-
1
-
-
33745187327
-
Histone H3 lysine 4 demethylation is a target of nonselective antidepressive medications
-
Lee MG, Wynder C, Schmidt DM, McCafferty DG, &, Shiekhattar R, (2006) Histone H3 lysine 4 demethylation is a target of nonselective antidepressive medications. Chem Biol 13, 563-567.
-
(2006)
Chem Biol
, vol.13
, pp. 563-567
-
-
Lee, M.G.1
Wynder, C.2
Schmidt, D.M.3
McCafferty, D.G.4
Shiekhattar, R.5
-
2
-
-
34147173308
-
Trans-2-Phenylcyclopropylamine is a mechanism-based inactivator of the histone demethylase LSD1
-
Schmidt DMZ, &, McCafferty DG, (2007) trans-2-Phenylcyclopropylamine is a mechanism-based inactivator of the histone demethylase LSD1. Biochemistry 46, 4408-4416.
-
(2007)
Biochemistry
, vol.46
, pp. 4408-4416
-
-
Schmidt, D.M.Z.1
McCafferty, D.G.2
-
3
-
-
33645307953
-
The therapeutic potential of monoamine oxidase inhibitors
-
Youdim MBH, Edmondson D, &, Tipton KF, (2006) The therapeutic potential of monoamine oxidase inhibitors. Nat Rev Neurosci 7, 295-309.
-
(2006)
Nat Rev Neurosci
, vol.7
, pp. 295-309
-
-
Youdim, M.B.H.1
Edmondson, D.2
Tipton, K.F.3
-
4
-
-
84878667982
-
An overview of phenylcyclopropylamine derivatives: Biochemical and biological significance and recent developments
-
Khan MNA, Suzuki T, &, Miyata N, (2013) An overview of phenylcyclopropylamine derivatives: biochemical and biological significance and recent developments. Med Res Rev 33, 873-910.
-
(2013)
Med Res Rev
, vol.33
, pp. 873-910
-
-
Khan, M.N.A.1
Suzuki, T.2
Miyata, N.3
-
5
-
-
77952355653
-
Biochemical, structural, and biological evaluation of tranylcypromine derivatives as inhibitors of histone demethylases LSD1 and LSD2
-
Binda C, Valente S, Romanenghi M, Pilotto S, Cirilli R, Karytinos A, Ciossani G, Botrugno OA, Forneris F, Tardugno M, et al,. (2010) Biochemical, structural, and biological evaluation of tranylcypromine derivatives as inhibitors of histone demethylases LSD1 and LSD2. J Am Chem Soc 132, 6827-6833.
-
(2010)
J Am Chem Soc
, vol.132
, pp. 6827-6833
-
-
Binda, C.1
Valente, S.2
Romanenghi, M.3
Pilotto, S.4
Cirilli, R.5
Karytinos, A.6
Ciossani, G.7
Botrugno, O.A.8
Forneris, F.9
Tardugno, M.10
Al, E.11
-
6
-
-
37549022689
-
Crystal structure of histone demethylase LSD1 and tranylcypromine at 2.25 Å
-
Mimasu S, Sengoku T, Fukuzawa S, Umehara T, &, Yokoyama S, (2008) Crystal structure of histone demethylase LSD1 and tranylcypromine at 2.25 Å. Biochem Biophys Res Commun 366, 15-22.
-
(2008)
Biochem Biophys Res Commun
, vol.366
, pp. 15-22
-
-
Mimasu, S.1
Sengoku, T.2
Fukuzawa, S.3
Umehara, T.4
Yokoyama, S.5
-
7
-
-
34250203607
-
Mechanistic analysis of a suicide inactivator of histone demethylase LSD1
-
Szewczuk LM, Culhane JC, Yang M, Majumdar A, Yu H, &, Cole PA, (2007) Mechanistic analysis of a suicide inactivator of histone demethylase LSD1. Biochemistry 46, 6892-6902.
-
(2007)
Biochemistry
, vol.46
, pp. 6892-6902
-
-
Szewczuk, L.M.1
Culhane, J.C.2
Yang, M.3
Majumdar, A.4
Yu, H.5
Cole, P.A.6
-
8
-
-
34447338875
-
Structural basis for the inhibition of the LSD1 histone demethylase by the antidepressant trans-2-phenylcyclopropylamine
-
Yang M, Culhane JC, Szewczuk LM, Jalili P, Ball HL, Machius M, Cole PA, &, Yu H, (2007) Structural basis for the inhibition of the LSD1 histone demethylase by the antidepressant trans-2-phenylcyclopropylamine. Biochemistry 46, 8058-8065.
