-
1
-
-
77949336151
-
Alzheimers disease facts and figures
-
Alzheimers Association. 194
-
Alzheimers Association. Alzheimers disease facts and figures. Alzheimers Dementia 2010, 6, 158, 194.
-
(2010)
Alzheimers Dementia
, vol.6
, pp. 158
-
-
-
2
-
-
0037135111
-
The amyloid hypothesis of Alzheimers disease: Progress and problems on the road to therapeutics
-
Hardy, J.; Selkoe, D. J. The amyloid hypothesis of Alzheimers disease: progress and problems on the road to therapeutics Science 2002, 297, 353-356
-
(2002)
Science
, vol.297
, pp. 353-356
-
-
Hardy, J.1
Selkoe, D.J.2
-
3
-
-
0033518251
-
Purification and cloning of amyloid precursor protein β-secretase from human brain
-
Sinha, S.; Anderson, J. P.; Barbour, R.; Basi, G. S.; Caccavello, R.; Davis, D.; Doan, M.; Dovey, H. F.; Frigon, N.; Hong, J.; Jacobson-Croak, K.; Jewett, N.; Keim, P.; Knops, J.; Lieberburg, I.; Power, M.; Tan, H.; Tatsuno, G.; Tung, J.; Schenk, D.; Seubert, P.; Suomensaari, S. M.; Wang, S.; Walker, D.; Zhao, J.; McConlogue, L.; John, V. Purification and cloning of amyloid precursor protein β-secretase from human brain Nature 1999, 402, 537-540
-
(1999)
Nature
, vol.402
, pp. 537-540
-
-
Sinha, S.1
Anderson, J.P.2
Barbour, R.3
Basi, G.S.4
Caccavello, R.5
Davis, D.6
Doan, M.7
Dovey, H.F.8
Frigon, N.9
Hong, J.10
Jacobson-Croak, K.11
Jewett, N.12
Keim, P.13
Knops, J.14
Lieberburg, I.15
Power, M.16
Tan, H.17
Tatsuno, G.18
Tung, J.19
Schenk, D.20
Seubert, P.21
Suomensaari, S.M.22
Wang, S.23
Walker, D.24
Zhao, J.25
McConlogue, L.26
John, V.27
more..
-
4
-
-
0033595706
-
β-secretase cleavage of Alzheimers amyloid precursor protein by the transmembrane aspartic protease BACE
-
Vassar, R.; Bennett, B. D.; Babu-Khan, S.; Kahn, S.; Mendiaz, E. A.; Denis, P.; Teplow, D. B.; Ross, S.; Amarante, P.; Loeloff, R.; Luo, Y.; Fisher, S.; Fuller, J.; Edenson, S.; Lile, J.; Jarosinski, M. A.; Biere, A. L.; Curran, E.; Burgess, T.; Louis, J. C.; Collins, F.; Treanor, J.; Rogers, G.; Citron, M. β-secretase cleavage of Alzheimers amyloid precursor protein by the transmembrane aspartic protease BACE Science 1999, 286, 735-741
-
(1999)
Science
, vol.286
, pp. 735-741
-
-
Vassar, R.1
Bennett, B.D.2
Babu-Khan, S.3
Kahn, S.4
Mendiaz, E.A.5
Denis, P.6
Teplow, D.B.7
Ross, S.8
Amarante, P.9
Loeloff, R.10
Luo, Y.11
Fisher, S.12
Fuller, J.13
Edenson, S.14
Lile, J.15
Jarosinski, M.A.16
Biere, A.L.17
Curran, E.18
Burgess, T.19
Louis, J.C.20
Collins, F.21
Treanor, J.22
Rogers, G.23
Citron, M.24
more..
-
5
-
-
70350455062
-
The β-secretase enzyme in health and Alzheimers disease: Regulation, cell biology, function, and therapeutic potential
-
Vassar, R.; Kovacs, D. M.; Yan, R.; Wong, P. C. The β-secretase enzyme in health and Alzheimers disease: regulation, cell biology, function, and therapeutic potential J. Neurosci. 2009, 29, 12787-12794
-
(2009)
J. Neurosci.
, vol.29
, pp. 12787-12794
-
-
Vassar, R.1
Kovacs, D.M.2
Yan, R.3
Wong, P.C.4
-
6
-
-
0035116273
-
Mice deficient in BACE1, the Alzheimers β-secretase, have normal phenotype and abolished β-amyloid generation
-
Luo, Y.; Bolon, B.; Kahn, S.; Bennett, B. D.; Babu-Khan, S.; Denis, P.; Fan, W.; Kha, H.; Zhang, J.; Gong, Y.; Martin, L.; Louis, J.-C.; Yan, Q.; Richards, W. G.; Citron, M.; Vassar, R. Mice deficient in BACE1, the Alzheimers β-secretase, have normal phenotype and abolished β-amyloid generation Nat. Neurosci. 2001, 4, 231-232
-
(2001)
Nat. Neurosci.
, vol.4
, pp. 231-232
-
-
Luo, Y.1
Bolon, B.2
Kahn, S.3
Bennett, B.D.4
Babu-Khan, S.5
Denis, P.6
Fan, W.7
Kha, H.8
Zhang, J.9
Gong, Y.10
Martin, L.11
Louis, J.-C.12
Yan, Q.13
Richards, W.G.14
Citron, M.15
Vassar, R.16
-
7
-
-
17344388652
-
BACE knockout mice are healthy despite lacking the primary β-secretase activity in brain: Implications for Alzheimers disease therapeutics
-
Roberds, S. L.; Anderson, J.; Basi, G.; Bienkowski, M. J.; Branstetter, D. G.; Chen, K. S.; Freedman, S. B.; Frigon, N. L.; Games, D.; Hu, K.; Johnson-Wood, K.; Kappenman, K. E.; Kawabe, T. T.; Kola, I.; Kuehn, R.; Lee, M.; Liu, W.; Motter, R.; Nichols, N. F.; Power, M.; Robertson, D. W.; Schenk, D.; Schoor, M.; Shopp, G. M.; Shuck, M. E.; Sinha, S.; Svensson, K. A.; Tatsuno, G.; Tintrup, H.; Wijsman, J.; Wright, S.; McConlogue, L. BACE knockout mice are healthy despite lacking the primary β-secretase activity in brain: implications for Alzheimers disease therapeutics Hum. Mol. Genet. 2001, 10, 1317-1324
-
(2001)
Hum. Mol. Genet.
