-
1
-
-
0029986131
-
Molecular cloning and functional expression of a new human CC-chemokine receptor gene
-
Samson, M.; Labbe, O.; Mollereau, C.; Vassart, G.; Parmentier, M. Molecular cloning and functional expression of a new human CC-chemokine receptor gene Biochemistry 1996, 35, 3362-3367
-
(1996)
Biochemistry
, vol.35
, pp. 3362-3367
-
-
Samson, M.1
Labbe, O.2
Mollereau, C.3
Vassart, G.4
Parmentier, M.5
-
2
-
-
0030018156
-
CC CKR5: A RANTES, MIP-1α, MIP-1β receptor as a fusion cofactor for macrophage-tropic HIV-1
-
Alkhatib, G.; Combadiere, C.; Broder, C. C.; Feng, Y.; Kennedy, P. E.; Murphy, P. M.; Berger, E. A. CC CKR5: A RANTES, MIP-1α, MIP-1β receptor as a fusion cofactor for macrophage-tropic HIV-1 Science 1996, 272, 1955-1958
-
(1996)
Science
, vol.272
, pp. 1955-1958
-
-
Alkhatib, G.1
Combadiere, C.2
Broder, C.C.3
Feng, Y.4
Kennedy, P.E.5
Murphy, P.M.6
Berger, E.A.7
-
3
-
-
15844419153
-
Identification of a major co-receptor for primary isolates of HIV-1
-
Deng, H.; Liu, R.; Ellmeier, W.; Choe, S.; Unutmaz, D.; Burkhart, M.; DiMarzio, P.; Marmon, S.; Sutton, R. E.; Hill, C. M.; Littman, D.; Landau, N. R. Identification of a major co-receptor for primary isolates of HIV-1 Nature 1996, 381, 661-666
-
(1996)
Nature
, vol.381
, pp. 661-666
-
-
Deng, H.1
Liu, R.2
Ellmeier, W.3
Choe, S.4
Unutmaz, D.5
Burkhart, M.6
Dimarzio, P.7
Marmon, S.8
Sutton, R.E.9
Hill, C.M.10
Littman, D.11
Landau, N.R.12
-
4
-
-
15844389650
-
+ cells is mediated by the chemokine receptor CC CKR-5
-
+ cells is mediated by the chemokine receptor CC CKR-5 Nature 1996, 381, 667-673
-
(1996)
Nature
, vol.381
, pp. 667-673
-
-
Dragic, T.1
Litwin, V.2
Allaway, G.P.3
Martin, S.R.4
Huang, Y.5
Nagashima, K.A.6
Cayanan, C.7
Maddon, P.J.8
Koup, R.A.9
Moore, J.P.10
Paxton, W.A.11
-
5
-
-
15844388931
-
Homozygous defect in HIV-1 coreceptor accounts for resistance of some multiple-exposed individuals to HIV-1 infection
-
Liu, R.; Paxton, W. A.; Choe, S.; Ceradini, D.; Martin, S. R.; Horuk, R.; Macdonald, M. E.; Stuhlmann, H.; Koup, R. A.; Landau, N. R. Homozygous defect in HIV-1 coreceptor accounts for resistance of some multiple-exposed individuals to HIV-1 infection Cell 1996, 86, 367-377
-
(1996)
Cell
, vol.86
, pp. 367-377
-
-
Liu, R.1
Paxton, W.A.2
Choe, S.3
Ceradini, D.4
Martin, S.R.5
Horuk, R.6
MacDonald, M.E.7
Stuhlmann, H.8
Koup, R.A.9
Landau, N.R.10
-
6
-
-
0031041571
-
The role of viral phenotype and CCR-5 gene defects in HIV-1 transmission and disease progression
-
Michael, N. L.; Chang, G.; Louie, L. G.; Mascola, J. R.; Dondero, D.; Birx, D. L.; Sheppard, H. W. The role of viral phenotype and CCR-5 gene defects in HIV-1 transmission and disease progression Nat. Med. 1997, 3, 338-340
-
(1997)
Nat. Med.
