-
1
-
-
53649106470
-
Selective inhibitors of picornavirus replication
-
De Palma, A. M.; Vliegen, I.; De Clercq, E.; Neyts, J. Selective inhibitors of picornavirus replication. Med. Res. Rev. 2008, 28, 823-884.
-
(2008)
Med. Res. Rev
, vol.28
, pp. 823-884
-
-
De Palma, A.M.1
Vliegen, I.2
De Clercq, E.3
Neyts, J.4
-
2
-
-
56649085335
-
Development of antiviral agents for enteroviruses
-
Chen, T. C.; Weng, K. F.; Chang, S. C.; Lin, J. Y.; Huang, P. N.; Shih, S. R. Development of antiviral agents for enteroviruses. J. Antimicrob. Chemother. 2008, 62, 1169-1173.
-
(2008)
J. Antimicrob. Chemother
, vol.62
, pp. 1169-1173
-
-
Chen, T.C.1
Weng, K.F.2
Chang, S.C.3
Lin, J.Y.4
Huang, P.N.5
Shih, S.R.6
-
3
-
-
43649086328
-
CVB infection and mechanisms of viral cardiomyopathy
-
Knowlton, K. U. CVB infection and mechanisms of viral cardiomyopathy. In Group B Coxsackieviruses, 2008; Vol. 323, pp 315-335.
-
(2008)
Group B Coxsackieviruses
, vol.323
, pp. 315-335
-
-
Knowlton, K.U.1
-
4
-
-
0033514987
-
From myocarditis to cardiomyopathy: Mechanisms of inflammation and cell death: Learning from the past for the future
-
Kawai, C. From myocarditis to cardiomyopathy: Mechanisms of inflammation and cell death: Learning from the past for the future. Circulation 1999, 99, 1091-1100.
-
(1999)
Circulation
, vol.99
, pp. 1091-1100
-
-
Kawai, C.1
-
5
-
-
43649102881
-
The CVB and etiology of type 1 diabetes
-
Springer-Verlag: New York
-
Drescher, K. M.; Tracy, S. M. The CVB and etiology of type 1 diabetes. In Group B Coxsackieviruses; Springer-Verlag: New York, 2008; Vol. 323, pp 259-274.
-
(2008)
Group B Coxsackieviruses
, vol.323
, pp. 259-274
-
-
Drescher, K.M.1
Tracy, S.M.2
-
6
-
-
4544240699
-
Coxsackievirus-induced pancreatitis
-
Huber, S.; Ramsingh, A. I. Coxsackievirus-induced pancreatitis. Viral Immunol. 2004, 17, 358-369.
-
(2004)
Viral Immunol
, vol.17
, pp. 358-369
-
-
Huber, S.1
Ramsingh, A.I.2
-
7
-
-
33744990410
-
Current status of anti-picornavirus therapies
-
Barnard, D. L. Current status of anti-picornavirus therapies. Curr. Pharm. Des. 2006, 12, 1379-1390.
-
(2006)
Curr. Pharm. Des
, vol.12
, pp. 1379-1390
-
-
Barnard, D.L.1
-
8
-
-
48149103755
-
3 antagonist binding
-
3 antagonist binding. ChemMedChem 2008, 3, 111-119.
-
(2008)
ChemMedChem
, vol.3
, pp. 111-119
-
-
Priego, E.M.1
Pérez-Pérez, M.J.2
Kuenzel, J.3
de Vries, H.4
Ijzerman, A.P.5
Camarasa, M.J.6
Martín-Santamaría, S.7
-
9
-
-
33748537737
-
5′-O-Tritylinosine and analogues as allosteric inhibitors of human thymidine phosphorylase
-
Casanova, E.; Hernández, A. I.; Priego, E. M.; Liekens, S.; Camarasa, M. J.; Balzarini, J.; Pérez-Pérez, M. J. 5′-O-Tritylinosine and analogues as allosteric inhibitors of human thymidine phosphorylase. J. Med. Chem. 2006, 49, 5562-5570.
