-
1
-
-
72149101615
-
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
-
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
-
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
-
4
-
-
33749247103
-
Novel pharmacological targets for the treatment of Parkinson's disease
-
Schapira, A.H.V.; Bezard, E.; Brotchie, J.; Calon, F.; Collingridge, G.L.; Ferger, B.; Hengerer, B.; Hirsch, E.; Jenner, P.; Novere, N.L.; Obeso, J.A.; Schwarzschild, M.A.; Spampinato, U.; Davidai, G., Novel pharmacological targets for the treatment of Parkinson's disease. Nat. Rev. Drug Discov., 2006, 5, (10), 845-854.
-
(2006)
Nat. Rev. Drug Discov
, vol.5
, Issue.10
, pp. 845-854
-
-
Schapira, A.H.V.1
Bezard, E.2
Brotchie, J.3
Calon, F.4
Collingridge, G.L.5
Ferger, B.6
Hengerer, B.7
Hirsch, E.8
Jenner, P.9
Novere, N.L.10
Obeso, J.A.11
Schwarzschild, M.A.12
Spampinato, U.13
Davidai, G.14
-
5
-
-
5444270967
-
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
-
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
-
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
-
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
-
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
-
10
-
-
0036920279
-
Management of Parkinson's Disease: An Evidence-Based Review: Levodopa
-
Goetz, C.G.; Koller, W.C.; Poewe, W.; Rascol, O.; Sampaio, C.; Brin, M.F.; Lees, A.J.; LeWitt, P.; Lozano, A.; Mizuno, Y.; Nutt, J.; Oertel, W.; Olanow, C.W.; Tolosa, E. Management of Parkinson's Disease: An Evidence-Based Review: Levodopa. Movement Disord., 2002, 17(S4), S23-S37.
-
(2002)
Movement Disord
, vol.17
, Issue.S4
-
-
Goetz, C.G.1
Koller, W.C.2
Poewe, W.3
Rascol, O.4
Sampaio, C.5
Brin, M.F.6
Lees, A.J.7
Lewitt, P.8
Lozano, A.9
Mizuno, Y.10
Nutt, J.11
Oertel, W.12
Olanow, C.W.13
Tolosa, E.14
-
11
-
-
0015501193
-
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
-
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
-
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
-
14
-
-
17144465591
-
Management of Parkinson's Disease: An Evidence-Based Review: DA agonists Overview
-
Goetz, C.G.; Koller, W.C.; Poewe, W.; Rascol, O.; Sampaio, C.; Brin, M.F.; Lees, A.J.; LeWitt, P.; Lozano, A.; Mizuno, Y.; Nutt, J.; Oertel, W.; Olanow, C.W.; Tolosa, E. Management of Parkinson's Disease: An Evidence-Based Review: DA agonists Overview. Movement Disord., 2002, 17(S4), S52-S52.
-
(2002)
Movement Disord
, vol.17
, Issue.S4
-
-
Goetz, C.G.1
Koller, W.C.2
Poewe, W.3
Rascol, O.4
Sampaio, C.5
Brin, M.F.6
Lees, A.J.7
Lewitt, P.8
Lozano, A.9
Mizuno, Y.10
Nutt, J.11
Oertel, W.12
Olanow, C.W.13
Tolosa, E.14
-
15
-
-
58349085532
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
24
-
-
0020627065
-
Compa rison of pergolide and bromocriptine therapy in parkinsonism
-
LeWitt, P.A.; Ward, C.D.; Larsen, T.A.; Raphaelson, M.I.; Newman, R.P.; Foster, N.; Dambrosia, J.M.; Calne, D.B. Compa rison of pergolide and bromocriptine therapy in parkinsonism. Neurology, 1983, 33(8), 1009-1014.