-
(2007)
Biochemistry
, vol.46
, pp. 8058-8065
-
-
Yang, M.1
Culhane, J.C.2
Szewczuk, L.M.3
Jalili, P.4
Ball, H.L.5
Machius, M.6
Cole, P.A.7
Yu, H.8
-
9
-
-
84906839626
-
Synthesis, biological activity and mechanistic insights of 1-substituted cyclopropylamine derivatives: A novel class of irreversible inhibitors of histone demethylase KDM1A
-
Vianello P, Botrugno OA, Cappa A, Ciossani G, Dessanti P, Mai A, Mattevi A, Meroni G, Minucci S, Thaler F, et al,. (2014) Synthesis, biological activity and mechanistic insights of 1-substituted cyclopropylamine derivatives: a novel class of irreversible inhibitors of histone demethylase KDM1A. Eur J Med Chem 86, 352-363.
-
(2014)
Eur J Med Chem
, vol.86
, pp. 352-363
-
-
Vianello, P.1
Botrugno, O.A.2
Cappa, A.3
Ciossani, G.4
Dessanti, P.5
Mai, A.6
Mattevi, A.7
Meroni, G.8
Minucci, S.9
Thaler, F.10
Al, E.11
-
10
-
-
0014430109
-
Mitochondrial monoamine oxidase. II. Action of various inhibitors for the bovine kidney enzyme. Catalytic mechanism
-
Hellerman L, &, Erwin VG, (1968) Mitochondrial monoamine oxidase. II. Action of various inhibitors for the bovine kidney enzyme. Catalytic mechanism. J Biol Chem 243, 5234-5243.
-
(1968)
J Biol Chem
, vol.243
, pp. 5234-5243
-
-
Hellerman, L.1
Erwin, V.G.2
-
11
-
-
0015509630
-
Multiple forms of monoamine oxidase. Comparison of in vitro and in vivo inhibition patterns
-
Collins GG, Youdim MB, &, Sandler M, (1972) Multiple forms of monoamine oxidase. Comparison of in vitro and in vivo inhibition patterns. Biochem Pharmacol 21, 1995-1998.
-
(1972)
Biochem Pharmacol
, vol.21
, pp. 1995-1998
-
-
Collins, G.G.1
Youdim, M.B.2
Sandler, M.3
-
12
-
-
0016152101
-
Efficacy of antidepressant drugs - A review of research (1958 to 1972)
-
Morris JB, &, Beck AT, (1974) Efficacy of antidepressant drugs-a review of research (1958 to 1972). Arch Gen Psychiatry 30, 667-674.
-
(1974)
Arch Gen Psychiatry
, vol.30
, pp. 667-674
-
-
Morris, J.B.1
Beck, A.T.2
-
13
-
-
77949421463
-
Comparative analysis of small molecules and histone substrate analogues as LSD1 lysine demethylase inhibitors
-
Culhane JC, Wang D, Yen PM, &, Cole PA, (2010) Comparative analysis of small molecules and histone substrate analogues as LSD1 lysine demethylase inhibitors. J Am Chem Soc 132, 3164-3176.
-
(2010)
J Am Chem Soc
, vol.132
, pp. 3164-3176
-
-
Culhane, J.C.1
Wang, D.2
Yen, P.M.3
Cole, P.A.4
-
14
-
-
84939243063
-
New substituted cyclopropylamine compounds useful for treating cancer E.G. Glioblastomas, Bannayan-Zonana syndrome, Cowden disease, inflammatory breast cancer, Wilm's tumor, Ewing's sarcoma, and giant cell tumor of bone and thyroid
-
Johnson NW, Kasparec J, Miller WH, Rouse MB, Suarez D, Tian X, Dominic S, Jiri K, Meagan RB, Neil JW, et al,. (2012) New substituted cyclopropylamine compounds useful for treating cancer e.g. glioblastomas, Bannayan-Zonana syndrome, Cowden disease, inflammatory breast cancer, Wilm's tumor, Ewing's sarcoma, and giant cell tumor of bone and thyroid. WO2012135113-A2; Glaxosmithkline Llc (GLAX-C).