-
(2006)
J. Med. Chem
, vol.49
, pp. 5562-5570
-
-
Casanova, E.1
Hernández, A.I.2
Priego, E.M.3
Liekens, S.4
Camarasa, M.J.5
Balzarini, J.6
Pérez-Pérez, M.J.7
-
11
-
-
0027262226
-
Nucleosides. 5. Synthesis of guanine and formycin B derivatives as potential inhibitors of purine nucleoside phosphorylase
-
Chern, J. W.; Lee, H. Y.; Chen, C. S.; Shewach, D. S.; Daddona, P. E.; Townsend, L. B. Nucleosides. 5. Synthesis of guanine and formycin B derivatives as potential inhibitors of purine nucleoside phosphorylase. J. Med. Chem. 1993, 36, 1024-1031.
-
(1993)
J. Med. Chem
, vol.36
, pp. 1024-1031
-
-
Chern, J.W.1
Lee, H.Y.2
Chen, C.S.3
Shewach, D.S.4
Daddona, P.E.5
Townsend, L.B.6
-
12
-
-
0037013427
-
9-[(Hydroxymethyl) phenyl]adenines: New aryladenine substrates of adenosine deaminase
-
Brakta, M.; Murthy, D.; Ellis, L.; Phadtare, S. 9-[(Hydroxymethyl) phenyl]adenines: new aryladenine substrates of adenosine deaminase. Bioorg. Med. Chem. Lett. 2002, 12, 1489-1492.
-
(2002)
Bioorg. Med. Chem. Lett
, vol.12
, pp. 1489-1492
-
-
Brakta, M.1
Murthy, D.2
Ellis, L.3
Phadtare, S.4
-
13
-
-
25444444803
-
Synthesis and properties of nucleic acid analogues consisting of a benzene-phosphate backbone
-
Ueno, Y.; Kato, T.; Sato, K.; Ito, Y.; Yoshida, M.; Inoue, T.; Shibata, A.; Ebihara, M.; Kitade, Y. Synthesis and properties of nucleic acid analogues consisting of a benzene-phosphate backbone. J. Org. Chem. 2005, 70, 7925-7935.
-
(2005)
J. Org. Chem
, vol.70
, pp. 7925-7935
-
-
Ueno, Y.1
Kato, T.2
Sato, K.3
Ito, Y.4
Yoshida, M.5
Inoue, T.6
Shibata, A.7
Ebihara, M.8
Kitade, Y.9
-
14
-
-
0001579456
-
Potential purine antagonists XXI. Preparation of some 9-phenyl-6-substituted purines
-
Greenberg, S. M.; Ross, L. O.; Robins, R. K. Potential purine antagonists XXI. Preparation of some 9-phenyl-6-substituted purines. J. Org. Chem. 1959, 24, 1314-1317.
-
(1959)
J. Org. Chem
, vol.24
, pp. 1314-1317
-
-
Greenberg, S.M.1
Ross, L.O.2
Robins, R.K.3
-
15
-
-
0035842155
-
Expanding the diversity of purine libraries
-
Ding, S.; Gray, N. S.; Ding, Q.; Schultz, P. G. Expanding the diversity of purine libraries. Tetrahedron Lett. 2001, 42, 8751-8755.
-
(2001)
Tetrahedron Lett
, vol.42
, pp. 8751-8755
-
-
Ding, S.1
Gray, N.S.2
Ding, Q.3
Schultz, P.G.4
-
16
-
-
0037436939
-
Regioselective N-9 arylation of purines employing arylboronic acids in the presence of Cu(II)
-
Bakkestuen, A. K.; Gundersen, L. L. Regioselective N-9 arylation of purines employing arylboronic acids in the presence of Cu(II). Tetrahedron Lett. 2003, 44, 3359-3362.
