메뉴 건너뛰기




Volumn 89, Issue , 2015, Pages 349-361

Design, synthesis, and biological evaluation of 2-arylethenylquinoline derivatives as multifunctional agents for the treatment of Alzheimer's disease

Author keywords

2 Arylethenylquinoline derivatives; Alzheimer's disease; Antioxidant; A aggregation; Metal chelating

Indexed keywords

4 (4 METHOXYANILINO) 2 (4 DIETHYLAMINO STYRYL)QUINOLINE; 4 (4 METHOXYANILINO) 2 (4 DIMETHYLAMINO STYRYL)QUINOLINE; 4 (4 METHYLPIPERAZIN 1 YL) 2 (2 METHOXYSTYRYL)QUINOLINE; 4 (4 METHYLPIPERAZIN 1 YL) 2 (4 CHLOROSTYRYL)QUINOLINE; 4 (4 METHYLPIPERAZIN 1 YL) 2 (4 DIETHYLAMINO STYRYL)QUINOLINE; 4 (4 METHYLPIPERAZIN 1 YL) 2 (4 DIMETHYLAMINO STYRYL)QUINOLINE; 4 (4 METHYLPIPERAZIN 1 YL) 2 (4 FLUOROSTYRYL)QUINOLINE; 4 (4 METHYLPIPERAZIN 1 YL) 2 (4 METHOXYSTYRYL)QUINOLINE; 4 (4 METHYLPIPERAZIN 1 YL) 2 (4 NITROSTYRYL)QUINOLINE; 4 (4 METHYLPIPERAZIN 1 YL) 2 STYRYL QUINOLINE; 4 (4 METHYLPIPERAZIN 1 YL) 2 [(1H INDOL 3 YL)ETHENYL]QUINOLINE; 4 (4 METHYLPIPERAZIN 1 YL) 2 [(9 ETHYL 9H CARBAZOL 3YL)ETHENYL]QUINOLINE; 4 (4 METHYLPIPERAZIN 1 YL) 2 [4 (METHYLPIPERAZIN 1 YL)STYRYL]QUINOLINE; 4 (4 METHYLPIPERAZIN 1 YL) 2 [4 (MORPHOLIN 1 YL)STYRYL]QUINOLINE; 4 (PIPERID 1 YL) 2 (4 NITROSTYRYL)QUINOLINE; 4 (PIPERID 1 YL) 2 [(9 ETHYL 9H CARBAZOL 3 YL)ETHENYL]QUINOLINE; 4 PIPERIDYL 2 (2 METHOXYSTYRYL)QUINOLINE; 4 PIPERIDYL 2 (4 CHLOROSTYRYL)QUINOLINE; 4 PIPERIDYL 2 (4 DIETHYLAMINO STYRYL)QUINOLINE; 4 PIPERIDYL 2 (4 DIMETHYLAMINO STYRYL)QUINOLINE; 4 PIPERIDYL 2 (4 METHOXYSTYRYL)QUINOLINE; 4 PIPERIDYL 2 (4 MORPHOLIN 1 YL STYRYL)QUINOLINE; ACETYLCHOLINESTERASE; AMYLOID BETA PROTEIN[1-42]; ANTIOXIDANT; CHELATING AGENT; CHOLINESTERASE; QUINOLINE DERIVATIVE; TROLOX C; UNCLASSIFIED DRUG; UNINDEXED DRUG; AMYLOID BETA PROTEIN; AMYLOID BETA-PROTEIN (1-42); CHOLINESTERASE INHIBITOR; PEPTIDE FRAGMENT; STILBENE DERIVATIVE;

EID: 84928630909     PISSN: 02235234     EISSN: 17683254     Source Type: Journal    
DOI: 10.1016/j.ejmech.2014.10.018     Document Type: Article
Times cited : (60)

References (61)
  • 1
    • 17344385275 scopus 로고    scopus 로고
    • Clinical features of Alzheimer's disease
    • H. Forstl, A. Kurz, Clinical features of Alzheimer's disease, Eur. Arch. Psychiatry Clin. N. 249 (1999) 288-290.
