-
1
-
-
84875732362
-
-
http://www.who.int/malaria/publications/atoz/9789241564106/en/index.html.
-
-
-
-
2
-
-
15044338866
-
The global distribution of clinical episodes of Plasmodium falciparum malaria
-
Snow, R. W.; Guerra, C. A.; Noor, A. M.; Myint, H. Y.; Hay, S. I. The global distribution of clinical episodes of Plasmodium falciparum malaria Nature 2005, 434 (7030) 214-217
-
(2005)
Nature
, vol.434
, Issue.7030
, pp. 214-217
-
-
Snow, R.W.1
Guerra, C.A.2
Noor, A.M.3
Myint, H.Y.4
Hay, S.I.5
-
3
-
-
80053065245
-
The threat of artemesinin-resistant malaria
-
Dondorp, A. M.; Fairhurst, R. M.; Slutsker, L.; Macarthur, J. R.; Breman, J. G.; Guerin, P. J.; Wellems, T. E.; Ringwald, P.; Newman, R. D.; Plowe, C. V. The threat of artemesinin-resistant malaria N. Eng. J. Med. 2011, 365 (12) 1073-1075
-
(2011)
N. Eng. J. Med.
, vol.365
, Issue.12
, pp. 1073-1075
-
-
Dondorp, A.M.1
Fairhurst, R.M.2
Slutsker, L.3
MacArthur, J.R.4
Breman, J.G.5
Guerin, P.J.6
Wellems, T.E.7
Ringwald, P.8
Newman, R.D.9
Plowe, C.V.10
-
4
-
-
0033043155
-
Inhibition of the in vitro growth of Plasmodium falciparum by acyclic nucleoside phosphonates
-
Smeijsters, L. J.; Franssen, F. F.; Naesens, L.; de Vries, E.; Holý, A.; Balzarini, J.; de Clercq, E.; Overdulve, J. P. Inhibition of the in vitro growth of Plasmodium falciparum by acyclic nucleoside phosphonates Int. J. Antimicrob. Agents 1999, 12 (1) 53-61
-
(1999)
Int. J. Antimicrob. Agents
, vol.12
, Issue.1
, pp. 53-61
-
-
Smeijsters, L.J.1
Franssen, F.F.2
Naesens, L.3
De Vries, E.4
Holý, A.5
Balzarini, J.6
De Clercq, E.7
Overdulve, J.P.8
-
5
-
-
67650745021
-
Inhibition of hypoxanthine-guanine phosphoribosyltransferase by acyclic nucleoside phosphonates: A new class of antimalarial therapeutics
-
Keough, D. T.; Hocková, D.; Holý, A.; Naesens, L. M.; Skinner-Adams, T. S.; Jersey, J.; Guddat, L. W. Inhibition of hypoxanthine-guanine phosphoribosyltransferase by acyclic nucleoside phosphonates: a new class of antimalarial therapeutics J. Med. Chem. 2009, 52 (14) 4391-4399
-
(2009)
J. Med. Chem.
, vol.52
, Issue.14
, pp. 4391-4399
-
-
Keough, D.T.1
Hocková, D.2
Holý, A.3
Naesens, L.M.4
Skinner-Adams, T.S.5
Jersey, J.6
Guddat, L.W.7
-
6
-
-
77955624880
-
Inhibitors of the purine salvage pathway: A valuable approach for antiprotozoal chemotherapy?
-
Berg, M.; Van der Veken, P.; Goeminne, A.; Haemers, A.; Augustyns, K. Inhibitors of the purine salvage pathway: a valuable approach for antiprotozoal chemotherapy? Curr. Med. Chem. 2010, 17 (23) 2456-2481
-
(2010)
Curr. Med. Chem.
, vol.17
, Issue.23
, pp. 2456-2481
-
-
Berg, M.1
Van Der Veken, P.2
Goeminne, A.3
Haemers, A.4
Augustyns, K.5
-
7
-
-
80051681004
-
6-Oxopurine phosphoribosyltransferase: A target for the development of antimalarial drugs
-
de Jersey, J.; Holý, A.; Hocková, D.; Naesens, L.; Keough, D. T.; Guddat, L. W. 6-Oxopurine phosphoribosyltransferase: a target for the development of antimalarial drugs Curr. Top. Med Chem. 2011, 11 (16) 2085-2102
-
(2011)
Curr. Top. Med Chem.
