메뉴 건너뛰기




Volumn 12, Issue 20, 2012, Pages 2116-2130

Parkinson's disease management. part iidiscovery of mao-b inhibitors based on nitrogen heterocycles and analogues

Author keywords

Hydrazinylthiazoles; Indoles; Isatins and phthalimides; Mao b inhibitors; Nitrogen heterocycles; Parkinson's disease and therapy; Pyridazine; Pyrimidine and pyrazole derivatives; Quinazolinones

Indexed keywords

AMANTADINE; AMINE OXIDASE (FLAVIN CONTAINING) ISOENZYME B; BENSERAZIDE; BENZATROPINE; BIPERIDEN; BIPHENYL; CARBIDOPA; CATECHOL METHYLTRANSFERASE INHIBITOR; CHOLINERGIC RECEPTOR BLOCKING AGENT; CHROMONE DERIVATIVE; COUMARIN DERIVATIVE; DOPAMINE RECEPTOR STIMULATING AGENT; ENTACAPONE; GLUTAMATE RECEPTOR ANTAGONIST; HYDRAZINE; INDOLE DERIVATIVE; LEVODOPA; MONOAMINE OXIDASE B INHIBITOR; PROCYCLIDINE; PROFENAMINE; PYRAZOLE; RASAGILINE; SELEGILINE; THIAZOLE; TOLCAPONE; TRIHEXYPHENIDYL; XANTHONE DERIVATIVE;

EID: 84874913282     PISSN: 15680266     EISSN: 18734294     Source Type: Journal    
DOI: 10.2174/156802612805220020     Document Type: Review
Times cited : (18)

References (101)
  • 1
    • 72149101615 scopus 로고    scopus 로고
    • Initial clinical manifestations of Parkinson's disease: Features and pathophysiological mecha nisms
    • Rodriguez-Oroz, M.C.; Jahanshahi, M.; Krack, P.; Litvan, I.; Macias, R.; Bezard, E.; Obeso, J.A. Initial clinical manifestations of Parkinson's disease: features and pathophysiological mecha nisms. Lancet Neurol., 2009, 8(12), 1128-1139.
    • (2009) Lancet Neurol , vol.8 , Issue.12 , pp. 1128-1139
    • Rodriguez-Oroz, M.C.1    Jahanshahi, M.2    Krack, P.3    Litvan, I.4    Macias, R.5    Bezard, E.6    Obeso, J.A.7
  • 2
    • 0000015266 scopus 로고
    • The occurrence, distribution and physiological role of catecholamines in the nervous system
    • Carlsson, A. The occurrence, distribution and physiological role of catecholamines in the nervous system. Pharmacol. Rev., 1959, 11(2, Part 2), 490-493.
    • (1959) Pharmacol. Rev , vol.11 , Issue.2 , pp. 490-493
    • Carlsson, A.1
  • 3
    • 0022474468 scopus 로고
    • Virtuoso design of drugs
    • Snyder, S.H. Virtuoso design of drugs. Nature, 1986, 323(6086), 292-293.
    • (1986) Nature , vol.323 , Issue.6086 , pp. 292-293
    • Snyder, S.H.1
  • 5
    • 5444270967 scopus 로고    scopus 로고
    • Neuronal pathology in Parkin son's disease
    • Schulz, J.B.; Falkenburger, B.H., Neuronal pathology in Parkin son's disease. Cell Tissue Res., 2004, 318(1), 135-147.
    • (2004) Cell Tissue Res , vol.318 , Issue.1 , pp. 135-147
    • Schulz, J.B.1    Falkenburger, B.H.2
  • 6
    • 33344461775 scopus 로고    scopus 로고
    • Protein aggregation in the pathogenesis of familial and sporadic Parkinson's disease
    • McNaught, K.S.P.; Olanow, C.W. Protein aggregation in the pathogenesis of familial and sporadic Parkinson's disease. Neuro biol. Aging, 2006, 27(4), 530-545.
    • (2006) Neuro Biol. Aging , vol.27 , Issue.4 , pp. 530-545
    • McNaught, K.S.P.1    Olanow, C.W.2
  • 7
    • 0034973443 scopus 로고    scopus 로고
    • An algorithm (decision tree) for the management of Parkinson's disease (2001): Treatment guidelines
    • Olanow, C.W.; Watts, R.L.; Koller, W.C. An algorithm (decision tree) for the management of Parkinson's disease (2001): treatment guidelines. Neurology, 2001, 56, (11 Suppl 5), S1-S88.
    • (2001) Neurology , vol.56 , Issue.11
    • Olanow, C.W.1    Watts, R.L.2    Koller, W.C.3
  • 8
    • 0029883235 scopus 로고    scopus 로고
    • The response to levodopa in parkinson's disease: Imposing pharmacological law and order
    • Nutt, J.G.; Holford, N.H.G. The response to levodopa in parkinson's disease: Imposing pharmacological law and order. Ann. Neurol., 1996, 39(5), 561-573.
    • (1996) Ann. Neurol , vol.39 , Issue.5 , pp. 561-573
    • Nutt, J.G.1    Holford, N.H.G.2
  • 9
    • 58149120928 scopus 로고    scopus 로고
    • L-dopa therapy for Parkinson's disease: Past, present, and future
    • Nagatsua, T.; Sawadab, M. L-dopa therapy for Parkinson's disease: past, present, and future. Parkinsonism Relat. Disord., 2009, 15 Suppl 1, S3-8.