, vol.10
, pp. 1317-1324
-
-
Roberds, S.L.1
Anderson, J.2
Basi, G.3
Bienkowski, M.J.4
Branstetter, D.G.5
Chen, K.S.6
Freedman, S.B.7
Frigon, N.L.8
Games, D.9
Hu, K.10
Johnson-Wood, K.11
Kappenman, K.E.12
Kawabe, T.T.13
Kola, I.14
Kuehn, R.15
Lee, M.16
Liu, W.17
Motter, R.18
Nichols, N.F.19
Power, M.20
Robertson, D.W.21
Schenk, D.22
Schoor, M.23
Shopp, G.M.24
Shuck, M.E.25
Sinha, S.26
Svensson, K.A.27
Tatsuno, G.28
Tintrup, H.29
Wijsman, J.30
Wright, S.31
McConlogue, L.32
more..
-
8
-
-
77951776829
-
Alzheimers disease: Strategies for disease modification
-
Citron, M. Alzheimers disease: strategies for disease modification Nat. Rev. Drug Discovery 2010, 9, 387-398
-
(2010)
Nat. Rev. Drug Discovery
, vol.9
, pp. 387-398
-
-
Citron, M.1
-
9
-
-
80052266213
-
The amyloid cascade hypothesis for Alzheimers disease: An appraisal for the development of therapeutics
-
Karran, E.; Mercken, M.; De Strooper, B. The amyloid cascade hypothesis for Alzheimers disease: an appraisal for the development of therapeutics Nat. Rev. Drug Discovery 2011, 10, 698-712
-
(2011)
Nat. Rev. Drug Discovery
, vol.10
, pp. 698-712
-
-
Karran, E.1
Mercken, M.2
De Strooper, B.3
-
10
-
-
84859788625
-
Discovery of cyclic sulfone hydroxyethylamines as potent and selective β-site APP-cleaving enzyme 1 (BACE1) inhibitors: Structure-based design and in vivo reduction of amyloid β-peptides
-
Rueeger, H.; Lueoend, R.; Rogel, O.; Rondeau, J.-M.; Mobitz, H.; Machauer, R.; Jacobson, L.; Staufenbiel, M.; Desrayaud, S.; Neumann, U. Discovery of cyclic sulfone hydroxyethylamines as potent and selective β-site APP-cleaving enzyme 1 (BACE1) inhibitors: structure-based design and in vivo reduction of amyloid β-peptides J. Med. Chem. 2012, 55, 3364-3386
-
(2012)
J. Med. Chem.
, vol.55
, pp. 3364-3386
-
-
Rueeger, H.1
Lueoend, R.2
Rogel, O.3
Rondeau, J.-M.4
Mobitz, H.5
MacHauer, R.6
Jacobson, L.7
Staufenbiel, M.8
Desrayaud, S.9
Neumann, U.10
-
11
-
-
84867516398
-
Design and preparation of a potent series of hydroxyethylamine containing β-secretase inhibitors that demonstrate robust reduction of central β-amyloid
-
in press
-
Weiss, M. M.; Williamson, T.; Babu-Khan, S.; Bartberger, M. D.; Brown, J.; Chen, K.; Cheng, Y.; Citron, M.; Croghan, M. D.; Dineen, T. A.; Esmay, J.; Graceffa, R. F.; Harried, S. S.; Hickman, D.; Hitchcock, S. A.; Horne, D. B.; Huang, H.; Imbeah-Ampiah, R.; Judd, T.; Kaller, M. R.; Kreiman, C. R.; La, D. S.; Li, V.; Lopez, P.; Louie, S.; Monenschein, H.; Nguyen, T. T.; Pennington, L. D.; Rattan, C.; San Miguel, T.; Sickmier, E. A.; Wahl, R. C.; Wen, P. H.; Wood, S.; Xue, Q.; Yang, B. H.; Patel, V. F.; Zhong, W. Design and preparation of a potent series of hydroxyethylamine containing β-secretase inhibitors that demonstrate robust reduction of central β-amyloid. J. Med. Chem. 2012, in press.
-
(2012)
J. Med. Chem.
-
-
Weiss, M.M.1
Williamson, T.2
Babu-Khan, S.3
Bartberger, M.D.4
Brown, J.5
Chen, K.6
Cheng, Y.7
Citron, M.8
Croghan, M.D.9
Dineen, T.A.10
Esmay, J.11
Graceffa, R.F.12
Harried, S.S.13
Hickman, D.14
Hitchcock, S.A.15
Horne, D.B.16
Huang, H.17
Imbeah-Ampiah, R.18
Judd, T.19
Kaller, M.R.20
Kreiman, C.R.21
La, D.S.22
Li, V.23
Lopez, P.24
Louie, S.25
Monenschein, H.26
Nguyen, T.T.27
Pennington, L.D.28
Rattan, C.29
San Miguel, T.30
Sickmier, E.A.31
Wahl, R.C.32
Wen, P.H.33
Wood, S.34
Xue, Q.35
Yang, B.H.36
Patel, V.F.37
Zhong, W.38
more..
-
12
-
-
33750132225
-
Acylguanidines as small-molecule β-secretase inhibitors
-
Cole, D. C.; Manas, E.; S.; Stock, J. R.; Condon, J. S.; Jennings, L. D.; Aulabaugh, A.; Chopra, R.; Cowling, R.; Ellingboe, J. W.; Fan, K. Y.; Harrison, B. L.; Hu, Y.; Jacobsen, S.; Jin, G.; Lin, L.; Lovering, F. E.; Malamas, M. S.; Stahl, J.; Strand, J.; Sukhedo, M. N.; Svenson, K.; Turner, M. J.; Wagner, E.; Wu, J.; Zhou, P.; Bard, J. Acylguanidines as small-molecule β-secretase inhibitors J. Med. Chem. 2006, 49, 6158-6161
-
(2006)
J. Med. Chem.
, vol.49
, pp. 6158-6161
-
-
Cole, D.C.1
Manas, E.2
Stock, J.R.3
Condon, J.S.4
Jennings, L.D.5
Aulabaugh, A.6
Chopra, R.7
Cowling, R.8
Ellingboe, J.W.9
Fan, K.Y.10
Harrison, B.L.11
Hu, Y.12
Jacobsen, S.13
Jin, G.14
Lin, L.15
Lovering, F.E.16
Malamas, M.S.17
Stahl, J.18
Strand, J.19
Sukhedo, M.N.20
Svenson, K.21
Turner, M.J.22
Wagner, E.23
Wu, J.24
Zhou, P.25
Bard, J.26
more..
