-
1
-
-
75449102536
-
Alzheimer's disease
-
[CrossRef] [PubMed]
-
Querfurth, H.W.; LaFerla, F.M. Alzheimer's disease. N. Engl. J. Med. 2010, 362, 329-344. [CrossRef] [PubMed]
-
(2010)
N. Engl. J. Med.
, vol.362
, pp. 329-344
-
-
Querfurth, H.W.1
LaFerla, F.M.2
-
2
-
-
0034304034
-
Cholinesterase inhibitors stabilize Alzheimer's disease
-
[CrossRef] [PubMed]
-
Giacobini, E. Cholinesterase inhibitors stabilize Alzheimer's disease. Neurochem. Res. 2000, 25, 1185-1190. [CrossRef] [PubMed]
-
(2000)
Neurochem. Res.
, vol.25
, pp. 1185-1190
-
-
Giacobini, E.1
-
3
-
-
20844460621
-
The molecular basis of memantine action in Alzheimer's disease and other neurologic disorders: Low-affinity, uncompetitive antagonism
-
[CrossRef] [PubMed]
-
Lipton, S.A. The molecular basis of memantine action in Alzheimer's disease and other neurologic disorders: Low-affinity, uncompetitive antagonism. Curr. Alzheimer Res. 2005, 2, 155-165. [CrossRef] [PubMed]
-
(2005)
Curr. Alzheimer Res.
, vol.2
, pp. 155-165
-
-
Lipton, S.A.1
-
4
-
-
84887972850
-
The multifactorial nature of Alzheimer's disease for developing potential therapeutics
-
[CrossRef] [PubMed]
-
Carreiras, M.C.; Mendes, E.; Perry, M.J.; Francisco, A.P.; Marco-Contelles, J. The multifactorial nature of Alzheimer's disease for developing potential therapeutics. Curr. Top. Med. Chem. 2013, 13, 1745-1770. [CrossRef] [PubMed]
-
(2013)
Curr. Top. Med. Chem.
, vol.13
, pp. 1745-1770
-
-
Carreiras, M.C.1
Mendes, E.2
Perry, M.J.3
Francisco, A.P.4
Marco-Contelles, J.5
-
5
-
-
84871094408
-
Recent advances in the multitarget-directed ligands approach for the treatment of Alzheimer's disease
-
[CrossRef] [PubMed]
-
Leon, R.; Garcia, A.G.; Marco-Contelles, J. Recent advances in the multitarget-directed ligands approach for the treatment of Alzheimer's disease. Med. Res. Rev. 2013, 33, 139-189. [CrossRef] [PubMed]
-
(2013)
Med. Res. Rev.
, vol.33
, pp. 139-189
-
-
Leon, R.1
Garcia, A.G.2
Marco-Contelles, J.3
-
6
-
-
84890136755
-
Successes and failures for drugs in late-stage development for Alzheimer's disease
-
[CrossRef] [PubMed]
-
Berk, C.; Sabbagh, M.N. Successes and failures for drugs in late-stage development for Alzheimer's disease. Drugs Aging 2013, 30, 783-792. [CrossRef] [PubMed]
-
(2013)
Drugs Aging
, vol.30
, pp. 783-792
-
-
Berk, C.1
Sabbagh, M.N.2
-
7
-
-
45249120152
-
Enhanced oxidative stress is an early event during development of Alzheimer-like pathologies in presenilin conditional knock-out mice
-
[CrossRef] [PubMed]
-
Gu, F.; Zhu, M.; Shi, J.; Hu, Y.; Zhao, Z. Enhanced oxidative stress is an early event during development of Alzheimer-like pathologies in presenilin conditional knock-out mice. Neurosci. Lett. 2008, 440, 44-48. [CrossRef] [PubMed]
-
(2008)
Neurosci. Lett.