-
(1983)
Neurology
, vol.33
, Issue.8
, pp. 1009-1014
-
-
Lewitt, P.A.1
Ward, C.D.2
Larsen, T.A.3
Raphaelson, M.I.4
Newman, R.P.5
Foster, N.6
Dambrosia, J.M.7
Calne, D.B.8
-
25
-
-
24144502098
-
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
-
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
-
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
-
-
-
28
-
-
0014684012
-
Amantadine in the Treatment of Parkinson's Disease
-
Robert S. Schwab, M.; Albert C. England Jr., M.; David C. Poskanzer, M.; Robert R. Young, M. Amantadine in the Treatment of Parkinson's Disease. JAMA, 1969, 208(7), 1168-1170.
-
(1969)
JAMA
, vol.208
, Issue.7
, pp. 1168-1170
-
-
Robert, S.1
Schwab, M.2
Albert, C.3
England, M.4
David, C.5
Poskanzer, M.6
Robert, R.7
Young, M.8
-
29
-
-
0027500750
-
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
-
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
-
31
-
-
0023639778
-
Amantadine and Motor Fluctuations in Chronic Parkinson's Disease
-
Shannon, K.M.; Goetz, C.G.; Carroll, V.S.; Tanner, C.M.; Klawans, H.L. Amantadine and Motor Fluctuations in Chronic Parkinson's Disease. Clin. Neuropharmacol., 1987, 10(6), 522-526.
-
(1987)
Clin. Neuropharmacol
, vol.10
, Issue.6
, pp. 522-526
-
-
Shannon, K.M.1
Goetz, C.G.2
Carroll, V.S.3
Tanner, C.M.4
Klawans, H.L.5
-
32
-
-
0036924325
-
Amantadine and other antiglutamate agents
-
Goetz, C.G.; Koller, W.C.; Poewe, W.; Rascol, O.; Sampaio, C.; Brin, M.F.; Lees, A.J.; LeWitt, P.; Lozano, A.; Mizuno, Y.; Nutt, J.; Oertel, W.; Olanow, C.W.; Tolosa, E., Amantadine and other antiglutamate agents. Movement Disord., 2002, 17, (Suppl 4), S13-S22.
-
(2002)
Movement Disord
, vol.17
, Issue.SUPPL. 4
-
-
Goetz, C.G.1
Koller, W.C.2
Poewe, W.3
Rascol, O.4
Sampaio, C.5
Brin, M.F.6
Lees, A.J.7
Lewitt, P.8
Lozano, A.9
Mizuno, Y.10
Nutt, J.11
Oertel, W.12
Olanow, C.W.13
Tolosa, E.14
-
33
-
-
7944236868
-
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
-
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
-
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
-
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
-
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
-
38
-
-
79960651250
-
Privileged Scaffold for the Development of Monoamine Oxidase Inhibitors
-
Gaspar, A.; Silva, T.; Yáñez, M.; Vina, D.; Orallo, F.; Ortuso, F.; Uriarte, E.; Alcaro, S.; Borges, F., Chromone, A. Privileged Scaffold for the Development of Monoamine Oxidase Inhibitors. J. Med. Chem., 2011, 54(14), 5165-5173.
-
(2011)
J. Med. Chem
, vol.54
, Issue.14
, pp. 5165-5173
-
-
Gaspar, A.1
Silva, T.2
Yáñez, M.3
Vina, D.4
Orallo, F.5
Ortuso, F.6
Uriarte, E.7
Alcaro, S.8
Borges, F.9
Chromone, A.10
-
39
-
-
0033991079
-
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
-
40
-
-
0036920181
-
Management of Parkinson's Disease: An Evidence-Based Review: MAO-B inhibitors for the treatment of Parkinson's disease
-
Goetz, C.G.; Koller, W.C.; Poewe, W.; Rascol, O.; Sampaio, C; Brin, M.F.; Lees, A.J.; LeWitt, P.; Lozano, A.; Mizuno, Y.; Nutt, J.; Oertel, W.; Olanow, C.W.; Tolosa, E., Management of Parkinson's Disease: An Evidence-Based Review: MAO-B inhibitors for the treatment of Parkinson's disease. Movement Disord., 2002, 17(S4), S38-S44.