-
13
-
-
70350050829
-
Aminoimidazoles as potent and selective human β-secretase (BACE1) inhibitors
-
Malamas, M. S.; Erdei, J.; Gunawan, I.; Barnes, K.; Johnson, M.; Hui, Y.; Turner, J.; Hu, Y.; Wagner, E.; Fan, K.; Olland, A.; Bard, J.; Robichaud, A. J. Aminoimidazoles as potent and selective human β-secretase (BACE1) inhibitors J. Med. Chem. 2009, 52, 6314-6323
-
(2009)
J. Med. Chem.
, vol.52
, pp. 6314-6323
-
-
Malamas, M.S.1
Erdei, J.2
Gunawan, I.3
Barnes, K.4
Johnson, M.5
Hui, Y.6
Turner, J.7
Hu, Y.8
Wagner, E.9
Fan, K.10
Olland, A.11
Bard, J.12
Robichaud, A.J.13
-
14
-
-
34548510854
-
2-Amino-3,4-dihydroquinazolines as inhibitors of BACE-1 (β-site APP cleaving enzyme): Use of structure based design to convert a micromolar hit into a nanomolar lead
-
Baxter, E. W.; Conway, K. A.; Kennis, L.; Bischoff, F.; Mercken, M. H.; Winter, H. L.; Reynolds, C. H.; Tounge, B. A.; Luo, C.; Scott, M. K.; Huang, Y.; Braeken, M.; Pieters, S. M.; Berthelot, D. J.; Masure, S.; Bruinzeel, W. D.; Jordan, A. D.; Parker, M. H.; Boyd, R. E.; Qu, J.; Alexander, R. S.; Brenneman, D. E.; Reitz, A. B. 2-Amino-3,4-dihydroquinazolines as inhibitors of BACE-1 (β-site APP cleaving enzyme): use of structure based design to convert a micromolar hit into a nanomolar lead J. Med. Chem. 2007, 50, 4261-4264
-
(2007)
J. Med. Chem.
, vol.50
, pp. 4261-4264
-
-
Baxter, E.W.1
Conway, K.A.2
Kennis, L.3
Bischoff, F.4
Mercken, M.H.5
Winter, H.L.6
Reynolds, C.H.7
Tounge, B.A.8
Luo, C.9
Scott, M.K.10
Huang, Y.11
Braeken, M.12
Pieters, S.M.13
Berthelot, D.J.14
Masure, S.15
Bruinzeel, W.D.16
Jordan, A.D.17
Parker, M.H.18
Boyd, R.E.19
Qu, J.20
Alexander, R.S.21
Brenneman, D.E.22
Reitz, A.B.23
more..
-
15
-
-
77249100811
-
Discovery of cyclic acylguanidines as highly potent and selective β-site amyloid cleaving enzyme (BACE) inhibitors: Part I-inhibitor design and validation
-
Zhu, Z.; Sun, Z.-Y.; Ye, Y.; Voigt, J.; Strickland, C.; Smith, E. M.; Cumming, J.; Wang, L.; Wong, J.; Wang, Y.-S.; Wyss, D. F.; Chen, X.; Kuvelkar, R.; Kennedy, M. E.; Favreau, L.; Parker, E.; McKittrick, B. A.; Stamford, A.; Czarniecki, M.; Greenlee, W.; Hunter, J. C. Discovery of cyclic acylguanidines as highly potent and selective β-site amyloid cleaving enzyme (BACE) inhibitors: part I-inhibitor design and validation J. Med. Chem. 2010, 53, 951-965
-
(2010)
J. Med. Chem.
, vol.53
, pp. 951-965
-
-
Zhu, Z.1
Sun, Z.-Y.2
Ye, Y.3
Voigt, J.4
Strickland, C.5
Smith, E.M.6
Cumming, J.7
Wang, L.8
Wong, J.9
Wang, Y.-S.10
Wyss, D.F.11
Chen, X.12
Kuvelkar, R.13
Kennedy, M.E.14
Favreau, L.15
Parker, E.16
McKittrick, B.A.17
Stamford, A.18
Czarniecki, M.19
Greenlee, W.20
Hunter, J.C.21
more..
-
16
-
-
84867795789
-
-
Patent WO2007058602
-
Berg, S.; Burrows, J.; Chessari, G.; Congreve, M. S.; Hedström, J.; Hellberg, S.; Högdin, K.; Kihlström, J.; Kolmodin, K.; Lindström, J.; Murray, C.; Patel, S. Novel 2-amino-imidazole-4-one compounds and their use in the manufacture of a medicament to be used in the treatment of cognitive impairment, Alzheimers disease, neurodegeneration and dementia. Patent WO2007058602, 2007.
-
(2007)
Novel 2-amino-imidazole-4-one Compounds and Their Use in the Manufacture of A Medicament to Be Used in the Treatment of Cognitive Impairment, Alzheimers Disease, Neurodegeneration and Dementia
-
-
Berg, S.1
Burrows, J.2
Chessari, G.3
Congreve, M.S.4
Hedström, J.5
Hellberg, S.6
Högdin, K.7
Kihlström, J.8
Kolmodin, K.9
Lindström, J.10
Murray, C.11
Patel, S.12
-
17
-
-
33947636525
-
Application of fragment screening by X-ray crystallography to the discovery of aminopyridines as inhibitors of β-secretase
-
Congreve, M.; Aharony, D.; Albert, J.; Callaghan, O.; Campbell, J.; Carr, R. A. E.; Chessari, G.; Cowan, S.; Edwards, P. D.; Frederickson, M.; McMenamin, R.; Murray, C. W.; Patel, S.; Wallis, N. Application of fragment screening by X-ray crystallography to the discovery of aminopyridines as inhibitors of β-secretase J. Med. Chem. 2007, 50, 1124-1132
-
(2007)
J. Med. Chem.
, vol.50
, pp. 1124-1132
-
-
Congreve, M.1
Aharony, D.2
Albert, J.3
Callaghan, O.4
Campbell, J.5
Carr, R.A.E.6
Chessari, G.7
Cowan, S.8
Edwards, P.D.9
Frederickson, M.10
McMenamin, R.11
Murray, C.W.12
Patel, S.13
Wallis, N.14
-
18
-
-
37849043411
-
Application of fragment-based lead generation to the discovery of novel, cyclic amidine β-secretase inhibitors with nanomolar potency, cellular activity, and high ligand efficiency
-
Edwards, P. D.; Albert, J. S.; Sylvester, M.; Aharony, D.; Andisik, D.; Callaghan, O.; Campbell, J. B.; Carr, R. A.; Chessari, G.; Congreve, M.; Frederickson, M.; Folmer, R. H.; Geschwindner, S.; Koether, G.; Kolmodin, K.; Krumrine, J.; Mauger, R. C.; Murray, C. W.; Olsson, L.-L.; Patel, S.; Spear, N.; Tian, G. Application of fragment-based lead generation to the discovery of novel, cyclic amidine β-secretase inhibitors with nanomolar potency, cellular activity, and high ligand efficiency J. Med. Chem. 2007, 50, 5912-5925
-
(2007)
J. Med. Chem.
, vol.50
, pp. 5912-5925
-
-
Edwards, P.D.1
Albert, J.S.2
Sylvester, M.3
Aharony, D.4
Andisik, D.5
Callaghan, O.6
Campbell, J.B.7
Carr, R.A.8
Chessari, G.9
Congreve, M.10
Frederickson, M.11
Folmer, R.H.12
Geschwindner, S.13
Koether, G.14
Kolmodin, K.15
Krumrine, J.16
Mauger, R.C.17
Murray, C.W.18
Olsson, L.-L.19
Patel, S.20
Spear, N.21
Tian, G.22
more..
