-
1
-
-
70349638299
-
Advances in tau-focused drug discovery for Alzheimer's disease and related tauopathies
-
K.R. Brunden, J.Q. Trojanowski, and V.M.Y. Lee Advances in tau-focused drug discovery for Alzheimer's disease and related tauopathies Nat. Rev. Drug Discov. 8 2009 783 793
-
(2009)
Nat. Rev. Drug Discov.
, vol.8
, pp. 783-793
-
-
Brunden, K.R.1
Trojanowski, J.Q.2
Lee, V.M.Y.3
-
2
-
-
84863337843
-
Alzheimer mechanisms and therapeutic strategies
-
Y.D. Huang, and L. Mucke Alzheimer mechanisms and therapeutic strategies Cell 148 2012 1204 1222
-
(2012)
Cell
, vol.148
, pp. 1204-1222
-
-
Huang, Y.D.1
Mucke, L.2
-
3
-
-
84859755505
-
Alzheimer's disease and the amyloid cascade hypothesis: A critical review
-
R. Christiane Alzheimer's disease and the amyloid cascade hypothesis: a critical review Int. J. Alzheimers Dis. 2012 2012 1 11
-
(2012)
Int. J. Alzheimers Dis.
, vol.2012
, pp. 1-11
-
-
Christiane, R.1
-
4
-
-
14844303721
-
Inhibition of heparin-induced tau filament formation by phenothiazines, polyphenols, and porphyrins
-
DOI 10.1074/jbc.M408714200
-
S. Taniguchi, N. Suzuki, M. Masuda, S. Hisanaga, T. Iwatsubo, M. Goedert, and M. Hasegawa Inhibition of heparin-induced tau filament formation by phenothiazines, polyphenols, and porphyrins J. Biol. Chem. 280 2005 7614 7623 (Pubitemid 40349654)
-
(2005)
Journal of Biological Chemistry
, vol.280
, Issue.9
, pp. 7614-7623
-
-
Taniguchi, S.1
Suzuki, N.2
Masuda, M.3
Hisanaga, S.-I.4
Iwatsubo, T.5
Goedert, M.6
Hasegawa, M.7
-
5
-
-
0029742937
-
Selective inhibition of Alzheimer disease-like tau aggregation by phenothiazines
-
DOI 10.1073/pnas.93.20.11213
-
C.M. Wischik, P.C. Edwards, R.Y.K. Lai, M. Roth, and C.R. Harrington Selective inhibition of Alzheimer disease-like tau aggregation by phenothiazines Proc. Natl. Acad. Sci. U. S. A. 93 1996 11213 11218 (Pubitemid 26333144)
-
(1996)
Proceedings of the National Academy of Sciences of the United States of America
, vol.93
, Issue.20
, pp. 11213-11218
-
-
Wischik, C.M.1
Edwards, P.C.2
Lai, R.Y.K.3
Roth, M.4
Harrington, C.R.5
-
6
-
-
84867830552
-
Design, synthesis and biological evaluation of benzo[e][1,2,4]triazin- 7(1H)-one and [1,2,4]-triazino[5,6,1-jk]carbazol-6-one derivatives as dual inhibitors of beta-amyloid aggregation and acetyl/butyryl cholinesterase
-
M. Catto, A.A. Berezin, D. Lo Re, G. Loizou, M. Demetriades, A. De Stradis, F. Campagna, P.A. Koutentis, and A. Carotti Design, synthesis and biological evaluation of benzo[e][1,2,4]triazin-7(1H)-one and [1,2,4]-triazino[5,6,1-jk]carbazol-6-one derivatives as dual inhibitors of beta-amyloid aggregation and acetyl/butyryl cholinesterase Eur. J. Med. Chem. 58 2012 84 97
-
(2012)
Eur. J. Med. Chem.