, vol.11
, Issue.16
, pp. 2085-2102
-
-
De Jersey, J.1
Holý, A.2
Hocková, D.3
Naesens, L.4
Keough, D.T.5
Guddat, L.W.6
-
8
-
-
84862749642
-
Acyclic immucillin phosphonates: Second-generation inhibitors of Plasmodium falciparum hypoxanthine-guanine-xanthine phosphoribosyltransferase
-
Hazleton, K. Z.; Ho, M. C.; Cassera, M. B.; Clinch, K.; Crump, D. R.; Rosario, I., Jr.; Merino, E. F.; Almo, S. C.; Tyler, P. C.; Schramm, V. L. Acyclic immucillin phosphonates: second-generation inhibitors of Plasmodium falciparum hypoxanthine-guanine-xanthine phosphoribosyltransferase Chem. Biol. 2012, 19 (6) 721-730
-
(2012)
Chem. Biol.
, vol.19
, Issue.6
, pp. 721-730
-
-
Hazleton, K.Z.1
Ho, M.C.2
Cassera, M.B.3
Clinch, K.4
Crump, D.R.5
Rosario Jr., I.6
Merino, E.F.7
Almo, S.C.8
Tyler, P.C.9
Schramm, V.L.10
-
9
-
-
53649104458
-
Comparative genomics of the neglected human malaria parasite Plasmodium vivax
-
Carlton, J. M.; Adams, J. H.; Silva, J. C.; Bidwell, S. L.; Lorenzi, H.; Caler, E.; Crabtree, J.; Angiuoli, S. V.; Merino, E. F.; Amedeo, P.; Cheng, Q.; Coulson, R. M. R.; Crabb, B. S.; del Portillo, H. A.; Essien, K.; Feldblyum, T. V.; Fernandez-Becerra, C.; Gilson, P. R.; Gueye, A. H.; Guo, X.; Kang'a, S.; Kooij, T. W. A.; Korsinczky, M.; Meyer, E. V. S.; Nene, V.; Paulsen, I.; White, O.; Ralph, S. A.; Ren, Q. H.; Sargeant, T. J.; Salzberg, S. L.; Stoeckert, C. J.; Sullivan, S. A.; Yamamoto, M. M.; Hoffman, S. L.; Wortman, J. R.; Gardner, M. J.; Galinski, M. R.; Barnwell, J. W.; Fraser-Liggett, C. M. Comparative genomics of the neglected human malaria parasite Plasmodium vivax Nature 2008, 455 (7214) 757-763
-
(2008)
Nature
, vol.455
, Issue.7214
, pp. 757-763
-
-
Carlton, J.M.1
Adams, J.H.2
Silva, J.C.3
Bidwell, S.L.4
Lorenzi, H.5
Caler, E.6
Crabtree, J.7
Angiuoli, S.V.8
Merino, E.F.9
Amedeo, P.10
Cheng, Q.11
Coulson, R.M.R.12
Crabb, B.S.13
Del Portillo, H.A.14
Essien, K.15
Feldblyum, T.V.16
Fernandez-Becerra, C.17
Gilson, P.R.18
Gueye, A.H.19
Guo, X.20
Kang'A, S.21
Kooij, T.W.A.22
Korsinczky, M.23
Meyer, E.V.S.24
Nene, V.25
Paulsen, I.26
White, O.27
Ralph, S.A.28
Ren, Q.H.29
Sargeant, T.J.30
Salzberg, S.L.31
Stoeckert, C.J.32
Sullivan, S.A.33
Yamamoto, M.M.34
Hoffman, S.L.35
Wortman, J.R.36
Gardner, M.J.37
Galinski, M.R.38
Barnwell, J.W.39
Fraser-Liggett, C.M.40
more..
-
10
-
-
0345138983
-
Phosphonomethoxyalkyl analogs of nucleotides
-
Holý, A. Phosphonomethoxyalkyl analogs of nucleotides Curr. Pharm. Des. 2003, 9 (31) 2567-2592
-
(2003)
Curr. Pharm. Des.
