-
1
-
-
33750603844
-
Alzheimer's centennial legacy: Prospects for rational therapeutic intervention targeting the Aβ amyloid pathway
-
Masters CL, Beyreuther K. Alzheimer's centennial legacy: Prospects for rational therapeutic intervention targeting the Aβ amyloid pathway. Brain 2006; 129: 2823-39.
-
(2006)
Brain
, vol.129
, pp. 2823-2839
-
-
Masters, C.L.1
Beyreuther, K.2
-
2
-
-
13944276825
-
Twenty years of the Alzheimer's disease amyloid hypothesis: A genetic perspective
-
Tanzi R, Bertram L. Twenty years of the Alzheimer's disease amyloid hypothesis: A genetic perspective. Cell 2005; 120: 545-55.
-
(2005)
Cell
, vol.120
, pp. 545-555
-
-
Tanzi, R.1
Bertram, L.2
-
3
-
-
67649641916
-
Alternative Aβ immunotherapy approaches for Alzheimer's disease
-
Town T. Alternative Aβ immunotherapy approaches for Alzheimer's disease. CNS Neurol Disord Drug Targets 2009; 8: 114-27.
-
(2009)
CNS Neurol Disord Drug Targets
, vol.8
, pp. 114-127
-
-
Town, T.1
-
4
-
-
48949098573
-
Safety, efficacy, and biomarker findings of PBT2 in targeting Aβ as a modifying therapy for Alzheimer's disease: A phase IIa, double-blind, randomised, placebo-controlled trial
-
Lannfelt L, Blennow K, Zetterberg H, Batsman S, Ames D, Harrison J, et al. Safety, efficacy, and biomarker findings of PBT2 in targeting Aβ as a modifying therapy for Alzheimer's disease: A phase IIa, double-blind, randomised, placebo-controlled trial. Lancet Neurol 2008; 7: 779-86.
-
(2008)
Lancet Neurol
, vol.7
, pp. 779-786
-
-
Lannfelt, L.1
Blennow, K.2
Zetterberg, H.3
Batsman, S.4
Ames, D.5
Harrison, J.6
-
5
-
-
77957038341
-
3-Hydroxy-3-methylglutaryl-coenzyme A reductase inhibitors in the treatment of central nervous system diseases
-
Willey J, Elkind, MS. 3-Hydroxy-3-methylglutaryl-coenzyme A reductase inhibitors in the treatment of central nervous system diseases. Arch Neurol 2010; 67: 1062-7.
-
(2010)
Arch Neurol
, vol.67
, pp. 1062-1067
-
-
Willey, J.1
Elkind, M.S.2
-
6
-
-
78049374467
-
Novel research horizons for presenilins and γ-secretases in cell biology and disease
-
De Strooper B, Annaert W. Novel research horizons for presenilins and γ-secretases in cell biology and disease. Annu Rev Cell Dev Biol 2010: 235-60.
-
(2010)
Annu Rev Cell Dev Biol
, pp. 235-260
-
-
de Strooper, B.1
Annaert, W.2
-
7
-
-
76849086405
-
The secretases: Enzymes with therapeutic potential in Alzheimer disease
-
De Strooper B, Vassar R, Golde T. The secretases: Enzymes with therapeutic potential in Alzheimer disease. Nat Rev Neurol 2010; 6: 99-107.
-
(2010)
Nat Rev Neurol
, vol.6
, pp. 99-107
-
-
de Strooper, B.1
Vassar, R.2
Golde, T.3
-
8
-
-
0035997231
-
Biogenesis and metabolism of Alzheimer's disease Aβ amyloid peptides
-
Evin G, Weidemann A. Biogenesis and metabolism of Alzheimer's disease Aβ amyloid peptides. Peptides 2002; 23: 1285-97.
-
(2002)
Peptides
, vol.23
, pp. 1285-1297
-
-
Evin, G.1
Weidemann, A.2
-
9
-
-
79954458099
-
EHT0202 in Alzheimer's disease: A 3-month, randomized, placebo-controlled, double-blind study
-
Jan 11. [Epub ahead of print]; PMID: 21222604 [
-
Vellas B, Sol O, Snyder PJ, Ousset PJ, Haddad R, Maurin M, et al. EHT0202 in Alzheimer's Disease: A 3-Month, Randomized, Placebo-Controlled, Double-Blind Study. Curr Alzheimer Res 2011: Jan 11. [Epub ahead of print]; PMID: 21222604 [
-
(2011)
Curr Alzheimer Res
-
-
Vellas, B.1
Sol, O.2
Snyder, P.J.3
Ousset, P.J.4
Haddad, R.5
Maurin, M.6
-
11
-
-
55849121517
-
γ -Secretase modulators: Hopes and setbacks for the future of Alzheimer's treatment
-
Evin G. γ -Secretase modulators: hopes and setbacks for the future of Alzheimer's treatment. Expert Rev Neurother 2008; 8: 1611-3.
-
(2008)
Expert Rev Neurother
, vol.8
, pp. 1611-1613
-
-
Evin, G.1
-
12
-
-
0035116273
-
Mice deficient in BACE1, the Alzheimer's β-secretase, have normal phenotype and abolished β -amyloid generation
-
Luo Y, Bolon B, Kahn S, Bennett B, Babu-Khan S, Denis P, et al. Mice deficient in BACE1, the Alzheimer's β-secretase, have normal phenotype and abolished β -amyloid generation. Nat Neurosci 2001; 4: 231-2.
-
(2001)
Nat Neurosci
, vol.4
, pp. 231-232
-
-
Luo, Y.1
Bolon, B.2
Kahn, S.3
Bennett, B.4
Babu-Khan, S.5
Denis, P.6
-
13
-
-
24744449320
-
Phenotypic and biochemical analyses of BACE1- and BACE2-deficient mice
-
Dominguez D, Tournoy J, Hartmann D, Huth T, Cryns K, Deforce S, et al. Phenotypic and biochemical analyses of BACE1- and BACE2-deficient mice. J Biol Chem 2005; 280: 30797-806.
-
(2005)
J Biol Chem
, vol.280
, pp. 30797-30806
-
-
Dominguez, D.1
Tournoy, J.2
Hartmann, D.3
Huth, T.4
Cryns, K.5
Deforce, S.6
-
14
-
-
77955792343
-
BACE1-/- mice exhibit seizure activity that does not correlate with sodium channel level or axonal localization
-
Hitt B, Jaramillo T, Chetkovich D, Vassar R. BACE1-/- mice exhibit seizure activity that does not correlate with sodium channel level or axonal localization. Mol Neurodegener 2010; 5: 31.
-
(2010)
Mol Neurodegener
, vol.5
, pp. 31
-
-
Hitt, B.1
Jaramillo, T.2
Chetkovich, D.3
Vassar, R.4
-
15
-
-
77954394162
-
BACE1 deficiency causes altered neuronal activity and neurodegeneration
-
Hu X, Zhou X, He W, Yang J, Xiong W, Wong P, et al. BACE1 deficiency causes altered neuronal activity and neurodegeneration. J Neurosci 2010; 30: 8819-29.
-
(2010)
J Neurosci
, vol.30
, pp. 8819-8829
-
-
Hu, X.1
Zhou, X.2
He, W.3
Yang, J.4
Xiong, W.5
Wong, P.6
-
16
-
-
78149286187
-
BACE: Therapeutic target and potential biomarker for Alzheimer's disease
-
Evin G, Barakat A, Masters CL. BACE: Therapeutic target and potential biomarker for Alzheimer's disease. Int J Biochem Cell Biol 2010; 42: 1923-6.
-
(2010)
Int J Biochem Cell Biol
, vol.42
, pp. 1923-1926
-
-
Evin, G.1
Barakat, A.2
Masters, C.L.3
-
17
-
-
77953922271
-
Lentivirus-Expressed siRNA Vectors Against Alzheimer Disease
-
Peng KA, Masliah E. Lentivirus-Expressed siRNA Vectors Against Alzheimer Disease. Methods in Molecular Biology 2010; 614: 215-24.
-
(2010)
Methods in Molecular Biology
, vol.614
, pp. 215-224
-
-
Peng, K.A.1
Masliah, E.2
-
18
-
-
27744588007
-
Targeting BACE1 with siRNAs ameliorates Alzheimer disease neuropathology in a transgenic model
-
Singer O, Marr R, Rockenstein E, Crews L, Coufal N, Gage F, et al. Targeting BACE1 with siRNAs ameliorates Alzheimer disease neuropathology in a transgenic model. Nat Neurosci 2005; 8: 1343-9.
-
(2005)
Nat Neurosci
, vol.8
, pp. 1343-1349
-
-
Singer, O.1
Marr, R.2
Rockenstein, E.3
Crews, L.4
Coufal, N.5
Gage, F.6
-
19
-
-
77955863408
-
A noncompetitive BACE1 inhibitor TAK-070 ameliorates Aβ pathology and behavioral deficits in a mouse model of Alzheimer's disease
-
Fukumoto H, Takahashi H, Tarui N, Matsui J, Tomita T, Hirode M, et al. A noncompetitive BACE1 inhibitor TAK-070 ameliorates Aβ pathology and behavioral deficits in a mouse model of Alzheimer's disease. J Neurosci 2010; 30: 11157-66.
