메뉴 건너뛰기




Volumn 12, Issue 10, 2012, Pages 907-919

Discovery of MAO-B inhibitors - present status and future directions part I: Oxygen heterocycles and analogs

Author keywords

Chalcones; Chromones; Coumarins; MAO inhibitors; Multi target; Parkinson's disease; SAR

Indexed keywords

7 (3,4 DIFLUOROBENZYLOXY) 3,4 DIMETHYLCOUMARIN; 7 (BENZYLOXY) 3,4 DIMETHYLCOUMARIN DERIVATIVE; ACETYLCHOLINESTERASE; AMINE OXIDASE (FLAVIN CONTAINING) ISOENZYME B; AROMATASE; CATECHOL METHYLTRANSFERASE INHIBITOR; CHALCONE DERIVATIVE; CHROMONE DERIVATIVE; CLORGYLINE; COUMARIN 3 ACYL CHLORIDE DERIVATIVE; COUMARIN 3 CARBOXYLIC ACID; COUMARIN DERIVATIVE; DOPAMINE; HETEROCYCLIC COMPOUND; LADOSTIGIL; LEVODOPA; MOCLOBEMIDE; MONOAMINE OXIDASE B INHIBITOR; NW 1772; RASAGILINE; RIVASTIGMINE; SAFINAMIDE; SELEGILINE; UNCLASSIFIED DRUG; XANTHONE DERIVATIVE;

EID: 84866449811     PISSN: 13895575     EISSN: 18755607     Source Type: Journal    
DOI: 10.2174/138955712802762301     Document Type: Review
Times cited : (43)

References (84)
  • 1
    • 34547698945 scopus 로고    scopus 로고
    • Structural insights into the mechanism of amine oxidation by monoamine oxidases A and B
    • Edmondson, D.E.; Binda, C.; Mattevi, A. Structural insights into the mechanism of amine oxidation by monoamine oxidases A and B. Arch Biochem Biophys, 2007, 464, (2), 269-276.
    • (2007) Arch Biochem Biophys , vol.464 , Issue.2 , pp. 269-276
    • Edmondson, D.E.1    Binda, C.2    Mattevi, A.3
  • 2
    • 56749085833 scopus 로고    scopus 로고
    • The increasing role of monoamine oxidase type B inhibitors in Parkinson's disease therapy
    • Elmer, L.W.; Bertoni, J.M. The increasing role of monoamine oxidase type B inhibitors in Parkinson's disease therapy. Expert Opin Pharmacother, 2008, 9, (16), 2759-2772.
    • (2008) Expert Opin Pharmacother , vol.9 , Issue.16 , pp. 2759-2772
    • Elmer, L.W.1    Bertoni, J.M.2
  • 3
    • 0027300857 scopus 로고
    • Spectral and kinetic studies of imine product formation in the oxidation of p- (N,N-dimethylamino)-benzylamine analogs by monoamine oxidase B
    • Edmondson, D.E.; Bhattacharyya, A.K.; Walker, M.C. Spectral and kinetic studies of imine product formation in the oxidation of p- (N,N-dimethylamino)-benzylamine analogs by monoamine oxidase B. Biochemistry, 1993, 32, 5196-5202.
    • (1993) Biochemistry , vol.32 , pp. 5196-5202
    • Edmondson, D.E.1    Bhattacharyya, A.K.2    Walker, M.C.3
  • 4
    • 51249118269 scopus 로고    scopus 로고
    • Monoamine oxidase inactivation: From pathophysiology to therapeutics
    • Bortolato, M.; Chen, K.; Shih, J.C. Monoamine oxidase inactivation: from pathophysiology to therapeutics. Adv Drug Deliv Rev, 2008, 60, (13/14), 1527-1533.
    • (2008) Adv Drug Deliv Rev , vol.60 , Issue.13-14 , pp. 1527-1533
    • Bortolato, M.1    Chen, K.2    Shih, J.C.3
  • 5
    • 36749021653 scopus 로고    scopus 로고
    • Comprehensive review of rasagiline, a second-generation monoamine oxidase inhibitor, for the treatment of Parkinson's disease
    • Chen, J.J.; Swope, D.M.; Dashtipour, K. Comprehensive review of rasagiline, a second-generation monoamine oxidase inhibitor, for the treatment of Parkinson's disease. Clin Ther, 2007, 29, (9), 1825-1849.
    • (2007) Clin Ther , vol.29 , Issue.9 , pp. 1825-1849
    • Chen, J.J.1    Swope, D.M.2    Dashtipour, K.3
  • 6
    • 33645307953 scopus 로고    scopus 로고
    • The therapeutic potential of monoamine oxidase inhibitors
    • Youdim, M.B.; Edmondson, D.; Tipton, K.F. The therapeutic potential of monoamine oxidase inhibitors. Nat Rev Neurosci, 2006, 7, (4), 295-309.
    • (2006) Nat Rev Neurosci , vol.7 , Issue.4 , pp. 295-309
    • Youdim, M.B.1    Edmondson, D.2    Tipton, K.F.3
  • 7
    • 36848999737 scopus 로고    scopus 로고
    • Pharmacotherapy for Parkinson's disease
    • Chen, J.J.; Swope, D.M. Pharmacotherapy for Parkinson's disease. Pharmacotherapy, 2007, 27, (12 Pt 2), 161S-173S.