-
(2012)
Glaxosmithkline LLC (GLAX-C)
-
-
Johnson, N.W.1
Kasparec, J.2
Miller, W.H.3
Rouse, M.B.4
Suarez, D.5
Tian, X.6
Dominic, S.7
Jiri, K.8
Meagan, R.B.9
Neil, J.W.10
Al, E.11
-
15
-
-
84939233768
-
New (hetero)aryl cyclopropylamine compound, useful for treating cancer, Alzheimer's disease, Huntington disease, Parkinson's disease, herpesvirus infection and viral reactivation after latency
-
Ortega Munoz A, Fyfe MCT, Martinell Pedemonte M, Estiarte Martinez MDL, Valls Vidal N, Kurz G, Castro Palomino Laria JC, Ortega MA, Martinell PM, Estiarte MMDL, et al,. (2013) New (hetero)aryl cyclopropylamine compound, useful for treating cancer, Alzheimer's disease, Huntington disease, Parkinson's disease, herpesvirus infection and viral reactivation after latency. WO2013057322-A1; Oryzon Genomics SA (ORYZ-Non-standard).
-
(2013)
Oryzon Genomics SA (ORYZ-Non-standard)
-
-
Ortega Munoz, A.1
Fyfe, M.C.T.2
Martinell Pedemonte, M.3
Estiarte Martinez, M.D.L.4
Valls Vidal, N.5
Kurz, G.6
Castro Palomino Laria, J.C.7
Ortega, M.A.8
Martinell, P.M.9
Estiarte, M.10
Al, E.11
-
16
-
-
84869455559
-
LSD1 inhibition: A therapeutic strategy in cancer?
-
Lynch JT, Harris WJ, &, Somervaille TCP, (2012) LSD1 inhibition: a therapeutic strategy in cancer? Exp Opin Therap Targ 16, 1239-1249.
-
(2012)
Exp Opin Therap Targ
, vol.16
, pp. 1239-1249
-
-
Lynch, J.T.1
Harris, W.J.2
Somervaille, T.C.P.3
-
17
-
-
84882700612
-
Effects of the monoamine oxidase inhibitors pargyline and tranylcypromine on cellular proliferation in human prostate cancer cells
-
Lee HT, Choi MR, Doh MS, Jung KH, &, Chai YG, (2013) Effects of the monoamine oxidase inhibitors pargyline and tranylcypromine on cellular proliferation in human prostate cancer cells. Oncol Rep 30, 1587-1592.
-
(2013)
Oncol Rep
, vol.30
, pp. 1587-1592
-
-
Lee, H.T.1
Choi, M.R.2
Doh, M.S.3
Jung, K.H.4
Chai, Y.G.5
-
18
-
-
0003321976
-
Amine oxidases. XIX. Inhibition of monoamine oxidase by phenylcyclopropylamines and iproniazid
-
Zeller EA, &, Sarkar S, (1962) Amine oxidases. XIX. Inhibition of monoamine oxidase by phenylcyclopropylamines and iproniazid. J Biol Chem 237, 2333-2336.
-
(1962)
J Biol Chem
, vol.237
, pp. 2333-2336
-
-
Zeller, E.A.1
Sarkar, S.2
-
19
-
-
77952375043
-
2-Substituted cyclopropylamines. II. Effect of structure upon monoamine oxidase-inhibitory activity as measured in vivo by potentiation of tryptamine convulsions
-
Zirkle CL, Kaiser C, Tedeschi DH, Tedeschi RE, &, Burger A, (1962) 2-Substituted cyclopropylamines. II. Effect of structure upon monoamine oxidase-inhibitory activity as measured in vivo by potentiation of tryptamine convulsions. J Med Pharmaceut Chem 91, 1265-1284.
-
(1962)
J Med Pharmaceut Chem
, vol.91
, pp. 1265-1284
-
-
Zirkle, C.L.1
Kaiser, C.2
Tedeschi, D.H.3
Tedeschi, R.E.4
Burger, A.5
-
20
-
-
0025148750
-
Quantitative structure-activity relationships in MAO-inhibitory 2-phenylcyclopropylamines: Insights into the topography of MAO-A and MAO-B
-
Kang GI, &, Hong SK, (1990) Quantitative structure-activity relationships in MAO-inhibitory 2-phenylcyclopropylamines: insights into the topography of MAO-A and MAO-B. Arch Pharmacal Res (Seoul) 13, 82-96.
