메뉴 건너뛰기




Volumn 18, Issue 30, 2011, Pages 4568-4587

Targeting monoamine oxidases with multipotent ligands: An emerging strategy in the search of new drugs against neurodegenerative diseases

Author keywords

Acetylcholinesterase inhibition; Alzheimer's disease; Monoamine oxidase inhibition; Multi target directed ligands; Neurodegenerative diseases; Parkinson's disease

Indexed keywords

ACETYLCHOLINESTERASE; ADENOSINE A2A RECEPTOR ANTAGONIST; AMINE OXIDASE (FLAVIN CONTAINING) ISOENZYME A; AMINE OXIDASE (FLAVIN CONTAINING) ISOENZYME B; BROFAROMINE; CHOLINESTERASE INHIBITOR; CLORGYLINE; DONEPEZIL; DOPAMINE; IPRONIAZID; ISOCARBOXAZID; LAZABEMIDE; LEVODOPA; MOCLOBEMIDE; MONOAMINE OXIDASE INHIBITOR; MUSCARINIC AGENT; NITRIC OXIDE SYNTHASE; NORADRENALIN; PHENELZINE; PROTEIN BCL 2; PROTEIN BCL XL; RASAGILINE; REACTIVE OXYGEN METABOLITE; SELEGILINE; SEROTONIN; SEROTONIN UPTAKE INHIBITOR; TOLOXATONE; TRANYLCYPROMINE; TRICYCLIC ANTIDEPRESSANT AGENT; UNINDEXED DRUG;

EID: 80053462390     PISSN: 09298673     EISSN: 1875533X     Source Type: Journal    
DOI: 10.2174/092986711797379302     Document Type: Review
Times cited : (80)

References (171)
  • 1
    • 41549108420 scopus 로고    scopus 로고
    • From single- to multi-target drugs in cancer therapy: When aspecificity becomes an advantage
    • DOI 10.2174/092986708783503212
    • Petrelli, A.; Giordano, S. From single- to multi-target drugs in cancertherapy: when aspecificity becomes an advantage. Curr. Med. Chem., 2008, 15, 422-432. (Pubitemid 351472408)
    • (2008) Current Medicinal Chemistry , vol.15 , Issue.5 , pp. 422-432
    • Petrelli, A.1    Giordano, S.2
  • 3
    • 3242794178 scopus 로고    scopus 로고
    • From magic bullets to designed multipleligands
    • Morphy, R.; Kay, C.; Rankovic, Z. From magic bullets to designed multipleligands. Drug Discov. Today, 2004, 9, 641-651.
    • (2004) Drug Discov. Today , vol.9 , pp. 641-651
    • Morphy, R.1    Kay, C.2    Rankovic, Z.3
  • 5
    • 79953695916 scopus 로고    scopus 로고
    • In silicorepositioning of approved drugs for rare and neglected diseases
    • (a) Ekins, S.; Williams, A.J.; Krasowski, M.D.; Freundlich, J.S. In silicorepositioning of approved drugs for rare and neglected diseases. DrugDiscov. Today, 2011, 16, 298-310
    • (2011) DrugDiscov. Today , vol.16 , pp. 298-310
    • Ekins, S.1    Williams, A.J.2    Krasowski, M.D.3    Freundlich, J.S.4
  • 6
    • 4344668661 scopus 로고    scopus 로고
    • Drug repositioning: Identifying and developing new uses for existing drugs
    • (b)Ashburn, T.T.; Thor, K.B. Drugrepositioning: identifying and developing new uses for existing drugs. Nat.Rev. Drug Discov., 2004, 3, 673-683. (Pubitemid 39173508)
    • (2004) Nature Reviews Drug Discovery , vol.3 , Issue.8 , pp. 673-683
    • Ashburn, T.T.1    Thor, K.B.2
  • 7
    • 27144449695 scopus 로고    scopus 로고
    • Designed multiple ligands. An emerging drug discovery paradigm
    • DOI 10.1021/jm058225d
    • Morphy, R.; Rankovic, Z. Designed multiple ligands. An emerging drugdiscovery paradigm. J. Med. Chem., 2005, 48, 6523-6543. (Pubitemid 41504710)
    • (2005) Journal of Medicinal Chemistry , vol.48 , Issue.21 , pp. 6523-6543
    • Morphy, R.1    Rankovic, Z.2
  • 9
    • 34548619267 scopus 로고    scopus 로고
    • Amine oxidases and monooxygenases in the in vivo metabolism of xenobiotic amines in humans: Has the involvement of amine oxidases been neglected?
    • DOI 10.1111/j.1472-8206.2007.00498.x
    • Strolin-Benedetti, M.; Tipton, K.F.; Whomsley, R. Amine oxidases andmonooxygenases in the in vivo metabolism of xenobiotic amines in humans:has the involvement of amine oxidases been neglected? Fundam. Clin. Pharmacol., 2007, 21, 467-479. (Pubitemid 47404324)
    • (2007) Fundamental and Clinical Pharmacology , vol.21 , Issue.5 , pp. 467-479
    • Strolin Benedetti, M.1    Tipton, K.F.2    Whomsley, R.3
  • 11
    • 0034642217 scopus 로고    scopus 로고
    • Structure-activity relations in theoxidation of phenethylamine analogues by recombinant human livermonoamine oxidase A
    • Nandigama, R.K.; Edmondson, D.E. Structure-activity relations in theoxidation of phenethylamine analogues by recombinant human livermonoamine oxidase A. Biochemistry, 2000, 39, 15258-15265.
    • (2000) Biochemistry , vol.39 , pp. 15258-15265
    • Nandigama, R.K.1    Edmondson, D.E.2
  • 12
    • 0024995831 scopus 로고
    • Tissue distribution ofhuman monoamine oxidase-A and oxidase-B messenger-RNA
    • Grimsby, J.; lan, N.C.; Neve, R.; Chen, K.; Shih, J.C. Tissue distribution ofhuman monoamine oxidase-A and oxidase-B messenger-RNA. J.Neurochem., 1990, 55, 1166-1169.
    • (1990) J.Neurochem. , vol.55 , pp. 1166-1169
    • Grimsby, J.1    Lan, N.C.2    Neve, R.3    Chen, K.4    Shih, J.C.5
  • 13
    • 0021250642 scopus 로고
    • Selective inhibitors of monoamine oxidase A and B: Biochemical, pharmacological, and clinical properties
    • Fowler, C.J.; Ross, S.B. Selective inhibitors of monoamine oxidase A and B:biochemical, pharmacological, and clinical properties. Med. Res. Rev., 1984, 4, 323-358. (Pubitemid 14073188)
    • (1984) Medicinal Research Reviews , vol.4 , Issue.3 , pp. 323-358
    • Fowler, C.J.1    Ross, S.B.2
  • 14
    • 0017088112 scopus 로고
    • Studies on monoamine oxidase. XVIII. Enzymatic properties ofplacental monoamine oxidase
    • Egashira, T. Studies on monoamine oxidase. XVIII. Enzymatic properties ofplacental monoamine oxidase. Jap. J. Pharmac., 1976, 26, 493-500.
    • (1976) Jap. J. Pharmac. , vol.26 , pp. 493-500
    • Egashira, T.1
  • 15
    • 0017329403 scopus 로고
    • Substrate-and inhibitor-related characteristicsof human platelet monoamine oxidase
    • Donnelly, C.H.; Murphy, D.L. Substrate- and inhibitor-related characteristicsof human platelet monoamine oxidase. Biochem. Pharmacol., 1977, 26, 852-858.
    • (1977) Biochem. Pharmacol. , vol.26 , pp. 852-858
    • Donnelly, C.H.1    Murphy, D.L.2
  • 16
    • 0026550390 scopus 로고
    • Quantitative enzymeradioautography with 3H-Ro 41-1049 and 3HRo 19-6327 in vitro:localization and abundance of MAO-A and MAO-B in rat CNS, peripheralorgans, and human brain
    • Saura, J.; Kettler, R.; Da Prada, M.; Richards, J.G. Quantitative enzymeradioautography with 3H-Ro 41-1049 and 3HRo 19-6327 in vitro:localization and abundance of MAO-A and MAO-B in rat CNS, peripheralorgans, and human brain. J. Neurosci., 1992, 12, 1977-1999.
    • (1992) J. Neurosci. , vol.12 , pp. 1977-1999
    • Saura, J.1    Kettler, R.2    Da Prada, M.3    Richards, J.G.4
  • 17
    • 33645307953 scopus 로고    scopus 로고
    • The therapeutic potentialof monoamine oxidase inhibitors
    • (a) Youdim, M.B.; Edmondson, D.E.; Tipton, K.F. The therapeutic potentialof monoamine oxidase inhibitors. Nat. Rev. Neurosci., 2006, 7, 295-309
    • (2006) Nat. Rev. Neurosci. , vol.7 , pp. 295-309
    • Youdim, M.B.1    Edmondson, D.E.2    Tipton, K.F.3
  • 18
    • 0346154805 scopus 로고    scopus 로고
    • Clinical pharmacology of MAO inhibitors: Safetyand future
    • (b)Yamada, M.; Yasuhara, H. Clinical pharmacology of MAO inhibitors: safetyand future. Neurotoxicology, 2004, 25, 215-221.
    • Neurotoxicology , vol.2004 , Issue.25 , pp. 215-221
    • Yamada, M.1    Yasuhara, H.2
  • 19
    • 0020672172 scopus 로고
    • Selective MAO A and B inhibitors: Their mechanism of action and pharmacology
    • DOI 10.1016/0028-3908(83)90194-6
    • Finberg, J.P.M.; Youdim, M.B.H. Selective MAO-A and MAO-B inhibitors:their mechanism of action and pharmacology. Neuropharmacology, 1983, 22, 441-446. (Pubitemid 13152056)
    • (1983) Neuropharmacology , vol.22 , Issue.3 B , pp. 441-446
    • Finberg, J.P.M.1    Youdim, M.B.H.2
  • 20
    • 36849055017 scopus 로고    scopus 로고
    • Monoamine oxidase-B inhibition in thetreatment of Parkinson's disease
    • Fernandez, H.H.; Chen, J.J. Monoamine oxidase-B inhibition in thetreatment of Parkinson's disease. Pharmacotherapy, 2007, 27, S174-S185.
    • (2007) Pharmacotherapy , vol.27
    • Fernandez, H.H.1    Chen, J.J.2
  • 22
    • 77953383270 scopus 로고    scopus 로고
    • Early pharmacologic treatment in Parkinson's disease
    • Hauser, R.A. Early pharmacologic treatment in Parkinson's disease. Am. J.Manag. Care, 2010, 16, S100-S107.
    • (2010) Am. J.Manag. Care , vol.16
    • Hauser, R.A.1
  • 23
    • 59349103130 scopus 로고    scopus 로고
    • Genotoxic stress in plants:shedding light on DNA damage, repair and DNA repair helicases
    • Tuteja, N.; Ahmad, P.; Panda, B.B.; Tuteja, R. Genotoxic stress in plants:shedding light on DNA damage, repair and DNA repair helicases. Mut. Res-Rev. Mutat., 2009, 681, 134-149.