-
19
-
-
80051860673
-
From fragment screening to in vivo efficacy: Optimization of a series of 2-aminoquinolines as potent inhibitors of β-site amyloid precursor protein cleaving enzyme 1 (BACE1)
-
Cheng, Y.; Judd, T. C.; Bartberger, M. D.; Brown, J.; Chen, K.; Fremeau, R. T.; Hickman, D.; Hitchcock, S. A.; Jordan, B.; Li, V.; Lopez, P.; Louie, S. W.; Luo, Y.; Michelsen, K.; Nixey, T.; Powers, T. S.; Rattan, C.; Sickmier, E. A., St; Jean, D. J., Jr.; Wahl, R. C.; Wen, P. H.; Wood, S. From fragment screening to in vivo efficacy: optimization of a series of 2-aminoquinolines as potent inhibitors of β-site amyloid precursor protein cleaving enzyme 1 (BACE1) J. Med. Chem. 2011, 54, 5836-5857
-
(2011)
J. Med. Chem.
, vol.54
, pp. 5836-5857
-
-
Cheng, Y.1
Judd, T.C.2
Bartberger, M.D.3
Brown, J.4
Chen, K.5
Fremeau, R.T.6
Hickman, D.7
Hitchcock, S.A.8
Jordan, B.9
Li, V.10
Lopez, P.11
Louie, S.W.12
Luo, Y.13
Michelsen, K.14
Nixey, T.15
Powers, T.S.16
Rattan, C.17
St, A.S.E.18
Jean, Jr.D.J.19
Wahl, R.C.20
Wen, P.H.21
Wood, S.22
more..
-
20
-
-
34547566031
-
Discovery of isonicotinamide derived β-secretase inhibitors: In vivo reduction of β-amyloid
-
Stanton, M. G.; Stauffer, S. R.; Gregro, A. R.; Steinbeiser, M.; Nantermet, P.; Sankaranarayanan, S.; Price, E. A.; Wu, G.; Crouthamel, M.-C.; Ellis, J.; Lai, M.-T.; Espeseth, A. S.; Shi, X.-P.; Jin, L.; Colussi, D.; Pietrak, B.; Huang, Q.; Xu, M.; Simon, A. J.; Graham, S. L.; Vacca, J. P.; Selnick, H. Discovery of isonicotinamide derived β-secretase inhibitors: in vivo reduction of β-amyloid J. Med. Chem. 2007, 50, 3431-3433
-
(2007)
J. Med. Chem.
, vol.50
, pp. 3431-3433
-
-
Stanton, M.G.1
Stauffer, S.R.2
Gregro, A.R.3
Steinbeiser, M.4
Nantermet, P.5
Sankaranarayanan, S.6
Price, E.A.7
Wu, G.8
Crouthamel, M.-C.9
Ellis, J.10
Lai, M.-T.11
Espeseth, A.S.12
Shi, X.-P.13
Jin, L.14
Colussi, D.15
Pietrak, B.16
Huang, Q.17
Xu, M.18
Simon, A.J.19
Graham, S.L.20
Vacca, J.P.21
Selnick, H.22
more..
-
21
-
-
59149083352
-
First demonstration of cerebrospinal fluid and plasma Aβ lowering with oral administration of a β-site amyloid precursor protein-cleaving enzyme 1 inhibitor in nonhuman primates
-
Sankaranarayanan, S; Holahan, M. A.; Colussi, D.; Crouthamel, M.-C.; Devanarayan, V.; Ellis, J.; Espeseth, A.; Gates, A. T.; Graham, S. L.; Gregro, A. R.; Hazuda, D.; Hochman, J. H.; Holloway, K.; Jin, L.; Kahana, J.; Lai, M.-T.; Lineberger, J.; McGaughey, G.; Moore, K. P.; Nantermet, P.; Pietrak, B.; Price, E. A.; Rajapakse, H.; Stauffer, S.; Steinbeiser, M. A.; Seabrook, G.; Selnick, H. G.; Shi, X.-P.; Stanton, M. G.; Swestock, J.; Tugusheva, K.; Tyler, K. X.; Vacca, J. P.; Wong, J.; Wu, G.; Xu, M.; Cook, J. J.; Simon, A. J. First demonstration of cerebrospinal fluid and plasma Aβ lowering with oral administration of a β-site amyloid precursor protein-cleaving enzyme 1 inhibitor in nonhuman primates J. Pharmacol. Exp. Ther. 2009, 328, 131-140
-
(2009)
J. Pharmacol. Exp. Ther.
, vol.328
, pp. 131-140
-
-
Sankaranarayanan, S.1
Holahan, M.A.2
Colussi, D.3
Crouthamel, M.-C.4
Devanarayan, V.5
Ellis, J.6
Espeseth, A.7
Gates, A.T.8
Graham, S.L.9
Gregro, A.R.10
Hazuda, D.11
Hochman, J.H.12
Holloway, K.13
Jin, L.14
Kahana, J.15
Lai, M.-T.16
Lineberger, J.17
McGaughey, G.18
Moore, K.P.19
Nantermet, P.20
Pietrak, B.21
Price, E.A.22
Rajapakse, H.23
Stauffer, S.24
Steinbeiser, M.A.25
Seabrook, G.26
Selnick, H.G.27
Shi, X.-P.28
Stanton, M.G.29
Swestock, J.30
Tugusheva, K.31
Tyler, K.X.32
Vacca, J.P.33
Wong, J.34
Wu, G.35
Xu, M.36
Cook, J.J.37
Simon, A.J.38
more..
-
22
-
-
76649097630
-
Rapid P1 SAR of brain penetrant tertiary carbinamine derived BACE inhibitors
-
Zhu, H.; Young, M. B.; Nantermet, P. G.; Graham, S. L.; Colussi, D.; Lai, M.-T.; Pietrak, B.; Price, E. A.; Sankaranarayanan, S.; Shi, X. P.; Tugusheva, K.; Holahan, M. A.; Michener, M. S.; Cook, J. J.; Simon, A.; Hazuda, D. J.; Vacca, J. P.; Rajapakse, H. A. Rapid P1 SAR of brain penetrant tertiary carbinamine derived BACE inhibitors Bioorg. Med. Chem. Lett. 2010, 20, 1779-1782
-
(2010)
Bioorg. Med. Chem. Lett.
