-
1
-
-
41549108420
-
From single- to multi-target drugs in cancer therapy: When aspecificity becomes an advantage
-
DOI 10.2174/092986708783503212
-
Petrelli, A.; Giordano, S. From single- to multi-target drugs in cancertherapy: when aspecificity becomes an advantage. Curr. Med. Chem., 2008, 15, 422-432. (Pubitemid 351472408)
-
(2008)
Current Medicinal Chemistry
, vol.15
, Issue.5
, pp. 422-432
-
-
Petrelli, A.1
Giordano, S.2
-
2
-
-
34548065794
-
How todesign multi-target drugs: Target search options in cellular networks
-
Korcsmáros, T.; Szalay, M.S.; Böde, C.; Kovács, I. A.; Csermely, P. How todesign multi-target drugs: Target search options in cellular networks. ExpertOpin. Drug Disc., 2007, 2, 1-10.
-
(2007)
ExpertOpin. Drug Disc.
, vol.2
, pp. 1-10
-
-
Korcsmáros, T.1
Szalay, M.S.2
Böde, C.3
Kovács, I.A.4
Csermely, P.5
-
3
-
-
3242794178
-
From magic bullets to designed multipleligands
-
Morphy, R.; Kay, C.; Rankovic, Z. From magic bullets to designed multipleligands. Drug Discov. Today, 2004, 9, 641-651.
-
(2004)
Drug Discov. Today
, vol.9
, pp. 641-651
-
-
Morphy, R.1
Kay, C.2
Rankovic, Z.3
-
4
-
-
39149091398
-
Multi-target-directed ligands to combatneurodegenerative diseases
-
Cavalli, A.; Bolognesi, M.L.; Minarini, A.; Rosini, M.; Tumiatti, V.;Recanatini, M.; Melchiorre, C. Multi-target-directed ligands to combatneurodegenerative diseases. J. Med. Chem., 2008, 51, 347-372.
-
(2008)
J. Med. Chem.
, vol.51
, pp. 347-372
-
-
Cavalli, A.1
Bolognesi, M.L.2
Minarini, A.3
Rosini, M.4
Tumiatti, V.5
Recanatini, M.6
Melchiorre, C.7
-
5
-
-
79953695916
-
In silicorepositioning of approved drugs for rare and neglected diseases
-
(a) Ekins, S.; Williams, A.J.; Krasowski, M.D.; Freundlich, J.S. In silicorepositioning of approved drugs for rare and neglected diseases. DrugDiscov. Today, 2011, 16, 298-310
-
(2011)
DrugDiscov. Today
, vol.16
, pp. 298-310
-
-
Ekins, S.1
Williams, A.J.2
Krasowski, M.D.3
Freundlich, J.S.4
-
6
-
-
4344668661
-
Drug repositioning: Identifying and developing new uses for existing drugs
-
(b)Ashburn, T.T.; Thor, K.B. Drugrepositioning: identifying and developing new uses for existing drugs. Nat.Rev. Drug Discov., 2004, 3, 673-683. (Pubitemid 39173508)
-
(2004)
Nature Reviews Drug Discovery
, vol.3
, Issue.8
, pp. 673-683
-
-
Ashburn, T.T.1
Thor, K.B.2
-
7
-
-
27144449695
-
Designed multiple ligands. An emerging drug discovery paradigm
-
DOI 10.1021/jm058225d
-
Morphy, R.; Rankovic, Z. Designed multiple ligands. An emerging drugdiscovery paradigm. J. Med. Chem., 2005, 48, 6523-6543. (Pubitemid 41504710)
-
(2005)
Journal of Medicinal Chemistry
, vol.48
, Issue.21
, pp. 6523-6543
-
-
Morphy, R.1
Rankovic, Z.2
-
8
-
-
34547484265
-
Molecular hybridization: A useful tool in the design of new drug prototypes
-
DOI 10.2174/092986707781058805
-
Viegas-Junior, C.; Danuello, A.; da Silva Bolzani, V.; Barreiro, E.J.; Fraga, C.A.M. Molecular hybridization: a useful tool in the design of new drugprototypes. Curr. Med. Chem., 2007, 14, 1829-1852. (Pubitemid 47163402)
-
(2007)
Current Medicinal Chemistry
, vol.14
, Issue.17
, pp. 1829-1852
-
-
Viegas-Junior, C.1
Danuello, A.2
Da Silva Bolzani, V.3
Barreiro, E.J.4
Fraga, C.A.M.5
-
9
-
-
34548619267
-
Amine oxidases and monooxygenases in the in vivo metabolism of xenobiotic amines in humans: Has the involvement of amine oxidases been neglected?
-
DOI 10.1111/j.1472-8206.2007.00498.x
-
Strolin-Benedetti, M.; Tipton, K.F.; Whomsley, R. Amine oxidases andmonooxygenases in the in vivo metabolism of xenobiotic amines in humans:has the involvement of amine oxidases been neglected? Fundam. Clin. Pharmacol., 2007, 21, 467-479. (Pubitemid 47404324)
-
(2007)
Fundamental and Clinical Pharmacology
, vol.21
, Issue.5
, pp. 467-479
-
-
Strolin Benedetti, M.1
Tipton, K.F.2
Whomsley, R.3
-
10
-
-
3242781888
-
Structure andmechanism of monoamine oxidases
-
Edmondson, D.E.; Mattevi, A.; Binda, C.; Li, M.; Hubalek, F. Structure andmechanism of monoamine oxidases. Curr. Med. Chem., 2004, 11, 1983-1993.
-
(2004)
Curr. Med. Chem.
, vol.11
, pp. 1983-1993
-
-
Edmondson, D.E.1
Mattevi, A.2
Binda, C.3
Li, M.4
Hubalek, F.5
-
11
-
-
0034642217
-
Structure-activity relations in theoxidation of phenethylamine analogues by recombinant human livermonoamine oxidase A
-
Nandigama, R.K.; Edmondson, D.E. Structure-activity relations in theoxidation of phenethylamine analogues by recombinant human livermonoamine oxidase A. Biochemistry, 2000, 39, 15258-15265.
-
(2000)
Biochemistry
, vol.39
, pp. 15258-15265
-
-
Nandigama, R.K.1
Edmondson, D.E.2
-
12
-
-
0024995831
-
Tissue distribution ofhuman monoamine oxidase-A and oxidase-B messenger-RNA
-
Grimsby, J.; lan, N.C.; Neve, R.; Chen, K.; Shih, J.C. Tissue distribution ofhuman monoamine oxidase-A and oxidase-B messenger-RNA. J.Neurochem., 1990, 55, 1166-1169.
-
(1990)
J.Neurochem.
, vol.55
, pp. 1166-1169
-
-
Grimsby, J.1
Lan, N.C.2
Neve, R.3
Chen, K.4
Shih, J.C.5
-
13
-
-
0021250642
-
Selective inhibitors of monoamine oxidase A and B: Biochemical, pharmacological, and clinical properties
-
Fowler, C.J.; Ross, S.B. Selective inhibitors of monoamine oxidase A and B:biochemical, pharmacological, and clinical properties. Med. Res. Rev., 1984, 4, 323-358. (Pubitemid 14073188)
-
(1984)
Medicinal Research Reviews
, vol.4
, Issue.3
, pp. 323-358
-
-
Fowler, C.J.1
Ross, S.B.2
-
14
-
-
0017088112
-
Studies on monoamine oxidase. XVIII. Enzymatic properties ofplacental monoamine oxidase
-
Egashira, T. Studies on monoamine oxidase. XVIII. Enzymatic properties ofplacental monoamine oxidase. Jap. J. Pharmac., 1976, 26, 493-500.
-
(1976)
Jap. J. Pharmac.
, vol.26
, pp. 493-500
-
-
Egashira, T.1
-
15
-
-
0017329403
-
Substrate-and inhibitor-related characteristicsof human platelet monoamine oxidase
-
Donnelly, C.H.; Murphy, D.L. Substrate- and inhibitor-related characteristicsof human platelet monoamine oxidase. Biochem. Pharmacol., 1977, 26, 852-858.
-
(1977)
Biochem. Pharmacol.
, vol.26
, pp. 852-858
-
-
Donnelly, C.H.1
Murphy, D.L.2
-
16
-
-
0026550390
-
Quantitative enzymeradioautography with 3H-Ro 41-1049 and 3HRo 19-6327 in vitro:localization and abundance of MAO-A and MAO-B in rat CNS, peripheralorgans, and human brain
-
Saura, J.; Kettler, R.; Da Prada, M.; Richards, J.G. Quantitative enzymeradioautography with 3H-Ro 41-1049 and 3HRo 19-6327 in vitro:localization and abundance of MAO-A and MAO-B in rat CNS, peripheralorgans, and human brain. J. Neurosci., 1992, 12, 1977-1999.
-
(1992)
J. Neurosci.
, vol.12
, pp. 1977-1999
-
-
Saura, J.1
Kettler, R.2
Da Prada, M.3
Richards, J.G.4
-
17
-
-
33645307953
-
The therapeutic potentialof monoamine oxidase inhibitors
-
(a) Youdim, M.B.; Edmondson, D.E.; Tipton, K.F. The therapeutic potentialof monoamine oxidase inhibitors. Nat. Rev. Neurosci., 2006, 7, 295-309
-
(2006)
Nat. Rev. Neurosci.
, vol.7
, pp. 295-309
-
-
Youdim, M.B.1
Edmondson, D.E.2
Tipton, K.F.3
-
18
-
-
0346154805
-
Clinical pharmacology of MAO inhibitors: Safetyand future
-
(b)Yamada, M.; Yasuhara, H. Clinical pharmacology of MAO inhibitors: safetyand future. Neurotoxicology, 2004, 25, 215-221.
-
Neurotoxicology
, vol.2004
, Issue.25
, pp. 215-221
-
-
Yamada, M.1
Yasuhara, H.2
-
19
-
-
0020672172
-
Selective MAO A and B inhibitors: Their mechanism of action and pharmacology
-
DOI 10.1016/0028-3908(83)90194-6
-
Finberg, J.P.M.; Youdim, M.B.H. Selective MAO-A and MAO-B inhibitors:their mechanism of action and pharmacology. Neuropharmacology, 1983, 22, 441-446. (Pubitemid 13152056)
-
(1983)
Neuropharmacology
, vol.22
, Issue.3 B
, pp. 441-446
-
-
Finberg, J.P.M.1
Youdim, M.B.H.2
-
20
-
-
36849055017
-
Monoamine oxidase-B inhibition in thetreatment of Parkinson's disease
-
Fernandez, H.H.; Chen, J.J. Monoamine oxidase-B inhibition in thetreatment of Parkinson's disease. Pharmacotherapy, 2007, 27, S174-S185.
-
(2007)
Pharmacotherapy
, vol.27
-
-
Fernandez, H.H.1
Chen, J.J.2
-
21
-
-
78650364351
-
MAO inhibitors: Risks, benefits, and lore
-
Wimbiscus, M.; Kostenko, O.; Malone, D. MAO inhibitors: risks, benefits, and lore. Cleve. Clin. J. Med., 2010, 77, 859-882.
-
(2010)
Cleve. Clin. J. Med.
, vol.77
, pp. 859-882
-
-
Wimbiscus, M.1
Kostenko, O.2
Malone, D.3
-
22
-
-
77953383270
-
Early pharmacologic treatment in Parkinson's disease
-
Hauser, R.A. Early pharmacologic treatment in Parkinson's disease. Am. J.Manag. Care, 2010, 16, S100-S107.
-
(2010)
Am. J.Manag. Care
, vol.16
-
-
Hauser, R.A.1
-
23
-
-
59349103130
-
Genotoxic stress in plants:shedding light on DNA damage, repair and DNA repair helicases
-
Tuteja, N.; Ahmad, P.; Panda, B.B.; Tuteja, R. Genotoxic stress in plants:shedding light on DNA damage, repair and DNA repair helicases. Mut. Res-Rev. Mutat., 2009, 681, 134-149.
-
(2009)
Mut. Res-Rev. Mutat.
, vol.681
, pp. 134-149
-
-
Tuteja, N.1
Ahmad, P.2
Panda, B.B.3
Tuteja, R.4
-
24
-
-
78449282609
-
Metals oxidativestress and neurodegenerative disorders
-
Jomova, K.; Vondrakova, D.; Lawson, M.; Valko, M. Metals, oxidativestress and neurodegenerative disorders. Mol. Cell. Biochem., 2010, 345, 91-104.
-
(2010)
Mol. Cell. Biochem.
, vol.345
, pp. 91-104
-
-
Jomova, K.1
Vondrakova, D.2
Lawson, M.3
Valko, M.4
-
25
-
-
29044438902
-
The crucial role of metal ions in neurodegeneration: The basis for a promising therapeutic strategy
-
DOI 10.1038/sj.bjp.0706416
-
Gaeta, A.; Hider, R.C. The crucial role of metal ions in neurodegeneration:the basis for a promising therapeutic strategy. Br. J. Pharmacol., 2005, 146, 1041-1059. (Pubitemid 41786957)
-
(2005)
British Journal of Pharmacology
, vol.146
, Issue.8
, pp. 1041-1059
-
-
Gaeta, A.1
Hider, R.C.2
-
26
-
-
0037264120
-
Unfolding the role of protein misfolding in neurodegenerative diseases
-
DOI 10.1038/nrn1007
-
Soto, C. Unfolding the role of protein misfolding in neurodegenerativediseases. Nat. Rev. Neurosci., 2003, 4, 49-60. (Pubitemid 37271088)
-
(2003)
Nature Reviews Neuroscience
, vol.4
, Issue.1
, pp. 49-60
-
-
Soto, C.1
-
27
-
-
33750347347
-
Mitochondrial dysfunction and oxidative stress in neurodegenerative diseases
-
DOI 10.1038/nature05292, PII NATURE05292
-
Lin, M.T.; Beal, M.F. Mitochondrial dysfunction and oxidative stress inneurodegenerative diseases. Nature, 2006, 443, 787-795. (Pubitemid 44622683)
-
(2006)
Nature
, vol.443
, Issue.7113
, pp. 787-795
-
-
Lin, M.T.1
Beal, M.F.2
-
28
-
-
0031596711
-
(R)(+)-N-propargyl-1-aminoindan (rasagiline) andderivatives: Highly selective and potent inhibitors of monoamine oxidase B
-
Sterling, J.; Veinberg, A.; Lerner, D.; Goldenberg, W.; Levy, R.; Youdim, M.; Finberg, J. (R)(+)-N-propargyl-1-aminoindan (rasagiline) andderivatives: Highly selective and potent inhibitors of monoamine oxidase B.J. Neural Transm.-Supp., 1998, 52, 301-305.