    • (1999) Eur. Arch. Psychiatry Clin. N. , vol.249 , pp. 288-290
    • Forstl, H.1    Kurz, A.2
  • 2
    • 78650462753 scopus 로고    scopus 로고
    • Alzheimer's disease: A general introduction and pathomechanism
    • V.H. Finder, Alzheimer's disease: a general introduction and pathomechanism, J. Alzheimers Dis. 22 (2010) 5-19.
    • (2010) J. Alzheimers Dis. , vol.22 , pp. 5-19
    • Finder, V.H.1
  • 3
    • 33750731675 scopus 로고    scopus 로고
    • 100 years and counting: Prospects for defeating Alzheimer's disease
    • E.D. Roberson, L. Mucke, 100 years and counting: prospects for defeating Alzheimer's disease, Science 314 (2006) 781-784.
    • (2006) Science , vol.314 , pp. 781-784
    • Roberson, E.D.1    Mucke, L.2
  • 7
    • 0042433479 scopus 로고    scopus 로고
    • The cholinergic hypothesis of age and Alzheimer's disease-related cognitive deficits: Recent challenges and their implications for novel drug development
    • A.V. Terry, J.J. Buccafusco, The cholinergic hypothesis of age and Alzheimer's disease-related cognitive deficits: recent challenges and their implications for novel drug development, J. Pharmacol. Exp. Ther. 306 (2003) 821-827.
    • (2003) J. Pharmacol. Exp. Ther. , vol.306 , pp. 821-827
    • Terry, A.V.1    Buccafusco, J.J.2
  • 8
    • 67651180986 scopus 로고    scopus 로고
    • The amyloid hypothesis for Alzheimer's disease: A critical reappraisal
    • J. Hardy, The amyloid hypothesis for Alzheimer's disease: a critical reappraisal, J. Neurochem. 110 (2009) 1129-1134.
    • (2009) J. Neurochem. , vol.110 , pp. 1129-1134
    • Hardy, J.1
  • 9
    • 0033600274 scopus 로고    scopus 로고
    • Translating cell biology into therapeutic advances in Alzheimer's disease
    • D.J. Selkoe, Translating cell biology into therapeutic advances in Alzheimer's disease, Nature 399 (1999) A23-A31.
    • (1999) Nature , vol.399 , pp. A23-A31
    • Selkoe, D.J.1
  • 10
    • 0037135111 scopus 로고    scopus 로고
    • The amyloid hypothesis of Alzheimer's disease: Progress and problems on the road to therapeutics
    • J. Hardy, D.J. Selkoe, The amyloid hypothesis of Alzheimer's disease: progress and problems on the road to therapeutics, Science 297 (2002) 353-356.
    • (2002) Science , vol.297 , pp. 353-356
    • Hardy, J.1    Selkoe, D.J.2
  • 12
    • 1542364225 scopus 로고    scopus 로고
    • Curcumin has potent antiamyloidogenic effects for Alzheimer's beta-amyloid fibrils in vitro
    • K. Ono, K. Hasegawa, H. Naiki, M. Yamada, Curcumin has potent antiamyloidogenic effects for Alzheimer's beta-amyloid fibrils in vitro, Neurosci. Res. 75 (2004) 742-750.
    • (2004) Neurosci. Res. , vol.75 , pp. 742-750
    • Ono, K.1    Hasegawa, K.2    Naiki, H.3    Yamada, M.4
  • 15
    • 34347263391 scopus 로고    scopus 로고
    • Curcumin derivatives inhibit or modulate beta-amyloid precursor protein metabolism
    • R. Narlawar, K. Baumann, R. Schubenel, B. Schmidt, Curcumin derivatives inhibit or modulate beta-amyloid precursor protein metabolism, Neurodegener. Dis. 4 (2007) 88-93.
