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Volumn 7, Issue 5, 2015, Pages 609-629

Propargylamine as functional moiety in the design of multifunctional drugs for neurodegenerative disorders: MAO inhibition and beyond

Author keywords

[No Author keywords available]

Indexed keywords

AMINE OXIDASE (FLAVIN CONTAINING); METAL; MONOAMINE OXIDASE INHIBITOR; PROPARGYLAMINE; RASAGILINE; SELEGILINE; UNCLASSIFIED DRUG; PARGYLINE; PROPYLAMINE;

EID: 84930004627     PISSN: 17568919     EISSN: 17568927     Source Type: Journal    
DOI: 10.4155/fmc.15.12     Document Type: Review
Times cited : (85)

References (158)
  • 3
    • 0141741347 scopus 로고    scopus 로고
    • Parkinsons disease: Mechanisms and models
    • Dauer W, Przedborski S. Parkinsons disease: mechanisms and models. Neuron 39(6), 889-909 (2003).
    • (2003) Neuron , vol.39 , Issue.6 , pp. 889-909
    • Dauer, W.1    Przedborski, S.2
  • 4
    • 0024517999 scopus 로고
    • Biogenic amines and their metabolites in Alzheimers disease: Noradrenaline, 5-hydroxytryptamine and 5-hydroxyindole-3-Acetic acid are depleted in the hippocampus but not in substantia innominata
    • Baker GB, Reynolds GP. Biogenic amines and their metabolites in Alzheimers disease: noradrenaline, 5-hydroxytryptamine and 5-hydroxyindole-3-Acetic acid are depleted in the hippocampus but not in substantia innominata. Neurosci. Lett. 100(1-3), 335-339 (1989).
    • (1989) Neurosci. Lett , vol.100 , Issue.1-3 , pp. 335-339
    • Baker, G.B.1    Reynolds, G.P.2
  • 5
    • 0025650794 scopus 로고
    • Serotonin in Alzheimer type dementia and other dementing illnesses
    • Cross AJ. Serotonin in Alzheimer type dementia and other dementing illnesses. Ann. NY Acad. Sci. 600, 405-415 (1990).
    • (1990) Ann. NY Acad. Sci , vol.600 , pp. 405-415
    • Cross, A.J.1
  • 6
    • 67649687124 scopus 로고    scopus 로고
    • The Alzheimers disease mitochondrial cascade hypotheses: An update
    • Swerdlow RH, Khan SM. The Alzheimers disease mitochondrial cascade hypotheses: an update. Exp. Neurol. 218(2), 308-315 (2009).
    • (2009) Exp. Neurol , vol.218 , Issue.2 , pp. 308-315
    • Swerdlow, R.H.1    Khan, S.M.2
  • 7
    • 0027686249 scopus 로고
    • Oxidative stress, glutamate and neurodegenerative disorders
    • Coyle JT, Puttfarcken P. Oxidative stress, glutamate and neurodegenerative disorders. Science 262(5134), 689-695 (1993).
    • (1993) Science , vol.262 , Issue.5134 , pp. 689-695
    • Coyle, J.T.1    Puttfarcken, P.2
  • 8
    • 1842504323 scopus 로고    scopus 로고
    • Redoxactive metals, oxidative stress and Alzheimers disease pathology
    • Huang X, Moir RD, Tanzi RE, Bush AI, Rogers JT. Redoxactive metals, oxidative stress and Alzheimers disease pathology. Ann. NY Acad. Sci. 1012, 153-163 (2004).
    • (2004) Ann. NY 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
  • 9
    • 80155142267 scopus 로고    scopus 로고
    • Future treatments for Parkinsons disease: Surfing the PD pipeline
    • Hauser RA. Future treatments for Parkinsons disease: surfing the PD pipeline. Int. J. Neurosci. 121(2), 53-62 (2011).
    • (2011) Int. J. Neurosci , vol.121 , Issue.2 , pp. 53-62
    • Hauser, R.A.1
  • 10
    • 0032861496 scopus 로고    scopus 로고
    • The neuroprotective effect of a new serotonin receptor agonist, BAY X3702, upon focal ischemic brain damage caused by acute subdural hematoma in the rat
    • Alessandri B, Tsuchida E, Bullock RM. The neuroprotective effect of a new serotonin receptor agonist, BAY X3702, upon focal ischemic brain damage caused by acute subdural hematoma in the rat. Brain Res. 845(2), 232-235 (1999).
    • (1999) Brain Res , vol.845 , Issue.2 , pp. 232-235
    • Alessandri, B.1    Tsuchida, E.2    Bullock, R.M.3
  • 11
    • 0035951899 scopus 로고    scopus 로고
    • New 5-HT1A receptor agonists possessing 1, 4-benzoxazepine scaffold exhibit highly potent anti-ischemic effects
    • Kamei K, Maeda N, Ogino R et al. New 5-HT1A receptor agonists possessing 1, 4-benzoxazepine scaffold exhibit highly potent anti-ischemic effects. Bioorg. Med. Chem. Lett. 11(4), 595-598 (2001).
    • (2001) Bioorg. Med. Chem. Lett , vol.11 , Issue.4 , pp. 595-598
    • Kamei, K.1    Maeda, N.2    Ogino, R.3
  • 12
    • 23044439727 scopus 로고    scopus 로고
    • Dopamine agonist-induced yawning in rats: A dopamine D3 receptormediated behavior
    • Collins GT, Witkin JM, Newman AH et al. Dopamine agonist-induced yawning in rats: a dopamine D3 receptormediated behavior. J. Pharmacol. Exp. Ther. 314(1), 310-319 (2005).
    • (2005) J. Pharmacol. Exp. Ther , vol.314 , Issue.1 , pp. 310-319
    • Collins, G.T.1    Witkin, J.M.2    Newman, A.H.3
  • 13
    • 84871094408 scopus 로고    scopus 로고
    • Recent advances in the multitarget-directed ligands approach for the treatment of Alzheimers disease
    • Leoacute;n R, García AG, Marco-Contelles J. Recent advances in the multitarget-directed ligands approach for the treatment of Alzheimers disease. Med. Res. Rev. 33(1), 139-189 (2013).
    • (2013) Med. Res. Rev , vol.33 , Issue.1 , pp. 139-189
    • Leoacute1    n, R.2    García, A.G.3    Marco-Contelles, J.4
  • 14
    • 17644375125 scopus 로고    scopus 로고
    • CNS Targets for multifunctional drugs in the treatment of Alzheimers and Parkinsons diseases
    • Youdim MHB, Buccafusco JJ. CNS Targets for multifunctional drugs in the treatment of Alzheimers and Parkinsons diseases. J. Neural. Transm. 112(4), 519-537 (2005).
    • (2005) J. Neural. Transm , vol.112 , Issue.4 , pp. 519-537
    • Mhb, Y.1    Buccafusco, J.J.2
  • 15
    • 0037153195 scopus 로고    scopus 로고
    • Novel dual inhibitors of AChE and MAO derived from hydroxy aminoindan and phenethylamine as potential treatment for Alzheimers disease
    • Sterling J, Herzig Y, Goren T et al. Novel dual inhibitors of AChE and MAO derived from hydroxy aminoindan and phenethylamine as potential treatment for Alzheimers disease. J. Med. Chem. 45(24), 5260-5279 (2002).
    • (2002) J. Med. Chem , vol.45 , Issue.24 , pp. 5260-5279
    • Sterling, J.1    Herzig, Y.2    Goren, T.3
  • 16
    • 0029951445 scopus 로고    scopus 로고
    • Does monoamine oxidase type B play a role in dopaminergic nerve cell death in Parkinsons disease?
    • Damier P, Kastner A, Agid Y, Hirsch EC. Does monoamine oxidase type B play a role in dopaminergic nerve cell death in Parkinsons disease? Neurology 46(5), 1262-1269 (1996).
    • (1996) Neurology , vol.46 , Issue.5 , pp. 1262-1269
    • Damier, P.1    Kastner, A.2    Agid, Y.3    Hirsch, E.C.4
  • 17
    • 84929994885 scopus 로고    scopus 로고
    • Design Synthesis and pharmacological evaluation of new coumarin derivatives as monoamine oxidase A and B inhibitors
    • Matos MJ, Santana L, Janeiro P. Design, Synthesis and pharmacological evaluation of new coumarin derivatives as monoamine oxidase A and B inhibitors. ECSOC 12, 1-30 (2008).
    • (2008) ECSOC , vol.12 , pp. 1-30
    • Matos, M.J.1    Santana, L.2    Janeiro, P.3
  • 18
    • 84874527492 scopus 로고    scopus 로고
    • Novel (coumarin- 3-yl)carbamates as selective MAO-B inhibitors: Synthesis, in vitro and in vivo assays, theoretical evaluation of ADME properties and docking study
    • Matos MJ, Vilar S, Gonzalez-Franco R et al. Novel (coumarin- 3-yl)carbamates as selective MAO-B inhibitors: synthesis, in vitro and in vivo assays, theoretical evaluation of ADME properties and docking study. Eur. J. Med. Chem. 63, 151-161 (2013).
    • (2013) Eur. J. Med. Chem , vol.63 , pp. 151-161
    • Matos, M.J.1    Vilar, S.2    Gonzalez-Franco, R.3
  • 19
    • 84878683397 scopus 로고    scopus 로고
    • Propargylamine-derived multitarget-directed ligands: Fighting Alzheimers disease with monoamine oxidase inhibitors
    • Bolea I, Gella A, Unzeta M. Propargylamine-derived multitarget-directed ligands: fighting Alzheimers disease with monoamine oxidase inhibitors. J. Neural. Transm. 120(6), 893-902 (2013).
    • (2013) J. Neural. Transm , vol.120 , Issue.6 , pp. 893-902
    • Bolea, I.1    Gella, A.2    Unzeta, M.3
  • 20
    • 77956092544 scopus 로고    scopus 로고
    • Rasagiline: A novel anti-Parkinsonian monoamine oxidase-B inhibitor with neuroprotective activity
    • Weinreb O, Amit T, Bar-Am O, Youdim MBH. Rasagiline: a novel anti-Parkinsonian monoamine oxidase-B inhibitor with neuroprotective activity. Prog. Neurobiol. 92(3), 330-344 (2010).
    • (2010) Prog. Neurobiol , vol.92 , Issue.3 , pp. 330-344
    • Weinreb, O.1    Amit, T.2    Bar-Am, O.3    Mbh, Y.4
  • 21
    • 12244296145 scopus 로고    scopus 로고
    • Rasagiline: Neurodegeneration, neuroprotection, and mitochondrial permeability transition
    • Youdim MBH, Bar-Am O, Yogev-Falach M et al. Rasagiline: neurodegeneration, neuroprotection, and mitochondrial permeability transition. J. Neurosci. Res. 79(1-2), 172-179 (2005).
    • (2005) J. Neurosci. Res , vol.79 , Issue.1-2 , pp. 172-179
    • Mbh, Y.1    Bar-Am, O.2    Yogev-Falach, M.3
  • 22
    • 0036719861 scopus 로고    scopus 로고
    • Neuroprotection by propargylamines in Parkinsons disease: Suppression of apoptosis and induction of prosurvival genes
    • Maruyama W, Akao Y, Carrillo MC, Kitani K, Youdium MBH, Naoi M. Neuroprotection by propargylamines in Parkinsons disease: suppression of apoptosis and induction of prosurvival genes. Neurotoxicol. Teratol. 24(5), 675-682 (2002).