, vol.9
, Issue.31
, pp. 2567-2592
-
-
Holý, A.1
-
11
-
-
27844455955
-
Acyclic nucleoside phosphonates: A key class of antiviral drugs
-
De Clercq, E.; Holý, A. Acyclic nucleoside phosphonates: a key class of antiviral drugs Nat. Rev. Drug Discovery 2005, 4 (11) 928-940
-
(2005)
Nat. Rev. Drug Discovery
, vol.4
, Issue.11
, pp. 928-940
-
-
De Clercq, E.1
Holý, A.2
-
12
-
-
68649085928
-
Synthesis of branched 9-[2-(2-phosphonoethoxy)ethyl]purines as a new class of acyclic nucleoside phosphonates which inhibit Plasmodium falciparum hypoxanthine-guanine-xanthine phosphoribosyltransferase
-
Hocková, D.; Holý, A.; Masojídková, M.; Keough, D. T.; de Jersey, J.; Guddat, L. W. Synthesis of branched 9-[2-(2-phosphonoethoxy)ethyl]purines as a new class of acyclic nucleoside phosphonates which inhibit Plasmodium falciparum hypoxanthine-guanine-xanthine phosphoribosyltransferase Bioorg. Med. Chem. 2009, 17 (17) 6218-6232
-
(2009)
Bioorg. Med. Chem.
, vol.17
, Issue.17
, pp. 6218-6232
-
-
Hocková, D.1
Holý, A.2
Masojídková, M.3
Keough, D.T.4
De Jersey, J.5
Guddat, L.W.6
-
13
-
-
77954761602
-
Plasmodium vivax hypoxanthine-guanine phosphoribosyltransferase: A target for anti-malarial chemotherapy
-
Keough, D. T.; Hocková, D.; Krečmerová, M.; Česnek, M.; Holý, A.; Naesens, L.; Brereton, I. M.; Winzor, D. J.; De Jersey, J.; Guddat, L. W. Plasmodium vivax hypoxanthine-guanine phosphoribosyltransferase: a target for anti-malarial chemotherapy Mol. Biochem. Parasitol. 2010, 173 (2) 165-169
-
(2010)
Mol. Biochem. Parasitol.
, vol.173
, Issue.2
, pp. 165-169
-
-
Keough, D.T.1
Hocková, D.2
Krečmerová, M.3
Česnek, M.4
Holý, A.5
Naesens, L.6
Brereton, I.M.7
Winzor, D.J.8
De Jersey, J.9
Guddat, L.W.10
-
14
-
-
84856233989
-
Synthesis of purine N9-[2-hydroxy-3-O-(phosphonomethoxy)propyl] derivatives and their side-chain modified analogues as potential antimalarial agentss
-
Krečmerová, M.; Dračínský, M.; Hocková, D.; Holý, A.; Keough, D. T.; Guddat, L. W. Synthesis of purine N9-[2-hydroxy-3-O-(phosphonomethoxy)propyl] derivatives and their side-chain modified analogues as potential antimalarial agentss Bioorg. Med. Chem. 2012, 20, 1222-1230
-
(2012)
Bioorg. Med. Chem.
, vol.20
, pp. 1222-1230
-
-
Krečmerová, M.1
Dračínský, M.2
Hocková, D.3
Holý, A.4
Keough, D.T.5
Guddat, L.W.6
-
15
-
-
84855784224
-
Synthesis of 9-phosphonoalkyl and 9-phosphonoalkoxyalkyl purines: Evaluation of their ability to act as inhibitors of Plasmodium falciparum, Plasmodium vivax and human hypoxanthine-guanine-(xanthine) phosphoribosyltransferases
-
Česnek, M.; Hocková, D.; Holý, A.; Dračínský, M.; Baszczyňski, O.; de Jersey, J.; Keough, D. T.; Guddat, L. W. Synthesis of 9-phosphonoalkyl and 9-phosphonoalkoxyalkyl purines: evaluation of their ability to act as inhibitors of Plasmodium falciparum, Plasmodium vivax and human hypoxanthine-guanine- (xanthine) phosphoribosyltransferases Bioorg. Med. Chem. 2012, 20 (2) 1076-1089
-
(2012)
Bioorg. Med. Chem.