    • (2009) Parkinsonism Relat. Disord , vol.15 , Issue.SUPPL. 1
    • Nagatsua, T.1    Sawadab, M.2
  • 11
    • 0015501193 scopus 로고
    • Levodopa combined with peripheral decarboxylase inhibition in Parkinson's disease
    • Barbeau, A.; Mars, H.; Botez, M.I.; Joubert, M. Levodopa combined with peripheral decarboxylase inhibition in Parkinson's disease. Can. Med. Assoc. J., 1972, 106(11), 1169-1174.
    • (1972) Can. Med. Assoc. J , vol.106 , Issue.11 , pp. 1169-1174
    • Barbeau, A.1    Mars, H.2    Botez, M.I.3    Joubert, M.4
  • 12
    • 0030741788 scopus 로고    scopus 로고
    • Attempts to obtain neuroprotection in Parkinson's disease
    • Olanow, C.W. Attempts to obtain neuroprotection in Parkinson's disease. Neurology, 1997, 49, (1 Suppl 1), S26-33.
    • (1997) Neurology , vol.49 , Issue.1 SUPPL. 1
    • Olanow, C.W.1
  • 13
    • 58349083886 scopus 로고    scopus 로고
    • Dopamine and impulse control disorders in Parkinson's disease
    • Weintraub, D. Dopamine and impulse control disorders in Parkinson's disease. Ann. Neurol., 2008, 64(S2), S93-S100.
    • (2008) Ann. Neurol , vol.64 , Issue.S2
    • Weintraub, D.1
  • 15
    • 58349085532 scopus 로고    scopus 로고
    • Drug selection and timing of initiation of treatment in early Parkinson's disease
    • Schapira, A.H.V.; Olanow, C.W. Drug selection and timing of initiation of treatment in early Parkinson's disease. Ann. Neurol., 2008, 64(S2), S47-S55.
    • (2008) Ann. Neurol , vol.64 , Issue.S2
    • Schapira, A.H.V.1    Olanow, C.W.2
  • 16
    • 34250647459 scopus 로고    scopus 로고
    • Current pharmacotherapeutic treatment options in Parkinson's Disease
    • Rezak, M. Current pharmacotherapeutic treatment options in Parkinson's Disease. Disease-a-Month, 2007, 53(4), 214-222.
    • (2007) Disease-a-Month , vol.53 , Issue.4 , pp. 214-222
    • Rezak, M.1
  • 17
    • 80053213044 scopus 로고    scopus 로고
    • Pharmacological Therapy in Parkinson's Disease: Focus on Neuroprotection
    • Kincses, Z.T.; Vecsei, L. Pharmacological Therapy in Parkinson's Disease: Focus on Neuroprotection. CNS Neurosci. Ther., 2011, 17(5), 345-367.
    • (2011) CNS Neurosci. Ther , vol.17 , Issue.5 , pp. 345-367
    • Kincses, Z.T.1    Vecsei, L.2
  • 18
    • 0037378032 scopus 로고    scopus 로고
    • Rationale for the use of dopamine agonists as neuroprotective agents in Parkinson's disease
    • Schapira, A.H.; Olanow, C.W. Rationale for the use of dopamine agonists as neuroprotective agents in Parkinson's disease. Ann. Neurol., 2003, 53 Suppl 3, S149-S157.
    • (2003) Ann. Neurol , vol.53 , Issue.3
    • Schapira, A.H.1    Olanow, C.W.2
  • 19
    • 0036018104 scopus 로고    scopus 로고
    • The dopamine agonist cabergoline provides neuroprotection by activation of the glutathione system and scavenging free radicals
    • Yoshioka, M.; Tanaka, K.I.; Miyazaki, I.; Fujita, N.; Higashi, Y.; Asanuma, M.; Ogawa, N. The dopamine agonist cabergoline provides neuroprotection by activation of the glutathione system and scavenging free radicals. Neurosci. Res., 2002, 43(3), 259-267.
    • (2002) Neurosci. Res , vol.43 , Issue.3 , pp. 259-267
    • Yoshioka, M.1    Tanaka, K.I.2    Miyazaki, I.3    Fujita, N.4    Higashi, Y.5    Asanuma, M.6    Ogawa, N.7
  • 20
    • 0028068121 scopus 로고
    • Bromocriptine protects mice against 6hydroxydopamine and scavenges hydroxyl free radicals in vitro
    • Ogawa, N.; Tanaka, K.I.; Asanuma, M.; Kawai, M.; Masumizu, T.; Kohno, M.; Mori, A., Bromocriptine protects mice against 6hydroxydopamine and scavenges hydroxyl free radicals in vitro. Brain Res., 1994, 657(1-2), 207-213.
    • (1994) Brain Res , vol.657 , Issue.1-2 , pp. 207-213
    • Ogawa, N.1    Tanaka, K.I.2    Asanuma, M.3    Kawai, M.4    Masumizu, T.5    Kohno, M.6    Mori, A.7
  • 21
    • 36248974676 scopus 로고    scopus 로고
    • Future directions in the treatment of Parkinson's disease
    • Schapira, A.H.V. Future directions in the treatment of Parkinson's disease. Movement Disord., 2007, 22(S17), S385-S391.