-
(2003)
Tetrahedron Lett
, vol.44
, pp. 3359-3362
-
-
Bakkestuen, A.K.1
Gundersen, L.L.2
-
17
-
-
0032492942
-
-
Chan, D. M. T.; Monaco, K. L.; Wang, R. P.; Winters, M. P. New N- and O-arylations with phenylboronic acids and cupric acetate. Tetrahedron Lett. 1998, 39, 2933-2936.
-
Chan, D. M. T.; Monaco, K. L.; Wang, R. P.; Winters, M. P. New N- and O-arylations with phenylboronic acids and cupric acetate. Tetrahedron Lett. 1998, 39, 2933-2936.
-
-
-
-
18
-
-
0032493017
-
New aryl/heteroaryl C-N bond crosscoupling reactions via arylboronic acid cupric acetate arylation
-
Lam, P. Y. S.; Clark, C. G.; Saubern, S.; Adams, J.; Winters, M. P.; Chan, D. M. T.; Combs, A. New aryl/heteroaryl C-N bond crosscoupling reactions via arylboronic acid cupric acetate arylation. Tetrahedron Lett. 1998, 39, 2941-2944.
-
(1998)
Tetrahedron Lett
, vol.39
, pp. 2941-2944
-
-
Lam, P.Y.S.1
Clark, C.G.2
Saubern, S.3
Adams, J.4
Winters, M.P.5
Chan, D.M.T.6
Combs, A.7
-
19
-
-
0032492980
-
Synthesis of diaryl ethers through the copper-promoted arylation of phenols with arylboronic acids. An expedient synthesis of thyroxine
-
Evans, D. A.; Katz, J. L.; West, T. R. Synthesis of diaryl ethers through the copper-promoted arylation of phenols with arylboronic acids. An expedient synthesis of thyroxine. Tetrahedron Lett. 1998, 39, 2937-2940.
-
(1998)
Tetrahedron Lett
, vol.39
, pp. 2937-2940
-
-
Evans, D.A.1
Katz, J.L.2
West, T.R.3
-
20
-
-
34047220034
-
Microwave-assisted rapid synthesis of 2,6,9-substituted purines
-
Huang, H.; Liu, H.; Chen, K. X.; Jiang, H. L. Microwave-assisted rapid synthesis of 2,6,9-substituted purines. J. Comb. Chem. 2007, 9, 197-199.
-
(2007)
J. Comb. Chem
, vol.9
, pp. 197-199
-
-
Huang, H.1
Liu, H.2
Chen, K.X.3
Jiang, H.L.4
-
21
-
-
67549132235
-
Synthesis and properties of a novel molecular beacon containing a benzene-phosphate backbone at its stem moiety
-
Ueno, Y.; Kawamura, A.; Takasu, K.; Komatsuzaki, S.; Kato, T.; Kuboe, S.; Kitamura, Y.; Kitade, Y. Synthesis and properties of a novel molecular beacon containing a benzene-phosphate backbone at its stem moiety. Org. Biomol. Chem. 2009, 7, 2761-2769.
-
(2009)
Org. Biomol. Chem
, vol.7
, pp. 2761-2769
-
-
Ueno, Y.1
Kawamura, A.2
Takasu, K.3
Komatsuzaki, S.4
Kato, T.5
Kuboe, S.6
Kitamura, Y.7
Kitade, Y.8
-
22
-
-
0345708168
-
Modern synthetic methods for coppermediated C(aryl)-O, C(aryl)-N, and C(aryl)-S bond formation
-
Ley, S. V.; Thomas, A. W. Modern synthetic methods for coppermediated C(aryl)-O, C(aryl)-N, and C(aryl)-S bond formation. Angew. Chem., Int. Ed. 2003, 42, 5400-5449.