-
(2010)
J Neurosci
, vol.30
, pp. 11157-11166
-
-
Fukumoto, H.1
Takahashi, H.2
Tarui, N.3
Matsui, J.4
Tomita, T.5
Hirode, M.6
-
20
-
-
33846261909
-
Oral administration of a potent and selective non-peptidic BACE-1 inhibitor decreases β -cleavage of amyloid precursor protein and amyloid- β production in vivo
-
Hussain I, Hawkins J, Harrison D, Hille C, Wayne G, Cutler L, et al. Oral administration of a potent and selective non-peptidic BACE-1 inhibitor decreases β -cleavage of amyloid precursor protein and amyloid- β production in vivo. J Neurochem 2007; 100: 802-9.
-
(2007)
J Neurochem
, vol.100
, pp. 802-809
-
-
Hussain, I.1
Hawkins, J.2
Harrison, D.3
Hille, C.4
Wayne, G.5
Cutler, L.6
-
21
-
-
40849083795
-
In vivo β -secretase 1 inhibition leads to brain Aβ lowering and increased β -secretase processing of Amyloid Precursor Protein without effect on Neuregulin-1
-
Sankaranarayanan S, Price EA, Wu G, Crouthamel M-C, Shi X-P, Tugusheva K, et al. In vivo β -secretase 1 inhibition leads to brain Aβ lowering and increased β -secretase processing of Amyloid Precursor Protein without effect on Neuregulin-1. J Pharmacol Exp Ther 2008; 324: 957-69.
-
(2008)
J Pharmacol Exp Ther
, vol.324
, pp. 957-969
-
-
Sankaranarayanan, S.1
Price, E.A.2
Wu, G.3
Crouthamel, M.-C.4
Shi, X.-P.5
Tugusheva, K.6
-
22
-
-
34249088593
-
-
Ghosh AK, Kumaragurubaran N, Hong L, Kulkarni SS, Xu X, Chang W, et al. J Med Chem 2007; 50:2399-407.
-
(2007)
J Med Chem
, vol.50
, pp. 2399-2407
-
-
Ghosh, A.K.1
Kumaragurubaran, N.2
Hong, L.3
Kulkarni, S.S.4
Xu, X.5
Chang, W.6
-
24
-
-
0034613320
-
Structure of the protease domain of memapsin 2 (β -secretase) complexed with inhibitor
-
Hong L, Koelsch G, Lin X, Wu S, Terzyan S, Ghosh A, et al. Structure of the protease domain of memapsin 2 (β -secretase) complexed with inhibitor. Sci 2000; 290: 150-3.
-
(2000)
Sci
, vol.290
, pp. 150-153
-
-
Hong, L.1
Koelsch, G.2
Lin, X.3
Wu, S.4
Terzyan, S.5
Ghosh, A.6
-
25
-
-
38749146862
-
Potent memapsin 2 (β -secretase) inhibitors: Design, synthesis, protein-ligand X-ray structure, and in vivo evaluation
-
Ghosh AK, Kumaragurubaran N, Hong L, Kulkarni S, Xu X, Miller HB, et al. Potent memapsin 2 (β -secretase) inhibitors: Design, synthesis, protein-ligand X-ray structure, and in vivo evaluation. Bioorg Med Chem Lett 2008; 18: 1031-6.
-
(2008)
Bioorg Med Chem Lett
, vol.18
, pp. 1031-1036
-
-
Ghosh, A.K.1
Kumaragurubaran, N.2
Hong, L.3
Kulkarni, S.4
Xu, X.5
Miller, H.B.6
-
26
-
-
79959369108
-
-
US7504420
-
Ghosh, A.K., Kumaragurubaran, N., Liu, C., Devasamudram, T., Lei, H., Swanson, L,M., Ankala, S.V., Tang, J.J.N., Bilcer, G.M. Compounds which inhibit β -secretase activity and methods of use. US7504420 (2009).
-
(2009)
Compounds Which Inhibit β -secretase Activity and Methods of Use
-
-
Ghosh, A.K.1
Kumaragurubaran, N.2
Liu, C.3
Devasamudram, T.4
Lei, H.5
Swanson, L.M.6
Ankala, S.V.7
Tang, J.J.N.8
Bilcer, G.M.9
-
27
-
-
79551633353
-
β -Secretase inhibitor GRL-8234 rescues age-related cognitive decline in APP transgenic mice
-
Chang W-P, Huang X, Downs D, Cirrito J, Koelsch G, Holtzman DM, et al. β -Secretase inhibitor GRL-8234 rescues age-related cognitive decline in APP transgenic mice. FASEB J 2010; 25: 775-784.
-
(2010)
FASEB J
, vol.25
, pp. 775-784
-
-
Chang, W.-P.1
Huang, X.2
Downs, D.3
Cirrito, J.4
Koelsch, G.5
Holtzman, D.M.6
-
28
-
-
79959330125
-
-
WO2010042892
-
Bilcer, G.M., Devasamudram, T., Ankala, S.V., Lilly, J.C., Liu, C., Lei, H., Ghosh, A.K., Inoue, M. Pyrrolidine compounds which inhibit β -secretase activity and methods of use thereof. WO2010042892 (2010).
-
(2010)
Pyrrolidine Compounds Which Inhibit β -secretase Activity and Methods of Use Thereof
-
-
Bilcer, G.M.1
Devasamudram, T.2
Ankala, S.V.3
Lilly, J.C.4
Liu, C.5
Lei, H.6
Ghosh, A.K.7
Inoue, M.8
-
29
-
-
79959366321
-
-
US20070185144
-
Zhong, W., Hitchcock, S., lbrecht, B.K., Bartberger, M.D., Brown, J., Brown, R., Chaffee, S.C., Cheng, Y., Croghan, M., Graceffa, R., Harried, S., Hitchcock, S., Hungate, R., Judd, T., Kaller, M., Kreiman, C., La, D., Lopez, P., Masse, C., Monenschein, H., Nguyen, T., Nixey, T., Patel, V.F., Pennington, L., Weiss, M., Yang, B., Zhong, W. β -Secretase modulators and methods of use. US20070185144 (2007).
-
(2007)
β -secretase modulators and methods of use
-
-
Zhong, W.1
Hitchcock, S.2
Lbrecht, B.K.3
Bartberger, M.D.4
Brown, J.5
Brown, R.6
Chaffee, S.C.7
Cheng, Y.8
Croghan, M.9
Graceffa, R.10
Harried, S.11
Hitchcock, S.12
Hungate, R.13
Judd, T.14
Kaller, M.15
Kreiman, C.16
La, D.17
Lopez, P.18
Masse, C.19
Monenschein, H.20
Nguyen, T.21
Nixey, T.22
Patel, V.F.23
Pennington, L.24
Weiss, M.25
Yang, B.26
Zhong, W.27
more..
-
30
-
-
85038384558
-
-
US20090036478
-
Zhong, W., Hitchcock, S., Patel, V.F., Croghan M, Dineen T, Harried, S., Horne D, Judd, T., Kaller, M., Kreiman, C., Lopez, P., Monenschein, H., Nguyen, T., Weiss, M., Xue, Q., Yang, B. Substituted hydroxyethyl amine compounds as β -secretase modulators and methods of use. US20090036478 (2009).
-
(2009)
Substituted Hydroxyethyl Amine Compounds as β -secretase Modulators and Methods of Use
-
-
Zhong, W.1
Hitchcock, S.2
Patel, V.F.3
Croghan, M.4
Dineen, T.5
Harried, S.6
Horne, D.7
Judd, T.8
Kaller, M.9
Kreiman, C.10
Lopez, P.11
Monenschein, H.12
Nguyen, T.13
Weiss, M.14
Xue, Q.15
Yang, B.16
-
31
-
-
79959364680
-
-
US20100222338
-
Zhong, W., Hitchcock, S., Albrecht, B.K., Bartberger, M.D., Brown, J.M., Brown, R., Chaffee, S.C, Cheng, Y., Croghan, M., Graceffa, R., Harried, S., Hickman, D., Horne, D., Hunbgate R., Judd, T., Kaller, M., Kreiman, C., La, D., Lopez, P., Masse, C.E., Nixey, T., Patel, V.F., Pennington, L., Weiss, M., Xue, Q., Yang, B., Monenschein, H., Nguyen, T., β -secretase modulators and methods of use. US20100222338 (2010).
-
(2010)
β -secretase Modulators and Methods of Use
-
-
Zhong, W.1
Hitchcock, S.2
Albrecht, B.K.3
Bartberger, M.D.4
Brown, J.M.5
Brown, R.6
Chaffee, S.C.7
Cheng, Y.8
Croghan, M.9
Graceffa, R.10
Harried, S.11
Hickman, D.12
Horne, D.13
Hunbgate, R.14
Judd, T.15
Kaller, M.16
Kreiman, C.17
La, D.18
Lopez, P.19
Masse, C.E.20
Nixey, T.21
Patel, V.F.22
Pennington, L.23
Weiss, M.24
Xue, Q.25
Yang, B.26
Monenschein, H.27
Nguyen, T.28
more..