    • (2007) Pharmacotherapy , vol.27 , Issue.12 PT 2
    • Chen, J.J.1    Swope, D.M.2
  • 11
    • 0344443765 scopus 로고    scopus 로고
    • Oxidative alphaketoglutarate dehydrogenase inhibition via subtle elevations in monoamine oxidase B levels results in loss of spare respiratory capacity: Implications for Parkinson's disease
    • Kumar, M.J.; Nicholls, D.G.; Andersen, J.K. Oxidative alphaketoglutarate dehydrogenase inhibition via subtle elevations in monoamine oxidase B levels results in loss of spare respiratory capacity: implications for Parkinson's disease. J Biol Chem, 2003, 278, (47), 46432-46439.
    • (2003) J Biol Chem , vol.278 , Issue.47 , pp. 46432-46439
    • Kumar, M.J.1    Nicholls, D.G.2    Andersen, J.K.3
  • 12
    • 61949458087 scopus 로고    scopus 로고
    • Molecular and clinical pathways to neuroprotection of dopaminergic drugs in Parkinson disease
    • Schapira, A.H. Molecular and clinical pathways to neuroprotection of dopaminergic drugs in Parkinson disease. Neurology, 2009, 72, (7 Suppl), S44-50.
    • (2009) Neurology , vol.72 , Issue.7 SUPPL. , pp. 44-50
    • Schapira, A.H.1
  • 14
    • 41249095982 scopus 로고    scopus 로고
    • Current status of symptomatic medical therapy in Parkinson's disease
    • Factor, S.A. Current status of symptomatic medical therapy in Parkinson's disease. Neurotherapeutics, 2008, 5, (2), 164-180.
    • (2008) Neurotherapeutics , vol.5 , Issue.2 , pp. 164-180
    • Factor, S.A.1
  • 15
    • 0033770513 scopus 로고    scopus 로고
    • (-)Deprenyl (Selegiline): Past, present and future
    • Knoll, J. (-)Deprenyl (Selegiline): past, present and future. Neurobiology (Bp.), 2000, 8, 179-199.
    • (2000) Neurobiology (Bp.) , vol.8 , pp. 179-199
    • Knoll, J.1
  • 16
    • 33645307953 scopus 로고    scopus 로고
    • The Therapeutic Potential of Monoamine Oxidase Inhibitors
    • Youdim, M.B.; Edmondson, D.E.; Tipton, K.F. The Therapeutic Potential of 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
  • 17
    • 33744980931 scopus 로고    scopus 로고
    • Rationale for Considering that Propargylamines Might Be Neuroprotective in Parkinson's Disease
    • Olanow, C.W. Rationale for Considering that Propargylamines Might Be Neuroprotective in Parkinson's Disease. Neurology, 2006, 66, S69-S79.
    • (2006) Neurology , vol.66
    • Olanow, C.W.1
  • 18
    • 61949442910 scopus 로고    scopus 로고
    • Can we achieve neuroprotection with currently available anti-parkinsonian interventions?
    • Olanow, C.W. Can we achieve neuroprotection with currently available anti-parkinsonian interventions? Neurology, 2009, 72, (7 Suppl), S59-64.
    • (2009) Neurology , vol.72 , Issue.7 SUPPL. , pp. 59-64
    • Olanow, C.W.1
  • 19
    • 58349122472 scopus 로고    scopus 로고
    • Why have we failed to achieve neuroprotection in Parkinson's disease?
    • Olanow, C.W.; Kieburtz, K.; Schapira, A.H. Why have we failed to achieve neuroprotection in Parkinson's disease? Ann Neurol, 2008, 64 Suppl 2, S101-110.
    • (2008) Ann Neurol , vol.64 , Issue.SUPPL. 2 , pp. 101-110
    • Olanow, C.W.1    Kieburtz, K.2    Schapira, A.H.3
  • 20
    • 58349085532 scopus 로고    scopus 로고
    • Drug selection and timing of initiation of treatment in early Parkinson's disease
    • Schapira, A.H.; Olanow, C.W. Drug selection and timing of initiation of treatment in early Parkinson's disease. Ann Neurol, 2008, 64 Suppl 2, S47-S55.
    • (2008) Ann Neurol , vol.64 , Issue.SUPPL. 2 , pp. 47-55
    • Schapira, A.H.1    Olanow, C.W.2
  • 21
    • 55749086674 scopus 로고    scopus 로고
    • Rasagiline in daily clinical use. Results of a treatment study of Parkinson patients with a combination treatment
    • Jost, W.H.; Klasser, M.; Reichmann, H. [Rasagiline in daily clinical use. Results of a treatment study of Parkinson patients with a combination treatment]. Fortschr Neurol Psychiatr, 2008, 76, (10), 594-599.
    • (2008) Fortschr Neurol Psychiatr , vol.76 , Issue.10 , pp. 594-599
    • Jost, W.H.1    Klasser, M.2    Reichmann, H.3
  • 22
    • 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, M.B. Rasagiline: a novel anti-Parkinsonian monoamine oxidase-B inhibitor with neuroprotective activity. Prog Neurobiol, 2010, 92, (3), 330-344.