, vol.20
, pp. 1779-1782
-
-
Zhu, H.1
Young, M.B.2
Nantermet, P.G.3
Graham, S.L.4
Colussi, D.5
Lai, M.-T.6
Pietrak, B.7
Price, E.A.8
Sankaranarayanan, S.9
Shi, X.P.10
Tugusheva, K.11
Holahan, M.A.12
Michener, M.S.13
Cook, J.J.14
Simon, A.15
Hazuda, D.J.16
Vacca, J.P.17
Rajapakse, H.A.18
-
23
-
-
84862777524
-
Structure based design of iminohydantoin BACE1 inhibitors: Identification of an orally available, centrally active BACE1 inhibitor
-
Cumming, J. N.; Smith, E. M.; Wang, L.; Misiaszek, J.; Durkin, J.; Pan, J.; Iserloh, U.; Wu, Y.; Zhu, Z.; Strickland, C.; Voigt, J.; Chen, X.; Kennedy, M. E.; Kuvelkar, R.; Hyde, L. A.; Cox, K.; Favreau, L.; Czarniecki, M. F.; Greenlee, W. J.; McKittrick, B. A.; Parker, E. M.; Stamford, A. W. Structure based design of iminohydantoin BACE1 inhibitors: identification of an orally available, centrally active BACE1 inhibitor Bioorg. Med. Chem. Lett. 2012, 22, 2444-2449
-
(2012)
Bioorg. Med. Chem. Lett.
, vol.22
, pp. 2444-2449
-
-
Cumming, J.N.1
Smith, E.M.2
Wang, L.3
Misiaszek, J.4
Durkin, J.5
Pan, J.6
Iserloh, U.7
Wu, Y.8
Zhu, Z.9
Strickland, C.10
Voigt, J.11
Chen, X.12
Kennedy, M.E.13
Kuvelkar, R.14
Hyde, L.A.15
Cox, K.16
Favreau, L.17
Czarniecki, M.F.18
Greenlee, W.J.19
McKittrick, B.A.20
Parker, E.M.21
Stamford, A.W.22
more..
-
24
-
-
81255143061
-
Robust central reduction of amyloid-β in humans with an orally available, non-peptidic β-secretase inhibitor
-
May, P. C.; Dean, R. A.; Lowe, S. L.; Martenyi, F.; Sheehan, S. M.; Boggs, L. N.; Monk, S. A.; Mathes, B. M.; Mergott, D. J.; Watson, B. M.; Stout, S. L.; Timm, D. E.; Smith Labell, E.; Gonzales, C. R.; Nakano, M.; Jhee, S. S.; Yen, M.; Ereshefsky, L.; Lindstrom, T. D.; Calligaro, D. O.; Cocke, P. J.; Hall, G. D.; Friedrich, S.; Citron, M.; Audia, J. E. Robust central reduction of amyloid-β in humans with an orally available, non-peptidic β-secretase inhibitor J. Neurosci. 2011, 31, 16507-16516
-
(2011)
J. Neurosci.
, vol.31
, pp. 16507-16516
-
-
May, P.C.1
Dean, R.A.2
Lowe, S.L.3
Martenyi, F.4
Sheehan, S.M.5
Boggs, L.N.6
Monk, S.A.7
Mathes, B.M.8
Mergott, D.J.9
Watson, B.M.10
Stout, S.L.11
Timm, D.E.12
Smith Labell, E.13
Gonzales, C.R.14
Nakano, M.15
Jhee, S.S.16
Yen, M.17
Ereshefsky, L.18
Lindstrom, T.D.19
Calligaro, D.O.20
Cocke, P.J.21
Hall, G.D.22
Friedrich, S.23
Citron, M.24
Audia, J.E.25
more..
-
25
-
-
84857365050
-
Aminoimidazoles as BACE-1 inhibitors: The challenge to achieve in vivo brain efficacy
-
Swahn, B.-M.; Holenz, J.; Kihlström, J.; Kolmodin, K.; Lindström, J.; Plobeck, N.; Rotticci, D.; Sehgelmeble, F.; Sundström, M.; von Berg, S.; Fälting, J.; Georgievska, B.; Gustavsson, S.; Neelissen, J.; Ek, M.; Olsson, L.-L.; Berg, S. Aminoimidazoles as BACE-1 inhibitors: the challenge to achieve in vivo brain efficacy Bioorg. Med. Chem. Lett. 2012, 22, 1854-1859
-
(2012)
Bioorg. Med. Chem. Lett.
, vol.22
, pp. 1854-1859
-
-
Swahn, B.-M.1
Holenz, J.2
Kihlström, J.3
Kolmodin, K.4
Lindström, J.5
Plobeck, N.6
Rotticci, D.7
Sehgelmeble, F.8
Sundström, M.9
Von Berg, S.10
Fälting, J.11
Georgievska, B.12
Gustavsson, S.13
Neelissen, J.14
Ek, M.15
Olsson, L.-L.16
Berg, S.17
-
26
-
-
1442306232
-
Drug-induced prolongation of the QT interval
-
Roden, D. M. Drug-induced prolongation of the QT interval N. Engl. J. Med. 2004, 350, 1013-1022
-
(2004)
N. Engl. J. Med.
, vol.350
, pp. 1013-1022
-
-
Roden, D.M.1
-
27
-
-
50249105403
-
Early clinical development: Evaluation of drug-induced torsades de pointes risk
-
Vik, T.; Pollard, C.; Sager, P. Early clinical development: evaluation of drug-induced torsades de pointes risk Pharmacol Ther. 2008, 119, 210-214
-
(2008)
Pharmacol Ther.
, vol.119
, pp. 210-214
-
-
Vik, T.1
Pollard, C.2
Sager, P.3
-
28
-
-
2042507954
-
Palladium-catalyzed cross-coupling reactions of organoboron compounds
-
Miyaura, N.; Suzuki, A. Palladium-catalyzed cross-coupling reactions of organoboron compounds Chem. Rev. 1995, 95, 2457-2483
-
(1995)
Chem. Rev.