    • (2007) Neurodegener. Dis. , vol.4 , pp. 88-93
    • Narlawar, R.1    Baumann, K.2    Schubenel, R.3    Schmidt, B.4
  • 16
    • 84879690631 scopus 로고    scopus 로고
    • Selective inhibition of human acetylcholinesterase by xanthine derivatives: In vitro inhibition and molecular modeling investigations
    • T. Mohamed, W. Osmana, G. Tina, P.P. Raoa, Selective inhibition of human acetylcholinesterase by xanthine derivatives: in vitro inhibition and molecular modeling investigations, Bioorg. Med. Chem. Lett. 23 (2013) 4336-4341.
    • (2013) Bioorg. Med. Chem. Lett. , vol.23 , pp. 4336-4341
    • Mohamed, T.1    Osmana, W.2    Tina, G.3    Raoa, P.P.4
  • 17
    • 35748978820 scopus 로고    scopus 로고
    • Recent developments in cholinesterases inhibitors for Alzheimer's disease treatment
    • A. Musial, M. Bajda, B. Malawska, Recent developments in cholinesterases inhibitors for Alzheimer's disease treatment, Curr. Med. Chem. 14 (2007) 2654-2679.
    • (2007) Curr. Med. Chem. , vol.14 , pp. 2654-2679
    • Musial, A.1    Bajda, M.2    Malawska, B.3
  • 18
    • 0032078728 scopus 로고    scopus 로고
    • Invited review: Cholinesterase inhibitors for Alzheimer's disease therapy: From tacrine to future applications
    • E. Giacobini, Invited review: cholinesterase inhibitors for Alzheimer's disease therapy: from tacrine to future applications, Neurochem. Int. 32 (1998) 413-419.
    • (1998) Neurochem. Int. , vol.32 , pp. 413-419
    • Giacobini, E.1
  • 19
    • 0346656610 scopus 로고    scopus 로고
    • Acetylcholinesterase inhibition in Alzheimer's disease
    • B. Ibach, E. Haen, Acetylcholinesterase inhibition in Alzheimer's disease, Curr. Pharm. Des. 10 (2004) 231-251.
    • (2004) Curr. Pharm. Des. , vol.10 , pp. 231-251
    • Ibach, B.1    Haen, E.2
  • 21
    • 84655161993 scopus 로고    scopus 로고
    • Butyrylcholinesterase is associated with β-amyloid plaques in the transgenic APP SWE/PSEN1d-9 mouse model of alzheimer disease
    • S. Darvesh, M.K. Cash, G.A. Reid, E. Martin, A. Mitnitski, C. Geula, Butyrylcholinesterase is associated with β-amyloid plaques in the transgenic APP SWE/PSEN1d-9 mouse model of alzheimer disease, J. Neuropathol. Exp. Neurol. 71 (2012) 2-14.
    • (2012) J. Neuropathol. Exp. Neurol. , vol.71 , pp. 2-14
    • Darvesh, S.1    Cash, M.K.2    Reid, G.A.3    Martin, E.4    Mitnitski, A.5    Geula, C.6
  • 24
    • 56349145099 scopus 로고    scopus 로고
    • Oxidative stress hypothesis in Alzheimer's disease: A reappraisal
    • D. Praticò, Oxidative stress hypothesis in Alzheimer's disease: a reappraisal, Trends Pharmacol. Sci. 29 (2008) 609-615.
    • (2008) Trends Pharmacol. Sci. , vol.29 , pp. 609-615
    • Praticò, D.1
  • 25
    • 54249103057 scopus 로고    scopus 로고
    • Drug development based on the metals hypothesis of Alzheimer's disease
    • A.I. Bush, Drug development based on the metals hypothesis of Alzheimer's disease, J. Alzheimers Dis. 15 (2008) 223-240.