    • (2010) Prog Neurobiol , vol.92 , Issue.3 , pp. 330-344
    • Weinreb, O.1    Amit, T.2    Bar-Am, O.3    Youdim, M.B.4
  • 23
    • 75949114175 scopus 로고    scopus 로고
    • The neuroprotective mechanism of 1-(R)-aminoindan, the major metabolite of the anti-parkinsonian drug rasagiline
    • Bar-Am, O.; Weinreb, O.; Amit, T.; Youdim, M.B. The neuroprotective mechanism of 1-(R)-aminoindan, the major metabolite of the anti-parkinsonian drug rasagiline. J Neurochem, 2010, 112, (5), 1131-1137.
    • (2010) J Neurochem , vol.112 , Issue.5 , pp. 1131-1137
    • Bar-Am, O.1    Weinreb, O.2    Amit, T.3    Youdim, M.B.4
  • 25
    • 0346154805 scopus 로고    scopus 로고
    • Clinical Pharmacology of MAO Inhibitors: Safety and Future
    • Yamada, M.; Yasuhara, H. Clinical Pharmacology of MAO Inhibitors: Safety and Future. Neurotoxicol., 2004, 25, 215-221.
    • (2004) Neurotoxicol , vol.25 , pp. 215-221
    • Yamada, M.1    Yasuhara, H.2
  • 26
    • 66149173641 scopus 로고    scopus 로고
    • Molecular and Mechanistic Properties of the Membrane-Bound Mitochondrial Monoamine Oxidases
    • Edmondson, D.E.; Binda, C.; Wang, J.; Upadhyay, A.K.; Mattevi, A. Molecular and Mechanistic Properties of the Membrane-Bound Mitochondrial Monoamine Oxidases. Biochemistry, 2009, 48(20), 4220-4230.
    • (2009) Biochemistry , vol.48 , Issue.20 , pp. 4220-4230
    • Edmondson, D.E.1    Binda, C.2    Wang, J.3    Upadhyay, A.K.4    Mattevi, A.5
  • 27
    • 33846076665 scopus 로고    scopus 로고
    • The path from anti Parkinson drug selegiline and rasagiline to multifunctional neuroprotective anti Alzheimer drugs ladostigil and m30
    • Youdim, M.B. The path from anti Parkinson drug selegiline and rasagiline to multifunctional neuroprotective anti Alzheimer drugs ladostigil and m30. Curr Alzheimer Res, 2006, 3, (5), 541-550.
    • (2006) Curr Alzheimer Res , vol.3 , Issue.5 , pp. 541-550
    • Youdim, M.B.1
  • 28
    • 33846873905 scopus 로고    scopus 로고
    • Rasagiline (TVP-1012): A new selective monoamine oxidase inhibitor for Parkinson's disease
    • Guay, D.R. Rasagiline (TVP-1012): a new selective monoamine oxidase inhibitor for Parkinson's disease. Am J Geriatr Pharmacother, 2006, 4, (4), 330-346.
    • (2006) Am J Geriatr Pharmacother , vol.4 , Issue.4 , pp. 330-346
    • Guay, D.R.1
  • 30
    • 0034649564 scopus 로고    scopus 로고
    • Inhibition of Monoamine Oxidases by Functionalized Coumarin Derivatives: Biological Activities, QSARs, and 3D-QSARs
    • Gnerre, C.; Catto, M.; Leonetti, F.; Weber, P.; Carrupt, P.A.; Altomare, C.; Carotti, A.; Testa, B. Inhibition of Monoamine Oxidases by Functionalized Coumarin Derivatives: Biological Activities, QSARs, and 3D-QSARs. J. Med. Chem., 2000, 43, 4747-4758.
    • (2000) J. Med. Chem , vol.43 , 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
  • 32
    • 68349155549 scopus 로고    scopus 로고
    • Synthesis and evaluation of 6-methyl-3-phenylcoumarins as potent and selective MAO-B inhibitors
    • Matos, M.J.; Vina, D.; Picciau, C.; Orallo, F.; Santana, L.; Uriarte, E. Synthesis and evaluation of 6-methyl-3-phenylcoumarins as potent and selective MAO-B inhibitors. Bioorg Med Chem Lett, 2009, 19, (17), 5053-5055.