-
32
-
-
79959341234
-
-
US20100120774
-
Graceffa, R., Kaller, M., La, D., Lopez, P., Patel, V.F., Zhong, W. Substituted pyrano [2,3-b] pyridinamine compounds as β -secretase modulators and methods of use. US20100120774 (2010).
-
(2010)
Substituted Pyrano [2,3-b] Pyridinamine Compounds as β -secretase Modulators and Methods of Use
-
-
Graceffa, R.1
Kaller, M.2
La, D.3
Lopez, P.4
Patel, V.F.5
Zhong, W.6
-
33
-
-
79959326356
-
-
US20070185103
-
Albrecht, B.K., Andersen, D.L., Bartberger M., Brown, J., Brown, R., Chaffee, S.C., Cheng, Y., Croghan, M., Graceffa, R., Harried, S., Hitchcock, S., Hunbgate, R., Judd, T., Kaller, M., Kreiman, C., La, D., Lopez, P., Masse, C.E., Monenschein, H., Nguyen, T., Nixey, T., Patel, V.F., Pennington, L., Weiss, M., Xue, Q., Yang, B., Zhong, W. β -secretase modulators and methods of use. US20070185103 (2007).
-
(2007)
β -secretase Modulators and Methods of Use
-
-
Albrecht, B.K.1
Andersen, D.L.2
Bartberger, M.3
Brown, J.4
Brown, R.5
Chaffee, S.C.6
Cheng, Y.7
Croghan, M.8
Graceffa, R.9
Harried, S.10
Hitchcock, S.11
Hunbgate, R.12
Judd, T.13
Kaller, M.14
Kreiman, C.15
La, D.16
Lopez, P.17
Masse, C.E.18
Monenschein, H.19
Nguyen, T.20
Nixey, T.21
Patel, V.F.22
Pennington, L.23
Weiss, M.24
Xue, Q.25
Yang, B.26
Zhong, W.27
more..
-
34
-
-
78650517324
-
Synthesis and SAR of indole-and 7-azaindole-1,3- dicarboxamide hydroxyethylamine inhibitors of BACE-1
-
In Press, Accepted Manuscript
-
Marcin LR, Higgins MA, Zusi FC, Zhang Y, Dee MF, Parker MF, et al. Synthesis and SAR of indole-and 7-azaindole-1,3- dicarboxamide hydroxyethylamine inhibitors of BACE-1. Bioorg Med Chem Lett 2010; In Press, Accepted Manuscript.
-
(2010)
Bioorg Med Chem Lett
-
-
Marcin, L.R.1
Higgins, M.A.2
Zusi, F.C.3
Zhang, Y.4
Dee, M.F.5
Parker, M.F.6
-
35
-
-
10644249886
-
Structure-based design of potent and selective cell-permeable inhibitors of human β -secretase (BACE-1)
-
Stachel S, Coburn C, Steele T, Jones K, Loutzenhiser E, Gregro A, et al. Structure-based design of potent and selective cell-permeable inhibitors of human β -secretase (BACE-1). J Med Chem 2004; 47: 6447-50.
-
(2004)
J Med Chem
, vol.47
, pp. 6447-6450
-
-
Stachel, S.1
Coburn, C.2
Steele, T.3
Jones, K.4
Loutzenhiser, E.5
Gregro, A.6
-
36
-
-
33845515686
-
BACE1 inhibition reduces endogenous Aβ and alters APP processing in wild-type mice
-
Nishitomi K, Sakaguchi G, Horikoshi Y, Gray AJ, Maeda M, Hirata-Fukae C, et al. BACE1 inhibition reduces endogenous Aβ and alters APP processing in wild-type mice. J Neurochem 2006; 99: 1555-63.
-
(2006)
J Neurochem
, vol.99
, pp. 1555-1563
-
-
Nishitomi, K.1
Sakaguchi, G.2
Horikoshi, Y.3
Gray, A.J.4
Maeda, M.5
Hirata-Fukae, C.6
-
37
-
-
66249122925
-
-
US20080153846
-
Coburn, C.A., Nantermet, P.G., Rajapakse, H.A., Selnick, H.G., Stauffer, S.R. Aminomethyl β -secretase inhibitors for the treatment of Alzheimer's disease. US20080153846 (2008).
-
(2008)
Aminomethyl β -secretase Inhibitors for the Treatment of Alzheimer's Disease
-
-
Coburn, C.A.1
Nantermet, P.G.2
Rajapakse, H.A.3
Selnick, H.G.4
Stauffer, S.R.5
-
38
-
-
33746509102
-
BACE-1 inhibition by a series of psi[CH2NH] reduced amide isosteres
-
Coburn C, Stachel S, Jones K, Steele T, Rush D, DiMuzio JP, et al. BACE-1 inhibition by a series of psi[CH2NH] reduced amide isosteres. Bioorg Med Chem Lett 2006; 16: 3635-8.
-
(2006)
Bioorg Med Chem Lett
, vol.16
, pp. 3635-3638
-
-
Coburn, C.1
Stachel, S.2
Jones, K.3
Steele, T.4
Rush, D.5
Dimuzio, J.P.6
-
39
-
-
33750128392
-
Macrocyclic inhibitors of β-secretase: Functional activity in an animal model
-
Stachel S, Coburn C, Sankaranarayanan S, Price E, Wu G, Crouthamel M, et al. Macrocyclic inhibitors of β-secretase: functional activity in an animal model. J Med Chem 2006; 49: 6147-50.
-
(2006)
J Med Chem
, vol.49
, pp. 6147-6150
-
-
Stachel, S.1
Coburn, C.2
Sankaranarayanan, S.3
Price, E.4
Wu, G.5
Crouthamel, M.6
-
40
-
-
84883303306
-
-
US20100029701
-
Nantermet, P.G., Holloway, K.M., Moore, K.P., Stauffer, S.R. Macrocyclic spiropiperidine β-secretase inhibitors for the treatment of Alzheimer's disease. US20100029701 (2010).
-
(2010)
Macrocyclic Spiropiperidine β-secretase Inhibitors for the Treatment of Alzheimer's Disease
-
-
Nantermet, P.G.1
Holloway, K.M.2
Moore, K.P.3
Stauffer, S.R.4
-
43
-
-
79959344825
-
-
US20107713961
-
Eickmeier, C., Peters, S., Fuchs, K., Heine, N., Handschuh, S., Dorner-Ciossek, C., Klinder, K., Kostka, M. Substituted 1,2- ethylenediamines, methods for preparing them and uses thereof. US20107713961 (2010).
-
(2010)
Substituted 1,2- Ethylenediamines, Methods for Preparing Them and Uses Thereof
-
-
Eickmeier, C.1
Peters, S.2
Fuchs, K.3
Heine, N.4
Handschuh, S.5
Dorner-Ciossek, C.6
Klinder, K.7
Kostka, M.8
-
45
-
-
79959347600
-
-
US20107772221
-
Marcin, L.R., Good, A.C., Wu, Y.-J.Z., Dmitry, S., Olson, R.E., Wang, N. Diaminopropane derived macrocycles as inhibitors of β- amyloid production. US20107772221 (2010).
-
(2010)
Diaminopropane Derived Macrocycles as Inhibitors of β- Amyloid Production
-
-
Marcin, L.R.1
Good, A.C.2
Wu, Y.-J.Z.3
Dmitry, S.4
Olson, R.E.5
Wang, N.6
-
46
-
-
79959347825
-
-
US20100048590
-
Gailunas, A., Tucker, J.A., Tenbrink, R., Mickelson, J. N-(3- amino-2-hydroxy-propyl)substituted alkylamide compounds. US20100048590 (2010).
-
(2010)
N-(3- Amino-2-hydroxy-propyl)substituted Alkylamide Compounds
-
-
Gailunas, A.1
Tucker, J.A.2
Tenbrink, R.3
Mickelson, J.4
-
47
-
-
79959353379
-
-
US20100145056
-
John, V., Maillard, M., Beck, J.P., Baldwin, E.T., Hughes, R., Pulley, S.R., TenBrink, T. Acetyl 2-hydroxy-1.3-diaminoalkanes. US20100145056 (2010).
-
(2010)
Acetyl 2-hydroxy-1.3-diaminoalkanes
-
-
John, V.1
Maillard, M.2
Beck, J.P.3
Baldwin, E.T.4
Hughes, R.5
Pulley, S.R.6
Tenbrink, T.7
-
48
-
-
33847368052
-
Design, synthesis, and crystal structure of hydroxyethyl secondary amine-based peptidomimetic inhibitors of human β- secretase
-
Maillard M, Hom R, Benson T, Moon J, Mamo S, Bienkowski M, et al. Design, synthesis, and crystal structure of hydroxyethyl secondary amine-based peptidomimetic inhibitors of human β- secretase. J Med Chem 2007; 50: 776-81.
-
(2007)
J Med Chem
, vol.50
, pp. 776-781
-
-
Maillard, M.1
Hom, R.2
Benson, T.3
Moon, J.4
Mamo, S.5
Bienkowski, M.6
-
49
-
-
71049138619
-
Design and synthesis of cell potent BACE-1 inhibitors: Structureactivity relationship of P1' substituents
-
Sealy JM, Truong AP, Tso L, Probst GD, Aquino J, Hom RK, et al. Design and synthesis of cell potent BACE-1 inhibitors: Structureactivity relationship of P1' substituents. Bioorg Med Chem Lett 2009; 19: 6386-91.