    • (2007) Movement Disord , vol.22 , Issue.S17
    • Schapira, A.H.V.1
  • 22
    • 33847105184 scopus 로고    scopus 로고
    • Advances in the treatment of Parkinson's disease
    • Singh, N.; Pillay, V.; Choonara, Y.E. Advances in the treatment of Parkinson's disease. Prog. Neurobiol., 2007, 81(1), 29-44.
    • (2007) Prog. Neurobiol , vol.81 , Issue.1 , pp. 29-44
    • Singh, N.1    Pillay, V.2    Choonara, Y.E.3
  • 23
    • 0023831051 scopus 로고
    • Effects of antiparkin sonian drugs on muscarinic receptor binding in rat brain, heart and lung
    • Syvalahti, E.K.; Kunelius, R.; Lauren, L. Effects of antiparkin sonian drugs on muscarinic receptor binding in rat brain, heart and lung. Pharmacol. Toxicol., 1988, 62(2), 90-94.
    • (1988) Pharmacol. Toxicol , vol.62 , Issue.2 , pp. 90-94
    • Syvalahti, E.K.1    Kunelius, R.2    Lauren, L.3
  • 25
    • 24144502098 scopus 로고    scopus 로고
    • Alternatives to levodopa in the initial treatment of early Parkinson's disease
    • Lees, A. Alternatives to levodopa in the initial treatment of early Parkinson's disease. Drugs Aging, 2005, 22(9), 731-740.
    • (2005) Drugs Aging , vol.22 , Issue.9 , pp. 731-740
    • Lees, A.1
  • 26
    • 0037378912 scopus 로고    scopus 로고
    • Neuroprotection for Parkinson's disease: Prospects and promises
    • Olanow, C.W.; Schapira, A.H.V.; Agid, Y. Neuroprotection for Parkinson's disease: prospects and promises. Ann. Neurol., 2003, 53(Suppl 3), S1-2.
    • (2003) Ann. Neurol , vol.53 , Issue.SUPPL. 3
    • Olanow, C.W.1    Schapira, A.H.V.2    Agid, Y.3
  • 27
    • 0033123308 scopus 로고    scopus 로고
    • Anticholinergic drugs used in Parkinson's disease: An overlooked class of drugs from a pharmacokinetic perspective
    • D.R. Anticholinergic drugs used in Parkinson's disease: An overlooked class of drugs from a pharmacokinetic perspective. J. Pharm. Pharm. Sci., 1999, 2(2), 39-46.
    • (1999) J. Pharm. Pharm. Sci , vol.2 , Issue.2 , pp. 39-46
  • 29
    • 0027500750 scopus 로고
    • Treatment of Parkinson's disease
    • Calne, D.B. Treatment of Parkinson's disease. N. Engl. J. Med., 1993, 329(14), 1021-1027.
    • (1993) N. Engl. J. Med , vol.329 , Issue.14 , pp. 1021-1027
    • Calne, D.B.1
  • 30
    • 0030957828 scopus 로고    scopus 로고
    • Amantadine in advanced Parkinson's disease: Good use of an old drug
    • Adler, C.H.; Stern, M.B.; Vernon, G.; Hurtig, H.I. Amantadine in advanced Parkinson's disease: good use of an old drug. J. Neurol., 1997, 244(5), 336-337.
    • (1997) J. Neurol , vol.244 , Issue.5 , pp. 336-337
    • Adler, C.H.1    Stern, M.B.2    Vernon, G.3    Hurtig, H.I.4
  • 33
    • 7944236868 scopus 로고    scopus 로고
    • Clinical advantages of COMT inhibition with entacapone a review
    • Gordin, A.; Kaakkola, S.; Teravainen, H. Clinical advantages of COMT inhibition with entacapone a review. J. Neural. Transm., 2004, 111(10-11), 1343-1363.
    • (2004) J. Neural. Transm , vol.111 , Issue.10-11 , pp. 1343-1363
    • Gordin, A.1    Kaakkola, S.2    Teravainen, H.3
  • 34
    • 0033574342 scopus 로고    scopus 로고
    • Entacapone: Is it useful as complimentary treatment with levodopa?
    • Burguera, J.A. Entacapone: is it useful as complimentary treatment with levodopa?. Rev Neurologia, 1999, 28(8), 817-834.
    • (1999) Rev Neurologia , vol.28 , Issue.8 , pp. 817-834
    • Burguera, J.A.1
  • 35
    • 19244365858 scopus 로고    scopus 로고
    • Efficacy and tolerability of entacapone in patients with Parkinson's disease treated with levodopa plus a dopamine agonist and experiencing wearing-off motor fluctuations. A randomized, double-blind, multicentre study
    • Fénelon, G.; Giménez-Roldán, S.; Montastruc, J.L.; Bermejo, F.; Durif, F.; Bourdeix, I.; Péré, J.J.; Galiano, L.; Schadrack, J. Efficacy and tolerability of entacapone in patients with Parkinson's disease treated with levodopa plus a dopamine agonist and experiencing wearing-off motor fluctuations. A randomized, double-blind, multicentre study. J. Neural. Transmission, 2003, 110(3), 239-251.