-
(2003)
Angew. Chem., Int. Ed
, vol.42
, pp. 5400-5449
-
-
Ley, S.V.1
Thomas, A.W.2
-
23
-
-
0026752346
-
Synthesis and anti-HIV activity of isonucleosides
-
Huryn, D. M.; Sluboski, B. C.; Tam, S. Y.; Weigele, M.; Sim, I.; Anderson, B. D.; Mitsuya, H.; Broder, S. Synthesis and anti-HIV activity of isonucleosides. J. Med. Chem. 1992, 35, 2347-2354.
-
(1992)
J. Med. Chem
, vol.35
, pp. 2347-2354
-
-
Huryn, D.M.1
Sluboski, B.C.2
Tam, S.Y.3
Weigele, M.4
Sim, I.5
Anderson, B.D.6
Mitsuya, H.7
Broder, S.8
-
24
-
-
0025058715
-
Synthesis and antiviral activity of 9-alkoxypurines. 1. 9-(3-Hydroxypropoxy)-purines and 9-[3-hydroxy-2-(hydroxymethyl)propoxy]purines
-
Harnden, M. R.; Wyatt, P. G.; Boyd, M. R.; Sutton, D. Synthesis and antiviral activity of 9-alkoxypurines. 1. 9-(3-Hydroxypropoxy)-purines and 9-[3-hydroxy-2-(hydroxymethyl)propoxy]purines. J. Med. Chem. 1990, 33, 187-196.
-
(1990)
J. Med. Chem
, vol.33
, pp. 187-196
-
-
Harnden, M.R.1
Wyatt, P.G.2
Boyd, M.R.3
Sutton, D.4
-
25
-
-
0036420227
-
Synthesis, kinetics, and molecular docking of novel 9-(2-hydroxypropyl) purine nucleoside analogs as ligands of herpesviral thymidine kinases
-
Pospisil, P.; Pilger, B. D.; Marveggio, S.; Schelling, P.; Wurth, C.; Scapozza, L.; Folkers, G.; Pongracic, M.; Mintas, M.; Malic, S. R. Synthesis, kinetics, and molecular docking of novel 9-(2-hydroxypropyl) purine nucleoside analogs as ligands of herpesviral thymidine kinases. Helv. Chim. Acta 2002, 85, 3237-3250.
-
(2002)
Helv. Chim. Acta
, vol.85
, pp. 3237-3250
-
-
Pospisil, P.1
Pilger, B.D.2
Marveggio, S.3
Schelling, P.4
Wurth, C.5
Scapozza, L.6
Folkers, G.7
Pongracic, M.8
Mintas, M.9
Malic, S.R.10
-
26
-
-
64949164162
-
Microwave-assisted synthesis of 9-arylpurines
-
Aguado,L.;Camarasa,M. J.; Pérez-Pérez, M. J. Microwave-assisted synthesis of 9-arylpurines. J. Comb. Chem. 2009, 11, 210-212.
-
(2009)
J. Comb. Chem
, vol.11
, pp. 210-212
-
-
Aguado, L.1
Camarasa, M.J.2
Pérez-Pérez, M.J.3
-
27
-
-
0037687843
-
Synthesis of fluorinated 1-(3-morpholin-4-yl-phenyl)-ethylamines
-
Wu, Y. J.; He, H.; Sun, L. Q.; Wu, D. D.; Gao, Q.; Li, H. Y. Synthesis of fluorinated 1-(3-morpholin-4-yl-phenyl)-ethylamines. Bioorg. Med. Chem. Lett. 2003, 13, 1725-1728.
-
(2003)
Bioorg. Med. Chem. Lett
, vol.13
, pp. 1725-1728
-
-
Wu, Y.J.1
He, H.2
Sun, L.Q.3
Wu, D.D.4
Gao, Q.5
Li, H.Y.6
-
28
-
-
0001261573
-
Synthesis of alpha-amino ketone hydrochlorides via chemoselective hydrogenation of alphanitro ketones
-
Tamura, R.; Oda, D.; Kurokawa, H. Synthesis of alpha-amino ketone hydrochlorides via chemoselective hydrogenation of alphanitro ketones. Tetrahedron Lett. 1986, 27, 5759-5762.
