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Volumn 17, Issue 3, 2013, Pages 320-328

Inhibitors of BACE for treating alzheimer's disease: A fragment-based drug discovery story

Author keywords

[No Author keywords available]

Indexed keywords

BETA SECRETASE 1; BETA SECRETASE INHIBITOR;

EID: 84878886764     PISSN: 13675931     EISSN: 18790402     Source Type: Journal    
DOI: 10.1016/j.cbpa.2013.04.016     Document Type: Review
Times cited : (53)

References (50)
  • 1
    • 0037135111 scopus 로고    scopus 로고
    • The amyloid hypothesis of Alzheimer's disease: progress and problems on the road to therapeutics
    • Hardy J., Selkoe D.J. The amyloid hypothesis of Alzheimer's 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
  • 2
    • 80052266213 scopus 로고    scopus 로고
    • The amyloid cascade hypothesis for Alzheimer's disease: an appraisal for the development of therapeutics
    • Karran E., Mercken M., De Strooper B. The amyloid cascade hypothesis for Alzheimer's disease: an appraisal for the development of therapeutics. Nat Rev Drug Discov 2011, 10:698-711.
    • (2011) Nat Rev Drug Discov , vol.10 , pp. 698-711
    • Karran, E.1    Mercken, M.2    De Strooper, B.3
  • 8
    • 0034652309 scopus 로고    scopus 로고
    • Human aspartic protease memapsin 2 cleaves the beta-secretase site of beta-amyloid precursor protein
    • Lin X., Koelsch G., Wu S., Downs D., Dashti A., Tang J. Human aspartic protease memapsin 2 cleaves the beta-secretase site of beta-amyloid precursor protein. Proc Natl Acad Sci USA 2000, 97:1456-1460.
    • (2000) Proc Natl Acad Sci USA , vol.97 , pp. 1456-1460
    • Lin, X.1    Koelsch, G.2    Wu, S.3    Downs, D.4    Dashti, A.5    Tang, J.6
  • 10
    • 64349109443 scopus 로고    scopus 로고
    • Progress toward the development of a viable BACE-1 inhibitor
    • Stachel S.J. Progress toward the development of a viable BACE-1 inhibitor. Drug Dev Res 2009, 70:101-110.
    • (2009) Drug Dev Res , vol.70 , pp. 101-110
    • Stachel, S.J.1
  • 11
    • 84861512510 scopus 로고    scopus 로고
    • Small-molecule BACE1 inhibitors: a patent literature review (2006-2011)
    • Probst G., Xu Y.-Z Small-molecule BACE1 inhibitors: a patent literature review (2006-2011). Expert Opin Ther Patents 2012, 22:511-540.
    • (2012) Expert Opin Ther Patents , vol.22 , pp. 511-540
    • Probst, G.1    Xu, Y.-Z.2
  • 13
    • 37849043411 scopus 로고    scopus 로고
    • 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., 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, 50:5912-5925.
    • (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
  • 14
    • 77249094569 scopus 로고    scopus 로고
    • 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 S., Voigt J.H., Kennedy M.E., Beyer B.M., Senior M.M., Smith E.M., Nechuta T.L., Madison V.S., Czarniecki M., 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 2010, 53:942-950.
    • (2010) J Med Chem , vol.53 , pp. 942-950
    • Wang, Y.-S.1    Strickland, S.2    Voigt, J.H.3    Kennedy, M.E.4    Beyer, B.M.5    Senior, M.M.6    Smith, E.M.7    Nechuta, T.L.8    Madison, V.S.9    Czarniecki, M.10
  • 15
    • 77249100811 scopus 로고    scopus 로고
    • 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., 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 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
  • 17
    • 0029836953 scopus 로고    scopus 로고
    • Discovering high-affinity ligands for proteins: SAR by NMR