, vol.20
, Issue.2
, pp. 1076-1089
-
-
Česnek, M.1
Hocková, D.2
Holý, A.3
Dračí nský, M.4
Baszczyňski, O.5
De Jersey, J.6
Keough, D.T.7
Guddat, L.W.8
-
16
-
-
84863826337
-
Synthesis of novel N-branched acyclic nucleoside phosphonates as potent and selective inhibitors of human, Plasmodium falciparum and Plasmodium vivax 6-oxopurine phosphoribosyltransferases
-
Hocková, D.; Keough, D. T.; Janeba, Z.; Wang, T. H.; de Jersey, J.; Guddat, L. W. Synthesis of novel N-branched acyclic nucleoside phosphonates as potent and selective inhibitors of human, Plasmodium falciparum and Plasmodium vivax 6-oxopurine phosphoribosyltransferases J. Med. Chem. 2012, 55 (13) 6209-6223
-
(2012)
J. Med. Chem.
, vol.55
, Issue.13
, pp. 6209-6223
-
-
Hocková, D.1
Keough, D.T.2
Janeba, Z.3
Wang, T.H.4
De Jersey, J.5
Guddat, L.W.6
-
17
-
-
19444364011
-
Prodrug strategies in the design of nucleoside and nucleotide antiviral therapeutics
-
Mackman, R. L.; Cihlar, T. Prodrug strategies in the design of nucleoside and nucleotide antiviral therapeutics Annu. Rep. Med. Chem. 2004, 39, 305-321
-
(2004)
Annu. Rep. Med. Chem.
, vol.39
, pp. 305-321
-
-
MacKman, R.L.1
Cihlar, T.2
-
18
-
-
43049112098
-
Prodrugs of phosphates and phosphonates
-
Hecker, S. J.; Erion, M. D. Prodrugs of phosphates and phosphonates J. Med. Chem. 2008, 51 (8) 2328-2345
-
(2008)
J. Med. Chem.
, vol.51
, Issue.8
, pp. 2328-2345
-
-
Hecker, S.J.1
Erion, M.D.2
-
19
-
-
34548045528
-
Bifunctional acyclic nucleoside phosphonates: 2. Symmetrical 2-{[bis(phosphono)methoxy]methyl}ethyl derivatives of purines and pyrimidines
-
Vrbková, S.; Dračínský, M.; Holý, A. Bifunctional acyclic nucleoside phosphonates: 2. Symmetrical 2-{[bis(phosphono)methoxy]methyl}ethyl derivatives of purines and pyrimidines Collect. Czech. Chem. Commun. 2007, 72 (7) 965-983
-
(2007)
Collect. Czech. Chem. Commun.
, vol.72
, Issue.7
, pp. 965-983
-
-
Vrbková, S.1
Dračínský, M.2
Holý, A.3
-
20
-
-
33744963162
-
Bifunctional acyclic nucleoside phosphonates. 1. Symmetrical 1,3-bis[(phosphonomethoxy) propan-2-yl] derivatives of purines and pyrimidines
-
Vrbovská, S.; Holý, A.; Pohl, R.; Masojídková , M. Bifunctional acyclic nucleoside phosphonates. 1. Symmetrical 1,3-bis[(phosphonomethoxy) propan-2-yl] derivatives of purines and pyrimidines Collect. Czech. Chem. Commun. 2006, 71 (4) 543-566
-
(2006)
Collect. Czech. Chem. Commun.
, vol.71
, Issue.4
, pp. 543-566
-
-
Vrbovská, S.1
Holý, A.2
Pohl, R.3
Masojídková, M.4
-
21
-
-
0033520243
-
Synthesis and cytostatic activity of nucleosides and acyclic nucleoside analogues derived from 6-(trifluoromethyl)purines
-
Hocková, D.; Hocek, M.; Dvořáková, H.; Votruba, I. Synthesis and cytostatic activity of nucleosides and acyclic nucleoside analogues derived from 6-(trifluoromethyl)purines Tetrahedron 1999, 55 (36) 11109-11118
-
(1999)
Tetrahedron
, vol.55
, Issue.36
, pp. 11109-11118
-
-
Hocková, D.1
Hocek, M.2
Dvořáková, H.3
Votruba, I.4
-
22
-
-
84875693078
-
-
Fujifilm Corporation. Glycerophosphoric acid ester derivative having polyfunctional metal chelate structure. Eur. Patent EP1795208 A1.
