chemokine and coreceptor function. J. Biol. Chem. 274:9617-9626.
-
(1999)
J. Biol. Chem.
, vol.274
, pp. 9617-9626
-
-
Lee, B.1
Sharron, M.2
Blanpain, C.3
Doranz, B.J.4
Vakili, J.5
Setoh, P.6
Berg, E.7
Liu, G.8
Guy, H.R.9
Durell, S.R.10
Parmentier, M.11
Chang, C.N.12
Price, K.13
Tsang, M.14
Doms, R.W.15
-
18
-
-
15844388931
-
Homozygous defect in HIV-1 coreceptor accounts for resistance of some multiply-exposed individuals to HIV-1 infection
-
Liu, R., W. Paxton, S. Choe, D. Ceradini, S. Martin, R. Horuk, M. MacDonald, H. Stuhlmann, R. Koup, and N. Landau. 1996. Homozygous defect in HIV-1 coreceptor accounts for resistance of some multiply-exposed individuals to HIV-1 infection. Cell 86:367-378.
-
(1996)
Cell
, vol.86
, pp. 367-378
-
-
Liu, R.1
Paxton, W.2
Choe, S.3
Ceradini, D.4
Martin, S.5
Horuk, R.6
MacDonald, M.7
Stuhlmann, H.8
Koup, R.9
Landau, N.10
-
19
-
-
0032575620
-
N-terminal peptides of stromal cell-derived factor-1 with CXC chemokine receptor 4 agonist and antagonist activities
-
Loetscher, P., J. H. Gong, B. Dewald, M. Baggiolini, and I. Clark-Lewis. 1998. N-terminal peptides of stromal cell-derived factor-1 with CXC chemokine receptor 4 agonist and antagonist activities. J. Biol. Chem. 273:22279-22283.
-
(1998)
J. Biol. Chem.
, vol.273
, pp. 22279-22283
-
-
Loetscher, P.1
Gong, J.H.2
Dewald, B.3
Baggiolini, M.4
Clark-Lewis, I.5
-
20
-
-
0034304841
-
New targets for inhibitors of HIV-1 replication
-
Moore, J. P., and M. Stevenson. 2000. New targets for inhibitors of HIV-1 replication. Nat. Rev. Mol. Cell. Biol. 1:40-49.
-
(2000)
Nat. Rev. Mol. Cell. Biol.
, vol.1
, pp. 40-49
-
-
Moore, J.P.1
Stevenson, M.2
-
21
-
-
0033647217
-
The effect of genetic variation in chemokines and their receptors on HIV transmission and progression to AIDS
-
O'Brien, S. J., and J. P. Moore. 2000. The effect of genetic variation in chemokines and their receptors on HIV transmission and progression to AIDS. Immunol. Rev. 177:99-111.
-
(2000)
Immunol. Rev.
, vol.177
, pp. 99-111
-
-
O'Brien, S.J.1
Moore, J.P.2
-
22
-
-
0032902710
-
Differential inhibition of human immunodeficiency virus type 1 fusion, gp120 binding, and CC-chemokine activity by monoclonal antibodies to CCR5
-
Olson, W. C., G. E. Rabut, K. A. Nagashima, D. N. Tran, D. J. Anselma, S. P. Monard, J. P. Segal, D. A. Thompson, F. Kajumo, Y. Guo, J. P. Moore, P. J. Maddon, and T. Dragic. 1999. Differential inhibition of human immunodeficiency virus type 1 fusion, gp120 binding, and CC-chemokine activity by monoclonal antibodies to CCR5. J. Virol. 73:4145-4155.
-
(1999)
J. Virol.
, vol.73
, pp. 4145-4155
-
-
Olson, W.C.1
Rabut, G.E.2
Nagashima, K.A.3
Tran, D.N.4
Anselma, D.J.5
Monard, S.P.6
Segal, J.P.7
Thompson, D.A.8
Kajumo, F.9
Guo, Y.10
Moore, J.P.11
Maddon, P.J.12
Dragic, T.13
-
23
-
-
0035846074
-
Discovery of 4-[(Z)-(4-bromophenyl)-(ethoxyimino)methyl]-1′-[(2,4-dimethyl-3- pyridinyl) carbonyl]-4′-methyl-1,4′-bi-piperidine N-oxide (SCH 351125): An orally bioavailable human CCR5 antagonist for the treatment of HIV infection
-
Palani, A., S. Shapiro, J. W. Clader, W. J. Greenlee, K. Cox, J. Strizki, M. Endres, and B. M. Baroudy. 2001. Discovery of 4-[(Z)-(4-bromophenyl)-(ethoxyimino)methyl]-1′-[(2,4-dimethyl-3- pyridinyl) carbonyl]-4′-methyl-1,4′-bi-piperidine N-oxide (SCH 351125): an orally bioavailable human CCR5 antagonist for the treatment of HIV infection. J. Med. Chem. 44:3339-3342.