-
(1990)
Arch Pharmacal Res (Seoul)
, vol.13
, pp. 82-96
-
-
Kang, G.I.1
Hong, S.K.2
-
21
-
-
0019505669
-
Anti-depressant efficacy of tranylcypromine isomers - A controlled study
-
Moises HW, &, Beckmann H, (1981) Anti-depressant efficacy of tranylcypromine isomers-a controlled study. J Neural Transm 50, 185-192.
-
(1981)
J Neural Transm
, vol.50
, pp. 185-192
-
-
Moises, H.W.1
Beckmann, H.2
-
22
-
-
79958247128
-
Enantioselective synthesis of tranylcypromine analogues as lysine demethylase (LSD1) inhibitors
-
Benelkebir H, Hodgkinson C, Duriez PJ, Hayden AL, Bulleid RA, Crabb SJ, Packham G, &, Ganesan A, (2011) Enantioselective synthesis of tranylcypromine analogues as lysine demethylase (LSD1) inhibitors. Bioorg Med Chem 19, 3709-3716.
-
(2011)
Bioorg Med Chem
, vol.19
, pp. 3709-3716
-
-
Benelkebir, H.1
Hodgkinson, C.2
Duriez, P.J.3
Hayden, A.L.4
Bulleid, R.A.5
Crabb, S.J.6
Packham, G.7
Ganesan, A.8
-
23
-
-
84875424030
-
Synthesis of cis-2-alkoxycyclopropylamines via intramolecular cyclization of 2-azaallylic anions derived from alkoxybrominated N-(arylidene)-2-methyl-2-propenylamines
-
Mangelinckx S, Kadam ST, Semina E, Callebaut G, Colpaert F, De Smaele D, &, De Kimpe N, (2013) Synthesis of cis-2-alkoxycyclopropylamines via intramolecular cyclization of 2-azaallylic anions derived from alkoxybrominated N-(arylidene)-2-methyl-2-propenylamines. Tetrahedron 69, 3728-3735.
-
(2013)
Tetrahedron
, vol.69
, pp. 3728-3735
-
-
Mangelinckx, S.1
Kadam, S.T.2
Semina, E.3
Callebaut, G.4
Colpaert, F.5
De Smaele, D.6
De Kimpe, N.7
-
24
-
-
0015530606
-
Human brain monoamine oxidase: Multiple forms and selective inhibitors
-
Youdim MB, Collins GG, Sandler M, Bevan Jones AB, Pare CM, &, Nicholson WJ, (1972) Human brain monoamine oxidase: multiple forms and selective inhibitors. Nature 236, 225-228.
-
(1972)
Nature
, vol.236
, pp. 225-228
-
-
Youdim, M.B.1
Collins, G.G.2
Sandler, M.3
Bevan Jones, A.B.4
Pare, C.M.5
Nicholson, W.J.6
-
25
-
-
0025583472
-
Ring-substituted analogues of tranylcypromine as monoamine oxidase inhibitors
-
Sherry RL, Baker GB, Coutts RT, &, Mousseau DD, (1990) Ring-substituted analogues of tranylcypromine as monoamine oxidase inhibitors. J Neural Transm (Suppl) 32, 107-112.
-
(1990)
J Neural Transm (Suppl)
, vol.32
, pp. 107-112
-
-
Sherry, R.L.1
Baker, G.B.2
Coutts, R.T.3
Mousseau, D.D.4
-
26
-
-
78049530845
-
Potentiation of ligand binding through cooperative effects in monoamine oxidase B
-
Bonivento D, Milczek EM, McDonald GR, Binda C, Holt A, Edmondson DE, &, Mattevi A, (2010) Potentiation of ligand binding through cooperative effects in monoamine oxidase B. J Biol Chem 285, 36849-36856.
-
(2010)
J Biol Chem
, vol.285
, pp. 36849-36856
-
-
Bonivento, D.1
Milczek, E.M.2
McDonald, G.R.3
Binda, C.4
Holt, A.5
Edmondson, D.E.6
Mattevi, A.7
-
27
-
-
78049526876
-
On the formation and nature of the imidazoline I(2) binding site on human monoamine oxidase-B
-
McDonald GR, Olivieri A, Ramsay RR, &, Holt A, (2010) On the formation and nature of the imidazoline I(2) binding site on human monoamine oxidase-B. Pharmacol Res 62, 475-488.