-
(2009)
Bioorg Med Chem Lett
, vol.19
, pp. 6386-6391
-
-
Sealy, J.M.1
Truong, A.P.2
Tso, L.3
Probst, G.D.4
Aquino, J.5
Hom, R.K.6
-
50
-
-
77955428346
-
Improving the permeability of the hydroxyethylamine BACE-1 inhibitors: Structure-activity relationship of P2' substituents
-
Truong AP, Probst GD, Aquino J, Fang L, Brogley L, Sealy JM, et al. Improving the permeability of the hydroxyethylamine BACE-1 inhibitors: Structure-activity relationship of P2' substituents. Bioorg Med Chem Lett 2010; 20: 4789-94.
-
(2010)
Bioorg Med Chem Lett
, vol.20
, pp. 4789-4794
-
-
Truong, A.P.1
Probst, G.D.2
Aquino, J.3
Fang, L.4
Brogley, L.5
Sealy, J.M.6
-
51
-
-
77957882573
-
Design of an orally efficacious hydroxyethylamine (HEA) BACE-1 inhibitor in a preclinical animal model
-
Truong AP, Tóth G, Probst GD, Sealy JM, Bowers S, Wone DWG, et al. Design of an orally efficacious hydroxyethylamine (HEA) BACE-1 inhibitor in a preclinical animal model. Bioorg Med Chem Lett 2010; 20: 6231-6.
-
(2010)
Bioorg Med Chem Lett
, vol.20
, pp. 6231-6236
-
-
Truong, A.P.1
Tóth, G.2
Probst, G.D.3
Sealy, J.M.4
Bowers, S.5
Wone, D.W.G.6
-
52
-
-
79959351764
-
-
WO2005108391
-
Bueno-Melendo, A.B., Chen, S.-h., Erickson, J.A., Gonzalez-Garcia, M.R., Guo, D., Marcos-LLorente, A., Mccarthy, J.R., Sheperd, T.A., Sheehan, S.M., Yip, Y.Y.M. Amides as BACE inhibitors. WO2005108391 (2005).
-
(2005)
Amides as BACE Inhibitors
-
-
Bueno-Melendo, A.B.1
Chen, S.-H.2
Erickson, J.A.3
Gonzalez-Garcia, M.R.4
Guo, D.5
Marcos-Llorente, A.6
McCarthy, J.R.7
Sheperd, T.A.8
Sheehan, S.M.9
Yip, Y.Y.M.10
-
53
-
-
79959372319
-
-
US20097618978
-
Bueno-Melendo, A.B., Chen, S.-H., Gonzalez-Garcia, M.R., Mccarthy, J.R. Amides as BACE inhibitors. US20097618978 (2009).
-
(2009)
Amides as BACE Inhibitors
-
-
Bueno-Melendo, A.B.1
Chen, S.-H.2
Gonzalez-Garcia, M.R.3
McCarthy, J.R.4
-
54
-
-
79959343797
-
-
US20107745438
-
Broughton, H.B., Dally, R.D., Durham, T.B., Gonzalez-Garcia, M.R., Hahn, P.J., Henry, Jr.K.J., Kohn, T.J., Mccarthy, J.R., Shepherd, T.A., Erickson, J.A., Bueno Melendo, A.B. 3-(2- acylamino-1-hydroxyethyl)-morpholine derivatives and their use as BACE inhibitors. US20107745438 (2010).
-
(2010)
3-(2- Acylamino-1-hydroxyethyl)-morpholine Derivatives and Their Use as BACE Inhibitors
-
-
Broughton, H.B.1
Dally, R.D.2
Durham, T.B.3
Gonzalez-Garcia, M.R.4
Hahn, P.J.5
Henry, K.J.6
Kohn, T.J.7
McCarthy, J.R.8
Shepherd, T.A.9
Erickson, J.A.10
Bueno Melendo, A.B.11
-
55
-
-
60449109719
-
Macrocyclic peptidomimetic β- secretase (BACE-1) inhibitors with activity in vivo
-
Machauer R, Laumen K, Veenstra S, Rondeau J-M, Tintelnot-Blomley M, Betschart C, et al. Macrocyclic peptidomimetic β- secretase (BACE-1) inhibitors with activity in vivo. Bioorg Med Chem Lett 2009; 19: 1366-70.
-
(2009)
Bioorg Med Chem Lett
, vol.19
, pp. 1366-1370
-
-
Machauer, R.1
Laumen, K.2
Veenstra, S.3
Rondeau, J.-M.4
Tintelnot-Blomley, M.5
Betschart, C.6
-
56
-
-
79959344248
-
-
US20090312370
-
Laumen, K., Machauer, R., Tintelnot-Blomley, M., Veenstra, S.J. Macrocyclic compounds useful as BACE inhibitors. US20090312370 (2009).
-
(2009)
Macrocyclic Compounds Useful as BACE Inhibitors
-
-
Laumen, K.1
Machauer, R.2
Tintelnot-Blomley, M.3
Veenstra, S.J.4
-
57
-
-
79959348309
-
-
US20080214526
-
Lerchner, A., Machauer, R., Tintelnot-Blomley, M., Simic, O. Macrocyclic compounds and compositions useful as BACE inhibitors. US20080214526 (2008).
-
(2008)
Macrocyclic Compounds and Compositions Useful as BACE Inhibitors
-
-
Lerchner, A.1
Machauer, R.2
Tintelnot-Blomley, M.3
Simic, O.4
-
59
-
-
72249103808
-
Macrocyclic BACE-1 inhibitors acutely reduce Aβ in brain after po application
-
Lerchner A, Machauer R, Betschart C, Veenstra S, Rueeger H, McCarthy C, et al. Macrocyclic BACE-1 inhibitors acutely reduce Aβ in brain after po application. Bioorg Med Chem Lett 2010; 20: 603-7.
-
(2010)
Bioorg Med Chem Lett
, vol.20
, pp. 603-607
-
-
Lerchner, A.1
Machauer, R.2
Betschart, C.3
Veenstra, S.4
Rueeger, H.5
McCarthy, C.6
-
60
-
-
37549069915
-
Discovery of an orally efficaceous 4-phenoxypyrrolidinebased BACE-1 inhibitor
-
Iserloh U, Pan J, Stamford AW, Kennedy ME, Zhang Q, Zhang L, et al. Discovery of an orally efficaceous 4-phenoxypyrrolidinebased BACE-1 inhibitor. Bioorg Med Chem Lett 2008; 18: 418-22.
-
(2008)
Bioorg Med Chem Lett
, vol.18
, pp. 418-422
-
-
Iserloh, U.1
Pan, J.2
Stamford, A.W.3
Kennedy, M.E.4
Zhang, Q.5
Zhang, L.6
-
61
-
-
37549010299
-
Potent pyrrolidine- and piperidine-based BACE-1 inhibitors
-
Iserloh U, Wu Y, Cumming JN, Pan J, Wang LY, Stamford AW, et al. Potent pyrrolidine- and piperidine-based BACE-1 inhibitors. Bioorg Med Chem Lett 2008; 18: 414-7.
-
(2008)
Bioorg Med Chem Lett
, vol.18
, pp. 414-417
-
-
Iserloh, U.1
Wu, Y.2
Cumming, J.N.3
Pan, J.4
Wang, L.Y.5
Stamford, A.W.6
-
62
-
-
79959356477
-
-
US20100152138
-
Cumming, J.N., Iserloh, U., Stamford, A., Strickland, C., Voigt, J.H., Wu Y., Huang, Y., Xia, Y., Chackalamannil, S., Guo, T., Hobbs, D.W., Le, X., Thuy, H., Lowrie, J.F., Saionz, K.W., Babu, S.D. Cyclic amine BACE-1 inhibitors having a benzamide substituent. US20100152138 (2010).
-
(2010)
Cyclic Amine BACE-1 Inhibitors Having a Benzamide Substituent
-
-
Cumming, J.N.1
Iserloh, U.2
Stamford, A.3
Strickland, C.4
Voigt, J.H.5
Wu, Y.6
Huang, Y.7
Xia, Y.8
Chackalamannil, S.9
Guo, T.10
Hobbs, D.W.11
Le, X.12
Thuy, H.13
Lowrie, J.F.14
Saionz, K.W.15
Babu, S.D.16
-
63
-
-
78649344112
-
-
WO2009131974
-
Stamford, A.W., Zhu, Z., Mandal, M., Liu, X. Thiophenyl substituted 2-amino-3-methyl pyrrolopyrimidinone compounds as BACE-1 inhbitors, compositions and their use. WO2009131974 (2009).
-
(2009)
Thiophenyl Substituted 2-amino-3-methyl Pyrrolopyrimidinone Compounds as BACE-1 Inhbitors, Compositions and Their Use
-
-
Stamford, A.W.1
Zhu, Z.2
Mandal, M.3
Liu, X.4
-
64
-
-
44149095259
-
Rational design of novel, potent piperazinone and imidazolidinone BACE1 inhibitors
-
Cumming JN, Le TX, Babu S, Carroll C, Chen X, Favreau L, et al. Rational design of novel, potent piperazinone and imidazolidinone BACE1 inhibitors. Bioorg Med Chem Lett 2008; 18: 3236-41.