-
(2002)
Movement Disord
, vol.17
, Issue.S4
-
-
Goetz, C.G.1
Koller, W.C.2
Poewe, W.3
Rascol, O.4
Sampaio, C.5
Brin, M.F.6
Lees, A.J.7
Lewitt, P.8
Lozano, A.9
Mizuno, Y.10
Nutt, J.11
Oertel, W.12
Olanow, C.W.13
Tolosa, E.14
-
41
-
-
33645307953
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
50
-
-
11144358502
-
Synthesis and selective inhibitory activity of 1-acetyl3,5-diphenyl-4,5-dihydro-(1H)-pyrazole derivatives against mono amine oxidase
-
Chimenti, F.; Bolasco, A.; Manna, F.; Secci, D.; Chimenti, P.; Befani, O.; Turini, P.; Giovannini, V.; Mondovì, B.; Cirilli, R.; La Torre, F., Synthesis and selective inhibitory activity of 1-acetyl3,5-diphenyl-4,5-dihydro-(1H)-pyrazole derivatives against mono amine oxidase. J. Med. Chem., 2004, 47(8), 2071-2074.
-
(2004)
J. Med. Chem
, vol.47
, Issue.8
, pp. 2071-2074
-
-
Chimenti, F.1
Bolasco, A.2
Manna, F.3
Secci, D.4
Chimenti, P.5
Befani, O.6
Turini, P.7
Giovannini, V.8
Mondovì, B.9
Cirilli, R.10
la Torre, F.11
-
51
-
-
71049173711
-
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
-
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
-
53
-
-
65749116833
-
A new series of 3-phenyl coumarins as potent and selective MAO-B inhibitors
-
Matos, M.J.; Viña, D.; Quezada, E.; Picciau, C; Delogu, G.; Orallo, F.; Santana, L.; Uriarte, E., A new series of 3-phenyl coumarins as potent and selective MAO-B inhibitors. Bioorg. Med. Chem. Lett, 2009, 19(12), 3268-3270.
-
(2009)
Bioorg. Med. Chem. Lett
, vol.19
, Issue.12
, pp. 3268-3270
-
-
Matos, M.J.1
Viña, D.2
Quezada, E.3
Picciau, C.4
Delogu, G.5
Orallo, F.6
Santana, L.7
Uriarte, E.8
-
54
-
-
69249111386
-
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
-
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
-
56
-
-
78651257725
-
Chromone 3-phenylcarboxamides as potent and selective MAO-B inhibitors
-
Gaspar, A.; Reis, J.; Fonseca, A.; Milhazes, N.; Viña, D.; Uriarte, E.; Borges, F., Chromone 3-phenylcarboxamides as potent and selective MAO-B inhibitors. Bioorg. Med. Chem. Lett., 2011, 21(2), 707-709.
-
(2011)
Bioorg. Med. Chem. Lett
, vol.21
, Issue.2
, pp. 707-709
-
-
Gaspar, A.1
Reis, J.2
Fonseca, A.3
Milhazes, N.4
Viña, D.5
Uriarte, E.6
Borges, F.7
-
57
-
-
77950954802
-
Chromone-2and -3-carboxylic acids inhibit differently monoamine oxidases A and B
-
Alcaro, S.; Gaspar, A.; Ortuso, F.; Milhazes, N.; Orallo, F.; Uriarte, E.; Yáñez, M.; Borges, F., Chromone-2and -3-carboxylic acids inhibit differently monoamine oxidases A and B. Bioorg. Med. Chem. Lett., 2010, 20(9), 2709-2712.