-
Fujifilm Corporation. Glycerophosphoric acid ester derivative having polyfunctional metal chelate structure. Eur. Patent EP1795208 A1, 2007.
-
(2007)
-
-
-
23
-
-
84859131422
-
An efficient oxa-Michael addition to diethyl vinylphosphonate under mild reaction conditions
-
Baszczyňski, O.; Jansa, P.; Dračínský, M.; Kaiser, M. M.; Špaček, P.; Janeba, Z. An efficient oxa-Michael addition to diethyl vinylphosphonate under mild reaction conditions RSC Adv. 2012, 2 (4) 1282-1284
-
(2012)
RSC Adv.
, vol.2
, Issue.4
, pp. 1282-1284
-
-
Baszczyňski, O.1
Jansa, P.2
Dračínský, M.3
Kaiser, M.M.4
Špaček, P.5
Janeba, Z.6
-
24
-
-
85077634689
-
The use of diethyl azodicarboxylate and triphenylphosphine in synthesis and transformation of natural products
-
Mitsunobu, O. The use of diethyl azodicarboxylate and triphenylphosphine in synthesis and transformation of natural products Synthesis 1981, 1, 1-28
-
(1981)
Synthesis
, vol.1
, pp. 1-28
-
-
Mitsunobu, O.1
-
26
-
-
33645125227
-
Synthesis of aminopropyl phosphonate nucleosides with purine and pyrimidine bases
-
Zhou, D.; Lagoja, I. M.; Van Aerschot, A.; Herdewijn, P. Synthesis of aminopropyl phosphonate nucleosides with purine and pyrimidine bases Collect. Czech. Chem. Commun. 2006, 71 (1) 15-34
-
(2006)
Collect. Czech. Chem. Commun.
, vol.71
, Issue.1
, pp. 15-34
-
-
Zhou, D.1
Lagoja, I.M.2
Van Aerschot, A.3
Herdewijn, P.4
-
27
-
-
80052929778
-
A novel and efficient one-pot synthesis of symmetrical diamide (bis-amidate) prodrugs of acyclic nucleoside phosphonates and evaluation of their biological activities
-
Jansa, P.; Baszczyňski, O.; Dračínský, M.; Votruba, I.; Zidek, Z.; Bahador, G.; Stepan, G.; Cihlar, T.; Mackman, R.; Holý, A.; Janeba, Z. A novel and efficient one-pot synthesis of symmetrical diamide (bis-amidate) prodrugs of acyclic nucleoside phosphonates and evaluation of their biological activities Eur. J. Med. Chem. 2011, 46 (9) 3748-3754
-
(2011)
Eur. J. Med. Chem.
, vol.46
, Issue.9
, pp. 3748-3754
-
-
Jansa, P.1
Baszczyňski, O.2
Dračínský, M.3
Votruba, I.4
Zidek, Z.5
Bahador, G.6
Stepan, G.7
Cihlar, T.8
MacKman, R.9
Holý, A.10
Janeba, Z.11
-
28
-
-
0033519996
-
The 2.0 Å structure of malarial purine phosphoribosyltransferase in complex with a transition-state analogue inhibitor
-
Shi, W.; Li, C. M.; Tyler, P. C.; Furneaux, R. H.; Cahill, S. M.; Girvin, M. E.; Grubmeyer, C.; Schramm, V. L.; Almo, S. C. The 2.0 Å structure of malarial purine phosphoribosyltransferase in complex with a transition-state analogue inhibitor Biochemistry 1999, 38 (31) 9872-9880
-
(1999)
Biochemistry
, vol.38
, Issue.31
, pp. 9872-9880
-
-
Shi, W.1
Li, C.M.2
Tyler, P.C.3
Furneaux, R.H.4
Cahill, S.M.5
Girvin, M.E.6
Grubmeyer, C.7
Schramm, V.L.8
Almo, S.C.9
-
29
-
-
0028083309
-
The crystal structure of human hypoxanthine-guanine phosphoribosyltransferase with bound GMP
-
Eads, J. C.; Scapin, G.; Xu, Y.; Grubmeyer, C.; Sacchettini, J. C. The crystal structure of human hypoxanthine-guanine phosphoribosyltransferase with bound GMP Cell 1994, 78 (2) 325-334
-
(1994)
Cell
, vol.78
, Issue.2
, pp. 325-334
-
-
Eads, J.C.1
Scapin, G.2
Xu, Y.3
Grubmeyer, C.4
Sacchettini, J.C.5
-
30
-
-
33845509641
-
Lead compounds for antimalarial chemotherapy: Purine base analogs discriminate between human and P. falciparum 6-oxopurine phosphoribosyltransferases
-
Keough, D. T.; Skinner-Adams, T.; Jones, M. K.; Ng, A. L.; Brereton, I. M.; Guddat, L. W.; de Jersey, J. Lead compounds for antimalarial chemotherapy: purine base analogs discriminate between human and P. falciparum 6-oxopurine phosphoribosyltransferases J. Med. Chem. 2006, 49 (25) 7479-7486
-
(2006)