-
(1998)
J. Neural Transm.-Supp.
, vol.52
, pp. 301-305
-
-
Sterling, J.1
Veinberg, A.2
Lerner, D.3
Goldenberg, W.4
Levy, R.5
Youdim, M.6
Finberg, J.7
-
29
-
-
0030300167
-
Pharmacology and neuroprotective properties of rasagiline
-
(a) Finberg, J.P.; Lamensdorf, I.; Commissiong, J.W.; Youdim, M.B.H.Pharmacology and neuroprotective properties of rasagiline. J. NeuralTransm.-Supp., 1996, 48, 95-101 (Pubitemid 26423350)
-
(1996)
Journal of Neural Transmission, Supplement
, Issue.48
, pp. 95-101
-
-
Finberg, J.P.M.1
Lamensdorf, I.2
Commissiong, J.W.3
Youdim, M.B.H.4
-
30
-
-
0032609072
-
Pharmacology of rasagiline(N-propargyl-1R-aminoindan
-
(b) Finberg, J.P.; Lamensdorf, I.;Weinstock, M.; Schwartz, M.; Youdim, M.B.H. Pharmacology of rasagiline(N-propargyl-1R-aminoindan). Adv. Neurol., 1999, 80, 495-499
-
(1999)
Adv. Neurol.
, vol.80
, pp. 495-499
-
-
Finberg, J.P.1
Lamensdorf, I.2
Weinstock, M.3
Schwartz, M.4
Youdim, M.B.H.5
-
31
-
-
30444437749
-
Monoamine oxidase: Isoforms and inhibitors in Parkinson's disease and depressive illness
-
DOI 10.1038/sj.bjp.0706464, PII 0706464
-
(c) Youdim, M.B.H.; Bakhle, Y.S. Monoamine oxidase: isoforms and inhibitors inParkinson's disease and depressive illness. Br. J. Pharmacol., 2006, 147, S287-S296 (Pubitemid 43077287)
-
(2006)
British Journal of Pharmacology
, vol.147
, Issue.SUPPL. 1
-
-
Youdim, M.B.H.1
Bakhle, Y.S.2
-
32
-
-
33645307953
-
Thetherapeutic potential of monoamine oxidase inhibitors
-
(d) Youdim, M.B.H.; Edmondson, D.; Tipton, K.F. Thetherapeutic potential of monoamine oxidase inhibitors. Nat. Rev. Neurosci., 2006, 7, 295-309.
-
(2006)
Nat. Rev. Neurosci.
, vol.7
, pp. 295-309
-
-
Youdim, M.B.H.1
Edmondson, D.2
Tipton, K.F.3
-
33
-
-
0018068203
-
Amphetamine and 2-phenylethylamine in post-mortem parkinsonian brain after (-)deprenyl administration
-
Reynolds, G.P.; Riederer, P.; Sandler, M.; Jellinger, K.; Seemann, D.Amphetamine and 2-phenylethylamine in post-mortem Parkinsonian brainafter (L)-deprenyl administration. J. Neural Transm., 1978, 43, 271-277. (Pubitemid 9050088)
-
(1978)
Journal of Neural Transmission - General Section
, vol.43
, Issue.3-4
, pp. 271-277
-
-
Reynolds, G.P.1
Riederer, P.2
Sandler, M.3
-
34
-
-
0019462668
-
Tyramine antagonistic properties of AGN 1135, an irreversible inhibitor of monoamine oxidase type B
-
(a) Finberg, J.P.; Tenne, M.; Youdim, M.B.H. Tyramine antagonisticproperties of AGN 1135, an irreversible inhibitor of monoamine oxidase typeB. Br. J. Pharmacol., 1981, 73, 65-74 (Pubitemid 11104761)
-
(1981)
British Journal of Pharmacology
, vol.73
, Issue.1
, pp. 65-74
-
-
Finberg, J.P.M.1
Tenne, M.2
Youdim, M.B.H.3
-
35
-
-
0018139965
-
Evidence that deprenyl, a type B monoamine oxidase inhibitor, is an indirectly acting sympathomimetic amine
-
DOI 10.1016/0006-2952(78)90490-2
-
(b) Simpson, L.L. Evidence thatdeprenyl, a type B monoamine oxidase inhibitor, is an indirectly actingsympathomimetic amine. Biochem. Pharmacol., 1978, 27, 1591-1595. (Pubitemid 8406839)
-
(1978)
Biochemical Pharmacology
, vol.27
, Issue.11
, pp. 1591-1595
-
-
Simpson, L.L.1
-
36
-
-
0036206323
-
The anti-parkinson drug, rasagiline, prevents apoptotic DNA damage induced by peroxynitrite in human dopaminergic neuroblastoma SH-SY5Y cells
-
DOI 10.1007/s007020200038
-
Maruyama, W.; Takahashi, T.; Youdim, M.B.H.; Naoi, M. The antiparkinsondrug, rasagiline, prevents apoptotic DNA damage induced byperoxynitrite in human dopaminergic neuroblastoma SH-SY5Y cells. J.Neural Transm., 2002, 109, 467-481. (Pubitemid 34280405)
-
(2002)
Journal of Neural Transmission
, vol.109
, Issue.4
, pp. 467-481
-
-
Maruyama, W.1
Takahashi, T.2
Youdim, M.3
Naoi, M.4
-
37
-
-
0022378166
-
Prevention of MPTP-induced neurotoxicity by AGN-1133 and AGN-1135, selective inhibitors of monoamine oxidase-B
-
DOI 10.1016/0014-2999(85)90168-2
-
Heikkila, R.E.; Duvoisin, R.C.; Finberg, J.P.; Youdim, M.B.H. Prevention ofMPTP-induced neurotoxicity by AGN-1133 and AGN-1135, selectiveinhibitors of monoamine oxidase-B. Eur. J. Pharmacol., 1985, 116, 313-317. (Pubitemid 16191823)
-
(1985)
European Journal of Pharmacology
, vol.116
, Issue.3
, pp. 313-317
-
-
Heikkila, R.E.1
Duvoisin, R.C.2
Finberg, J.P.M.3
Youdim, M.B.H.4
-
38
-
-
0034525891
-
Neurotoxins induce apoptosis in dopamine neurons: Protection by N-propargylamine-1(R)- and (S)-aminoindan, rasagiline and TV1022
-
Maruyama, W.; Akao, Y.; Youdim, M.B.H.; Naoi, M. Neurotoxins induceapoptosis in dopamine neurons: protection by N-propargylamine-1(R)- and(S)-aminoindan, rasagiline and TV1022. J. Neural Transm.-Supp., 2000, 60, 171-186. (Pubitemid 32037192)
-
(2000)
Journal of Neural Transmission, Supplement
, Issue.60
, pp. 171-186
-
-
Maruyama, W.1
Akao, Y.2
Youdim, M.B.H.3
Naoi, M.4
-
39
-
-
0036677312
-
Mitochondrialpermeability transition mediates apoptosis induced by N-methyl-(R)-salsolinol, an endogenous neurotoxin, and is inhibited by Bcl-2 andrasagiline, N-propargyl-1(R)- aminoindan
-
Akao, Y.; Maruyama, W.; Shimizu, S.; Yi, H.; Nakagawa, Y.; Shamoto-Nagai, M.; Youdim, M.B.; Tsujimoto, Y.; Naoi, M. Mitochondrialpermeability transition mediates apoptosis induced by N-methyl-(R)-salsolinol, an endogenous neurotoxin, and is inhibited by Bcl-2 andrasagiline, N-propargyl-1(R)- aminoindan. J. Neurochem., 2002, 82, 913-923.
-
(2002)
J. Neurochem.
, vol.82
, pp. 913-923
-
-
Akao, Y.1
Maruyama, W.2
Shimizu, S.3
Yi, H.4
Nakagawa, Y.5
Shamoto-Nagai, M.6
Youdim, M.B.7
Tsujimoto, Y.8
Naoi, M.9
-
40
-
-
0032999575
-
Neuroprotective effect of rasagiline, a selective monoamine oxidase-B inhibitor, against closed head injury in the mouse
-
DOI 10.1016/S0014-2999(98)00929-7, PII S0014299998009297
-
Huang, W.; Chen, Y.; Shohami, E.; Weinstock, M. Neuroprotective effect ofrasagiline, a selective monoamine oxidase-B inhibitor, against closed headinjury in the mouse. Eur. J. Pharmacol., 1999, 366, 127-135. (Pubitemid 29080775)
-
(1999)
European Journal of Pharmacology
, vol.366
, Issue.2-3
, pp. 127-135
-
-
Huang, W.1
Chen, Y.2
Shohami, E.3
Weinstock, M.4
-
41
-
-
0035130289
-
Rasagiline [N-propargyl-1R(+)-aminoindan], a selective and potent inhibitor of mitochondrial monoamine oxidase B
-
Youdim, M.B.H.; Gross, A.; Finberg, J.P.M. Rasagiline [N-propargyl-1R(+)aminoindan], a selective and potent inhibitor of mitochondrialmonoamine oxidase B. Br. J. Pharmacol., 2001, 132, 500-506. (Pubitemid 32142364)
-
(2001)
British Journal of Pharmacology
, vol.132
, Issue.2
, pp. 500-506
-
-
Youdim, M.B.H.1
Gross, A.2
Finberg, J.P.M.3
-
42
-
-
0035568344
-
Molecular basis of neuroprotective activities of rasagiline and the anti-Alzheimer drug TV3326 [(N-propargyl-(3R)aminoindan-5-YL)-ethyl methyl carbamate]
-
DOI 10.1023/A:1015131516649
-
Youdim, M.B.H.; Weinstock, M. Molecular basis of neuroprotectiveactivities of rasagiline and the anti Alzheimer drug, TV3326, [(N-propargyl-(3R)-aminoindan-5-yl)-ethyl methyl carbamate]. Cell. Mol. Neurobiol., 2002, 21, 555-573. (Pubitemid 34538855)
-
(2001)
Cellular and Molecular Neurobiology
, vol.21
, Issue.6
, pp. 555-573
-
-
Youdim, M.B.H.1
Weinstock, M.2
-
43
-
-
6944242126
-
Neuroprotection via pro-survival protein kinase C isoforms associated with Bcl-2 family members
-
DOI 10.1096/fj.04-1916fje
-
(a) Weinreb, O.; Bar-Am, O.; Amit, T.; Chillag-Talmor, O.; Youdim, M.B.H.Neuroprotection via pro-survival protein kinase C isoforms associated withBcl-2 family members. FASEB J., 2004, 18, 1471-1473 (Pubitemid 39561618)
-
(2004)
FASEB Journal
, vol.18
, Issue.12
, pp. 1471-1473
-
-
Weinreb, O.1
Bar-Am, O.2
Amit, T.3
Chillag-Talmor, O.4
Youdim, M.B.H.5
-
44
-
-
0036229947
-
Propargylamines induce antiapoptotic new protein synthesis in serum- and nerve growth factor (NGF)-withdrawn, NGF-differentiated PC-12 cells
-
DOI 10.1124/jpet.301.2.753
-
(b) Tatton, W.G.;Chalmers-Redman, R.M.; Ju, W.J.; Mammen, M.; Carlile, G.W.; Pong, A.W.; Tatton, N.A. Propargylamines induce antiapoptotic new proteinsynthesis inserum-and nerve growth factor(NGF)-withdrawn, NGFdifferentiatedPC-12 cells. J. Pharmacol. Exp. Ther., 2002, 301, 753-764 (Pubitemid 34429993)
-
(2002)
Journal of Pharmacology and Experimental Therapeutics
, vol.301
, Issue.2
, pp. 753-764
-
-
Tatton, W.G.1
Chalmers-Redman, R.M.E.2
Ju, W.J.H.3
Mammen, M.4
Carlile, G.W.5
Pong, A.W.6
Tatton, N.A.7
-
45
-
-
27744486071
-
Regulation of Bcl-2 family proteins, neutrophic factors, and APP processing in the neurorescue activity of propargylamine
-
DOI 10.1096/fj.05-3794fje
-
(c)Bar-Am, O.; Weinreb, O.; Amit, T.; Youdim, M. B. Regulation of Bcl-2family proteins, neurotrophic factors, and APP processing in the neurorescueactivity of propargylamine. FASEB J., 2005, 19, 1899-1901. (Pubitemid 41598788)
-
(2005)
FASEB Journal
, vol.19
, Issue.13
, pp. 1899-1901
-
-
Bar-Am, O.1
Weinreb, O.2
Amit, T.3
Youdim, M.B.H.4
-
46
-
-
0034884148
-
Transfection-enforced Bcl-2 overexpression and an anti-Parkinson drug, rasagiline, prevent nuclear accumulation of glyceraldehyde-3-phosphate dehydrogenase induced by an endogenous dopaminergic neurotoxin, N-methyl(R)salsolinol
-
DOI 10.1046/j.1471-4159.2001.00448.x
-
(a) Maruyama, W.; Akao, Y.; Youdim, M.B.H.; Davis, B.A.; Naoi, M.Transfection-enforced Bcl-2 overexpression and an anti-Parkinson drug, rasagiline, prevent nuclear accumulation of glyceraldehyde-3- phosphatedehydrogenase induced by an endogenous dopaminergic neurotoxin, Nmethyl-(R)-salsolinol. J. Neurochem., 2001, 78, 727-735 (Pubitemid 32777974)
-
(2001)
Journal of Neurochemistry
, vol.78
, Issue.4
, pp. 727-735
-
-
Maruyama, W.1
Akao, Y.2
Youdim, M.B.H.3
Davis, B.A.4
Naoi, M.5
-
47
-
-
0345308381
-
Rasagiline: An anti-Parkinson drug with neuroprotective activity
-
DOI 10.1586/14737175.3.6.737
-
(b) Youdim, M.B.H. Rasagiline: an anti-Parkinson drug with neuroprotective activity.Expert Rev. Neurother., 2003, 3, 737-749. (Pubitemid 37462173)
-
(2003)
Expert Review of Neurotherapeutics
, vol.3
, Issue.6
, pp. 737-749
-
-
Youdim, M.B.H.1
-
48
-
-
0642303109
-
The importance of propargylamine moiety in the anti-Parkinson drug rasagiline and its derivatives in MAPK-dependent amyloid precursor protein processing
-
DOI 10.1096/fj.03-0078fje
-
(a) Yogev-Falach, M.; Amit, T.; Bar-Am, O.; Youdim, M.B.H. Theimportance of propargylamine moiety in the anti-Parkinson drug rasagilineand its derivatives for MAPK-dependent amyloid precursor proteinprocessing. FASEB J., 2003, 17, 2325-2327 (Pubitemid 39561481)
-
(2003)
FASEB Journal
, vol.17
, Issue.15
, pp. 2325-2327
-
-
Yogev-Falach, M.1
Amit, T.2
Bar-Am, O.3
Youdim, M.B.H.4
-
49
-
-
2642529309
-
Regulation of protein kinase C by the anti-Parkinson drug, MAO-B inhibitor, rasagiline and its derivatives, in vivo
-
DOI 10.1111/j.1471-4159.2004.02425.x
-
(b) Bar-Am, O.; Yogev-Falach, M.; Amit, T.; Sagi, Y.; Youdim, M.B.H. Regulation of protein kinase C bythe anti-Parkinson drug, MAO-B inhibitor, rasagiline and its derivatives, invivo. J. Neurochem., 2004, 89, 1119-1125. (Pubitemid 38715829)
-
(2004)
Journal of Neurochemistry
, vol.89
, Issue.5
, pp. 1119-1125
-
-
Bar-Am, O.1
Yogev-Falach, M.2
Amit, T.3
Sagi, Y.4
Youdim, M.B.H.5
-
50
-
-
0025295039
-
Cleavage of amyloid beta peptideduring constitutive processing of its precursor
-
(a) Esch, F.S.; Keim, P.S.; Beattie, E.C.; Blacher, R.W.; Culwell, A.R.;Oltersdorf, T.; McClure, D.; Ward, P.J. Cleavage of amyloid beta peptideduring constitutive processing of its precursor. Science, 1990, 248, 1122-1124
-
(1990)
Science
, vol.248
, pp. 1122-1124
-
-
Esch, F.S.1
Keim, P.S.2
Beattie, E.C.3
Blacher, R.W.4
Culwell, A.R.5
Oltersdorf, T.6
McClure, D.7
Ward, P.J.8
-
51
-
-
0025373508
-
Evidence that beta amyloid protein in Alzheimer's disease is not derived bynormal processing
-
(b) Sisodia, S.S.; Koo, E.H.; Beyreuther, K.; Unterbeck, A.; Price, D.L.Evidence that beta amyloid protein in Alzheimer's disease is not derived bynormal processing. Science, 1990, 248, 492-495.