    • (2009) Mut. Res-Rev. Mutat. , vol.681 , pp. 134-149
    • Tuteja, N.1    Ahmad, P.2    Panda, B.B.3    Tuteja, R.4
  • 24
  • 25
    • 29044438902 scopus 로고    scopus 로고
    • The crucial role of metal ions in neurodegeneration: The basis for a promising therapeutic strategy
    • DOI 10.1038/sj.bjp.0706416
    • Gaeta, A.; Hider, R.C. The crucial role of metal ions in neurodegeneration:the basis for a promising therapeutic strategy. Br. J. Pharmacol., 2005, 146, 1041-1059. (Pubitemid 41786957)
    • (2005) British Journal of Pharmacology , vol.146 , Issue.8 , pp. 1041-1059
    • Gaeta, A.1    Hider, R.C.2
  • 26
    • 0037264120 scopus 로고    scopus 로고
    • Unfolding the role of protein misfolding in neurodegenerative diseases
    • DOI 10.1038/nrn1007
    • Soto, C. Unfolding the role of protein misfolding in neurodegenerativediseases. Nat. Rev. Neurosci., 2003, 4, 49-60. (Pubitemid 37271088)
    • (2003) Nature Reviews Neuroscience , vol.4 , Issue.1 , pp. 49-60
    • Soto, C.1
  • 27
    • 33750347347 scopus 로고    scopus 로고
    • Mitochondrial dysfunction and oxidative stress in neurodegenerative diseases
    • DOI 10.1038/nature05292, PII NATURE05292
    • Lin, M.T.; Beal, M.F. Mitochondrial dysfunction and oxidative stress inneurodegenerative diseases. Nature, 2006, 443, 787-795. (Pubitemid 44622683)
    • (2006) Nature , vol.443 , Issue.7113 , pp. 787-795
    • Lin, M.T.1    Beal, M.F.2
  • 28
    • 0031596711 scopus 로고    scopus 로고
    • (R)(+)-N-propargyl-1-aminoindan (rasagiline) andderivatives: Highly selective and potent inhibitors of monoamine oxidase B
    • Sterling, J.; Veinberg, A.; Lerner, D.; Goldenberg, W.; Levy, R.; Youdim, M.; Finberg, J. (R)(+)-N-propargyl-1-aminoindan (rasagiline) andderivatives: Highly selective and potent inhibitors of monoamine oxidase B.J. Neural Transm.-Supp., 1998, 52, 301-305.
    • (1998) J. Neural Transm.-Supp. , vol.52 , pp. 301-305
    • Sterling, J.1    Veinberg, A.2    Lerner, D.3    Goldenberg, W.4    Levy, R.5    Youdim, M.6    Finberg, J.7
  • 31
    • 30444437749 scopus 로고    scopus 로고
    • Monoamine oxidase: Isoforms and inhibitors in Parkinson's disease and depressive illness
    • DOI 10.1038/sj.bjp.0706464, PII 0706464
    • (c) Youdim, M.B.H.; Bakhle, Y.S. Monoamine oxidase: isoforms and inhibitors inParkinson's disease and depressive illness. Br. J. Pharmacol., 2006, 147, S287-S296 (Pubitemid 43077287)
    • (2006) British Journal of Pharmacology , vol.147 , Issue.SUPPL. 1
    • Youdim, M.B.H.1    Bakhle, Y.S.2
  • 32
    • 33645307953 scopus 로고    scopus 로고
    • Thetherapeutic potential of monoamine oxidase inhibitors
    • (d) Youdim, M.B.H.; Edmondson, D.; Tipton, K.F. Thetherapeutic potential of monoamine oxidase inhibitors. Nat. Rev. Neurosci., 2006, 7, 295-309.
    • (2006) Nat. Rev. Neurosci. , vol.7 , pp. 295-309
    • Youdim, M.B.H.1    Edmondson, D.2    Tipton, K.F.3
  • 33
    • 0018068203 scopus 로고
    • Amphetamine and 2-phenylethylamine in post-mortem parkinsonian brain after (-)deprenyl administration
    • Reynolds, G.P.; Riederer, P.; Sandler, M.; Jellinger, K.; Seemann, D.Amphetamine and 2-phenylethylamine in post-mortem Parkinsonian brainafter (L)-deprenyl administration. J. Neural Transm., 1978, 43, 271-277. (Pubitemid 9050088)
    • (1978) Journal of Neural Transmission - General Section , vol.43 , Issue.3-4 , pp. 271-277
    • Reynolds, G.P.1    Riederer, P.2    Sandler, M.3
  • 34
    • 0019462668 scopus 로고
    • Tyramine antagonistic properties of AGN 1135, an irreversible inhibitor of monoamine oxidase type B
    • (a) Finberg, J.P.; Tenne, M.; Youdim, M.B.H. Tyramine antagonisticproperties of AGN 1135, an irreversible inhibitor of monoamine oxidase typeB. Br. J. Pharmacol., 1981, 73, 65-74 (Pubitemid 11104761)
    • (1981) British Journal of Pharmacology , vol.73 , Issue.1 , pp. 65-74
    • Finberg, J.P.M.1    Tenne, M.2    Youdim, M.B.H.3
  • 35
    • 0018139965 scopus 로고
    • Evidence that deprenyl, a type B monoamine oxidase inhibitor, is an indirectly acting sympathomimetic amine
    • DOI 10.1016/0006-2952(78)90490-2
    • (b) Simpson, L.L. Evidence thatdeprenyl, a type B monoamine oxidase inhibitor, is an indirectly actingsympathomimetic amine. Biochem. Pharmacol., 1978, 27, 1591-1595. (Pubitemid 8406839)
    • (1978) Biochemical Pharmacology , vol.27 , Issue.11 , pp. 1591-1595
    • Simpson, L.L.1
  • 36
    • 0036206323 scopus 로고    scopus 로고
    • The anti-parkinson drug, rasagiline, prevents apoptotic DNA damage induced by peroxynitrite in human dopaminergic neuroblastoma SH-SY5Y cells
    • DOI 10.1007/s007020200038
    • Maruyama, W.; Takahashi, T.; Youdim, M.B.H.; Naoi, M. The antiparkinsondrug, rasagiline, prevents apoptotic DNA damage induced byperoxynitrite in human dopaminergic neuroblastoma SH-SY5Y cells. J.Neural Transm., 2002, 109, 467-481. (Pubitemid 34280405)
    • (2002) Journal of Neural Transmission , vol.109 , Issue.4 , pp. 467-481
    • Maruyama, W.1    Takahashi, T.2    Youdim, M.3    Naoi, M.4
  • 37
    • 0022378166 scopus 로고
    • Prevention of MPTP-induced neurotoxicity by AGN-1133 and AGN-1135, selective inhibitors of monoamine oxidase-B
    • DOI 10.1016/0014-2999(85)90168-2
    • Heikkila, R.E.; Duvoisin, R.C.; Finberg, J.P.; Youdim, M.B.H. Prevention ofMPTP-induced neurotoxicity by AGN-1133 and AGN-1135, selectiveinhibitors of monoamine oxidase-B. Eur. J. Pharmacol., 1985, 116, 313-317. (Pubitemid 16191823)
    • (1985) European Journal of Pharmacology , vol.116 , Issue.3 , pp. 313-317
    • Heikkila, R.E.1    Duvoisin, R.C.2    Finberg, J.P.M.3    Youdim, M.B.H.4
  • 38
    • 0034525891 scopus 로고    scopus 로고
    • Neurotoxins induce apoptosis in dopamine neurons: Protection by N-propargylamine-1(R)- and (S)-aminoindan, rasagiline and TV1022
    • Maruyama, W.; Akao, Y.; Youdim, M.B.H.; Naoi, M. Neurotoxins induceapoptosis in dopamine neurons: protection by N-propargylamine-1(R)- and(S)-aminoindan, rasagiline and TV1022. J. Neural Transm.-Supp., 2000, 60, 171-186. (Pubitemid 32037192)
    • (2000) Journal of Neural Transmission, Supplement , Issue.60 , pp. 171-186
    • Maruyama, W.1    Akao, Y.2    Youdim, M.B.H.3    Naoi, M.4
  • 39
    • 0036677312 scopus 로고    scopus 로고
    • Mitochondrialpermeability transition mediates apoptosis induced by N-methyl-(R)-salsolinol, an endogenous neurotoxin, and is inhibited by Bcl-2 andrasagiline, N-propargyl-1(R)- aminoindan
    • Akao, Y.; Maruyama, W.; Shimizu, S.; Yi, H.; Nakagawa, Y.; Shamoto-Nagai, M.; Youdim, M.B.; Tsujimoto, Y.; Naoi, M. Mitochondrialpermeability transition mediates apoptosis induced by N-methyl-(R)-salsolinol, an endogenous neurotoxin, and is inhibited by Bcl-2 andrasagiline, N-propargyl-1(R)- aminoindan. J. Neurochem., 2002, 82, 913-923.