    • (2003) J. Neural. Transmission , vol.110 , Issue.3 , pp. 239-251
    • Fénelon, G.1    Giménez-Roldán, S.2    Montastruc, J.L.3    Bermejo, F.4    Durif, F.5    Bourdeix, I.6    Péré, J.J.7    Galiano, L.8    Schadrack, J.9
  • 36
    • 0033977448 scopus 로고    scopus 로고
    • Tolcapone and Hepatotoxic Effects
    • Olanow, C.W. Tolcapone and Hepatotoxic Effects. Arch. Neurol, 2000, 57(2), 263-267.
    • (2000) Arch. Neurol , vol.57 , Issue.2 , pp. 263-267
    • Olanow, C.W.1
  • 37
    • 0014314486 scopus 로고
    • Some observations upon a new inhibitor of monoamine oxidase in brain tissue
    • Johnston, J.P. Some observations upon a new inhibitor of monoamine oxidase in brain tissue. Biochem. Pharmacol, 1968, 17(7), 1285-1297.
    • (1968) Biochem. Pharmacol , vol.17 , Issue.7 , pp. 1285-1297
    • Johnston, J.P.1
  • 39
    • 0033991079 scopus 로고    scopus 로고
    • MAO-B inhibitors: Multiple roles in the therapy of neurodegenerative disorders?
    • Foley, P.; Gerlach, M.; Youdim, M.B.; Riederer, P. MAO-B inhibitors: multiple roles in the therapy of neurodegenerative disorders? Parkinsonism Relat. Disord., 2000, 6(1), 25-47.
    • (2000) Parkinsonism Relat. Disord , vol.6 , Issue.1 , pp. 25-47
    • Foley, P.1    Gerlach, M.2    Youdim, M.B.3    Riederer, P.4
  • 41
    • 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
  • 42
    • 30444437749 scopus 로고    scopus 로고
    • Monoamine oxidase: Isoforms and inhibitors in Parkinson's disease and depressive illness
    • Youdim, M.B.; Bakhle, Y.S. Monoamine oxidase: isoforms and inhibitors in Parkinson's disease and depressive illness. Br. J. Pharmacol, 2006, 147 Suppl 1, S287-296.
    • (2006) Br. J. Pharmacol , vol.147 , Issue.1
    • Youdim, M.B.1    Bakhle, Y.S.2
  • 43
    • 31044453010 scopus 로고    scopus 로고
    • Effects of selegiline on antioxidant systems in the nigrostriatum in rat
    • Takahata, K.; Shimazu, S.; Katsuki, H.; Yoneda, F.; Akaike, A., Effects of selegiline on antioxidant systems in the nigrostriatum in rat. J. Neural. Transm., 2006, 113(2), 151-158.
    • (2006) J. Neural. Transm , vol.113 , Issue.2 , pp. 151-158
    • Takahata, K.1    Shimazu, S.2    Katsuki, H.3    Yoneda, F.4    Akaike, A.5
  • 44
    • 0032938038 scopus 로고    scopus 로고
    • Treating and preventing levodopa-induced dyskinesias: Current and future strategies
    • F. Treating and preventing levodopa-induced dyskinesias: current and future strategies. Drugs Aging, 1999, 14(5), 337-345.
    • (1999) Drugs Aging , vol.14 , Issue.5 , pp. 337-345
  • 46
    • 0037789491 scopus 로고    scopus 로고
    • Early and persistent alterations in prefrontal cortex MAO A and B in Alzheimer's disease
    • Kennedy, B.P.; Ziegler, M.G.; Alford, M.; Hansen, L.A.; Thal, L.J.; Masliah, E. Early and persistent alterations in prefrontal cortex MAO A and B in Alzheimer's disease. J. Neural. Transm., 2003, 110(7), 789-801.
    • (2003) J. Neural. Transm , vol.110 , Issue.7 , pp. 789-801
    • Kennedy, B.P.1    Ziegler, M.G.2    Alford, M.3    Hansen, L.A.4    Thal, L.J.5    Masliah, E.6
  • 47
    • 15844386001 scopus 로고    scopus 로고
    • Rasagiline as an adjunct to levodopa in patients with Parkinson's disease and motor fluctuations (LARGO, Lasting effect in Adjunct therapy with Rasagiline Given Once daily, study): A randomised, double-blind, parallel-group trial
    • Rascol, O.; Brooks, D.J.; Melamed, E.; Oertel, W.; Poewe, W.; Stocchi, F.; Tolosa, E. Rasagiline as an adjunct to levodopa in patients with Parkinson's disease and motor fluctuations (LARGO, Lasting effect in Adjunct therapy with Rasagiline Given Once daily, study): a randomised, double-blind, parallel-group trial. Lancet, 2005, 365, (9463), 947-954.
    • (2005) Lancet , vol.365 , Issue.9463 , pp. 947-954
    • Rascol, O.1    Brooks, D.J.2    Melamed, E.3    Oertel, W.4    Poewe, W.5    Stocchi, F.6    Tolosa, E.7
  • 48
    • 23144441835 scopus 로고    scopus 로고
    • Neuropharmacological, neuroprotective and amyloid precursor processing properties of selective MAO-B inhibitor antiparkinsonian drug, rasagiline
    • Youdim, M.B.; Maruyama, W.; Naoi, M. Neuropharmacological, neuroprotective and amyloid precursor processing properties of selective MAO-B inhibitor antiparkinsonian drug, rasagiline. Drugs Today, 2005, 41(6), 369-391.