    • (2008) J. Alzheimers Dis. , vol.15 , pp. 223-240
    • Bush, A.I.1
  • 26
    • 67649392464 scopus 로고    scopus 로고
    • Alzheimer's disease, metal ions and metal homeostatic therapy
    • P. Zatta, D. Drago, S. Bolognin, S.L. Sensi, Alzheimer's disease, metal ions and metal homeostatic therapy, Trends Pharmacol. Sci. 30 (2009) 346-355.
    • (2009) Trends Pharmacol. Sci. , vol.30 , pp. 346-355
    • Zatta, P.1    Drago, D.2    Bolognin, S.3    Sensi, S.L.4
  • 28
    • 1842504323 scopus 로고    scopus 로고
    • Redox-active metals, oxidative stress, and Alzheimer's disease pathology
    • X. Huang, R.D. Moir, R.E. Tanzi, A.I. Bush, J.T. Rogers, Redox-active metals, oxidative stress, and Alzheimer's disease pathology, Ann. N. Y. Acad. Sci. 1012 (2004) 153-163.
    • (2004) Ann. N. Y. Acad. Sci. , vol.1012 , pp. 153-163
    • Huang, X.1    Moir, R.D.2    Tanzi, R.E.3    Bush, A.I.4    Rogers, J.T.5
  • 30
    • 10744224267 scopus 로고    scopus 로고
    • Metal-protein attenuation with iodochlorhydroxyquin (clioquinol) targeting Abeta amyloid deposition and toxicity in Alzheimer disease: A pilot phase 2 clinical trial
    • C.W. Ritchie, et al., Metal-protein attenuation with iodochlorhydroxyquin (clioquinol) targeting Abeta amyloid deposition and toxicity in Alzheimer disease: a pilot phase 2 clinical trial, Arch. Neurol. 60 (2003) 1685-1691.
    • (2003) Arch. Neurol. , vol.60 , pp. 1685-1691
    • Ritchie, C.W.1
  • 33
    • 84918793217 scopus 로고    scopus 로고
    • Multi-target design strategies in the context of Alzheimer's disease: Acetylcholinesterase inhibition and NMDA receptor antagonism as the driving forces
    • M. Rosini, E. Simoni, A. Minarini, C. Melchiorre, Multi-target design strategies in the context of Alzheimer's disease: acetylcholinesterase inhibition and NMDA receptor antagonism as the driving forces, Neurochem. Res. 39 (2014) 1914-1923.
    • (2014) Neurochem. Res. , vol.39 , pp. 1914-1923
    • Rosini, M.1    Simoni, E.2    Minarini, A.3    Melchiorre, C.4
  • 35
    • 14844318072 scopus 로고    scopus 로고
    • Chemotherapeutic potential of the chemopreventive phytoalexin resveratrol
    • S. Pervaiz, Chemotherapeutic potential of the chemopreventive phytoalexin resveratrol, Drug Resist. Updates 7 (2004) 333-344.
    • (2004) Drug Resist. Updates , vol.7 , pp. 333-344
    • Pervaiz, S.1
  • 36
    • 33745962138 scopus 로고    scopus 로고
    • Therapeutic potential of resveratrol: The in vivo evidence
    • J.A. Baur, D.A. Sinclair, Therapeutic potential of resveratrol: the in vivo evidence, Nat. Rev. Drug Discov. 5 (2006) 493-506.
    • (2006) Nat. Rev. Drug Discov. , vol.5 , pp. 493-506
    • Baur, J.A.1    Sinclair, D.A.2
  • 37
    • 0141642253 scopus 로고    scopus 로고
    • Potent anti-amyloidogenic and fibril-destabilizing effects of poly phenols in vitro: Implications for the prevention and therapeutics of Alzheimer's disease
    • K. Ono, Y. Yoshiike, A. Takashima, K. Hasegawa, H. Naiki, M. Yamada, Potent anti-amyloidogenic and fibril-destabilizing effects of poly phenols in vitro: implications for the prevention and therapeutics of Alzheimer's disease, J. Neurochem. 87 (2003) 172-181.