    • (2002) J. Neurochem. , vol.82 , pp. 913-923
    • Akao, Y.1    Maruyama, W.2    Shimizu, S.3    Yi, H.4    Nakagawa, Y.5    Shamoto-Nagai, M.6    Youdim, M.B.7    Tsujimoto, Y.8    Naoi, M.9
  • 40
    • 0032999575 scopus 로고    scopus 로고
    • Neuroprotective effect of rasagiline, a selective monoamine oxidase-B inhibitor, against closed head injury in the mouse
    • DOI 10.1016/S0014-2999(98)00929-7, PII S0014299998009297
    • Huang, W.; Chen, Y.; Shohami, E.; Weinstock, M. Neuroprotective effect ofrasagiline, a selective monoamine oxidase-B inhibitor, against closed headinjury in the mouse. Eur. J. Pharmacol., 1999, 366, 127-135. (Pubitemid 29080775)
    • (1999) European Journal of Pharmacology , vol.366 , Issue.2-3 , pp. 127-135
    • Huang, W.1    Chen, Y.2    Shohami, E.3    Weinstock, M.4
  • 41
    • 0035130289 scopus 로고    scopus 로고
    • Rasagiline [N-propargyl-1R(+)-aminoindan], a selective and potent inhibitor of mitochondrial monoamine oxidase B
    • Youdim, M.B.H.; Gross, A.; Finberg, J.P.M. Rasagiline [N-propargyl-1R(+)aminoindan], a selective and potent inhibitor of mitochondrialmonoamine oxidase B. Br. J. Pharmacol., 2001, 132, 500-506. (Pubitemid 32142364)
    • (2001) British Journal of Pharmacology , vol.132 , Issue.2 , pp. 500-506
    • Youdim, M.B.H.1    Gross, A.2    Finberg, J.P.M.3
  • 42
    • 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]
    • DOI 10.1023/A:1015131516649
    • Youdim, M.B.H.; Weinstock, M. Molecular basis of neuroprotectiveactivities of rasagiline and the anti Alzheimer drug, TV3326, [(N-propargyl-(3R)-aminoindan-5-yl)-ethyl methyl carbamate]. Cell. Mol. Neurobiol., 2002, 21, 555-573. (Pubitemid 34538855)
    • (2001) Cellular and Molecular Neurobiology , vol.21 , Issue.6 , pp. 555-573
    • Youdim, M.B.H.1    Weinstock, M.2
  • 43
    • 6944242126 scopus 로고    scopus 로고
    • Neuroprotection via pro-survival protein kinase C isoforms associated with Bcl-2 family members
    • DOI 10.1096/fj.04-1916fje
    • (a) Weinreb, O.; Bar-Am, O.; Amit, T.; Chillag-Talmor, O.; Youdim, M.B.H.Neuroprotection via pro-survival protein kinase C isoforms associated withBcl-2 family members. FASEB J., 2004, 18, 1471-1473 (Pubitemid 39561618)
    • (2004) FASEB Journal , vol.18 , Issue.12 , pp. 1471-1473
    • Weinreb, O.1    Bar-Am, O.2    Amit, T.3    Chillag-Talmor, O.4    Youdim, M.B.H.5
  • 45
    • 27744486071 scopus 로고    scopus 로고
    • Regulation of Bcl-2 family proteins, neutrophic factors, and APP processing in the neurorescue activity of propargylamine
    • DOI 10.1096/fj.05-3794fje
    • (c)Bar-Am, O.; Weinreb, O.; Amit, T.; Youdim, M. B. Regulation of Bcl-2family proteins, neurotrophic factors, and APP processing in the neurorescueactivity of propargylamine. FASEB J., 2005, 19, 1899-1901. (Pubitemid 41598788)
    • (2005) FASEB Journal , vol.19 , Issue.13 , pp. 1899-1901
    • Bar-Am, O.1    Weinreb, O.2    Amit, T.3    Youdim, M.B.H.4
  • 46
    • 0034884148 scopus 로고    scopus 로고
    • Transfection-enforced Bcl-2 overexpression and an anti-Parkinson drug, rasagiline, prevent nuclear accumulation of glyceraldehyde-3-phosphate dehydrogenase induced by an endogenous dopaminergic neurotoxin, N-methyl(R)salsolinol
    • DOI 10.1046/j.1471-4159.2001.00448.x
    • (a) Maruyama, W.; Akao, Y.; Youdim, M.B.H.; Davis, B.A.; Naoi, M.Transfection-enforced Bcl-2 overexpression and an anti-Parkinson drug, rasagiline, prevent nuclear accumulation of glyceraldehyde-3- phosphatedehydrogenase induced by an endogenous dopaminergic neurotoxin, Nmethyl-(R)-salsolinol. J. Neurochem., 2001, 78, 727-735 (Pubitemid 32777974)
    • (2001) Journal of Neurochemistry , vol.78 , Issue.4 , pp. 727-735
    • Maruyama, W.1    Akao, Y.2    Youdim, M.B.H.3    Davis, B.A.4    Naoi, M.5
  • 47
    • 0345308381 scopus 로고    scopus 로고
    • Rasagiline: An anti-Parkinson drug with neuroprotective activity
    • DOI 10.1586/14737175.3.6.737
    • (b) Youdim, M.B.H. Rasagiline: an anti-Parkinson drug with neuroprotective activity.Expert Rev. Neurother., 2003, 3, 737-749. (Pubitemid 37462173)
    • (2003) Expert Review of Neurotherapeutics , vol.3 , Issue.6 , pp. 737-749
    • Youdim, M.B.H.1
  • 48
    • 0642303109 scopus 로고    scopus 로고
    • The importance of propargylamine moiety in the anti-Parkinson drug rasagiline and its derivatives in MAPK-dependent amyloid precursor protein processing
    • DOI 10.1096/fj.03-0078fje
    • (a) Yogev-Falach, M.; Amit, T.; Bar-Am, O.; Youdim, M.B.H. Theimportance of propargylamine moiety in the anti-Parkinson drug rasagilineand its derivatives for MAPK-dependent amyloid precursor proteinprocessing. FASEB J., 2003, 17, 2325-2327 (Pubitemid 39561481)
    • (2003) FASEB Journal , vol.17 , Issue.15 , pp. 2325-2327
    • Yogev-Falach, M.1    Amit, T.2    Bar-Am, O.3    Youdim, M.B.H.4
  • 49
    • 2642529309 scopus 로고    scopus 로고
    • Regulation of protein kinase C by the anti-Parkinson drug, MAO-B inhibitor, rasagiline and its derivatives, in vivo
    • DOI 10.1111/j.1471-4159.2004.02425.x
    • (b) Bar-Am, O.; Yogev-Falach, M.; Amit, T.; Sagi, Y.; Youdim, M.B.H. Regulation of protein kinase C bythe anti-Parkinson drug, MAO-B inhibitor, rasagiline and its derivatives, invivo. J. Neurochem., 2004, 89, 1119-1125. (Pubitemid 38715829)
    • (2004) Journal of Neurochemistry , vol.89 , Issue.5 , pp. 1119-1125
    • Bar-Am, O.1    Yogev-Falach, M.2    Amit, T.3    Sagi, Y.4    Youdim, M.B.H.5
  • 51
    • 0025373508 scopus 로고
    • Evidence that beta amyloid protein in Alzheimer's disease is not derived bynormal processing
    • (b) Sisodia, S.S.; Koo, E.H.; Beyreuther, K.; Unterbeck, A.; Price, D.L.Evidence that beta amyloid protein in Alzheimer's disease is not derived bynormal processing. Science, 1990, 248, 492-495.
    • (1990) Science , vol.248 , pp. 492-495
    • Sisodia, S.S.1    Koo, E.H.2    Beyreuther, K.3    Unterbeck, A.4    Price, D.L.5
  • 52
    • 75949114175 scopus 로고    scopus 로고
    • The neuroprotectivemechanism of 1-(R)-aminoindan, the major metabolite of the antiparkinsoniandrug rasagiline
    • Bar-Am, O.; Weinreb, O.; Amit, T.; Youdim, M.B.H. The neuroprotectivemechanism of 1-(R)-aminoindan, the major metabolite of the antiparkinsoniandrug rasagiline. J. Neurochem., 2010, 112, 1131-1137.
    • (2010) J. Neurochem. , vol.112 , pp. 1131-1137
    • Bar-Am, O.1    Weinreb, O.2    Amit, T.3    Youdim, M.B.H.4
  • 53
    • 36749021653 scopus 로고    scopus 로고
    • Comprehensive review of rasagiline, a second-generation monoamine oxidase inhibitor, for the treatment of Parkinson's Disease
    • DOI 10.1016/j.clinthera.2007.09.021, PII S0149291807003025
    • Chen, J.J.; Swope, D.M. ; Dashtipour, K. Comprehensive review ofrasagiline, a second-generation monoamine oxidase inhibitor, for thetreatment of Parkinson's disease. Clin. Ther., 2007, 29, 1825-1849. (Pubitemid 350212811)
    • (2007) Clinical Therapeutics , vol.29 , Issue.9 , pp. 1825-1849
    • Chen, J.J.1    Swope, D.M.2    Dashtipour, K.3
  • 54
    • 0000293742 scopus 로고
    • Uber eine eigenartige Erkrankung der Hirnrinde
    • Alzheimer A. Uber eine eigenartige Erkrankung der Hirnrinde. Allg. Z.Psychiat., 1907, 64, 146-148.
    • (1907) Allg. Z.Psychiat. , vol.64 , pp. 146-148
    • Alzheimer, A.1
  • 55
    • 75449102536 scopus 로고    scopus 로고
    • Mechanisms of disease: Alzheimer'sdisease
    • Querfurth, H.W.; LaFerla, F.M. Mechanisms of disease: Alzheimer'sdisease. New Engl. J. Med., 2010, 362, 329-344.
    • (2010) New Engl. J. Med. , vol.362 , pp. 329-344
    • Querfurth, H.W.1    Laferla, F.M.2
  • 56
    • 33746489936 scopus 로고    scopus 로고
    • Towards a unifying hypothesis of Alzheimer's disease: Cholinergic system linked to plaques, tangles and neuroinflammation
    • DOI 10.2174/092986706777935203
    • Sivaprakasam, K. Towards a unifying hypothesis of Alzheimer's disease:cholinergic system linked to plaques, tangles and neuroinflammation. Curr.Med. Chem., 2006, 13, 2179-2188. (Pubitemid 44132608)
    • (2006) Current Medicinal Chemistry , vol.13 , Issue.18 , pp. 2179-2188
    • Sivaprakasam, K.1
  • 59
  • 60
    • 77954369899 scopus 로고    scopus 로고
    • Beyond the cholinergic hypothesis: Docurrent drugs work in Alzheimer's disease?
    • Martorana, A.; Esposito, Z.; Koch, G. Beyond the cholinergic hypothesis: docurrent drugs work in Alzheimer's disease? CNS Neurosci. Ther., 2010, 16, 235-245.
    • (2010) CNS Neurosci. Ther. , vol.16 , pp. 235-245
    • Martorana, A.1    Esposito, Z.2    Koch, G.3
  • 62
    • 36749073565 scopus 로고    scopus 로고
    • BACE inhibitors as potential therapeutics for Alzheimer's disease
    • DOI 10.2174/157488907782411783
    • Evin, G.; Kenche, V.B. BACE inhibitors as potential therapeutics forAlzheimer's disease. Recent Pat. CNS Drug Discov., 2007, 2, 188-199. (Pubitemid 350200291)
    • (2007) Recent Patents on CNS Drug Discovery , vol.2 , Issue.3 , pp. 188-199
    • Evin, G.1    Kenche, V.B.2
  • 63
    • 33846922600 scopus 로고    scopus 로고
    • γ-Secretase: A complex target for Alzheimer's disease
    • DOI 10.1016/j.coph.2006.10.002, PII S1471489206001998, Neurosciences
    • Lundkvist, J.; Naslund, J. Gamma-secretase: a complex target forAlzheimer's disease. Curr. Opin. Pharmacol., 2007, 7, 112-118. (Pubitemid 46238041)
    • (2007) Current Opinion in Pharmacology , vol.7 , Issue.1 , pp. 112-118
    • Lundkvist, J.1    Naslund, J.2
  • 65
    • 76849091134 scopus 로고    scopus 로고
    • Can Alzheimer disease be prevented by amyloid-βimmunotherapy?
    • Lemere, C.A.; Masliah, E. Can Alzheimer disease be prevented by amyloid-βimmunotherapy? Nat. Rev. Neurol., 2010, 6, 108-119.