, vol.440
, pp. 44-48
-
-
Gu, F.1
Zhu, M.2
Shi, J.3
Hu, Y.4
Zhao, Z.5
-
8
-
-
80053462390
-
Targeting monoamine oxidases with multipotent ligands: An emerging strategy in the search of new drugs against neurodegenerative diseases
-
[CrossRef] [PubMed]
-
Pisani, L.; Catto, M.; Leonetti, F.; Nicolotti, O.; Stefanachi, A.; Campagna, F.; Carotti, A. Targeting monoamine oxidases with multipotent ligands: An emerging strategy in the search of new drugs against neurodegenerative diseases. Curr. Med. Chem. 2011, 18, 4568-4587. [CrossRef] [PubMed]
-
(2011)
Curr. Med. Chem.
, vol.18
, pp. 4568-4587
-
-
Pisani, L.1
Catto, M.2
Leonetti, F.3
Nicolotti, O.4
Stefanachi, A.5
Campagna, F.6
Carotti, A.7
-
9
-
-
24644437716
-
Three-dimensional structure of human monoamine oxidase A (MAO-A): Relation to the structures of rat MAO-A and human MAO-B
-
[CrossRef] [PubMed]
-
De Colibus, L.; Li, M.; Binda, C.; Lustig, A.; Edmondson, D.E.; Mattevi, A. Three-dimensional structure of human monoamine oxidase A (MAO-A): Relation to the structures of rat MAO-A and human MAO-B. Proc. Natl. Acad. Sci. USA 2005, 102, 12684-12689. [CrossRef] [PubMed]
-
(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
-
10
-
-
0348046385
-
Monoamine oxidase-B inhibition in Alzheimer's disease
-
[CrossRef]
-
Riederer, P.; Danielczyk, W.; Gruenblatt, E. Monoamine oxidase-B inhibition in Alzheimer's disease. Neurotoxicology 2004, 1-2, 271-277. [CrossRef]
-
(2004)
Neurotoxicology
, vol.1-2
, pp. 271-277
-
-
Riederer, P.1
Danielczyk, W.2
Gruenblatt, E.3
-
11
-
-
84887272848
-
Fine molecular tuning at position 4 of 2H-chromen-2-one derivatives in the search of potent and selective monoamine oxidase B inhibitors
-
[CrossRef] [PubMed]
-
Pisani, L.; Catto, M.; Nicolotti, O.; Grossi, G.; di Braccio, M.; Soto-Otero, R.; Mendez-Alvarez, E.; Stefanachi, A.; Gadaleta, D.; Carotti, A. Fine molecular tuning at position 4 of 2H-chromen-2-one derivatives in the search of potent and selective monoamine oxidase B inhibitors. Eur. J. Med. Chem. 2013, 70, 723-739. [CrossRef] [PubMed]
-
(2013)
Eur. J. Med. Chem.
, vol.70
, pp. 723-739
-
-
Pisani, L.1
Catto, M.2
Nicolotti, O.3
Grossi, G.4
Di Braccio, M.5
Soto-Otero, R.6
Mendez-Alvarez, E.7
Stefanachi, A.8
Gadaleta, D.9
Carotti, A.10
-
12
-
-
71049173711
-
Discovery of a novel class of potent coumarin monoamine oxidase B inhibitors: Development and biopharmacological profiling of 7-[(3-chlorobenzyl)oxy]-4-[(methylamino)methyl]-2H-chromen-2-one methanesulfonate (NW-1772) as a highly potent, selective, reversible, and orally active monoamine oxidase B inhibitor
-
Pisani, L.; Muncipinto, G.; Miscioscia, T.F.; Nicolotti, O.; Leonetti, F.; Catto, M.; Caccia, C.; Salvati, P.; Soto-Otero, R.; Mendez-Alvarez, E.; et al. Discovery of a novel class of potent coumarin monoamine oxidase B inhibitors: Development and biopharmacological profiling of 7-[(3-chlorobenzyl)oxy]-4-[(methylamino)methyl]-2H-chromen-2-one methanesulfonate (NW-1772) as a highly potent, selective, reversible, and orally active monoamine oxidase B inhibitor. J. Med. Chem. 2009, 52, 6685-6706.