    • (2002) Neurotoxicol. Teratol , vol.24 , Issue.5 , pp. 675-682
    • Maruyama, W.1    Akao, Y.2    Carrillo, M.C.3    Kitani, K.4    Mbh, Y.5    Naoi, M.6
  • 23
    • 0037153195 scopus 로고    scopus 로고
    • Novel dual inhibitors of AChE and MAO derived from hydroxy aminoindan and phenethylamine as potential treatment for Alzheimers disease
    • Sterling J, Herzig Y, Goren T et al. Novel dual inhibitors of AChE and MAO derived from hydroxy aminoindan and phenethylamine as potential treatment for Alzheimers disease. J. Med. Chem. 45(24), 5260-5279 (2002).
    • (2002) J. Med. Chem , vol.45 , Issue.24 , pp. 5260-5279
    • Sterling, J.1    Herzig, Y.2    Goren, T.3
  • 24
    • 33845669856 scopus 로고    scopus 로고
    • A multifunctional, neuroprotective drug, ladostigil (TV3326), regulates holo-APP translation and processing
    • Yogev-Falach M, Bar-Am O, Amit T, Weinreb O, Youdim MB. A multifunctional, neuroprotective drug, ladostigil (TV3326), regulates holo-APP translation and processing. FASEB J. 20(12), 2177-2179 (2006).
    • (2006) FASEB J , vol.20 , Issue.12 , pp. 2177-2179
    • Yogev-Falach, M.1    Bar-Am, O.2    Amit, T.3    Weinreb, O.4    Youdim, M.B.5
  • 25
    • 0035568344 scopus 로고    scopus 로고
    • Molecular basis of neuroprotective activities of rasagiline and the anti-Alzheimer drug TV3326 [(N-propargyl-(3R)aminoindan-5-YL)-ethyl methyl carbamate]
    • Youdim MB, Weinstock M. Molecular basis of neuroprotective activities of rasagiline and the anti-Alzheimer drug TV3326 [(N-propargyl-(3R)aminoindan-5-YL)-ethyl methyl carbamate]. Cell. Mol. Neurobiol. 21(6), 555-573 (2002).
    • (2002) Cell. Mol. Neurobiol , vol.21 , Issue.6 , pp. 555-573
    • Youdim, M.B.1    Weinstock, M.2
  • 26
    • 77957374286 scopus 로고    scopus 로고
    • Propargylamine containing compounds as modulators of proteolytic cleavage of amyloid-beta protein precursor: Involvement of MAPK and PKC activation
    • Bar-Am O, Amit T, Weinreb O, Youdim MB, Mandel S. Propargylamine containing compounds as modulators of proteolytic cleavage of amyloid-beta protein precursor: involvement of MAPK and PKC activation. J. Alzheimers Dis. 21(2), 361-371 (2010).
    • (2010) J. Alzheimers Dis , vol.21 , Issue.2 , pp. 361-371
    • Bar-Am, O.1    Amit, T.2    Weinreb, O.3    Youdim, M.B.4    Mandel, S.5
  • 27
    • 80053488353 scopus 로고
    • Monoamine oxidase inhibitor antidepressants
    • Grahame-Smith DG, Cowen PJ (Eds). Excerpta Medica, Amsterdam
    • Youdim MBH, Finberg JPM. Monoamine oxidase inhibitor antidepressants. In: Preclinical Psychopharmacology (Part 1). Grahame-Smith DG, Cowen PJ (Eds). Excerpta Medica, Amsterdam, 38-70 (1983).
    • (1983) Preclinical Psychopharmacology (Part 1) , pp. 38-70
    • Mbh, Y.1    Jpm, F.2
  • 28
    • 0000083255 scopus 로고
    • Amine oxidases
    • Weiner N, Trendelenburg U (Eds). Springer-Verlag, Berlin
    • Youdim MBH, Finberg JPM, Tipton KF. Amine oxidases. In:Handbook of Experimental Pharmacology. Weiner N, Trendelenburg U (Eds). Springer-Verlag, Berlin, 119-92 (1988).
    • (1988) Handbook of Experimental Pharmacology , pp. 119-192
    • Mbh, Y.1    Jpm, F.2    Tipton, K.F.3
  • 29
    • 0346154810 scopus 로고    scopus 로고
    • Monoamine oxidase expression during development and aging
    • Nicotra A, Pierucci F, Parvez H, Senatori O. Monoamine oxidase expression during development and aging. Neurotoxicology 25(1-2), 155-165 (2004).
    • (2004) Neurotoxicology , vol.25 , Issue.1-2 , pp. 155-165
    • Nicotra, A.1    Pierucci, F.2    Parvez, H.3    Senatori, O.4
  • 30
    • 0030768730 scopus 로고    scopus 로고
    • Age-related increases in brain monoamine oxidase B in living healthy human subjects
    • Fowler JS, Volkow ND, Wang GJ et al. Age-related increases in brain monoamine oxidase B in living healthy human subjects. Neurobiol. Aging 18(4), 431-435 (1997).
    • (1997) Neurobiol. Aging , vol.18 , Issue.4 , pp. 431-435
    • Fowler, J.S.1    Volkow, N.D.2    Wang, G.J.3
  • 31
    • 18044366925 scopus 로고    scopus 로고
    • Effects of depression, cigarette smoking, and age on monoamine oxidase B in amygdaloid nuclei
    • Karolewicz B, Klimek V, Zhu H et al. Effects of depression, cigarette smoking, and age on monoamine oxidase B in amygdaloid nuclei. Brain Res. 1043(1-2), 57-64 (2005).
    • (2005) Brain Res , vol.1043 , Issue.1-2 , pp. 57-64
    • Karolewicz, B.1    Klimek, V.2    Zhu, H.3
  • 32
    • 84896806282 scopus 로고    scopus 로고
    • Pharmacology of rasagiline, a new MAO-B inhibitor drug for the treatment of Parkinsons disease with neuroprotective potential
    • Finberg JP. Pharmacology of rasagiline, a new MAO-B inhibitor drug for the treatment of Parkinsons disease with neuroprotective potential. Rambam Maimonides Med. J. 1(1), e0003 (2010).
    • (2010) Rambam Maimonides Med. J , vol.1 , Issue.1 , pp. e0003
    • Finberg, J.P.1
  • 33
    • 84873725851 scopus 로고    scopus 로고
    • Inhibition of monoamine oxidase by phthalide analogues
    • Strydom B, Bergh JJ, Petzer JP. Inhibition of monoamine oxidase by phthalide analogues. Bioorg Med. Chem. Lett. 23(5), 1269-1273 (2013).
    • (2013) Bioorg Med. Chem. Lett , vol.23 , Issue.5 , pp. 1269-1273
    • Strydom, B.1    Bergh, J.J.2    Petzer, J.P.3
  • 34
    • 0035871771 scopus 로고    scopus 로고
    • Selective dopaminergic vulnerability: 3, 4-dihydroxyphenylacetaldehyde targets mitochondria
    • Kristal BS, Conway AD, Brown AM et al. Selective dopaminergic vulnerability: 3, 4-dihydroxyphenylacetaldehyde targets mitochondria. Free Radic. Biol. Med. 30(8), 924-931 (2001).
    • (2001) Free Radic. Biol. Med , vol.30 , Issue.8 , pp. 924-931
    • Kristal, B.S.1    Conway, A.D.2    Brown, A.M.3
  • 35
    • 9144224220 scopus 로고    scopus 로고
    • Neurotoxicity of MAO metabolites of catecholamine neurotransmitters: Role in neurodegenerative diseases
    • Burke WJ, Li SW, Chung HD et al. Neurotoxicity of MAO metabolites of catecholamine neurotransmitters: role in neurodegenerative diseases. Neurotoxicology 25(1-2), 101-115 (2004).
    • (2004) Neurotoxicology , vol.25 , Issue.1-2 , pp. 101-115
    • Burke, W.J.1    Li, S.W.2    Chung, H.D.3
  • 36
    • 33750705653 scopus 로고    scopus 로고
    • A century of Alzheimers disease
    • Goedert M, Spillantini MG. A century of Alzheimers disease. Science 314(5800), 777-781 (2006).
    • (2006) Science , vol.314 , Issue.5800 , pp. 777-781
    • Goedert, M.1    Spillantini, M.G.2
  • 37
    • 0032914318 scopus 로고    scopus 로고
    • Monoamine oxidase: From genes to behavior
    • Shih JC, Chen K, Ridd MJ. Monoamine oxidase: from genes to behavior. Annu. Rev. Neurosci.22, 197-217 (1999).
    • (1999) Annu. Rev. Neurosci , vol.22 , pp. 197-217
    • Shih, J.C.1    Chen, K.2    Ridd, M.J.3
  • 38
    • 0042020173 scopus 로고    scopus 로고
    • Treatment of Alzheimers disease: Current status and new perspectives
    • Scarpini E, Scheltens P, Feldman H. Treatment of Alzheimers disease: current status and new perspectives. Lancet Neurol. 2(9), 539-547 (2003).
    • (2003) Lancet Neurol , vol.2 , Issue.9 , pp. 539-547
    • Scarpini, E.1    Scheltens, P.2    Feldman, H.3
  • 39
    • 0029863697 scopus 로고    scopus 로고
    • Acetylcholinesterase accelerates assembly of amyloidbeta- peptides into Alzheimers fibrils: Possible role of the peripheral site of the enzyme
    • Inestrosa NC, Alvarez A, Pérez CA et al. Acetylcholinesterase accelerates assembly of amyloidbeta- peptides into Alzheimers fibrils: possible role of the peripheral site of the enzyme. Neuron 16(4), 881-891 (1996).
    • (1996) Neuron , vol.16 , Issue.4 , pp. 881-891
    • Inestrosa, N.C.1    Alvarez, A.2    Pérez, C.A.3
  • 40
    • 0141818332 scopus 로고    scopus 로고
    • Cholinergic function and Alzheimers disease
    • Giacobini E. Cholinergic function and Alzheimers disease. Int. J. Geriatr. Psychiatry 18(Suppl. 1), S1-S5 (2003).
    • (2003) Int. J. Geriatr. Psychiatry , vol.18 , pp. S1-S5
    • Giacobini, E.1
  • 41
    • 0033836376 scopus 로고    scopus 로고
    • Abundant tissue butyrylcholinesterase and its possible function in the acetylcholinesterase knockout mouse
    • Li B, Stribley J, Ticu A et al. Abundant tissue butyrylcholinesterase and its possible function in the acetylcholinesterase knockout mouse. J. Neurochem. 75(3), 1320-1331 (2000).
    • (2000) J. Neurochem , vol.75 , Issue.3 , pp. 1320-1331
    • Li, B.1    Stribley, J.2    Ticu, A.3
  • 42
    • 0037318283 scopus 로고    scopus 로고
    • Neurobiology of butyrylcholinesterase
    • Darvesh S, Hopkins D, Geula C. Neurobiology of butyrylcholinesterase. Nat. Rev. Neurosci. 4(2), 131-138 (2003).
    • (2003) Nat. Rev. Neurosci , vol.4 , Issue.2 , pp. 131-138
    • Darvesh, S.1    Hopkins, D.2    Geula, C.3
  • 44
    • 0036315026 scopus 로고    scopus 로고
    • Inhibition of acetyl- and butyryl-cholinesterase in the cerebrospinal fluid of patients with Alzheimers disease by rivastigmine: Correlation with cognitive benefit
    • Giacobini E, Spiegel R, Enz A, Veroff A, Cutler NR. Inhibition of acetyl- and butyryl-cholinesterase in the cerebrospinal fluid of patients with Alzheimers disease by rivastigmine: correlation with cognitive benefit. J. Neural Trans. 109(7-8), 1053-1065 (2002).