, vol.95
, pp. 2457-2483
-
-
Miyaura, N.1
Suzuki, A.2
-
29
-
-
77249128954
-
Design and synthesis of 5,5′-disubstituted aminohydantoins as potent and selective human β-secretase (BACE1) inhibitors
-
Malamas, M. S.; Erdei, J.; Gunawan, I.; Turner, J.; Hu, Y.; Wagner, E.; Fan, K.; Chopra, R.; Olland, A.; Bard, J.; Jacobsen, S.; Magolda, R. L.; Pangalos, M.; Robichaud, A. J. Design and synthesis of 5,5′-disubstituted aminohydantoins as potent and selective human β-secretase (BACE1) inhibitors J. Med. Chem. 2010, 53, 1146-1158
-
(2010)
J. Med. Chem.
, vol.53
, pp. 1146-1158
-
-
Malamas, M.S.1
Erdei, J.2
Gunawan, I.3
Turner, J.4
Hu, Y.5
Wagner, E.6
Fan, K.7
Chopra, R.8
Olland, A.9
Bard, J.10
Jacobsen, S.11
Magolda, R.L.12
Pangalos, M.13
Robichaud, A.J.14
-
30
-
-
0034613320
-
Structure of the protease domain of memapsin 2 (β-secretase) complexed with inhibitor
-
Hong, L.; Koelsch, G.; Lin, X. L.; Wu, S. L.; Terzyan, S.; Ghosh, A. K.; Zhang, X. C.; Tang, J. Structure of the protease domain of memapsin 2 (β-secretase) complexed with inhibitor Science 2000, 290, 150-153
-
(2000)
Science
, vol.290
, pp. 150-153
-
-
Hong, L.1
Koelsch, G.2
Lin, X.L.3
Wu, S.L.4
Terzyan, S.5
Ghosh, A.K.6
Zhang, X.C.7
Tang, J.8
-
31
-
-
84863398102
-
Balancing hERG affinity and absorption in the discovery of AZD5672, an orally active CCR5 antagonist for the treatment of rheumatoid arthritis
-
Cumming, J. G.; Tucker, H.; Oldfield, J.; Fielding, C.; Highton, A.; Faull, A.; Wild, M.; Brown, D.; Wells, S.; Shaw, J. Balancing hERG affinity and absorption in the discovery of AZD5672, an orally active CCR5 antagonist for the treatment of rheumatoid arthritis Bioorg. Med. Chem. Lett. 2012, 22, 1655-1659
-
(2012)
Bioorg. Med. Chem. Lett.
, vol.22
, pp. 1655-1659
-
-
Cumming, J.G.1
Tucker, H.2
Oldfield, J.3
Fielding, C.4
Highton, A.5
Faull, A.6
Wild, M.7
Brown, D.8
Wells, S.9
Shaw, J.10
-
32
-
-
77957806868
-
Reducing the risk of drug attrition associated with physicochemical properties
-
Leeson, P. D.; Empfield, J. R. Reducing the risk of drug attrition associated with physicochemical properties Annu. Rep. Med. Chem. 2010, 45, 393-407
-
(2010)
Annu. Rep. Med. Chem.
, vol.45
, pp. 393-407
-
-
Leeson, P.D.1
Empfield, J.R.2
-
33
-
-
77749315417
-
Lipophilicity in drug discovery
-
Waring, M. J. Lipophilicity in drug discovery Expert Opin. Drug Discovery 2010, 5, 235-248
-
(2010)
Expert Opin. Drug Discovery
, vol.5
, pp. 235-248
-
-
Waring, M.J.1
-
34
-
-
0032541986
-
Pyrimidinylimidazole inhibitors of CSBP/p38 kinase demonstrating decreased inhibition of hepatic cytochrome P450 enzymes
-
Adams, J. L.; Boehm, J. C.; Kassis, S.; Gorycki, P. D.; Webb, E. F.; Hall, R.; Sorenson, M.; Lee, J. C.; Ayrton, A.; Griswold, D. E.; Gallagher, T. F. Pyrimidinylimidazole inhibitors of CSBP/p38 kinase demonstrating decreased inhibition of hepatic cytochrome P450 enzymes Bioorg. Med. Chem. Lett. 1998, 8, 3111-3116
-
(1998)
Bioorg. Med. Chem. Lett.
, vol.8
, pp. 3111-3116
-
-
Adams, J.L.1
Boehm, J.C.2
Kassis, S.3
Gorycki, P.D.4
Webb, E.F.5
Hall, R.6
Sorenson, M.7
Lee, J.C.8
Ayrton, A.9
Griswold, D.E.10
Gallagher, T.F.11
-
35
-
-
65149086462
-
Discovery of aminoheterocycles as a novel β-secretase inhibitor class: PH dependence on binding activity part 1
-
Stachel, S. J.; Coburn, C. A.; Rush, D.; Jones, K. L. G.; Zhu, H.; Rajapakse, H.; Graham, S. L.; Simon, A.; Holloway, M. K.; Allison, T. J.; Munshi, S. K.; Espeseth, A. S.; Zuck, P.; Colussi, D.; Wolfe, A.; Pietrak, B. L.; Lai, M.-T.; Vacca, J. P. Discovery of aminoheterocycles as a novel β-secretase inhibitor class: pH dependence on binding activity part 1 Bioorg. Med. Chem. Lett. 2009, 19, 2977-2980
-
(2009)
Bioorg. Med. Chem. Lett.
, vol.19
, pp. 2977-2980
-
-
Stachel, S.J.1
Coburn, C.A.2
Rush, D.3
Jones, K.L.G.4
Zhu, H.5
Rajapakse, H.6
Graham, S.L.7
Simon, A.8
Holloway, M.K.9
Allison, T.J.10
Munshi, S.K.11
Espeseth, A.S.12
Zuck, P.13
Colussi, D.14
Wolfe, A.15
Pietrak, B.L.16
Lai, M.-T.17
Vacca, J.P.18
-
36
-
-
77956013896
-
Effect of the protonation state of the titratable residues on the inhibitor affinity to BACE-1
-
Dominguez, J. L.; Christopeit, T.; Villaverde, M. C.; Gossas, T.; Otero, J. M.; Nystrom, S.; Baraznenok, V.; Lindstrom, E.; Danielson, U. H.; Sussman, F. Effect of the protonation state of the titratable residues on the inhibitor affinity to BACE-1 Biochemistry 2010, 49, 7255-7263
-
(2010)
Biochemistry
, vol.49
, pp. 7255-7263
-
-
Dominguez, J.L.1
Christopeit, T.2
Villaverde, M.C.3
Gossas, T.4
Otero, J.M.5
Nystrom, S.6
Baraznenok, V.7
Lindstrom, E.8
Danielson, U.H.9
Sussman, F.10
-
37
-
-
33748129547
-
Optimisation and validation of a medium-throughput electrophysiology- based hERG assay using IonWorks HT
-
Bridgland-Taylor, M. H.; Hargreaves, A. C.; Easter, A.; Orme, A.; Henthorn, D. C.; Ding, M.; Davis, A. M.; Small, B. G.; Heapy, C. G.; Abi-Gerges, N.; Persson, F.; Jacobson, I.; Sullivan, M.; Albertson, N.; Hammond, T. G.; Sullivan, E.; Valentin, J. P.; Pollard, C. E. Optimisation and validation of a medium-throughput electrophysiology-based hERG assay using IonWorks HT J. Pharmacol. Toxicol. Methods 2006, 54, 189-199
-
(2006)
J. Pharmacol. Toxicol. Methods
, vol.54
, pp. 189-199
-
-
Bridgland-Taylor, M.H.1
Hargreaves, A.C.2
Easter, A.3
Orme, A.4
Henthorn, D.C.5
Ding, M.6
Davis, A.M.7
Small, B.G.8
Heapy, C.G.9
Abi-Gerges, N.10
Persson, F.11
Jacobson, I.12
Sullivan, M.13
Albertson, N.14
Hammond, T.G.15
Sullivan, E.16
Valentin, J.P.17
Pollard, C.E.18
-
38
-
-
0041888478
-
IonWorks: A new high-throughput electrophysiology measurement platform
-
Schroeder, K.; Neagle, B.; Trezise, D. J.; Worley, J. IonWorks: a new high-throughput electrophysiology measurement platform J. Biomol. Screening 2003, 8, 50-64
-
(2003)
J. Biomol. Screening
, vol.8
, pp. 50-64
-
-
Schroeder, K.1
Neagle, B.2
Trezise, D.J.3
Worley, J.4
-
39
-
-
11244269638
-
The use of a cocktail of probe substrates for drug-metabolizing enzymes for the assessment of the metabolic capacity of hepatocyte preparations
-
Floby, E.; Briem, S.; Terelius, Y.; Sohlenius-Sternbeck, A.-K. The use of a cocktail of probe substrates for drug-metabolizing enzymes for the assessment of the metabolic capacity of hepatocyte preparations Xenobiotica 2004, 34, 949-959
-
(2004)
Xenobiotica
, vol.34
, pp. 949-959
-
-
Floby, E.1
Briem, S.2
Terelius, Y.3
Sohlenius-Sternbeck, A.-K.4
-
40
-
-
0019226759
-
Phenotypic stability of adult rat hepatocytes in primary monolayer culture
-
Bissell, D. M.; Guzelian, P. S. Phenotypic stability of adult rat hepatocytes in primary monolayer culture Ann. N. Y. Acad. Sci. 1980, 249, 85-98
-
(1980)
Ann. N. Y. Acad. Sci.