-
(2001)
J. Med. Chem.
, vol.44
, pp. 3339-3342
-
-
Palani, A.1
Shapiro, S.2
Clader, J.W.3
Greenlee, W.J.4
Cox, K.5
Strizki, J.6
Endres, M.7
Baroudy, B.M.8
-
24
-
-
0037019271
-
Synthesis, SAR, and biological evaluation of oximino-piperidino-piperidine amides. I. Orally bioavailable CCR5 receptor antagonists with potent anti-HIV activity
-
Palani, A., S. Shapiro, H. Josien, T. Bara, J. W. Clader, W. J. Greenlee, K. Cox, J. M. Strizki, and B. M. Baroudy. 2002. Synthesis, SAR, and biological evaluation of oximino-piperidino-piperidine amides. I. Orally bioavailable CCR5 receptor antagonists with potent anti-HIV activity. J. Med. Chem. 45:3143-3160.
-
(2002)
J. Med. Chem.
, vol.45
, pp. 3143-3160
-
-
Palani, A.1
Shapiro, S.2
Josien, H.3
Bara, T.4
Clader, J.W.5
Greenlee, W.J.6
Cox, K.7
Strizki, J.M.8
Baroudy, B.M.9
-
25
-
-
0034604451
-
Crystal structure of rhodopsin: A G protein-coupled receptor
-
Palczewski, K., T. Kumasaka, T. Hori, C. A. Behnke, H. Motoshima, B. A. Fox, I. Le Trong, D. C. Teller, T. Okada, R. E. Stenkamp, M. Yamamoto, and M. Miyano. 2000. Crystal structure of rhodopsin: a G protein-coupled receptor. Science 289:739-745.
-
(2000)
Science
, vol.289
, pp. 739-745
-
-
Palczewski, K.1
Kumasaka, T.2
Hori, T.3
Behnke, C.A.4
Motoshima, H.5
Fox, B.A.6
Le Trong, I.7
Teller, D.C.8
Okada, T.9
Stenkamp, R.E.10
Yamamoto, M.11
Miyano, M.12
-
26
-
-
0032565314
-
+ lymphocytes from exposed-uninfected individuals: Association with low expression of CCR5 and high production of beta-chemokines
-
+ lymphocytes from exposed-uninfected individuals: association with low expression of CCR5 and high production of beta-chemokines. Virology 244:66-73.
-
(1998)
Virology
, vol.244
, pp. 66-73
-
-
Paxton, W.A.1
Liu, R.2
Kang, S.3
Wu, L.4
Gingeras, T.R.5
Landau, N.R.6
Mackay, C.R.7
Koup, R.A.8
-
27
-
-
0031900659
-
Alanine substitutions of polar and nonpolar residues in the amino-terminal domain of CCR5 differently impair entry of macrophage- and dual-tropic isolates of human immunodeficiency virus type 1
-
Rabut, G. E., J. A. Konner, F. Kajumo, J. P. Moore, and T. Dragic. 1998. Alanine substitutions of polar and nonpolar residues in the amino-terminal domain of CCR5 differently impair entry of macrophage- and dual-tropic isolates of human immunodeficiency virus type 1. J. Virol. 72:3464-3468.
-
(1998)
J. Virol.
, vol.72
, pp. 3464-3468
-
-
Rabut, G.E.1
Konner, J.A.2
Kajumo, F.3
Moore, J.P.4
Dragic, T.5
-
28
-
-
0035912249
-
HIV chemotherapy
-
Richman, D. D. 2001. HIV chemotherapy. Nature 410:995-1001.