    • (2010) Nat. Rev. Neurol. , vol.6 , pp. 108-119
    • Lemere, C.A.1    Masliah, E.2
  • 66
    • 0031773098 scopus 로고    scopus 로고
    • Oxidative stress and neurodegenerative disorders
    • Sun, A.Y.; Chen, Y.M. Oxidative stress and neurodegenerative disorders. J.Biomed. Sci., 1998, 5, 401-414. (Pubitemid 28559104)
    • (1998) Journal of Biomedical Science , vol.5 , Issue.6 , pp. 401-414
    • Sun, A.Y.1    Chen, Y.-M.2
  • 68
    • 34248549035 scopus 로고    scopus 로고
    • Involvement of type A monoamine oxidase in neurodegeneration: Regulation of mitochondrial signaling leading to cell death or neuroprotection
    • (b)Naoi, M.; Maruyama, W.; Akao, Y.; Yi, H.; Yamaoka, T. Involvement oftype A monoamine oxidase in neurodegeneration: regulation ofmitochondrial signaling leading to cell death or neuroprotection. J. NeuralTransm. Suppl., 2006, 71, 67-77. (Pubitemid 351412108)
    • (2006) Journal of Neural Transmission, Supplement , Issue.71 , pp. 67-77
    • Naoi, M.1    Maruyama, W.2    Akao, Y.3    Yi, H.4    Yamaoka, Y.5
  • 69
    • 0028145566 scopus 로고
    • Increased monoamine oxidase B activity in plaque-associated astrocytes of Alzheimer brains revealed by quantitative enzyme radioautography
    • DOI 10.1016/0306-4522(94)90311-5
    • Saura, J.; Luque, J.M.; Cesura, A.M.; Da Prada, M.; Chan-Palay, V.; Huber, G.; Loffler, J.; Richards, J.G. Increased monoamine oxidase B activity inplaque-associated astrocytes of Alzheimer brains revealed by quantitativeenzyme radioautography. Neuroscience, 1994, 62, 15-30. (Pubitemid 24287342)
    • (1994) Neuroscience , vol.62 , Issue.1 , pp. 15-30
    • Saura, J.1
  • 70
    • 33750462391 scopus 로고    scopus 로고
    • Multifunctional drugs with different CNS targets for neuropsychiatric disorders
    • DOI 10.1111/j.1471-4159.2006.04141.x
    • (a) Van der Schyf, C.J.; Geldenhuys, W.J.; Youdim, M.B.H. Multifunctionaldrugs with different CNS targets for neuropsychiatric disorders. J.Neurochem., 2006, 99, 1033-1048 (Pubitemid 44655271)
    • (2006) Journal of Neurochemistry , vol.99 , Issue.4 , pp. 1033-1048
    • Van Der Schyf, C.J.1    Geldenhuys, W.J.2    Youdim, M.B.H.3
  • 71
    • 11144245220 scopus 로고    scopus 로고
    • Multi-functional drugs for various CNS targets in the treatment of neurodegenerative disorders
    • DOI 10.1016/j.tips.2004.11.007, PII S016561470400313X
    • (b) Youdim, M.B.H.; Buccafusco, J.J.Multi-functional drugs for various CNS targets in the treatment ofneurodegenerative disorders. Trends Pharm. Sci., 2005, 26, 27-35. (Pubitemid 40052707)
    • (2005) Trends in Pharmacological Sciences , vol.26 , Issue.1 , pp. 27-35
    • Youdim, M.B.H.1    Buccafusco, J.J.2
  • 74
    • 0345435251 scopus 로고    scopus 로고
    • KA-672 inhibits rat brain acetylcholinesterase in vitro but not in vivo
    • DOI 10.1016/S0304-3940(99)00149-4, PII S0304394099001494
    • Hilgert, M.; Nöldner, M.; Chatterjee, S.S.; Klein, J. KA-672 inhibits rat brainacetylcholinesterase in vitro but not in vivo. Neurosci. Lett., 1999, 263, 193-196. (Pubitemid 29158961)
    • (1999) Neuroscience Letters , vol.263 , Issue.2-3 , pp. 193-196
    • Hilgert, M.1    Noldner, M.2    Chatterjee, S.S.3    Klein, J.4
  • 75
    • 0034649564 scopus 로고    scopus 로고
    • Inhibition of monoamine oxidases by functionalized coumarin derivatives: Biological activities, QSARs, and 3D-QSARs
    • DOI 10.1021/jm001028o
    • Gnerre, C.; Catto, M.; Leonetti, F.; Weber, P.; Carrupt, P.A.; Altomare, C.;Carotti, A.; Testa, B. Inhibition of monoamine oxidases by functionalizedcoumarin derivatives: biological activities, QSARs, and 3D-QSARs. J. Med.Chem., 2000, 43, 4747-4758. (Pubitemid 32002686)
    • (2000) Journal of Medicinal Chemistry , vol.43 , Issue.25 , pp. 4747-4758
    • Gnerre, C.1    Catto, M.2    Leonetti, F.3    Weber, P.4    Carrupt, P.-A.5    Altomare, C.6    Carotti, A.7    Testa, B.8
  • 77
    • 77956413632 scopus 로고    scopus 로고
    • Design synthesis and biological evaluation ofcoumarin derivatives tethered to an edrophonium-like fragment as highlypotent and selective dual binding site acetylcholinesterase inhibitors
    • Pisani, L.; Catto, M.; Giangreco, I.; Leonetti, F.; Nicolotti, O.; Stefanachi, A.; Cellamare, S.; Carotti, A. Design, synthesis and biological evaluation ofcoumarin derivatives tethered to an edrophonium-like fragment as highlypotent and selective dual binding site acetylcholinesterase inhibitors.ChemMedChem, 2010, 5, 1616-1630.
    • (2010) ChemMedChem , vol.5 , pp. 1616-1630
    • Pisani, L.1    Catto, M.2    Giangreco, I.3    Leonetti, F.4    Nicolotti, O.5    Stefanachi, A.6    Cellamare, S.7    Carotti, A.8
  • 79
    • 0036849156 scopus 로고    scopus 로고
    • Limited potentiation of blood pressure response to oral tyramine by brain-selective monoamine oxidase A-B inhibitor, TV-3326 in conscious rabbits
    • DOI 10.1016/S0028-3908(02)00176-4, PII S0028390802001764
    • Weinstock, M.; Gorodetsky, E.; Wang, R.H.; Fross, A.; Weinreb, O.;Youdim, M.B.H. Limited potentiation of blood pressure response to oraltyramine by brain-selective monoamine oxidase A-B inhibitor, TV-3326 inconscious rabbits. Neuropharmacology, 2002, 43, 999-1005. (Pubitemid 35341235)
    • (2002) Neuropharmacology , vol.43 , Issue.6 , pp. 999-1005
    • Weinstock, M.1    Gorodetsky, E.2    Wang, R.H.3    Gross, A.4    Weinreb, O.5    Youdim, M.B.H.6
  • 80
    • 0038012567 scopus 로고    scopus 로고
    • A novel cholinesterase and brain-selective monoamine oxidase inhibitor for the treatment of dementia comorbid with depression and Parkinson's disease
    • DOI 10.1016/S0278-5846(03)00053-8
    • Weinstock, M.; Gorodetsky, E.; Poltyrev, T.; Gross, A.; Sagi, Y.; Youdim, M.B.H. A novel cholinesterase and brain-selective monoamine oxidaseinhibitor for the treatment of dementia comorbid with depression andParkinson's disease. Prog. Neuropsychopharmacol. Biol. Psychiatry, 2003, 27, 555-561. (Pubitemid 36645054)
    • (2003) Progress in Neuro-Psychopharmacology and Biological Psychiatry , vol.27 , Issue.4 , pp. 555-561
    • Weinstock, M.1    Gorodetsky, E.2    Poltyrev, T.3    Gross, A.4    Sagi, Y.5    Youdim, M.6
  • 81
    • 0038155162 scopus 로고    scopus 로고
    • Attenuation of MPTP-induced dopaminergic neurotoxicity by TV3326, a cholinesterase-monoamine oxidase inhibitor
    • DOI 10.1046/j.1471-4159.2003.01801.x
    • Sagi, Y.; Weinstock, M.; Youdim, M.B.H. Attenuation of MPTP-induceddopaminergic neurotoxicity by TV3326, a cholinesterase- monoamineoxidase inhibitor. J. Neurochem., 2003, 86, 290-297. (Pubitemid 36842429)
    • (2003) Journal of Neurochemistry , vol.86 , Issue.2 , pp. 290-297
    • Sagi, Y.1    Weinstock, M.2    Youdim, M.B.H.3
  • 82
    • 0344989342 scopus 로고    scopus 로고
    • Neuroprotectiveand neurorescue properties of rasagiline and TV3326 in MPTP model ofParkinson's disease
    • Sagi, Y.; O. Weinreb, O.; Weinstock, M.; Youdim, M.B.H. Neuroprotectiveand neurorescue properties of rasagiline and TV3326 in MPTP model ofParkinson's disease. Neural Plasticity, 2001, 8, 197-198.
    • (2001) Neural Plasticity , vol.8 , pp. 197-198
    • Sagi, Y.1    Weinreb, O.O.2    Weinstock, M.3    Youdim, M.B.H.4
  • 84
    • 77957968479 scopus 로고    scopus 로고
    • Monoamine oxidase inhibitors as neuroprotectiveagents in age-dependent neurodegenerative disorders
    • Naoi, M.; Maruyama, W. Monoamine oxidase inhibitors as neuroprotectiveagents in age-dependent neurodegenerative disorders. Curr. Pharm. Design, 2010, 16, 2799-2817.
    • (2010) Curr. Pharm. Design , vol.16 , pp. 2799-2817
    • Naoi, M.1    Maruyama, W.2
  • 85
    • 17444449069 scopus 로고    scopus 로고
    • 1-N-substituted thiocarbamoyl-3-phenyl-5-thienyl-2-pyrazolines: Synthesis and evaluation as MAO inhibitors
    • DOI 10.1002/ardp.200300732
    • Gökhan, N.; Yesilada, A.; Uçar, G.; Erol, K.; Bilgin, A. 1-N-Substitutedthiocarbamoyl-3-phenyl-5-thienyl-2-pyrazolines: synthesis and evaluation asMAO inhibitors. Arch. Pharm. Pharm. Med. Chem., 2003, 336, 362-371. (Pubitemid 37127992)
    • (2003) Archiv der Pharmazie , vol.336 , Issue.8 , pp. 362-371
    • Gokhan, N.1    Yesilada, A.2    Ucar, G.3    Erol, K.4    Bilgin, A.A.5
  • 86
    • 19544390899 scopus 로고    scopus 로고
    • 1-N-Substituted thiocarbamoyl-3-phenyl-5-thienyl-2-pyrazolines: A novel cholinesterase and selective monoamine oxidase B inhibitors for the treatment of Parkinson's and Alzheimer's diseases
    • DOI 10.1016/j.neulet.2005.03.028, PII S0304394005003216
    • Uçar, G.; Gökhan, N.; Yesilada, A.; Bilgin, A.A. 1-N-Substitutedthiocarbamoyl-3-phenyl-5-thienyl-2-pyrazolines: A novel cholinesterase andselective monoamine oxidase B inhibitors for the treatment of Parkinson'sand Alzheimer's diseases. Neurosci. Lett., 2005, 382, 327-331. (Pubitemid 40733646)
    • (2005) Neuroscience Letters , vol.382 , Issue.3 , pp. 327-331
    • Ucar, G.1    Gokhan, N.2    Yesilada, A.3    Bilgin, A.A.4
  • 87
    • 25844529207 scopus 로고    scopus 로고
    • Screening of non-alkaloidal natural compounds as acetylcholinesteraseinhibitors
    • (a) Bruhlmann, C.; Marston, A.; Hostettmann, K.; Carrupt, P.A.; Testa, B.Screening of non-alkaloidal natural compounds as acetylcholinesteraseinhibitors. Chem. Biodivers., 2004, 1, 819-829
    • (2004) Chem. Biodivers. , vol.1 , pp. 819-829
    • Bruhlmann, C.1    Marston, A.2    Hostettmann, K.3    Carrupt, P.A.4    Testa, B.5
  • 89
    • 41149163183 scopus 로고    scopus 로고
    • Parkinson's disease: Clinical features and diagnosis
    • DOI 10.1136/jnnp.2007.131045
    • Jankovic, J. Parkinson's disease: clinical features and diagnosis. J. Neurol.Neurosurg. Psychiatry, 2008, 79, 368-376. (Pubitemid 351441488)
    • (2008) Journal of Neurology, Neurosurgery and Psychiatry , vol.79 , Issue.4 , pp. 368-376
    • Jankovic, J.1
  • 90
    • 37149050857 scopus 로고    scopus 로고
    • Disease-modifying drugs andParkinson's disease
    • Allain, H.; Bentué-Ferrer, D.; Akwa, Y. Disease-modifying drugs andParkinson's disease. Prog. Neurobiol., 2008, 84, 25-39.