    • (2003) J. Neurochem. , vol.87 , pp. 172-181
    • Ono, K.1    Yoshiike, Y.2    Takashima, A.3    Hasegawa, K.4    Naiki, H.5    Yamada, M.6
  • 39
    • 77649208936 scopus 로고    scopus 로고
    • Consuming a diet supplemented with resveratrol reduced infection-related neuroinflammation and deficits in working memory in aged mice
    • J. Abraham, R.W. Johnson, Consuming a diet supplemented with resveratrol reduced infection-related neuroinflammation and deficits in working memory in aged mice, Rejuvenation Res. 12 (2009) 445-453.
    • (2009) Rejuvenation Res. , vol.12 , pp. 445-453
    • Abraham, J.1    Johnson, R.W.2
  • 40
    • 84907494997 scopus 로고    scopus 로고
    • Antioxidant and anti-inflammatory effects of selected natural compounds contained in a dietary supplement on two human immortalized keratinocyte lines
    • (Epub)
    • E. Fasano, S. Serini, N. Mondella, S. Trombino, L. Celleno, P. Lanza, A. Cittadini, G. Calviello, Antioxidant and anti-inflammatory effects of selected natural compounds contained in a dietary supplement on two human immortalized keratinocyte lines. Biomed. Res. Int., http://dx.doi.org/10.1155/2014/327452 (Epub 2014).
    • (2014) Biomed. Res. Int.
    • Fasano, E.1    Serini, S.2    Mondella, N.3    Trombino, S.4    Celleno, L.5    Lanza, P.6    Cittadini, A.7    Calviello, G.8
  • 42
    • 79961047423 scopus 로고    scopus 로고
    • Resveratrol and health a comprehensive review of human clinical trials
    • J.M. Smoliga, J.A. Baur, H.A. Hausenblas, Resveratrol and health a comprehensive review of human clinical trials, Mol. Nutr. Food Res. 55 (2011) 1129-1141.
    • (2011) Mol. Nutr. Food Res. , vol.55 , pp. 1129-1141
    • Smoliga, J.M.1    Baur, J.A.2    Hausenblas, H.A.3
  • 43
    • 84867413445 scopus 로고    scopus 로고
    • Automated synthesis of [18F]florbetaben as Alzheimer's disease imaging agent based on a synthesis module system
    • H.L. Wang, X.Y. Guo, S.D. Jiang, G.H. Tang, Automated synthesis of [18F]florbetaben as Alzheimer's disease imaging agent based on a synthesis module system, Appl. Radiat. Isotopes 71 (2013) 41-46.
    • (2013) Appl. Radiat. Isotopes , vol.71 , pp. 41-46
    • Wang, H.L.1    Guo, X.Y.2    Jiang, S.D.3    Tang, G.H.4
  • 44
    • 84863077449 scopus 로고    scopus 로고
    • 81F-labeled styryltriazole and resveratrol derivatives for β-amyloid plaque imaging
    • 81F-labeled styryltriazole and resveratrol derivatives for β-amyloid plaque imaging, J. Med. Chem. 55 (2012) 883-892.
    • (2012) J. Med. Chem. , vol.55 , pp. 883-892
    • Lee, I.1    Choe, Y.S.2    Choi, J.Y.3    Lee, K.H.4    Kim, B.T.5
  • 46
    • 0025907011 scopus 로고
    • Tacrine: A pharmacological review
    • S.E. Freeman, R.M. Dawson, Tacrine: a pharmacological review, Prog. Neurobiol. 36 (1991) 257-277.
    • (1991) Prog. Neurobiol. , vol.36 , pp. 257-277
    • Freeman, S.E.1    Dawson, R.M.2
  • 47
    • 70350597464 scopus 로고    scopus 로고
    • Effects of clioquinol on metaltriggered amyloid-β aggregation revisited
    • A.M. Mancino, S.S. Hindo, A. Kochi, M.H. Lim, Effects of clioquinol on metaltriggered amyloid-β aggregation revisited, Inorg. Chem. 48 (2009) 9596-9598.