-
(2001)
Nature
, vol.410
, pp. 995-1001
-
-
Richman, D.D.1
-
29
-
-
16044373004
-
Resistance to HIV-1 infection in Caucasian individuals bearing mutant alleles of the CCR-5 chemokine receptor gene
-
Samson, M., F. Libert, B. J. Doranz, J. Rucker, C. Liesnard, C. M. Farber, S. Saragosti, C. Lapoumeroulie, J. Cognaux, C. Forceille, G. Muyldermans, C. Verhofstede, G. Burtonboy, M. Georges, T. Imai, S. Rana, Y. Yi, R. J. Smyth, R. G. Collman, R. W. Doms, G. Vassart, and M. Parmentier. 1996. Resistance to HIV-1 infection in Caucasian individuals bearing mutant alleles of the CCR-5 chemokine receptor gene. Nature 382:722-725.
-
(1996)
Nature
, vol.382
, pp. 722-725
-
-
Samson, M.1
Libert, F.2
Doranz, B.J.3
Rucker, J.4
Liesnard, C.5
Farber, C.M.6
Saragosti, S.7
Lapoumeroulie, C.8
Cognaux, J.9
Forceille, C.10
Muyldermans, G.11
Verhofstede, C.12
Burtonboy, G.13
Georges, M.14
Imai, T.15
Rana, S.16
Yi, Y.17
Smyth, R.J.18
Collman, R.G.19
Doms, R.W.20
Vassart, G.21
Parmentier, M.22
more..
-
30
-
-
0030830661
-
Inhibition of T-tropic HIV strains by selective antagonization of the chemokine receptor CXCR4
-
Schols, D., S. Struyf, J. Van Damme, J. A. Este, G. Henson, and E. De Clercq. 1997. Inhibition of T-tropic HIV strains by selective antagonization of the chemokine receptor CXCR4. J. Exp. Med. 186:1383-1388.
-
(1997)
J. Exp. Med.
, vol.186
, pp. 1383-1388
-
-
Schols, D.1
Struyf, S.2
Van Damme, J.3
Este, J.A.4
Henson, G.5
De Clercq, E.6
-
31
-
-
0036561677
-
New therapeutics that modulate chemokine networks
-
Schwarz, M. K., and T. N. Wells. 2002. New therapeutics that modulate chemokine networks. Nat. Rev. Drug Disc. 1:347-358.
-
(2002)
Nat. Rev. Drug Disc.
, vol.1
, pp. 347-358
-
-
Schwarz, M.K.1
Wells, T.N.2
-
32
-
-
0030951442
-
Potent inhibition of HIV-1 infectivity in macrophages and lymphocytes by a novel CCR5 antagonist
-
Simmons, G., P. R. Clapham, L. Picard, R. E. Offord, M. M. Rosenkilde, T. W. Schwartz, R. Buser, T. N. C. Wells, and A. E. Proudfoot. 1997. Potent inhibition of HIV-1 infectivity in macrophages and lymphocytes by a novel CCR5 antagonist. Science 276:276-279.
-
(1997)
Science
, vol.276
, pp. 276-279
-
-
Simmons, G.1
Clapham, P.R.2
Picard, L.3
Offord, R.E.4
Rosenkilde, M.M.5
Schwartz, T.W.6
Buser, R.7
Wells, T.N.C.8
Proudfoot, A.E.9
-
33
-
-
0035940445
-
SCH-C (SCH 351125), an orally bioavailable, small molecule antagonist of the chemokine receptor CCR5, is a potent inhibitor of HIV-1 infection in vitro and in vivo
-
Strizki, J. M., S. Xu, N. E. Wagner, L. Wojcik, J. Liu, Y. Hou, M. Endres, A. Palani, S. Shapiro, J. W. Clader, W. J. Greenlee, J. R. Tagat, S. McCombie, K. Cox, A. B. Fawzi, C. C. Chou, C. Pugliese-Sivo, L. Davies, M. E. Moreno, D. D. Ho, A. Trkola, C. A. Stoddart, J. P. Moore, G. R. Reyes, and B. M. Baroudy. 2001. SCH-C (SCH 351125), an orally bioavailable, small molecule antagonist of the chemokine receptor CCR5, is a potent inhibitor of HIV-1 infection in vitro and in vivo. Proc. Natl. Acad. Sci. USA 98:12718-12723.
-
(2001)
Proc. Natl. Acad. Sci. USA
, vol.98
, pp. 12718-12723
-
-
Strizki, J.M.1
Xu, S.2
Wagner, N.E.3
Wojcik, L.4
Liu, J.5
Hou, Y.6
Endres, M.7
Palani, A.8
Shapiro, S.9
Clader, J.W.10
Greenlee, W.J.11
Tagat, J.R.12
McCombie, S.13
Cox, K.14
Fawzi, A.B.15
Chou, C.C.16
Pugliese-Sivo, C.17
Davies, L.18
Moreno, M.E.19
Ho, D.D.20
Trkola, A.21
Stoddart, C.A.22
Moore, J.P.23
Reyes, G.R.24
Baroudy, B.M.25
more..