    • (2008) Prog. Neurobiol. , vol.84 , pp. 25-39
    • Allain, H.1    Bentué-Ferrer, D.2    Akwa, Y.3
  • 92
    • 77955366745 scopus 로고    scopus 로고
    • Role of post-translationalmodifications in modulating the structure, function and toxicity of alphasynuclein:implications for Parkinson's disease pathogenesis and therapies
    • Oueslati, A.; Fournier, M.; Lashuel, H.A. Role of post- translationalmodifications in modulating the structure, function and toxicity of alphasynuclein:implications for Parkinson's disease pathogenesis and therapies.Prog. Brain Res., 2010, 183, 115-145.
    • (2010) Prog. Brain Res. , vol.183 , pp. 115-145
    • Oueslati, A.1    Fournier, M.2    Lashuel, H.A.3
  • 93
    • 0038711511 scopus 로고    scopus 로고
    • Effects of oxidative and nitrative challenges on α-synuclein fibrillogenesis involve distinct mechanisms of protein modifications
    • DOI 10.1074/jbc.M212436200
    • Norris, E.H.; Giasson, B.I.; Ischiropoulos, H.; Lee, V.M. Effects of oxidativeand nitrative challenges on alpha-synuclein fibrillogenesis involve distinctmechanisms of protein modifications. J. Biol. Chem., 2003, 278, 27230-27240. (Pubitemid 36876880)
    • (2003) Journal of Biological Chemistry , vol.278 , Issue.29 , pp. 27230-27240
    • Norris, E.H.1    Giasson, B.I.2    Ischiropoulos, H.3    Lee, V.M.-Y.4
  • 94
    • 77950644314 scopus 로고    scopus 로고
    • Copper binding regulatesintracellular alpha-synuclein localisation, aggregation and toxicity
    • Wang, X.; Moualla, D.; Wright, J.A.; Brown, D.R. Copper binding regulatesintracellular alpha-synuclein localisation, aggregation and toxicity. J.Neurochem., 2010, 113, 704-714.
    • (2010) J.Neurochem. , vol.113 , pp. 704-714
    • Wang, X.1    Moualla, D.2    Wright, J.A.3    Brown, D.R.4
  • 95
    • 72949084639 scopus 로고    scopus 로고
    • Interaction between alphasynucleinand metal ions, still looking for a role in the pathogenesis ofParkinson's disease
    • Bisaglia, M.; Tessari, I.; Mammi, S.; Bubacco, L. Interaction between alphasynucleinand metal ions, still looking for a role in the pathogenesis ofParkinson's disease. Neuromol. Med., 2009, 11, 239-251.
    • (2009) Neuromol. Med. , vol.11 , pp. 239-251
    • Bisaglia, M.1    Tessari, I.2    Mammi, S.3    Bubacco, L.4
  • 96
    • 80051632039 scopus 로고    scopus 로고
    • Increased iron levels correlatewith the selective nigral dopaminergic neuron degeneration in Parkinson'sdisease
    • Lv, Z.; Jiang, H.; Xu, H.; Song, N.; Xie, J. Increased iron levels correlatewith the selective nigral dopaminergic neuron degeneration in Parkinson'sdisease. J. Neural Transm., 2011, 118, 361-369.
    • (2011) J. Neural Transm. , vol.118 , pp. 361-369
    • Lv, Z.1    Jiang, H.2    Xu, H.3    Song, N.4    Xie, J.5
  • 97
    • 59149084113 scopus 로고    scopus 로고
    • Metal-dependentgeneration of reactive oxygen species from amyloid proteins implicated inneurodegenerative disease
    • Allsop, D.; Mayes, J.; Moore, S.; Masad, A.; Tabner, B.J. Metal-dependentgeneration of reactive oxygen species from amyloid proteins implicated inneurodegenerative disease. Biochem. Soc. Trans., 2008, 36, 1293-1298.
    • (2008) Biochem. Soc. Trans. , vol.36 , pp. 1293-1298
    • Allsop, D.1    Mayes, J.2    Moore, S.3    Masad, A.4    Tabner, B.J.5
  • 99
    • 11844255676 scopus 로고    scopus 로고
    • Design, synthesis, and evaluation of novel bifunctional iron-chelators as potential agents for neuroprotection in Alzheimer's, Parkinson's, and other neurodegenerative diseases
    • DOI 10.1016/j.bmc.2004.10.037, PII S0968089604008399
    • Zheng, H.; Weiner, L.M.; Bar-Am, O.; Epsztejn, S.; Cabantchik, Z.I.;Warshawsky, A.; Youdim, M.B.H.; Fridkin, M. Design, synthesis, andevaluation of novel bifunctional iron-chelators as potential agents forneuroprotection in Alzheimer's, Parkinson's, and other neurodegenerativediseases. Bioorg. Med. Chem., 2005, 13, 773-783. (Pubitemid 40093620)
    • (2005) Bioorganic and Medicinal Chemistry , vol.13 , Issue.3 , pp. 773-783
    • Zheng, H.1    Weiner, L.M.2    Bar-Am, O.3    Epsztejn, S.4    Cabantchik, Z.I.5    Warshawsky, A.6    Youdim, M.B.H.7    Fridkin, M.8
  • 100
    • 0346849912 scopus 로고    scopus 로고
    • Neuroprotection by a novel brain permeable iron chelator, VK-28, against 6-hydroxydopamine lession in rats
    • DOI 10.1016/j.neuropharm.2003.09.005
    • Ben Shachar, D.B.; Kahana, N.; Kampel, V.; Warshawsky, A.; Youdim, M.B.H. Neuroprotection by a novel brain permeable iron chelator, VK-28, against 6-hydroxydopamine lesion in rats. Neuropharmacology, 2004, 46, 254-263. (Pubitemid 37532833)
    • (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.H.5
  • 101
    • 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
    • DOI 10.1111/j.1471-4159.2005.03340.x
    • Zheng, H.; Gal, S.; Weiner, L.M.; Bar-Am, O.; Warshawsky, A.; Fridkin, M.; Youdim, M.B.H. Novel multifunctional neuroprotective iron chelatormonoamine oxidase inhibitor drugs for neurodegenerative diseases: in vitrostudies on antioxidant activity, prevention of lipid peroxide formation andmonoamine oxidase inhibition. J. Neurochem., 2005, 95, 68-78. (Pubitemid 41384426)
    • (2005) Journal of Neurochemistry , vol.95 , Issue.1 , pp. 68-78
    • Zheng, H.1    Gal, S.2    Weiner, L.M.3    Bar-Am, O.4    Warshawsky, A.5    Fridkin, M.6    Youdim, M.B.H.7
  • 102
    • 11144316146 scopus 로고    scopus 로고
    • Bifunctional drug derivatives of MAO-B inhibitor rasagiline and iron chelator VK-28 as a more effective approach to treatment of brain ageing and ageing neurodegenerative diseases
    • DOI 10.1016/j.mad.2004.08.023, PII S0047637404002064, The Voyage to Old Age: Searching for Human Longevity Genes
    • Youdim, M.B.H.; Fridkin, M.; Zheng, H. Bifunctional drug derivatives ofMAO-B inhibitor rasagiline and iron chelator VK-28 as a more effectiveapproach to treatment of brain ageing and ageing neurodegenerative diseases.Mech. Ageing Dev., 2005, 126, 317-326. (Pubitemid 40038353)
    • (2005) Mechanisms of Ageing and Development , vol.126 , Issue.2 , pp. 317-326
    • Youdim, M.B.H.1    Fridkin, M.2    Zheng, H.3
  • 103
    • 0037734329 scopus 로고    scopus 로고
    • Neuroprotection by deprenyl and other propargylamines: Glyceraldehyde-3-phosphate dehydrogenase rather than monoamine oxidase B
    • DOI 10.1007/s00702-002-0827-z
    • (a) Tatton, W.; Chalmers-Redman, R.; Tatton, N. Neuroprotection bydeprenyl and other propargylamines: glyceraldehyde-3-phosphatedehydrogenase rather than monoamine oxidase B. J. Neural Transm., 2003, 110, 509-515 (Pubitemid 36543282)
    • (2003) Journal of Neural Transmission , vol.110 , Issue.5 , pp. 509-515
    • Tatton, W.1    Chalmers-Redman, R.2    Tatton, N.3
  • 104
    • 0034939146 scopus 로고    scopus 로고
    • Antiapoptoticproperties of rasagiline, N-propargylamine-1(R)-aminoindan, and its optical(S)-isomer, TV1022
    • (b) Maruyama, W.; Youdim, M.B.H.; Naoi, M. Antiapoptoticproperties of rasagiline, N-propargylamine-1(R)-aminoindan, and its optical(S)-isomer, TV1022. Ann. N. Y. Acad. Sci., 2001, 939, 320-329.
    • (2001) Ann. N. Y. Acad. Sci. , vol.939 , pp. 320-329
    • Maruyama, W.1    Youdim, M.B.H.2    Naoi, M.3
  • 105
    • 33845879870 scopus 로고    scopus 로고
    • Therapeutic targets and potential of the novel brain- permeable multifunctional iron chelator-monoamine oxidase inhibitor drug, M-30, for the treatment of Alzheimer's disease
    • DOI 10.1111/j.1471-4159.2006.04258.x
    • Avramovich-Tirosh, Y.; Amit, T.; Bar-Am, O.; Zheng, H.; Fridkin, M.;Youdim, M.B.H. Therapeutic targets and potential of the novel brainpermeablemultifunctional iron chelator-monoamine oxidase inhibitor drug, M-30, for the treatment of Alzheimer's disease. J. Neurochem., 2007, 100, 490-502. (Pubitemid 46016026)
    • (2007) Journal of Neurochemistry , 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.H.6
  • 106
    • 77953864734 scopus 로고    scopus 로고
    • Site-activated chelators targetingacetylcholinesterase and monoamine oxidase for Alzheimer's therapy
    • Zheng, H.; Youdim, M.B.H.; Fridkin, M. Site-activated chelators targetingacetylcholinesterase and monoamine oxidase for Alzheimer's therapy. ACSChem. Biol., 2010, 5, 603-610.
    • (2010) ACSChem. Biol. , vol.5 , pp. 603-610
    • Zheng, H.1    Youdim, M.B.H.2    Fridkin, M.3
  • 107
    • 0035181291 scopus 로고    scopus 로고
    • Monoamine oxidase B and free radical scavenging activities of naturalflavonoids in melastoma candidum D. Don
    • Lee, M.H.; Lin, R.D.; Shen, L.Y.; Yang, L.L.; Yen, K.Y.; Hou, W.C.Monoamine oxidase B and free radical scavenging activities of naturalflavonoids in melastoma candidum D. Don. J. Agric. Food Chem., 2001, 49, 5551-5555.
    • (2001) J. Agric. Food Chem. , vol.49 , pp. 5551-5555
    • Lee, M.H.1    Lin, R.D.2    Shen, L.Y.3    Yang, L.L.4    Yen, K.Y.5    Hou, W.C.6
  • 109
    • 79958762778 scopus 로고    scopus 로고
    • Inhibition of the bioactivation of the neurotoxinMPTP by antioxidants, redox agents and monoamine oxidase inhibitors
    • Herraiz, T.; Guillén, H. Inhibition of the bioactivation of the neurotoxinMPTP by antioxidants, redox agents and monoamine oxidase inhibitors.Food Chem. Toxicol., 2011, 49, 1773-1781.