    • (2009) Inorg. Chem. , vol.48 , pp. 9596-9598
    • Mancino, A.M.1    Hindo, S.S.2    Kochi, A.3    Lim, M.H.4
  • 49
    • 80655146741 scopus 로고    scopus 로고
    • Benzenediolberberine hybrids: Multifunctional agents for Alzheimer's disease
    • H.L. Jiang, X. Wang, L. Huang, Z. Luo, T. Su, K. Ding, X. Li, Benzenediolberberine hybrids: multifunctional agents for Alzheimer's disease, Bioorg. Med. Chem. 19 (2011) 7228-7235.
    • (2011) Bioorg. Med. Chem. , vol.19 , pp. 7228-7235
    • Jiang, H.L.1    Wang, X.2    Huang, L.3    Luo, Z.4    Su, T.5    Ding, K.6    Li, X.7
  • 50
    • 28844431542 scopus 로고    scopus 로고
    • Search for dual function inhibitors for Alzheimer's disease: Synthesis and biological activity of acetylcholinesterase inhibitors of pyridinium-type and their Abeta fibril formation inhibition capacity
    • P. Kapková, V. Alptüzün, P. Frey, E. Erciyas, U. Holzgrabe, Search for dual function inhibitors for Alzheimer's disease: synthesis and biological activity of acetylcholinesterase inhibitors of pyridinium-type and their Abeta fibril formation inhibition capacity, Bioorg. Med. Chem. 14 (2006) 472-478.
    • (2006) Bioorg. Med. Chem. , vol.14 , pp. 472-478
    • Kapková, P.1    Alptüzün, V.2    Frey, P.3    Erciyas, E.4    Holzgrabe, U.5
  • 51
    • 84877582640 scopus 로고    scopus 로고
    • Facile syntheses of disubstituted bis(vinylquinolinium)benzene derivatives as G-quadruplex DNA binders
    • Z.Q. Liu, S.T. Zhuo, J.H. Tan, T.M. Ou, D. Li, L.Q. Gu, Z.S. Huang, Facile syntheses of disubstituted bis(vinylquinolinium)benzene derivatives as G-quadruplex DNA binders, Tetrahedron 69 (2013) 4922-4932.
    • (2013) Tetrahedron , vol.69 , pp. 4922-4932
    • Liu, Z.Q.1    Zhuo, S.T.2    Tan, J.H.3    Ou, T.M.4    Li, D.5    Gu, L.Q.6    Huang, Z.S.7
  • 52
    • 36849078628 scopus 로고    scopus 로고
    • Insight into the kinetic of amyloid beta (1-42) peptide self-aggregation: Elucidation of inhibitors' mechanism of action
    • M. Bartolini, C. Bertucci, M.L. Bolognesi, A. Cavalli, C. Melchiorre, V. Andrisano, Insight into the kinetic of amyloid beta (1-42) peptide self-aggregation: elucidation of inhibitors' mechanism of action, Chem BioChem 8 (2007) 2152-2161.
    • (2007) Chem BioChem , vol.8 , pp. 2152-2161
    • Bartolini, M.1    Bertucci, C.2    Bolognesi, M.L.3    Cavalli, A.4    Melchiorre, C.5    Andrisano, V.6
  • 53
    • 17344380047 scopus 로고    scopus 로고
    • Extending applicability of the oxygen radical absorbance capacity (ORAC-Fluorescein) assay
    • A. Davalos, C. Gómez-Cordoves, B. Bartolomě, Extending applicability of the oxygen radical absorbance capacity (ORAC-Fluorescein) assay, J. Agric. Food Chem. 52 (2003) 48-54.