, vol.3
, pp. 338-340
-
-
Michael, N.L.1
Chang, G.2
Louie, L.G.3
Mascola, J.R.4
Dondero, D.5
Birx, D.L.6
Sheppard, H.W.7
-
7
-
-
0034117636
-
Discovery of novel, potent, and selective small-molecule CCR5 antagonists as anti-HIV-1 agents: Synthesis and biological evaluation of anilide derivatives with a quaternary ammonium moiety
-
Shiraishi, M.; Aramaki, Y.; Seto, M.; Imoto, H.; Nishikawa, Y.; Kanzaki, N.; Okamoto, M.; Sawada, H.; Nishimura, O.; Baba, M.; Fujino, M. Discovery of novel, potent, and selective small-molecule CCR5 antagonists as anti-HIV-1 agents: Synthesis and biological evaluation of anilide derivatives with a quaternary ammonium moiety J. Med. Chem. 2000, 43, 2049-2063
-
(2000)
J. Med. Chem.
, vol.43
, pp. 2049-2063
-
-
Shiraishi, M.1
Aramaki, Y.2
Seto, M.3
Imoto, H.4
Nishikawa, Y.5
Kanzaki, N.6
Okamoto, M.7
Sawada, H.8
Nishimura, O.9
Baba, M.10
Fujino, M.11
-
8
-
-
33646755473
-
Discovery and development of small-molecule chemokine coreceptor CCR5 antagonists
-
Palani, A.; Tagat, J. R. Discovery and development of small-molecule chemokine coreceptor CCR5 antagonists J. Med. Chem. 2006, 49, 2851-2867
-
(2006)
J. Med. Chem.
, vol.49
, pp. 2851-2867
-
-
Palani, A.1
Tagat, J.R.2
-
9
-
-
27744548649
-
The discovery of the CCR5 receptor antagonist, UK-427,857, a new agent for the treatment of HIV infection and AIDS
-
Wood, A.; Armour, D. The discovery of the CCR5 receptor antagonist, UK-427,857, a new agent for the treatment of HIV infection and AIDS Prog. Med. Chem. 2005, 43, 239-271
-
(2005)
Prog. Med. Chem.
, vol.43
, pp. 239-271
-
-
Wood, A.1
Armour, D.2
-
10
-
-
27644510382
-
Maraviroc (UK-427,857), a potent, orally bioavailable, and selective small-molecule inhibitor of chemokine receptor CCR5 with broad-spectrum anti-human immunodeficiency virus type-I activity
-
Dorr, P.; Westby, M.; Dobbs, S.; Griffin, P.; Irvine, B.; Macartney, M.; Mori, J.; Rickett, G.; Smith-Burchnell, C.; Napier, C.; Webster, R.; Armour, D.; Price, D.; Stammen, B.; Wood, A.; Perros, M. Maraviroc (UK-427,857), a potent, orally bioavailable, and selective small-molecule inhibitor of chemokine receptor CCR5 with broad-spectrum anti-human immunodeficiency virus type-I activity Antimicrob. Agents Chemother. 2005, 49, 4721-4732
-
(2005)
Antimicrob. Agents Chemother.
, vol.49
, pp. 4721-4732
-
-
Dorr, P.1
Westby, M.2
Dobbs, S.3
Griffin, P.4
Irvine, B.5
MacArtney, M.6
Mori, J.7
Rickett, G.8
Smith-Burchnell, C.9
Napier, C.10
Webster, R.11
Armour, D.12
Price, D.13
Stammen, B.14
Wood, A.15
Perros, M.16
-
11
-
-
36849075379
-
Targeting of Th1-associated chemokine receptors CXCR3 and CCR5 as therapeutic strategy for inflammatory diseases
-
Turner, J. E.; Steinmetz, O. M.; Stahl, R. A.; Panzer, U. Targeting of Th1-associated chemokine receptors CXCR3 and CCR5 as therapeutic strategy for inflammatory diseases Mini-Rev. Med. Chem. 2007, 7, 1089-1096
-
(2007)
Mini-Rev. Med. Chem.
, vol.7
, pp. 1089-1096
-
-
Turner, J.E.1
Steinmetz, O.M.2
Stahl, R.A.3
Panzer, U.4
-
12
-
-
13444303844
-
Inhibition of the development of collagen-induced arthritis in rhesus monkeys by a small molecular weight antagonist of CCR5
-
Vierboom, M. P.; Zavodny, P. J.; Chou, C. C.; Tagat, J. R.; Pugliese-Sivo, C.; Strizki, J.; Steensma, R. W.; McCombie, S. W.; Celebi-Paul, L.; Remarque, E.; Jonker, M.; Narula, S. K.; Hart, B. Inhibition of the development of collagen-induced arthritis in rhesus monkeys by a small molecular weight antagonist of CCR5 Arthritis Rheum. 2005, 52, 627-636
-
(2005)
Arthritis Rheum.