-
(2010)
Bioorg. Med. Chem. Lett
, vol.20
, Issue.9
, pp. 2709-2712
-
-
Alcaro, S.1
Gaspar, A.2
Ortuso, F.3
Milhazes, N.4
Orallo, F.5
Uriarte, E.6
Yáñez, M.7
Borges, F.8
-
58
-
-
84866449811
-
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
-
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
-
60
-
-
82255192216
-
Thioand aminocaffeine analogues as inhibitors of human monoamine oxidase
-
Booysen, H.P.; Moraal, C.; Terre'Blanche, G.; Petzer, A.; Bergh, J.J.; Petzer, J.P., Thioand aminocaffeine analogues as inhibitors of human monoamine oxidase. Bioorg. Med. Chem., 2011, 19(24), 7507-7518.
-
(2011)
Bioorg. Med. Chem
, vol.19
, Issue.24
, pp. 7507-7518
-
-
Booysen, H.P.1
Moraal, C.2
Terre'Blanche, G.3
Petzer, A.4
Bergh, J.J.5
Petzer, J.P.6
-
61
-
-
79960928546
-
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
-
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
-
63
-
-
0038513715
-
Binding models of reversible inhibitors to type-B monoamine oxidase
-
Carrieri, A.; Carotti, A.; Barreca, M.L.; Altomare, C., Binding models of reversible inhibitors to type-B monoamine oxidase. J. Computer-Aided Mol. Des., 2002, 16, 769-778.
-
(2002)
J. Computer-Aided Mol. Des
, vol.16
, pp. 769-778
-
-
Carrieri, A.1
Carotti, A.2
Barreca, M.L.3
Altomare, C.4
-
64
-
-
56249144473
-
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
-
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
-
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
-
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
-
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
-
-
77956184314
-
Synthesis of new 3-aryl-4,5-dihydropyrazole-1-carbothioamide derivatives. An investigation on their ability to inhibit monoamine oxidase
-
Maccioni, E.; Alcaro, S.; Orallo, F.; Cardia, M.C.; Distinto, S.; Costa, G.; Yanez, M.; Sanna, M.L.; Vigo, S.; Meleddu, R.; Secci, D., Synthesis of new 3-aryl-4,5-dihydropyrazole-1-carbothioamide derivatives. An investigation on their ability to inhibit monoamine oxidase. Eur. J. Med. Chem., 2010, 45(10), 4490-4498.
-
(2010)
Eur. J. Med. Chem
, vol.45
, Issue.10
, pp. 4490-4498
-
-
Maccioni, E.1
Alcaro, S.2
Orallo, F.3
Cardia, M.C.4
Distinto, S.5
Costa, G.6
Yanez, M.7
Sanna, M.L.8
Vigo, S.9
Meleddu, R.10
Secci, D.11
-
70
-
-
77958059098
-
Synthesis and molecular modelling studies of prenylated pyrazolines as MAO-B inhibitors
-
Fioravanti, R.; Bolasco, A.; Manna, F.; Rossi, F.; Orallo, F.; Yanez, M.; Vitali, A.; Ortuso, F.; Alcaro, S., Synthesis and molecular modelling studies of prenylated pyrazolines as MAO-B inhibitors. Bioorg. Med. Chem. Lett., 2010, 20(22), 6479-6482.
-
(2010)
Bioorg. Med. Chem. Lett
, vol.20
, Issue.22
, pp. 6479-6482
-
-
Fioravanti, R.1
Bolasco, A.2
Manna, F.3
Rossi, F.4
Orallo, F.5
Yanez, M.6
Vitali, A.7
Ortuso, F.8
Alcaro, S.9
-
71
-
-
79959891957
-
Pyrazoline based MAO inhibitors: Synthesis, biological evaluation and SAR studies
-
Jagrat, M.; Behera, J.; Yabanoglu, S.; Ercan, A.; Ucar, G.; Sinha, B.N.; Sankaran, V.; Basu, A.; Jayaprakash, V., Pyrazoline based MAO inhibitors: Synthesis, biological evaluation and SAR studies. Bioorg. Med. Chem. Lett., 2011, 21(14), 4296-4300.