    • (2009) Bioorg Med Chem Lett , vol.19 , Issue.17 , pp. 5053-5055
    • Matos, M.J.1    Vina, D.2    Picciau, C.3    Orallo, F.4    Santana, L.5    Uriarte, E.6
  • 35
    • 71049173711 scopus 로고    scopus 로고
    • Discovery of a Novel Class of Potent Coumarin Monoamine Oxidase B Inhibitors: Development and Biopharmacological Profiling of 7-[(3-Chlorobenzyl)oxy]-4-[(methylamino)methyl]-2H-chromen-2-one Methanesulfonate (NW-1772) as a Highly Potent, Selective, Reversible, and Orally Active Monoamine Oxidase B Inhibitor
    • Pisani, L.; Muncipinto, G.; Miscioscia, T.F.; Nicolotti, O.; Leonetti, F.; Catto, M.; Caccia, C.; Salvati, P.; Soto-Otero, R.; Mendez-Alvarez, E.; Passeleu, C.; Carotti, A. Discovery of a Novel Class of Potent Coumarin Monoamine Oxidase B Inhibitors: Development and Biopharmacological Profiling of 7-[(3-Chlorobenzyl)oxy]-4-[(methylamino)methyl]-2H-chromen-2-one Methanesulfonate (NW-1772) as a Highly Potent, Selective, Reversible, and Orally Active Monoamine Oxidase B Inhibitor. J. Med. Chem., 2009, 52, (21), 6685-6706.
    • (2009) J. Med. Chem , vol.52 , Issue.21 , pp. 6685-6706
    • Pisani, L.1    Muncipinto, G.2    Miscioscia, T.F.3    Nicolotti, O.4    Leonetti, F.5    Catto, M.6    Caccia, C.7    Salvati, P.8    Soto-Otero, R.9    Mendez-Alvarez, E.10    Passeleu, C.11    Carotti, A.12
  • 36
    • 71049173711 scopus 로고    scopus 로고
    • Discovery of a novel class of potent coumarin monoamine oxidase B inhibitors: Development and biopharmacological profiling of 7-[(3-chlorobenzyl)oxy]-4- [(methylamino)methyl]-2H-chromen-2-one methanesulfonate (NW-1772) as a highly potent, selective, reversible, and orally active monoamine oxidase B inhibitor
    • Pisani, L.; Muncipinto, G.; Miscioscia, T.; Nicolott, I.O.; Leonetti, F.; Catto, M.; Caccia, C.; Salvati, P.; Soto-Otero, R.; Mendez-Alvarez, E.; Passeleu, C.; Carotti, A. Discovery of a novel class of potent coumarin monoamine oxidase B inhibitors: development and biopharmacological profiling of 7-[(3-chlorobenzyl)oxy]-4- [(methylamino)methyl]-2H-chromen-2-one methanesulfonate (NW-1772) as a highly potent, selective, reversible, and orally active monoamine oxidase B inhibitor. J Med Chem., 2009, 52(21). 6685-6706.
    • (2009) J Med Chem , vol.52 , Issue.21 , pp. 6685-6706
    • Pisani, L.1    Muncipinto, G.2    Miscioscia, T.3    Nicolott, I.O.4    Leonetti, F.5    Catto, M.6    Caccia, C.7    Salvati, P.8    Soto-Otero, R.9    Mendez-Alvarez, E.10    Passeleu, C.11    Carotti, A.12
  • 37
    • 0027265461 scopus 로고
    • Substituted xanthones as selective and reversible monoamine oxidase A (MAO-A) inhibitors
    • Thull, U.; Kneubühler, S.; Testa, B.; Borges, M.F.M.; Pinto, M.M.M. Substituted xanthones as selective and reversible monoamine oxidase A (MAO-A) inhibitors. Pharm. Res, 1993, 10, (8), 1187-1190.
    • (1993) Pharm. Res , vol.10 , Issue.8 , pp. 1187-1190
    • Thull, U.1    Kneubühler, S.2    Testa, B.3    Borges, M.F.M.4    Pinto, M.M.M.5
  • 38
    • 34547767187 scopus 로고    scopus 로고
    • QSAR of aromatic substances: MAO inhibitory activity of xanthone derivatives
    • Deeb, O.; Alfalah, S.; Clare, B.W. QSAR of aromatic substances: MAO inhibitory activity of xanthone derivatives. J. Enzym. Inhib. Med. Chem., 2007, 22, (3), 277-286.
    • (2007) J. Enzym. Inhib. Med. Chem , vol.22 , Issue.3 , pp. 277-286
    • Deeb, O.1    Alfalah, S.2    Clare, B.W.3
  • 41
    • 5144234432 scopus 로고    scopus 로고
    • QSAR modeling of the MAO inhibitory activity of xanthones derivatives
    • Núñez, M.B.; Maguna, F.P.; Okulika, N.B.; Castro, E.A. QSAR modeling of the MAO inhibitory activity of xanthones derivatives. Bioorg Med Chem Lett, 2004, 14, 5611-5617.
    • (2004) Bioorg Med Chem Lett , vol.14 , pp. 5611-5617
    • Núñez, M.B.1    Maguna, F.P.2    Okulika, N.B.3    Castro, E.A.4
  • 42
  • 43
    • 9144269994 scopus 로고    scopus 로고
    • Biochemical and biological characterization of a novel antiaromatase coumarin derivative
    • Chen, S.; Cho, M.; Karlsberg, K.; Zhou, D.; Yuan, Y.C. Biochemical and biological characterization of a novel antiaromatase coumarin derivative. J. Biol. Chem., 2004, 279, (46), 48071-48078.