    • (2003) J. Agric. Food Chem. , vol.52 , pp. 48-54
    • Davalos, A.1    Gómez-Cordoves, C.2    Bartolomě, B.3
  • 54
    • 0028008584 scopus 로고
    • Characterization of 2′,7′-dichloro-fluorescin fluorescence in dissociated mammalian brain neurons: Estimation on intra cellular content of hydrogen peroxide
    • Y. Oyama, A. Hayashi, T. Ueha, K. Maekawa, Y. Oyama, A. Hayashi, T. Ueha, K. Maekawa, Characterization of 2′,7′-dichloro-fluorescin fluorescence in dissociated mammalian brain neurons: estimation on intra cellular content of hydrogen peroxide, Brain Res. 635 (1994) 113-117.
    • (1994) Brain Res. , vol.635 , pp. 113-117
    • Oyama, Y.1    Hayashi, A.2    Ueha, T.3    Maekawa, K.4    Oyama, Y.5    Hayashi, A.6    Ueha, T.7    Maekawa, K.8
  • 55
    • 37349122146 scopus 로고    scopus 로고
    • Multi-target-directed drug design strategy: From a dual binding site acetylcholinesterase inhibitor to a trifunctional compound against Alzheimer's disease
    • M.L. Bolognesi, A. Cavalli, L. Valgimigli, M. Bartolini, M. Rosini, V. Andrisano, M. Recanatini, C. Melchiorre, Multi-target-directed drug design strategy: from a dual binding site acetylcholinesterase inhibitor to a trifunctional compound against Alzheimer's disease, J. Med. Chem. 50 (2007) 6446-6449.
    • (2007) J. Med. Chem. , vol.50 , pp. 6446-6449
    • Bolognesi, M.L.1    Cavalli, A.2    Valgimigli, L.3    Bartolini, M.4    Rosini, M.5    Andrisano, V.6    Recanatini, M.7    Melchiorre, C.8
  • 58
    • 84880915278 scopus 로고    scopus 로고
    • Design, synthesis, and evaluation of Multitarget-directed resveratrol derivatives for the treatment of alzheimer's disease
    • C.J. Lu, Y.Y. Guo, J. Yan, Z.H. Luo, H.B. Luo, M. Yan, L. Huang, X.S. Li, Design, synthesis, and evaluation of Multitarget-directed resveratrol derivatives for the treatment of alzheimer's disease, J. Med. Chem. 56 (2013) 5843-5859.
    • (2013) J. Med. Chem. , vol.56 , pp. 5843-5859
    • Lu, C.J.1    Guo, Y.Y.2    Yan, J.3    Luo, Z.H.4    Luo, H.B.5    Yan, M.6    Huang, L.7    Li, X.S.8
  • 59
    • 77955865110 scopus 로고    scopus 로고
    • Clicked bivalent ligands containing curcumin and cholesterol as multifunctional abeta oligomerization inhibitors: Design, synthesis, and biological characterization
    • J.A. Lenhart, X. Ling, R. Gandhi, T.L. Guo, P.M. Gerk, D.H. Brunzell, S. Zhang, "Clicked" bivalent ligands containing curcumin and cholesterol as multifunctional abeta oligomerization inhibitors: design, synthesis, and biological characterization, J. Med. Chem. 53 (2010) 6198-6209.
    • (2010) J. Med. Chem. , vol.53 , pp. 6198-6209
    • Lenhart, J.A.1    Ling, X.2    Gandhi, R.3    Guo, T.L.4    Gerk, P.M.5    Brunzell, D.H.6    Zhang, S.7
  • 61
    • 0021061819 scopus 로고
    • Rapid colorimetric assay for cellular growth and survival: Application to proliferation and cytotoxicity assays
    • T. Mosmann, Rapid colorimetric assay for cellular growth and survival: application to proliferation and cytotoxicity assays, J. Immunol. Methods 65 (1983) 55-63.
    • (1983) J. Immunol. Methods , vol.65 , pp. 55-63
    • Mosmann, T.1


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.