, vol.249
, pp. 85-98
-
-
Bissell, D.M.1
Guzelian, P.S.2
-
41
-
-
0345526990
-
High throughput screening of pKa values of pharmaceuticals by pressure-assisted capillary electrophoresis and mass spectrometry
-
Wan, H; Holmén, A; Wang, Y. D.; Lindberg, W; Englund, M; Någård, M; Thompson, R. High throughput screening of pKa values of pharmaceuticals by pressure-assisted capillary electrophoresis and mass spectrometry Rapid Commun. Mass Spectrom. 2003, 1, 2639-2648
-
(2003)
Rapid Commun. Mass Spectrom.
, vol.1
, pp. 2639-2648
-
-
Wan, H.1
Holmén, A.2
Wang, Y.D.3
Lindberg, W.4
Englund, M.5
Någård, M.6
Thompson, R.7
-
42
-
-
0037032612
-
Rapid screening of pKa values of pharmaceuticals by pressure-assisted capillary electrophoresis combined with short-end injection
-
Wan, H; Holmén, A; Någård, M; Lindberg, W. Rapid screening of pKa values of pharmaceuticals by pressure-assisted capillary electrophoresis combined with short-end injection J. Chromatogr., A 2002, 979, 369-377
-
(2002)
J. Chromatogr., A
, vol.979
, pp. 369-377
-
-
Wan, H.1
Holmén, A.2
Någård, M.3
Lindberg, W.4
-
43
-
-
0035913059
-
oct: A tool for lipophilicity determination in drug discovery. 2. Basic and neutral compounds
-
oct: a tool for lipophilicity determination in drug discovery. 2. Basic and neutral compounds J. Med. Chem. 2001, 44, 2490-2497
-
(2001)
J. Med. Chem.
, vol.44
, pp. 2490-2497
-
-
Lombardo, F.1
Shalaeva, M.Y.2
Tupper, K.A.3
Gao, F.4
-
44
-
-
67650763061
-
The pKBHX Database: Toward a better understanding of hydrogen-bond basicity for medicinal chemists
-
Laurence, C.; Brameld, K. A.; Graton, J.; Le Questel, J.-Y.; Renault, E. The pKBHX Database: toward a better understanding of hydrogen-bond basicity for medicinal chemists J. Med. Chem. 2009, 52, 4073-4086
-
(2009)
J. Med. Chem.
, vol.52
, pp. 4073-4086
-
-
Laurence, C.1
Brameld, K.A.2
Graton, J.3
Le Questel, J.-Y.4
Renault, E.5
-
45
-
-
77953631827
-
A medicinal chemists guide to molecular interactions
-
Bissantz, C.; Kuhn, B.; Stahl, M. A medicinal chemists guide to molecular interactions J. Med. Chem. 2010, 53, 5061-5084
-
(2010)
J. Med. Chem.
, vol.53
, pp. 5061-5084
-
-
Bissantz, C.1
Kuhn, B.2
Stahl, M.3
-
46
-
-
77949492453
-
Pyridinyl aminohydantoins as small molecule BACE1 inhibitors
-
Zhou, P.; Li, Y.; Fan, Y.; Wang, Z.; Chopra, R.; Olland, A.; Hu, Y.; Magolda, R. L.; Pangalos, M.; Reinhart, P. H.; Turner, M. J.; Bard, J.; Malamas, M. S.; Robichaud, A. J. Pyridinyl aminohydantoins as small molecule BACE1 inhibitors Bioorg. Med. Chem. Lett. 2010, 20, 2326-2329
-
(2010)
Bioorg. Med. Chem. Lett.
, vol.20
, pp. 2326-2329
-
-
Zhou, P.1
Li, Y.2
Fan, Y.3
Wang, Z.4
Chopra, R.5
Olland, A.6
Hu, Y.7
Magolda, R.L.8
Pangalos, M.9
Reinhart, P.H.10
Turner, M.J.11
Bard, J.12
Malamas, M.S.13
Robichaud, A.J.14
-
47
-
-
77958038910
-
Design and synthesis of aminohydantoins as potent and selective human β-secretase (BACE1) inhibitors with enhanced brain permeability
-
Malamas, M. S.; Robichaud, A.; Erdei, J.; Quagliato, D.; Solvibile, W.; Zhou, P.; Morris, K.; Turner, J.; Wagner, E.; Fan, K.; Olland, A.; Jacobsen, S.; Reinhart, P.; Riddell, D.; Pangalos, M. Design and synthesis of aminohydantoins as potent and selective human β-secretase (BACE1) inhibitors with enhanced brain permeability Bioorg. Med. Chem. Lett. 2010, 20, 6597-6605
-
(2010)
Bioorg. Med. Chem. Lett.