    • (2004) J. Biol. Chem , vol.279 , Issue.46 , pp. 48071-48078
    • Chen, S.1    Cho, M.2    Karlsberg, K.3    Zhou, D.4    Yuan, Y.C.5
  • 44
    • 11144224747 scopus 로고    scopus 로고
    • Design, synthesis, and 3D QSAR of novel potent and selective aromatase inhibitors
    • Leonetti, F.; Favia, A.; Rao, A.; Aliano, R.; Paluszcak, A.; Hartmann, R.W.; Carotti, A. Design, synthesis, and 3D QSAR of novel potent and selective aromatase inhibitors. J. Med. Chem., 2004, 47, (27), 6792-6803.
    • (2004) J. Med. Chem , vol.47 , Issue.27 , pp. 6792-6803
    • Leonetti, F.1    Favia, A.2    Rao, A.3    Aliano, R.4    Paluszcak, A.5    Hartmann, R.W.6    Carotti, A.7
  • 46
    • 33745126693 scopus 로고    scopus 로고
    • Synthesis, molecular modeling studies, and selective inhibitory activity against monoamine oxidase of N,N'-bis[2-oxo-2Hbenzopyran]-3-carboxamides Bioorg
    • Chimenti, F.; Secci, D.; Bolasco, A.; Chimenti, P.; Granese, A.; Carradori, S.; Befani, O.; Turini, P.; Alcaro, S.; Ortuso, F. Synthesis, molecular modeling studies, and selective inhibitory activity against monoamine oxidase of N,N'-bis[2-oxo-2Hbenzopyran]-3-carboxamides Bioorg. Med. Chem. Lett., 2006, 16, 4135-4140.
    • (2006) Med. Chem. Lett. , vol.16 , pp. 4135-4140
    • Chimenti, F.1    Secci, D.2    Bolasco, A.3    Chimenti, P.4    Granese, A.5    Carradori, S.6    Befani, O.7    Turini, P.8    Alcaro, S.9    Ortuso, F.10
  • 48
    • 33746933809 scopus 로고    scopus 로고
    • Structural insights into monoamine oxidase inhibitory potency and selectivity of 7- substituted coumarins from ligand- and target-based approaches
    • Catto, M.; Nicolotti, O.; Leonetti, F.; Carotti, A.; Favia, A.D.; Soto-Otero, R.; Méndez-Alvarez, E.; Carotti, A. Structural insights into monoamine oxidase inhibitory potency and selectivity of 7- substituted coumarins from ligand- and target-based approaches. J. Med. Chem., 2006, 49, 4912-4925.
    • (2006) J. Med. Chem , vol.49 , pp. 4912-4925
    • Catto, M.1    Nicolotti, O.2    Leonetti, F.3    Carotti, A.4    Favia, A.D.5    Soto-Otero, R.6    Méndez-Alvarez, E.7    Carotti, A.8
  • 49
    • 0033773601 scopus 로고    scopus 로고
    • High-level expression of human liver monoamine oxidase B in Pichia pastoris
    • Newton-Vinson, P.; Hubalek, F.; Edmondson, D.E. High-level expression of human liver monoamine oxidase B in Pichia pastoris. Protein Expression Purif., 2000, 20, 334-345.
    • (2000) Protein Expression Purif , vol.20 , pp. 334-345
    • Newton-Vinson, P.1    Hubalek, F.2    Edmondson, D.E.3
  • 50
    • 0042693016 scopus 로고    scopus 로고
    • Insights into the mode of inhibition of human mitochondrial monoamine oxidase B from high-resolution crystal structures
    • Binda, C.; Li, M.; Hubalek, F.; Restelli, N.; Edmondson, D.E.; Mattevi, A. Insights into the mode of inhibition of human mitochondrial monoamine oxidase B from high-resolution crystal structures. Proc. Natl. Acad. Sci. U.S.A., 2003, 100, 9750-9755.
    • (2003) Proc. Natl. Acad. Sci. U.S.A , vol.100 , pp. 9750-9755
    • Binda, C.1    Li, M.2    Hubalek, F.3    Restelli, N.4    Edmondson, D.E.5    Mattevi, A.6
  • 51
    • 38849116342 scopus 로고    scopus 로고
    • Comparison of the structural properties of the active site cavities of human and rat monoamine oxidase A and B in their soluble and membrane-bound forms
    • Upadhyay, A.K.; Wang, J.; Edmondson, D.E. Comparison of the structural properties of the active site cavities of human and rat monoamine oxidase A and B in their soluble and membrane-bound forms. Biochemistry, 2008, 47, 526-536.
    • (2008) Biochemistry , vol.47 , pp. 526-536
    • Upadhyay, A.K.1    Wang, J.2    Edmondson, D.E.3
  • 52
    • 24644437716 scopus 로고    scopus 로고
    • Three-dimensional structure of human monoamine oxidase A (MAO A): Relation to the structures of rat MAO A and human MAO B
    • De Colibus, L.; Li, M.; Binda, C.; Lustig, A.; Edmondson, D.E.; Mattevi, A. Three-dimensional structure of human monoamine oxidase A (MAO A): Relation to the structures of rat MAO A and human MAO B. Proc. Natl. Acad. Sci. U.S.A., 2005, 102, 12684-12689.