-
(1990)
Science
, vol.248
, pp. 492-495
-
-
Sisodia, S.S.1
Koo, E.H.2
Beyreuther, K.3
Unterbeck, A.4
Price, D.L.5
-
52
-
-
75949114175
-
The neuroprotectivemechanism of 1-(R)-aminoindan, the major metabolite of the antiparkinsoniandrug rasagiline
-
Bar-Am, O.; Weinreb, O.; Amit, T.; Youdim, M.B.H. The neuroprotectivemechanism of 1-(R)-aminoindan, the major metabolite of the antiparkinsoniandrug rasagiline. J. Neurochem., 2010, 112, 1131-1137.
-
(2010)
J. Neurochem.
, vol.112
, pp. 1131-1137
-
-
Bar-Am, O.1
Weinreb, O.2
Amit, T.3
Youdim, M.B.H.4
-
53
-
-
36749021653
-
Comprehensive review of rasagiline, a second-generation monoamine oxidase inhibitor, for the treatment of Parkinson's Disease
-
DOI 10.1016/j.clinthera.2007.09.021, PII S0149291807003025
-
Chen, J.J.; Swope, D.M. ; Dashtipour, K. Comprehensive review ofrasagiline, a second-generation monoamine oxidase inhibitor, for thetreatment of Parkinson's disease. Clin. Ther., 2007, 29, 1825-1849. (Pubitemid 350212811)
-
(2007)
Clinical Therapeutics
, vol.29
, Issue.9
, pp. 1825-1849
-
-
Chen, J.J.1
Swope, D.M.2
Dashtipour, K.3
-
54
-
-
0000293742
-
Uber eine eigenartige Erkrankung der Hirnrinde
-
Alzheimer A. Uber eine eigenartige Erkrankung der Hirnrinde. Allg. Z.Psychiat., 1907, 64, 146-148.
-
(1907)
Allg. Z.Psychiat.
, vol.64
, pp. 146-148
-
-
Alzheimer, A.1
-
55
-
-
75449102536
-
Mechanisms of disease: Alzheimer'sdisease
-
Querfurth, H.W.; LaFerla, F.M. Mechanisms of disease: Alzheimer'sdisease. New Engl. J. Med., 2010, 362, 329-344.
-
(2010)
New Engl. J. Med.
, vol.362
, pp. 329-344
-
-
Querfurth, H.W.1
Laferla, F.M.2
-
56
-
-
33746489936
-
Towards a unifying hypothesis of Alzheimer's disease: Cholinergic system linked to plaques, tangles and neuroinflammation
-
DOI 10.2174/092986706777935203
-
Sivaprakasam, K. Towards a unifying hypothesis of Alzheimer's disease:cholinergic system linked to plaques, tangles and neuroinflammation. Curr.Med. Chem., 2006, 13, 2179-2188. (Pubitemid 44132608)
-
(2006)
Current Medicinal Chemistry
, vol.13
, Issue.18
, pp. 2179-2188
-
-
Sivaprakasam, K.1
-
57
-
-
33745446987
-
Progress in acetylcholinesterase inhibitors for Alzheimer's disease
-
DOI 10.1517/13543776.16.6.811
-
Bolognesi, M.L.; Minarini, A.; Tumiatti, V.; Melchiorre, C. Progress inacetylcholinesterase inhibitors for Alzheimer's disease. Expert Opin. Ther.Pat., 2006, 16, 811-823. (Pubitemid 43949964)
-
(2006)
Expert Opinion on Therapeutic Patents
, vol.16
, Issue.6
, pp. 811-823
-
-
Bolognesi, M.L.1
Minarini, A.2
Tumiatti, V.3
Melchiorre, C.4
-
58
-
-
0034528416
-
M1 muscarinic agonists as potential disease-modifying agents in Alzheimer's disease: Rationale and perspectives
-
Fisher, A.; Michaelson, D.M.; Brandeis, R.; Haring, R.; Chapman, S.; Pittel, Z. M1 muscarinic agonists as potential disease-modifying agents inAlzheimer's disease. Rationale and perspectives. Ann. N. Y. Acad. Sci., 2000, 920, 315-320. (Pubitemid 32056587)
-
(2000)
Annals of the New York Academy of Sciences
, vol.920
, pp. 315-320
-
-
Fisher, A.1
Michaelson, D.M.2
Brandeis, R.3
Haring, R.4
Chapman, S.5
Pittel, Z.6
-
59
-
-
38549098085
-
Amyloid-cholinesterase interactions
-
Inestrosa, N.C.; Dinamarca, M.C.; Alvarez, A. Amyloid-cholinesterase interactions. FEBS J., 2008, 275, 625-632.
-
(2008)
FEBS J.
, vol.275
, pp. 625-632
-
-
Inestrosa, N.C.1
Dinamarca, M.C.2
Alvarez, A.3
-
60
-
-
77954369899
-
Beyond the cholinergic hypothesis: Docurrent drugs work in Alzheimer's disease?
-
Martorana, A.; Esposito, Z.; Koch, G. Beyond the cholinergic hypothesis: docurrent drugs work in Alzheimer's disease? CNS Neurosci. Ther., 2010, 16, 235-245.
-
(2010)
CNS Neurosci. Ther.
, vol.16
, pp. 235-245
-
-
Martorana, A.1
Esposito, Z.2
Koch, G.3
-
61
-
-
77949768182
-
Towards disease-modifying treatment of Alzheimer's disease:drugs targeting β-Amyloid
-
Frisardi, V.; Solfrizzi, V.; Imbimbo, P.B.; Capurso, C.; D'Introno, A.;Colacicco, A.M.; Vendemiale, G.; Seripa, D.; Pilotto, A.; Capurso, A.;Panza, F. Towards disease-modifying treatment of Alzheimer's disease:drugs targeting β-Amyloid. Curr. Alzheimer Res., 2010, 7, 40-55.
-
(2010)
Curr. Alzheimer Res.
, vol.7
, pp. 40-55
-
-
Frisardi, V.1
Solfrizzi, V.2
Imbimbo, P.B.3
Capurso, C.4
D'Introno, A.5
Colacicco, A.M.6
Vendemiale, G.7
Seripa, D.8
Pilotto, A.9
Capurso, A.10
Panza, F.11
-
62
-
-
36749073565
-
BACE inhibitors as potential therapeutics for Alzheimer's disease
-
DOI 10.2174/157488907782411783
-
Evin, G.; Kenche, V.B. BACE inhibitors as potential therapeutics forAlzheimer's disease. Recent Pat. CNS Drug Discov., 2007, 2, 188-199. (Pubitemid 350200291)
-
(2007)
Recent Patents on CNS Drug Discovery
, vol.2
, Issue.3
, pp. 188-199
-
-
Evin, G.1
Kenche, V.B.2
-
63
-
-
33846922600
-
γ-Secretase: A complex target for Alzheimer's disease
-
DOI 10.1016/j.coph.2006.10.002, PII S1471489206001998, Neurosciences
-
Lundkvist, J.; Naslund, J. Gamma-secretase: a complex target forAlzheimer's disease. Curr. Opin. Pharmacol., 2007, 7, 112-118. (Pubitemid 46238041)
-
(2007)
Current Opinion in Pharmacology
, vol.7
, Issue.1
, pp. 112-118
-
-
Lundkvist, J.1
Naslund, J.2
-
64
-
-
0041929529
-
Design strategies for antiamyloidagents
-
Mason, J.M.; Kokkoni, N.; Stott, K.; Doig, A.J. Design strategies for antiamyloidagents. Curr. Opin. Struc. Biol., 2003, 13, 526-532.
-
(2003)
Curr. Opin. Struc. Biol.
, vol.13
, pp. 526-532
-
-
Mason, J.M.1
Kokkoni, N.2
Stott, K.3
Doig, A.J.4
-
65
-
-
76849091134
-
Can Alzheimer disease be prevented by amyloid-βimmunotherapy?
-
Lemere, C.A.; Masliah, E. Can Alzheimer disease be prevented by amyloid-βimmunotherapy? Nat. Rev. Neurol., 2010, 6, 108-119.
-
(2010)
Nat. Rev. Neurol.
, vol.6
, pp. 108-119
-
-
Lemere, C.A.1
Masliah, E.2
-
66
-
-
0031773098
-
Oxidative stress and neurodegenerative disorders
-
Sun, A.Y.; Chen, Y.M. Oxidative stress and neurodegenerative disorders. J.Biomed. Sci., 1998, 5, 401-414. (Pubitemid 28559104)
-
(1998)
Journal of Biomedical Science
, vol.5
, Issue.6
, pp. 401-414
-
-
Sun, A.Y.1
Chen, Y.-M.2
-
67
-
-
0028182786
-
Monoamine oxidase inhibitors, cognitive functions and neurodegenerative diseases
-
(a) Delumeau, J.C.; Bentué-Ferrer, D.; Gandon, J.M.; Amrein, R.; Belliard, S.; Allain, H. Monoamine oxidase inhibitors, cognitive functions andneurodegenerative diseases. J. Neural Transm. Suppl., 1994, 41, 259-266 (Pubitemid 24215700)
-
(1994)
Journal of Neural Transmission, Supplement
, Issue.41
, pp. 259-266
-
-
Delumeau, J.C.1
Bentue-Ferrer, D.2
Gandon, J.M.3
Amrein, R.4
Belliard, S.5
Allain, H.6
-
68
-
-
34248549035
-
Involvement of type A monoamine oxidase in neurodegeneration: Regulation of mitochondrial signaling leading to cell death or neuroprotection
-
(b)Naoi, M.; Maruyama, W.; Akao, Y.; Yi, H.; Yamaoka, T. Involvement oftype A monoamine oxidase in neurodegeneration: regulation ofmitochondrial signaling leading to cell death or neuroprotection. J. NeuralTransm. Suppl., 2006, 71, 67-77. (Pubitemid 351412108)
-
(2006)
Journal of Neural Transmission, Supplement
, Issue.71
, pp. 67-77
-
-
Naoi, M.1
Maruyama, W.2
Akao, Y.3
Yi, H.4
Yamaoka, Y.5
-
69
-
-
0028145566
-
Increased monoamine oxidase B activity in plaque-associated astrocytes of Alzheimer brains revealed by quantitative enzyme radioautography
-
DOI 10.1016/0306-4522(94)90311-5
-
Saura, J.; Luque, J.M.; Cesura, A.M.; Da Prada, M.; Chan-Palay, V.; Huber, G.; Loffler, J.; Richards, J.G. Increased monoamine oxidase B activity inplaque-associated astrocytes of Alzheimer brains revealed by quantitativeenzyme radioautography. Neuroscience, 1994, 62, 15-30. (Pubitemid 24287342)
-
(1994)
Neuroscience
, vol.62
, Issue.1
, pp. 15-30
-
-
Saura, J.1
-
70
-
-
33750462391
-
Multifunctional drugs with different CNS targets for neuropsychiatric disorders
-
DOI 10.1111/j.1471-4159.2006.04141.x
-
(a) Van der Schyf, C.J.; Geldenhuys, W.J.; Youdim, M.B.H. Multifunctionaldrugs with different CNS targets for neuropsychiatric disorders. J.Neurochem., 2006, 99, 1033-1048 (Pubitemid 44655271)
-
(2006)
Journal of Neurochemistry
, vol.99
, Issue.4
, pp. 1033-1048
-
-
Van Der Schyf, C.J.1
Geldenhuys, W.J.2
Youdim, M.B.H.3
-
71
-
-
11144245220
-
Multi-functional drugs for various CNS targets in the treatment of neurodegenerative disorders
-
DOI 10.1016/j.tips.2004.11.007, PII S016561470400313X
-
(b) Youdim, M.B.H.; Buccafusco, J.J.Multi-functional drugs for various CNS targets in the treatment ofneurodegenerative disorders. Trends Pharm. Sci., 2005, 26, 27-35. (Pubitemid 40052707)
-
(2005)
Trends in Pharmacological Sciences
, vol.26
, Issue.1
, pp. 27-35
-
-
Youdim, M.B.H.1
Buccafusco, J.J.2
-
72
-
-
0029869159
-
Imino 1,2,3,4-tetrahydrocyclopent[b]indole carbamates as dual inhibitors of acetylcholinesterase and monoamine oxidase
-
DOI 10.1016/0960-894X(96)00072-8
-
Fink, D.M.; Palermo, M.G.; Bores, G.M.; Huger, F.P.; Kurys, B.E.;Merriman, M.C.; Olsen, G.E.; Petko, W.; O'Malley, G.J. Imino 1, 2, 3, 4-tetrahydrocyclopent [b]indole carbamates as dual inhibitors ofacetylcholinesterase and monoamine oxidase. Bioorg. Med. Chem. Lett., 1996, 6, 625-630. (Pubitemid 26107892)
-
(1996)
Bioorganic and Medicinal Chemistry Letters
, vol.6
, Issue.6
, pp. 625-630
-
-
Fink, D.M.1
Palermo, M.G.2
Bores, G.M.3
Huger, F.P.4
Kurys, B.E.5
Merriman, M.C.6
Olsen, G.E.7
Petko, W.8
O'Malley, G.J.9
-
73
-
-
80053527089
-
-
MEDI, abstract
-
O'Malley, G.J.; Bores, G.; Huger, F.; Kuris, B.E.; Merriman, M.C.; Olsen, G.; Petko, W.; Palermo, M.G. Abstract of the 205th American ChemicalSociety National Meeting 1993, MEDI, abstract.