    • (2002) J. Neural Trans , vol.109 , Issue.7-8 , pp. 1053-1065
    • Giacobini, E.1    Spiegel, R.2    Enz, A.3    Veroff, A.4    Cutler, N.R.5
  • 45
    • 84949125368 scopus 로고    scopus 로고
    • Historical strategies for lead generation
    • Morphy JR, Harris CJ (Eds). The Royal Society of Chemistry, Cambridge, UK
    • Morphy JR. Historical strategies for lead generation. In:Designing Multi-Target Drugs. Morphy JR, Harris CJ (Eds). The Royal Society of Chemistry, Cambridge, UK, 114-115 (2012).
    • (2012) Designing Multi-Target Drugs , pp. 114-115
    • Morphy, J.R.1
  • 46
    • 0033023543 scopus 로고    scopus 로고
    • Relevance of benzyloxy group in 2-indolyl methylamines in the selective MAO-B inhibition
    • Pérez V, Marco JL, Fernández-Alvarez E, Unzeta M. Relevance of benzyloxy group in 2-indolyl methylamines in the selective MAO-B inhibition. Br. J. Pharmacol. 127(4), 869-876 (1999).
    • (1999) Br. J. Pharmacol , vol.127 , Issue.4 , pp. 869-876
    • Pérez, V.1    Marco, J.L.2    Fernández-Alvarez, E.3    Unzeta, M.4
  • 47
    • 0035568344 scopus 로고    scopus 로고
    • Molecular basis of neuroprotective activities of rasagiline and the anti- Alzheimer drug TV3326 [(N-propargyl-(3R)aminoindan- 5-YL)-ethyl methyl carbamate]
    • Youdim MB, Weinstock M. Molecular basis of neuroprotective activities of rasagiline and the anti- Alzheimer drug TV3326 [(N-propargyl-(3R)aminoindan- 5-YL)-ethyl methyl carbamate]. Cell Mol. Neurobiol. 21(6), 555-73 (2001).
    • (2001) Cell Mol. Neurobiol , vol.21 , Issue.6 , pp. 555-573
    • Youdim, M.B.1    Weinstock, M.2
  • 48
    • 0034525115 scopus 로고    scopus 로고
    • TV3326, a novel neuroprotective drug with cholinesterase and monoamine oxidase inhibitory activities for the treatment of Alzheimers disease
    • Weinstock M, Bejar C, Wang RH et al. TV3326, a novel neuroprotective drug with cholinesterase and monoamine oxidase inhibitory activities for the treatment of Alzheimers disease. J. Neural Transm. Suppl. 2000(60), 157-169 (2000).
    • (2000) J. Neural Transm. Suppl , vol.2000 , Issue.60 , pp. 157-169
    • Weinstock, M.1    Bejar, C.2    Wang, R.H.3
  • 49
    • 57749108326 scopus 로고    scopus 로고
    • Multifunctional neuroprotective derivatives of rasagiline as anti- alzheimers Disease Drugs
    • Weinreb O, Mandel S, Bar-Am O. et al. Multifunctional Neuroprotective Derivatives of Rasagiline as Anti- Alzheimers Disease Drugs. Neurotherapeutics. 6(1), 163-174 (2009).
    • (2009) Neurotherapeutics , vol.6 , Issue.1 , pp. 163-174
    • Weinreb, O.1    Mandel, S.2    Bar-Am, O.3
  • 50
    • 0033809197 scopus 로고    scopus 로고
    • Development of a novel neuroprotective drug (TV3326) for the treatment of Alzheimers disease, with cholinesterase and monoamine oxidase inhibitory activities
    • Weinstock M, Goren T, Youdim MB. Development of a novel neuroprotective drug (TV3326) for the treatment of Alzheimers disease, with cholinesterase and monoamine oxidase inhibitory activities. Drug Dev. Res. 50, 216-222 (2000).
    • (2000) Drug Dev. Res , vol.50 , pp. 216-222
    • Weinstock, M.1    Goren, T.2    Youdim, M.B.3
  • 51
    • 77954947811 scopus 로고    scopus 로고
    • Neuroprotective multifunctional iron chelators: From redox-sensitive process to novel therapeutic opportunities
    • Weinreb O, Amit T, Mandel S, Kupershmidt L, Youdim MB. Neuroprotective multifunctional iron chelators: from redox-sensitive process to novel therapeutic opportunities. Antioxid. Redox Signal. 13(6), 919-49 (2010).
    • (2010) Antioxid. Redox Signal , vol.13 , Issue.6 , pp. 919-949
    • Weinreb, O.1    Amit, T.2    Mandel, S.3    Kupershmidt, L.4    Youdim, M.B.5
  • 52
    • 84857709982 scopus 로고    scopus 로고
    • Ladostigil: A novel multimodal neuroprotective drug with cholinesterase and brain-selective monoamine oxidase inhibitory activities for Alzheimers disease treatment
    • Weinreb O, Amit T, Bar-Am O, Youdim MB. Ladostigil: a novel multimodal neuroprotective drug with cholinesterase and brain-selective monoamine oxidase inhibitory activities for Alzheimers disease treatment. Curr. Drug Targets 13(4), 483-94 (2012).
    • (2012) Curr. Drug Targets , vol.13 , Issue.4 , pp. 483-494
    • Weinreb, O.1    Amit, T.2    Bar-Am, O.3    Youdim, M.B.4
  • 53
    • 0038155162 scopus 로고    scopus 로고
    • Attenuation of MPTP-induced dopaminergic neurotoxicity by TV3326, a cholinesterase-monoamine oxidase inhibitor
    • Sagi Y, Weinstock M, Youdim MB. Attenuation of MPTP-induced dopaminergic neurotoxicity by TV3326, a cholinesterase-monoamine oxidase inhibitor. J. Neurochem. 86(2), 290-297 (2003).
    • (2003) J. Neurochem , vol.86 , Issue.2 , pp. 290-297
    • Sagi, Y.1    Weinstock, M.2    Youdim, M.B.3
  • 54
    • 0020662487 scopus 로고
    • The deamination of dopamine by human brain monoamine oxidase. Specificity for the two enzyme forms in seven brain regions
    • OCarroll AM, Fowler CJ, Phillips JP, Tobbia I, Tipton KF. The deamination of dopamine by human brain monoamine oxidase. Specificity for the two enzyme forms in seven brain regions. Naunyn Schmiedebergs Arch. Pharmacol. 322(3), 198-202 (1983).
    • (1983) Naunyn Schmiedebergs Arch. Pharmacol , vol.322 , Issue.3 , pp. 198-202
    • Ocarroll, A.M.1    Fowler, C.J.2    Phillips, J.P.3    Tobbia, I.4    Tipton, K.F.5
  • 55
    • 0017755902 scopus 로고
    • Evidence for dopamine deamination by both type A and type B monoamine oxidase in rat brain in vivo and for the degree of inhibition of enzyme necessary for increased functional activity of dopamine and 5-hydroxytryptamine
    • Green AR, Mitchell BD, Tordoff AF, Youdim MB. Evidence for dopamine deamination by both type A and type B monoamine oxidase in rat brain in vivo and for the degree of inhibition of enzyme necessary for increased functional activity of dopamine and 5-hydroxytryptamine. Br. J. Pharmacol. 60(3), 343-349 (1977).
    • (1977) Br. J. Pharmacol , vol.60 , Issue.3 , pp. 343-349
    • Green, A.R.1    Mitchell, B.D.2    Tordoff, A.F.3    Youdim, M.B.4
  • 56
    • 33645307953 scopus 로고    scopus 로고
    • The therapeutic potential of monoamine oxidase inhibitors
    • Youdim MBH, Edmondson D, Tipton KF. The therapeutic potential of monoamine oxidase inhibitors. Nat. Rev. Neurosci. 7(4), 295-309 (2006).
    • (2006) Nat. Rev. Neurosci , vol.7 , Issue.4 , pp. 295-309
    • Mbh, Y.1    Edmondson, D.2    Tipton, K.F.3
  • 57
    • 0031910978 scopus 로고    scopus 로고
    • Donepezil use in Alzheimer disease
    • Barner EL, Gray SL. Donepezil use in Alzheimer disease. Ann. Pharmacother. 32(1), 70-77 (1998).
    • (1998) Ann. Pharmacother , vol.32 , Issue.1 , pp. 70-77
    • Barner, E.L.1    Gray, S.L.2
  • 58
    • 80052925179 scopus 로고    scopus 로고
    • Synthesis, biological assessment and molecular modeling of new multipotent MAO and cholinesterase inhibitors as potential drugs for the treatment of Alzheimers disease
    • Samadi A, Chioua M, Bolea I et al. Synthesis, biological assessment and molecular modeling of new multipotent MAO and cholinesterase inhibitors as potential drugs for the treatment of Alzheimers disease. Eur. J. Med. Chem. 46(9), 4665-4668 (2011).
    • (2011) Eur. J. Med. Chem , vol.46 , Issue.9 , pp. 4665-4668
    • Samadi, A.1    Chioua, M.2    Bolea, I.3
  • 59
    • 0037199660 scopus 로고    scopus 로고
    • Neuroprotective effect of the monoamine oxidase inhibitor PF 9601N [N-(2- propynyl)-2-(5-benzyloxy-indolyl) methylamine] on rat nigral neurons after 6-hydroxydopamine-striatal lesion
    • Cutillas B, Ambrosio S, Unzeta M. Neuroprotective effect of the monoamine oxidase inhibitor PF 9601N [N-(2- propynyl)-2-(5-benzyloxy-indolyl) methylamine] on rat nigral neurons after 6-hydroxydopamine-striatal lesion. Neurosci. Lett. 329(2), 165-168 (2002).
    • (2002) Neurosci. Lett , vol.329 , Issue.2 , pp. 165-168
    • Cutillas, B.1    Ambrosio, S.2    Unzeta, M.3
  • 60
    • 0034070031 scopus 로고    scopus 로고
    • The novel type B MAO inhibitor PF9601N enhances the duration of L-DOPA-induced contralateral turning in 6-hydroxydopamine lesioned rats
    • Prat G, Pérez V, Rubí A, Casas M, Unzeta M. The novel type B MAO inhibitor PF9601N enhances the duration of L-DOPA-induced contralateral turning in 6-hydroxydopamine lesioned rats. J. Neural. Transm. 107(4), 409-417 (2000).
    • (2000) J. Neural. Transm , vol.107 , Issue.4 , pp. 409-417
    • Prat, G.1    Pérez, V.2    Rubí, A.3    Casas, M.4    Unzeta, M.5
  • 61
    • 84055217642 scopus 로고    scopus 로고
    • Synthesis, biological evaluation, and molecular modeling of donepezil and N-[(5-(benzyloxy)-1-methyl-1H-indol-2-yl)methyl]- N-methylprop-2-yn-1-Amine hybrids as new multipotent cholinesterase/monoamine oxidase inhibitors for the treatment of Alzheimers disease
    • Bolea I, Juárez-Jiménez J, de los Ríos C et al. Synthesis, biological evaluation, and molecular modeling of donepezil and N-[(5-(benzyloxy)-1-methyl-1H-indol-2-yl)methyl]- N-methylprop-2-yn-1-Amine hybrids as new multipotent cholinesterase/monoamine oxidase inhibitors for the treatment of Alzheimers disease. J. Med. Chem. 54(24), 8251-8270 (2011).