    • (2005) Proc. Natl. Acad. Sci. U.S.A , vol.102 , pp. 12684-12689
    • de Colibus, L.1    Li, M.2    Binda, C.3    Lustig, A.4    Edmondson, D.E.5    Mattevi, A.6
  • 53
    • 18144423424 scopus 로고    scopus 로고
    • Demonstration of isoleucine 199 as a structural determinant for the selective inhibition of human monoamine oxidase B by specific reversible inhibitors
    • Hubalek, F.; Binda, C.; Khalil, A.; Li, M.; Mattevi, A.; Castagnoli, N.; Edmondson, D.E. Demonstration of isoleucine 199 as a structural determinant for the selective inhibition of human monoamine oxidase B by specific reversible inhibitors. J. Biol. Chem., 2005, 280, 15761-15766.
    • (2005) J. Biol. Chem , vol.280 , pp. 15761-15766
    • Hubalek, F.1    Binda, C.2    Khalil, A.3    Li, M.4    Mattevi, A.5    Castagnoli, N.6    Edmondson, D.E.7
  • 55
    • 56249083925 scopus 로고    scopus 로고
    • Quantitative Structure-Activity Relationship and Complex Network Approach to Monoamine Oxidase A and B Inhibitors
    • Santana, L.; González-Díaz, H.; Quezada, E.; Uriarte, E.; Yáñez, M.; Viña, D.; Orallo, F. Quantitative Structure-Activity Relationship and Complex Network Approach to Monoamine Oxidase A and B Inhibitors. J. Med. Chem., 2008, 51, 6740-6751.
    • (2008) J. Med. Chem , vol.51 , pp. 6740-6751
    • Santana, L.1    González-Díaz, H.2    Quezada, E.3    Uriarte, E.4    Yáñez, M.5    Viña, D.6    Orallo, F.7
  • 57
    • 31444457188 scopus 로고    scopus 로고
    • Design, synthesis, and evaluation of novel 6-chloro-/fluorochromone derivatives as potential topoisomerase inhibitor anticancer agents
    • Ishar, M.P.S.; Singh, G.; Singh, S.; Sreenivasan, K.K.; Singh, G. Design, synthesis, and evaluation of novel 6-chloro-/fluorochromone derivatives as potential topoisomerase inhibitor anticancer agents. Bioorg. Med. Chem. Lett., 2006, 16, 1366-1370.
    • (2006) Bioorg. Med. Chem. Lett , vol.16 , pp. 1366-1370
    • Ishar, M.P.S.1    Singh, G.2    Singh, S.3    Sreenivasan, K.K.4    Singh, G.5
  • 58
    • 0036453923 scopus 로고    scopus 로고
    • Interactions of a new 2-styrylchromone with mitochondrial oxidative phosphorylation
    • Peixoto, F.; Barros, A.I.R.N.A.; Silva, A.M.S. Interactions of a new 2-styrylchromone with mitochondrial oxidative phosphorylation. J. Biochem. Mol. Toxicol., 2002, 16, 220-226.
    • (2002) J. Biochem. Mol. Toxicol , vol.16 , pp. 220-226
    • Peixoto, F.1    Barros, A.I.R.N.A.2    Silva, A.M.S.3
  • 59
    • 79953066953 scopus 로고    scopus 로고
    • Towards the discovery of a novel class of monoamine oxidase inhibitors: Structure-property-activity and docking studies on chromone amides
    • Gaspar, A.; Teixeira, F.; Uriarte, E.; Milhazes, N.; Melo, A.; Cordeiro, M.N.; Ortuso, F.; Alcaro, S.; Borges, F. Towards the discovery of a novel class of monoamine oxidase inhibitors: structure-property-activity and docking studies on chromone amides. ChemMedChem, 2011, 6, (4), 628-632.
    • (2011) ChemMedChem , vol.6 , Issue.4 , pp. 628-632
    • Gaspar, A.1    Teixeira, F.2    Uriarte, E.3    Milhazes, N.4    Melo, A.5    Cordeiro, M.N.6    Ortuso, F.7    Alcaro, S.8    Borges, F.9
  • 62
    • 33646092535 scopus 로고    scopus 로고
    • Inhibitory effects of cisand trans-resveratrol on noradrenaline and 5-hydroxytryptamine uptake and on monoamine oxidase activity
    • Yanez, M.; Fraiz, N.; Cano, E.; Orallo, F. Inhibitory effects of cisand trans-resveratrol on noradrenaline and 5-hydroxytryptamine uptake and on monoamine oxidase activity. Biochem Biophys Res Commun, 2006, 344, (2), 688-695.
    • (2006) Biochem Biophys Res Commun , vol.344 , Issue.2 , pp. 688-695
    • Yanez, M.1    Fraiz, N.2    Cano, E.3    Orallo, F.4
  • 63
    • 20144367578 scopus 로고    scopus 로고
    • Chalcones: An update on cytotoxic and chemoprotective properties
    • Go, M.L.; Wu, X.; Liu, X.L. Chalcones: an update on cytotoxic and chemoprotective properties. Curr. Med. Chem., 2005, 12, 481-499.