, vol.20
, pp. 6597-6605
-
-
Malamas, M.S.1
Robichaud, A.2
Erdei, J.3
Quagliato, D.4
Solvibile, W.5
Zhou, P.6
Morris, K.7
Turner, J.8
Wagner, E.9
Fan, K.10
Olland, A.11
Jacobsen, S.12
Reinhart, P.13
Riddell, D.14
Pangalos, M.15
-
48
-
-
4644364822
-
Apo and inhibitor complex structures of BACE (β-secretase)
-
Patel, S.; Vuillard, L.; Cleasby, A.; Murray, C. W.; Yon, J. Apo and inhibitor complex structures of BACE (β-secretase) J. Mol. Biol. 2004, 343, 407-416
-
(2004)
J. Mol. Biol.
, vol.343
, pp. 407-416
-
-
Patel, S.1
Vuillard, L.2
Cleasby, A.3
Murray, C.W.4
Yon, J.5
-
49
-
-
0000243829
-
PROCHECK: A program to check the stereochemical quality of protein structures
-
Laskowski, R. A.; MacArthur, M. W.; Moss, D. S.; Thornton, J. M. PROCHECK: a program to check the stereochemical quality of protein structures J. Appl. Crystallogr. 1993, 26, 283-291
-
(1993)
J. Appl. Crystallogr.
, vol.26
, pp. 283-291
-
-
Laskowski, R.A.1
MacArthur, M.W.2
Moss, D.S.3
Thornton, J.M.4
-
50
-
-
82755187127
-
In vivo analysis using a presenilin-1-specific inhibitor. Presenilin-1-containing gamma;-secretase complexes mediate the majority of CNS Aβ production in the mouse
-
Borgegård, T.; Minidis, A.; Juréus, A.; Malmborg, J.; Rosqvist, S.; Gruber, S.; Almqvist, H.; Yan, H.; Bogstedt, A.; Olsson, F.; Dahlström, J.; Ray, C.; Närhi, K.; Malinowsky, D.; Hagström, E.; Jin, S.; Malmberg, A.; Lendahl, U.; Lundkvist, J. In vivo analysis using a presenilin-1-specific inhibitor. Presenilin-1-containing gamma;-secretase complexes mediate the majority of CNS Aβ production in the mouse Alzheimer Dis. Res. J. 2011, 3, 29-45
-
(2011)
Alzheimer Dis. Res. J.
, vol.3
, pp. 29-45
-
-
Borgegård, T.1
Minidis, A.2
Juréus, A.3
Malmborg, J.4
Rosqvist, S.5
Gruber, S.6
Almqvist, H.7
Yan, H.8
Bogstedt, A.9
Olsson, F.10
Dahlström, J.11
Ray, C.12
Närhi, K.13
Malinowsky, D.14
Hagström, E.15
Jin, S.16
Malmberg, A.17
Lendahl, U.18
Lundkvist, J.19
-
51
-
-
34548071206
-
In vitro methods for estimating unbound drug concentrations in the brain interstitial and intracellular fluids
-
Friden, M.; Gupta, A.; Antonsson, M.; Bredberg, U.; Hammarlund-Udenaes, M. In vitro methods for estimating unbound drug concentrations in the brain interstitial and intracellular fluids Drug Metab. Dispos. 2007, 35, 1711
-
(2007)
Drug Metab. Dispos.
, vol.35
, pp. 1711
-
-
Friden, M.1
Gupta, A.2
Antonsson, M.3
Bredberg, U.4
Hammarlund-Udenaes, M.5
-
52
-
-
0003076963
-
Recent changes to the MOSFLM package for processing film and image plate data
-
Leslie, A. G. W. Recent changes to the MOSFLM package for processing film and image plate data. Joint CCP4 + ESF-EAMCB Newsl. Protein Crystallogr. 1992, No. 26.
-
(1992)
Joint CCP4 + ESF-EAMCB Newsl. Protein Crystallogr.
, Issue.26
-
-
Leslie, A.G.W.1
-
53
-
-
0028103275
-
Collaborative Computational Project, number 4. The CCP4 suite: Programs for protein crystallography
-
Collaborative Computational Project, number 4. The CCP4 suite: programs for protein crystallography. Acta Crystallogr., Sect. D: Biol. Crystallogr. 1994, D50, 760-763.
-
(1994)
Acta Crystallogr., Sect. D: Biol. Crystallogr.
, vol.50
, pp. 760-763
-
-
-
54
-
-
79953733151
-
Data processing and analysis with the autoPROC toolbox
-
Vonrhein, C.; Flensburg, C.; Keller, P.; Sharff, A.; Smart, O. S.; Paciorek, W.; Womack, T. O.; Bricogne, G. Data processing and analysis with the autoPROC toolbox Acta Crystallogr., Sect. D: Biol. Crystallogr. 2011, D67, 293-302
-
(2011)
Acta Crystallogr., Sect. D: Biol. Crystallogr.
, vol.67
, pp. 293-302
-
-
Vonrhein, C.1
Flensburg, C.2
Keller, P.3
Sharff, A.4
Smart, O.S.5
Paciorek, W.6
Womack, T.O.7
Bricogne, G.8
-
56
-
-
0030924992
-
Refinement of macromolecular structures by the maximum-likelihood method
-
Murshudov, G. N.; Vagin, A. A.; Dodson, E. J. Refinement of macromolecular structures by the maximum-likelihood method Acta Crystallogr., Sect. D: Biol. Crystallogr. 1997, D53, 240-255
-
(1997)
Acta Crystallogr., Sect. D: Biol. Crystallogr.
, vol.53
, pp. 240-255
-
-
Murshudov, G.N.1
Vagin, A.A.2
Dodson, E.J.3
-
57
-
-
84858642798
-
-
version 2.11.1; Global Phasing Ltd. Cambridge, U.K
-
Bricogne, G.; Blanc, E.; Brandl, M.; Flensburg, C.; Keller, P.; Paciorek, W.; Roversi, P.; Sharff, A.; Smart, O. S.; Vonrhein, C.; Womack, T. O. BUSTER, version 2.11.1; Global Phasing Ltd.: Cambridge, U.K., 2011.
-
(2011)
BUSTER
-
-
Bricogne, G.1
Blanc, E.2
Brandl, M.3
Flensburg, C.4
Keller, P.5
Paciorek, W.6
Roversi, P.7
Sharff, A.8
Smart, O.S.9
Vonrhein, C.10
Womack, T.O.11
-
58
-
-
13244281317
-
Coot: Model-building tools for molecular graphics
-
Emsley, P.; Cowtan, K. Coot: model-building tools for molecular graphics Acta Crystallogr., Sect. D: Biol. Crystallogr. 2004, D60, 2126-2132
-
(2004)
Acta Crystallogr., Sect. D: Biol. Crystallogr.
, vol.60
, pp. 2126-2132
-
-
Emsley, P.1
Cowtan, K.2
|