-
(2008)
Bioorg Med Chem Lett
, vol.18
, pp. 3236-3241
-
-
Cumming, J.N.1
Le, T.X.2
Babu, S.3
Carroll, C.4
Chen, X.5
Favreau, L.6
-
65
-
-
77649180798
-
Structure-based design and synthesis of novel P2/P3 modified, non-peptidic β-secretase (BACE-1) inhibitors
-
Hanessian S, Shao Z, Betschart C, Rondeau JM, Neumann U, Tintelnot-Blomley M. Structure-based design and synthesis of novel P2/P3 modified, non-peptidic β-secretase (BACE-1) inhibitors. Bioorg Med Chem Lett 2010; 20: 1924-7.
-
(2010)
Bioorg Med Chem Lett
, vol.20
, pp. 1924-1927
-
-
Hanessian, S.1
Shao, Z.2
Betschart, C.3
Rondeau, J.M.4
Neumann, U.5
Tintelnot-Blomley, M.6
-
66
-
-
38749086822
-
BACE-1 inhibitors part 1: Identification of novel hydroxy ethylamines (HEAs)
-
Clarke B, Demont E, Dingwall C, Dunsdon R, Faller A, Hawkins J, et al. BACE-1 inhibitors part 1: Identification of novel hydroxy ethylamines (HEAs). Bioorg Med Chem Lett 2008; 18: 1011-6.
-
(2008)
Bioorg Med Chem Lett
, vol.18
, pp. 1011-1016
-
-
Clarke, B.1
Demont, E.2
Dingwall, C.3
Dunsdon, R.4
Faller, A.5
Hawkins, J.6
-
67
-
-
38749138124
-
BACE-1 inhibitors part 2: Identification of hydroxy ethylamines (HEAs) with reduced peptidic character
-
Clarke B, Demont E, Dingwall C, Dunsdon R, Faller A, Hawkins J, et al. BACE-1 inhibitors part 2: Identification of hydroxy ethylamines (HEAs) with reduced peptidic character. Bioorg Med Chem Lett 2008; 18: 1017-21.
-
(2008)
Bioorg Med Chem Lett
, vol.18
, pp. 1017-1021
-
-
Clarke, B.1
Demont, E.2
Dingwall, C.3
Dunsdon, R.4
Faller, A.5
Hawkins, J.6
-
68
-
-
38749097747
-
BACE-1 inhibitors part 3: Identification of hydroxy ethylamines (HEAs) with nanomolar potency in cells
-
Beswick P, Charrier N, Clarke B, Demont E, Dingwall C, Dunsdon R, et al. BACE-1 inhibitors part 3: Identification of hydroxy ethylamines (HEAs) with nanomolar potency in cells. Bioorg Med Chem Lett 2008; 18: 1022-6.
-
(2008)
Bioorg Med Chem Lett
, vol.18
, pp. 1022-1026
-
-
Beswick, P.1
Charrier, N.2
Clarke, B.3
Demont, E.4
Dingwall, C.5
Dunsdon, R.6
-
69
-
-
33750132225
-
Acylguanidines as small-molecule β-secretase inhibitors
-
Cole D, Manas E, Stock J, Condon J, Jennings L, Aulabaugh A, et al. Acylguanidines as small-molecule β-secretase inhibitors. J Med Chem 2006; 49: 6158-61.
-
(2006)
J Med Chem
, vol.49
, pp. 6158-6161
-
-
Cole, D.1
Manas, E.2
Stock, J.3
Condon, J.4
Jennings, L.5
Aulabaugh, A.6
-
70
-
-
38749095202
-
Acylguanidine inhibitors of [beta]-secretase: Optimization of the pyrrole ring substituents extending into the S1 and S3 substrate binding pockets
-
Cole DC, Stock JR, Chopra R, Cowling R, Ellingboe JW, Fan KY, et al. Acylguanidine inhibitors of [beta]-secretase: Optimization of the pyrrole ring substituents extending into the S1 and S3 substrate binding pockets. Bioorg Med Chem Lett 2008; 18: 1063-6.
-
(2008)
Bioorg Med Chem Lett
, vol.18
, pp. 1063-1066
-
-
Cole, D.C.1
Stock, J.R.2
Chopra, R.3
Cowling, R.4
Ellingboe, J.W.5
Fan, K.Y.6
-
71
-
-
38149128145
-
Acylguanidine inhibitors of β-secretase: Optimization of the pyrrole ring substituents extending into the substrate binding pocket
-
Jennings LD, Cole DC, Stock JR, Sukhdeo MN, Ellingboe JW, Cowling R, et al. Acylguanidine inhibitors of β-secretase: Optimization of the pyrrole ring substituents extending into the substrate binding pocket. Bioorg Med Chem Lett 2008; 18: 767-71.
-
(2008)
Bioorg Med Chem Lett
, vol.18
, pp. 767-771
-
-
Jennings, L.D.1
Cole, D.C.2
Stock, J.R.3
Sukhdeo, M.N.4
Ellingboe, J.W.5
Cowling, R.6
-
72
-
-
34548574654
-
Thiophene substituted acylguanidines as BACE1 inhibitors
-
Fobare WF, Solvibile WR, Robichaud AJ, Malamas MS, Manas E, Turner J, et al. Thiophene substituted acylguanidines as BACE1 inhibitors. Bioorg Med Chem Lett 2007; 17: 5353-6.
-
(2007)
Bioorg Med Chem Lett
, vol.17
, pp. 5353-5356
-
-
Fobare, W.F.1
Solvibile, W.R.2
Robichaud, A.J.3
Malamas, M.S.4
Manas, E.5
Turner, J.6
-
73
-
-
77949659631
-
Novel pyrrolyl 2-aminopyridines as potent and selective human β-secretase (BACE1) inhibitors
-
Malamas MS, Barnes K, Hui Y, Johnson M, Lovering F, Condon J, et al. Novel pyrrolyl 2-aminopyridines as potent and selective human β-secretase (BACE1) inhibitors. Bioorg Med Chem Lett 2010; 20: 2068-73.
-
(2010)
Bioorg Med Chem Lett
, vol.20
, pp. 2068-2073
-
-
Malamas, M.S.1
Barnes, K.2
Hui, Y.3
Johnson, M.4
Lovering, F.5
Condon, J.6
-
74
-
-
66249143922
-
-
US20060173049
-
Malamas, M.S., Fobare, W.F., Solvibile, Jr., William, R., Lovering, F.E., Condon, J.S., Robichaud, A.J. Amino-pyridines as inhibitors of β-secretase. US20060173049 (2006).
-
(2006)
Amino-pyridines as Inhibitors of β-secretase
-
-
Malamas, M.S.1
Fobare, W.F.2
Solvibile Jr., W.R.3
Lovering, F.E.4
Condon, J.S.5
Robichaud, A.J.6
-
75
-
-
66249143922
-
-
US20100204245
-
Malamas, M.S., Fobare, W.F., Solvibile, Jr.W.R., Lovering, F.E., Condon, J.S., Robichaud, A.J. Amino-pyridines as inhibitors of β- secretase. US20100204245 (2010).
-
(2010)
Amino-pyridines as Inhibitors of β- Secretase
-
-
Malamas, M.S.1
Fobare, W.F.2
Solvibile, W.R.3
Lovering, F.E.4
Condon, J.S.5
Robichaud, A.J.6
-
76
-
-
76449094443
-
Di-substituted pyridinyl aminohydantoins as potent and highly selective human β-secretase (BACE1) inhibitors
-
Malamas MS, Barnes K, Johnson M, Hui Y, Zhou P, Turner J, et al. Di-substituted pyridinyl aminohydantoins as potent and highly selective human β-secretase (BACE1) inhibitors. Bioorg Med Chem 2010; 18: 630-9.
-
(2010)
Bioorg Med Chem
, vol.18
, pp. 630-639
-
-
Malamas, M.S.1
Barnes, K.2
Johnson, M.3
Hui, Y.4
Zhou, P.5
Turner, J.6
-
77
-
-
79959333415
-
-
US20070015754
-
Gerritz, S., Good, A.C., Thompson III L. A., Zhai, W., Shi, S., Zhu, S. Acyl guanidines as β-secretase inhibitors. US20070015754 (2007).
-
(2007)
Acyl Guanidines as β-secretase Inhibitors
-
-
Gerritz, S.1
Good, A.C.2
Thompson III, L.A.3
Zhai, W.4
Shi, S.5
Zhu, S.6
-
78
-
-
79959371335
-
-
US20097612069
-
Gerritz, S., Zhai, W., Shi, S., Zhu, S., Good, A.C., Thompson III L.A. Acyl guanidines as β-secretase inhibitors. US20097612069 (2009).
-
(2009)
Acyl Guanidines as β-secretase Inhibitors
-
-
Gerritz, S.1
Zhai, W.2
Shi, S.3
Zhu, S.4
Good, A.C.5
Thompson III, L.A.6
-
79
-
-
64349113476
-
-
US20070232679
-
Boy, K.M., Zhu, S., Macor, J.E., Shi, S., Gerritz, S. N-aryl pyrrolidine derivatives as β-secretase inhibitors. US20070232679 (2007).