    • (2005) Drugs Today , vol.41 , Issue.6 , pp. 369-391
    • Youdim, M.B.1    Maruyama, W.2    Naoi, M.3
  • 49
    • 19944383467 scopus 로고    scopus 로고
    • Structure-activity relation ships for the design of small-molecule inhibitors
    • Andricopulo, A.D.; Montanari, C.A. Structure-activity relation ships for the design of small-molecule inhibitors. Mini Rev. Med. Chem., 2005, 5(6), 585-593.
    • (2005) Mini Rev. Med. Chem , vol.5 , Issue.6 , pp. 585-593
    • Andricopulo, A.D.1    Montanari, C.A.2
  • 51
    • 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.; MendezAlvarez, 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    Mendezalvarez, E.10    Passeleu, C.11    Carotti, A.12
  • 52
    • 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
  • 54
    • 69249111386 scopus 로고    scopus 로고
    • Synthesis and molecular modeling of some novel hexahydroindazole derivatives as potent monoamine oxidase inhibitors
    • Gökhan-Kelekçi, N.; Simsek, O.; Ercan, A; Yelekçi, K.; Sahin, Z.; Isik, S.; Uçar, G.; Bilgin, A. Synthesis and molecular modeling of some novel hexahydroindazole derivatives as potent monoamine oxidase inhibitors. Bioorg. Med. Chem., 2009, 17(18), 6761-6772.
    • (2009) Bioorg. Med. Chem , vol.17 , Issue.18 , pp. 6761-6772
    • Gökhan-Kelekçi, N.1    Simsek, O.2    Ercan, A.3    Yelekçi, K.4    Sahin, Z.5    Isik, S.6    Uçar, G.7    Bilgin, A.8
  • 55
    • 77956189112 scopus 로고    scopus 로고
    • Inhibition of monoamine oxidase by indole and benzofuran derivatives
    • Prins, L.H.; Petzer, J.P.; Malan, S.F., Inhibition of monoamine oxidase by indole and benzofuran derivatives. Eur. J. Med. Chem., 2010, 45(10), 4458-4466.
    • (2010) Eur. J. Med. Chem , vol.45 , Issue.10 , pp. 4458-4466
    • Prins, L.H.1    Petzer, J.P.2    Malan, S.F.3
  • 58
    • 84866449811 scopus 로고    scopus 로고
    • Discovery of MAO-B inhibitors present status and future directions. Part I: Oxygen heterocycles and analogues
    • Epub ahead of print
    • Helguera, A.M.; Perez-Machado, G.; Cordeiro, M.N.; Borges, F. Discovery of MAO-B inhibitors present status and future directions. Part I: Oxygen heterocycles and analogues. Mini-Rev. Med. Chem., 2012, [Epub ahead of print].
    • (2012) Mini-Rev. Med. Chem
    • Helguera, A.M.1    Perez-Machado, G.2    Cordeiro, M.N.3    Borges, F.4
  • 59
    • 84862799939 scopus 로고    scopus 로고
    • Design and synthesis of 8-substituted benzamido-phenylxanthine derivatives as MAO-B inhibitors
    • Song, B.; Xiao, T.; Qi, X.; Li, L.N.; Qin, K.; Nian, S.; Hu, G.X.; Yu, Y.; Liang, G.; Ye, F., Design and synthesis of 8-substituted benzamido-phenylxanthine derivatives as MAO-B inhibitors. Bioorg. Med. Chem. Lett., 2012, 22(4), 1739-1742.
    • (2012) Bioorg. Med. Chem. Lett , vol.22 , Issue.4 , pp. 1739-1742
    • Song, B.1    Xiao, T.2    Qi, X.3    Li, L.N.4    Qin, K.5    Nian, S.6    Hu, G.X.7    Yu, Y.8    Liang, G.9    Ye, F.10
  • 61
    • 79960928546 scopus 로고    scopus 로고
    • Structure-activity relationship and docking studies of thiazolidinedione-type compounds with monoamine oxidase B
    • Carroll, R.T.; Dluzen, D.E.; Stinnett, H.; Awale, P.S.; Funk, M.O.; Geldenhuys, W.J., Structure-activity relationship and docking studies of thiazolidinedione-type compounds with monoamine oxidase B. Bioorg. Med. Chem. Lett., 2011, 21(16), 4798-4803.
    • (2011) Bioorg. Med. Chem. Lett , vol.21 , Issue.16 , pp. 4798-4803
    • Carroll, R.T.1    Dluzen, D.E.2    Stinnett, H.3    Awale, P.S.4    Funk, M.O.5    Geldenhuys, W.J.6
  • 62
    • 0032563927 scopus 로고    scopus 로고
    • Inhibition of Monoamine Oxidase-B by Condensed Pyridazines and Pyrimidines: Effects of Lipophilicity and Structure-Activity Relationships
    • Altomare, C.; Cellamare, S.; Summo, L.; Catto, M.; Carotti, A. Inhibition of Monoamine Oxidase-B by Condensed Pyridazines and Pyrimidines: Effects of Lipophilicity and Structure-Activity Relationships. J. Med. Chem., 1998, 41, 3812-3820.