    • (2011) J. Med. Chem , vol.54 , Issue.24 , pp. 8251-8270
    • Bolea, I.1    Juárez-Jiménez, J.2    De Los Ríos, C.3
  • 62
    • 84908079484 scopus 로고    scopus 로고
    • Multipotent cholinesterase/monoamine oxidase inhibitors for the treatment of Alzheimers disease: Design, syn, biochemical evaluation, ADMET, molecular modeling, and QSAR analysis of novel donepezil-pyridylhybrids
    • Bautista-Aguilera OM, Esteban G, Chioua M et al. Multipotent cholinesterase/monoamine oxidase inhibitors for the treatment of Alzheimers disease: design, synthesis, biochemical evaluation, ADMET, molecular modeling, and QSAR analysis of novel donepezil-pyridylhybrids. Drug Des. Devel. Ther. 8, 1893-1910 (2014).
    • (2014) Drug Des. Devel. Ther , vol.8 , pp. 1893-1910
    • Bautista-Aguilera, O.M.1    Esteban, G.2    Chioua, M.3
  • 64
    • 84893943097 scopus 로고    scopus 로고
    • Design, syn thesis, pharmacological evaluation, QSAR analysis, molecular modeling and ADMET of novel donepezileindolyl hybrids as multipotent cholinesterase/ monoamine oxidase inhibitors for the potential treatment of Alzheimers disease
    • Bautista-Aguilera OM, Esteban G, Bolea I et al. Design, synthesis, pharmacological evaluation, QSAR analysis, molecular modeling and ADMET of novel donepezileindolyl hybrids as multipotent cholinesterase/ monoamine oxidase inhibitors for the potential treatment of Alzheimers disease. Eur. J. Med. Chem. 75, 82-95 (2014).
    • (2014) Eur. J. Med. Chem , vol.75 , pp. 82-95
    • Bautista-Aguilera, O.M.1    Esteban, G.2    Bolea, I.3
  • 65
    • 0031573408 scopus 로고    scopus 로고
    • A one-step fluorometric method for the continuous measurement of monoamine oxidase activity
    • Zhou M, Panchuk-Voloshina N. A one-step fluorometric method for the continuous measurement of monoamine oxidase activity. Anal. Biochem. 253(2), 169-174 (1997).
    • (1997) Anal. Biochem , vol.253 , Issue.2 , pp. 169-174
    • Zhou, M.1    Panchuk-Voloshina, N.2
  • 66
    • 76149120388 scopus 로고    scopus 로고
    • AutoDock Vina: Improving the speed and accuracy of docking with a new scoring function, efficient optimization, and multithreading
    • Trott O, Olson AJ. AutoDock Vina: improving the speed and accuracy of docking with a new scoring function, efficient optimization, and multithreading. J. Comput. Chem. 31(2), 455-461 (2010).
    • (2010) J. Comput. Chem , vol.31 , Issue.2 , pp. 455-461
    • Trott, O.1    Olson, A.J.2
  • 67
    • 0034603412 scopus 로고    scopus 로고
    • Monoamine oxidase B inhibitors in the treatment of Alzheimers disease
    • Thomas T. Monoamine oxidase B inhibitors in the treatment of Alzheimers disease. Neurobiol. Aging 21(2), 343-348 (2000).
    • (2000) Neurobiol. Aging , vol.21 , Issue.2 , pp. 343-348
    • Thomas, T.1
  • 68
    • 0348046385 scopus 로고    scopus 로고
    • Monoamine oxidase inhibition in Alzheimers disease
    • Riederer P, Danyelczyk W, Grunblat E. Monoamine oxidase inhibition in Alzheimers disease. Neurotoxicology 25(1-2), 271-277 (2004).
    • (2004) Neurotoxicology , vol.25 , Issue.1-2 , pp. 271-277
    • Riederer, P.1    Danyelczyk, W.2    Grunblat, E.3
  • 69
    • 33947546504 scopus 로고    scopus 로고
    • Implications of co-morbidity for etiology and treatment of neurodegenerative diseases with multifunctional neuroprotective-neurorescue drugs: Ladostigil
    • Youdim MB, Amit T, Bar-Am O, Weinreb O, Yogev-Falach M. Implications of co-morbidity for etiology and treatment of neurodegenerative diseases with multifunctional neuroprotective-neurorescue drugs: ladostigil. Neurotoxic Res. 10(3-4), 181-192 (2006).
    • (2006) Neurotoxic Res , vol.10 , Issue.3-4 , pp. 181-192
    • Youdim, M.B.1    Amit, T.2    Bar-Am, O.3    Weinreb, O.4    Yogev-Falach, M.5
  • 70
    • 42249083032 scopus 로고    scopus 로고
    • Synergistic effects of selegiline and donepezil on cognitive impaitment induced by amyloid beta (25-35)
    • Tsunekawa H, Noda Y, Mouri A, Yoneda F, Nameshiba T. Synergistic effects of selegiline and donepezil on cognitive impaitment induced by amyloid beta (25-35). Behav. Brain Res 190 2 224-232(2008).
    • (2008) Behav. Brain Res , vol.190 , Issue.2 , pp. 224-232
    • Tsunekawa, H.1    Noda, Y.2    Mouri, A.3    Yoneda, F.4    Nameshiba, T.5
  • 71
    • 55749115608 scopus 로고    scopus 로고
    • Synthesis and pharmacological evaluation of several ring-contracted amantadine analogs
    • Camps P, Duque MD, Vázquez S et al. Synthesis and pharmacological evaluation of several ring-contracted amantadine analogs. Bioorg. Med. Chem. 16(23), 9925-9936 (2008).
    • (2008) Bioorg. Med. Chem , vol.16 , Issue.23 , pp. 9925-9936
    • Camps, P.1    Duque, M.D.2    Vázquez, S.3
  • 72
    • 0037025273 scopus 로고    scopus 로고
    • The pharmacological manipulation of glutamate receptors and neuroprotection
    • Stone TW, Addae JI. The pharmacological manipulation of glutamate receptors and neuroprotection. Eur. J. Pharmacol. 447(2-3), 285-296 (2002).
    • (2002) Eur. J. Pharmacol , vol.447 , Issue.2-3 , pp. 285-296
    • Stone, T.W.1    Addae, J.I.2
  • 73
    • 0037466232 scopus 로고    scopus 로고
    • Combined nimodipine and citicoline reduce infarct size, attenuate apoptosis and increase bcl-2 expression after focal cerebral ischemia
    • Sobrado M, Loacute;pez MG, Carceller F, García AG, Roda JM. Combined nimodipine and citicoline reduce infarct size, attenuate apoptosis and increase bcl-2 expression after focal cerebral ischemia. Neuroscience 118(1), 107-113 (2003).
    • (2003) Neuroscience , vol.118 , Issue.1 , pp. 107-113
    • Sobrado, M.1    Loacute2    pez, M.G.3    Carceller, F.4    García, A.G.5    Roda, J.M.6
  • 74
    • 33645095476 scopus 로고    scopus 로고
    • Paradigm shift in neuroprotection by NMDA receptor blockade: Memantine and beyond
    • Lipton SA. Paradigm shift in neuroprotection by NMDA receptor blockade: memantine and beyond. Nat. Rev. Drug Discov. 5(2), 160-170 (2006).
    • (2006) Nat. Rev. Drug Discov , vol.5 , Issue.2 , pp. 160-170
    • Lipton, S.A.1
  • 75
    • 0026005169 scopus 로고
    • N-methyl-d-Aspartate antagonists in the treatment of Parkinsons disease
    • Greenamyre JT, OBrien CF. N-methyl-d-Aspartate antagonists in the treatment of Parkinsons disease. Arch. Neurol. 48(9), 977-981 (1991).
    • (1991) Arch. Neurol , vol.48 , Issue.9 , pp. 977-981
    • Greenamyre, J.T.1    Obrien, C.F.2
  • 76
    • 1542404521 scopus 로고    scopus 로고
    • Synthesis and biological evaluation of pentacyclo[5.4.0.02, 6.03, 10.05, 9]undecane derivatives as potential therapeutic agents in Parkinsons disease
    • Geldenhuys WJ, Malan SF, Murugesan T, van der Schyf CJ, Bloomquist JR. Synthesis and biological evaluation of pentacyclo[5.4.0.02, 6.03, 10.05, 9]undecane derivatives as potential therapeutic agents in Parkinsons disease. Bioorg. Med. Chem. 12(7), 1799-1806 (2004).
    • (2004) Bioorg. Med. Chem , vol.12 , Issue.7 , pp. 1799-1806
    • Geldenhuys, W.J.1    Malan, S.F.2    Murugesan, T.3    Van Der Schyf, C.J.4    Bloomquist, J.R.5
  • 77
    • 72149107359 scopus 로고    scopus 로고
    • New oxapolycyclic cage amines with NMDA receptor antagonist and trypanocidal activities
    • Duque MD, Camps P, Torres E et al. New oxapolycyclic cage amines with NMDA receptor antagonist and trypanocidal activities. Bioorg. Med. Chem. 18(1), 46-57 (2010).
    • (2010) Bioorg. Med. Chem , vol.18 , Issue.1 , pp. 46-57
    • Duque, M.D.1    Camps, P.2    Torres, E.3
  • 78
    • 84855800380 scopus 로고    scopus 로고
    • Synthesis of benzopolycyclic cage amines: NMDA receptor antagonist, trypanocidal and antiviral activities
    • Torres E, Duque MD, Loacute;pez-Querol M et al. Synthesis of benzopolycyclic cage amines: NMDA receptor antagonist, trypanocidal and antiviral activities. Bioorg. Med. Chem. 20(2), 942-948 (2012).
    • (2012) Bioorg. Med. Chem , vol.20 , Issue.2 , pp. 942-948
    • Torres, E.1    Duque, M.D.2    Loacute3    pez-Querol, M.4
  • 79
  • 81
    • 10344221023 scopus 로고    scopus 로고
    • Pharmacology and structure-Activity relationships of bioactive polycyclic cage compounds: A focus on pentacycloundecane derivatives
    • Geldenhuys WJ, Malan SF, Bloomquist JR, Marchand AP, van der Schyf CJ. Pharmacology and structure-Activity relationships of bioactive polycyclic cage compounds: a focus on pentacycloundecane derivatives. Med. Res. Rev. 25(1), 21-48 (2005).
    • (2005) Med. Res. Rev , vol.25 , Issue.1 , pp. 21-48
    • Geldenhuys, W.J.1    Malan, S.F.2    Bloomquist, J.R.3    Marchand, A.P.4    Van Der Schyf, C.J.5
  • 82
    • 33744797392 scopus 로고    scopus 로고
    • NGP1-01 is a brain permeable dual blocker of neuronal voltage-And ligand-operated calcium channels
    • Kiewert C, Hartmann J, Stoll J, Thekkumkara TJ, Geldenhuys WJ, Klein J. NGP1-01 is a brain permeable dual blocker of neuronal voltage-And ligand-operated calcium channels. Neurochem. Res. 31(3), 395-399 (2006).