, vol.58
, pp. 84-97
-
-
Catto, M.1
Berezin, A.A.2
Lo Re, D.3
Loizou, G.4
Demetriades, M.5
De Stradis, A.6
Campagna, F.7
Koutentis, P.A.8
Carotti, A.9
-
7
-
-
84884773453
-
Multifunctional tacrine-flavonoid hybrids with cholinergic, β-amyloid-reducing, and metal chelating properties for the treatment of Alzheimer's disease
-
S.-Y. Li, X.-B. Wang, S.-S. Xie, N. Jiang, K.D.G. Wang, H.-Q. Yao, H.-B. Sun, and L.-Y. Kong Multifunctional tacrine-flavonoid hybrids with cholinergic, β-amyloid-reducing, and metal chelating properties for the treatment of Alzheimer's disease Eur. J. Med. Chem. 69 2013 632 646
-
(2013)
Eur. J. Med. Chem.
, vol.69
, pp. 632-646
-
-
Li, S.-Y.1
Wang, X.-B.2
Xie, S.-S.3
Jiang, N.4
Wang, K.D.G.5
Yao, H.-Q.6
Sun, H.-B.7
Kong, L.-Y.8
-
8
-
-
42449147149
-
2,3-disubstituted thiophene-based organic dyes for solar cells
-
DOI 10.1021/cm702631r
-
K.R.J. Thomas, Y.C. Hsu, J.T. Lin, K.M. Lee, K.C. Ho, C.H. Lai, Y.M. Cheng, and P.T. Chou 2,3-Disubstituted thiophene-based organic dyes for solar cells Chem. Mater. 20 2008 1830 1840 (Pubitemid 351560844)
-
(2008)
Chemistry of Materials
, vol.20
, Issue.5
, pp. 1830-1840
-
-
Thomas, K.R.J.1
Hsu, Y.-C.2
Lin, J.T.3
Lee, K.-M.4
Ho, K.-C.5
Lai, C.-H.6
Cheng, Y.-M.7
Chou, P.-T.8
-
9
-
-
50649091316
-
Pyrrole-based organic dyes for dye-sensitized solar cells
-
Y.S. Yen, Y.C. Hsu, J.T. Lin, C.W. Chang, C.P. Hsu, and D.J. Yin Pyrrole-based organic dyes for dye-sensitized solar cells J. Phys. Chem. C 112 2008 12557 12567
-
(2008)
J. Phys. Chem. C
, vol.112
, pp. 12557-12567
-
-
Yen, Y.S.1
Hsu, Y.C.2
Lin, J.T.3
Chang, C.W.4
Hsu, C.P.5
Yin, D.J.6
-
10
-
-
65149102326
-
Dye-sensitized solar cell utilizing organic dyads containing triarylene conjugates
-
Y.J. Chang, and T.J. Chow Dye-sensitized solar cell utilizing organic dyads containing triarylene conjugates Tetrahedron 65 2009 4726 4734
-
(2009)
Tetrahedron
, vol.65
, pp. 4726-4734
-
-
Chang, Y.J.1
Chow, T.J.2
-
11
-
-
70349880505
-
Highly efficient organic sensitizers for solid-state dye-sensitized solar cells
-
S.J. Moon, J.H. Yum, R. Humphry-Baker, K.M. Karlsson, D.P. Hagberg, T. Marinado, A. Hagfeldt, L.C. Sun, M. Gratzel, and M.K. Nazeeruddin Highly efficient organic sensitizers for solid-state dye-sensitized solar cells J. Phys. Chem. C 113 2009 16816 16820
-
(2009)
J. Phys. Chem. C
, vol.113
, pp. 16816-16820
-
-
Moon, S.J.1
Yum, J.H.2
Humphry-Baker, R.3
Karlsson, K.M.4
Hagberg, D.P.5
Marinado, T.6
Hagfeldt, A.7
Sun, L.C.8
Gratzel, M.9
Nazeeruddin, M.K.10
-
12
-
-
84861532193
-
An iterative approach to the synthesis of thiophene-based organic dyes
-
S. Fuse, H. Yoshida, and T. Takahashi An iterative approach to the synthesis of thiophene-based organic dyes Tetrahedron Lett. 53 2012 3288 3291
-
(2012)
Tetrahedron Lett.
, vol.53
, pp. 3288-3291
-
-
Fuse, S.1
Yoshida, H.2
Takahashi, T.3
-
13
-
-
84870272212
-
Sequential coupling approach to the synthesis of nickel(II) complexes with N-aryl-2-amino phenolates
-
S. Fuse, H. Tago, M.M. Maitani, Y. Wada, and T. Takahashi Sequential coupling approach to the synthesis of nickel(II) complexes with N-aryl-2-amino phenolates ACS Combi. Sci. 14 2012 545 550
-
(2012)
ACS Combi. Sci.