-
(1993)
Abstract of the 205th American ChemicalSociety National Meeting
-
-
O'malley, G.J.1
Bores, G.2
Huger, F.3
Kuris, B.E.4
Merriman, M.C.5
Olsen, G.6
Petko, W.7
Palermo, M.G.8
-
74
-
-
0345435251
-
KA-672 inhibits rat brain acetylcholinesterase in vitro but not in vivo
-
DOI 10.1016/S0304-3940(99)00149-4, PII S0304394099001494
-
Hilgert, M.; Nöldner, M.; Chatterjee, S.S.; Klein, J. KA-672 inhibits rat brainacetylcholinesterase in vitro but not in vivo. Neurosci. Lett., 1999, 263, 193-196. (Pubitemid 29158961)
-
(1999)
Neuroscience Letters
, vol.263
, Issue.2-3
, pp. 193-196
-
-
Hilgert, M.1
Noldner, M.2
Chatterjee, S.S.3
Klein, J.4
-
75
-
-
0034649564
-
Inhibition of monoamine oxidases by functionalized coumarin derivatives: Biological activities, QSARs, and 3D-QSARs
-
DOI 10.1021/jm001028o
-
Gnerre, C.; Catto, M.; Leonetti, F.; Weber, P.; Carrupt, P.A.; Altomare, C.;Carotti, A.; Testa, B. Inhibition of monoamine oxidases by functionalizedcoumarin derivatives: biological activities, QSARs, and 3D-QSARs. J. Med.Chem., 2000, 43, 4747-4758. (Pubitemid 32002686)
-
(2000)
Journal of Medicinal Chemistry
, vol.43
, Issue.25
, pp. 4747-4758
-
-
Gnerre, C.1
Catto, M.2
Leonetti, F.3
Weber, P.4
Carrupt, P.-A.5
Altomare, C.6
Carotti, A.7
Testa, B.8
-
76
-
-
0035855832
-
Coumarins derivatives as dual inhibitors of acetylcholinesterase and monoamine oxidase
-
DOI 10.1021/jm010894d
-
Bruhlmann, C.; Ooms, F.; Carrupt, P.A.; Testa, B.; Catto, M.; Leonetti, F.;Altomare, C.; Carotti, A. Coumarins derivatives as dual inhibitors ofacetylcholinesterase and monoamine oxidase. J. Med. Chem., 2001, 44, 3195-3198. (Pubitemid 32862350)
-
(2001)
Journal of Medicinal Chemistry
, vol.44
, Issue.19
, pp. 3195-3198
-
-
Bruhlmann, C.1
Ooms, F.2
Carrupt, P.-A.3
Testa, B.4
Catto, M.5
Leonetti, F.6
Altomare, C.7
Carotti, A.8
-
77
-
-
77956413632
-
Design synthesis and biological evaluation ofcoumarin derivatives tethered to an edrophonium-like fragment as highlypotent and selective dual binding site acetylcholinesterase inhibitors
-
Pisani, L.; Catto, M.; Giangreco, I.; Leonetti, F.; Nicolotti, O.; Stefanachi, A.; Cellamare, S.; Carotti, A. Design, synthesis and biological evaluation ofcoumarin derivatives tethered to an edrophonium-like fragment as highlypotent and selective dual binding site acetylcholinesterase inhibitors.ChemMedChem, 2010, 5, 1616-1630.
-
(2010)
ChemMedChem
, vol.5
, pp. 1616-1630
-
-
Pisani, L.1
Catto, M.2
Giangreco, I.3
Leonetti, F.4
Nicolotti, O.5
Stefanachi, A.6
Cellamare, S.7
Carotti, A.8
-
78
-
-
0037153195
-
Novel dual inhibitors of AChE and MAO derived from hydroxy aminoindan and phenethylamine as potential treatment for Alzheimer's disease
-
DOI 10.1021/jm020120c
-
Sterling, J.; Herzig, Y.; Goren, T.; Finkelstein, N.; Lerner, D.; Goldenberg, W.; Miskolczi, I.; Molnar, S.; Rantal, F.; Tamas, T.; Toth, G.; Zagyva, A.;Zekany, A.; Lavian, G.; Gross, A.; Friedman, R.; Razin, M.; Huang, W.;Krais, B.; Chorev, M.; Youdim, M.B.H.; Weinstock, M. Novel dualinhibitors of AChE and MAO derived from hydroxy aminoindan andphenethylamine as potential treatment for Alzheimer's disease. J. Med.Chem., 2002, 45, 5260-5279. (Pubitemid 35429165)
-
(2002)
Journal of Medicinal Chemistry
, vol.45
, Issue.24
, pp. 5260-5279
-
-
Sterling, J.1
Herzig, Y.2
Goren, T.3
Finkelstein, N.4
Lerner, D.5
Goldenberg, W.6
Miskolczi, I.7
Molnar, S.8
Rantal, F.9
Tamas, T.10
Toth, G.11
Zagyva, A.12
Zekany, A.13
Lavian, G.14
Gross, A.15
Friedman, R.16
Razin, M.17
Huang, W.18
Krais, B.19
Chorev, M.20
Youdim, M.B.21
Weinstock, M.22
more..
-
79
-
-
0036849156
-
Limited potentiation of blood pressure response to oral tyramine by brain-selective monoamine oxidase A-B inhibitor, TV-3326 in conscious rabbits
-
DOI 10.1016/S0028-3908(02)00176-4, PII S0028390802001764
-
Weinstock, M.; Gorodetsky, E.; Wang, R.H.; Fross, A.; Weinreb, O.;Youdim, M.B.H. Limited potentiation of blood pressure response to oraltyramine by brain-selective monoamine oxidase A-B inhibitor, TV-3326 inconscious rabbits. Neuropharmacology, 2002, 43, 999-1005. (Pubitemid 35341235)
-
(2002)
Neuropharmacology
, vol.43
, Issue.6
, pp. 999-1005
-
-
Weinstock, M.1
Gorodetsky, E.2
Wang, R.H.3
Gross, A.4
Weinreb, O.5
Youdim, M.B.H.6
-
80
-
-
0038012567
-
A novel cholinesterase and brain-selective monoamine oxidase inhibitor for the treatment of dementia comorbid with depression and Parkinson's disease
-
DOI 10.1016/S0278-5846(03)00053-8
-
Weinstock, M.; Gorodetsky, E.; Poltyrev, T.; Gross, A.; Sagi, Y.; Youdim, M.B.H. A novel cholinesterase and brain-selective monoamine oxidaseinhibitor for the treatment of dementia comorbid with depression andParkinson's disease. Prog. Neuropsychopharmacol. Biol. Psychiatry, 2003, 27, 555-561. (Pubitemid 36645054)
-
(2003)
Progress in Neuro-Psychopharmacology and Biological Psychiatry
, vol.27
, Issue.4
, pp. 555-561
-
-
Weinstock, M.1
Gorodetsky, E.2
Poltyrev, T.3
Gross, A.4
Sagi, Y.5
Youdim, M.6
-
81
-
-
0038155162
-
Attenuation of MPTP-induced dopaminergic neurotoxicity by TV3326, a cholinesterase-monoamine oxidase inhibitor
-
DOI 10.1046/j.1471-4159.2003.01801.x
-
Sagi, Y.; Weinstock, M.; Youdim, M.B.H. Attenuation of MPTP-induceddopaminergic neurotoxicity by TV3326, a cholinesterase- monoamineoxidase inhibitor. J. Neurochem., 2003, 86, 290-297. (Pubitemid 36842429)
-
(2003)
Journal of Neurochemistry
, vol.86
, Issue.2
, pp. 290-297
-
-
Sagi, Y.1
Weinstock, M.2
Youdim, M.B.H.3
-
82
-
-
0344989342
-
Neuroprotectiveand neurorescue properties of rasagiline and TV3326 in MPTP model ofParkinson's disease
-
Sagi, Y.; O. Weinreb, O.; Weinstock, M.; Youdim, M.B.H. Neuroprotectiveand neurorescue properties of rasagiline and TV3326 in MPTP model ofParkinson's disease. Neural Plasticity, 2001, 8, 197-198.
-
(2001)
Neural Plasticity
, vol.8
, pp. 197-198
-
-
Sagi, Y.1
Weinreb, O.O.2
Weinstock, M.3
Youdim, M.B.H.4
-
83
-
-
0034932067
-
Neuroprotective effects of novel cholinesterase inhibitors derived from rasagiline as potential anti-Alzheimer drugs
-
Weinstock, M.; Kirschbaum-Slager, N.; Lazarovici, P.; Bejar, C.; Youdim, M.B.H.; Shoham, S. Neuroprotective effects of novel cholinesteraseinhibitors derived from rasagiline as potential anti-Alzheimer drugs. Ann. N.Y. Acad. Sci., 2001, 939, 148-161. (Pubitemid 32620064)
-
(2001)
Annals of the New York Academy of Sciences
, vol.939
, pp. 148-161
-
-
Weinstock, M.1
Kirschbaum-Slager, N.2
Lazarovici, P.3
Bejar, C.4
Youdim, M.B.H.5
Shoham, S.6
-
84
-
-
77957968479
-
Monoamine oxidase inhibitors as neuroprotectiveagents in age-dependent neurodegenerative disorders
-
Naoi, M.; Maruyama, W. Monoamine oxidase inhibitors as neuroprotectiveagents in age-dependent neurodegenerative disorders. Curr. Pharm. Design, 2010, 16, 2799-2817.
-
(2010)
Curr. Pharm. Design
, vol.16
, pp. 2799-2817
-
-
Naoi, M.1
Maruyama, W.2
-
85
-
-
17444449069
-
1-N-substituted thiocarbamoyl-3-phenyl-5-thienyl-2-pyrazolines: Synthesis and evaluation as MAO inhibitors
-
DOI 10.1002/ardp.200300732
-
Gökhan, N.; Yesilada, A.; Uçar, G.; Erol, K.; Bilgin, A. 1-N-Substitutedthiocarbamoyl-3-phenyl-5-thienyl-2-pyrazolines: synthesis and evaluation asMAO inhibitors. Arch. Pharm. Pharm. Med. Chem., 2003, 336, 362-371. (Pubitemid 37127992)
-
(2003)
Archiv der Pharmazie
, vol.336
, Issue.8
, pp. 362-371
-
-
Gokhan, N.1
Yesilada, A.2
Ucar, G.3
Erol, K.4
Bilgin, A.A.5
-
86
-
-
19544390899
-
1-N-Substituted thiocarbamoyl-3-phenyl-5-thienyl-2-pyrazolines: A novel cholinesterase and selective monoamine oxidase B inhibitors for the treatment of Parkinson's and Alzheimer's diseases
-
DOI 10.1016/j.neulet.2005.03.028, PII S0304394005003216
-
Uçar, G.; Gökhan, N.; Yesilada, A.; Bilgin, A.A. 1-N-Substitutedthiocarbamoyl-3-phenyl-5-thienyl-2-pyrazolines: A novel cholinesterase andselective monoamine oxidase B inhibitors for the treatment of Parkinson'sand Alzheimer's diseases. Neurosci. Lett., 2005, 382, 327-331. (Pubitemid 40733646)
-
(2005)
Neuroscience Letters
, vol.382
, Issue.3
, pp. 327-331
-
-
Ucar, G.1
Gokhan, N.2
Yesilada, A.3
Bilgin, A.A.4
-
87
-
-
25844529207
-
Screening of non-alkaloidal natural compounds as acetylcholinesteraseinhibitors
-
(a) Bruhlmann, C.; Marston, A.; Hostettmann, K.; Carrupt, P.A.; Testa, B.Screening of non-alkaloidal natural compounds as acetylcholinesteraseinhibitors. Chem. Biodivers., 2004, 1, 819-829
-
(2004)
Chem. Biodivers.
, vol.1
, pp. 819-829
-
-
Bruhlmann, C.1
Marston, A.2
Hostettmann, K.3
Carrupt, P.A.4
Testa, B.5
-
88
-
-
0035048669
-
Natural and synthetic xanthones as monoamine oxidase inhibitors: Biological assay and 3D-QSAR
-
DOI 10.1002/1522-2675(20010321)84:3<552::AID-HLCA552>3.0.CO;2-X
-
(b) Gnerre, C.; Thull, U.;Gaillard, P.; Carrupt, P.-A.; Testa, B.; Fernandes, E.; Silva, F.; Pinto, M.;Pinto, M.M.M.; Wolfender, J.-L.; Hostettmann, K.; Cruciani, G. Natural andsynthetic xanthones as monoamine oxidase inhibitors: biological assay and3D-QSAR. Helv. Chim. Acta, 2001, 84, 552-570. (Pubitemid 32299308)
-
(2001)
Helvetica Chimica Acta
, vol.84
, Issue.3
, pp. 552-570
-
-
Guerre, C.1
Thull, U.2
Gaillard, P.3
Carrupt, P.-A.4
Testa, B.5
Fernandes, E.6
Silva, F.7
Pinto, M.8
Pinto, M.M.M.9
Wolfender, J.-L.10
Hostettmann, K.11
Cruciani, G.12
-
89
-
-
41149163183
-
Parkinson's disease: Clinical features and diagnosis
-
DOI 10.1136/jnnp.2007.131045
-
Jankovic, J. Parkinson's disease: clinical features and diagnosis. J. Neurol.Neurosurg. Psychiatry, 2008, 79, 368-376. (Pubitemid 351441488)
-
(2008)
Journal of Neurology, Neurosurgery and Psychiatry
, vol.79
, Issue.4
, pp. 368-376
-
-
Jankovic, J.1
-
90
-
-
37149050857
-
Disease-modifying drugs andParkinson's disease
-
Allain, H.; Bentué-Ferrer, D.; Akwa, Y. Disease-modifying drugs andParkinson's disease. Prog. Neurobiol., 2008, 84, 25-39.
-
(2008)
Prog. Neurobiol.
, vol.84
, pp. 25-39
-
-
Allain, H.1
Bentué-Ferrer, D.2
Akwa, Y.3
-
91
-
-
0030882856
-
α-Synuclein in Lewy bodies
-
Spillantini, M.G.; Schmidt, M.L.; Lee, V.M.-Y.; Trojanowski, J.Q.; Jakes, R.; Goedert, M. α-Synuclein in Lewy bodies. Nature, 1997, 388, 839-840.
-
(1997)
Nature
, vol.388
, pp. 839-840
-
-
Spillantini, M.G.1
Schmidt, M.L.2
Lee, V.M.-Y.3
Trojanowski, J.Q.4
Jakes, R.5
Goedert, M.6
-
92
-
-
77955366745
-
Role of post-translationalmodifications in modulating the structure, function and toxicity of alphasynuclein:implications for Parkinson's disease pathogenesis and therapies
-
Oueslati, A.; Fournier, M.; Lashuel, H.A. Role of post- translationalmodifications in modulating the structure, function and toxicity of alphasynuclein:implications for Parkinson's disease pathogenesis and therapies.Prog. Brain Res., 2010, 183, 115-145.