-
(1986)
Tetrahedron Lett
, vol.27
, pp. 5759-5762
-
-
Tamura, R.1
Oda, D.2
Kurokawa, H.3
-
29
-
-
0029146072
-
Synthesis and anticonvulsant activity of N-benzylpyrrolo[2, 3-d]pyrimidines, N-benzylpyrazolo[3,4-d]pyrimidines, and N-benzyltriazolo[4,5-d]pyrimidine: Imidazole ringmodified analogs of 9-(2-flurobenzyl)-6-(methylamino)-9H-purine
-
Kelley, J. L.; Davis, R. G.; McLean, E. W.; Glen, R. C.; Soroko, F. E.; Cooper, B. R. Synthesis and anticonvulsant activity of N-benzylpyrrolo[2, 3-d]pyrimidines, N-benzylpyrazolo[3,4-d]pyrimidines, and N-benzyltriazolo[4,5-d]pyrimidine: imidazole ringmodified analogs of 9-(2-flurobenzyl)-6-(methylamino)-9H-purine. J. Med. Chem. 1995, 38, 3884-3888.
-
(1995)
J. Med. Chem
, vol.38
, pp. 3884-3888
-
-
Kelley, J.L.1
Davis, R.G.2
McLean, E.W.3
Glen, R.C.4
Soroko, F.E.5
Cooper, B.R.6
-
30
-
-
17144376741
-
Synthesis, biological activity, and SAR of antimycobacterial 9-aryl-, 9-arylsulfonyl-, and 9-benzyl-6-(2-furyl)purines
-
Bakkestuen, A. K.; Gundersen, L. L.; Utenova, B. T. Synthesis, biological activity, and SAR of antimycobacterial 9-aryl-, 9-arylsulfonyl-, and 9-benzyl-6-(2-furyl)purines. J. Med. Chem. 2005, 48, 2710-2723.
-
(2005)
J. Med. Chem
, vol.48
, pp. 2710-2723
-
-
Bakkestuen, A.K.1
Gundersen, L.L.2
Utenova, B.T.3
-
32
-
-
33645393217
-
Synthesis and biological evaluation of novel 9-substituted-8-hydroxyadenine derivatives as potent interferon inducers
-
Isobe, Y.; Kurimoto, A.; Tobe, M.; Hashimoto, K.; Nakamura, T.; Norimura, K.; Ogita, H.; Takaku, H. Synthesis and biological evaluation of novel 9-substituted-8-hydroxyadenine derivatives as potent interferon inducers. J. Med. Chem. 2006, 49, 2088-2095.
-
(2006)
J. Med. Chem
, vol.49
, pp. 2088-2095
-
-
Isobe, Y.1
Kurimoto, A.2
Tobe, M.3
Hashimoto, K.4
Nakamura, T.5
Norimura, K.6
Ogita, H.7
Takaku, H.8
-
33
-
-
63149175990
-
2-Azidoalkoxy-7-hydro-8-oxoadenine derivatives as TLR7 agonists inducing dendritic cell maturation
-
Weterings, J. J.; Khan, S.; van Noort, G. J. V.; Melief, C. J. M.; Overkleeft, H. S.; van der Burg, S. H.; Ossendorp, F.; van der Marel, G. A.; Filippov, D. V. 2-Azidoalkoxy-7-hydro-8-oxoadenine derivatives as TLR7 agonists inducing dendritic cell maturation. Bioorg. Med. Chem. Lett. 2009, 19, 2249-2251.