, vol.14
, pp. 545-550
-
-
Fuse, S.1
Tago, H.2
Maitani, M.M.3
Wada, Y.4
Takahashi, T.5
-
14
-
-
84879211315
-
Design and synthesis of 2-phenyl-1,4-dioxa-spiro[4.5]deca-6,9-dien-8-ones as potential anticancer agents starting from cytotoxic spiromamakone A
-
S. Fuse, K. Inaba, M. Takagi, M. Tanaka, T. Hirokawa, K. Johmoto, H. Uekusa, K. Shin-Ya, T. Takahashi, and T. Doi Design and synthesis of 2-phenyl-1,4-dioxa-spiro[4.5]deca-6,9-dien-8-ones as potential anticancer agents starting from cytotoxic spiromamakone A Eur. J. Med. Chem. 66 2013 180 184
-
(2013)
Eur. J. Med. Chem.
, vol.66
, pp. 180-184
-
-
Fuse, S.1
Inaba, K.2
Takagi, M.3
Tanaka, M.4
Hirokawa, T.5
Johmoto, K.6
Uekusa, H.7
Shin-Ya, K.8
Takahashi, T.9
Doi, T.10
-
15
-
-
84906069628
-
Elucidating the structure-property relationship of donor-π-acceptor dyes for DSSCs through rapid library synthesis via a one-pot procedure
-
10.1002/chem.201402093
-
S. Fuse, S. Sugiyama, M.M. Maitani, Y. Wada, Y. Ogomi, S. Hayase, R. Katoh, T. Kaiho, T. Takahashi, Elucidating the structure-property relationship of donor-π-acceptor dyes for DSSCs through rapid library synthesis via a one-pot procedure, Chem. Eur. J. Early View 10.1002/chem.201402093.
-
Chem. Eur. J. Early View
-
-
Fuse, S.1
Sugiyama, S.2
Maitani, M.M.3
Wada, Y.4
Ogomi, Y.5
Hayase, S.6
Katoh, R.7
Kaiho, T.8
Takahashi, T.9
-
16
-
-
84860361440
-
Sequential Suzuki/asymmetric aldol and Suzuki/Knoevenagel reactions under aqueous conditions
-
M. Gruttadauria, L.A. Bivona, P. Lo Meo, S. Riela, and R. Noto Sequential Suzuki/asymmetric aldol and Suzuki/Knoevenagel reactions under aqueous conditions Eur. J. Org. Chem. 2012 2012 2635 2642
-
(2012)
Eur. J. Org. Chem.
, vol.2012
, pp. 2635-2642
-
-
Gruttadauria, M.1
Bivona, L.A.2
Lo Meo, P.3
Riela, S.4
Noto, R.5
-
17
-
-
37049042977
-
Palladium(0) compounds. Part II. Compounds with triarylphosphines, triaryl phosphites, and triarylarsines
-
L. Malatesta, and M. Angoletta Palladium(0) compounds. Part II. Compounds with triarylphosphines, triaryl phosphites, and triarylarsines J. Chem. Soc. 1957 1186 1188
-
(1957)