-
34
-
-
0035921055
-
Piperazine-based CCR5 antagonists as HIV-1 inhibitors. I: 2(S)-methyl piperazine as a key pharmacophore element
-
Tagat, J. R., S. W. McCombie, R. W. Steensma, S. Lin, D. V. Nazareno, B. Baroudy, N. Vantuno, S. Xu, and J. Liu. 2001. Piperazine-based CCR5 antagonists as HIV-1 inhibitors. I: 2(S)-methyl piperazine as a key pharmacophore element. Bioorg. Med. Chem. Lett. 11:2143-2146.
-
(2001)
Bioorg. Med. Chem. Lett.
, vol.11
, pp. 2143-2146
-
-
Tagat, J.R.1
McCombie, S.W.2
Steensma, R.W.3
Lin, S.4
Nazareno, D.V.5
Baroudy, B.6
Vantuno, N.7
Xu, S.8
Liu, J.9
-
35
-
-
0035846070
-
Piperazine-based CCR5 antagonists as HIV-1 inhibitors. II. Discovery of 1-[(2,4-dimethyl-3-pyridinyl)carbonyl]-4-methyl-4-[3(S)-methyl-4-[1(S)- [4-(trifluoromethyl)phenyl]ethyl]-1-piperazinyl]-piperidine N1-oxide (Sch-350634), an orally bioavailable, potent CCR5 antagonist
-
Tagat, J. R., R. W. Steensma, S. W. McCombie, D. V. Nazareno, S. I. Lin, B. R. Neustadt, K. Cox, S. Xu, L. Wojcik, M. G. Murray, N. Vantuno, B. M. Baroudy, and J. M. Strizki. 2001. Piperazine-based CCR5 antagonists as HIV-1 inhibitors. II. Discovery of 1-[(2,4-dimethyl-3-pyridinyl)carbonyl]-4-methyl-4-[3(S)-methyl-4-[1(S)- [4-(trifluoromethyl)phenyl]ethyl]-1-piperazinyl]-piperidine N1-oxide (Sch-350634), an orally bioavailable, potent CCR5 antagonist. J. Med. Chem. 44:3343-3346.
-
(2001)
J. Med. Chem.
, vol.44
, pp. 3343-3346
-
-
Tagat, J.R.1
Steensma, R.W.2
McCombie, S.W.3
Nazareno, D.V.4
Lin, S.I.5
Neustadt, B.R.6
Cox, K.7
Xu, S.8
Wojcik, L.9
Murray, M.G.10
Vantuno, N.11
Baroudy, B.M.12
Strizki, J.M.13
-
36
-
-
0037039380
-
HIV-1 escape from a small molecule, CCR5-specific entry inhibitor does not involve CXCR4 use
-
Trkola, A., S. E. Kuhmann, J. M. Strizki, E. Maxwell, T. Ketas, T. Morgan, P. Pugach, S. Xu, L. Wojcik, J. Tagat, A. Palani, S. Shapiro, J. W. Clader, S. McCombie, G. R. Reyes, B. M. Baroudy, and J. P. Moore. 2002. HIV-1 escape from a small molecule, CCR5-specific entry inhibitor does not involve CXCR4 use. Proc. Natl. Acad. Sci. USA 99:395-400.
-
(2002)
Proc. Natl. Acad. Sci. USA
, vol.99
, pp. 395-400
-
-
Trkola, A.1
Kuhmann, S.E.2
Strizki, J.M.3
Maxwell, E.4
Ketas, T.5
Morgan, T.6
Pugach, P.7
Xu, S.8
Wojcik, L.9
Tagat, J.10
Palani, A.11
Shapiro, S.12
Clader, J.W.13
McCombie, S.14
Reyes, G.R.15
Baroudy, B.M.16
Moore, J.P.17
-
37
-
-
0031963975
-
Genetic subtype-independent inhibition of human immunodeficiency virus type 1 replication by CC and CXC chemokines
-
Trkola, A., W. A. Paxton, S. P. Monard, J. A. Hoxie, M. A. Siani, D. A. Thompson, L. Wu, C. R. Mackay, R. Horuk, and J. P. Moore. 1998. Genetic subtype-independent inhibition of human immunodeficiency virus type 1 replication by CC and CXC chemokines. J. Virol. 72:396-404.