, vol.52
, pp. 627-636
-
-
Vierboom, M.P.1
Zavodny, P.J.2
Chou, C.C.3
Tagat, J.R.4
Pugliese-Sivo, C.5
Strizki, J.6
Steensma, R.W.7
McCombie, S.W.8
Celebi-Paul, L.9
Remarque, E.10
Jonker, M.11
Narula, S.K.12
Hart, B.13
-
13
-
-
2342544143
-
Piperazine-based CCR5 antagonists as HIV-1 inhibitors. IV: Discovery of 1-[(4,6-dimethyl-5-pyrimidinyl)carbonyl]-4-[4-{2-methoxy-1(R) -4-(trifluoromethyl)-phenyl}ethyl-3(S)-methyl-1-piperazinyl]-4-methylpiperidine (Sch-417690/Sch-D), a potent, highly selective and orally bioavailable CCR5 antagonist
-
Tagat, J. R.; McCombie, S. W.; Nazareno, D.; Labroli, M. A.; Xiao, Y.; Steensma, R. W.; Strizki, J. M.; Baroudy, B. M.; Cox, K.; Lachowicz, J.; Varty, G.; Watkins, R. Piperazine-based CCR5 antagonists as HIV-1 inhibitors. IV: Discovery of 1-[(4,6-dimethyl-5-pyrimidinyl)carbonyl]-4-[4-{2-methoxy-1(R)-4- (trifluoromethyl)-phenyl}ethyl-3(S)-methyl-1-piperazinyl]-4-methylpiperidine (Sch-417690/Sch-D), a potent, highly selective and orally bioavailable CCR5 antagonist J. Med. Chem. 2004, 47, 2405-2408
-
(2004)
J. Med. Chem.
, vol.47
, pp. 2405-2408
-
-
Tagat, J.R.1
McCombie, S.W.2
Nazareno, D.3
Labroli, M.A.4
Xiao, Y.5
Steensma, R.W.6
Strizki, J.M.7
Baroudy, B.M.8
Cox, K.9
Lachowicz, J.10
Varty, G.11
Watkins, R.12
-
14
-
-
28944454412
-
Discovery and characterization of Vicriviroc (Sch-417690), a CCR5 antagonist with potent activity against human immunodeficiency virus type-1
-
Strizki, J. M.; Tremblay, C.; Xu, S.; Wojcki, L.; Wagner, N.; Gonsiorek, W.; Hipkin, W.; Chou, C.-C.; Pugliesie-Sivo, C.; Xiao, Y.; Tagat, J. R.; Cox, K.; Priestley, T.; Sorota, S.; Huang, W.; Hirsch, M.; Reyes, G. R.; Baroudy, B. M. Discovery and characterization of Vicriviroc (Sch-417690), a CCR5 antagonist with potent activity against human immunodeficiency virus type-1 Antimicrob. Agents Chemother. 2005, 49, 4911-4919
-
(2005)
Antimicrob. Agents Chemother.
, vol.49
, pp. 4911-4919
-
-
Strizki, J.M.1
Tremblay, C.2
Xu, S.3
Wojcki, L.4
Wagner, N.5
Gonsiorek, W.6
Hipkin, W.7
Chou, C.-C.8
Pugliesie-Sivo, C.9
Xiao, Y.10
Tagat, J.R.11
Cox, K.12
Priestley, T.13
Sorota, S.14
Huang, W.15
Hirsch, M.16
Reyes, G.R.17
Baroudy, B.M.18
-
15
-
-
84989536113
-
Highly enantioselective epoxidation catalysts derived from 1,2-diaminocyclohexane
-
Jacobsen, E. N.; Zhang, W.; Muci, A. R.; Ecker, J. R.; Deng, L. Highly enantioselective epoxidation catalysts derived from 1,2-diaminocyclohexane J. Am. Chem. Soc. 1991, 113, 7063-7064
-
(1991)
J. Am. Chem. Soc.
, vol.113
, pp. 7063-7064
-
-
Jacobsen, E.N.1
Zhang, W.2
Muci, A.R.3
Ecker, J.R.4
Deng, L.5
-
16
-
-
34250006524
-
Antiviral activity, pharmacokinetics and safety of vicriviroc, an oral CCR5 antagonist, during 14-day monotherapy in HIV-infected adults
-
Schürmann, D.; Fätkenheuer, G.; Reynes, J.; Michelet, C.; Raffi, F.; van Lier, J.; Caceres, M.; Keung, A.; Sansone-Parsons, A.; Dunkle, L. M.; Hoffmann, C. Antiviral activity, pharmacokinetics and safety of vicriviroc, an oral CCR5 antagonist, during 14-day monotherapy in HIV-infected adults AIDS 2007, 21, 1293-1299
-
(2007)
AIDS
, vol.21
, pp. 1293-1299
-
-
Schürmann, D.1
Fätkenheuer, G.2
Reynes, J.3
Michelet, C.4
Raffi, F.5
Van Lier, J.6
Caceres, M.7
Keung, A.8
Sansone-Parsons, A.9
Dunkle, L.M.10
Hoffmann, C.11
|