250 related articles for article (PubMed ID: 20650633)
21. 2-Arylthiomorpholine derivatives as potent and selective monoamine oxidase B inhibitors.
Lühr S; Vilches-Herrera M; Fierro A; Ramsay RR; Edmondson DE; Reyes-Parada M; Cassels BK; Iturriaga-Vásquez P
Bioorg Med Chem; 2010 Feb; 18(4):1388-95. PubMed ID: 20123154
[TBL] [Abstract][Full Text] [Related]
22. Fine molecular tuning at position 4 of 2H-chromen-2-one derivatives in the search of potent and selective monoamine oxidase B inhibitors.
Pisani L; Catto M; Nicolotti O; Grossi G; Di Braccio M; Soto-Otero R; Mendez-Alvarez E; Stefanachi A; Gadaleta D; Carotti A
Eur J Med Chem; 2013; 70():723-39. PubMed ID: 24231308
[TBL] [Abstract][Full Text] [Related]
23. Synthesis and inhibition study of monoamine oxidase, indoleamine 2,3-dioxygenase and tryptophan 2,3-dioxygenase by 3,8-substituted 5H-indeno[1,2-c]pyridazin-5-one derivatives.
Reniers J; Meinguet C; Moineaux L; Masereel B; Vincent SP; Frederick R; Wouters J
Eur J Med Chem; 2011 Dec; 46(12):6104-11. PubMed ID: 22018876
[TBL] [Abstract][Full Text] [Related]
24. Structure-activity study of the mechanism of 1-methyl-4-phenyl-1,2,3,6-tetrahydropyridine (MPTP)-induced neurotoxicity. I. Evaluation of the biological activity of MPTP analogs.
Youngster SK; Sonsalla PK; Sieber BA; Heikkila RE
J Pharmacol Exp Ther; 1989 Jun; 249(3):820-8. PubMed ID: 2786564
[TBL] [Abstract][Full Text] [Related]
25. Inhibition of monoamine oxidase by 8-phenoxymethylcaffeine derivatives.
Okaecwe T; Swanepoel AJ; Petzer A; Bergh JJ; Petzer JP
Bioorg Med Chem; 2012 Jul; 20(14):4336-47. PubMed ID: 22705191
[TBL] [Abstract][Full Text] [Related]
26. Sulfur-substituted alpha-alkyl phenethylamines as selective and reversible MAO-A inhibitors: biological activities, CoMFA analysis, and active site modeling.
Gallardo-Godoy A; Fierro A; McLean TH; Castillo M; Cassels BK; Reyes-Parada M; Nichols DE
J Med Chem; 2005 Apr; 48(7):2407-19. PubMed ID: 15801832
[TBL] [Abstract][Full Text] [Related]
27. Discovery, biological evaluation, and structure-activity and -selectivity relationships of 6'-substituted (E)-2-(benzofuran-3(2H)-ylidene)-N-methylacetamides, a novel class of potent and selective monoamine oxidase inhibitors.
Pisani L; Barletta M; Soto-Otero R; Nicolotti O; Mendez-Alvarez E; Catto M; Introcaso A; Stefanachi A; Cellamare S; Altomare C; Carotti A
J Med Chem; 2013 Mar; 56(6):2651-64. PubMed ID: 23437843
[TBL] [Abstract][Full Text] [Related]
28. Chromone, a 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
J Med Chem; 2011 Jul; 54(14):5165-73. PubMed ID: 21696156
[TBL] [Abstract][Full Text] [Related]
29. Characterization of N-methyl-4-phenyl-1,2,3,6-tetrahydropyridine (MPTP) binding sites in C57BL/6 mouse brain: mutual effects of monoamine oxidase inhibitors and sigma ligands on MPTP and sigma binding sites.