-
(1998)
J. Virol.
, vol.72
, pp. 396-404
-
-
Trkola, A.1
Paxton, W.A.2
Monard, S.P.3
Hoxie, J.A.4
Siani, M.A.5
Thompson, D.A.6
Wu, L.7
Mackay, C.R.8
Horuk, R.9
Moore, J.P.10
-
38
-
-
0030779808
-
Interaction of chemokine receptor CCR5 with its ligands: Multiple domains for HIV-1 gp120 binding and a single domain for chemokine binding
-
Wu, L., G. LaRosa, N. Kassam, C. J. Gordon, H. Heath, N. Ruffing, H. Chen, J. Humblias, M. Samson, M. Parmentier, J. P. Moore, and C. R. Mackay. 1997. Interaction of chemokine receptor CCR5 with its ligands: multiple domains for HIV-1 gp120 binding and a single domain for chemokine binding. J. Exp. Med. 186:1373-1381.
-
(1997)
J. Exp. Med.
, vol.186
, pp. 1373-1381
-
-
Wu, L.1
LaRosa, G.2
Kassam, N.3
Gordon, C.J.4
Heath, H.5
Ruffing, N.6
Chen, H.7
Humblias, J.8
Samson, M.9
Parmentier, M.10
Moore, J.P.11
Mackay, C.R.12
-
39
-
-
0030987288
-
CCR5 levels and expression pattern correlate with infectability by macrophage-tropic HIV-1 in vitro
-
Wu, L., W. Paxton, N. Kassam, N. Ruffing, J. Rottman, N. Sullivan, H. Choe, J. Sodroski, W. Newman, R. Koup, and C. Mackay. 1997. CCR5 levels and expression pattern correlate with infectability by macrophage-tropic HIV-1 in vitro. J. Exp. Med. 185:1681-1691.
-
(1997)
J. Exp. Med.
, vol.185
, pp. 1681-1691
-
-
Wu, L.1
Paxton, W.2
Kassam, N.3
Ruffing, N.4
Rottman, J.5
Sullivan, N.6
Choe, H.7
Sodroski, J.8
Newman, W.9
Koup, R.10
Mackay, C.11
-
40
-
-
0032990719
-
Enhanced inhibition of human immunodeficiency virus type 1 by Met-stromal-derived factor 1β correlates with down-modulation of CXCR4
-
Yang, O. O., S. L. Swanberg, Z. Lu, M. Dziejman, J. McCoy, A. D. Luster, B. D. Walker, and S. H. Herrmann. 1999. Enhanced inhibition of human immunodeficiency virus type 1 by Met-stromal-derived factor 1β correlates with down-modulation of CXCR4. J. Virol. 73:4582-4589.
-
(1999)
J. Virol.
, vol.73
, pp. 4582-4589
-
-
Yang, O.O.1
Swanberg, S.L.2
Lu, Z.3
Dziejman, M.4
McCoy, J.5
Luster, A.D.6
Walker, B.D.7
Herrmann, S.H.8
-
41
-
-
0032543650
-
Synthetic full-length and truncated RANTES inhibit HIV-1 infection of primary macrophages
-
Ylisastigui, L., J. Vizzavona, E. Drakopoulou, P. Paindavoine, C. F. Calvo, M. Parmentier, J. C. Gluckman, C. Vita, and A. Benjouad. 1998. Synthetic full-length and truncated RANTES inhibit HIV-1 infection of primary macrophages. AIDS 12:977-984.
-
(1998)
AIDS
, vol.12
, pp. 977-984
-
-
Ylisastigui, L.1
Vizzavona, J.2
Drakopoulou, E.3
Paindavoine, P.4
Calvo, C.F.5
Parmentier, M.6
Gluckman, J.C.7
Vita, C.8
Benjouad, A.9
-
42
-
-
0033008471
-
Will multiple coreceptors need to be targeted by inhibitors of human immunodeficiency virus type 1 entry?
-
Zhang, Y. J., and J. P. Moore. 1999. Will multiple coreceptors need to be targeted by inhibitors of human immunodeficiency virus type 1 entry? J. Virol. 73:3443-3448.
-
(1999)
J. Virol.
, vol.73
, pp. 3443-3448
-
-
Zhang, Y.J.1
Moore, J.P.2
|