-
(2009)
J. Med. Chem.
, vol.52
, pp. 6685-6706
-
-
Pisani, L.1
Muncipinto, G.2
Miscioscia, T.F.3
Nicolotti, O.4
Leonetti, F.5
Catto, M.6
Caccia, C.7
Salvati, P.8
Soto-Otero, R.9
Mendez-Alvarez, E.10
-
13
-
-
84908430587
-
In silico design of novel 2H-chromen-2-one derivatives as potent and selective MAO-B inhibitors
-
[CrossRef] [PubMed]
-
Pisani, L.; Farina, R.; Nicolotti, O.; Gadaleta, D.; Soto-Otero, R.; Catto, M.; di Braccio, M.; Mendez-Alvarez, E.; Carotti, A. In silico design of novel 2H-chromen-2-one derivatives as potent and selective MAO-B inhibitors. Eur. J. Med. Chem. 2015, 89, 98-105. [CrossRef] [PubMed]
-
(2015)
Eur. J. Med. Chem.
, vol.89
, pp. 98-105
-
-
Pisani, L.1
Farina, R.2
Nicolotti, O.3
Gadaleta, D.4
Soto-Otero, R.5
Catto, M.6
Di Braccio, M.7
Mendez-Alvarez, E.8
Carotti, A.9
-
14
-
-
84870943115
-
Design, synthesis and biological evaluation of coumarin alkylamines as potent and selective dual binding site inhibitors of acetylcholinesterase
-
[CrossRef] [PubMed]
-
Catto, M.; Pisani, L.; Leonetti, F.; Nicolotti, O.; Pesce, P.; Stefanachi, A.; Cellamare, S.; Carotti, A. Design, synthesis and biological evaluation of coumarin alkylamines as potent and selective dual binding site inhibitors of acetylcholinesterase. Bioorg. Med. Chem. 2013, 21, 146-152. [CrossRef] [PubMed]
-
(2013)
Bioorg. Med. Chem.
, vol.21
, pp. 146-152
-
-
Catto, M.1
Pisani, L.2
Leonetti, F.3
Nicolotti, O.4
Pesce, P.5
Stefanachi, A.6
Cellamare, S.7
Carotti, A.8
-
15
-
-
84937680699
-
Structure-based design and optimization of multitarget-directed 2H-chromen-2-one derivatives as potent inhibitors of monoamine oxidase B and cholinesterases
-
[CrossRef] [PubMed]
-
Farina, R.; Pisani, L.; Catto, M.; Nicolotti, O.; Gadaleta, D.; Denora, N.; Soto-Otero, R.; Mendez-Alvarez, E.; Passos, C.S.; Muncipinto, G.; et al. Structure-based design and optimization of multitarget-directed 2H-chromen-2-one derivatives as potent inhibitors of monoamine oxidase B and cholinesterases. J. Med. Chem. 2 2015, 58, 5561-5578. [CrossRef] [PubMed]
-
(2015)
J. Med. Chem. 2
, vol.58
, pp. 5561-5578
-
-
Farina, R.1
Pisani, L.2
Catto, M.3
Nicolotti, O.4
Gadaleta, D.5
Denora, N.6
Soto-Otero, R.7
Mendez-Alvarez, E.8
Passos, C.S.9
Muncipinto, G.10
-
16
-
-
77956413632
-
Design, synthesis and biological evaluation of coumarin derivatives tethered to an edrophonium-like fragment as highly potent and selective dual binding site acetylcholinesterase inhibitors
-
[CrossRef] [PubMed]
-
Pisani, L.; Catto, M.; Giangreco, I.; Leonetti, F.; Nicolotti, O.; Stefanachi, A.; Cellamare, S.; Carotti, A. Design, synthesis and biological evaluation of coumarin derivatives tethered to an edrophonium-like fragment as highly potent and selective dual binding site acetylcholinesterase inhibitors. Chem. Med. Chem. 2010, 5, 1616-1630. [CrossRef] [PubMed]
-
(2010)
Chem. Med. Chem.