J. Chem. Soc.
, pp. 1186-1188
-
-
Malatesta, L.1
Angoletta, M.2
-
19
-
-
0001029926
-
New diphosphine ligands based on heterocyclic aromatics inducing very high regioselectivity in rhodium-catalyzed hydroformylation - Effect of the bite angle
-
M. Kranenburg, Y.E.M. Vanderburgt, P.C.J. Kamer, P. Vanleeuwen, K. Goubitz, and J. Fraanje New diphosphine ligands based on heterocyclic aromatics inducing very high regioselectivity in rhodium-catalyzed hydroformylation - effect of the bite angle Organometallics 14 1995 3081 3089
-
(1995)
Organometallics
, vol.14
, pp. 3081-3089
-
-
Kranenburg, M.1
Vanderburgt, Y.E.M.2
Kamer, P.C.J.3
Vanleeuwen, P.4
Goubitz, K.5
Fraanje, J.6
-
20
-
-
0034600318
-
Versatile catalysts for the Suzuki cross-coupling of arylboronic acids with aryl and vinyl halides and triflates under mild conditions
-
DOI 10.1021/ja0002058
-
A.F. Littke, C.Y. Dai, and G.C. Fu Versatile catalysts for the Suzuki cross-coupling of arylboronic acids with aryl and vinyl halides and triflates under mild conditions J. Am. Chem. Soc. 122 2000 4020 4028 (Pubitemid 30304832)
-
(2000)
Journal of the American Chemical Society
, vol.122
, Issue.17
, pp. 4020-4028
-
-
Littke, A.F.1
Dai, C.2
Fu, G.C.3
-
22
-
-
82255192015
-
Arylcyanoacrylamides as inhibitors of the Dengue and West Nile virus proteases
-
C. Nitsche, C. Steuer, and C.D. Klein Arylcyanoacrylamides as inhibitors of the Dengue and West Nile virus proteases Bioorg. Med. Chem. 19 2011 7318 7337
-
(2011)
Bioorg. Med. Chem.
, vol.19
, pp. 7318-7337
-
-
Nitsche, C.1
Steuer, C.2
Klein, C.D.3
-
23
-
-
0027502784
-
Thioflavine-T interaction with synthetic Alzheimer's disease β-amyloid peptides - Detection of amyloid aggregation in solution
-
H. Levine Thioflavine-T interaction with synthetic Alzheimer's disease β-amyloid peptides - detection of amyloid aggregation in solution Protein Sci. 2 1993 404 410
-
(1993)
Protein Sci.
, vol.2
, pp. 404-410
-
-
Levine, H.1
-
24
-
-
70349481513
-
The thioflavin T fluorescence assay for amyloid fibril detection can be biased by the presence of exogenous compounds
-
S.A. Hudson, H. Ecroyd, T.W. Kee, and J.A. Carver The thioflavin T fluorescence assay for amyloid fibril detection can be biased by the presence of exogenous compounds FEBS J. 276 2009 5960 5972
-
(2009)
FEBS J.
, vol.276
, pp. 5960-5972
-
-
Hudson, S.A.1
Ecroyd, H.2
Kee, T.W.3
Carver, J.A.4
-
25
-
-
40749131329
-
Linkage-dependent contribution of repeat peptides to self-aggregation of three- or four-repeat microtubule-binding domains in tau protein
-
DOI 10.1111/j.1742-4658.2008.06312.x
-
K. Okuyama, C. Nishiura, F. Mizushima, K. Minoura, M. Sumida, T. Taniguchi, K. Tomoo, and T. Ishida Linkage-dependent contribution of repeat peptides to self-aggregation of three- or four-repeat microtubule-binding domains in tau protein FEBS J. 275 2008 1529 1539 (Pubitemid 351388799)
-
(2008)
FEBS Journal
, vol.275
, Issue.7
, pp. 1529-1539
-
-
Okuyama, K.1
Nishiura, C.2
Mizushima, F.3
Minoura, K.4
Sumida, M.5
Taniguchi, T.6
Tomoo, K.7
Ishida, T.8
-
26
-
-
84894029931
-
A new route towards fluorescent organic nanoparticles with red-shifted emission and increased colloidal stability
-
K. Amro, J. Daniel, G. Clermont, T. Bsaibess, M. Pucheault, E. Genin, M. Vaultier, and M. Blanchard-Desce A new route towards fluorescent organic nanoparticles with red-shifted emission and increased colloidal stability Tetrahedron 70 2014 1903 1909
-
(2014)
Tetrahedron
, vol.70
, pp. 1903-1909
-
-
Amro, K.1
Daniel, J.2
Clermont, G.3
Bsaibess, T.4
Pucheault, M.5
Genin, E.6
Vaultier, M.7
Blanchard-Desce, M.8
-
27
-
-
84876566725
-
Efficient planar organic semiconductors containing fused triphenylamine for solution processed small molecule organic solar cells
-
K. Do, C. Kim, K. Song, S.J. Yun, J.K. Lee, and J. Ko Efficient planar organic semiconductors containing fused triphenylamine for solution processed small molecule organic solar cells Sol. Energy Mater. Sol. Cells 115 2013 52 57
-
(2013)
Sol. Energy Mater. Sol. Cells
, vol.115
, pp. 52-57
-
-
Do, K.1
Kim, C.2
Song, K.3
Yun, S.J.4
Lee, J.K.5
Ko, J.6
-
28
-
-
84897971278
-
Hyper-bright" near-infrared emitting fluorescent organic nanoparticles for single particle tracking
-
E. Genin, Z. Gao, J.A. Varela, J. Daniel, T. Bsaibess, I. Gosse, L. Groc, L. Cognet, and M. Blanchard-Desce "Hyper-bright" near-infrared emitting fluorescent organic nanoparticles for single particle tracking Adv. Mater. 26 2014 2258 2261
-
(2014)
Adv. Mater.
