메뉴 건너뛰기




Volumn 85, Issue , 2014, Pages 228-234

Development of dual targeting inhibitors against aggregations of amyloid-β and tau protein

Author keywords

Aggregation; Alzheimer's disease; Amyloid ; Suzuki Miyaura coupling; Tau

Indexed keywords

ALDEHYDE DERIVATIVE; AMYLOID BETA PROTEIN; DYE; MALONONITRILE; METHYLENE BLUE; TAU PROTEIN; THIOPHENE DERIVATIVE; HETEROCYCLIC COMPOUND; AMYLOID BETA-PROTEIN (1-42); PEPTIDE FRAGMENT;

EID: 84905437056     PISSN: 02235234     EISSN: 17683254     Source Type: Journal    
DOI: 10.1016/j.ejmech.2014.07.095     Document Type: Article
Times cited : (46)

References (32)
  • 1
    • 70349638299 scopus 로고    scopus 로고
    • 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 scopus 로고    scopus 로고
    • 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 scopus 로고    scopus 로고
    • 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
  • 6
    • 84867830552 scopus 로고    scopus 로고
    • 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 scopus 로고    scopus 로고
    • 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
  • 10
    • 65149102326 scopus 로고    scopus 로고
    • 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
  • 12
    • 84861532193 scopus 로고    scopus 로고
    • 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 scopus 로고    scopus 로고
    • 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 scopus 로고    scopus 로고
    • 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 scopus 로고    scopus 로고
    • 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 scopus 로고    scopus 로고
    • 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 scopus 로고
    • 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
  • 18
  • 19
    • 0001029926 scopus 로고
    • 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 scopus 로고    scopus 로고
    • 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 scopus 로고    scopus 로고
    • 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 scopus 로고
    • 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 scopus 로고    scopus 로고
    • 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 scopus 로고    scopus 로고
    • 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
  • 27
    • 84876566725 scopus 로고    scopus 로고
    • 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
  • 29
    • 84863421792 scopus 로고    scopus 로고
    • 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
  • 31
    • 19544383985 scopus 로고    scopus 로고
    • 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 scopus 로고    scopus 로고
    • 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


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.