-
(2007)
N-aryl Pyrrolidine Derivatives as β-secretase Inhibitors
-
-
Boy, K.M.1
Zhu, S.2
Macor, J.E.3
Shi, S.4
Gerritz, S.5
-
80
-
-
79959362318
-
-
US20087408071
-
Boy, K.M., Zhu, S., Macor, J.E., Shi, S., Gerritz, S. N-aryl pyrrolidine derivatives as β-secretase inhibitors. US20087408071 (2008).
-
(2008)
N-aryl Pyrrolidine Derivatives as β-secretase Inhibitors
-
-
Boy, K.M.1
Zhu, S.2
Macor, J.E.3
Shi, S.4
Gerritz, S.5
-
81
-
-
79959356228
-
-
US20087390925
-
Wu, Y.-J., Gerritz, S., Shi, S., Zhu, S. Oxime-containing acyl guanidines as β-secretase inhibitors. US20087390925 (2008).
-
(2008)
Oxime-containing Acyl Guanidines as β-secretase Inhibitors
-
-
Wu, Y.-J.1
Gerritz, S.2
Shi, S.3
Zhu, S.4
-
82
-
-
85017440065
-
-
US20097601751
-
Thompson III L. A., Shi, J., Zusi, C.F., Dee Michael, F., Macor, John E. Indole acetic acid acyl guanidines as β-secretase inhibitors. US20097601751 (2009).
-
(2009)
Indole Acetic Acid Acyl Guanidines as β-secretase Inhibitors
-
-
Thompson III, L.A.1
Shi, J.2
Zusi, C.F.3
Dee, M.F.4
Macor, J.E.5
-
83
-
-
78650431356
-
-
US20107678784
-
Wu, Y.-J., Gerritz, S., Shi, S., Zhu, S. Oxime-containing macrocyclic acyl guanidines as β-secretase inhibitors. US20107678784 (2010).
-
(2010)
Oxime-containing Macrocyclic Acyl Guanidines as β-secretase Inhibitors
-
-
Wu, Y.-J.1
Gerritz, S.2
Shi, S.3
Zhu, S.4
-
86
-
-
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 EW, Conway KA, Kennis L, Bischoff F, Mercken MH, Winter HL, et al. 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: 4261-4.
-
(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
-
87
-
-
79959337670
-
-
US20090227581
-
Baxter, E., Creighton, C.J., Ho, C.Y., Huang, Y., Lu, T., Luo, C., Reitz, A.B., Reynolds, C.H., Ross, T.M., Siber-McMaster, E. 2- Amino-quinoline derivatives useful as inhibitors of β-secretase (BACE). US20090227581 (2009).
-
(2009)
2- Amino-quinoline Derivatives Useful as Inhibitors of β-secretase (BACE)
-
-
Baxter, E.1
Creighton, C.J.2
Ho, C.Y.3
Huang, Y.4
Lu, T.5
Luo, C.6
Reitz, A.B.7
Reynolds, C.H.8
Ross, T.M.9
Siber-McMaster, E.10
-
88
-
-
77952320391
-
Macrocyclic BACE inhibitors: Optimization of a micromolar hit to nanomolar leads
-
Huang Y, Strobel ED, Ho CY, Reynolds CH, Conway KA, Piesvaux JA, et al. Macrocyclic BACE inhibitors: Optimization of a micromolar hit to nanomolar leads. Bioorg Med Chem Lett 20: 3158-60.
-
Bioorg Med Chem Lett
, vol.20
, pp. 3158-3160
-
-
Huang, Y.1
Strobel, E.D.2
Ho, C.Y.3
Reynolds, C.H.4
Conway, K.A.5
Piesvaux, J.A.6
-
89
-
-
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, et al. Application of fragment screening by X-ray crystallography to the discovery of aminopyridines as inhibitors of β-secretase. J Med Chem 2007; 50: 1124-32.
-
(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.6
-
90
-
-
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 PD, Albert JS, Sylvester M, Aharony D, Andisik D, Callaghan O, et al. 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: 5912-25.
-
(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
-
91
-
-
79959349009
-
-
WO2009022961
-
Chessari, G., Congreve, M.S., Holenz, J., Murray, C., Patel, S., Rakos, L., Rotticci, D. Pyrrolopiridine derivatives and tehir use as BACE inhibitors. WO2009022961 (2009).
-
(2009)
Pyrrolopiridine Derivatives and Tehir Use as BACE Inhibitors
-
-
Chessari, G.1
Congreve, M.S.2
Holenz, J.3
Murray, C.4
Patel, S.5
Rakos, L.6
Rotticci, D.7
-
92
-
-
79959350820
-
-
US20097629356
-
Chessari, G., Congreve, M.S., Holenz, J., Murray, C., Patel, S., Rakos, L., Rotticci, D. Substituted pyrrolo[3,4-b]pyridinamines and pharmaceutical compositions. US20097629356 (2009).
-
(2009)
Substituted Pyrrolo[3,4-b]pyridinamines and Pharmaceutical Compositions
-
-
Chessari, G.1
Congreve, M.S.2
Holenz, J.3
Murray, C.4
Patel, S.5
Rakos, L.6
Rotticci, D.7
-
93
-
-
79959334882
-
-
US200811761130
-
Berg, S., Hogdin, K., Kihlstrom, J., Plobeck, N., Sehgelmeble, F., Wirstam, M. New Compounds 317. US200811761130 (2008).
-
(2008)
New Compounds 317
-
-
Berg, S.1
Hogdin, K.2
Kihlstrom, J.3
Plobeck, N.4
Sehgelmeble, F.5
Wirstam, M.6
-
94
-
-
79959328746
-
-
US20080058349
-
Berg, S., Holenz, J., Hogdin, K., Kihlstrom, J., Kolmodin, K., Lindstrom, J., Plobeck, N., Rotticci, D., Sehgelmeble, F., Wirstam, M. New Compounds 318. US20080058349 (2008).
-
(2008)
New Compounds 318
-
-
Berg, S.1
Holenz, J.2
Hogdin, K.3
Kihlstrom, J.4
Kolmodin, K.5
Lindstrom, J.6
Plobeck, N.7
Rotticci, D.8
Sehgelmeble, F.9
Wirstam, M.10
-
95
-
-
79959368178
-
-
US20080171771
-
Arnold, J., Edwards, P., Sylvester, M., Berg, S., Holenz, J., Kers, A., Kolmodin, K., Rakos, L., Ohberg, L., Rotticci, D., Chessari, G., Congreeve, M., Murray, C., Patel, S., New Compounds 391. US20080171771 (2008).
-
(2008)
New Compounds 391
-
-
Arnold, J.1
Edwards, P.2
Sylvester, M.3
Berg, S.4
Holenz, J.5
Kers, A.6
Kolmodin, K.7
Rakos, L.8
Ohberg, L.9
Rotticci, D.10
Chessari, G.11
Congreeve, M.12
Murray, C.13
Patel, S.14
-
96
-
-
33845500273
-
Discovery of oxadiazoyl tertiary carbinamine inhibitors of β-secretase (BACE-1)
-
Rajapakse H, Nantermet P, Selnick H, Munsh iS, McGaughey G, Lindsley S, et al. Discovery of oxadiazoyl tertiary carbinamine inhibitors of β-secretase (BACE-1). J Med Chem 2006; 49: 7270-3.
-
(2006)
J Med Chem
, vol.49
, pp. 7270-7273
-
-
Rajapakse, H.1
Nantermet, P.2
Selnick, H.3
Munsh, I.S.4
McGaughey, G.5
Lindsley, S.6
-
97
-
-
34250346394
-
Design, synthesis, and SAR of macrocyclic tertiary carbinamine BACE-1 inhibitors
-
Lindsley S, Moore K, Rajapakse H, Selnick H, Young M, Zhu H, et al. Design, synthesis, and SAR of macrocyclic tertiary carbinamine BACE-1 inhibitors. Bioorg Med Chem Lett 2007, 17: 4057-61.
-
(2007)
Bioorg Med Chem Lett
, vol.17
, pp. 4057-4061
-
-
Lindsley, S.1
Moore, K.2
Rajapakse, H.3
Selnick, H.4
Young, M.5
Zhu, H.6
-
98
-
-
34548855068
-
Strategies toward improving the brain penetration of macrocyclic tertiary carbinamine BACE-1 inhibitors
-
Moore KP, Zhu H, Rajapakse HA, McGaughey GB, Colussi D, Price EA, et al. Strategies toward improving the brain penetration of macrocyclic tertiary carbinamine BACE-1 inhibitors. Bioorg Med Chem Lett 2007; 17: 5831-5.
-
(2007)
Bioorg Med Chem Lett
, vol.17
, pp. 5831-5835
-
-
Moore, K.P.1
Zhu, H.2
Rajapakse, H.A.3
McGaughey, G.B.4
Colussi, D.5
Price, E.A.6
-
99
-
-
33846623654
-
β-Secretase (BACE-1) inhibitors: Accounting for 10s loop flexibility using rigid active sites
-
McGaughey GB, Colussi D, Graham SL, Lai M-T, Munshi SK, Nantermet PG, et al. β-Secretase (BACE-1) inhibitors: Accounting for 10s loop flexibility using rigid active sites. Bioorg Med Chem Lett. 2007; 17: 1117-21.