, 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
-
17
-
-
0001138103
-
A convenient synthesis of a simple coumarin from salicylaldehyde and Witting reagent (I): A synthesis of methoxy- and hydroxycoumarins
-
[CrossRef]
-
Harayama, T.; Katsuno, K.; Nishioka, N.; Fujii, M.; Nishita, Y.; Isii, H.; Kaneko, Y. A convenient synthesis of a simple coumarin from salicylaldehyde and Witting reagent (I): A synthesis of methoxy- and hydroxycoumarins. Heterocycles 1994, 39, 613-622. [CrossRef]
-
(1994)
Heterocycles
, vol.39
, pp. 613-622
-
-
Harayama, T.1
Katsuno, K.2
Nishioka, N.3
Fujii, M.4
Nishita, Y.5
Isii, H.6
Kaneko, Y.7
-
18
-
-
84870951777
-
Synthesis and biological evaluation of scopoletin derivatives
-
[CrossRef] [PubMed]
-
Cai, X.; Yang, J.; Zhou, J.; Lu, W.; Hu, C.; Gu, Z.; Huo, J.; Wang, X.; Cao, P. Synthesis and biological evaluation of scopoletin derivatives. Bioorg. Med. Chem. 2013, 21, 84-92. [CrossRef] [PubMed]
-
(2013)
Bioorg. Med. Chem.
, vol.21
, pp. 84-92
-
-
Cai, X.1
Yang, J.2
Zhou, J.3
Lu, W.4
Hu, C.5
Gu, Z.6
Huo, J.7
Wang, X.8
Cao, P.9
-
19
-
-
0035130289
-
Rasagiline [N-propargyl-1R(+)aminoindan], a selective and potent inhibitor of mitochondrial monoamine oxidase B
-
[CrossRef] [PubMed]
-
Youdim, M.B.H.; Gross, A.; Finberg, J.P.M. Rasagiline [N-propargyl-1R(+)aminoindan], a selective and potent inhibitor of mitochondrial monoamine oxidase B. Br. J. Pharmacol. 2001, 132, 500-506. [CrossRef] [PubMed]
-
(2001)
Br. J. Pharmacol.
, vol.132
, pp. 500-506
-
-
Youdim, M.B.H.1
Gross, A.2
Finberg, J.P.M.3
-
20
-
-
33644811612
-
A new and rapid colorimetric determination of acetylcholinesterase activity
-
[CrossRef]
-
Ellman, G.L.; Courtney, K.D.; Andres, V., Jr.; Feartherstone, R.M. A new and rapid colorimetric determination of acetylcholinesterase activity. Biochem. Pharmacol. 1961, 7, 88-95. [CrossRef]
-
(1961)
Biochem. Pharmacol.
, vol.7
, pp. 88-95
-
-
Ellman, G.L.1
Courtney, K.D.2
Andres, V.3
Feartherstone, R.M.4
-
21
-
-
84875721627
-
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
-
[CrossRef] [PubMed]
-
Pisani, L.; Barletta, M.; Soto-Otero, R.; Nicolotti, O.; Mendez-Alvarez, E.; Catto, M.; Introcaso, A.; Stefanachi, A.; Cellamare, S.; Altomare, C.D.; et al. Carotti, A.; et al. 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. J. Med. Chem. 2013, 56, 2651-2664. [CrossRef] [PubMed]
-
(2013)