, vol.26
, pp. 2258-2261
-
-
Genin, E.1
Gao, Z.2
Varela, J.A.3
Daniel, J.4
Bsaibess, T.5
Gosse, I.6
Groc, L.7
Cognet, L.8
Blanchard-Desce, M.9
-
29
-
-
84863421792
-
Absorption enhancement of oligothiophene dyes through the use of a cyanopyridone acceptor group in solution-processed organic solar cells
-
A. Gupta, A. Ali, A. Bilic, M. Gao, K. Hegedus, B. Singh, S.E. Watkins, G.J. Wilson, U. Bach, and R.A. Evans Absorption enhancement of oligothiophene dyes through the use of a cyanopyridone acceptor group in solution-processed organic solar cells Chem. Commun. 48 2012 1889 1891
-
(2012)
Chem. Commun.
, vol.48
, pp. 1889-1891
-
-
Gupta, A.1
Ali, A.2
Bilic, A.3
Gao, M.4
Hegedus, K.5
Singh, B.6
Watkins, S.E.7
Wilson, G.J.8
Bach, U.9
Evans, R.A.10
-
30
-
-
84876586916
-
Synthesis and characterization of 2D-D-π-A-type organic dyes bearing bis(3,6-di-tert-butylcarbazol-9-ylphenyl)aniline as donor moiety for dye-sensitized solar cells
-
T. Khanasa, N. Jantasing, S. Morada, N. Leesakul, R. Tarsang, S. Namuangruk, T. Kaewin, S. Jungsuttiwong, T. Sudyoadsuk, and V. Promarak Synthesis and characterization of 2D-D-π-A-type organic dyes bearing bis(3,6-di-tert-butylcarbazol-9-ylphenyl)aniline as donor moiety for dye-sensitized solar cells Eur. J. Org. Chem. 2013 2013 2608 2620
-
(2013)
Eur. J. Org. Chem.
, vol.2013
, pp. 2608-2620
-
-
Khanasa, T.1
Jantasing, N.2
Morada, S.3
Leesakul, N.4
Tarsang, R.5
Namuangruk, S.6
Kaewin, T.7
Jungsuttiwong, S.8
Sudyoadsuk, T.9
Promarak, V.10
-
31
-
-
19544383985
-
Organic dyes incorporating low-band-gap chromophores for dye-sensitized solar cells
-
DOI 10.1021/ol050417f
-
M. Velusamy, K.R.J. Thomas, J.T. Lin, Y.-C. Hsu, and K.-C. Ho Organic dyes incorporating low-band-gap chromophores for dye-sensitized solar cells Org. Lett. 7 2005 1899 1902 (Pubitemid 40732008)
-
(2005)
Organic Letters
, vol.7
, Issue.10
, pp. 1899-1902
-
-
Velusamy, M.1
Thomas, K.R.J.2
Lin, J.T.3
Hsu, Y.-C.4
Ho, K.-C.5
-
32
-
-
79951610276
-
Organic D-A-π-A solar cell sensitizers with improved stability and spectral response
-
W. Zhu, Y. Wu, S. Wang, W. Li, X. Li, J. Chen, Z.-S. Wang, and H. Tian Organic D-A-π-A solar cell sensitizers with improved stability and spectral response Adv. Funct. Mater. 21 2011 756 763
-
(2011)
Adv. Funct. Mater.
, vol.21
, pp. 756-763
-
-
Zhu, W.1
Wu, Y.2
Wang, S.3
Li, W.4
Li, X.5
Chen, J.6
Wang, Z.-S.7
Tian, H.8
|