    • (2005) Curr. Med. Chem , vol.12 , pp. 481-499
    • Go, M.L.1    Wu, X.2    Liu, X.L.3
  • 66
    • 57049108624 scopus 로고    scopus 로고
    • Evaluation of chalcones-a flavonoid subclass for their anxiolytic effect in rats using elevated plus maze and open field behaviour tests
    • Jamal, H.; Ansari, W.H.; Rizvi, S.J. Evaluation of chalcones-a flavonoid subclass for their anxiolytic effect in rats using elevated plus maze and open field behaviour tests. Fund. Clin. Pharmacol., 2008, 22, 673-681.
    • (2008) Fund. Clin. Pharmacol , vol.22 , pp. 673-681
    • Jamal, H.1    Ansari, W.H.2    Rizvi, S.J.3
  • 67
    • 0023103019 scopus 로고
    • Isolation of Monoamine Oxidase Inhibitors from Glycyrrhiza uralensis Roots and the Structure-Activity Relationship
    • Tanaka, S.; Kuwai, Y.; Tabata, M. Isolation of Monoamine Oxidase Inhibitors from Glycyrrhiza uralensis Roots and the Structure-Activity Relationship. Planta Med., 1987, 53, 5-8.
    • (1987) Planta Med , vol.53 , pp. 5-8
    • Tanaka, S.1    Kuwai, Y.2    Tabata, M.3
  • 68
    • 57749087002 scopus 로고    scopus 로고
    • Dual-target-directed drugs that block monoamine oxidase B and adenosine A(2A) receptors for Parkinson's disease
    • Petzer, J.P.; Castagnoli, N., Jr.; Schwarzschild, M.A.; Chen, J.F.; Van der Schyf, C.J. Dual-target-directed drugs that block monoamine oxidase B and adenosine A(2A) receptors for Parkinson's disease. Neurotherapeutics, 2009, 6, (1), 141-151.
    • (2009) Neurotherapeutics , vol.6 , Issue.1 , pp. 141-151
    • Petzer, J.P.1    Castagnoli Jr., N.2    Schwarzschild, M.A.3    Chen, J.F.4    van der Schyf, C.J.5
  • 70
    • 57749113203 scopus 로고    scopus 로고
    • Multifunctional pharmacotherapy: What can we learn from study of selective serotonin reuptake inhibitor augmentation of antipsychotics in negative-symptom schizophrenia?
    • Silver, H.; Chertkow, Y.; Weinreb, O.; Danovich, L.; Youdim, M. Multifunctional pharmacotherapy: what can we learn from study of selective serotonin reuptake inhibitor augmentation of antipsychotics in negative-symptom schizophrenia? Neurotherapeutics, 2009, 6, (1), 86-93.
    • (2009) Neurotherapeutics , vol.6 , Issue.1 , pp. 86-93
    • Silver, H.1    Chertkow, Y.2    Weinreb, O.3    Danovich, L.4    Youdim, M.5
  • 71
    • 57749085681 scopus 로고    scopus 로고
    • Multifunctional drugs as neurotherapeutics
    • Van der Schyf, C.J.; Youdim, M.B. Multifunctional drugs as neurotherapeutics. Neurotherapeutics, 2009, 6, (1), 1-3.
    • (2009) Neurotherapeutics , vol.6 , Issue.1 , pp. 1-3
    • van der Schyf, C.J.1    Youdim, M.B.2
  • 72
    • 77954947811 scopus 로고    scopus 로고
    • Neuroprotective multifunctional iron chelators: From redoxsensitive process to novel therapeutic opportunities
    • Weinreb, O.; Amit, T.; Mandel, S.; Kupershmidt, L.; Youdim, M.B. Neuroprotective multifunctional iron chelators: from redoxsensitive process to novel therapeutic opportunities. Antioxid Redox Signal, 2010, 13, (6), 919-949.
    • (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
  • 73
    • 38949111419 scopus 로고    scopus 로고
    • Why should we use multifunctional neuroprotective and neurorestorative drugs for Parkinson's disease?
    • Youdim, M.B.; Geldenhuys, W.J.; Van der Schyf, C.J. Why should we use multifunctional neuroprotective and neurorestorative drugs for Parkinson's disease? Parkinsonism Relat Disord, 2007, 13 Suppl 3, S281-S291.
    • (2007) Parkinsonism Relat Disord , vol.13 , Issue.SUPPL. 3
    • Youdim, M.B.1    Geldenhuys, W.J.2    van der Schyf, C.J.3
  • 74
    • 34848906324 scopus 로고    scopus 로고
    • Aminoindan and hydroxyaminoindan, metabolites of rasagiline and ladostigil, respectively, exert neuroprotective properties in vitro
    • Bar-Am, O.; Amit, T.; Youdim, M.B. Aminoindan and hydroxyaminoindan, metabolites of rasagiline and ladostigil, respectively, exert neuroprotective properties in vitro. J Neurochem, 2007, 103, (2), 500-508.
    • (2007) J Neurochem , vol.103 , Issue.2 , pp. 500-508
    • Bar-Am, O.1    Amit, T.2    Youdim, M.B.3
  • 75
    • 11144245220 scopus 로고    scopus 로고
    • Multi-functional drugs for various CNS targets in the treatment of neurodegenerative disorders
    • Youdim, M.B.H.; Buccafusco, J.J. Multi-functional drugs for various CNS targets in the treatment of neurodegenerative disorders. Trends Pharmacol. Sci., 2005, 26, 27-35.