J. Med. Chem.
, vol.49
, Issue.25
, pp. 7479-7486
-
-
Keough, D.T.1
Skinner-Adams, T.2
Jones, M.K.3
Ng, A.L.4
Brereton, I.M.5
Guddat, L.W.6
De Jersey, J.7
-
31
-
-
0032587578
-
The 2.0 Å structure of human hypoxanthine-guanine phosphoribosyltransferase in complex with a transition-state analog inhibitor
-
Shi, W.; Li, C. M.; Tyler, P. C.; Furneaux, R. H.; Grubmeyer, C.; Schramm, V. L.; Almo, S. C. The 2.0 Å structure of human hypoxanthine-guanine phosphoribosyltransferase in complex with a transition-state analog inhibitor Nat. Struct. Biol. 1999, 6 (6) 588-593
-
(1999)
Nat. Struct. Biol.
, vol.6
, Issue.6
, pp. 588-593
-
-
Shi, W.1
Li, C.M.2
Tyler, P.C.3
Furneaux, R.H.4
Grubmeyer, C.5
Schramm, V.L.6
Almo, S.C.7
-
32
-
-
0030935658
-
Kinetic mechanism of human hypoxanthine-guanine phosphoribosyltransferase: Rapid phosphoribosyl transfer chemistry
-
Xu, Y.; Eads, J.; Sacchettini, J. C.; Grubmeyer, C. Kinetic mechanism of human hypoxanthine-guanine phosphoribosyltransferase: rapid phosphoribosyl transfer chemistry Biochemistry 1997, 36 (12) 3700-3712
-
(1997)
Biochemistry
, vol.36
, Issue.12
, pp. 3700-3712
-
-
Xu, Y.1
Eads, J.2
Sacchettini, J.C.3
Grubmeyer, C.4
-
33
-
-
22044439547
-
The crystal structure of free human hypoxanthine-guanine phosphoribosyltransferase reveals extensive conformational plasticity throughout the catalytic cycle
-
Keough, D. T.; Brereton, I. M.; de Jersey, J.; Guddat, L. W. The crystal structure of free human hypoxanthine-guanine phosphoribosyltransferase reveals extensive conformational plasticity throughout the catalytic cycle J. Mol. Biol. 2005, 351 (1) 170-181
-
(2005)
J. Mol. Biol.
, vol.351
, Issue.1
, pp. 170-181
-
-
Keough, D.T.1
Brereton, I.M.2
De Jersey, J.3
Guddat, L.W.4
-
34
-
-
0030950226
-
Crystal structure of Escherichia coli xanthine phosphoribosyltransferase
-
Vos, S.; de Jersey, J.; Martin, J. L. Crystal structure of Escherichia coli xanthine phosphoribosyltransferase Biochemistry 1997, 36 (14) 4125-4134
-
(1997)
Biochemistry
, vol.36
, Issue.14
, pp. 4125-4134
-
-
Vos, S.1
De Jersey, J.2
Martin, J.L.3
-
35
-
-
0036084604
-
Crystal structures of free, IMP-, and GMP-bound Escherichia coli hypoxanthine phosphoribosyltransferase
-
Guddat, L. W.; Vos, S.; Martin, J. L.; Keough, D. T.; de Jersey, J. Crystal structures of free, IMP-, and GMP-bound Escherichia coli hypoxanthine phosphoribosyltransferase Protein Sci. 2002, 11 (7) 1626-1638
-
(2002)
Protein Sci.