    • (2011) Food Chem. Toxicol. , vol.49 , pp. 1773-1781
    • Herraiz, T.1    Guillén, H.2
  • 110
    • 0033791895 scopus 로고    scopus 로고
    • Antioxidant activity of eugenoland related monomeric and dimeric compounds
    • Ogata, M.; Hoshi, M.; Urano, S.; Endo, T. Antioxidant activity of eugenoland related monomeric and dimeric compounds. Chem. Pharm. Bull., 2000, 48, 1467-1469.
    • (2000) Chem. Pharm. Bull. , vol.48 , pp. 1467-1469
    • Ogata, M.1    Hoshi, M.2    Urano, S.3    Endo, T.4
  • 111
    • 20544463414 scopus 로고    scopus 로고
    • Eugenol and its structural analogs inhibit monoamine oxidase A and exhibit antidepressant-like activity
    • DOI 10.1016/j.bmc.2005.04.081, PII S0968089605004013
    • Tao, G.; Irie, Y.; Li, D.J.; Keung, W.M. Eugenol and its structural analogsinhibit monoamine oxidase A and exhibit antidepressant-like activity.Bioorg. Med. Chem., 2005, 13, 4777-4788. (Pubitemid 40848356)
    • (2005) Bioorganic and Medicinal Chemistry , vol.13 , Issue.15 , pp. 4777-4788
    • Tao, G.1    Irie, Y.2    Li, D.-J.3    Wing, M.K.4
  • 112
    • 0025883342 scopus 로고
    • Nitric oxide: Physiology, pathophysiology, and pharmacology
    • Moncada, S.; Palmer, R.M.J.; Higgs, E.A. Nitric oxide: physiology, pathophysiology, and pharmacology. Pharmacol. Rev., 1991, 43, 109-142.
    • (1991) Pharmacol. Rev. , vol.43 , pp. 109-142
    • Moncada, S.1    Palmer, R.M.J.2    Higgs, E.A.3
  • 114
    • 69949160564 scopus 로고    scopus 로고
    • Redox mechanisms in hepatic chronic wound healingand fibrogenesis
    • (a) Novo, E.; Parola, M. Redox mechanisms in hepatic chronic wound healingand fibrogenesis. Fibrogenesis Tissue Repair, 2008, 1, 5
    • (2008) Fibrogenesis Tissue Repair , vol.1 , pp. 5
    • Novo, E.1    Parola, M.2
  • 115
    • 79960433284 scopus 로고    scopus 로고
    • The effect of nNOSinhibitors on toxin-induced cell death in dopaminergic cell lines depends onthe extent of enzyme expression
    • (b) Brzozowski, M.J.; Alcantara, S.L.; Iravani, M.M.; Rose, S.; Jenner, P. The effect of nNOSinhibitors on toxin-induced cell death in dopaminergic cell lines depends onthe extent of enzyme expression. Brain Res., 2011, 1404, 21-30
    • (2011) Brain Res. , vol.1404 , pp. 21-30
    • Brzozowski, M.J.1    Alcantara, S.L.2    Iravani, M.M.3    Rose, S.4    Jenner, P.5
  • 116
    • 0029805172 scopus 로고    scopus 로고
    • Nitric oxide, superoxide, and peroxynitrite: The good, the bad, and ugly
    • (c) Beckman, J.S.; Koppenol, W.H. Nitric oxide, superoxide, and peroxynitrite: the good, the bad, and ugly. Am. J. Physiol., 1996, 271, C1424-1437.
    • (1996) Am. J. Physiol. , vol.271
    • Beckman, J.S.1    Koppenol, W.H.2
  • 117
    • 12344308106 scopus 로고    scopus 로고
    • Nitric oxide as a unique bioactive signaling messenger in physiology and pathophysiology
    • DOI 10.1155/S1110724304402034, PII S1110724304402034
    • Tuteja, N.; Chandra, M.; Tuteja, R.; Misra, M.K. Nitric oxide as a uniquebioactive signaling messenger in physiology and pathophysiology. J.Biomed. Biotech., 2004, 4, 227-237. (Pubitemid 40128959)
    • (2004) Journal of Biomedicine and Biotechnology , vol.2004 , Issue.4 , pp. 227-237
    • Tuteja, N.1    Chandra, M.2    Tuteja, R.3    Misra, M.K.4
  • 118
    • 65249163408 scopus 로고    scopus 로고
    • Design of selective neuronal nitric oxide synthase inhibitorsfor the prevention and treatment of neurodegenerative diseases
    • Silverman, R.B. Design of selective neuronal nitric oxide synthase inhibitorsfor the prevention and treatment of neurodegenerative diseases. Acc. Chem.Res., 2009, 42, 439-451.
    • (2009) Acc. Chem.Res. , vol.42 , pp. 439-451
    • Silverman, R.B.1
  • 119
    • 0023733428 scopus 로고
    • Acetylenic and allenic derivatives of 2-(1-methylindolyl) methylamine as selective inhibitors of the monoamine oxidases A and B
    • (a) Cruces, M.A.; Elorriaga, C.; Fernandez-Alvarez, E.; Lopez Chico, M.T.;Nieto Lopez, O. Acetylenic and allenic derivatives of 2-(1-methylindolyl) methylamine as selective inhibitors of the monoamineoxidases A and B. Farmaco Sci., 1988, 43, 567-573 (Pubitemid 18261461)
    • (1988) Farmaco, Edizione Scientifica , vol.43 , Issue.7-8 , pp. 567-573
    • Cruces, M.A.1    Elorriaga, C.2    Fernandez Alvarez, E.3    Lopez Chico, M.T.4    Nieto Lopez, O.5
  • 120
    • 0025823001 scopus 로고
    • Acetylenic and allenic derivatives of 2-(5-methoxyindolyl) and 2-(5-hydroxyindolyl)methylamines: Synthesis and invitro evaluation as monoamine oxidase inhibitors
    • (b) Cruces, M.A.;Elorriaga, C.; Fernandez-Alvarez, E. Acetylenic and allenic derivatives of 2-(5-methoxyindolyl) and 2-(5-hydroxyindolyl) methylamines: synthesis and invitro evaluation as monoamine oxidase inhibitors. Eur. J. Med. Chem., 1991, 26, 33-41
    • (1991) Eur. J. Med. Chem. , vol.26 , pp. 33-41
    • Cruces, M.A.1    Elorriaga, C.2    Fernandez-Alvarez, E.3
  • 121
    • 0027336573 scopus 로고
    • The effects of side chain substitution at positions 2 and 3 of the heterocyclic ring of N-acetylenic analogues of tryptamine as monoamine oxidase inhibitors
    • DOI 10.1016/0006-2952(93)90194-2
    • (c) Avila, M.; Balsa, M.D.; Fernandez-Alvarez, E.; Tipton, K. F.;Unzeta, M. The effect of side-chain substitution at positions 2 and 3 of theheterocyclic ring of N-acetylenic analogues of tryptamine as monoamineoxidase inhibitors. Biochem. Pharmacol., 1993, 45, 2231-2237 (Pubitemid 23171084)
    • (1993) Biochemical Pharmacology , 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
  • 122
    • 0025974835 scopus 로고
    • Monoamine oxidaseinhibitory potencies and selectivities of 2-[N-(2-propynyl)-aminomethyl]-1-methyl indole derivatives
    • (d) Balsa, D.;Fernandez-Alvarez, E.; Tipton, K.F.; Unzeta, M. Monoamine oxidaseinhibitory potencies and selectivities of 2-[N-(2-propynyl)-aminomethyl]- 1-methyl indole derivatives. Biochem. Soc. Trans., 1991, 19, 215-218.
    • (1991) Biochem. Soc. Trans. , vol.19 , pp. 215-218
    • Balsa, D.1    Fernandez-Alvarez, E.2    Tipton, K.F.3    Unzeta, M.4
  • 123
    • 0033023543 scopus 로고    scopus 로고
    • Relevance of benzyloxy group in 2-indolyl methylamines in the selective MAO-B inhibition
    • DOI 10.1038/sj.bjp.0702600
    • Perez, V.; Marco, J.L.; Fernandez-Alvarez, E.; Unzeta, M. Relevance of abenzyloxy group in 2-indolyl methylamines in the selective MAO-Binhibition. Br. J. Pharmacol., 1999, 127, 869-876. (Pubitemid 29295345)
    • (1999) British Journal of Pharmacology , vol.127 , Issue.4 , pp. 869-876
    • Perez, V.1    Marco, J.L.2    Fernandez-Alvarez, E.3    Unzeta, M.4
  • 124
    • 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
    • DOI 10.1016/S0197-0186(02)00091-8, PII S0197018602000918
    • (a) Perez, V.; Unzeta, M. PF9601N [N-(2-propynyl)-2-(5-benzyloxyindolyl) methylamine], a new MAO-B inhibitor, attenuates MPTP induced depletionof striatal dopamine levels in C57/BL mice. Neurochem. Intern., 2003, 42, 221-229 (Pubitemid 35335694)
    • (2003) Neurochemistry International , vol.42 , Issue.3 , pp. 221-229
    • Perez, V.1    Unzeta, M.2
  • 125
    • 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
    • DOI 10.1016/S0304-3940(02)00614-6, PII S0304394002006146
    • (b) Cutillas, B.; Ambrosio, S.; Unzeta, M. Neuroprotective effect ofthe monoamine oxidase inhibitor PF9601N [N-(2-propynyl)-2-(5-benzyloxyindolyl) methylamine] on rat nigral neurons after 6-OH-DA striatallesion. Neurosci. Lett., 2002, 329, 165-168 (Pubitemid 34880064)
    • (2002) Neuroscience Letters , vol.329 , Issue.2 , pp. 165-168
    • Cutillas, B.1    Ambrosio, S.2    Unzeta, M.3
  • 127
    • 33745310693 scopus 로고    scopus 로고
    • Protective effect of N-(2-propynyl)-2-(5-benzyloxy-indolyl) methylamine (PF9601N) on mitochondrial permeability transition
    • DOI 10.1007/s00018-006-6105-8
    • Battaglia, V.; Sanz, E.; Salvi, M.; Unzeta, M.; Toninello, A. Protective effectof N-(2-propynyl)-2-(5-benzyloxy-indolyl)methylamine (PF9601N) onmitochondrial permeability transition. Cell. Mol. Life Sci., 2006, 63, 1440-1448. (Pubitemid 43939023)
    • (2006) Cellular and Molecular Life Sciences , vol.63 , Issue.12 , pp. 1440-1448
    • Battaglia, V.1    Sanz, E.2    Salvi, M.3    Unzeta, M.4    Toninello, A.5
  • 128
    • 77956553922 scopus 로고    scopus 로고
    • Antioxidant properties of PF9601N, a novel MAO-B inhibitor: Assessment ofits ability to interact with reactive nitrose species
    • Bellik, L.; Dragoni, S.; Pessina, F.; Sanz, E.; Unzeta, M.; Valoti, M.Antioxidant properties of PF9601N, a novel MAO-B inhibitor: assessment ofits ability to interact with reactive nitrose species. Acta Biochim. Pol., 2010, 57, 235-239.