    • Shuker S.B., Hajduk P.J., Meadows R.P., Fesik S.W. Discovering high-affinity ligands for proteins: SAR by NMR. Science 1996, 274:1531-1534.
    • (1996) Science , vol.274 , pp. 1531-1534
    • Shuker, S.B.1    Hajduk, P.J.2    Meadows, R.P.3    Fesik, S.W.4
  • 18
    • 79958779889 scopus 로고    scopus 로고
    • Fragment-based drug design: tools, practical approaches, and examples
    • Kuo L. Fragment-based drug design: tools, practical approaches, and examples. Methods Enzymol 2011, 493:1-591.
    • (2011) Methods Enzymol , vol.493 , pp. 1-591
    • Kuo, L.1
  • 19
    • 84860511479 scopus 로고    scopus 로고
    • Experiences in fragment-based drug discovery
    • Murray C., Verdonk M., Rees D. Experiences in fragment-based drug discovery. Trends Pharm Sci 2012, 33:224-232.
    • (2012) Trends Pharm Sci , vol.33 , pp. 224-232
    • Murray, C.1    Verdonk, M.2    Rees, D.3
  • 20
    • 84856935181 scopus 로고    scopus 로고
    • Introduction to fragment-based drug discovery
    • Erlanson D. Introduction to fragment-based drug discovery. Top Curr Chem 2012, 317:1-32.
    • (2012) Top Curr Chem , vol.317 , pp. 1-32
    • Erlanson, D.1
  • 21
    • 84862869077 scopus 로고    scopus 로고
    • Fragment-based approaches in drug discovery and chemical biology
    • Scott D., Coyne A., Hudson S., Abell C. Fragment-based approaches in drug discovery and chemical biology. Biochemistry 2012, 51:4990-5003.
    • (2012) Biochemistry , vol.51 , pp. 4990-5003
    • Scott, D.1    Coyne, A.2    Hudson, S.3    Abell, C.4
  • 24
    • 80051860673 scopus 로고    scopus 로고
    • From fragment screening to in vivo efficacy: optimization of a series of 2-aminoquinolines as potent inhibitors of beta-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., et al. From fragment screening to in vivo efficacy: optimization of a series of 2-aminoquinolines as potent inhibitors of beta-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
  • 27
    • 84868570563 scopus 로고    scopus 로고
    • Acyl guanidine inhibitors of β-secretase (BACE-1): optimization of a micromolar hit to a nanomolar lead via iterative solid- and solution-phase library synthesis
    • Gerritz S.W., Zhai W., Shi S., Zhu S., Toyn J.H., Meredith J.E., Iben L.G., Burton C.R., Albright C.F., Good A.C., et al. Acyl guanidine inhibitors of β-secretase (BACE-1): optimization of a micromolar hit to a nanomolar lead via iterative solid- and solution-phase library synthesis. J Med Chem 2012, 55:9208-9223.
    • (2012) J Med Chem , vol.55 , pp. 9208-9223
    • Gerritz, S.W.1    Zhai, W.2    Shi, S.3    Zhu, S.4    Toyn, J.H.5    Meredith, J.E.6    Iben, L.G.7    Burton, C.R.8    Albright, C.F.9    Good, A.C.10
  • 29
    • 80955180214 scopus 로고    scopus 로고
    • Triazole-linked reduced amide isosteres: an approach for the fragment-based drug discovery of anti-Alzheimer's BACE1 inhibitors
    • Monceaux C., Hirata-Fukae C., Lam P., Totrov M., Matsuoka Y., Carlier P. Triazole-linked reduced amide isosteres: an approach for the fragment-based drug discovery of anti-Alzheimer's BACE1 inhibitors. Bioorg Med Chem Lett 2011, 21:3992-3996.
    • (2011) Bioorg Med Chem Lett , vol.21 , pp. 3992-3996
    • Monceaux, C.1    Hirata-Fukae, C.2    Lam, P.3    Totrov, M.4    Matsuoka, Y.5    Carlier, P.6
  • 36
    • 1942453243 scopus 로고    scopus 로고
    • Ligand efficiency: a useful metric for lead selection
    • Hopkins A.L., Groom C.R., Alex A. Ligand efficiency: a useful metric for lead selection. Drug Discov Today 2004, 9:430-431.