J. Med. Chem.
, vol.56
, pp. 2651-2664
-
-
Pisani, L.1
Barletta, M.2
Soto-Otero, R.3
Nicolotti, O.4
Mendez-Alvarez, E.5
Catto, M.6
Introcaso, A.7
Stefanachi, A.8
Cellamare, S.9
Altomare, C.D.10
Carotti, A.11
-
22
-
-
0022445670
-
Rapid colorimetric assay for cell growth and survival. Modifications to the tetrazolium dye procedure giving improved sensitivity and reliability
-
[CrossRef]
-
Denizot, F.; Lang, R. Rapid colorimetric assay for cell growth and survival. Modifications to the tetrazolium dye procedure giving improved sensitivity and reliability. J. Immunol. Methods 1986, 89, 271-277. [CrossRef]
-
(1986)
J. Immunol. Methods
, vol.89
, pp. 271-277
-
-
Denizot, F.1
Lang, R.2
-
23
-
-
0037424245
-
Mitochondrial complex I inhibitor rotenone induces apoptosis through enhancing mitochondrial reactive oxygen species production
-
[CrossRef] [PubMed]
-
Li, N.; Ragheb, K.; Lawler, G.; Sturgis, J.; Rajwa, B.; Melendez, J.A.; Robinson, J.P. Mitochondrial complex I inhibitor rotenone induces apoptosis through enhancing mitochondrial reactive oxygen species production. J. Biol. Chem. 2003, 278, 8516-8525. [CrossRef] [PubMed]
-
(2003)
J. Biol. Chem.
, vol.278
, pp. 8516-8525
-
-
Li, N.1
Ragheb, K.2
Lawler, G.3
Sturgis, J.4
Rajwa, B.5
Melendez, J.A.6
Robinson, J.P.7
-
24
-
-
78649910298
-
Translocator protein (TSPO) ligand-Ara-C (cytarabine) conjugates as a strategy to deliver antineoplastic drugs and to enhance drug clinical potential
-
[CrossRef] [PubMed]
-
Denora, N.; Laquintana, V.; Trapani, A.; Lopedota, A.; Latrofa, A.; Gallo, J.M.; Trapani, G. Translocator protein (TSPO) ligand-Ara-C (cytarabine) conjugates as a strategy to deliver antineoplastic drugs and to enhance drug clinical potential. Mol. Pharm. 2010, 7, 2255-2269. [CrossRef] [PubMed]
-
(2010)
Mol. Pharm.
, vol.7
, pp. 2255-2269
-
-
Denora, N.1
Laquintana, V.2
Trapani, A.3
Lopedota, A.4
Latrofa, A.5
Gallo, J.M.6
Trapani, G.7
-
25
-
-
84866743619
-
Novel codrugs with GABAergic activity for dopamine delivery in the brain
-
[CrossRef] [PubMed]
-
Denora, N.; Cassano, T.; Laquintana, V.; Lopalco, A.; Trapani, A.; Cimmino, C.S.; Laconca, L.; Giuffrida, A.; Trapani, G. Novel codrugs with GABAergic activity for dopamine delivery in the brain. Int. J. Pharm. 2012, 437, 221-231. [CrossRef] [PubMed]
-
(2012)
Int. J. Pharm.
, vol.437
, pp. 221-231
-
-
Denora, N.1
Cassano, T.2
Laquintana, V.3
Lopalco, A.4
Trapani, A.5
Cimmino, C.S.6
Laconca, L.7
Giuffrida, A.8
Trapani, G.9
-
26
-
-
11144224747
-
Design, synthesis, and 3D QSAR of novel potent and selective aromatase inhibitors
-
[CrossRef] [PubMed]
-
Leonetti, F.; Favia, A.; Rao, A.; Aliano, R.; Paluszcak, A.; Hartmann, R.W.; Carotti, A. Design, synthesis, and 3D QSAR of novel potent and selective aromatase inhibitors. J. Med. Chem. 2004, 47, 6792-6803. [CrossRef] [PubMed]
-
(2004)
J. Med. Chem.
, vol.47
, pp. 6792-6803
-
-
Leonetti, F.1
Favia, A.2
Rao, A.3
Aliano, R.4
Paluszcak, A.5
Hartmann, R.W.6
Carotti, A.7
-
27
-
-
84949115920
-
Novel one-pot asymmetric cascade approach toward densely substituted enantioenriched α-methylene-γ-lactams
-
[CrossRef]
-
Tan, Y.; Yang, X.D.; Liu, W.J.; Sun, X.W. Novel one-pot asymmetric cascade approach toward densely substituted enantioenriched α-methylene-γ-lactams. Tetrahedron Lett. 2014, 55, 6105-6108. [CrossRef]
-
(2014)
Tetrahedron Lett.