-
(2010)
Prog. Brain Res.
, vol.183
, pp. 115-145
-
-
Oueslati, A.1
Fournier, M.2
Lashuel, H.A.3
-
93
-
-
0038711511
-
Effects of oxidative and nitrative challenges on α-synuclein fibrillogenesis involve distinct mechanisms of protein modifications
-
DOI 10.1074/jbc.M212436200
-
Norris, E.H.; Giasson, B.I.; Ischiropoulos, H.; Lee, V.M. Effects of oxidativeand nitrative challenges on alpha-synuclein fibrillogenesis involve distinctmechanisms of protein modifications. J. Biol. Chem., 2003, 278, 27230-27240. (Pubitemid 36876880)
-
(2003)
Journal of Biological Chemistry
, vol.278
, Issue.29
, pp. 27230-27240
-
-
Norris, E.H.1
Giasson, B.I.2
Ischiropoulos, H.3
Lee, V.M.-Y.4
-
94
-
-
77950644314
-
Copper binding regulatesintracellular alpha-synuclein localisation, aggregation and toxicity
-
Wang, X.; Moualla, D.; Wright, J.A.; Brown, D.R. Copper binding regulatesintracellular alpha-synuclein localisation, aggregation and toxicity. J.Neurochem., 2010, 113, 704-714.
-
(2010)
J.Neurochem.
, vol.113
, pp. 704-714
-
-
Wang, X.1
Moualla, D.2
Wright, J.A.3
Brown, D.R.4
-
95
-
-
72949084639
-
Interaction between alphasynucleinand metal ions, still looking for a role in the pathogenesis ofParkinson's disease
-
Bisaglia, M.; Tessari, I.; Mammi, S.; Bubacco, L. Interaction between alphasynucleinand metal ions, still looking for a role in the pathogenesis ofParkinson's disease. Neuromol. Med., 2009, 11, 239-251.
-
(2009)
Neuromol. Med.
, vol.11
, pp. 239-251
-
-
Bisaglia, M.1
Tessari, I.2
Mammi, S.3
Bubacco, L.4
-
96
-
-
80051632039
-
Increased iron levels correlatewith the selective nigral dopaminergic neuron degeneration in Parkinson'sdisease
-
Lv, Z.; Jiang, H.; Xu, H.; Song, N.; Xie, J. Increased iron levels correlatewith the selective nigral dopaminergic neuron degeneration in Parkinson'sdisease. J. Neural Transm., 2011, 118, 361-369.
-
(2011)
J. Neural Transm.
, vol.118
, pp. 361-369
-
-
Lv, Z.1
Jiang, H.2
Xu, H.3
Song, N.4
Xie, J.5
-
97
-
-
59149084113
-
Metal-dependentgeneration of reactive oxygen species from amyloid proteins implicated inneurodegenerative disease
-
Allsop, D.; Mayes, J.; Moore, S.; Masad, A.; Tabner, B.J. Metal-dependentgeneration of reactive oxygen species from amyloid proteins implicated inneurodegenerative disease. Biochem. Soc. Trans., 2008, 36, 1293-1298.
-
(2008)
Biochem. Soc. Trans.
, vol.36
, pp. 1293-1298
-
-
Allsop, D.1
Mayes, J.2
Moore, S.3
Masad, A.4
Tabner, B.J.5
-
98
-
-
8344265251
-
Iron, brain ageing and neurodegenerative disorders
-
DOI 10.1038/nrn1537
-
Zecca, L.; Youdim, M.B.H.; Riederer, P.; Connor J.R.; Crichton, R.R. Iron, brain ageing and neurodegenerative disorders. Nat. Rev. Neurosci., 2004, 5, 863-873. (Pubitemid 39482155)
-
(2004)
Nature Reviews Neuroscience
, vol.5
, Issue.11
, pp. 863-873
-
-
Zecca, L.1
Youdim, M.B.H.2
Riederer, P.3
Connor, J.R.4
Crichton, R.R.5
-
99
-
-
11844255676
-
Design, synthesis, and evaluation of novel bifunctional iron-chelators as potential agents for neuroprotection in Alzheimer's, Parkinson's, and other neurodegenerative diseases
-
DOI 10.1016/j.bmc.2004.10.037, PII S0968089604008399
-
Zheng, H.; Weiner, L.M.; Bar-Am, O.; Epsztejn, S.; Cabantchik, Z.I.;Warshawsky, A.; Youdim, M.B.H.; Fridkin, M. Design, synthesis, andevaluation of novel bifunctional iron-chelators as potential agents forneuroprotection in Alzheimer's, Parkinson's, and other neurodegenerativediseases. Bioorg. Med. Chem., 2005, 13, 773-783. (Pubitemid 40093620)
-
(2005)
Bioorganic and Medicinal Chemistry
, vol.13
, Issue.3
, pp. 773-783
-
-
Zheng, H.1
Weiner, L.M.2
Bar-Am, O.3
Epsztejn, S.4
Cabantchik, Z.I.5
Warshawsky, A.6
Youdim, M.B.H.7
Fridkin, M.8
-
100
-
-
0346849912
-
Neuroprotection by a novel brain permeable iron chelator, VK-28, against 6-hydroxydopamine lession in rats
-
DOI 10.1016/j.neuropharm.2003.09.005
-
Ben Shachar, D.B.; Kahana, N.; Kampel, V.; Warshawsky, A.; Youdim, M.B.H. Neuroprotection by a novel brain permeable iron chelator, VK-28, against 6-hydroxydopamine lesion in rats. Neuropharmacology, 2004, 46, 254-263. (Pubitemid 37532833)
-
(2004)
Neuropharmacology
, vol.46
, Issue.2
, pp. 254-263
-
-
Shachar, D.B.1
Kahana, N.2
Kampel, V.3
Warshawsky, A.4
Youdim, M.B.H.5
-
101
-
-
25644461154
-
Novel multifunctional neuroprotective iron chelator-monoamine oxidase inhibitor drugs for neurodegenerative diseases: In vitro studies on antioxidant activity, prevention of lipid peroxide formation and monoamine oxidase inhibition
-
DOI 10.1111/j.1471-4159.2005.03340.x
-
Zheng, H.; Gal, S.; Weiner, L.M.; Bar-Am, O.; Warshawsky, A.; Fridkin, M.; Youdim, M.B.H. Novel multifunctional neuroprotective iron chelatormonoamine oxidase inhibitor drugs for neurodegenerative diseases: in vitrostudies on antioxidant activity, prevention of lipid peroxide formation andmonoamine oxidase inhibition. J. Neurochem., 2005, 95, 68-78. (Pubitemid 41384426)
-
(2005)
Journal of Neurochemistry
, vol.95
, Issue.1
, pp. 68-78
-
-
Zheng, H.1
Gal, S.2
Weiner, L.M.3
Bar-Am, O.4
Warshawsky, A.5
Fridkin, M.6
Youdim, M.B.H.7
-
102
-
-
11144316146
-
Bifunctional drug derivatives of MAO-B inhibitor rasagiline and iron chelator VK-28 as a more effective approach to treatment of brain ageing and ageing neurodegenerative diseases
-
DOI 10.1016/j.mad.2004.08.023, PII S0047637404002064, The Voyage to Old Age: Searching for Human Longevity Genes
-
Youdim, M.B.H.; Fridkin, M.; Zheng, H. Bifunctional drug derivatives ofMAO-B inhibitor rasagiline and iron chelator VK-28 as a more effectiveapproach to treatment of brain ageing and ageing neurodegenerative diseases.Mech. Ageing Dev., 2005, 126, 317-326. (Pubitemid 40038353)
-
(2005)
Mechanisms of Ageing and Development
, vol.126
, Issue.2
, pp. 317-326
-
-
Youdim, M.B.H.1
Fridkin, M.2
Zheng, H.3
-
103
-
-
0037734329
-
Neuroprotection by deprenyl and other propargylamines: Glyceraldehyde-3-phosphate dehydrogenase rather than monoamine oxidase B
-
DOI 10.1007/s00702-002-0827-z
-
(a) Tatton, W.; Chalmers-Redman, R.; Tatton, N. Neuroprotection bydeprenyl and other propargylamines: glyceraldehyde-3-phosphatedehydrogenase rather than monoamine oxidase B. J. Neural Transm., 2003, 110, 509-515 (Pubitemid 36543282)
-
(2003)
Journal of Neural Transmission
, vol.110
, Issue.5
, pp. 509-515
-
-
Tatton, W.1
Chalmers-Redman, R.2
Tatton, N.3
-
104
-
-
0034939146
-
Antiapoptoticproperties of rasagiline, N-propargylamine-1(R)-aminoindan, and its optical(S)-isomer, TV1022
-
(b) Maruyama, W.; Youdim, M.B.H.; Naoi, M. Antiapoptoticproperties of rasagiline, N-propargylamine-1(R)-aminoindan, and its optical(S)-isomer, TV1022. Ann. N. Y. Acad. Sci., 2001, 939, 320-329.
-
(2001)
Ann. N. Y. Acad. Sci.
, vol.939
, pp. 320-329
-
-
Maruyama, W.1
Youdim, M.B.H.2
Naoi, M.3
-
105
-
-
33845879870
-
Therapeutic targets and potential of the novel brain- permeable multifunctional iron chelator-monoamine oxidase inhibitor drug, M-30, for the treatment of Alzheimer's disease
-
DOI 10.1111/j.1471-4159.2006.04258.x
-
Avramovich-Tirosh, Y.; Amit, T.; Bar-Am, O.; Zheng, H.; Fridkin, M.;Youdim, M.B.H. Therapeutic targets and potential of the novel brainpermeablemultifunctional iron chelator-monoamine oxidase inhibitor drug, M-30, for the treatment of Alzheimer's disease. J. Neurochem., 2007, 100, 490-502. (Pubitemid 46016026)
-
(2007)
Journal of Neurochemistry
, vol.100
, Issue.2
, pp. 490-502
-
-
Avramovich-Tirosh, Y.1
Amit, T.2
Bar-Am, O.3
Zheng, H.4
Fridkin, M.5
Youdim, M.B.H.6
-
106
-
-
77953864734
-
Site-activated chelators targetingacetylcholinesterase and monoamine oxidase for Alzheimer's therapy
-
Zheng, H.; Youdim, M.B.H.; Fridkin, M. Site-activated chelators targetingacetylcholinesterase and monoamine oxidase for Alzheimer's therapy. ACSChem. Biol., 2010, 5, 603-610.
-
(2010)
ACSChem. Biol.
, vol.5
, pp. 603-610
-
-
Zheng, H.1
Youdim, M.B.H.2
Fridkin, M.3
-
107
-
-
0035181291
-
Monoamine oxidase B and free radical scavenging activities of naturalflavonoids in melastoma candidum D. Don
-
Lee, M.H.; Lin, R.D.; Shen, L.Y.; Yang, L.L.; Yen, K.Y.; Hou, W.C.Monoamine oxidase B and free radical scavenging activities of naturalflavonoids in melastoma candidum D. Don. J. Agric. Food Chem., 2001, 49, 5551-5555.
-
(2001)
J. Agric. Food Chem.
, vol.49
, pp. 5551-5555
-
-
Lee, M.H.1
Lin, R.D.2
Shen, L.Y.3
Yang, L.L.4
Yen, K.Y.5
Hou, W.C.6
-
108
-
-
33746514329
-
Quercetin as the active principle of Hypericum hircinum exerts a selective inhibitory activity against MAO-A: Extraction, biological analysis, and computational study
-
DOI 10.1021/np060015w
-
Chimenti, F.; Cottiglia, F.; Bonsignore, L.; Casu, L.; Casu, M.; Floris, C.;Secci, D.; Bolasco, A.; Chimenti, P.; Granese, A.; Befani, O.; Turini, P.;Alcaro, S.; Ortuso, F.; Trombetta, G.; Loizzo, A.; Guarino, I. Quercetin asthe active principle of Hypericum hircinum exerts a selective inhibitoryactivity against MAO-A: Extraction, biological analysis, and computationalstudy. J. Nat. Prod., 2006, 69, 945-949. (Pubitemid 44166270)
-
(2006)
Journal of Natural Products
, vol.69
, Issue.6
, pp. 945-949
-
-
Chimenti, F.1
Cottiglia, F.2
Bonsignore, L.3
Casu, L.4
Casu, M.5
Floris, C.6
Secci, D.7
Bolasco, A.8
Chimenti, P.9
Granese, A.10
Befani, O.11
Turini, P.12
Alcaro, S.13
Ortuso, F.14
Trombetta, G.15
Loizzo, A.16
Guarino, I.17
-
109
-
-
79958762778
-
Inhibition of the bioactivation of the neurotoxinMPTP by antioxidants, redox agents and monoamine oxidase inhibitors
-
Herraiz, T.; Guillén, H. Inhibition of the bioactivation of the neurotoxinMPTP by antioxidants, redox agents and monoamine oxidase inhibitors.Food Chem. Toxicol., 2011, 49, 1773-1781.
-
(2011)
Food Chem. Toxicol.
, vol.49
, pp. 1773-1781
-
-
Herraiz, T.1
Guillén, H.2
-
110
-
-
0033791895
-
Antioxidant activity of eugenoland related monomeric and dimeric compounds
-
Ogata, M.; Hoshi, M.; Urano, S.; Endo, T. Antioxidant activity of eugenoland related monomeric and dimeric compounds. Chem. Pharm. Bull., 2000, 48, 1467-1469.
-
(2000)
Chem. Pharm. Bull.
, vol.48
, pp. 1467-1469
-
-
Ogata, M.1
Hoshi, M.2
Urano, S.3
Endo, T.4
-
111
-
-
20544463414
-
Eugenol and its structural analogs inhibit monoamine oxidase A and exhibit antidepressant-like activity
-
DOI 10.1016/j.bmc.2005.04.081, PII S0968089605004013
-
Tao, G.; Irie, Y.; Li, D.J.; Keung, W.M. Eugenol and its structural analogsinhibit monoamine oxidase A and exhibit antidepressant-like activity.Bioorg. Med. Chem., 2005, 13, 4777-4788. (Pubitemid 40848356)
-
(2005)
Bioorganic and Medicinal Chemistry
, vol.13
, Issue.15
, pp. 4777-4788
-
-
Tao, G.1
Irie, Y.2
Li, D.-J.3
Wing, M.K.4
-
112
-
-
0025883342
-
Nitric oxide: Physiology, pathophysiology, and pharmacology
-
Moncada, S.; Palmer, R.M.J.; Higgs, E.A. Nitric oxide: physiology, pathophysiology, and pharmacology. Pharmacol. Rev., 1991, 43, 109-142.
-
(1991)
Pharmacol. Rev.