    • (2006) Neurochem. Res , vol.31 , Issue.3 , pp. 395-399
    • Kiewert, C.1    Hartmann, J.2    Stoll, J.3    Thekkumkara, T.J.4    Geldenhuys, W.J.5    Klein, J.6
  • 83
    • 39149141841 scopus 로고    scopus 로고
    • Neuroprotection in mice by NGP1-01 after transient focal brain ischemia
    • Hao J, Mdzinarishvili A, Abbruscato TJ et al. Neuroprotection in mice by NGP1-01 after transient focal brain ischemia. Brain Res. 1196, 113-120 (2008).
    • (2008) Brain Res , vol.1196 , pp. 113-120
    • Hao, J.1    Mdzinarishvili, A.2    Abbruscato, T.J.3
  • 84
    • 0029985871 scopus 로고    scopus 로고
    • Kineticsand mechanism of degradation of the heterocyclic cage compound NGP1-01 in aqueoussolution
    • Du Preez JL, Lotter AP, Guillory JK. Kineticsand mechanism of degradation of the heterocyclic cage compound NGP1-01 in aqueoussolution. Pharmazie 51, 223 (1996).
    • (1996) Pharmazie , vol.51 , pp. 223
    • Du Preez, J.L.1    Lotter, A.P.2    Guillory, J.K.3
  • 85
    • 0029824551 scopus 로고    scopus 로고
    • LC-MS identification of the degradates of NGP1-01 and subsequent development of a routine stability-indicating method of analysis
    • Du Preez JL, Lotter AP. LC-MS identification of the degradates of NGP1-01 and subsequent development of a routine stability-indicating method of analysis. Drug Dev. Ind. Pharm. 22, 1249 (1996).
    • (1996) Drug Dev. Ind. Pharm , vol.22 , pp. 1249
    • Du Preez, J.L.1    Lotter, A.P.2
  • 86
    • 0022260733 scopus 로고
    • Biochemical characterization of a filtered synaptoneurosome preparation from guinea pig cerebral cortex: Cyclic adenosine 3:5-monophosphategenerating systems, receptors, and enzymes
    • Hollingsworth EB, McNeal ET, Burton JL, Williams RJ, Daly JW, Creveling CR. Biochemical characterization of a filtered synaptoneurosome preparation from guinea pig cerebral cortex: cyclic adenosine 3:5-monophosphategenerating systems, receptors, and enzymes. J. Neurosci. 5(8), 2240-2253 (1985).
    • (1985) J. Neurosci , vol.5 , Issue.8 , pp. 2240-2253
    • Hollingsworth, E.B.1    McNeal, E.T.2    Burton, J.L.3    Williams, R.J.4    Daly, J.W.5    Creveling, C.R.6
  • 88
    • 84857763725 scopus 로고    scopus 로고
    • Polycyclic cage structures as lipophilic scaffolds for neuroactive drugs
    • Joubert J, Geldenhuys WJ, Van der Schyf CJ et al. Polycyclic cage structures as lipophilic scaffolds for neuroactive drugs. ChemMedChem 7(3), 375-84 (2012).
    • (2012) ChemMedChem , vol.7 , Issue.3 , pp. 375-384
    • Joubert, J.1    Geldenhuys, W.J.2    Van Der Schyf, C.J.3
  • 89
    • 0042623380 scopus 로고    scopus 로고
    • Physicochemical prediction of a brain-blood distribution profile in polycyclic amines
    • Zah J, TerreBlanche G, Erasmus E, Malan SF. Physicochemical prediction of a brain-blood distribution profile in polycyclic amines. Bioorg. Med. Chem. 11(17), 3569-3578 (2003).
    • (2003) Bioorg. Med. Chem , vol.11 , Issue.17 , pp. 3569-3578
    • Zah, J.1    Terreblanche, G.2    Erasmus, E.3    Malan, S.F.4
  • 90
    • 10344227370 scopus 로고
    • Introduction of pharmacophoric groups into polycyclic systems 4. Aziridine, oxiran, and tertiary betahydroxyethylamine derivatives of adamantine
    • Brookes KB, Hickmott PW, Jutle KK, Schreyer CA. Introduction of pharmacophoric groups into polycyclic systems 4. aziridine, oxiran, and tertiary betahydroxyethylamine derivatives of adamantine. S. Afr. J. Chem. 45, 8-11 (1992).
    • (1992) S. Afr. J. Chem , vol.45 , pp. 8-11
    • Brookes, K.B.1    Hickmott, P.W.2    Jutle, K.K.3    Schreyer, C.A.4
  • 91
    • 0033601338 scopus 로고    scopus 로고
    • Cu(II) potentiation of alzheimer abeta neurotoxicity. Correlation with cell-free hydrogen peroxide production and metal reduction
    • Huang X, Cuanjungco MP, Atwood CS et al. Cu(II) potentiation of alzheimer abeta neurotoxicity. Correlation with cell-free hydrogen peroxide production and metal reduction. J. Biol. Chem. 274(52), 37111-37116 (1999).
    • (1999) J. Biol. Chem , vol.274 , Issue.52 , pp. 37111-37116
    • Huang, X.1    Cuanjungco, M.P.2    Atwood, C.S.3
  • 92
    • 0023833858 scopus 로고
    • Tyrosine hydroxylase activity in caudate nucleus from Parkinsons disease: Effects of iron and phosphorylating agents
    • Rausch WD, Hirata Y, Nagatsu T, Riederer P, Jellinger K. Tyrosine hydroxylase activity in caudate nucleus from Parkinsons disease: effects of iron and phosphorylating agents. J. Neurochem. 50(1), 202-208 (1988).
    • (1988) J. Neurochem , vol.50 , Issue.1 , pp. 202-208
    • Rausch, W.D.1    Hirata, Y.2    Nagatsu, T.3    Riederer, P.4    Jellinger, K.5
  • 93
    • 84863639586 scopus 로고    scopus 로고
    • Chelators in the treatment of iron accumulation in parkinsons disease
    • Mounsey RB, Teismann P. Chelators in the treatment of iron accumulation in parkinsons disease. Int. J. Cell Biol. 9832, 45 (2012).
    • (2012) Int. J. Cell Biol , vol.9832 , Issue.45
    • Mounsey, R.B.1    Teismann, P.2
  • 94
    • 0023638828 scopus 로고
    • Increased nigral iron content in postmortem parkinsonian brain
    • Dexter DT, Wells FR, Agid F, Lees AJ, Jenner P, Marsden CD. Increased nigral iron content in postmortem parkinsonian brain. Lancet 2(8569), 1219-1220 (1987).
    • (1987) Lancet , vol.2 , Issue.8569 , pp. 1219-1220
    • Dexter, D.T.1    Wells, F.R.2    Agid, F.3    Lees, A.J.4    Jenner, P.5    Marsden, C.D.6
  • 95
    • 0023804321 scopus 로고
    • Increased iron (III) and total iron content in post mortem substantia nigra of Parkinsonian brain
    • Sofic E, Riederer P, Heinsen H et al. Increased iron (III) and total iron content in post mortem substantia nigra of Parkinsonian brain. J. Neural Transm. 74(3), 199-205 (1988).
    • (1988) J. Neural Transm , vol.74 , Issue.3 , pp. 199-205
    • Sofic, E.1    Riederer, P.2    Heinsen, H.3
  • 96
    • 0031687793 scopus 로고    scopus 로고
    • Understanding cell death in Parkinsons disease
    • Jenner P, Olanow CW. Understanding cell death in Parkinsons disease. Ann. Neurol. 44(3 Suppl. 1), S72-S84 (1998).
    • (1998) Ann. Neurol , vol.44 , Issue.3 , pp. S72-S84
    • Jenner, P.1    Olanow, C.W.2
  • 97
    • 1842608744 scopus 로고    scopus 로고
    • Ironing iron out in Parkinsons disease and other neurodegenerative diseases with iron chelators: A lesson from 6-hydroxydopamine and iron chelators, desferal and VK-28
    • Youdim MB, Stephenson G, Ben Shachar D. Ironing iron out in Parkinsons disease and other neurodegenerative diseases with iron chelators: a lesson from 6-hydroxydopamine and iron chelators, desferal and VK-28. Ann. NY Acad. Sci. 1012, 306-325 (2004).
    • (2004) Ann. NY Acad. Sci , vol.1012 , pp. 306-325
    • Youdim, M.B.1    Stephenson, G.2    Ben Shachar, D.3
  • 98
    • 0346849912 scopus 로고    scopus 로고
    • Neuroprotection by a novel brain permeable iron chelator, VK-28, against 6-hydroxydopamine lesion in rats
    • Shachar DB, Kahana N, Kampel V, Warshawsky A, Youdim MB. Neuroprotection by a novel brain permeable iron chelator, VK-28, against 6-hydroxydopamine lesion in rats. Neuropharmacology 46(2), 254-263 (2004).
    • (2004) Neuropharmacology , vol.46 , Issue.2 , pp. 254-263
    • Shachar, D.B.1    Kahana, N.2    Kampel, V.3    Warshawsky, A.4    Youdim, M.B.5
  • 99
    • 25644452043 scopus 로고    scopus 로고
    • Novel multifunctional neuroprotective iron chelator-monoamine oxidase inhibitor drugs for neurodegenerative diseases. in vivo selective brain monoamine oxidase inhibition and prevention of MPTP-induced striatal dopamine depletion
    • Gal S, Zheng H, Fridkin M, Youdim MB. Novel multifunctional neuroprotective iron chelator-monoamine oxidase inhibitor drugs for neurodegenerative diseases. In vivo selective brain monoamine oxidase inhibition and prevention of MPTP-induced striatal dopamine depletion. J. Neurochem. 95(1), 79-88 (2005).
    • (2005) J. Neurochem , vol.95 , Issue.1 , pp. 79-88
    • Gal, S.1    Zheng, H.2    Fridkin, M.3    Youdim, M.B.4
  • 100
    • 25644461154 scopus 로고    scopus 로고
    • Novel multifunctional neuroprotective iron chelator-monoamine oxidase inhibitor drugs for neurodegenerative diseases: In vitro studies on antioxidant activity, prevention of lipid peroxide formation and monoamine oxidase inhibition
    • Zheng H, Gal S, Weiner LM et al. Novel multifunctional neuroprotective iron chelator-monoamine oxidase inhibitor drugs for neurodegenerative diseases: in vitro studies on antioxidant activity, prevention of lipid peroxide formation and monoamine oxidase inhibition. J. Neurochem. 95(1), 68-78 (2005).
    • (2005) J. Neurochem , vol.95 , Issue.1 , pp. 68-78
    • Zheng, H.1    Gal, S.2    Weiner, L.M.3
  • 101
    • 79960895695 scopus 로고    scopus 로고
    • Novel molecular targets of the neuroprotective/neurorescue multimodal iron chelating drug M30 in the mouse brain
    • Kupershmidt L, Weinreb O, Amit T, Mandel S, Bar- Am O, Youdim MB. Novel molecular targets of the neuroprotective/neurorescue multimodal iron chelating drug M30 in the mouse brain. Neuroscience 189, 345-358 (2011).
    • (2011) Neuroscience , vol.189 , pp. 345-358
    • Kupershmidt, L.1    Weinreb, O.2    Amit, T.3    Mandel, S.4    Bar- Am, O.5    Youdim, M.B.6
  • 102
    • 84863896457 scopus 로고    scopus 로고
    • The novel multitarget iron chelating-radical scavenging compound M30 possesses beneficial effects on major hallmarks of Alzheimers disease
    • Kupershmidt L, Amit T, Bar-Am O, Youdim MB, Weinreb O. The novel multitarget iron chelating-radical scavenging compound M30 possesses beneficial effects on major hallmarks of Alzheimers disease. Antioxid. Redox Signal. 17(6), 860-77 (2012).
