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Volumn 70, Issue , 2013, Pages 233-247

A stereoselective approach to peptidomimetic BACE1 inhibitors

Author keywords

Alzheimer's disease; BACE1; Benzodiazepines; Inhibitors; Peptidomimetics

Indexed keywords

2 (BENZYLOXYCARBONYLAMINO) N (2 BENZOYL 5 (( 1 HYDROXY) 2 (BENZYL(TERT BUTOXYCARBONYLAMINO))ETHYL)PHENYL) 2 PHENYLACETAMIDE; 2 (BENZYLOXYCARBONYLAMINO) N (3 (( 1 HYDROXY) 2 ( 1 BENZYL 2 HYDROXYETHYL)AMINOETHYL)PHENYL) 2 PHENYLACETAMIDE; 2 (BENZYLOXYCARBONYLAMINO) N (3 (( 1 HYDROXY) 2 (( 1 PHENYL 2 HYDROXYETHYL)(TERT BUTOXYCARBONYLAMINO))ETHYL)PHENYL) 2 PHENYLACETAMIDE; 2 (BENZYLOXYCARBONYLAMINO) N(3 (( 1 HYDROXY) 2 (BENZYL(TERT BUTOXYCARBONYLAMINO))ETHYL)PHENYL) 2 PHENYLACETAMIDE; 3 PHENYL 9 (4 TERT BUTOXYCARBONYLPIPERAZIN 1 YL) 1,3 DIHYDROBENZO[E][1,4]DIAZEPIN 2 ONE; 3,6 DIPHENYL 9 (4 TERT BUTOXYCARBONYLPIPERAZIN 1 YL) 1,3 DIHYDROBENZO[E][1,4]DIAZEPIN 2 ONE; 3,6 DIPHENYL 9 (4 TERT BUTOXYCARBONYLPIPERAZIN 1 YL) 1,3,4,5 TETRAHYDROBENZO[E][1,4]DIAZEPIN 2 ONE; 3,6 DIPHENYL 9 (PIPERAZIN 1 YL) 1,3 DIHYDROBENZO[E] [1,4]DIAZEPIN 2 ONE; BENZODIAZEPINE DERIVATIVE; BETA SECRETASE INHIBITOR; LIGAND; N (3 (( 1 HYDROXY) 2 (BENZYL(TERT BUTOXYCARBONYLAMINO)) ETHYL)PHENYL) 1 NAPHTHAMIDE; UNCLASSIFIED DRUG; [2 ((9H FLUOREN 9 YLMETHOXYCARBONYLAMINO) 2 PHENYLACETAMIDO) 3 (4 TERT BUTOXYCARBONYLPIPERAZIN 1 YL) 6 PHENYL]BENZALDEHYDE; [2 (BENZYLOXYCARBONYLAMINO 2 PHENYLACETAMIDO) 3 (4 TERT BUTOXYCARBONYLPIPERAZIN 1 YL)]BENZALDEHYDE;

EID: 84886039061     PISSN: 02235234     EISSN: 17683254     Source Type: Journal    
DOI: 10.1016/j.ejmech.2013.09.056     Document Type: Article
Times cited : (16)