, vol.55
, pp. 6105-6108
-
-
Tan, Y.1
Yang, X.D.2
Liu, W.J.3
Sun, X.W.4
-
28
-
-
0343144860
-
Inhibition of brain monoamine oxidase by adducts of 1,2,3,4-tetrahydroisoquinoline with components of cigarette smoke
-
[CrossRef]
-
Mendez-Alvarez, E.; Soto-Otero, R.; Sanchez-Sellero, I.; Lopez-Rivadulla, L.M.; Lamas, M. Inhibition of brain monoamine oxidase by adducts of 1,2,3,4-tetrahydroisoquinoline with components of cigarette smoke. Life Sci. 1997, 60, 1719-1727. [CrossRef]
-
(1997)
Life Sci.
, vol.60
, pp. 1719-1727
-
-
Mendez-Alvarez, E.1
Soto-Otero, R.2
Sanchez-Sellero, I.3
Lopez-Rivadulla, L.M.4
Lamas, M.5
-
29
-
-
79955449571
-
Homodimeric bis-quaternary heterocyclic ammonium salts as potent acetyl- and butyrylcholinesterase inhibitors: A systematic investigation of the influence of linker and cationic heads over affinity and selectivity
-
[CrossRef] [PubMed]
-
Conejo-Garcia, A.; Pisani, L.; Nunez, M.C.; Catto, M.; Nicolotti, O.; Leonetti, F.; Campos, J.M.; Gallo, M.A.; Espinosa, A.; Carotti, A. Homodimeric bis-quaternary heterocyclic ammonium salts as potent acetyl- and butyrylcholinesterase inhibitors: A systematic investigation of the influence of linker and cationic heads over affinity and selectivity. J. Med. Chem. 2011, 54, 2627-2645. [CrossRef] [PubMed]
-
(2011)
J. Med. Chem.
, vol.54
, pp. 2627-2645
-
-
Conejo-Garcia, A.1
Pisani, L.2
Nunez, M.C.3
Catto, M.4
Nicolotti, O.5
Leonetti, F.6
Campos, J.M.7
Gallo, M.A.8
Espinosa, A.9
Carotti, A.10
-
30
-
-
29744451969
-
Binding of rasagiline-related inhibitors to human monoamine oxidases: A kinetic and crystallographic analysis
-
[CrossRef] [PubMed]
-
Binda, C.; Hubalek, F.; Li, M.; Herzig, Y.; Sterling, J.; Edmonson, D.E.; Mattevi, A. Binding of rasagiline-related inhibitors to human monoamine oxidases: A kinetic and crystallographic analysis. J. Med. Chem. 2005, 48, 8148-8154. [CrossRef] [PubMed]
-
(2005)
J. Med. Chem.
, vol.48
, pp. 8148-8154
-
-
Binda, C.1
Hubalek, F.2
Li, M.3
Herzig, Y.4
Sterling, J.5
Edmonson, D.E.6
Mattevi, A.7
-
31
-
-
84930004627
-
Propargylamine as functional moiety in the design of multifunctional drugs for neurodegenerative disorders: MAO inhibition and beyond
-
[CrossRef] [PubMed]
-
Zindo, F.T.; Joubert, J.; Malan, S.F. Propargylamine as functional moiety in the design of multifunctional drugs for neurodegenerative disorders: MAO inhibition and beyond. Future Med. Chem. 2015, 7, 609-629. [CrossRef] [PubMed]
-
(2015)
Future Med. Chem.
, vol.7
, pp. 609-629
-
-
Zindo, F.T.1
Joubert, J.2
Malan, S.F.3
|