, vol.43
, pp. 109-142
-
-
Moncada, S.1
Palmer, R.M.J.2
Higgs, E.A.3
-
113
-
-
70349970281
-
Oxidative stressand ischemic myocardial syndromes
-
Misra, M.K.; Sarwat, M.; Bhakuni, P.; Tuteja, R.; Tuteja, N. Oxidative stressand ischemic myocardial syndromes. Med. Sci. Monit., 2009, 15, RA209-219.
-
(2009)
Med. Sci. Monit.
, vol.15
-
-
Misra, M.K.1
Sarwat, M.2
Bhakuni, P.3
Tuteja, R.4
Tuteja, N.5
-
114
-
-
69949160564
-
Redox mechanisms in hepatic chronic wound healingand fibrogenesis
-
(a) Novo, E.; Parola, M. Redox mechanisms in hepatic chronic wound healingand fibrogenesis. Fibrogenesis Tissue Repair, 2008, 1, 5
-
(2008)
Fibrogenesis Tissue Repair
, vol.1
, pp. 5
-
-
Novo, E.1
Parola, M.2
-
115
-
-
79960433284
-
The effect of nNOSinhibitors on toxin-induced cell death in dopaminergic cell lines depends onthe extent of enzyme expression
-
(b) Brzozowski, M.J.; Alcantara, S.L.; Iravani, M.M.; Rose, S.; Jenner, P. The effect of nNOSinhibitors on toxin-induced cell death in dopaminergic cell lines depends onthe extent of enzyme expression. Brain Res., 2011, 1404, 21-30
-
(2011)
Brain Res.
, vol.1404
, pp. 21-30
-
-
Brzozowski, M.J.1
Alcantara, S.L.2
Iravani, M.M.3
Rose, S.4
Jenner, P.5
-
116
-
-
0029805172
-
Nitric oxide, superoxide, and peroxynitrite: The good, the bad, and ugly
-
(c) Beckman, J.S.; Koppenol, W.H. Nitric oxide, superoxide, and peroxynitrite: the good, the bad, and ugly. Am. J. Physiol., 1996, 271, C1424-1437.
-
(1996)
Am. J. Physiol.
, vol.271
-
-
Beckman, J.S.1
Koppenol, W.H.2
-
117
-
-
12344308106
-
Nitric oxide as a unique bioactive signaling messenger in physiology and pathophysiology
-
DOI 10.1155/S1110724304402034, PII S1110724304402034
-
Tuteja, N.; Chandra, M.; Tuteja, R.; Misra, M.K. Nitric oxide as a uniquebioactive signaling messenger in physiology and pathophysiology. J.Biomed. Biotech., 2004, 4, 227-237. (Pubitemid 40128959)
-
(2004)
Journal of Biomedicine and Biotechnology
, vol.2004
, Issue.4
, pp. 227-237
-
-
Tuteja, N.1
Chandra, M.2
Tuteja, R.3
Misra, M.K.4
-
118
-
-
65249163408
-
Design of selective neuronal nitric oxide synthase inhibitorsfor the prevention and treatment of neurodegenerative diseases
-
Silverman, R.B. Design of selective neuronal nitric oxide synthase inhibitorsfor the prevention and treatment of neurodegenerative diseases. Acc. Chem.Res., 2009, 42, 439-451.
-
(2009)
Acc. Chem.Res.
, vol.42
, pp. 439-451
-
-
Silverman, R.B.1
-
119
-
-
0023733428
-
Acetylenic and allenic derivatives of 2-(1-methylindolyl) methylamine as selective inhibitors of the monoamine oxidases A and B
-
(a) Cruces, M.A.; Elorriaga, C.; Fernandez-Alvarez, E.; Lopez Chico, M.T.;Nieto Lopez, O. Acetylenic and allenic derivatives of 2-(1-methylindolyl) methylamine as selective inhibitors of the monoamineoxidases A and B. Farmaco Sci., 1988, 43, 567-573 (Pubitemid 18261461)
-
(1988)
Farmaco, Edizione Scientifica
, vol.43
, Issue.7-8
, pp. 567-573
-
-
Cruces, M.A.1
Elorriaga, C.2
Fernandez Alvarez, E.3
Lopez Chico, M.T.4
Nieto Lopez, O.5
-
120
-
-
0025823001
-
Acetylenic and allenic derivatives of 2-(5-methoxyindolyl) and 2-(5-hydroxyindolyl)methylamines: Synthesis and invitro evaluation as monoamine oxidase inhibitors
-
(b) Cruces, M.A.;Elorriaga, C.; Fernandez-Alvarez, E. Acetylenic and allenic derivatives of 2-(5-methoxyindolyl) and 2-(5-hydroxyindolyl) methylamines: synthesis and invitro evaluation as monoamine oxidase inhibitors. Eur. J. Med. Chem., 1991, 26, 33-41
-
(1991)
Eur. J. Med. Chem.
, vol.26
, pp. 33-41
-
-
Cruces, M.A.1
Elorriaga, C.2
Fernandez-Alvarez, E.3
-
121
-
-
0027336573
-
The effects of side chain substitution at positions 2 and 3 of the heterocyclic ring of N-acetylenic analogues of tryptamine as monoamine oxidase inhibitors
-
DOI 10.1016/0006-2952(93)90194-2
-
(c) Avila, M.; Balsa, M.D.; Fernandez-Alvarez, E.; Tipton, K. F.;Unzeta, M. The effect of side-chain substitution at positions 2 and 3 of theheterocyclic ring of N-acetylenic analogues of tryptamine as monoamineoxidase inhibitors. Biochem. Pharmacol., 1993, 45, 2231-2237 (Pubitemid 23171084)
-
(1993)
Biochemical Pharmacology
, vol.45
, Issue.11
, pp. 2231-2237
-
-
Avila, M.1
Balsa, M.D.2
Fernandez-Alvarez, E.3
Tipton, K.F.4
Unzeta, M.5
-
122
-
-
0025974835
-
Monoamine oxidaseinhibitory potencies and selectivities of 2-[N-(2-propynyl)-aminomethyl]-1-methyl indole derivatives
-
(d) Balsa, D.;Fernandez-Alvarez, E.; Tipton, K.F.; Unzeta, M. Monoamine oxidaseinhibitory potencies and selectivities of 2-[N-(2-propynyl)-aminomethyl]- 1-methyl indole derivatives. Biochem. Soc. Trans., 1991, 19, 215-218.
-
(1991)
Biochem. Soc. Trans.
, vol.19
, pp. 215-218
-
-
Balsa, D.1
Fernandez-Alvarez, E.2
Tipton, K.F.3
Unzeta, M.4
-
123
-
-
0033023543
-
Relevance of benzyloxy group in 2-indolyl methylamines in the selective MAO-B inhibition
-
DOI 10.1038/sj.bjp.0702600
-
Perez, V.; Marco, J.L.; Fernandez-Alvarez, E.; Unzeta, M. Relevance of abenzyloxy group in 2-indolyl methylamines in the selective MAO-Binhibition. Br. J. Pharmacol., 1999, 127, 869-876. (Pubitemid 29295345)
-
(1999)
British Journal of Pharmacology
, vol.127
, Issue.4
, pp. 869-876
-
-
Perez, V.1
Marco, J.L.2
Fernandez-Alvarez, E.3
Unzeta, M.4
-
124
-
-
0037290217
-
PF 9601N [N-(2-propynyl)-2-(5-benzyloxy-indolyl) methylamine], a new MAO-B inhibitor, attenuates MPTP-induced depletion of striatal dopamine levels in C57/BL6 mice
-
DOI 10.1016/S0197-0186(02)00091-8, PII S0197018602000918
-
(a) Perez, V.; Unzeta, M. PF9601N [N-(2-propynyl)-2-(5-benzyloxyindolyl) methylamine], a new MAO-B inhibitor, attenuates MPTP induced depletionof striatal dopamine levels in C57/BL mice. Neurochem. Intern., 2003, 42, 221-229 (Pubitemid 35335694)
-
(2003)
Neurochemistry International
, vol.42
, Issue.3
, pp. 221-229
-
-
Perez, V.1
Unzeta, M.2
-
125
-
-
0037199660
-
Neuroprotective effect of the monoamine oxidase inhibitor PF 9601N [N-(2-propynyl)-2-(5-benzyloxy-indolyl) methylamine] on rat nigral neurons after 6-hydroxydopamine-striatal lesion
-
DOI 10.1016/S0304-3940(02)00614-6, PII S0304394002006146
-
(b) Cutillas, B.; Ambrosio, S.; Unzeta, M. Neuroprotective effect ofthe monoamine oxidase inhibitor PF9601N [N-(2-propynyl)-2-(5-benzyloxyindolyl) methylamine] on rat nigral neurons after 6-OH-DA striatallesion. Neurosci. Lett., 2002, 329, 165-168 (Pubitemid 34880064)
-
(2002)
Neuroscience Letters
, vol.329
, Issue.2
, pp. 165-168
-
-
Cutillas, B.1
Ambrosio, S.2
Unzeta, M.3
-
126
-
-
44649196507
-
+-treated SH-SY5Y human dopaminergic cells
-
DOI 10.1111/j.1471-4159.2008.05326.x
-
(c) Sanz, E.; Quintana, A.;Battaglia, V.; Toninello, A.; Hidalgo, J.; Ambrosio, S.; Valoti, M.; Marco, J.L.; Tipton, K.F.; Unzeta, M. Anti-apoptotic effect of MAO-B inhibitorPF9601N [N-(2-propynyl)-2-(5-benzyloxyindolyl) methylamine] is mediatedby p53 pathway inhibition in MPP+-treated SH-SY5Y human dopaminergiccells. J. Neurochem., 2008, 105, 2404-2417. (Pubitemid 351782267)
-
(2008)
Journal of Neurochemistry
, vol.105
, Issue.6
, pp. 2404-2417
-
-
Sanz, E.1
Quintana, A.2
Battaglia, V.3
Toninello, A.4
Hidalgo, J.5
Ambrosio, S.6
Valoti, M.7
Marco, J.L.8
Tipton, K.F.9
Unzeta, M.10
-
127
-
-
33745310693
-
Protective effect of N-(2-propynyl)-2-(5-benzyloxy-indolyl) methylamine (PF9601N) on mitochondrial permeability transition
-
DOI 10.1007/s00018-006-6105-8
-
Battaglia, V.; Sanz, E.; Salvi, M.; Unzeta, M.; Toninello, A. Protective effectof N-(2-propynyl)-2-(5-benzyloxy-indolyl)methylamine (PF9601N) onmitochondrial permeability transition. Cell. Mol. Life Sci., 2006, 63, 1440-1448. (Pubitemid 43939023)
-
(2006)
Cellular and Molecular Life Sciences
, vol.63
, Issue.12
, pp. 1440-1448
-
-
Battaglia, V.1
Sanz, E.2
Salvi, M.3
Unzeta, M.4
Toninello, A.5
-
128
-
-
77956553922
-
Antioxidant properties of PF9601N, a novel MAO-B inhibitor: Assessment ofits ability to interact with reactive nitrose species
-
Bellik, L.; Dragoni, S.; Pessina, F.; Sanz, E.; Unzeta, M.; Valoti, M.Antioxidant properties of PF9601N, a novel MAO-B inhibitor: assessment ofits ability to interact with reactive nitrose species. Acta Biochim. Pol., 2010, 57, 235-239.
-
(2010)
Acta Biochim. Pol.
, vol.57
, pp. 235-239
-
-
Bellik, L.1
Dragoni, S.2
Pessina, F.3
Sanz, E.4
Unzeta, M.5
Valoti, M.6
-
129
-
-
73949123501
-
Synthesis and in vitro evaluation ofpteridine analogues as monoamine oxidase B and nitric oxide synthaseinhibitors
-
Prins, L.H.A.; Petzer, J.P.; Malan, S.F. Synthesis and in vitro evaluation ofpteridine analogues as monoamine oxidase B and nitric oxide synthaseinhibitors. Bioorg. Med. Chem., 2009, 17, 7523-7530.
-
(2009)
Bioorg. Med. Chem.
, vol.17
, pp. 7523-7530
-
-
Prins, L.H.A.1
Petzer, J.P.2
Malan, S.F.3
-
130
-
-
0033582238
-
Nitric oxide synthase in cardiac sarcoplasmic reticulum
-
DOI 10.1073/pnas.96.2.657
-
Xu, K.Y.; Huso, D.L.; Dawson, T.M.; Bredt, D.S.; Becker, L.C. Nitric oxidesynthase in cardiac sarcoplasmic reticulum. Proc. Natl. Acad. Sci. USA, 1999, 96, 657-662. (Pubitemid 29061264)
-
(1999)
Proceedings of the National Academy of Sciences of the United States of America
, vol.96
, Issue.2
, pp. 657-662
-
-
Xu, K.Y.1
Huso, D.L.2
Dawson, T.M.3
Bredt, D.S.4
Becker, L.C.5
-
131
-
-
70450228608
-
Nitroindazole compounds inhibit theoxidative activation of 1-methyl-4-phenyl-1, 2, 3, 6-tetrahydropyridine(MPTP) neurotoxin to neurotoxic pyridinium cations by human monoamineoxidase (MAO
-
Herraiz, T.; Aran, V. J.; Guillen, H. Nitroindazole compounds inhibit theoxidative activation of 1-methyl-4-phenyl-1, 2, 3, 6-tetrahydropyridine(MPTP) neurotoxin to neurotoxic pyridinium cations by human monoamineoxidase (MAO). Free Radical Res., 2009, 43, 975-984.
-
(2009)
Free Radical Res.
, vol.43
, pp. 975-984
-
-
Herraiz, T.1
Aran, V.J.2
Guillen, H.3
-
132
-
-
0030938169
-
The neuronal nitric oxide synthase inhibitor 7-nitroindazole also inhibits the monoamine oxidase-B-catalyzed oxidation of 1 -methyl-4-phenyl- 1,2,3,6-tetrahydropyridine
-
DOI 10.1021/tx970001d
-
Castagnoli, K.; Palmer, S.; Anderson, A.; Bueters, T.; Castagnoli, N.Jr. Theneuronal nitric oxide synthase inhibitor 7-nitroindazole also inhibits themonoamine oxidase-B-catalyzed oxidation of 1-methyl-4-phenyl-1, 2, 3, 6-tetrahydropyridine. Chem. Res. Toxicol., 1997, 10, 364-368. (Pubitemid 27176296)
-
(1997)
Chemical Research in Toxicology
, vol.10
, Issue.4
, pp. 364-368
-
-
Castagnoli, K.1
Palmer, S.2
Anderson, A.3
Bueters, T.4
Castagnoli Jr., N.5
-
133
-
-
40949144116
-
In vitro and in vivoevidences that antioxidant action contributes to the neuroprotective effects ofthe neuronal nitric oxide synthase and monoamine oxidase-B inhibitor, 7-nitroindazole
-
Thomas, B.; Saravanan, K.S.; Mohanakumar, K.P. In vitro and in vivoevidences that antioxidant action contributes to the neuroprotective effects ofthe neuronal nitric oxide synthase and monoamine oxidase-B inhibitor, 7-nitroindazole. Neurochem. Int., 2008, 52, 990-1001.