-
(2007)
Bioorg Med Chem Lett
, vol.17
, pp. 1117-1121
-
-
McGaughey, G.B.1
Colussi, D.2
Graham, S.L.3
Lai, M.-T.4
Munshi, S.K.5
Nantermet, P.G.6
-
100
-
-
34547566031
-
Discovery of isonicotinamide derived β- secretase inhibitors: In vivo Reduction of β-amyloid
-
Stanton MG, Stauffer SR, Gregro AR, Steinbeiser M, Nantermet P, Sankaranarayanan S, et al. Discovery of isonicotinamide derived β- secretase inhibitors: in vivo Reduction of β-amyloid. J Med Chem 2007; 50: 3431-3.
-
(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
-
101
-
-
58549102936
-
Evolution of tertiary carbinamine BACE-1 inhibitors: Aβ reduction in rhesus CSF upon oral dosing
-
Nantermet PG, Rajapakse HA, Stanton MG, Stauffer SR, Barrow JC, Gregro AR, et al. Evolution of tertiary carbinamine BACE-1 inhibitors: Aβ reduction in rhesus CSF upon oral dosing. Chem Med Chem 2009; 4: 37-40.
-
(2009)
Chem Med Chem
, vol.4
, pp. 37-40
-
-
Nantermet, P.G.1
Rajapakse, H.A.2
Stanton, M.G.3
Stauffer, S.R.4
Barrow, J.C.5
Gregro, A.R.6
-
102
-
-
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 MA, Colussi D, Crouthamel MC, Devanarayan V, Ellis J, et al. 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: 131-40.
-
(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
-
103
-
-
76649097630
-
Rapid P1 SAR of brain penetrant tertiary carbinamine derived BACE inhibitors
-
Zhu H, Young MB, Nantermet PG, Graham SL, Colussi D, Lai MT, et al. Rapid P1 SAR of brain penetrant tertiary carbinamine derived BACE inhibitors. Bioorg Med Chem Lett 2010; 20: 1779-82.
-
(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
-
104
-
-
77549087611
-
SAR of tertiary carbinamine derived BACE1 inhibitors: Role of aspartate ligand amine pKa in enzyme inhibition
-
Rajapakse HA, Nantermet PG, Selnick HG, Barrow JC, McGaughey GB, Munshi S, et al. SAR of tertiary carbinamine derived BACE1 inhibitors: Role of aspartate ligand amine pKa in enzyme inhibition. Bioorg Med Chem Lett 2010; 20: 1885-9.
-
(2010)
Bioorg Med Chem Lett
, vol.20
, pp. 1885-1889
-
-
Rajapakse, H.A.1
Nantermet, P.G.2
Selnick, H.G.3
Barrow, J.C.4
McGaughey, G.B.5
Munshi, S.6
-
105
-
-
33845500273
-
Discovery of oxadiazoyl tertiary carbinamine inhibitors of β-secretase (BACE-1)
-
Rajapakse H, Nantermet P, Selnick H, Munshi S, McGaughey G, Lindsley S, et al. Discovery of oxadiazoyl tertiary carbinamine inhibitors of β-secretase (BACE-1). J Med Chem 2006; 49: 7270-3.
-
(2006)
J Med Chem
, vol.49
, pp. 7270-7273
-
-
Rajapakse, H.1
Nantermet, P.2
Selnick, H.3
Munshi, S.4
McGaughey, G.5
Lindsley, S.6
-
106
-
-
77249094569
-
Application of fragment-based NMR screening, X-ray crystallography, structure-based design, and focused chemical library design to identify novel μM leads for the development of nM BACE-1 (β-Site APP Cleaving Enzyme 1) inhibitors
-
Wang Y-S, Strickland C, Voigt JH, Kennedy ME, Beyer BM, Senior MM, et al. Application of fragment-based NMR screening, X-ray crystallography, structure-based design, and focused chemical library design to identify novel μM leads for the development of nM BACE-1 (β-Site APP Cleaving Enzyme 1) inhibitors. J Med Chem 2009; 53: 942-50.
-
(2009)
J Med Chem
, vol.53
, pp. 942-950
-
-
Wang, Y.-S.1
Strickland, C.2
Voigt, J.H.3
Kennedy, M.E.4
Beyer, B.M.5
Senior, M.M.6
-
107
-
-
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 ZY, Ye Y, Voigt J, Strickland C, Smith EM, et al. 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; 53: 951-65.
-
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
-
108
-
-
70449586603
-
Fragment-Based Discovery of BACE1 Inhibitors Using Functional Assays
-
Godemann R, Madden J, KraÃàmer J, Smith M, Fritz U, Hesterkamp T, et al. Fragment-Based Discovery of BACE1 Inhibitors Using Functional Assays. Biochemistry 2009; 48: 10743-51.
-
(2009)
Biochemistry
, vol.48
, pp. 10743-10751
-
-
Godemann, R.1
Madden, J.2
Kraãàmer, J.3
Smith, M.4
Fritz, U.5
Hesterkamp, T.6
-
109
-
-
77955655180
-
Fragment-based discovery and optimization of BACE1 inhibitors
-
Madden J, Dod JR, Godemann R, Kraemer J, Smith M, Biniszkiewicz M, et al. Fragment-based discovery and optimization of BACE1 inhibitors. Bioorg Med Chem Lett 2010; 20: 5329-33.
-
(2010)
Bioorg Med Chem Lett
, vol.20
, pp. 5329-5333
-
-
Madden, J.1
Dod, J.R.2
Godemann, R.3
Kraemer, J.4
Smith, M.5
Biniszkiewicz, M.6
-
110
-
-
70350050829
-
Aminoimidazoles as Potent and Selective Human β-ecretase (BACE1) inhibitors
-
Malamas MS, Erdei J, Gunawan I, Barnes K, Johnson M, Hui Y, et al. Aminoimidazoles as Potent and Selective Human β-ecretase (BACE1) inhibitors. J Med Chem 2009; 52: 6314-23.
-
(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
-
111
-
-
79959337175
-
-
WO/2007/005366
-
Malamas, M., Zhou, P., Fobare, W., Solvibile, W., Gunawan, I., Erdei, J.J., Yan, Y., Andrae, P.M., Quagliato, D.A. Amino-5-(5- membered)hetero-arylimidazolone compounds and the use thereof for β-secretase modulation. WO/2007/005366 (2007).
-
(2007)
Amino-5-(5- Membered)hetero-arylimidazolone Compounds and The Use Thereof for β-secretase Modulation
-
-
Malamas, M.1
Zhou, P.2
Fobare, W.3
Solvibile, W.4
Gunawan, I.5
Erdei, J.J.6
Yan, Y.7
Andrae, P.M.8
Quagliato, D.A.9
-
112
-
-
77249122570
-
-
US20107700602
-
Malamas, M.S., Erdei, J.J., Gunawan, I.S., Zhou, P.Y.Y., Quagliato, D.A. Amino-5,5-diphenylimidazolone derivatives for the inhibition of β-secretase. US20107700602 (2010).
-
(2010)
Amino-5,5-diphenylimidazolone Derivatives for the Inhibition of β-secretase
-
-
Malamas, M.S.1
Erdei, J.J.2
Gunawan, I.S.3
Zhou, P.Y.Y.4
Quagliato, D.A.5
-
113
-
-
79959329883
-
-
US20070004730
-
Zhou, P., Malamas, M., Li, Y., Robichaud, A., Quagliato, D. Amino-5-(6-membered)heteroarylimidazolone compounds and the use thereof for β-secretase modulation. US20070004730 (2007).
-
(2007)
Amino-5-(6-membered)heteroarylimidazolone Compounds and The Use Thereof for β-secretase Modulation
-
-
Zhou, P.1
Malamas, M.2
Li, Y.3
Robichaud, A.4
Quagliato, D.5
-
114
-
-
84867752600
-
-
US20097582667
-
Quagliato, D.A., Andrae, P.M., Fan, Y. Dihydrospiro[dibenzo [a,d][7]annulene-5,4'-imidazol] compounds for the inhibition of β- secretase. US20097582667 (2009).
-
(2009)
Dihydrospiro[dibenzo [a,d][7]annulene-5,4'-imidazol] Compounds for the Inhibition of β- Secretase
-
-
Quagliato, D.A.1
Andrae, P.M.2
Fan, Y.3
-
116
-
-
72249088155
-
Discovery and initial optimization of 5,5'-disubstituted aminohydantoins as potent β-secretase (BACE1) inhibitors
-
Nowak P, Cole DC, Aulabaugh A, Bard J, Chopra R, Cowling R, et al. Discovery and initial optimization of 5,5'-disubstituted aminohydantoins as potent β-secretase (BACE1) inhibitors. Bioorg Med Chem Lett 2010; 20: 632-5.