, vol.11
, Issue.7
, pp. 1626-1638
-
-
Guddat, L.W.1
Vos, S.2
Martin, J.L.3
Keough, D.T.4
De Jersey, J.5
-
36
-
-
84865796528
-
Synthesis and antiviral activities of hexadecyloxypropyl prodrugs of acyclic nucleoside phosphonates containing guanine or hypoxanthine and a (S)-HPMP or PEE acyclic moiety
-
Tichý, T.; Andrei, G.; Snoeck, R.; Balzarini, J.; Dračínský, M.; Krečmerová, M. Synthesis and antiviral activities of hexadecyloxypropyl prodrugs of acyclic nucleoside phosphonates containing guanine or hypoxanthine and a (S)-HPMP or PEE acyclic moiety Eur. J. Med. Chem. 2012, 55, 307-314
-
(2012)
Eur. J. Med. Chem.
, vol.55
, pp. 307-314
-
-
Tichý, T.1
Andrei, G.2
Snoeck, R.3
Balzarini, J.4
Dračí nský, M.5
Krečmerová, M.6
-
37
-
-
84875691910
-
-
Phosphonates, monophosphonamidates, bisphosphonamidates for the treatment of viral diseases. Patent WO 2005066189 A1.
-
Cheng, X.; He, G.; Lee, W. A.; Wang, J.; Yang, Z.; Rohloff, J. C.; Kim, C. U.; Doerffler, E.; Cook, G. P.; Desai, M. C. Phosphonates, monophosphonamidates, bisphosphonamidates for the treatment of viral diseases. Patent WO 2005066189 A1, 2005.
-
(2005)
-
-
Cheng, X.1
He, G.2
Lee, W.A.3
Wang, J.4
Yang, Z.5
Rohloff, J.C.6
Kim, C.U.7
Doerffler, E.8
Cook, G.P.9
Desai, M.C.10
-
38
-
-
67349157073
-
Alkoxyalkyl prodrugs of acyclic nucleoside phosphonates enhance oral antiviral activity and reduce toxicity: Current state of the art
-
Hostetler, K. Y. Alkoxyalkyl prodrugs of acyclic nucleoside phosphonates enhance oral antiviral activity and reduce toxicity: Current state of the art Antiviral Res. 2009, 82 (2) A84-A98
-
(2009)
Antiviral Res.
, vol.82
, Issue.2
-
-
Hostetler, K.Y.1
-
39
-
-
79955529468
-
Role of cathepsin A and lysosomes in the intracellular activation of novel antipapillomavirus agent GS-9191
-
Birkus, G.; Kutty, N.; Frey, C. R.; Shribata, R.; Chou, T.; Wagner, C.; McDermott, M.; Cihlar, T. Role of cathepsin A and lysosomes in the intracellular activation of novel antipapillomavirus agent GS-9191 Antimicrob. Agents Chemother. 2011, 55 (5) 2166-2173
-
(2011)
Antimicrob. Agents Chemother.
, vol.55
, Issue.5
, pp. 2166-2173
-
-
Birkus, G.1
Kutty, N.2
Frey, C.R.3
Shribata, R.4
Chou, T.5
Wagner, C.6
McDermott, M.7
Cihlar, T.8
-
41
-
-
34447508216
-
Phaser crystallographic software
-
McCoy, A. J.; Grosse-Kunstleve, R. W.; Adams, P. D.; Winn, M. D.; Storoni, L. C.; Read, R. J. Phaser crystallographic software J. Appl. Crystallogr. 2007, 40, 658-674
-
(2007)