    • (1998) J. Med. Chem , vol.41 , pp. 3812-3820
    • Altomare, C.1    Cellamare, S.2    Summo, L.3    Catto, M.4    Carotti, A.5
  • 64
    • 56249144473 scopus 로고    scopus 로고
    • Pyrazolinebased mycobactin analogues as MAO-inhibitors
    • Jayaprakash, V.; Sinha, B.N.; Ucar, G.; Ercan, A., Pyrazolinebased mycobactin analogues as MAO-inhibitors. Bioorg. Med. Chem. Lett., 2008, 18(24), 6362-6368.
    • (2008) Bioorg. Med. Chem. Lett , vol.18 , Issue.24 , pp. 6362-6368
    • Jayaprakash, V.1    Sinha, B.N.2    Ucar, G.3    Ercan, A.4
  • 65
    • 58549107997 scopus 로고    scopus 로고
    • New pyrazoline bearing 4(3H)-quinazolinone inhibitors of monoamine oxidase: Synthesis, biological evaluation, and structural deter minants of MAO-A and MAO-B selectivity
    • Gokhan-Kelekci, N.; Koyunoglu, S.; Yabanoglu, S.; Yelekci, K.; Ozgen, O.; Ucar, G.; Erol, K.; Kendi, E.; Yesilada, A. New pyrazoline bearing 4(3H)-quinazolinone inhibitors of monoamine oxidase: synthesis, biological evaluation, and structural deter minants of MAO-A and MAO-B selectivity. Bioorg. Med. Chem., 2009, 17, (2), 675-689.
    • (2009) Bioorg. Med. Chem , vol.17 , Issue.2 , pp. 675-689
    • Gokhan-Kelekci, N.1    Koyunoglu, S.2    Yabanoglu, S.3    Yelekci, K.4    Ozgen, O.5    Ucar, G.6    Erol, K.7    Kendi, E.8    Yesilada, A.9
  • 66
    • 34447280369 scopus 로고    scopus 로고
    • A new therapeutic approach in Alzheimer disease: Some novel pyrazole derivatives as dual MAO-B inhibitors and anti inflammatory analgesics
    • Gokhan-Kelekci, N.; Yabanoglu, S.; Kupeli, E.; Salgin, U.; Ozgen, O.; Ucar, G.; Yesilada, E.; Kendi, E.; Yesilada, A.; Bilgin, A.A., A new therapeutic approach in Alzheimer disease: some novel pyrazole derivatives as dual MAO-B inhibitors and anti inflammatory analgesics. Bioorg. Med. Chem., 2007, 15(17), 5775-5786.
    • (2007) Bioorg. Med. Chem , 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
  • 67
    • 79952484009 scopus 로고    scopus 로고
    • Development of selective and reversible pyrazoline based MAO-B inhibitors: Virtual screening, synthesis and biological evaluation
    • Mishra, N.; Sasmal, D., Development of selective and reversible pyrazoline based MAO-B inhibitors: Virtual screening, synthesis and biological evaluation. Bioorg. Med. Chem. Lett., 2011, 21(7), 1969-1973.
    • (2011) Bioorg. Med. Chem. Lett , vol.21 , Issue.7 , pp. 1969-1973
    • Mishra, N.1    Sasmal, D.2
  • 68
    • 72149094342 scopus 로고    scopus 로고
    • Towards development of selective and reversible pyrazoline based MAO-inhibitors: Synthesis, biological evaluation and docking studies
    • Sahoo, A.; Yabanoglu, S.; Sinha, B.N.; Ucar, G.; Basu, A.; Jayaprakash, V. Towards development of selective and reversible pyrazoline based MAO-inhibitors: Synthesis, biological evaluation and docking studies. Bioorg. Med. Chem. Lett., 2010, 20(1), 132-136.
    • (2010) Bioorg. Med. Chem. Lett , vol.20 , Issue.1 , pp. 132-136
    • Sahoo, A.1    Yabanoglu, S.2    Sinha, B.N.3    Ucar, G.4    Basu, A.5    Jayaprakash, V.6
  • 69
  • 74
    • 34250847887 scopus 로고    scopus 로고
    • Interaction of rat lung SSAO with the novel 1-Nsubstituted thiocarbamoyl-3-substituted phenyl-5-(2-pyrolyl)-2pyrazoline derivatives
    • Yabanoglu, S.; Ucar, G.; Gokhan, N.; Salgin, U.; Yesilada, A.; Bilgin, A. A. Interaction of rat lung SSAO with the novel 1-Nsubstituted thiocarbamoyl-3-substituted phenyl-5-(2-pyrolyl)-2pyrazoline derivatives. J. Neural. Transm., 2007, 114(6), 769-773.
    • (2007) J. Neural. Transm , vol.114 , Issue.6 , pp. 769-773
    • Yabanoglu, S.1    Ucar, G.2    Gokhan, N.3    Salgin, U.4    Yesilada, A.5    Bilgin, A.A.6
  • 76
    • 73549097080 scopus 로고    scopus 로고
    • Synthesis and inhibitory activity against human monoamine oxidase of N1thiocarbamoyl-3,5-di(hetero)aryl-4,5-dihydro-(1H)-pyrazole derivatives
    • Chimenti, F.; Carradori, S.; Secci, D.; Bolasco, A.; Bizzarri, B.; Chimenti, P.; Granese, A.; Yanez, M.; Orallo, F., Synthesis and inhibitory activity against human monoamine oxidase of N1thiocarbamoyl-3,5-di(hetero)aryl-4,5-dihydro-(1H)-pyrazole derivatives. Eur. J. Med. Chem., 2010, 45(2), 800-804.