    • (2012) Antioxid. Redox Signal , vol.17 , Issue.6 , pp. 860-877
    • Kupershmidt, L.1    Amit, T.2    Bar-Am, O.3    Youdim, M.B.4    Weinreb, O.5
  • 103
    • 84868093104 scopus 로고    scopus 로고
    • Multi-target, neuroprotective and neurorestorative M30 improves cognitive impairment and reduces Alzheimers-like neuropathology and age-related alterations in mice
    • Kupershmidt L, Amit T, Bar-Am O, Weinreb O, Youdim MB. Multi-target, neuroprotective and neurorestorative M30 improves cognitive impairment and reduces Alzheimers-like neuropathology and age-related alterations in mice. Mol. Neurobiol. 46(1), 217-220 (2012).
    • (2012) Mol. Neurobiol , vol.46 , Issue.1 , pp. 217-220
    • Kupershmidt, L.1    Amit, T.2    Bar-Am, O.3    Weinreb, O.4    Youdim, M.B.5
  • 104
    • 84887970188 scopus 로고    scopus 로고
    • Promises of novel multi-target neuroprotective and neurorestorative drugs for Parkinsons disease
    • Youdim MB, Kupershmidt L, Amit T, Weinreb O. Promises of novel multi-target neuroprotective and neurorestorative drugs for Parkinsons disease. Parkinsonism Relat. Disord. 20(Suppl. 1), S132-S136 (2014).
    • (2014) Parkinsonism Relat. Disord , vol.20 , pp. S132-S136
    • Youdim, M.B.1    Kupershmidt, L.2    Amit, T.3    Weinreb, O.4
  • 105
    • 84900532421 scopus 로고    scopus 로고
    • Donepezil + propargylamine + 8-hydroxyquinoline hybrids as new multifunctional metal-chelators, ChE and MAO inhibitors for the potential treatment of Alzheimers disease
    • Wang L, Esteban G, Ojima M et al. Donepezil + propargylamine + 8-hydroxyquinoline hybrids as new multifunctional metal-chelators, ChE and MAO inhibitors for the potential treatment of Alzheimers disease. Eur. J. Med. Chem. 80, 543-561 (2014).
    • (2014) Eur. J. Med. Chem , vol.80 , pp. 543-561
    • Wang, L.1    Esteban, G.2    Ojima, M.3
  • 106
    • 11844255676 scopus 로고    scopus 로고
    • Design, synthesis, and evaluation of novel bifunctional iron-chelators as potential agents for neuroprotection in Alzheimers, Parkinsons, and other neurodegenerative diseases
    • Zheng H, Weiner LM, Bar-Am O et al. Design, synthesis, and evaluation of novel bifunctional iron-chelators as potential agents for neuroprotection in Alzheimers, Parkinsons, and other neurodegenerative diseases. Bioorg. Med. Chem. 13(3), 773-83 (2005).
    • (2005) Bioorg. Med. Chem , vol.13 , Issue.3 , pp. 773-783
    • Zheng, H.1    Weiner, L.M.2    Bar-Am, O.3
  • 107
    • 36849044036 scopus 로고    scopus 로고
    • Prevention and restoration of lactacystin-induced nigrostriatal dopamine neuron degeneration by novel brain-permeable iron chelators
    • Zhu W, Xie W, Pan T et al. Prevention and restoration of lactacystin-induced nigrostriatal dopamine neuron degeneration by novel brain-permeable iron chelators. FASEB J. 21(14), 3835-3844 (2007).
    • (2007) FASEB J , vol.21 , Issue.14 , pp. 3835-3844
    • Zhu, W.1    Xie, W.2    Pan, T.3
  • 108
    • 0019812049 scopus 로고
    • Concentration dependence of the oxidation of tyramine by the two forms of rat liver mitochondrial monoamine oxidase
    • Fowler CJ, Tipton KF. Concentration dependence of the oxidation of tyramine by the two forms of rat liver mitochondrial monoamine oxidase. Biochem. Pharmacol. 30(24), 3329-3332 (1981).
    • (1981) Biochem. Pharmacol , vol.30 , Issue.24 , pp. 3329-3332
    • Fowler, C.J.1    Tipton, K.F.2
  • 109
    • 33845879870 scopus 로고    scopus 로고
    • Therapeutic targets and potential of the novel brain- permeable multifunctional iron chelatormonoamine oxidase inhibitor drug, M-30, for the treatment of Alzheimers disease
    • Avramovich-Tirosh Y, Amit T, Bar-Am O, Zheng H, Fridkin M, Youdim MB. Therapeutic targets and potential of the novel brain- permeable multifunctional iron chelatormonoamine oxidase inhibitor drug, M-30, for the treatment of Alzheimers disease. J. Neurochem. 100(2), 490-502 (2007).
    • (2007) J. Neurochem , vol.100 , Issue.2 , pp. 490-502
    • Avramovich-Tirosh, Y.1    Amit, T.2    Bar-Am, O.3    Zheng, H.4    Fridkin, M.5    Youdim, M.B.6
  • 110
    • 0030912161 scopus 로고    scopus 로고
    • Inhibition of monoamine oxidase A and B activities by imidazol(ine)/guanidine drugs, nature of the interaction and distinction from I2-imidazoline receptors in rat liver
    • Ozaita A, Olmos G, Boronat MA, Lizcano JM, Unzeta M, García-Sevilla JA. Inhibition of monoamine oxidase A and B activities by imidazol(ine)/guanidine drugs, nature of the interaction and distinction from I2-imidazoline receptors in rat liver. Br. J. Pharmacol. 121(5), 901-912 (1997).
    • (1997) Br. J. Pharmacol , vol.121 , Issue.5 , pp. 901-912
    • Ozaita, A.1    Olmos, G.2    Boronat, M.A.3    Lizcano, J.M.4    Unzeta, M.5    García-Sevilla, J.A.6
  • 111
    • 0033023543 scopus 로고    scopus 로고
    • Relevance of benzyloxy group in 2-indolyl methylamines in the selective MAO-B inhibition
    • Pérez V, Marco JL, Fernández-A lvarez E, Unzeta M. Relevance of benzyloxy group in 2-indolyl methylamines in the selective MAO-B inhibition. Br. J. Pharmacol. 127(4), 869-876 (1999).
    • (1999) Br. J. Pharmacol , vol.127 , Issue.4 , pp. 869-876
    • Pérez, V.1    Marco, J.L.2    Fernández-A Lvarez, E.3    Unzeta, M.4
  • 112
    • 0020440236 scopus 로고
    • Determination of binding stoichiometry by the continuous variation method: The job plot
    • Huang CY. Determination of binding stoichiometry by the continuous variation method: the job plot. Methods Enzymol. 87, 509-525 (1982).
    • (1982) Methods Enzymol , vol.87 , pp. 509-525
    • Huang, C.Y.1
  • 113
    • 0030990079 scopus 로고    scopus 로고
    • In vitro permeability across Caco-2 cells (colonic) can predict in vivo (small intestinal) absorption in man - Fact or myth
    • Yee S. In vitro permeability across Caco-2 cells (colonic) can predict in vivo (small intestinal) absorption in man - fact or myth. Pharm. Res. 14(6), 763-766 (1997).
    • (1997) Pharm. Res , vol.14 , Issue.6 , pp. 763-766
    • Yee, S.1
  • 114
    • 0035782650 scopus 로고    scopus 로고
    • Reactive oxygen species and mitochondrial diseases
    • Kirkinezos IG, Moraes CT. Reactive oxygen species and mitochondrial diseases. Semin. Cell Dev. Biol. 12(6), 449-457 (2001).
    • (2001) Semin. Cell Dev. Biol , vol.12 , Issue.6 , pp. 449-457
    • Kirkinezos, I.G.1    Moraes, C.T.2
  • 115
    • 0028796770 scopus 로고
    • Inhibition of neuronal nitric oxide synthase by 7-nitroindazole protects against MPTP-induced neurotoxicity in mice
    • Schulz JB, Matthews RT, Muqit MM, Browne SE, Beal MF. Inhibition of neuronal nitric oxide synthase by 7-nitroindazole protects against MPTP-induced neurotoxicity in mice. J. Neurochem. 64(2), 936-939 (1995).
    • (1995) J. Neurochem , vol.64 , Issue.2 , pp. 936-939
    • Schulz, J.B.1    Matthews, R.T.2    Muqit, M.M.3    Browne, S.E.4    Beal, M.F.5
  • 116
    • 0029844003 scopus 로고    scopus 로고
    • Inhibition of neuronal nitric oxide synthase prevents MPTP-induced parkinsonism in baboons
    • Hantraye P, Brouillet E, Ferrante R et al. Inhibition of neuronal nitric oxide synthase prevents MPTP-induced parkinsonism in baboons. Nat. Med. 2(9), 1017-1102 (1996).
    • (1996) Nat. Med , vol.2 , Issue.9 , pp. 1017-1102
    • Hantraye, P.1    Brouillet, E.2    Ferrante, R.3
  • 117
    • 0025189864 scopus 로고
    • Apparent hydroxyl radical production by peroxynitrite: Implications for endothelial injury from nitric oxide and superoxide
    • Beckman JS, Beckman TW, Chen J, Marshall PA, Freeman BA. Apparent hydroxyl radical production by peroxynitrite: implications for endothelial injury from nitric oxide and superoxide. Proc. Natl Acad. Sci. USA 87(4), 1620-1624 (1990).
    • (1990) Proc. Natl Acad. Sci. USA , vol.87 , Issue.4 , pp. 1620-1624
    • Beckman, J.S.1    Beckman, T.W.2    Chen, J.3    Marshall, P.A.4    Freeman, B.A.5
  • 118
    • 0027336573 scopus 로고
    • The effect of side-chain substitution at positions 2 and 3 of the heterocyclic ring of N-Acetylenic analogues of tryptamine as monoamine oxidase inhibitors
    • Avila M, Balsa MD, Fernandez-Alvarez E, Tipton KF, Unzeta M. The effect of side-chain substitution at positions 2 and 3 of the heterocyclic ring of N-Acetylenic analogues of tryptamine as monoamine oxidase inhibitors. Biochem. Pharmacol. 45(11), 2231-2237 (1993).
    • (1993) Biochem. Pharmacol , vol.45 , Issue.11 , pp. 2231-2237
    • Avila, M.1    Balsa, M.D.2    Fernandez-Alvarez, E.3    Tipton, K.F.4    Unzeta, M.5
  • 119
    • 80053530118 scopus 로고    scopus 로고
    • NovelMAO-B inhibitors: Potential therapeutic use of the selective MAO-B inhibitor PF9601N in Parkinsons disease
    • Unzeta M, Sanz E, NovelMAO-B inhibitors: potential therapeutic use of the selective MAO-B inhibitor PF9601N in Parkinsons disease. Int. Rev. Neurobiol 100, 217-236 (2011).
    • (2011) Int. Rev. Neurobiol , vol.100 , pp. 217-236
    • Unzeta, M.1    Sanz, E.2
  • 120
    • 0037290217 scopus 로고    scopus 로고
    • PF 9601N [N-(2-propynyl)-2-(5- benzyloxy-indolyl) methylamine], a new MAO-B inhibitor, attenuates MPTP-induced depletion of striatal dopamine levels in C57/BL6 mice
    • Perez V, Unzeta M. PF 9601N [N-(2-propynyl)-2-(5- benzyloxy-indolyl) methylamine], a new MAO-B inhibitor, attenuates MPTP-induced depletion of striatal dopamine levels in C57/BL6 mice. Neurochem. Int. 42(3), 221-229 (2003).