    • (2004) Drug Discov Today , vol.9 , pp. 430-431
    • Hopkins, A.L.1    Groom, C.R.2    Alex, A.3
  • 37
    • 77953680038 scopus 로고    scopus 로고
    • Defining desirable central nervous system drug space through the alignment of molecular properties, in vitro ADME, and safety attributes
    • Wager T.T., Chandrasekaran R.Y., Hou X., Troutman M.D., Verhoest P.R., Villalobos A., Will Y. Defining desirable central nervous system drug space through the alignment of molecular properties, in vitro ADME, and safety attributes. ACS Chem Neurosci 2010, 1:420-434.
    • (2010) ACS Chem Neurosci , vol.1 , pp. 420-434
    • Wager, T.T.1    Chandrasekaran, R.Y.2    Hou, X.3    Troutman, M.D.4    Verhoest, P.R.5    Villalobos, A.6    Will, Y.7
  • 39
    • 84868590120 scopus 로고    scopus 로고
    • Design and validation of bicyclic iminopyrimidinones as beta amyloid cleaving enzyme-1 (BACE1) inhibitors: conformational constraint to favor a bioactive conformation
    • Mandal M., Zhu Z., Cumming J.N., Liu X., Strickland S., Mazzola R.D., Caldwell J.P., Leach P., Grzelak M., Hyde L., et al. Design and validation of bicyclic iminopyrimidinones as beta amyloid cleaving enzyme-1 (BACE1) inhibitors: conformational constraint to favor a bioactive conformation. J Med Chem 2012, 55:9331-9345.
    • (2012) J Med Chem , vol.55 , pp. 9331-9345
    • Mandal, M.1    Zhu, Z.2    Cumming, J.N.3    Liu, X.4    Strickland, S.5    Mazzola, R.D.6    Caldwell, J.P.7    Leach, P.8    Grzelak, M.9    Hyde, L.10
  • 42
    • 84868562686 scopus 로고    scopus 로고
    • Design and synthesis of β-site amyloid precursor protein cleaving enzyme (BACE1) inhibitors with in vivo brain reduction of β-amyloid peptides
    • Swahn B.-M., Kolmodin K., Karlstrom S., von Berg S., Soderman P., Holenz J., Berg S., Lindstrom J., Sundstrom M., Turek D., et al. Design and synthesis of β-site amyloid precursor protein cleaving enzyme (BACE1) inhibitors with in vivo brain reduction of β-amyloid peptides. J Med Chem 2012, 55:9346-9361.
    • (2012) J Med Chem , vol.55 , pp. 9346-9361
    • Swahn, B.-M.1    Kolmodin, K.2    Karlstrom, S.3    von Berg, S.4    Soderman, P.5    Holenz, J.6    Berg, S.7    Lindstrom, J.8    Sundstrom, M.9    Turek, D.10
  • 46
    • 84867590210 scopus 로고    scopus 로고
    • Design and synthesis of potent, orally efficacious hydroxyethylamine derived β-site amyloid precursor protein cleaving enzyme (BACE1) inhibitors
    • Dineen T.A., Weiss M.M., Williamson T., Acton P., Babu-Khan S., Bartberger M.D., Brown J., Chen K., Cheng Y., Citron M., et al. Design and synthesis of potent, orally efficacious hydroxyethylamine derived β-site amyloid precursor protein cleaving enzyme (BACE1) inhibitors. J Med Chem 2012, 55:9025-9044.
    • (2012) J Med Chem , vol.55 , pp. 9025-9044
    • Dineen, T.A.1    Weiss, M.M.2    Williamson, T.3    Acton, P.4    Babu-Khan, S.5    Bartberger, M.D.6    Brown, J.7    Chen, K.8    Cheng, Y.9    Citron, M.10
  • 47
    • 0034613320 scopus 로고    scopus 로고
    • Structure of the protease domain of memapsin 2 (beta-secretase) complexed with inhibitor
    • Hong L., Koelsch G., Lin X., Wu S., Terzyan S., Ghosh A.K., Zhang X.C., Tang J. Structure of the protease domain of memapsin 2 (beta-secretase) complexed with inhibitor. Science 2000, 290:150-153.
    • (2000) Science , vol.290 , pp. 150-153
    • Hong, L.1    Koelsch, G.2    Lin, X.3    Wu, S.4    Terzyan, S.5    Ghosh, A.K.6    Zhang, X.C.7    Tang, J.8


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