    • (2005) Trends Pharmacol. Sci , vol.26 , pp. 27-35
    • Youdim, M.B.H.1    Buccafusco, J.J.2
  • 76
    • 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, M.B.; 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.
    • 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
  • 77
    • 61549111876 scopus 로고    scopus 로고
    • The novel cholinesterase-monoamine oxidase inhibitor and antioxidant, ladostigil, confers neuroprotection in neuroblastoma cells and aged rats
    • Bar-Am, O.; Weinreb, O.; Amit, T.; Youdim, M.B. The novel cholinesterase-monoamine oxidase inhibitor and antioxidant, ladostigil, confers neuroprotection in neuroblastoma cells and aged rats. J Mol Neurosci, 2009, 37, (2), 135-145.
    • (2009) J Mol Neurosci , vol.37 , Issue.2 , pp. 135-145
    • Bar-Am, O.1    Weinreb, O.2    Amit, T.3    Youdim, M.B.4
  • 79
    • 38349081326 scopus 로고    scopus 로고
    • CSC, an adenosine A(2A) receptor antagonist and MAO B inhibitor, reverses behavior, monoamine neurotransmission, and amino acid alterations in the 6-OHDAlesioned rats
    • Aguiar, L.M.; Macedo, D.S.; Vasconcelos, S.M.; Oliveira, A.A.; de Sousa, F.C.; Viana, G.S. CSC, an adenosine A(2A) receptor antagonist and MAO B inhibitor, reverses behavior, monoamine neurotransmission, and amino acid alterations in the 6-OHDAlesioned rats. Brain Res, 2008, 1191, 192-199.
    • (2008) Brain Res , vol.1191 , pp. 192-199
    • Aguiar, L.M.1    Macedo, D.S.2    Vasconcelos, S.M.3    Oliveira, A.A.4    de Sousa, F.C.5    Viana, G.S.6
  • 80
    • 30344455384 scopus 로고    scopus 로고
    • E)-8-(3-Chlorostyryl)-1,3,7-trimethylxanthine, a caffeine derivative acting both as antagonist of adenosine A2A receptors and as inhibitor of MAO-B
    • Frederick, R.; Ooms, F.; Castagnoli, N., Jr.; Petzer, J.P.; Feng, J.F.; Schwarzschild, M.A.; Van der Schyf, C.J.; Wouters, J. (E)-8-(3-Chlorostyryl)-1,3,7-trimethylxanthine, a caffeine derivative acting both as antagonist of adenosine A2A receptors and as inhibitor of MAO-B. Acta Crystallogr C, 2005, 61, (Pt 9), o531-o532.
    • (2005) Acta Crystallogr C , vol.61 , Issue.Pt 9
    • Frederick, R.1    Ooms, F.2    Castagnoli Jr., N.3    Petzer, J.P.4    Feng, J.F.5    Schwarzschild, M.A.6    van der Schyf, C.J.7    Wouters, J.8
  • 81
    • 20544477648 scopus 로고    scopus 로고
    • Other pharmacological treatments for motor complications and dyskinesias
    • Waters, C. Other pharmacological treatments for motor complications and dyskinesias. Mov Disord, 2005, 20 Suppl 11, S38-S44.
    • (2005) Mov Disord , vol.20 , Issue.SUPPL. 11
    • Waters, C.1
  • 83
    • 33645870453 scopus 로고    scopus 로고
    • Inhibition of monoamine oxidase B by analogs of the adenosine A2A receptor antagonist (E)-8-(3-chlorostyryl)caffeine (CSC)
    • Vlok, N.; Malan, S.F.; Castagnoli, N., Jr.; Bergh, J.J.; Petzer, J.P. Inhibition of monoamine oxidase B by analogs of the adenosine A2A receptor antagonist (E)-8-(3-chlorostyryl)caffeine (CSC). Bioorg Med Chem, 2006, 14, (10), 3512-3521.
    • (2006) Bioorg Med Chem , vol.14 , Issue.10 , pp. 3512-3521
    • Vlok, N.1    Malan, S.F.2    Castagnoli Jr., N.3    Bergh, J.J.4    Petzer, J.P.5
  • 84
    • 51449101712 scopus 로고    scopus 로고
    • Dual inhibition of monoamine oxidase B and antagonism of the adenosine A(2A) receptor by (E,E)-8-(4-phenylbutadien-1- yl)caffeine analogs
    • Pretorius, J.; Malan, S.F.; Castagnoli, N., Jr.; Bergh, J.J.; Petzer, J.P. Dual inhibition of monoamine oxidase B and antagonism of the adenosine A(2A) receptor by (E,E)-8-(4-phenylbutadien-1- yl)caffeine analogs. Bioorg Med Chem, 2008, 16, (18), 8676-8684.
    • (2008) Bioorg Med Chem , vol.16 , Issue.18 , pp. 8676-8684
    • Pretorius, J.1    Malan, S.F.2    Castagnoli Jr., N.3    Bergh, J.J.4    Petzer, J.P.5


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.