    • (2003) Neurochem. Int , vol.42 , Issue.3 , pp. 221-229
    • Perez, V.1    Unzeta, M.2
  • 121
    • 0037199660 scopus 로고    scopus 로고
    • Neuroprotective effect of the monoamine oxidase inhibitor PF9601N [N-(2-propynyl)- 2-(5-benzyloxy- indolyl) methylamine] on rat nigral neurons after 6-OH-DA striatal lesion
    • Cutillas B, Ambrosio S, Unzeta M. Neuroprotective effect of the monoamine oxidase inhibitor PF9601N [N-(2-propynyl)- 2-(5-benzyloxy- indolyl) methylamine] on rat nigral neurons after 6-OH-DA striatal lesion. Neuroscience Lett. 329(2), 165-168 (2002).
    • (2002) Neuroscience Lett , vol.329 , Issue.2 , pp. 165-168
    • Cutillas, B.1    Ambrosio, S.2    Unzeta, M.3
  • 122
    • 13944274899 scopus 로고    scopus 로고
    • Indolalkylamines derivatives as antioxidant and neuroprotective agents in an experimental model of Parkinsons disease
    • Sanz E, Romera M, Bellik L, Marco JI, Unzeta M. Indolalkylamines derivatives as antioxidant and neuroprotective agents in an experimental model of Parkinsons disease. Med. Sci. Monit. 10(12), BR477-BR484 (2004).
    • (2004) Med. Sci. Monit , vol.10 , Issue.12 , pp. BR477-BR484
    • Sanz, E.1    Romera, M.2    Bellik, L.3    Marco, J.I.4    Unzeta, M.5
  • 123
    • 77956553922 scopus 로고    scopus 로고
    • Antioxidant properties of PF9601N, a novel MAO-B inhibitor: Assessment of its ability to interact with reactive nitrogen species
    • Bellik L, Dragoni S, Pessina F, Sanz E, Unzeta M, Valoti M. Antioxidant properties of PF9601N, a novel MAO-B inhibitor: assessment of its ability to interact with reactive nitrogen species. Acta Biochim. Pol. 57(2), 235-239 (2010).
    • (2010) Acta Biochim. Pol , vol.57 , Issue.2 , pp. 235-239
    • Bellik, L.1    Dragoni, S.2    Pessina, F.3    Sanz, E.4    Unzeta, M.5    Valoti, M.6
  • 124
    • 44649196507 scopus 로고    scopus 로고
    • Anti-Apoptotic effect of Mao-B inhibitor PF9601N [N-(2-propynyl)-2-(5- benzyloxyindolyl) methylamine] is mediated by p53 pathway inhibition in MPP+-treated SH-SY5Y human dopaminergic cells
    • Sanz E, Quintana A, Battaglia V et al. Anti-Apoptotic effect of Mao-B inhibitor PF9601N [N-(2-propynyl)-2-(5- benzyloxyindolyl) methylamine] is mediated by p53 pathway inhibition in MPP+-treated SH-SY5Y human dopaminergic cells. J. Neurochem. 105(6), 2404-2417 (2008).
    • (2008) J. Neurochem , vol.105 , Issue.6 , pp. 2404-2417
    • Sanz, E.1    Quintana, A.2    Battaglia, V.3
  • 125
    • 33846607750 scopus 로고    scopus 로고
    • Expression, microsomal and mitochondrial activities of cytochrome P450 enzymes in brain regions from control and phenobarbital-treated rabbits
    • Marini S, Nannelli A, Sodini D et al. Expression, microsomal and mitochondrial activities of cytochrome P450 enzymes in brain regions from control and phenobarbital-treated rabbits. Life Sci. 80(10), 910-917 (2007).
    • (2007) Life Sci , vol.80 , Issue.10 , pp. 910-917
    • Marini, S.1    Nannelli, A.2    Sodini, D.3
  • 126
    • 50549101921 scopus 로고    scopus 로고
    • A novel adenosine A(1) and A(2A) receptor antagonist ASP5854 ameliorates motor impairment in MPTP-treated marmosets: Comparison with existing anti-Parkinsons disease drugs
    • Mihara T, Iwashita A, Matsuoka N. A novel adenosine A(1) and A(2A) receptor antagonist ASP5854 ameliorates motor impairment in MPTP-treated marmosets: comparison with existing anti-Parkinsons disease drugs. Behav. Brain Res. 194(2), 152-161 (2008).
    • (2008) Behav. Brain Res , vol.194 , Issue.2 , pp. 152-161
    • Mihara, T.1    Iwashita, A.2    Matsuoka, N.3
  • 127
    • 78649499608 scopus 로고    scopus 로고
    • In vivo characterization of a dual adenosine A2A/A1 receptor antagonist in animal models of Parkinsons disease
    • Shook BC, Rassnick S, Osborne MC et al. In vivo characterization of a dual adenosine A2A/A1 receptor antagonist in animal models of Parkinsons disease. J. Med. Chem. 53(22), 8104-8115 (2010).
    • (2010) J. Med. Chem , vol.53 , Issue.22 , pp. 8104-8115
    • Shook, B.C.1    Rassnick, S.2    Osborne, M.C.3
  • 128
    • 35548950937 scopus 로고    scopus 로고
    • Pharmacological characterization of a novel, potent adenosine A1 and A2A receptor dual antagonist, 5-[5-Amino-3-(4-fluorophenyl) pyrazin-2-yl]-1-isopropylpyridine-2(1H)-one (ASP5854), in models of Parkinsons disease and cognition
    • Mihara T, Mihara K, Yarimizu J et al. Pharmacological characterization of a novel, potent adenosine A1 and A2A receptor dual antagonist, 5-[5-Amino-3-(4-fluorophenyl) pyrazin-2-yl]-1-isopropylpyridine-2(1H)-one (ASP5854), in models of Parkinsons disease and cognition. J. Pharmacol. Exp. Ther. 323(2), 708-719 (2007).
    • (2007) J. Pharmacol. Exp. Ther , vol.323 , Issue.2 , pp. 708-719
    • Mihara, T.1    Mihara, K.2    Yarimizu, J.3
  • 129
    • 84878952850 scopus 로고    scopus 로고
    • Istradefylline: First global approval
    • Dungo R, Deeks ED. Istradefylline: first global approval. Drugs 73(8), 875-882 (2013).
    • (2013) Drugs , vol.73 , Issue.8 , pp. 875-882
    • Dungo, R.1    Deeks, E.D.2
  • 130
    • 34248355605 scopus 로고    scopus 로고
    • Blocking striatal adenosine A2A receptors: A new strategy for basal ganglia disorders
    • Muller CE, Ferré S. Blocking striatal adenosine A2A receptors: a new strategy for basal ganglia disorders. Recent Pat. CNS Drug Discov. 2(1), 1-21 (2007).
    • (2007) Recent Pat. CNS Drug Discov , vol.2 , Issue.1 , pp. 1-21
    • Muller, C.E.1    Ferré, S.2
  • 131
    • 57749087002 scopus 로고    scopus 로고
    • Dual-target-directed drugs that block monoamine oxidase B and adenosine A(2A) receptors for Parkinsons disease
    • Petzer JP, Castagnoli N Jr, Schwarzschild MA, Chen JF, Van der Schyf CJ. Dual-target-directed drugs that block monoamine oxidase B and adenosine A(2A) receptors for Parkinsons disease. Neurotherapeutics 6(1), 141 (2009).
    • (2009) Neurotherapeutics , vol.6 , Issue.1 , pp. 141
    • Petzer, J.P.1    Castagnoli, Jr.N.2    Schwarzschild, M.A.3    Chen, J.F.4    Van Der Schyf, C.J.5
  • 132
    • 84886952444 scopus 로고    scopus 로고
    • Symptomatic and neuroprotective effects of a2a receptor antagonists in Parkinsons disease
    • Masino S, Boison D (Eds). Springer, NY, USA
    • Pinna A, Simola N, Frau L, Morelli M. Symptomatic and neuroprotective effects of a2a receptor antagonists in Parkinsons disease. In:Adenosine: A Key Link Between Metabolism and Brain Activity. Masino S, Boison D (Eds). Springer, NY, USA, 361-384 (2013).
    • (2013) Adenosine: A Key Link between Metabolism and Brain Activity , pp. 361-384
    • Pinna, A.1    Simola, N.2    Frau, L.3    Morelli, M.4
  • 133
    • 41849085227 scopus 로고    scopus 로고
    • Adenosine A2A receptor antagonists exert motor and neuroprotective effects by distinct cellular mechanisms
    • Yu L, Shen HY, Coelho JE et al. Adenosine A2A receptor antagonists exert motor and neuroprotective effects by distinct cellular mechanisms. Ann. Neurol. 63(3), 338-346 (2008).
    • (2008) Ann. Neurol , vol.63 , Issue.3 , pp. 338-346
    • Yu, L.1    Shen, H.Y.2    Coelho, J.E.3
  • 134
    • 84870251836 scopus 로고    scopus 로고
    • Monoamine oxidase inhibitors and neuroprotection: A review
    • Al-Nuaimi SK, Mackenzie EM, Baker GB. Monoamine oxidase inhibitors and neuroprotection: a review. Am. J. Ther. 19(6), 436-448 (2012).
    • (2012) Am. J. Ther , vol.19 , Issue.6 , pp. 436-448
    • Al-Nuaimi, S.K.1    Mackenzie, E.M.2    Baker, G.B.3
  • 135
    • 84865640480 scopus 로고    scopus 로고
    • Adenosine A2A antagonists in Parkinsons disease: Whats next?
    • Hickey P, Stacy M. Adenosine A2A antagonists in Parkinsons disease: whats next? Curr. Neurol. Neurosci. Rep. 12(4), 376-385 (2012).
    • (2012) Curr. Neurol. Neurosci. Rep , vol.12 , Issue.4 , pp. 376-385
    • Hickey, P.1    Stacy, M.2
  • 136
    • 84886946282 scopus 로고    scopus 로고
    • 1, 3-Dialkylsubstituted tetrahydropyrimido[1, 2-f ]purine-2, 4-diones as multiple target drugs for the potential treatment of neurodegenerative diseases
    • Koch P, Akkari R, Brunschweiger A et al. 1, 3-Dialkylsubstituted tetrahydropyrimido[1, 2-f ]purine-2, 4-diones as multiple target drugs for the potential treatment of neurodegenerative diseases. Bioorg. Med. Chem. 21(23), 7435-7452 (2013).
    • (2013) Bioorg. Med. Chem , vol.21 , Issue.23 , pp. 7435-7452
    • Koch, P.1    Akkari, R.2    Brunschweiger, A.3
  • 137
    • 33748740645 scopus 로고    scopus 로고
    • Synthesis and biological activity of tricyclic aryloimidazo-, pyrimido-, and diazepinopurinediones
    • Drabczyñska A, Müller CE, Lacher SK et al. Synthesis and biological activity of tricyclic aryloimidazo-, pyrimido-, and diazepinopurinediones. Bioorg. Med. Chem. 14(21), 7258-7281 (2006).