    • (2010) Acta Biochim. Pol. , vol.57 , pp. 235-239
    • Bellik, L.1    Dragoni, S.2    Pessina, F.3    Sanz, E.4    Unzeta, M.5    Valoti, M.6
  • 129
    • 73949123501 scopus 로고    scopus 로고
    • Synthesis and in vitro evaluation ofpteridine analogues as monoamine oxidase B and nitric oxide synthaseinhibitors
    • Prins, L.H.A.; Petzer, J.P.; Malan, S.F. Synthesis and in vitro evaluation ofpteridine analogues as monoamine oxidase B and nitric oxide synthaseinhibitors. Bioorg. Med. Chem., 2009, 17, 7523-7530.
    • (2009) Bioorg. Med. Chem. , vol.17 , pp. 7523-7530
    • Prins, L.H.A.1    Petzer, J.P.2    Malan, S.F.3
  • 131
    • 70450228608 scopus 로고    scopus 로고
    • Nitroindazole compounds inhibit theoxidative activation of 1-methyl-4-phenyl-1, 2, 3, 6-tetrahydropyridine(MPTP) neurotoxin to neurotoxic pyridinium cations by human monoamineoxidase (MAO
    • Herraiz, T.; Aran, V. J.; Guillen, H. Nitroindazole compounds inhibit theoxidative activation of 1-methyl-4-phenyl-1, 2, 3, 6-tetrahydropyridine(MPTP) neurotoxin to neurotoxic pyridinium cations by human monoamineoxidase (MAO). Free Radical Res., 2009, 43, 975-984.
    • (2009) Free Radical Res. , vol.43 , pp. 975-984
    • Herraiz, T.1    Aran, V.J.2    Guillen, H.3
  • 132
    • 0030938169 scopus 로고    scopus 로고
    • The neuronal nitric oxide synthase inhibitor 7-nitroindazole also inhibits the monoamine oxidase-B-catalyzed oxidation of 1 -methyl-4-phenyl- 1,2,3,6-tetrahydropyridine
    • DOI 10.1021/tx970001d
    • Castagnoli, K.; Palmer, S.; Anderson, A.; Bueters, T.; Castagnoli, N.Jr. Theneuronal nitric oxide synthase inhibitor 7-nitroindazole also inhibits themonoamine oxidase-B-catalyzed oxidation of 1-methyl-4-phenyl-1, 2, 3, 6-tetrahydropyridine. Chem. Res. Toxicol., 1997, 10, 364-368. (Pubitemid 27176296)
    • (1997) Chemical Research in Toxicology , vol.10 , Issue.4 , pp. 364-368
    • Castagnoli, K.1    Palmer, S.2    Anderson, A.3    Bueters, T.4    Castagnoli Jr., N.5
  • 133
    • 40949144116 scopus 로고    scopus 로고
    • In vitro and in vivoevidences that antioxidant action contributes to the neuroprotective effects ofthe neuronal nitric oxide synthase and monoamine oxidase-B inhibitor, 7-nitroindazole
    • Thomas, B.; Saravanan, K.S.; Mohanakumar, K.P. In vitro and in vivoevidences that antioxidant action contributes to the neuroprotective effects ofthe neuronal nitric oxide synthase and monoamine oxidase-B inhibitor, 7-nitroindazole. Neurochem. Int., 2008, 52, 990-1001.
    • (2008) Neurochem. Int. , vol.52 , pp. 990-1001
    • Thomas, B.1    Saravanan, K.S.2    Mohanakumar, K.P.3
  • 134
    • 0027323351 scopus 로고
    • Inhibition of rat cerebellar nitric oxide synthase by 7-nitro indazole and related substituted indazoles
    • Babbedge, R.C.; Bland-Ward, P.A.; Hart, S.L.; Moore, P.K. Inhibition of ratcerebellar nitric oxide synthase by 7-nitroindazole and related substitutedindazoles. Br. J. Pharmacol., 1993, 110, 225-228. (Pubitemid 23257783)
    • (1993) British Journal of Pharmacology , vol.110 , Issue.1 , pp. 225-228
    • Babbedge, R.C.1    Bland-Ward, P.A.2    Hart, S.L.3    Moore, P.K.4
  • 135
    • 0036451888 scopus 로고    scopus 로고
    • Non-cholinergic strategies for treating and preventing Alzheimer's disease
    • Doraiswamy, P.M. Non-cholinergic strategies for treating and preventingAlzheimer's disease. CNS Drugs, 2002, 16, 811-824. (Pubitemid 35440615)
    • (2002) CNS Drugs , vol.16 , Issue.12 , pp. 811-824
    • Doraiswamy, P.M.1
  • 136
    • 0030035582 scopus 로고    scopus 로고
    • Neurodegenerative disease: Searching for drugs that combatAlzheimer's
    • Marx, J. Neurodegenerative disease: searching for drugs that combatAlzheimer's. Science, 1996, 273, 50.
    • (1996) Science , vol.273 , pp. 50
    • Marx, J.1
  • 137
    • 0036812560 scopus 로고    scopus 로고
    • From epidemiology to therapeutic trials with anti-inflammatory drugs in Alzheimer's disease: The role of NSAIDs and cyclooxygenase in β-amyloidosis and clinical dementia
    • Pasinetti, G.M. From epidemiology to therapeutic trials with antiinflammatorydrugs in Alzheimer's disease: the role of NSAIDs andcyclooxygenase in beta-amyloidosis and clinical dementia. J. Alzheimer'sDis., 2002, 4, 435-445. (Pubitemid 35397809)
    • (2002) Journal of Alzheimer's Disease , vol.4 , Issue.5 , pp. 435-445
    • Pasinetti, G.M.1
  • 139
    • 34447280369 scopus 로고    scopus 로고
    • A new therapeutic approach in Alzheimer disease: Some novel pyrazole derivatives as dual MAO-B inhibitors and antiinflammatory analgesics
    • DOI 10.1016/j.bmc.2007.06.004, PII S0968089607005287
    • Gökhan-Kelekçi, N.; Yabanoǧlu, S.; Küpeli, E.; Salg?n, U.; Özgen, Ö.; Uçar, G.; Yeşilada, E.; Kendi, E.; Yeşilada, A.; Bilgin, A.A. A new therapeuticapproach in Alzheimer disease: Some novel pyrazole derivatives as dualMAO-B inhibitors and anti-inflammatory analgesics. Bioorg. Med. Chem., 2007, 15, 5775-5786. (Pubitemid 47043476)
    • (2007) Bioorganic and Medicinal Chemistry , vol.15 , Issue.17 , pp. 5775-5786
    • Gokhan-Kelekci, N.1    Yabanoglu, S.2    Kupeli, E.3    Salgin, U.4    Ozgen, O.5    Ucar, G.6    Yesilada, E.7    Kendi, E.8    Yesilada, A.9    Bilgin, A.A.10
  • 142
    • 0042141599 scopus 로고    scopus 로고
    • 2A antagonist prevents dopamine agonist-induced motor complications in animal models of Parkinson's disease
    • DOI 10.1016/S0014-4886(03)00250-4
    • Bibbiani, F.; Oh, J.D.; Petzer, J.P.; Castagnoli, N.Jr.; Chen, J.F.;Schwarzschild, M.A.; Chase, T.N. A2A antagonist prevents dopamineagonist-induced motor complications in animal models of Parkinson'sdisease. Exp. Neurol., 2003, 184, 285-294. (Pubitemid 37444038)
    • (2003) Experimental Neurology , vol.184 , Issue.1 , pp. 285-294
    • Bibbiani, F.1    Oh, J.D.2    Petzer, J.P.3    Castagnoli Jr., N.4    Chen, J.-F.5    Schwarzschild, M.A.6    Chase, T.N.7
  • 143
    • 33750171348 scopus 로고    scopus 로고
    • 2A receptors in Parkinson's disease
    • DOI 10.1016/j.tins.2006.09.004, PII S0166223606002219
    • (a) Schwarzschild, M.A.; Agnati, L.; Fuxe, K.; Chen, J.F.; Morelli, M.Targeting adenosine A2A receptors in Parkinson's disease. Trends Neurosci., 2006, 29, 647-654 (Pubitemid 44602262)
    • (2006) Trends in Neurosciences , vol.29 , Issue.11 , pp. 647-654
    • Schwarzschild, M.A.1    Agnati, L.2    Fuxe, K.3    Chen, J.-F.4    Morelli, M.5
  • 144
    • 14544288232 scopus 로고    scopus 로고
    • 2A receptor antagonists in Parkinson's disease
    • DOI 10.1016/j.pharmthera.2004.10.007
    • (b) Xu, K.; Bastia, E.; Schwarzschild, M. Therapeuticpotential of adenosine A(2A) receptor antagonists in Parkinson's disease.Pharmacol. Ther., 2005, 105, 267-310. (Pubitemid 40297894)
    • (2005) Pharmacology and Therapeutics , vol.105 , Issue.3 , pp. 267-310
    • Xu, K.1    Bastia, E.2    Schwarzschild, M.3
  • 145
    • 0028100413 scopus 로고
    • Differential age-related changes of MAO-A and MAO-B in mouse brain and peripheral organs
    • DOI 10.1016/0197-4580(94)90071-X
    • (a) Saura, J.; Richards, J.G.; Mahy, N. Differential age-related changes ofMAO-A and MAO-B in mouse brain and peripheral organs. Neurobiol.Aging, 1994, 15, 399-408 (Pubitemid 24241808)
    • (1994) Neurobiology of Aging , vol.15 , Issue.4 , pp. 399-408
    • Saura, J.1    Richards, J.G.2    Mahy, N.3
  • 146
    • 0030768730 scopus 로고    scopus 로고
    • Age-related increases in brain monoamine oxidase B in living healthy human subjects
    • DOI 10.1016/S0197-4580(97)00037-7, PII S0197458097000377
    • (b) Fowler, J.S.; Volkow, N.D.; Wang, G.-J.;Logan, J.; Pappas, N.; Shea, C.; Macgregor, R. Age-related increases in brainmonoamine oxidase B in living healthy human subjects. Neurobiol. Aging, 1997, 18, 431-435. (Pubitemid 27435085)
    • (1997) Neurobiology of Aging , vol.18 , Issue.4 , pp. 431-435
    • Fowler, J.S.1    Volkow, N.D.2    Wang, G.-J.3    Logan, J.4    Pappas, N.5    Shea, C.6    MacGregor, R.7
  • 150
    • 51449101712 scopus 로고    scopus 로고
    • Dualinhibition of monoamine oxidase B and antagonism of the adenosine A2Areceptor by (E, E)-8-(4-phenylbutadien-1-yl)caffeine analogues
    • Pretorius, J.; Malan, S.F.; Castagnoli, N.Jr.; Bergh, J.J.; Petzer, J.P. Dualinhibition of monoamine oxidase B and antagonism of the adenosine A2Areceptor by (E, E)-8-(4-phenylbutadien-1-yl)caffeine analogues. Bioorg. Med.Chem., 2008, 16, 8676-8684.