-
(2009)
Bioorg. Med. Chem. Lett
, vol.19
, pp. 2249-2251
-
-
Weterings, J.J.1
Khan, S.2
van Noort, G.J.V.3
Melief, C.J.M.4
Overkleeft, H.S.5
van der Burg, S.H.6
Ossendorp, F.7
van der Marel, G.A.8
Filippov, D.V.9
-
34
-
-
33845992478
-
Anti-enterovirus activity and structure-activity relationship of a series of 2,6-dihalophenyl-substituted 1H,3H-thiazolo[3,4-a] benzimidazoles
-
De Palma, A. M.; Heggermont, W.; Leyssen, P.; Purstinger, G.; Wimmer, E.; De Clercq, E.; Rao, A.; Monforte, A. M.; Chimirri, A.; Neyts, J. Anti-enterovirus activity and structure-activity relationship of a series of 2,6-dihalophenyl-substituted 1H,3H-thiazolo[3,4-a] benzimidazoles. Biochem. Biophys. Res. Commun. 2007, 353, 628-632.
-
(2007)
Biochem. Biophys. Res. Commun
, vol.353
, pp. 628-632
-
-
De Palma, A.M.1
Heggermont, W.2
Leyssen, P.3
Purstinger, G.4
Wimmer, E.5
De Clercq, E.6
Rao, A.7
Monforte, A.M.8
Chimirri, A.9
Neyts, J.10
-
35
-
-
0029126203
-
Inhibition of the enteroviruses that cause acute hemorrhagic conjunctivitis (Ahc) by benzimidazoles-enviroxime (Ly-122772) and enviradone (Ly-127123)
-
Langford, M. P.; Ball, W. A.; Ganley, J. P. Inhibition of the enteroviruses that cause acute hemorrhagic conjunctivitis (Ahc) by benzimidazoles-enviroxime (Ly-122772) and enviradone (Ly-127123). Antiviral Res. 1995, 27, 355-365.
-
(1995)
Antiviral Res
, vol.27
, pp. 355-365
-
-
Langford, M.P.1
Ball, W.A.2
Ganley, J.P.3
-
37
-
-
43249108208
-
The thiazolobenzimidazole TBZE-029 inhibits enterovirus replication by targeting a short region immediately downstream from motifCin the nonstructural protein 2C
-
De Palma, A. M.; Heggermont, W.; Lanke, K.; Coutard, B.; Bergmann, M.; Monforte, A. M.; Canard, B.; De Clercq, E.; Chimirri, A.; Purstinger, G.; Rohayem, J.; van Kuppeveld, F.; Neyts, J. The thiazolobenzimidazole TBZE-029 inhibits enterovirus replication by targeting a short region immediately downstream from motifCin the nonstructural protein 2C. J. Virol. 2008, 82, 4720-4730.
-
(2008)
J. Virol
, vol.82
, pp. 4720-4730
-
-
De Palma, A.M.1
Heggermont, W.2
Lanke, K.3
Coutard, B.4
Bergmann, M.5
Monforte, A.M.6
Canard, B.7
De Clercq, E.8
Chimirri, A.9
Purstinger, G.10
Rohayem, J.11
van Kuppeveld, F.12
Neyts, J.13
-
38
-
-
66149154626
-
Mutations in the Nonstructural Protein 3A Confer Resistance to the Novel Enterovirus Replication Inhibitor TTP-8307
-
De Palma, A. M.; Thibaut, H. J.; van der Linden, L.; Lanke, K.; Heggermont, W.; Ireland, S.; Andrews, R.; Arimilli, M.; Al-Tel, T. H.; De Clercq, E.; van Kuppeveld, F.; Neyts, J. Mutations in the Nonstructural Protein 3A Confer Resistance to the Novel Enterovirus Replication Inhibitor TTP-8307. Antimicrob. Agents Chemother. 2009, 53, 1850-1857.
-
(2009)
Antimicrob. Agents Chemother
, vol.53
, pp. 1850-1857
-
-
De Palma, A.M.1
Thibaut, H.J.2
van der Linden, L.3
Lanke, K.4
Heggermont, W.5
Ireland, S.6
Andrews, R.7
Arimilli, M.8
Al-Tel, T.H.9
De Clercq, E.10
van Kuppeveld, F.11
Neyts, J.12
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