-
(2008)
Neurochem. Int.
, vol.52
, pp. 990-1001
-
-
Thomas, B.1
Saravanan, K.S.2
Mohanakumar, K.P.3
-
134
-
-
0027323351
-
Inhibition of rat cerebellar nitric oxide synthase by 7-nitro indazole and related substituted indazoles
-
Babbedge, R.C.; Bland-Ward, P.A.; Hart, S.L.; Moore, P.K. Inhibition of ratcerebellar nitric oxide synthase by 7-nitroindazole and related substitutedindazoles. Br. J. Pharmacol., 1993, 110, 225-228. (Pubitemid 23257783)
-
(1993)
British Journal of Pharmacology
, vol.110
, Issue.1
, pp. 225-228
-
-
Babbedge, R.C.1
Bland-Ward, P.A.2
Hart, S.L.3
Moore, P.K.4
-
135
-
-
0036451888
-
Non-cholinergic strategies for treating and preventing Alzheimer's disease
-
Doraiswamy, P.M. Non-cholinergic strategies for treating and preventingAlzheimer's disease. CNS Drugs, 2002, 16, 811-824. (Pubitemid 35440615)
-
(2002)
CNS Drugs
, vol.16
, Issue.12
, pp. 811-824
-
-
Doraiswamy, P.M.1
-
136
-
-
0030035582
-
Neurodegenerative disease: Searching for drugs that combatAlzheimer's
-
Marx, J. Neurodegenerative disease: searching for drugs that combatAlzheimer's. Science, 1996, 273, 50.
-
(1996)
Science
, vol.273
, pp. 50
-
-
Marx, J.1
-
137
-
-
0036812560
-
From epidemiology to therapeutic trials with anti-inflammatory drugs in Alzheimer's disease: The role of NSAIDs and cyclooxygenase in β-amyloidosis and clinical dementia
-
Pasinetti, G.M. From epidemiology to therapeutic trials with antiinflammatorydrugs in Alzheimer's disease: the role of NSAIDs andcyclooxygenase in beta-amyloidosis and clinical dementia. J. Alzheimer'sDis., 2002, 4, 435-445. (Pubitemid 35397809)
-
(2002)
Journal of Alzheimer's Disease
, vol.4
, Issue.5
, pp. 435-445
-
-
Pasinetti, G.M.1
-
138
-
-
0037638809
-
Effects of Rofecoxib or Naproxen vs Placebo on Alzheimer Disease Progression: A Randomized Controlled Trial
-
Aisen, P.S.; Schafer, K.A.; Grundman, M.; Pfeiffer, E.; Sano, M.; Davis, K.L.; Farlow, M.R.; Jin, S.; Thomas, R.G.; Thal, L.J. Effects of rofecoxib ornaproxen vs placebo on Alzheimer disease progression: a randomizedcontrolled trial. JAMA, 2003, 289, 2819-2826. (Pubitemid 37430117)
-
(2003)
Journal of the American Medical Association
, vol.289
, Issue.21
, pp. 2819-2826
-
-
Aisen, P.S.1
Schafer, K.A.2
Grundman, M.3
Pfeiffer, E.4
Sano, M.5
Davis, K.L.6
Farlow, M.R.7
Jin, S.8
Thomas, R.G.9
Thal, L.J.10
-
139
-
-
34447280369
-
A new therapeutic approach in Alzheimer disease: Some novel pyrazole derivatives as dual MAO-B inhibitors and antiinflammatory analgesics
-
DOI 10.1016/j.bmc.2007.06.004, PII S0968089607005287
-
Gökhan-Kelekçi, N.; Yabanoǧlu, S.; Küpeli, E.; Salg?n, U.; Özgen, Ö.; Uçar, G.; Yeşilada, E.; Kendi, E.; Yeşilada, A.; Bilgin, A.A. A new therapeuticapproach in Alzheimer disease: Some novel pyrazole derivatives as dualMAO-B inhibitors and anti-inflammatory analgesics. Bioorg. Med. Chem., 2007, 15, 5775-5786. (Pubitemid 47043476)
-
(2007)
Bioorganic and Medicinal Chemistry
, vol.15
, Issue.17
, pp. 5775-5786
-
-
Gokhan-Kelekci, N.1
Yabanoglu, S.2
Kupeli, E.3
Salgin, U.4
Ozgen, O.5
Ucar, G.6
Yesilada, E.7
Kendi, E.8
Yesilada, A.9
Bilgin, A.A.10
-
140
-
-
21044435784
-
Pathogenesis of levodopa-induced dyskinesia: Focus on D1 and D3 dopamine receptors
-
DOI 10.1016/j.parkreldis.2004.11.005, PII S1353802005000386
-
Guigoni, C.; Aubert, I.; Li, Q.; Gurevich, V.V.; Benovic, J.L.; Ferry, S.;Mach, U.; Stark, H.; Leriche, L.; Hakansson, K.; Bioulac, B.H.; Gross, C.E.;Sokoloff, P.; Fisone, G.; Gurevich, E.V.; Bloch, B.; Bezard, E. Pathogenesisof levodopa-induced dyskinesia: focus on D1 and D3 dopamine receptors.Parkinsonism Relat. D., 2005, 1, S25-S29. (Pubitemid 40693574)
-
(2005)
Parkinsonism and Related Disorders
, vol.11
, Issue.SUPPL. 1
-
-
Guigoni, C.1
Aubert, I.2
Li, Q.3
Gurevich, V.V.4
Benovic, J.L.5
Ferry, S.6
Mach, U.7
Stark, H.8
Leriche, L.9
Hakansson, K.10
Bioulac, B.H.11
Gross, C.E.12
Sokoloff, P.13
Fisone, G.14
Gurevich, E.V.15
Bloch, B.16
Bezard, E.17
-
141
-
-
0035874345
-
Neuroprotection by caffeine and A(2A) adenosine receptor inactivation in amodel of Parkinson's disease
-
Chen, J.F.; Xu, K.; Petzer, J.P.; Staal, R.; Xu, Y.H.; Beilstein, M.; Sonsalla, P.K.; Castagnoli, K.; Castagnoli, N.Jr.; Schwarzschild, M.A.Neuroprotection by caffeine and A(2A) adenosine receptor inactivation in amodel of Parkinson's disease. J. Neurosci., 2001, 21, RC143.
-
(2001)
J. Neurosci.
, vol.21
-
-
Chen, J.F.1
Xu, K.2
Petzer, J.P.3
Staal, R.4
Xu, Y.H.5
Beilstein, M.6
Sonsalla, P.K.7
Castagnoli, K.8
Castagnoli Jr., N.9
Schwarzschild, M.A.10
-
142
-
-
0042141599
-
2A antagonist prevents dopamine agonist-induced motor complications in animal models of Parkinson's disease
-
DOI 10.1016/S0014-4886(03)00250-4
-
Bibbiani, F.; Oh, J.D.; Petzer, J.P.; Castagnoli, N.Jr.; Chen, J.F.;Schwarzschild, M.A.; Chase, T.N. A2A antagonist prevents dopamineagonist-induced motor complications in animal models of Parkinson'sdisease. Exp. Neurol., 2003, 184, 285-294. (Pubitemid 37444038)
-
(2003)
Experimental Neurology
, vol.184
, Issue.1
, pp. 285-294
-
-
Bibbiani, F.1
Oh, J.D.2
Petzer, J.P.3
Castagnoli Jr., N.4
Chen, J.-F.5
Schwarzschild, M.A.6
Chase, T.N.7
-
143
-
-
33750171348
-
2A receptors in Parkinson's disease
-
DOI 10.1016/j.tins.2006.09.004, PII S0166223606002219
-
(a) Schwarzschild, M.A.; Agnati, L.; Fuxe, K.; Chen, J.F.; Morelli, M.Targeting adenosine A2A receptors in Parkinson's disease. Trends Neurosci., 2006, 29, 647-654 (Pubitemid 44602262)
-
(2006)
Trends in Neurosciences
, vol.29
, Issue.11
, pp. 647-654
-
-
Schwarzschild, M.A.1
Agnati, L.2
Fuxe, K.3
Chen, J.-F.4
Morelli, M.5
-
144
-
-
14544288232
-
2A receptor antagonists in Parkinson's disease
-
DOI 10.1016/j.pharmthera.2004.10.007
-
(b) Xu, K.; Bastia, E.; Schwarzschild, M. Therapeuticpotential of adenosine A(2A) receptor antagonists in Parkinson's disease.Pharmacol. Ther., 2005, 105, 267-310. (Pubitemid 40297894)
-
(2005)
Pharmacology and Therapeutics
, vol.105
, Issue.3
, pp. 267-310
-
-
Xu, K.1
Bastia, E.2
Schwarzschild, M.3
-
145
-
-
0028100413
-
Differential age-related changes of MAO-A and MAO-B in mouse brain and peripheral organs
-
DOI 10.1016/0197-4580(94)90071-X
-
(a) Saura, J.; Richards, J.G.; Mahy, N. Differential age-related changes ofMAO-A and MAO-B in mouse brain and peripheral organs. Neurobiol.Aging, 1994, 15, 399-408 (Pubitemid 24241808)
-
(1994)
Neurobiology of Aging
, vol.15
, Issue.4
, pp. 399-408
-
-
Saura, J.1
Richards, J.G.2
Mahy, N.3
-
146
-
-
0030768730
-
Age-related increases in brain monoamine oxidase B in living healthy human subjects
-
DOI 10.1016/S0197-4580(97)00037-7, PII S0197458097000377
-
(b) Fowler, J.S.; Volkow, N.D.; Wang, G.-J.;Logan, J.; Pappas, N.; Shea, C.; Macgregor, R. Age-related increases in brainmonoamine oxidase B in living healthy human subjects. Neurobiol. Aging, 1997, 18, 431-435. (Pubitemid 27435085)
-
(1997)
Neurobiology of Aging
, vol.18
, Issue.4
, pp. 431-435
-
-
Fowler, J.S.1
Volkow, N.D.2
Wang, G.-J.3
Logan, J.4
Pappas, N.5
Shea, C.6
MacGregor, R.7
-
147
-
-
0027189806
-
2-selective adenosine antagonists
-
DOI 10.1021/jm00062a005
-
Jacobson, K.A.; Gallo-Rodriguez, C.; Melman, N.; Fischer, B.; Maillard, M.;van Bergen, A.; van Galen, P.J.; Karton, Y. Structure-activity relationshipsof 8-styrylxanthines as A2-selective adenosine antagonists. J. Med. Chem., 1993, 36, 1333-1342. (Pubitemid 23164489)
-
(1993)
Journal of Medicinal Chemistry
, vol.36
, Issue.10
, pp. 1333-1342
-
-
Jacobson, K.A.1
Gallo-Rodriguez, C.2
Melman, N.3
Fischer, B.4
Maillard, M.5
Van Bergen, A.6
Van Galen, P.J.M.7
Karton, Y.8
-
148
-
-
0037184039
-
8-(3-Chlorostyryl)caffeine may attenuate MPTP neurotoxicity through dualactions of monoamine oxidase inhibition and A2A receptor antagonism
-
Chen, J.F.; Steyn, S.; Staal, R.; Petzer, J.P.; Xu, K.; Van Der Schyf, C.J.;Castagnoli, K.; Sonsalla, P.K.; Castagnoli, N.Jr.; Schwarzschild, M.A. 8-(3-Chlorostyryl)caffeine may attenuate MPTP neurotoxicity through dualactions of monoamine oxidase inhibition and A2A receptor antagonism. J. Biol. Chem., 2002, 277, 36040-36044.
-
(2002)
J. Biol. Chem.
, vol.277
, pp. 36040-36044
-
-
Chen, J.F.1
Steyn, S.2
Staal, R.3
Petzer, J.P.4
Xu, K.5
Van Der Schyf, C.J.6
Castagnoli, K.7
Sonsalla, P.K.8
Castagnoli Jr., N.9
Schwarzschild, M.A.10
-
149
-
-
0037375621
-
2A receptor antagonists
-
DOI 10.1016/S0968-0896(02)00648-X
-
Petzer, J.P.; Steyn, S.; Castagnoli, K.P.; Chen, J.F.; Schwarzschild, M.A.;Van der Schyf, C.J.; Castagnoli, N. Inhibition of monoamine oxidase B byselective adenosine A2A receptor antagonists. Bioorg. Med. Chem., 2003, 11, 1299-1310. (Pubitemid 36293525)
-
(2003)
Bioorganic and Medicinal Chemistry
, vol.11
, Issue.7
, pp. 1299-1310
-
-
Petzer, J.P.1
Steyn, S.2
Castagnoli, K.P.3
Chen, J.-F.4
Schwarzschild, M.A.5
Van Der Schyf, C.J.6
Castagnoli, N.7
-
150
-
-
51449101712
-
Dualinhibition of monoamine oxidase B and antagonism of the adenosine A2Areceptor by (E, E)-8-(4-phenylbutadien-1-yl)caffeine analogues
-
Pretorius, J.; Malan, S.F.; Castagnoli, N.Jr.; Bergh, J.J.; Petzer, J.P. Dualinhibition of monoamine oxidase B and antagonism of the adenosine A2Areceptor by (E, E)-8-(4-phenylbutadien-1-yl)caffeine analogues. Bioorg. Med.Chem., 2008, 16, 8676-8684.
-
(2008)
Bioorg. Med.Chem.
, vol.16
, pp. 8676-8684
-
-
Pretorius, J.1
Malan, S.F.2
Castagnoli Jr., N.3
Bergh, J.J.4
Petzer, J.P.5
-
151
-
-
0027453490
-
Activation of protein kinase C inhibits cellular production of the amyloid β-protein
-
(a) Hung, A.Y.; Haass, C.; Nitsch, R.M.; Qiu, W.Q.; Citron, M.; Wurtman, R.J.; Growdon, J.H.; Selkoe, D.J. Activation of protein kinase C inhibitscellular production of the amyloid beta-protein. J. Biol. Chem., 1993, 268, 22959-22962 (Pubitemid 23327996)
-
(1993)
Journal of Biological Chemistry
, vol.268
, Issue.31
, pp. 22959-22962
-
-
Hung, A.Y.1
Haass, C.2
Nitsch, R.M.3
Wei Qiao Qiu4
Citron, M.5
Wurtman, R.J.6
Growdon, J.H.7
Selkoe, D.J.8
-
152
-
-
36749037180
-
Role of the APP non-amyloidogenic signaling pathway and targeting α-secretase as an alternative drug target for treatment of Alzheimer's diseases
-
DOI 10.2174/092986707782360060
-
(b) Bandyopadhyay, S.; Goldstein, L.E.; Lahiri, D.K.; Rogers, J.T. Role of the APP non-amyloidogenic signaling pathway and targetingalpha-secretase as an alternative drug target for treatment of Alzheimer'sdisease. Curr. Med. Chem., 2007, 14, 2848-2864 (Pubitemid 350201652)
-
(2007)
Current Medicinal Chemistry
, vol.14
, Issue.27
, pp. 2848-2864
-
-
Bandyopadhyay, S.1
Goldstein, L.E.2
Lahiri, D.K.3
Rogers, J.T.4
-
153
-
-
77957374286
-
Propargylamine containingcompounds as modulators of proteolytic cleavage of amyloid-beta proteinprecursor: Involvement of MAPK and PKC activation
-
(c) Bar-Am, O.; Amit, T.;Weinreb, O.; Youdim, M.B.H.; Mandel, S. Propargylamine containingcompounds as modulators of proteolytic cleavage of amyloid-beta proteinprecursor: involvement of MAPK and PKC activation. J. Alzheimer's Dis., 2010, 21, 361-371.