Itzhak Y; Mash D; Zhang SH; Stein I
Mol Pharmacol; 1991 Mar; 39(3):385-93. PubMed ID: 1848660
[TBL] [Abstract][Full Text] [Related]
30. Inhibition of monoamine oxidase B by selected benzimidazole and caffeine analogues.
van den Berg D; Zoellner KR; Ogunrombi MO; Malan SF; Terre'Blanche G; Castagnoli N; Bergh JJ; Petzer JP
Bioorg Med Chem; 2007 Jun; 15(11):3692-702. PubMed ID: 17416530
[TBL] [Abstract][Full Text] [Related]
31. New pyrrole inhibitors of monoamine oxidase: synthesis, biological evaluation, and structural determinants of MAO-A and MAO-B selectivity.
La Regina G; Silvestri R; Artico M; Lavecchia A; Novellino E; Befani O; Turini P; Agostinelli E
J Med Chem; 2007 Mar; 50(5):922-31. PubMed ID: 17256833
[TBL] [Abstract][Full Text] [Related]
32. Chromone 3-phenylcarboxamides as potent and selective MAO-B inhibitors.
Gaspar A; Reis J; Fonseca A; Milhazes N; Viña D; Uriarte E; Borges F
Bioorg Med Chem Lett; 2011 Jan; 21(2):707-9. PubMed ID: 21194943
[TBL] [Abstract][Full Text] [Related]
33. Monoamine oxidase inhibition by selected anilide derivatives.
Legoabe L; Kruger J; Petzer A; Bergh JJ; Petzer JP
Eur J Med Chem; 2011 Oct; 46(10):5162-74. PubMed ID: 21899930
[TBL] [Abstract][Full Text] [Related]
34. Novel sulfanylphthalimide analogues as highly potent inhibitors of monoamine oxidase B.
Van der Walt MM; Terre'Blanche G; Petzer A; Petzer JP
Bioorg Med Chem Lett; 2012 Nov; 22(21):6632-5. PubMed ID: 23010267
[TBL] [Abstract][Full Text] [Related]
35. Synthesis, structure-activity relationships and molecular modeling studies of new indole inhibitors of monoamine oxidases A and B.
La Regina G; Silvestri R; Gatti V; Lavecchia A; Novellino E; Befani O; Turini P; Agostinelli E
Bioorg Med Chem; 2008 Nov; 16(22):9729-40. PubMed ID: 18951803
[TBL] [Abstract][Full Text] [Related]
36. Nitroindazole compounds inhibit the oxidative activation of 1-methyl-4-phenyl-1,2,3,6-tetrahydropyridine (MPTP) neurotoxin to neurotoxic pyridinium cations by human monoamine oxidase (MAO).
Herraiz T; Arán VJ; Guillén H
Free Radic Res; 2009 Oct; 43(10):975-84. PubMed ID: 19669997
[TBL] [Abstract][Full Text] [Related]
37. Synthesis and evaluation of β-carboline derivatives as potential monoamine oxidase inhibitors.
Reniers J; Robert S; Frederick R; Masereel B; Vincent S; Wouters J
Bioorg Med Chem; 2011 Jan; 19(1):134-44. PubMed ID: 21183355
[TBL] [Abstract][Full Text] [Related]
38. New halogenated 3-phenylcoumarins as potent and selective MAO-B inhibitors.
Matos MJ; Viña D; Janeiro P; Borges F; Santana L; Uriarte E
Bioorg Med Chem Lett; 2010 Sep; 20(17):5157-60. PubMed ID: 20659799
[TBL] [Abstract][Full Text] [Related]
39. Synthesis and selective human monoamine oxidase B inhibition of heterocyclic hybrids based on hydrazine and thiazole scaffolds.
Carradori S; D'Ascenzio M; De Monte C; Secci D; Yáñez M
Arch Pharm (Weinheim); 2013 Jan; 346(1):17-22. PubMed ID: 23065686
[TBL] [Abstract][Full Text] [Related]
40. Thio- and aminocaffeine analogues as inhibitors of human monoamine oxidase.
Booysen HP; Moraal C; Terre'Blanche G; Petzer A; Bergh JJ; Petzer JP
Bioorg Med Chem; 2011 Dec; 19(24):7507-18. PubMed ID: 22055712
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]