J. Appl. Crystallogr.
, vol.40
, pp. 658-674
-
-
McCoy, A.J.1
Grosse-Kunstleve, R.W.2
Adams, P.D.3
Winn, M.D.4
Storoni, L.C.5
Read, R.J.6
-
42
-
-
76449098262
-
PHENIX: A comprehensive Python-based system for macromolecular structure solution
-
Adams, P. D.; Afonine, P. V.; Bunkoczi, G.; Chen, V. B.; Davis, I. W.; Echols, N.; Headd, J. J.; Hung, L. W.; Kapral, G. J.; Grosse-Kunstleve, R. W.; McCoy, A. J.; Moriarty, N. W.; Oeffner, R.; Read, R. J.; Richardson, D. C.; Richardson, J. S.; Terwilliger, T. C.; Zwart, P. H. PHENIX: a comprehensive Python-based system for macromolecular structure solution Acta Crystallogr. D 2010, 66, 213-221
-
(2010)
Acta Crystallogr. D
, vol.66
, pp. 213-221
-
-
Adams, P.D.1
Afonine, P.V.2
Bunkoczi, G.3
Chen, V.B.4
Davis, I.W.5
Echols, N.6
Headd, J.J.7
Hung, L.W.8
Kapral, G.J.9
Grosse-Kunstleve, R.W.10
McCoy, A.J.11
Moriarty, N.W.12
Oeffner, R.13
Read, R.J.14
Richardson, D.C.15
Richardson, J.S.16
Terwilliger, T.C.17
Zwart, P.H.18
-
43
-
-
77949535720
-
Features and development of Coot
-
Emsley, P.; Lohkamp, B.; Scott, W. G.; Cowtan, K. Features and development of Coot Acta Crystallogr. D 2010, 66, 486-501
-
(2010)
Acta Crystallogr. D
, vol.66
, pp. 486-501
-
-
Emsley, P.1
Lohkamp, B.2
Scott, W.G.3
Cowtan, K.4
-
44
-
-
7544226311
-
PRODRG: A tool for high-throughput crystallography of protein-ligand complexes
-
Schuttelkopf, A. W.; van Aalten, D. M. F. PRODRG: a tool for high-throughput crystallography of protein-ligand complexes Acta Crystallogr. D 2004, 60, 1355-1363
-
(2004)
Acta Crystallogr. D
, vol.60
, pp. 1355-1363
-
-
Schuttelkopf, A.W.1
Van Aalten, D.M.F.2
-
45
-
-
0017311840
-
Human malaria parasites in continuous culture
-
Trager, W.; Jensen, J. B. Human malaria parasites in continuous culture Science 1976, 193 (4254) 673-675
-
(1976)
Science
, vol.193
, Issue.4254
, pp. 673-675
-
-
Trager, W.1
Jensen, J.B.2
-
46
-
-
0018704491
-
Synchronization of Plasmodium falciparum erythrocytic stages in culture
-
Lambros, C.; Vanderberg, J. P. Synchronization of Plasmodium falciparum erythrocytic stages in culture J. Parasitol. 1979, 65 (3) 418-420
-
(1979)
J. Parasitol.
, vol.65
, Issue.3
, pp. 418-420
-
-
Lambros, C.1
Vanderberg, J.P.2
-
47
-
-
0018606732
-
Quantitative assessment of anti-malarial activity in vitro by a semiautomated microdilution technique
-
Desjardins, R. E.; Canfield, C. J.; Haynes, J. D.; Chulay, J. D. Quantitative assessment of anti-malarial activity in vitro by a semiautomated microdilution technique Antimicrob. Agents Chemother. 1979, 16 (6) 710-718
-
(1979)
Antimicrob. Agents Chemother.
, vol.16
, Issue.6
, pp. 710-718
-
-
Desjardins, R.E.1
Canfield, C.J.2
Haynes, J.D.3
Chulay, J.D.4
-
48
-
-
0020521697
-
Chromosome changes in 6-TG-resistant mutant strains derived from a karyotypically stable human line, C32
-
Chen, T. R. Chromosome changes in 6-TG-resistant mutant strains derived from a karyotypically stable human line, C32 Cytogenet. Cell Genet. 1983, 35 (3) 181-189
-
(1983)
Cytogenet. Cell Genet.
, vol.35
, Issue.3
, pp. 181-189
-
-
Chen, T.R.1
|