-
(2011)
Bioorg. Med. Chem. Lett
, vol.21
, Issue.14
, pp. 4296-4300
-
-
Jagrat, M.1
Behera, J.2
Yabanoglu, S.3
Ercan, A.4
Ucar, G.5
Sinha, B.N.6
Sankaran, V.7
Basu, A.8
Jayaprakash, V.9
-
72
-
-
28544443174
-
Synthesis, molecular modeling studies, and selective inhibitory activity against monoamine oxidase of 1-thiocarbamoyl-3,5-diaryl-4,5-dihydro (1H)pyrazole derivatives
-
Chimenti, F.; Maccioni, E.; Secci, D.; Bolasco, A.; Chimenti, P.; Granese, A.; Befani, O.; Turini, P.; Alcaro, S.; Ortuso, F.; Cirilli, R.; La Torre, F.; Cardia, M.C.; Distinto, S. Synthesis, molecular modeling studies, and selective inhibitory activity against monoamine oxidase of 1-thiocarbamoyl-3,5-diaryl-4,5-dihydro (1H)pyrazole derivatives. J. Med. Chem., 2005, 48(23), 7113-7122.
-
(2005)
J. Med. Chem
, vol.48
, Issue.23
, pp. 7113-7122
-
-
Chimenti, F.1
Maccioni, E.2
Secci, D.3
Bolasco, A.4
Chimenti, P.5
Granese, A.6
Befani, O.7
Turini, P.8
Alcaro, S.9
Ortuso, F.10
Cirilli, R.11
la Torre, F.12
Cardia, M.C.13
Distinto, S.14
-
73
-
-
33847420851
-
Selective inhibitory activity against MAO and molecular modeling studies of 2-thiazolylhydrazone derivatives
-
Chimenti, F.; Maccioni, E.; Secci, D.; Bolasco, A.; Chimenti, P.; Granese, A.; Befani, O.; Turini, P.; Alcaro, S.; Ortuso, F.; Cardia, M.C.; Distinto, S., Selective inhibitory activity against MAO and molecular modeling studies of 2-thiazolylhydrazone derivatives. J. Med. Chem., 2007, 50(4), 707-712.
-
(2007)
J. Med. Chem
, vol.50
, Issue.4
, pp. 707-712
-
-
Chimenti, F.1
Maccioni, E.2
Secci, D.3
Bolasco, A.4
Chimenti, P.5
Granese, A.6
Befani, O.7
Turini, P.8
Alcaro, S.9
Ortuso, F.10
Cardia, M.C.11
Distinto, S.12
-
74
-
-
34250847887
-
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
-
75
-
-
33646507688
-
Synthesis, biological evaluation and 3DQSAR of 1,3,5-trisubstituted-4,5-dihydro-(1H)-pyrazole deriva tives as potent and highly selective monoamine oxidase A inhibitors
-
Chimenti, F.; Bolasco, A.; Manna, F.; Secci, D.; Chimenti, P.; Granese, A.; Befani, O.; Turini, P.; Cirilli, R.; La Torre, F.; Alcaro, S.; Ortuso, F.; Langer, T., Synthesis, biological evaluation and 3DQSAR of 1,3,5-trisubstituted-4,5-dihydro-(1H)-pyrazole deriva tives as potent and highly selective monoamine oxidase A inhibitors. Curr. Med. Chem., 2006, 13(12), 1411-1428.
-
(2006)
Curr. Med. Chem
, vol.13
, Issue.12
, pp. 1411-1428
-
-
Chimenti, F.1
Bolasco, A.2
Manna, F.3
Secci, D.4
Chimenti, P.5
Granese, A.6
Befani, O.7
Turini, P.8
Cirilli, R.9
la Torre, F.10
Alcaro, S.11
Ortuso, F.12
Langer, T.13
-
76
-
-
73549097080
-
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
-
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
-
78
-
-
2942527408
-
Inhibition of monoamine oxidases by coumarin-3-acyl derivatives: Biological activity and computational study
-
Chimenti, F.; Secci, D.; Bolasco, A.; Chimenti, P.; Granese, A.; Befani, O.; Turini, P.; Alcaro, S.; Ortuso, F., Inhibition of monoamine oxidases by coumarin-3-acyl derivatives: biological activity and computational study. Bioorg. Med. Chem. Lett., 2004, 14(14), 3697-3703.