    • (2006) Bioorg. Med. Chem , vol.14 , Issue.21 , pp. 7258-7281
    • Drabczyñska, A.1    Müller, C.E.2    Lacher, S.K.3
  • 138
    • 78650757374 scopus 로고    scopus 로고
    • Cholinergic and neuroprotective drugs for the treatment of Alzheimer and neuronal vascular diseases. II. Syn thesis, biological assessment, and molecular modelling of new tacrine analogues from highly substituted 2-Aminopyridine-3- carbonitriles
    • Samadi A, Valderas C, de los Ríos C et al. Cholinergic and neuroprotective drugs for the treatment of Alzheimer and neuronal vascular diseases. II. Synthesis, biological assessment, and molecular modelling of new tacrine analogues from highly substituted 2-Aminopyridine-3- carbonitriles. Bioorg. Med. Chem. 19(1), 122-133 (2011).
    • (2011) Bioorg. Med. Chem , vol.19 , Issue.1 , pp. 122-133
    • Samadi, A.1    Valderas, C.2    De Los Ríos, C.3
  • 139
    • 57649148545 scopus 로고    scopus 로고
    • N-Acetylcysteine for antioxidant therapy: Pharmacology and clinical utility
    • Dodd S, Dean O, Copolov DL, Malhi GS, Berk M. N-Acetylcysteine for antioxidant therapy: pharmacology and clinical utility. Expert Opin. Biol. Ther. 8(12), 1955-1962 (2008).
    • (2008) Expert Opin. Biol. Ther , vol.8 , Issue.12 , pp. 1955-1962
    • Dodd, S.1    Dean, O.2    Copolov, D.L.3    Malhi, G.S.4    Berk, M.5
  • 140
    • 84892179731 scopus 로고    scopus 로고
    • Synthesis and studies of calcium channel blocking and antioxidant activities of novel 4-pyridinium and/or N-propargyl substituted 1, 4-dihydropyridine derivatives
    • Rucins M, Kaldre D, Pajuste K et al. Synthesis and studies of calcium channel blocking and antioxidant activities of novel 4-pyridinium and/or N-propargyl substituted 1, 4-dihydropyridine derivatives. C. R. Chimie 17, 69-80 (2014).
    • (2014) C. R. Chimie , vol.17 , pp. 69-80
    • Rucins, M.1    Kaldre, D.2    Pajuste, K.3
  • 141
    • 77249089823 scopus 로고    scopus 로고
    • Synthesis of dihydrofuroaporphine derivatives: Identification of a potent and selective serotonin 5-HT 1A receptor agonist
    • Liu Z, Zhang H, Ye N et al. Synthesis of dihydrofuroaporphine derivatives: identification of a potent and selective serotonin 5-HT 1A receptor agonist. J. Med. Chem. 53(3), 1319-1328 (2010).
    • (2010) J. Med. Chem , vol.53 , Issue.3 , pp. 1319-1328
    • Liu, Z.1    Zhang, H.2    Ye, N.3
  • 142
    • 0024360932 scopus 로고
    • 1, 4-Dihydropyridines - A basis for developing new drugs
    • Bossert F, Vater W. 1, 4-Dihydropyridines - a basis for developing new drugs. Med. Res. Rev. 9(3), 291-324 (1989).
    • (1989) Med. Res. Rev , vol.9 , Issue.3 , pp. 291-324
    • Bossert, F.1    Vater, W.2
  • 143
    • 34249049430 scopus 로고    scopus 로고
    • Calcium channel antagonists: Clinical uses - Past, present and future
    • Triggle DJ. Calcium channel antagonists: clinical uses - past, present and future. Biochem. Pharmacol. 74(1), 1-9 (2007).
    • (2007) Biochem. Pharmacol , vol.74 , Issue.1 , pp. 1-9
    • Triggle, D.J.1
  • 144
    • 44449155992 scopus 로고    scopus 로고
    • Dihydropyridine derivatives as bioprotectors
    • Duburs G, Vigante B, Plotniece A et al. Dihydropyridine derivatives as bioprotectors. Chim. Oggi. 26, 68-70 (2008).
    • (2008) Chim. Oggi , vol.26 , pp. 68-70
    • Duburs, G.1    Vigante, B.2    Plotniece, A.3
  • 145
    • 0034741123 scopus 로고    scopus 로고
    • Dopamine D3 receptor as a therapeutic target for antipsychotic and antiparkinsonian drugs
    • Joyce JN. Dopamine D3 receptor as a therapeutic target for antipsychotic and antiparkinsonian drugs. Pharmacol. Ther. 90(2-3), 231-259 (2001).
    • (2001) Pharmacol. Ther , vol.90 , Issue.2-3 , pp. 231-259
    • Joyce, J.N.1
  • 146
    • 0033595283 scopus 로고    scopus 로고
    • Selective inhibition of cocaine-seeking behaviour by a partial dopamine D3 receptor agonist
    • Pilla M, Perachon S, Sautel F et al. Selective inhibition of cocaine-seeking behaviour by a partial dopamine D3 receptor agonist. Nature 400(6742), 371-375 (1999).
    • (1999) Nature , vol.400 , Issue.6742 , pp. 371-375
    • Pilla, M.1    Perachon, S.2    Sautel, F.3
  • 147
    • 0032841418 scopus 로고    scopus 로고
    • Cocaine addiction therapy - Are we partially there?
    • Koob GF, Caine SB. Cocaine addiction therapy - are we partially there? Nat. Med. 5(9), 993-995 (1999).
    • (1999) Nat. Med , vol.5 , Issue.9 , pp. 993-995
    • Koob, G.F.1    Caine, S.B.2
  • 148
    • 0033596820 scopus 로고    scopus 로고
    • Restless legs syndrome improved by pramipexole: A doubleblind randomized trial
    • Montplaisir J, Nicolas A, Denesle R, Gomez-Mancilla B. Restless legs syndrome improved by pramipexole: a doubleblind randomized trial. Neurology 52(5), 938-943 (1999).
    • (1999) Neurology , vol.52 , Issue.5 , pp. 938-943
    • Montplaisir, J.1    Nicolas, A.2    Denesle, R.3    Gomez-Mancilla, B.4
  • 149
    • 0030610305 scopus 로고    scopus 로고
    • The D3 dopamine receptor: Neurobiology and potential clinical relevance
    • Levant B. The D3 dopamine receptor: neurobiology and potential clinical relevance. Pharmacol. Rev. 49(3), 231-252 (1997).
    • (1997) Pharmacol. Rev , vol.49 , Issue.3 , pp. 231-252
    • Levant, B.1
  • 150
    • 20144378943 scopus 로고    scopus 로고
    • Dopamine D3 receptor partial agonists and antagonists as potential drug abuse therapeutic agents
    • Newman AH, Grundt P, Nader MA. Dopamine D3 receptor partial agonists and antagonists as potential drug abuse therapeutic agents. J. Med. Chem. 48(11), 3663-3679 (2005).
    • (2005) J. Med. Chem , vol.48 , Issue.11 , pp. 3663-3679
    • Newman, A.H.1    Grundt, P.2    Nader, M.A.3
  • 151
    • 34347391256 scopus 로고    scopus 로고
    • Yawning and hypothermia in rats: Effects of dopamine D3 and D2 agonists and antagonists
    • Collins GT, Newman AH, Grundt P et al. Yawning and hypothermia in rats: effects of dopamine D3 and D2 agonists and antagonists. Psychopharmacology (Berl.) 193(2), 159-170 (2007).
    • (2007) Psychopharmacology (Berl.) , vol.193 , Issue.2 , pp. 159-170
    • Collins, G.T.1    Newman, A.H.2    Grundt, P.3
  • 152
    • 0032861496 scopus 로고    scopus 로고
    • The neuroprotective effect of a new serotonin receptor agonist, BAY X3702, upon focal ischemic brain damage caused by acute subdural hematoma in the rat
    • Alessandri B, Tsuchida E, Bullock RM. The neuroprotective effect of a new serotonin receptor agonist, BAY X3702, upon focal ischemic brain damage caused by acute subdural hematoma in the rat. Brain Res. 845(2), 232-235 (1999).
    • (1999) Brain Res , vol.845 , Issue.2 , pp. 232-235
    • Alessandri, B.1    Tsuchida, E.2    Bullock, R.M.3
  • 153
    • 0035951899 scopus 로고    scopus 로고
    • New 5-HT1A receptor agonists possessing 1, 4-benzoxazepine scaffold exhibit highly potent anti-ischemic effects
    • Kamei K, Maeda N, Ogino R et al. New 5-HT1A receptor agonists possessing 1, 4-benzoxazepine scaffold exhibit highly potent anti-ischemic effects. Bioorg. Med. Chem. Lett. 11(4), 595-598 (2001).
    • (2001) Bioorg. Med. Chem. Lett , vol.11 , Issue.4 , pp. 595-598
    • Kamei, K.1    Maeda, N.2    Ogino, R.3
  • 154
    • 0035960558 scopus 로고    scopus 로고
    • Serotonin 5-HT1A agonist improves motor complications in rodent and primate parkinsonian models
    • Bibbiani F, Oh JD, Chase TN. Serotonin 5-HT1A agonist improves motor complications in rodent and primate parkinsonian models. Neurology 57(10), 1829 (2001).
    • (2001) Neurology , vol.57 , Issue.10 , pp. 1829
    • Bibbiani, F.1    Oh, J.D.2    Chase, T.N.3
  • 155
    • 0029689597 scopus 로고    scopus 로고
    • Involvement of serotonin in clinical features of Parkinsons disease and complications of L-DOPA therapy
    • Melamed E, Zoldan J, Friedberg G, Ziv I, Weizmann A. Involvement of serotonin in clinical features of Parkinsons disease and complications of L-DOPA therapy. Adv. Neurol. 69, 545-550 (1996).
    • (1996) Adv. Neurol , vol.69 , pp. 545-550
    • Melamed, E.1    Zoldan, J.2    Friedberg, G.3    Ziv, I.4    Weizmann, A.5
  • 156
    • 0030906167 scopus 로고    scopus 로고
    • 8-OH-DPAT, a 5-HT1A agonist and ritanserin, a 5-HT2A/C antagonist, reverse haloperidolinduced catalepsy in rats independently of striatal dopamine release
    • Lucas G, Bonhomme N, De Deurwaerdere P, Le Moal M, Spampinato U. 8-OH-DPAT, a 5-HT1A agonist and ritanserin, a 5-HT2A/C antagonist, reverse haloperidolinduced catalepsy in rats independently of striatal dopamine release. Psychopharmacology (Berl.) 131(1), 57-63 (1997).
    • (1997) Psychopharmacology (Berl.) , vol.131 , Issue.1 , pp. 57-63
    • Lucas, G.1    Bonhomme, N.2    De Deurwaerdere, P.3    Le Moal, M.4    Spampinato, U.5
  • 157
    • 0036460744 scopus 로고    scopus 로고
    • 5-hydroxytryptamine (5-HT, serotonin) and Parkinsons disease - Opportunities for novel therapeutics to reduce the problems of levodopa therapy
    • Nicholson SL, Brotchie JM. 5-hydroxytryptamine (5-HT, serotonin) and Parkinsons disease - opportunities for novel therapeutics to reduce the problems of levodopa therapy. Eur. J. Neurol. 9(Suppl. 3), 1-6 (2002).
    • (2002) Eur. J. Neurol , vol.9 , pp. 1-6
    • Nicholson, S.L.1    Brotchie, J.M.2


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