References (34)
  • 2
    • 77951776829 scopus 로고    scopus 로고
    • Alzheimer's disease: Strategies for disease modification
    • M. Citron Alzheimer's disease: strategies for disease modification Nat. Rev. Drug Discovery 9 2010 387 398
    • (2010) Nat. Rev. Drug Discovery , vol.9 , pp. 387-398
    • Citron, M.1
  • 3
    • 84867477898 scopus 로고    scopus 로고
    • The amyloid beta peptide: A chemist's perspective. Role in Alzheimer's and fibrillization
    • I.W. Hamley The amyloid beta peptide: a chemist's perspective. Role in Alzheimer's and fibrillization Chem. Rev. 112 2012 5147 5192
    • (2012) Chem. Rev. , vol.112 , pp. 5147-5192
    • Hamley, I.W.1
  • 4
    • 84857642949 scopus 로고    scopus 로고
    • The toxic Abeta oligomer and Alzheimer's disease: An emperor in need of clothes
    • I. Benilova, E. Karran, and B. De Strooper The toxic Abeta oligomer and Alzheimer's disease: an emperor in need of clothes Nat. Neurosci. 15 2012 349 357
    • (2012) Nat. Neurosci. , vol.15 , pp. 349-357
    • Benilova, I.1    Karran, E.2    De Strooper, B.3
  • 5
    • 34248190279 scopus 로고    scopus 로고
    • A beta oligomers - A decade of discovery
    • D.M. Walsh, and D.J. Selkoe A beta oligomers - a decade of discovery J. Neurochem. 101 2007 1172 1184
    • (2007) J. Neurochem. , vol.101 , pp. 1172-1184
    • Walsh, D.M.1    Selkoe, D.J.2
  • 6
    • 0027374493 scopus 로고
    • Normal cellular processing of the β-amyloid precursor protein results in the secretion of the amyloid β peptide and related molecules
    • DOI 10.1111/j.1749-6632.1993.tb23037.x
    • C. Haass, A.Y. Hung, M.G. Schlossmacher, T. Oltersdorf, D.B. Teplow, and D.J. Selkoe Normal cellular processing of the beta-amyloid precursor protein results in the secretion of the amyloid beta peptide and related molecules Ann. N. Y. Acad. Sci. 695 1993 109 116 (Pubitemid 23348246)
    • (1993) Annals of the New York Academy of Sciences , vol.695 , pp. 109-116
    • Haass, C.1    Hung, A.Y.2    Schlossmacher, M.G.3    Oltersdorf, T.4    Teplow, D.B.5    Selkoe, D.J.6
  • 9
    • 34347326512 scopus 로고    scopus 로고
    • Disease modifying approaches for Alzheimer's pathology
    • DOI 10.2174/138161207781039788
    • M. Sadowski, and T. Wisniewski Disease modifying approaches for Alzheimer's pathology Curr. Pharm. Des. 13 2007 1943 1954 (Pubitemid 47040494)
    • (2007) Current Pharmaceutical Design , vol.13 , Issue.19 , pp. 1943-1954
    • Sadowski, M.1    Wisniewski, T.2
  • 10
    • 84887026379 scopus 로고    scopus 로고
    • The structural evolution of beta-secretase inhibitors: A focus on the development of small-molecule inhibitors
    • S. Butini, S. Brogi, E. Novellino, G. Campiani, A.K. Ghosh, M. Brindisi, and S. Gemma The structural evolution of beta-secretase inhibitors: a focus on the development of small-molecule inhibitors Curr. Top. Med. Chem. 13 2013 1787 1807
    • (2013) Curr. Top. Med. Chem. , vol.13 , pp. 1787-1807
    • Butini, S.1    Brogi, S.2    Novellino, E.3    Campiani, G.4    Ghosh, A.K.5    Brindisi, M.6    Gemma, S.7
  • 11
    • 77951060145 scopus 로고    scopus 로고
    • Proteases and proteolysis in Alzheimer disease: A multifactorial view on the disease process
    • B. De Strooper Proteases and proteolysis in Alzheimer disease: a multifactorial view on the disease process Physiol. Rev. 90 2010 465 494
    • (2010) Physiol. Rev. , vol.90 , pp. 465-494
    • De Strooper, B.1
  • 14
    • 0347694970 scopus 로고    scopus 로고
    • Determination of the Active Site Protonation State of β-Secretase from Molecular Dynamics Simulation and Docking Experiment: Implications for Structure-Based Inhibitor Design
    • DOI 10.1021/ja0304493
    • H. Park, and S. Lee Determination of the active site protonation state of beta-secretase from molecular dynamics simulation and docking experiment: implications for structure-based inhibitor design J. Am. Chem. Soc. 125 2003 16416 16422 (Pubitemid 38020666)
    • (2003) Journal of the American Chemical Society , vol.125 , Issue.52 , pp. 16416-16422
    • Park, H.1    Lee, S.2
  • 15
    • 4644364822 scopus 로고    scopus 로고
    • Apo and inhibitor complex structures of BACE (β-secretase)
    • DOI 10.1016/j.jmb.2004.08.018, PII S0022283604009866
    • S. Patel, L. Vuillard, A. Cleasby, C.W. Murray, and J. Yon Apo and inhibitor complex structures of BACE (beta-secretase) J. Mol. Biol. 343 2004 407 416 (Pubitemid 39296874)
    • (2004) Journal of Molecular Biology , vol.343 , Issue.2 , pp. 407-416
    • Patel, S.1    Vuillard, L.2    Cleasby, A.3    Murray, C.W.4    Yon, J.5
  • 16
    • 0037366605 scopus 로고    scopus 로고
    • The combinatorial synthesis of bicyclic privileged structures or privileged substructures
    • D.A. Horton, G.T. Bourne, and M.L. Smythe The combinatorial synthesis of bicyclic privileged structures or privileged substructures Chem. Rev. 103 2003 893 930
    • (2003) Chem. Rev. , vol.103 , pp. 893-930
    • Horton, D.A.1    Bourne, G.T.2    Smythe, M.L.3
  • 19
    • 0027967498 scopus 로고
    • A mechanistically designed mono-cinchona alkaloid is an excellent catalyst for the enantioselective dihydroxylation of olefins
    • DOI 10.1016/S0040-4039(00)78237-2
    • E.J. Corey, M.C. Noe, and M.J. Grogan A mechanistically designed mono-cinchona alkaloid is an excellent catalyst for the enantioselective dihydroxylation of olefins Tetrahedron Lett. 35 1994 6427 6430 (Pubitemid 24270778)
    • (1994) Tetrahedron Letters , vol.35 , Issue.35 , pp. 6427-6430
    • Corey, E.J.1    Noe, M.C.2    Grogan, M.J.3
  • 24
    • 79951503684 scopus 로고    scopus 로고
    • Assignment of absolute configuration using chiral reagents and NMR spectroscopy
    • T.J. Wenzel, and C.D. Chisholm Assignment of absolute configuration using chiral reagents and NMR spectroscopy Chirality 23 2011 190 214
    • (2011) Chirality , vol.23 , pp. 190-214
    • Wenzel, T.J.1    Chisholm, C.D.2
  • 25
    • 23144446231 scopus 로고    scopus 로고
    • A continuous time-resolved fluorescence assay for identification of BACE1 inhibitors
    • DOI 10.1089/adt.2005.3.287
    • V. Porcari, L. Magnoni, G.C. Terstappen, and W. Fecke A continuous time-resolved fluorescence assay for identification of BACE1 inhibitors Assay Drug Dev. Technol. 3 2005 287 297 (Pubitemid 41079126)
    • (2005) Assay and Drug Development Technologies , vol.3 , Issue.3 , pp. 287-297
    • Porcari, V.1    Magnoni, L.2    Terstappen, G.C.3    Fecke, W.4
  • 27
  • 29
    • 77949825974 scopus 로고    scopus 로고
    • Schrodinger, LLC New York
    • Glide, Version 5.5 2009 Schrodinger, LLC New York
    • (2009) Glide, Version 5.5
  • 30
    • 79953072107 scopus 로고    scopus 로고
    • Schrodinger, LLC New York
    • Maestro, Version 9.0.211 2009 Schrodinger, LLC New York
    • (2009) Maestro, Version 9.0.211


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.