-
(2004)
Bioorg. Med. Chem. Lett
, vol.14
, Issue.14
, pp. 3697-3703
-
-
Chimenti, F.1
Secci, D.2
Bolasco, A.3
Chimenti, P.4
Granese, A.5
Befani, O.6
Turini, P.7
Alcaro, S.8
Ortuso, F.9
-
79
-
-
33745126693
-
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
-
80
-
-
64549137053
-
Synthesis, molecular modeling, and selective inhibitory activity against human monoamine oxidases of 3-carboxamido-7substituted coumarins
-
Chimenti, F.; Secci, D.; Bolasco, A.; Chimenti, P.; Bizzarri, B.; Granese, A.; Carradori, S.; Yanez, M.; Orallo, F.; Ortuso, F.; Alcaro, S., Synthesis, molecular modeling, and selective inhibitory activity against human monoamine oxidases of 3-carboxamido-7substituted coumarins. J. Med. Chem., 2009, 52(7), 1935-1942.
-
(2009)
J. Med. Chem
, vol.52
, Issue.7
, pp. 1935-1942
-
-
Chimenti, F.1
Secci, D.2
Bolasco, A.3
Chimenti, P.4
Bizzarri, B.5
Granese, A.6
Carradori, S.7
Yanez, M.8
Orallo, F.9
Ortuso, F.10
Alcaro, S.11
-
81
-
-
50249143998
-
Synthesis, stereochemical identification, and selective inhibitory activity against human monoamine oxidase-B of 2-methylcyclohexylidene(4-arylthiazol-2-yl)hydrazones
-
Chimenti, F.; Maccioni, E.; Secci, D.; Bolasco, A.; Chimenti, P.; Granese, A.; Carradori, S.; Alcaro, S.; Ortuso, F.; Yanez, M.; Orallo, F.; Cirilli, R.; Ferretti, R.; La Torre, F., Synthesis, stereochemical identification, and selective inhibitory activity against human monoamine oxidase-B of 2-methylcyclohexylidene(4-arylthiazol-2-yl)hydrazones. J. Med. Chem., 2008, 51(16), 4874-4880.
-
(2008)
J. Med. Chem
, vol.51
, Issue.16
, pp. 4874-4880
-
-
Chimenti, F.1
Maccioni, E.2
Secci, D.3
Bolasco, A.4
Chimenti, P.5
Granese, A.6
Carradori, S.7
Alcaro, S.8
Ortuso, F.9
Yanez, M.10
Orallo, F.11
Cirilli, R.12
Ferretti, R.13
la Torre, F.14
-
82
-
-
77955325332
-
Synthesis, semipreparative HPLC separation, biological evaluation, and 3D-QSAR of hydrazothiazole derivatives as human monoamine oxidase B inhibitors
-
Chimenti, F.; Secci, D.; Bolasco, A.; Chimenti, P.; Granese, A.; Carradori, S.; Maccioni, E.; Cardia, M.C.; Yanez, M.; Orallo, F.; Alcaro, S.; Ortuso, F.; Cirilli, R.; Ferretti, R.; Distinto, S.; Kirchmair, J.; Langer, T., Synthesis, semipreparative HPLC separation, biological evaluation, and 3D-QSAR of hydrazothiazole derivatives as human monoamine oxidase B inhibitors. Bioorg. Med. Chem., 2010, 18(14), 5063-5070.