    • (2008) Bioorg. Med.Chem. , vol.16 , pp. 8676-8684
    • Pretorius, J.1    Malan, S.F.2    Castagnoli Jr., N.3    Bergh, J.J.4    Petzer, J.P.5
  • 152
    • 36749037180 scopus 로고    scopus 로고
    • Role of the APP non-amyloidogenic signaling pathway and targeting α-secretase as an alternative drug target for treatment of Alzheimer's diseases
    • DOI 10.2174/092986707782360060
    • (b) Bandyopadhyay, S.; Goldstein, L.E.; Lahiri, D.K.; Rogers, J.T. Role of the APP non-amyloidogenic signaling pathway and targetingalpha-secretase as an alternative drug target for treatment of Alzheimer'sdisease. Curr. Med. Chem., 2007, 14, 2848-2864 (Pubitemid 350201652)
    • (2007) Current Medicinal Chemistry , vol.14 , Issue.27 , pp. 2848-2864
    • Bandyopadhyay, S.1    Goldstein, L.E.2    Lahiri, D.K.3    Rogers, J.T.4
  • 153
    • 77957374286 scopus 로고    scopus 로고
    • Propargylamine containingcompounds as modulators of proteolytic cleavage of amyloid-beta proteinprecursor: Involvement of MAPK and PKC activation
    • (c) Bar-Am, O.; Amit, T.;Weinreb, O.; Youdim, M.B.H.; Mandel, S. Propargylamine containingcompounds as modulators of proteolytic cleavage of amyloid-beta proteinprecursor: involvement of MAPK and PKC activation. J. Alzheimer's Dis., 2010, 21, 361-371.
    • (2010) J. Alzheimer's Dis. , vol.21 , pp. 361-371
    • Bar-Am, O.1    Amit, T.2    Weinreb, O.3    Youdim, M.B.H.4    Mandel, S.5
  • 154
    • 0036777108 scopus 로고    scopus 로고
    • Involvement of MAP kinase in the regulation of amyloid precursor proteinprocessing by novel cholinesterase inhibitors derived from rasagiline
    • Yogev-Falach, M.; Amit, T.; Bar-Am, O.; Weinstock, M.; Youdim, M.B.H.Involvement of MAP kinase in the regulation of amyloid precursor proteinprocessing by novel cholinesterase inhibitors derived from rasagiline. FASEBJ., 2002, 16, 1674-1676.
    • (2002) FASEBJ. , vol.16 , pp. 1674-1676
    • Yogev-Falach, M.1    Amit, T.2    Bar-Am, O.3    Weinstock, M.4    Youdim, M.B.H.5
  • 155
    • 38949121975 scopus 로고    scopus 로고
    • New 1, 2, 3, 4-tetrahydroisoquinoline derivatives as modulators ofproteolytic cleavage of amyloid precursor proteins
    • Hu, M.K.; Liao, Y.F.; Chen, J.F.; Wang, B.J.; Tung, Y.T.; Lin, H.C.; Lee, K.P. New 1, 2, 3, 4-tetrahydroisoquinoline derivatives as modulators ofproteolytic cleavage of amyloid precursor proteins. Bioorg. Med. Chem., 2008, 16, 1957-1965.
    • (2008) Bioorg. Med. Chem. , vol.16 , pp. 1957-1965
    • Hu, M.K.1    Liao, Y.F.2    Chen, J.F.3    Wang, B.J.4    Tung, Y.T.5    Lin, H.C.6    Lee, K.P.7
  • 157
    • 34548431717 scopus 로고    scopus 로고
    • Clinical pharmacology and mechanism of action of zonisamide
    • DOI 10.1097/wnf.0b013e3180413d7d, PII 0000282620070700000007
    • Biton, V. Clinical pharmacology and mechanism of action of zonisamide.Clin. Neuropharmacol., 2007, 30, 230-240. (Pubitemid 47356720)
    • (2007) Clinical Neuropharmacology , vol.30 , Issue.4 , pp. 230-240
    • Biton, V.1
  • 158
    • 73949095157 scopus 로고    scopus 로고
    • Protective effects of a novel anti-parkinsonianagent zonisamide on dopamine quinone-related neurotoxicity
    • Asanuma, M.; Miyazaki, I. Protective effects of a novel anti-parkinsonianagent zonisamide on dopamine quinone-related neurotoxicity. Society forNeuroscience Program Nol 158, 2007, 1.
    • (2007) Society ForNeuroscience Program Nol , vol.158 , pp. 1
    • Asanuma, M.1    Miyazaki, I.2
  • 160
    • 73949127414 scopus 로고    scopus 로고
    • The antiepileptic drugzonisamide inhibits MAO-B and attenuates MPTP toxicity in mice: Clinicalrelevance
    • Sonsalla, P. K.; Wong, L.-Y.; Winnik, B.; Buckley, B. The antiepileptic drugzonisamide inhibits MAO-B and attenuates MPTP toxicity in mice: Clinicalrelevance. Exp. Neurol., 2010, 221, 329-334.
    • (2010) Exp. Neurol. , vol.221 , pp. 329-334
    • Sonsalla, P.K.1    Wong, L.-Y.2    Winnik, B.3    Buckley, B.4
  • 161
    • 79851502469 scopus 로고    scopus 로고
    • Interactions ofmonoamine oxidases with the antiepileptic drug zonisamide: Specificity ofinhibition and structure of the human monoamine oxidase B complex
    • Binda, C.; Aldeco, M.; Mattevi, A.; Edmondson, D.E. Interactions ofmonoamine oxidases with the antiepileptic drug zonisamide: Specificity ofinhibition and structure of the human monoamine oxidase B complex. J.Med. Chem., 2011, 54, 909-912.
    • (2011) J.Med. Chem. , vol.54 , pp. 909-912
    • Binda, C.1    Aldeco, M.2    Mattevi, A.3    Edmondson, D.E.4
  • 162
    • 20444499367 scopus 로고    scopus 로고
    • Acute treatment with the PPARγ agonist pioglitazone and ibuprofen reduces glial inflammation and Aβ1-42 levels in APPV717I transgenic mice
    • DOI 10.1093/brain/awh452
    • Heneka, M.T.; Sastre, M.; Dumitrescu-Ozimek, L.; Hanke, A.; Dewachter, I.;Kuiperi, C.; O'Banion, K.; Klockgether, T.; Van Leuven, F.; Landreth, G.E.Acute treatment with the PPARg agonist pioglitazone and ibuprofen reducesglial inflammation and Ab 1-42 levels in APPV7171 transgenic mice. Brain, 2005, 128, 1442-1453. (Pubitemid 40826196)
    • (2005) Brain , vol.128 , Issue.6 , pp. 1442-1453
    • Heneka, M.T.1    Sastre, M.2    Dumitrescu-Ozimek, L.3    Hanke, A.4    Dewachter, I.5    Kuiperi, C.6    O'Banion, K.7    Klockgether, T.8    Van Leuven, F.9    Landreth, G.E.10
  • 163
    • 0036326074 scopus 로고    scopus 로고
    • Protective action of the peroxisome proliferator-activated receptor-γ agonist pioglitazone in a mouse model of Parkinson's disease
    • DOI 10.1046/j.1471-4159.2002.00990.x
    • Breidert, T.; Callebert, J.; Heneka, M.T.; Landreth, G.; Launay, J.M.; Hirsch, E.C. Protective action of the peroxisome proliferator-activated receptor-γagonist pioglitazone in a mouse model of Parkinson's disease. J.Neurochem., 2002, 82, 615-624. (Pubitemid 34831499)
    • (2002) Journal of Neurochemistry , vol.82 , Issue.3 , pp. 615-624
    • Breidert, T.1    Callebert, J.2    Heneka, M.T.3    Landreth, G.4    Launay, J.M.5    Hirsch, E.C.6
  • 164
    • 0347087323 scopus 로고    scopus 로고
    • Protection by pioglitazone in the MPTP model of Parkinson's disease correlates with IκBα induction and block of NFκB and iNOS activation
    • Dehmer, T.; Heneka, M.T.; Sastre, M.; Dichgans, J.; Schultz, J.B. Protectionby pioglitazone in the MPTP model of Parkinson's disease correlates withIkBa induction and block of NFkB and iNOS activation. J. Neurochem., 2004, 88, 494-501. (Pubitemid 38084565)
    • (2004) Journal of Neurochemistry , vol.88 , Issue.2 , pp. 494-501
    • Dehmer, T.1    Heneka, M.T.2    Sastre, M.3    Dichgans, J.4    Schulz, J.B.5
  • 165
    • 42949100802 scopus 로고    scopus 로고
    • The PPARγ agonist pioglitazone is effective in the MPTP mouse model of Parkinson's disease through inhibition of monoamine oxidase B
    • DOI 10.1038/bjp.2008.78, PII BJP200878
    • Quinn, L.P.; Crook, B.; Hows, M.E.; Vidgeon-Hart, M.; Chapman, H.;Upton, N.; Medhurst, A.D.; Virley, D.J. The PPARγ agonist pioglitazone iseffective in the MPTP mouse model of Parkinson's disease throughinhibition of monoamine oxidase B. Br. J. Pharmacol., 2008, 154, 226-233. (Pubitemid 351620404)
    • (2008) British Journal of Pharmacology , vol.154 , Issue.1 , pp. 226-233
    • Quinn, L.P.1    Crook, B.2    Hows, M.E.3    Vidgeon-Hart, M.4    Chapman, H.5    Upton, N.6    Medhurst, A.D.7    Virley, D.J.8
  • 166
    • 0034651101 scopus 로고    scopus 로고
    • Inflammatory mechanisms in Alzheimer's disease: Inhibition of β- amyloid-stimulated proinflammatory responses and neurotoxicity by PPARγ agonists
    • (a) Combs, C.K.; Johnson, D.E.; Karlo, J.C.; Cannady, S.B.; Landreth, G.E.Inflammatory mechanisms in Alzheimer's disease: inhibition of betaamyloid-stimulated proinflammatory responses and neurotoxicity byPPARgamma agonists. J. Neurosci., 2000, 2, 558-567 (Pubitemid 30225558)
    • (2000) Journal of Neuroscience , vol.20 , Issue.2 , pp. 558-567
    • Combs, C.K.1    Johnson, D.E.2    Karlo, J.C.3    Cannady, S.B.4    Landreth, G.E.5
  • 167
    • 13644271368 scopus 로고    scopus 로고
    • Peroxisome proliferator-activated receptor γ is expressed in hippocampal neurons and its activation prevents β-amyloid neurodegeneration: Role of Wnt signaling
    • DOI 10.1016/j.yexcr.2004.09.032
    • (b) Inestrosa, N.C.;Godoy, J.A.; Quintanilla, R.A.; Koenig, C.S.; Bronfman, M. Peroxisomeproliferator-activated receptor gamma is expressed in hippocampal neuronsand its activation prevents beta-amyloid neurodegeneration: role of Wntsignalling. Exp. Cell Res., 2005, 304, 91-104. (Pubitemid 40227422)
    • (2005) Experimental Cell Research , vol.304 , Issue.1 , pp. 91-104
    • Inestrosa, N.C.1    Godoy, J.A.2    Quintanilla, R.A.3    Koenig, C.S.4    Bronfman, M.5
  • 169
    • 0002036701 scopus 로고    scopus 로고
    • 3D QSAR in drug design: Recent advances
    • Kluwer Academic Publishers: Dordrecht, The Netherlands
    • (a) 3D QSAR in drug design: recent advances. In: Perspectives in drugdiscovery and design, vol. 12-14; Kubinyi, H.; Folkers, G.; Martin, Y.C.Eds.; Kluwer Academic Publishers: Dordrecht, The Netherlands, 1998
    • (1998) Perspectives in Drugdiscovery and Design , vol.12-14
    • Kubinyi, H.1    Folkers, G.2    Martin, Y.C.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.