-
(2010)
Pharmacol Res
, vol.62
, pp. 475-488
-
-
McDonald, G.R.1
Olivieri, A.2
Ramsay, R.R.3
Holt, A.4
-
28
-
-
84899813177
-
Computational comparison of imidazoline association with the 12 binding site in human monoamine oxidases
-
Basile L, Pappalardo M, Guccione S, Milardi D, &, Ramsay RR, (2014) Computational comparison of imidazoline association with the 12 binding site in human monoamine oxidases. J Chem Inf Model 54, 1200-1207.
-
(2014)
J Chem Inf Model
, vol.54
, pp. 1200-1207
-
-
Basile, L.1
Pappalardo, M.2
Guccione, S.3
Milardi, D.4
Ramsay, R.R.5
-
29
-
-
69249111386
-
Synthesis and molecular modeling of some novel hexahydroindazole derivatives as potent monoamine oxidase inhibitors
-
Gokhan-Kelekci N, Simsek OO, Ercan A, Yelekci K, Sahin ZS, Isik S, Ucar G, &, Bilgin AA, (2009) Synthesis and molecular modeling of some novel hexahydroindazole derivatives as potent monoamine oxidase inhibitors. Bioorg Med Chem 17, 6761-6772.
-
(2009)
Bioorg Med Chem
, vol.17
, pp. 6761-6772
-
-
Gokhan-Kelekci, N.1
Simsek, O.O.2
Ercan, A.3
Yelekci, K.4
Sahin, Z.S.5
Isik, S.6
Ucar, G.7
Bilgin, A.A.8
-
30
-
-
11644261806
-
Automated docking using a Lamarckian genetic algorithm and empirical binding free energy function
-
Morris GM, Goodsell DS, Halliday RS, Huey R, Hart WE, Belew RK, &, Olson AJ, (1998) Automated docking using a Lamarckian genetic algorithm and empirical binding free energy function. J Comp Chem 19, 1639-1662.
-
(1998)
J Comp Chem
, vol.19
, pp. 1639-1662
-
-
Morris, G.M.1
Goodsell, D.S.2
Halliday, R.S.3
Huey, R.4
Hart, W.E.5
Belew, R.K.6
Olson, A.J.7
-
31
-
-
76149120388
-
AutoDock Vina: Improving the speed and accuracy of docking with a new scoring function, efficient optimization, and multithreading
-
Trott O, &, Olson AJ, (2010) AutoDock Vina: improving the speed and accuracy of docking with a new scoring function, efficient optimization, and multithreading. J Comput Chem 31, 455-461.
-
(2010)
J Comput Chem
, vol.31
, pp. 455-461
-
-
Trott, O.1
Olson, A.J.2
-
32
-
-
80051634935
-
An improved approach to steady-state analysis of monoamine oxidases
-
Ramsay RR, Olivieri A, &, Holt A, (2011) An improved approach to steady-state analysis of monoamine oxidases. J Neural Transm 118, 1003-1019.
-
(2011)
J Neural Transm
, vol.118
, pp. 1003-1019
-
-
Ramsay, R.R.1
Olivieri, A.2
Holt, A.3
-
33
-
-
73649151319
-
Esters of methanesulfonic acid as irreversible inhibitors of acetylcholinesterase
-
Kitz R, &, Wilson IB, (1962) Esters of methanesulfonic acid as irreversible inhibitors of acetylcholinesterase. J Biol Chem 237, 3245-3249.
-
(1962)
J Biol Chem
, vol.237
, pp. 3245-3249
-
-
Kitz, R.1
Wilson, I.B.2
-
34
-
-
34547698945
-
Structural insights into the mechanism of amine oxidation by monoamine oxidases A and B
-
Edmondson DE, Binda C, &, Mattevi A, (2007) Structural insights into the mechanism of amine oxidation by monoamine oxidases A and B. Arch Biochem Biophys 464, 269-276.
-
(2007)
Arch Biochem Biophys
, vol.464
, pp. 269-276
-
-
Edmondson, D.E.1
Binda, C.2
Mattevi, A.3
-
35
-
-
0036140732
-
Structure of human monoamine oxidase B, a drug target for the treatment of neurological disorders
-
Binda C, Newton-Vinson P, Hubalek F, Edmondson DE, &, Mattevi A, (2002) Structure of human monoamine oxidase B, a drug target for the treatment of neurological disorders. Nat Struct Biol 9, 22-26.