-
(2010)
Bioorg. Med. Chem
, vol.18
, Issue.14
, pp. 5063-5070
-
-
Chimenti, F.1
Secci, D.2
Bolasco, A.3
Chimenti, P.4
Granese, A.5
Carradori, S.6
Maccioni, E.7
Cardia, M.C.8
Yanez, M.9
Orallo, F.10
Alcaro, S.11
Ortuso, F.12
Cirilli, R.13
Ferretti, R.14
Distinto, S.15
Kirchmair, J.16
Langer, T.17
-
83
-
-
0015361603
-
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
-
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
-
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
-
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
-
87
-
-
66349115617
-
Synthesis and Biological Evaluation of Novel Conjugated Coumarin-Thiazole Systems
-
Chimenti, F.; Carradori, S.; Secci, D.; Bolasco, A.; Chimenti, P.; Granese, A.; Bizzarri, B. Synthesis and Biological Evaluation of Novel Conjugated Coumarin-Thiazole Systems. J. Heterocyclic. Chem., 2009, 46(3), 575-578.
-
(2009)
J. Heterocyclic. Chem
, vol.46
, Issue.3
, pp. 575-578
-
-
Chimenti, F.1
Carradori, S.2
Secci, D.3
Bolasco, A.4
Chimenti, P.5
Granese, A.6
Bizzarri, B.7
-
88
-
-
33746196499
-
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
-
89
-
-
0025654482
-
Inhibition of MAO by substituted tryptamine analogues
-
Balsa, D.; Fernandez-Alvarez, E.; Tipton, K.F.; Unzeta, M. Inhibition of MAO by substituted tryptamine analogues. J. Neural. Transm. Suppl., 1990, 32, 103-105.
-
(1990)
J. Neural. Transm. Suppl
, vol.32
, pp. 103-105
-
-
Balsa, D.1
Fernandez-Alvarez, E.2
Tipton, K.F.3
Unzeta, M.4
-
90
-
-
0025974835
-
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
-
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
-
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
-
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
-
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
-
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
-
96
-
-
64249159149
-
Inhibition of monoamine oxidase by (E)-styrylisatin analogues
-
Van der Walt, E.M.; Milczek, E.M.; Malan, S.F.; Edmondson, D.E.; Castagnoli Jr, N.; Bergh, J.J.; Petzer, J.P. Inhibition of monoamine oxidase by (E)-styrylisatin analogues. Bioorg. Med. Chem. Lett., 2009, 19(9), 2509-2513.
-
(2009)
Bioorg. Med. Chem. Lett
, vol.19
, Issue.9
, pp. 2509-2513
-
-
van der Walt, E.M.1
Milczek, E.M.2
Malan, S.F.3
Edmondson, D.E.4
Castagnoli, N.5
Bergh, J.J.6
Petzer, J.P.7
-
97
-
-
79961170657
-
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
-
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
-
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
-
-
75149186558
-
Inhibition of monoamine oxidase by 8-benzyloxycaffeine analogues
-
Strydom, B.; Malan, S.F.; Castagnoli Jr, N.; Bergh, J.J.; Petzer, J.P. Inhibition of monoamine oxidase by 8-benzyloxycaffeine analogues. Bioorg. Med. Chem., 2010, 18(3), 1018-1028.
-
(2010)
Bioorg. Med. Chem
, vol.18
, Issue.3
, pp. 1018-1028
-
-
Strydom, B.1
Malan, S.F.2
Castagnoli, N.3
Bergh, J.J.4
Petzer, J.P.5
-
101
-
-
33750124443
-
Impact of speciesdependent differences on screening, design, and development of MAO B inhibitors
-
Novaroli, L.; Daina, A.; Favre, E.; Bravo, J.; Carotti, A.; Leonetti, F.; Catto, M.; Carrupt, P. A.; Reist, M., Impact of speciesdependent differences on screening, design, and development of MAO B inhibitors. J. Med. Chem., 2006, 49, 6264-6272.
-
(2006)
J. Med. Chem
, vol.49
, pp. 6264-6272
-
-
Novaroli, L.1
Daina, A.2
Favre, E.3
Bravo, J.4
Carotti, A.5
Leonetti, F.6
Catto, M.7
Carrupt, P.A.8
Reist, M.9
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