    • (2010) Eur. J. Med. Chem , vol.45 , Issue.2 , pp. 800-804
    • Chimenti, F.1    Carradori, S.2    Secci, D.3    Bolasco, A.4    Bizzarri, B.5    Chimenti, P.6    Granese, A.7    Yanez, M.8    Orallo, F.9
  • 77
    • 77955418391 scopus 로고    scopus 로고
    • Investigations on the 2-thiazolylhydrazyne scaffold: Synthesis and molecular modeling of selective human monoamine oxidase inhibitors
    • Chimenti, F.; Bolasco, A.; Secci, D.; Chimenti, P.; Granese, A.; Carradori, S.; Yanez, M.; Orallo, F.; Ortuso, F.; Alcaro, S., Investigations on the 2-thiazolylhydrazyne scaffold: synthesis and molecular modeling of selective human monoamine oxidase inhibitors. Bioorg. Med. Chem., 2010, 18(15), 5715-5723.
    • (2010) Bioorg. Med. Chem , vol.18 , Issue.15 , pp. 5715-5723
    • Chimenti, F.1    Bolasco, A.2    Secci, D.3    Chimenti, P.4    Granese, A.5    Carradori, S.6    Yanez, M.7    Orallo, F.8    Ortuso, F.9    Alcaro, S.10
  • 79
    • 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
    • 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(15), 4135-4140.
    • (2006) Bioorg. Med. Chem. Lett , vol.16 , Issue.15 , 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
  • 83
    • 0015361603 scopus 로고
    • Inhibition of monoamine oxidase by substituted hydrazines
    • Tipton, K.F., Inhibition of monoamine oxidase by substituted hydrazines. Biochem. J., 1972, 128(4), 913-919.
    • (1972) Biochem. J , vol.128 , Issue.4 , pp. 913-919
    • Tipton, K.F.1
  • 84
    • 22544453906 scopus 로고    scopus 로고
    • Inhibition of monoamine oxidase-A activity in rat brain by synthetic hydrazines: Structure-activity relationship (SAR)
    • Dar, A.; Khan, K.M.; Ateeq, H.S.; Khan, S.; Rahat, S.; Perveen, S.; Supuran, C.T., Inhibition of monoamine oxidase-A activity in rat brain by synthetic hydrazines: structure-activity relationship (SAR). J. Enzyme Inhib. Med. Chem., 2005, 20(3), 269-274.
    • (2005) J. Enzyme Inhib. Med. Chem , vol.20 , Issue.3 , pp. 269-274
    • Dar, A.1    Khan, K.M.2    Ateeq, H.S.3    Khan, S.4    Rahat, S.5    Perveen, S.6    Supuran, C.T.7
  • 85
    • 43949123265 scopus 로고    scopus 로고
    • Structural and mechanistic studies of arylalkylhydrazine inhibition of human monoamine oxidases A and B
    • Binda, C.; Wang, J.; Li, M.; Hubalek, F.; Mattevi, A.; Edmondson, D.E. Structural and mechanistic studies of arylalkylhydrazine inhibition of human monoamine oxidases A and B. Biochemistry, 2008, 47(20), 5616-5625.
    • (2008) Biochemistry , vol.47 , Issue.20 , pp. 5616-5625
    • Binda, C.1    Wang, J.2    Li, M.3    Hubalek, F.4    Mattevi, A.5    Edmondson, D.E.6
  • 86
    • 77956325073 scopus 로고    scopus 로고
    • Synthesis and selective inhibition of human monoamine oxidases of a large scaffold of (4,5-substituted-thiazol-2-yl)hydrazones
    • Chimenti, F.; Secci, D.; Bolasco, A.; Chimenti, P.; Granese, A.; Carradori, S.; D'Ascenzio, M.; Yanez, M.; Orallo, F., Synthesis and selective inhibition of human monoamine oxidases of a large scaffold of (4,5-substituted-thiazol-2-yl)hydrazones. Med. Chem. Comm., 2010, 1(1), 61-72.
    • (2010) Med. Chem. Comm , vol.1 , Issue.1 , pp. 61-72
    • Chimenti, F.1    Secci, D.2    Bolasco, A.3    Chimenti, P.4    Granese, A.5    Carradori, S.6    D'Ascenzio, M.7    Yanez, M.8    Orallo, F.9
  • 88
    • 33746196499 scopus 로고    scopus 로고
    • Synthesis and evaluation of phenoxy acetic acid derivatives as anti-mycobacterial agents
    • Shaharyar, M.; Siddiqui, A.A.; Ali, M.A. Synthesis and evaluation of phenoxy acetic acid derivatives as anti-mycobacterial agents. Bioorg. Med. Chem. Lett., 2006, 16(17), 4571-4574.