-
(2002)
Nat Struct Biol
, vol.9
, pp. 22-26
-
-
Binda, C.1
Newton-Vinson, P.2
Hubalek, F.3
Edmondson, D.E.4
Mattevi, A.5
-
36
-
-
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 DE, &, Mattevi A, (2005) 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 USA 102, 12684-12689.
-
(2005)
Proc Natl Acad Sci USA
, vol.102
, pp. 12684-12689
-
-
De Colibus, L.1
Li, M.2
Binda, C.3
Lustig, A.4
Edmondson, D.E.5
Mattevi, A.6
-
37
-
-
24944456335
-
Subtle differences between MAO A and its cysteine 374 mutant during mechanism-based inactivation by cyclopropylamines
-
In (Chapman S.K. Perham R.N. & Scrutton N.S. eds), Rudolph Weber, Berlin.
-
Vintem A-PB, Ramsay RR, &, Silverman RB, (2002) Subtle differences between MAO A and its cysteine 374 mutant during mechanism-based inactivation by cyclopropylamines. In Flavins and Flavoproteins 2002 (, Chapman SK, Perham RN, &, Scrutton NS, eds), pp. 911-915. Rudolph Weber, Berlin.
-
(2002)
Flavins and Flavoproteins 2002
, pp. 911-915
-
-
Vintem, A.-P.1
Ramsay, R.R.2
Silverman, R.B.3
-
38
-
-
84898656900
-
Kinetic and structural analysis of the irreversible inhibition of human monoamine oxidases by ASS234, a multi-target compound designed for use in Alzheimer's disease
-
Esteban G, Allan J, Samadi A, Mattevi A, Unzeta M, Marco-Contelles J, Binda C, &, Ramsay RR, (2014) Kinetic and structural analysis of the irreversible inhibition of human monoamine oxidases by ASS234, a multi-target compound designed for use in Alzheimer's disease. Biochim Biophys Acta 1844, 1104-1110.
-
(2014)
Biochim Biophys Acta
, vol.1844
, pp. 1104-1110
-
-
Esteban, G.1
Allan, J.2
Samadi, A.3
Mattevi, A.4
Unzeta, M.5
Marco-Contelles, J.6
Binda, C.7
Ramsay, R.R.8
-
39
-
-
17444368018
-
Mutation of surface cysteine 374 to alanine in monoamine oxidase A alters substrate turnover and inactivation by cyclopropylamines
-
Vintem APB, Price NT, Silverman RB, &, Ramsay RR, (2005) Mutation of surface cysteine 374 to alanine in monoamine oxidase A alters substrate turnover and inactivation by cyclopropylamines. Bioorg Med Chem 13, 3487-3495.
-
(2005)
Bioorg Med Chem
, vol.13
, pp. 3487-3495
-
-
Vintem, A.P.B.1
Price, N.T.2
Silverman, R.B.3
Ramsay, R.R.4
-
40
-
-
0035833067
-
Inactivation of monoamine oxidase B by 1-phenylcyclopropylamine: Mass spectral evidence for the flavin adduct
-
Mitchell DJ, Nikolic D, van Breemen RB, &, Silverman RB, (2001) Inactivation of monoamine oxidase B by 1-phenylcyclopropylamine: mass spectral evidence for the flavin adduct. Bioorg Med Chem Lett 11, 1757-1760.
-
(2001)
Bioorg Med Chem Lett
, vol.11
, pp. 1757-1760
-
-
Mitchell, D.J.1
Nikolic, D.2
Van Breemen, R.B.3
Silverman, R.B.4
-
41
-
-
0001319451
-
Radical ideas about monoamine-oxidase
-
Silverman RB, (1995) Radical ideas about monoamine-oxidase. Accounts Chem Res 28, 335-342.
-
(1995)
Accounts Chem Res
, vol.28
, pp. 335-342
-
-
Silverman, R.B.1
-
42
-
-
77955025931
-
Structurally designed trans-2-phenylcyclopropylamine derivatives potently inhibit histone demethylase LSDI/KDM1
-
Mimasu S, Umezawa N, Sato S, Higuchi T, Umehara T, &, Yokoyama S, (2010) Structurally designed trans-2-phenylcyclopropylamine derivatives potently inhibit histone demethylase LSDI/KDM1. Biochemistry 49, 6494-6503.