-
(2010)
Bioorg Med Chem Lett
, vol.20
, pp. 632-635
-
-
Nowak, P.1
Cole, D.C.2
Aulabaugh, A.3
Bard, J.4
Chopra, R.5
Cowling, R.6
-
117
-
-
77949492453
-
Pyridinyl aminohydantoins as small molecule BACE1 inhibitors
-
Zhou P, Li Y, Fan Y, Wang Z, Chopra R, Olland A, et al. Pyridinyl aminohydantoins as small molecule BACE1 inhibitors. Bioorg Med Chem Lett 2010; 20: 2326-9.
-
(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
-
118
-
-
77249128954
-
Design and Synthesis of 5,5'-disubstituted aminohydantoins as potent and selective human β-secretase (BACE1) inhibitors
-
Malamas MS, Erdei J, Gunawan I, Turner J, Hu Y, Wagner E, et al. Design and Synthesis of 5,5'-disubstituted aminohydantoins as potent and selective human β-secretase (BACE1) inhibitors. J Med Chem 2010; 53: 1146-58.
-
(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
-
119
-
-
79959350250
-
-
US20090247577
-
Rogel, O., Rondeau, J.-M., Rueeger, H., Simic, O., Sirockin, F. Tintelnot-Blomley M. Pyrrolidine derivatives useful as BACE inhibitors. US20090247577 (2009).
-
(2009)
Pyrrolidine Derivatives Useful as BACE Inhibitors
-
-
Rogel, O.1
Rondeau, J.-M.2
Rueeger, H.3
Simic, O.4
Sirockin, F.5
Tintelnot-Blomley, M.6
-
120
-
-
79959332676
-
-
WO/2009/024615
-
Briard, E., Lueoend, R., Machauer, R., Moebitz, H., Rogel, O., Rondeau, J., Rueger, H., Tintelnot-Blomley, M., Veenstra, S.J. Aminobenzyl substituted cyclic sulfones useful as BACE inhibitors. WO/2009/024615 (2009).
-
(2009)
Aminobenzyl Substituted Cyclic Sulfones Useful as BACE Inhibitors
-
-
Briard, E.1
Lueoend, R.2
Machauer, R.3
Moebitz, H.4
Rogel, O.5
Rondeau, J.6
Rueger, H.7
Tintelnot-Blomley, M.8
Veenstra, S.J.9
-
121
-
-
79959332418
-
-
20100056490
-
Briard, E., Lueoend, R.M., Machauer, R., Moebitz, H., Rogel, O., Rondeau, J.-M., Rueger, H., Tintelnot-Blomley, M., Veenstra, S.J. Cyclic sulfones with aminobenzyl substitution useful as BACE inhibitors. 20100056490 (2010).
-
(2010)
Cyclic Sulfones with Aminobenzyl Substitution Useful as BACE Inhibitors
-
-
Briard, E.1
Lueoend, R.M.2
Machauer, R.3
Moebitz, H.4
Rogel, O.5
Rondeau, J.-M.6
Rueger, H.7
Tintelnot-Blomley, M.8
Veenstra, S.J.9
-
122
-
-
79959363479
-
-
US20100075957
-
Tamura, Y., Suzuki, S., Tada, Y., Yonezawa, S., Fujikoshi, C., Matsumoto, S., Kooriyama, Y., Ueno, T. Aminodihydrothiazine derivatives substituted with a cyclic group. US20100075957 (2010).
-
(2010)
Aminodihydrothiazine Derivatives Substituted with a Cyclic Group
-
-
Tamura, Y.1
Suzuki, S.2
Tada, Y.3
Yonezawa, S.4
Fujikoshi, C.5
Matsumoto, S.6
Kooriyama, Y.7
Ueno, T.8
-
123
-
-
79959342377
-
-
Audia, J., Edmund, M.D., James, S.S., Martin, W.B.M. Aminodihydrothiazime derivatives as BACE inhibitors for the treatment of Alzheimer's disease. (2009).
-
(2009)
Aminodihydrothiazime Derivatives as BACE Inhibitors for the Treatment of Alzheimer's Disease
-
-
Audia, J.1
Edmund, M.D.2
James, S.S.3
Martin, W.B.M.4
-
124
-
-
79959362521
-
-
US20107648983
-
Audia, J.E., Mergott, D.J., Sheehan, S.M., Watson, B.M. BACE inhibitors. US20107648983 (2010).
-
(2010)
BACE Inhibitors
-
-
Audia, J.E.1
Mergott, D.J.2
Sheehan, S.M.3
Watson, B.M.4
-
125
-
-
79959351540
-
-
US20100087429
-
White, R., Amegadzie, A., Bryan, M.C., Chen, J.J., Cheng, A.C., Dineen, T., Epstein, O., Gore, V.K., Hua, Z, Human, J.B., Huang, H., Kreiman, C., La, D., Liu, Q., Ma, V.V., Marx, I, Patel, V.F., Qian, W., Weiss, M, Yuan, C. Spiro-tricyclic ring compounds as β- secretase imodulators and methods of use. US20100087429 (2010).
-
(2010)
Spiro-tricyclic Ring Compounds as β- Secretase Imodulators and Methods of Use
-
-
White, R.1
Amegadzie, A.2
Bryan, M.C.3
Chen, J.J.4
Cheng, A.C.5
Dineen, T.6
Epstein, O.7
Gore, V.K.8
Hua, Z.9
Human, J.B.10
Huang, H.11
Kreiman, C.12
La, D.13
Liu, Q.14
Ma, V.V.15
Marx, I.16
Patel, V.F.17
Qian, W.18
Weiss, M.19
Yuan, C.20
more..
-
126
-
-
78049286290
-
Ameliorative effects of a non-competitive BACE1 inhibitor TAK-070 on Aβ peptide levels and impaired learning behavior in aged rats
-
Takahashi, H., Fukumoto, H., Maeda, R., Terauchi, J., Kato, K., Miyamoto, M. Ameliorative effects of a non-competitive BACE1 inhibitor TAK-070 on Aβ peptide levels and impaired learning behavior in aged rats. Brain Res 2010.
-
(2010)
Brain Res
-
-
Takahashi, H.1
Fukumoto, H.2
Maeda, R.3
Terauchi, J.4
Kato, K.5
Miyamoto, M.6
-
127
-
-
42549148456
-
Efficient inhibition of the Alzheimer's disease β-secretase by membrane targeting
-
Rajendran L, Schneider A, Schlechtingen G, Weidlich S, Ries J, Braxmeier T, et al. Efficient inhibition of the Alzheimer's disease β-secretase by membrane targeting. Sci 2008; 320: 520-3.
-
(2008)
Sci
, vol.320
, pp. 520-523
-
-
Rajendran, L.1
Schneider, A.2
Schlechtingen, G.3
Weidlich, S.4
Ries, J.5
Braxmeier, T.6
-
128
-
-
34249942064
-
Levels of β-secretase (BACE1) in cerebrospinal fluid as a predictor of risk in mild cognitive impairment
-
Zhong Z, Ewers M, Teipel S, Burger K, Wallin A, Blennow K, et al. Levels of β-secretase (BACE1) in cerebrospinal fluid as a predictor of risk in mild cognitive impairment. Arch Gen Psychiatry 2007; 64: 718-26.
-
(2007)
Arch Gen Psychiatry
, vol.64
, pp. 718-726
-
-
Zhong, Z.1
Ewers, M.2
Teipel, S.3
Burger, K.4
Wallin, A.5
Blennow, K.6
-
129
-
-
0036260892
-
Increased expression of the amyloid precursor β-secretase in Alzheimer's disease
-
Holsinger R, McLean, CA, Beyreuther, K, Masters, CL, Evin, G. Increased expression of the amyloid precursor β-secretase in Alzheimer's disease. Ann Neurol 2002; 51: 783-6.
-
(2002)
Ann Neurol
, vol.51
, pp. 783-786
-
-
Holsinger, R.1
McLean, C.A.2
Beyreuther, K.3
Masters, C.L.4
Evin, G.5
-
130
-
-
0036718272
-
β-Secretase protein and activity are increased in the neocortex in Alzheimer disease
-
Fukumoto H, Cheung BS, Hyman BT, Irizarry MC. β-Secretase protein and activity are increased in the neocortex in Alzheimer disease. Arch Neurol 2002; 59: 1381-9.
-
(2002)
Arch Neurol
, vol.59
, pp. 1381-1389
-
-
Fukumoto, H.1
Cheung, B.S.2
Hyman, B.T.3
Irizarry, M.C.4
-
131
-
-
79955944449
-
Decreased expression of GGA3 Protein in Alzheimer's disease frontal cortex and increased co-distribution of BACE with the amyloid precursor protein
-
Santosa C, Rasche S, Barakat A, Bellingham SA, Ho M, Tan J, Hill AF, Masters CL, McLean C, Evin G. Decreased expression of GGA3 Protein in Alzheimer's disease frontal cortex and increased co-distribution of BACE with the amyloid precursor protein. Neurobiol Dis 2011; 43: 176-83.
-
(2011)
Neurobiol Dis
, vol.43
, pp. 176-183
-
-
Santosa, C.1
Rasche, S.2
Barakat, A.3
Bellingham, S.A.4
Ho, M.5
Tan, J.6
Hill, A.F.7
Masters, C.L.8
McLean, C.9
Evin, G.10
|