-
(2010)
J. Alzheimer's Dis.
, vol.21
, pp. 361-371
-
-
Bar-Am, O.1
Amit, T.2
Weinreb, O.3
Youdim, M.B.H.4
Mandel, S.5
-
154
-
-
0036777108
-
Involvement of MAP kinase in the regulation of amyloid precursor proteinprocessing by novel cholinesterase inhibitors derived from rasagiline
-
Yogev-Falach, M.; Amit, T.; Bar-Am, O.; Weinstock, M.; Youdim, M.B.H.Involvement of MAP kinase in the regulation of amyloid precursor proteinprocessing by novel cholinesterase inhibitors derived from rasagiline. FASEBJ., 2002, 16, 1674-1676.
-
(2002)
FASEBJ.
, vol.16
, pp. 1674-1676
-
-
Yogev-Falach, M.1
Amit, T.2
Bar-Am, O.3
Weinstock, M.4
Youdim, M.B.H.5
-
155
-
-
38949121975
-
New 1, 2, 3, 4-tetrahydroisoquinoline derivatives as modulators ofproteolytic cleavage of amyloid precursor proteins
-
Hu, M.K.; Liao, Y.F.; Chen, J.F.; Wang, B.J.; Tung, Y.T.; Lin, H.C.; Lee, K.P. New 1, 2, 3, 4-tetrahydroisoquinoline derivatives as modulators ofproteolytic cleavage of amyloid precursor proteins. Bioorg. Med. Chem., 2008, 16, 1957-1965.
-
(2008)
Bioorg. Med. Chem.
, vol.16
, pp. 1957-1965
-
-
Hu, M.K.1
Liao, Y.F.2
Chen, J.F.3
Wang, B.J.4
Tung, Y.T.5
Lin, H.C.6
Lee, K.P.7
-
156
-
-
33846054367
-
Zonisamide improves motor function in Parkinson disease: A randomized, double-blind study
-
DOI 10.1212/01.wnl.0000250236.75053.16, PII 0000611420070102000014
-
Murata, M.; Hasegawa, K.; Kanazawa, I.; Murata, M.; Hasegawa, K.;Kanazawa, I. The Japan Zonisamide on, P. D. S. G. Zonisamide improvesmotor function in Parkinson disease: a randomized, double-blind study.Neurology, 2007, 68, 45-50. (Pubitemid 46058551)
-
(2007)
Neurology
, vol.68
, Issue.1
, pp. 45-50
-
-
Murata, M.1
Hasegawa, K.2
Kanazawa, I.3
Aizawa, H.4
Kimura, T.5
Kikuchi, S.6
Baba, M.7
Chida, K.8
Hisanaga, K.9
Toyoshima, I.10
Kurita, K.11
Suzuki, Y.12
Yoshizawa, K.13
Shoji, S.14
Nakano, I.15
Hirata, K.16
Kamakura, K.17
Shimizu, T.18
Nogawa, S.19
Utsumi, H.20
Mizusawa, H.21
Yokochi, F.22
Hirabayashi, K.23
Hasegawa, K.24
Takahashi, Y.25
Kuroiwa, Y.26
Kameyama, S.27
Komai, K.28
Hashimoto, T.29
Mizoguchi, K.30
Mitake, S.31
Yasuda, T.32
Washimi, Y.33
Tatsuoka, Y.34
Matsumoto, S.35
Abe, K.36
Fujimura, H.37
Hashiguchi, H.38
Nakashima, K.39
Takamatsu, K.40
Yamada, T.41
Nomoto, M.42
Yuhi, T.43
Yamada, T.44
Ikezoe, K.45
Sato, A.46
Matsuo, H.47
Tsuruta, K.48
Arimura, K.49
Yuasa, T.50
Kawashima, N.51
Ishikawa, A.52
Yoshikawa, N.53
Higashi, Y.54
Ohnishi, H.55
Yoshinaga, J.56
Fujita, H.57
Katagi, R.58
Miyajima, H.59
Ojika, K.60
Kawamura, M.61
more..
-
157
-
-
34548431717
-
Clinical pharmacology and mechanism of action of zonisamide
-
DOI 10.1097/wnf.0b013e3180413d7d, PII 0000282620070700000007
-
Biton, V. Clinical pharmacology and mechanism of action of zonisamide.Clin. Neuropharmacol., 2007, 30, 230-240. (Pubitemid 47356720)
-
(2007)
Clinical Neuropharmacology
, vol.30
, Issue.4
, pp. 230-240
-
-
Biton, V.1
-
158
-
-
73949095157
-
Protective effects of a novel anti-parkinsonianagent zonisamide on dopamine quinone-related neurotoxicity
-
Asanuma, M.; Miyazaki, I. Protective effects of a novel anti-parkinsonianagent zonisamide on dopamine quinone-related neurotoxicity. Society forNeuroscience Program Nol 158, 2007, 1.
-
(2007)
Society ForNeuroscience Program Nol
, vol.158
, pp. 1
-
-
Asanuma, M.1
Miyazaki, I.2
-
159
-
-
0033794452
-
In vivo evaluation of hippocampalanti-oxidant ability of zonisamide in rats
-
Tokumaru, J.; Ueda, Y.; Yokoyama, H.; Nakajima, A.; Doi, T.; Mitsuyama, Y.; Ohya-Nishiguchi, H.; Kamada, H. In vivo evaluation of hippocampalanti- oxidant ability of zonisamide in rats. Neurochem. Res., 2000, 25, 1107-1111.
-
(2000)
Neurochem. Res.
, vol.25
, pp. 1107-1111
-
-
Tokumaru, J.1
Ueda, Y.2
Yokoyama, H.3
Nakajima, A.4
Doi, T.5
Mitsuyama, Y.6
Ohya-Nishiguchi, H.7
Kamada, H.8
-
160
-
-
73949127414
-
The antiepileptic drugzonisamide inhibits MAO-B and attenuates MPTP toxicity in mice: Clinicalrelevance
-
Sonsalla, P. K.; Wong, L.-Y.; Winnik, B.; Buckley, B. The antiepileptic drugzonisamide inhibits MAO-B and attenuates MPTP toxicity in mice: Clinicalrelevance. Exp. Neurol., 2010, 221, 329-334.
-
(2010)
Exp. Neurol.
, vol.221
, pp. 329-334
-
-
Sonsalla, P.K.1
Wong, L.-Y.2
Winnik, B.3
Buckley, B.4
-
161
-
-
79851502469
-
Interactions ofmonoamine oxidases with the antiepileptic drug zonisamide: Specificity ofinhibition and structure of the human monoamine oxidase B complex
-
Binda, C.; Aldeco, M.; Mattevi, A.; Edmondson, D.E. Interactions ofmonoamine oxidases with the antiepileptic drug zonisamide: Specificity ofinhibition and structure of the human monoamine oxidase B complex. J.Med. Chem., 2011, 54, 909-912.
-
(2011)
J.Med. Chem.
, vol.54
, pp. 909-912
-
-
Binda, C.1
Aldeco, M.2
Mattevi, A.3
Edmondson, D.E.4
-
162
-
-
20444499367
-
Acute treatment with the PPARγ agonist pioglitazone and ibuprofen reduces glial inflammation and Aβ1-42 levels in APPV717I transgenic mice
-
DOI 10.1093/brain/awh452
-
Heneka, M.T.; Sastre, M.; Dumitrescu-Ozimek, L.; Hanke, A.; Dewachter, I.;Kuiperi, C.; O'Banion, K.; Klockgether, T.; Van Leuven, F.; Landreth, G.E.Acute treatment with the PPARg agonist pioglitazone and ibuprofen reducesglial inflammation and Ab 1-42 levels in APPV7171 transgenic mice. Brain, 2005, 128, 1442-1453. (Pubitemid 40826196)
-
(2005)
Brain
, vol.128
, Issue.6
, pp. 1442-1453
-
-
Heneka, M.T.1
Sastre, M.2
Dumitrescu-Ozimek, L.3
Hanke, A.4
Dewachter, I.5
Kuiperi, C.6
O'Banion, K.7
Klockgether, T.8
Van Leuven, F.9
Landreth, G.E.10
-
163
-
-
0036326074
-
Protective action of the peroxisome proliferator-activated receptor-γ agonist pioglitazone in a mouse model of Parkinson's disease
-
DOI 10.1046/j.1471-4159.2002.00990.x
-
Breidert, T.; Callebert, J.; Heneka, M.T.; Landreth, G.; Launay, J.M.; Hirsch, E.C. Protective action of the peroxisome proliferator-activated receptor-γagonist pioglitazone in a mouse model of Parkinson's disease. J.Neurochem., 2002, 82, 615-624. (Pubitemid 34831499)
-
(2002)
Journal of Neurochemistry
, vol.82
, Issue.3
, pp. 615-624
-
-
Breidert, T.1
Callebert, J.2
Heneka, M.T.3
Landreth, G.4
Launay, J.M.5
Hirsch, E.C.6
-
164
-
-
0347087323
-
Protection by pioglitazone in the MPTP model of Parkinson's disease correlates with IκBα induction and block of NFκB and iNOS activation
-
Dehmer, T.; Heneka, M.T.; Sastre, M.; Dichgans, J.; Schultz, J.B. Protectionby pioglitazone in the MPTP model of Parkinson's disease correlates withIkBa induction and block of NFkB and iNOS activation. J. Neurochem., 2004, 88, 494-501. (Pubitemid 38084565)
-
(2004)
Journal of Neurochemistry
, vol.88
, Issue.2
, pp. 494-501
-
-
Dehmer, T.1
Heneka, M.T.2
Sastre, M.3
Dichgans, J.4
Schulz, J.B.5
-
165
-
-
42949100802
-
The PPARγ agonist pioglitazone is effective in the MPTP mouse model of Parkinson's disease through inhibition of monoamine oxidase B
-
DOI 10.1038/bjp.2008.78, PII BJP200878
-
Quinn, L.P.; Crook, B.; Hows, M.E.; Vidgeon-Hart, M.; Chapman, H.;Upton, N.; Medhurst, A.D.; Virley, D.J. The PPARγ agonist pioglitazone iseffective in the MPTP mouse model of Parkinson's disease throughinhibition of monoamine oxidase B. Br. J. Pharmacol., 2008, 154, 226-233. (Pubitemid 351620404)
-
(2008)
British Journal of Pharmacology
, vol.154
, Issue.1
, pp. 226-233
-
-
Quinn, L.P.1
Crook, B.2
Hows, M.E.3
Vidgeon-Hart, M.4
Chapman, H.5
Upton, N.6
Medhurst, A.D.7
Virley, D.J.8
-
166
-
-
0034651101
-
Inflammatory mechanisms in Alzheimer's disease: Inhibition of β- amyloid-stimulated proinflammatory responses and neurotoxicity by PPARγ agonists
-
(a) Combs, C.K.; Johnson, D.E.; Karlo, J.C.; Cannady, S.B.; Landreth, G.E.Inflammatory mechanisms in Alzheimer's disease: inhibition of betaamyloid-stimulated proinflammatory responses and neurotoxicity byPPARgamma agonists. J. Neurosci., 2000, 2, 558-567 (Pubitemid 30225558)
-
(2000)
Journal of Neuroscience
, vol.20
, Issue.2
, pp. 558-567
-
-
Combs, C.K.1
Johnson, D.E.2
Karlo, J.C.3
Cannady, S.B.4
Landreth, G.E.5
-
167
-
-
13644271368
-
Peroxisome proliferator-activated receptor γ is expressed in hippocampal neurons and its activation prevents β-amyloid neurodegeneration: Role of Wnt signaling
-
DOI 10.1016/j.yexcr.2004.09.032
-
(b) Inestrosa, N.C.;Godoy, J.A.; Quintanilla, R.A.; Koenig, C.S.; Bronfman, M. Peroxisomeproliferator-activated receptor gamma is expressed in hippocampal neuronsand its activation prevents beta-amyloid neurodegeneration: role of Wntsignalling. Exp. Cell Res., 2005, 304, 91-104. (Pubitemid 40227422)
-
(2005)
Experimental Cell Research
, vol.304
, Issue.1
, pp. 91-104
-
-
Inestrosa, N.C.1
Godoy, J.A.2
Quintanilla, R.A.3
Koenig, C.S.4
Bronfman, M.5
-
168
-
-
85073159603
-
Recent advances in QSAR studies. Methods and applications
-
Springer: Dordrecht, TheNetherlands
-
Recent advances in QSAR studies. Methods and applications. In: Challengesand Advances in Computational Chemistry and Physics, 1st ed., vol. 8.;Puzyn, T.; Leszczynski, J.; Cronin, M.T.D. Eds.; Springer: Dordrecht, TheNetherlands, 2010.
-
(2010)
Challengesand Advances in Computational Chemistry and Physics, 1st Ed.
, vol.8
-
-
Puzyn, T.1
Leszczynski, J.2
Cronin, M.T.D.3
-
169
-
-
0002036701
-
3D QSAR in drug design: Recent advances
-
Kluwer Academic Publishers: Dordrecht, The Netherlands
-
(a) 3D QSAR in drug design: recent advances. In: Perspectives in drugdiscovery and design, vol. 12-14; Kubinyi, H.; Folkers, G.; Martin, Y.C.Eds.; Kluwer Academic Publishers: Dordrecht, The Netherlands, 1998
-
(1998)
Perspectives in Drugdiscovery and Design
, vol.12-14
-
-
Kubinyi, H.1
Folkers, G.2
Martin, Y.C.3
-
170
-
-
0003476917
-
-
Kluwer AcademicPublishers: Dordrecht, The Netherlands
-
(b) 3DQSAR in drug design: ligand-protein interactions and molecular similarity, vol. 2; Kubinyi, H.; Folkers, G.; Martin, Y.C. Eds.; Kluwer AcademicPublishers: Dordrecht, The Netherlands, 1998.
-
(1998)
3DQSAR in Drug Design: Ligand-protein Interactions and Molecular Similarity
, vol.2
-
-
Kubinyi, H.1
Folkers, G.2
Martin, Y.C.3
|