-
(2010)
Biochemistry
, vol.49
, pp. 6494-6503
-
-
Mimasu, S.1
Umezawa, N.2
Sato, S.3
Higuchi, T.4
Umehara, T.5
Yokoyama, S.6
-
43
-
-
84902462712
-
Tranylcypromine substituted cis-hydroxycyclobutylnaphthamides as potent and selective dopamine D3 receptor antagonists
-
Chen J, Levant B, Jiang C, Keck TM, Newman AH, &, Wang S, (2014) Tranylcypromine substituted cis-hydroxycyclobutylnaphthamides as potent and selective dopamine D3 receptor antagonists. J Med Chem 57, 4962-4968.
-
(2014)
J Med Chem
, vol.57
, pp. 4962-4968
-
-
Chen, J.1
Levant, B.2
Jiang, C.3
Keck, T.M.4
Newman, A.H.5
Wang, S.6
-
44
-
-
66149173641
-
Molecular and mechanistic properties of the membrane-bound mitochondrial monoamine oxidases
-
Edmondson DE, Binda C, Wang J, Upadhyay AK, &, Mattevi A, (2009) Molecular and mechanistic properties of the membrane-bound mitochondrial monoamine oxidases. Biochemistry 48, 4220-4230.
-
(2009)
Biochemistry
, vol.48
, pp. 4220-4230
-
-
Edmondson, D.E.1
Binda, C.2
Wang, J.3
Upadhyay, A.K.4
Mattevi, A.5
-
45
-
-
84939215648
-
Nuclear magnetic resonance and mass spectroscopic evidence for the flavin-1-phenylcyclopropylamine inactivator adduct of monoamine oxidase
-
BIOL
-
Mitchell DJ, Silverman RB, Singer TP, Sablin SO, van Breemen RB, Nikolic D, &, Rivera E, (2000) Nuclear magnetic resonance and mass spectroscopic evidence for the flavin-1-phenylcyclopropylamine inactivator adduct of monoamine oxidase. Abstr Pap Am Chem Soc. 219, 52- BIOL.
-
(2000)
Abstr Pap Am Chem Soc
, vol.219
, pp. 52
-
-
Mitchell, D.J.1
Silverman, R.B.2
Singer, T.P.3
Sablin, S.O.4
Breemen Van, R.B.5
Nikolic, D.6
Rivera, E.7
-
46
-
-
0031573408
-
A one-step fluorometric method for the continuous measurement of monoamine oxidase activity
-
Zhou MJ, &, PanchukVoloshina N, (1997) A one-step fluorometric method for the continuous measurement of monoamine oxidase activity. Anal Biochem 253, 169-174.
-
(1997)
Anal Biochem
, vol.253
, pp. 169-174
-
-
Zhou, M.J.1
PanchukVoloshina, N.2
-
47
-
-
34250791622
-
A peroxidase-coupled continuous absorbance plate-reader assay for flavin monoamine oxidases, copper-containing amine oxidases and related enzymes
-
Holt A, &, Palcic MM, (2006) A peroxidase-coupled continuous absorbance plate-reader assay for flavin monoamine oxidases, copper-containing amine oxidases and related enzymes. Nat Protoc 1, 2498-2505.
-
(2006)
Nat Protoc
, vol.1
, pp. 2498-2505
-
-
Holt, A.1
Palcic, M.M.2
-
48
-
-
84872329515
-
Effects of novel neuroprotective and neurorestorative multifunctional drugs on iron chelation and glucose metabolism
-
Pollak Y, Mechlovich D, Amit T, Bar-Am O, Manov I, Mandel SA, Weinreb O, Meyron-Holtz EG, Iancu TC, &, Youdim MBH, (2013) Effects of novel neuroprotective and neurorestorative multifunctional drugs on iron chelation and glucose metabolism. J Neural Transm 120, 37-48.
-
(2013)
J Neural Transm
, vol.120
, pp. 37-48
-
-
Pollak, Y.1
Mechlovich, D.2
Amit, T.3
Bar-Am, O.4
Manov, I.5
Mandel, S.A.6
Weinreb, O.7
Meyron-Holtz, E.G.8
Iancu, T.C.9
Youdim, M.B.H.10
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