    • (2006) Bioorg. Med. Chem. Lett , vol.16 , Issue.17 , pp. 4571-4574
    • Shaharyar, M.1    Siddiqui, A.A.2    Ali, M.A.3
  • 90
    • 0025974835 scopus 로고
    • Monoamine oxidase inhibitory potencies and selectivities of 2-[N(2-propynyl)-aminomethyl]-1-methyl indole derivatives
    • Balsa, D.; Fernandez-Alverez, E.; Tipton, K.F.; Unzeta, M., Monoamine oxidase inhibitory potencies and selectivities of 2-[N(2-propynyl)-aminomethyl]-1-methyl indole derivatives. Biochem. Soc. Trans., 1991, 19(1), 215-218.
    • (1991) Biochem. Soc. Trans , vol.19 , Issue.1 , pp. 215-218
    • Balsa, D.1    Fernandez-Alverez, E.2    Tipton, K.F.3    Unzeta, M.4
  • 91
    • 0027066886 scopus 로고
    • Acetylenic and allenic derivatives of 2-(5-methoxy-1-methylin dolyl) alkylamines: Synthesis and evaluation as selective inhibitors of the monoamine oxidases A and B
    • Fernández García, C.; Marco, J.L.; Fernández-Alvarez, E., Acetylenic and allenic derivatives of 2-(5-methoxy-1-methylin dolyl) alkylamines: Synthesis and evaluation as selective inhibitors of the monoamine oxidases A and B. Eur. J. Med. Chem., 1992, 27(9), 909-918.
    • (1992) Eur. J. Med. Chem , vol.27 , Issue.9 , pp. 909-918
    • Fernández García, C.1    Marco, J.L.2    Fernández-Alvarez, E.3
  • 92
    • 84961984929 scopus 로고    scopus 로고
    • Molecular determinants of MAO selectivity in a series of indolylmethylamine derivatives: Biological activities, 3D-QSAR/ CoMFA analysis, and computational simulation of ligand recognition
    • Moron, J.A.; Campillo, M.; Perez, V.; Unzeta, M.; Pardo, L. Molecular determinants of MAO selectivity in a series of indolylmethylamine derivatives: biological activities, 3D-QSAR/ CoMFA analysis, and computational simulation of ligand recognition. J. Med. Chem., 2000, 43(9), 1684-1691.
    • (2000) J. Med. Chem , vol.43 , Issue.9 , pp. 1684-1691
    • Moron, J.A.1    Campillo, M.2    Perez, V.3    Unzeta, M.4    Pardo, L.5
  • 93
    • 0033023543 scopus 로고    scopus 로고
    • Relevance of benzyloxy group in 2-indolyl methylamines in the selective MAO-B inhibition
    • Perez, V.; Marco, J.L.; Fernandez-Alvarez, E.; Unzeta, M., Relevance of benzyloxy group in 2-indolyl methylamines in the selective MAO-B inhibition. Br. J. Pharmacol., 1999, 127(4), 869-876.
    • (1999) Br. J. Pharmacol , vol.127 , Issue.4 , pp. 869-876
    • Perez, V.1    Marco, J.L.2    Fernandez-Alvarez, E.3    Unzeta, M.4
  • 94
    • 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(16), 15761-15766.
    • (2005) J. Biol. Chem , vol.280 , Issue.16 , 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
  • 95
    • 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(36), 12684-12689.
    • (2005) Proc. Natl. Acad. Sci. U S A , vol.102 , Issue.36 , pp. 12684-12689
    • de Colibus, L.1    Li, M.2    Binda, C.3    Lustig, A.4    Edmondson, D.E.5    Mattevi, A.6
  • 97
    • 79961170657 scopus 로고    scopus 로고
    • Inhibition of monoamine oxidase by C5-substituted phthalimide analogues
    • Manley-King, C.I.; Bergh, J.J.; Petzer, J.P. Inhibition of monoamine oxidase by C5-substituted phthalimide analogues. Bioorg. Med. Chem., 2011, 19(16), 4829-4840.
    • (2011) Bioorg. Med. Chem , vol.19 , Issue.16 , pp. 4829-4840
    • Manley-King, C.I.1    Bergh, J.J.2    Petzer, J.P.3
  • 98
    • 78650729131 scopus 로고    scopus 로고
    • Inhibition of monoamine oxidase by selected C5and C6-substituted isatin analogues
    • Manley-King, C.I.; Bergh, J.J.; Petzer, J.P., Inhibition of monoamine oxidase by selected C5and C6-substituted isatin analogues. Bioorg. Med. Chem., 2011, 19(1), 261-274.
    • (2011) Bioorg. Med. Chem , vol.19 , Issue.1 , pp. 261-274
    • Manley-King, C.I.1    Bergh, J.J.2    Petzer, J.P.3
  • 99
    • 84887410071 scopus 로고    scopus 로고
    • Inhibition of monoamine oxidase by selected C5and C6-substituted isatin analogues
    • Manley-King, C.I.; Bergh., J.J.; Petzer, J.P. Inhibition of monoamine oxidase by selected C5and C6-substituted isatin analogues. Russ. J. Org. Chem., 2006, 42, 261-274.
    • (2006) Russ. J. Org. Chem , vol.42 , pp. 261-274
    • Manley-King, C.I.1    Bergh, J.J.2    Petzer, J.P.3
  • 100


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.