
A Concise Review on Cyclin Dependent Kinase 5 (CDK5) Inhibitors
Abstract
Keywords
Full Text:
PDFReferences
D. Silva, M. Chioua, A. Samadi, P. Agostinho, P. Garcao, R. Lajarin-Cuesta, C. de los Rios, I. Iriepa, I. Moraleda, L. Gonzalez-Lafuente, E. Mendes, C. Perez, M.I. Rodriguez-Franco, J. Marco-Contelles, M.C. Carreiras. Synthesis, Pharmacological Assessment, and Molecular Modelling of Acetylcholinestrase/Butyrylcholinestrase Inhibitor: Effect against Amyloid- β-Induced Neurotoxicity. ACS Chem.Neurosci. 2013, 4, 547-565.
C.P. Ferri, M. Prince, C. Brayne, H. Brodaty, L. Fratiglioni, M. Ganguly, K. Hall, K. Hasegawa, H. Hendris, Y. Huang, A. Jorm, C. Mathers, P.R. Menezes, E. Rimmer, M. Scazufca. Lancet. 2005, 366, 2112-2117.
H.W. Querfurth, F.M.N. LaFerla. Engl.J.Med. 2010, 362, 329.
M. Citron. Nat Rev. Drug Disc. 2010, 9, 387.
A. Lleo, S. M. Greenberg, J. H. Growdon. Annu. Rev. Med. 2006, 57, 513.
L.E. Herbert, P.A. Scherr, J.L. Bienias, A.D. Bennett. Arch. Neurol. 2003, 60, 1119.
R. Dhavan, Li-Huei. Tsai. A Decade of CDK5. Mol.Cell.Biol. 2001, 2, 749.
M. Malumbres, M. Barbacid. Trends in Biochem.Sci. 2006, 30, 630.
J. Lew, K. Beaudette, C.M.E. Litwin, J.H. Wang. Purification and characterization of a novel proline-directed protein kinase from bovine brain. J.Biol.Chem. 1992, 267, 13383-13390.
M. Meyerson et al. A family of human cdc2-related protein kinase. EMBO. J. 1992, 11, 2909-2917.
A. Gupta, Li-Huei.Tsai. Cyclin dependent kinase 5 and neuronal migration in the neocortex. Neurosignals. 2003, 12, 173-179.
T. Ohshima, J.M. Ward, C.G. Huh, G. Longenecker, Veeranna et al. Targeted disruption of cyclin dependent kinase 5 gene results in abnormal corticogenesis, neuronal pathology and perinatal death. Proc. Natl. Acad. Sci. U.S.A. 1996, 93, 11173-11178.
E.C. Gilmore, T. Ohshima, A.M. Goffinet, A.B. Kulkarni, K. Herrup. Cyclin-dependent kinase 5 defecient mice demonstrate novel development arrest in cerebral cortex. J. Neurosci. 1998, 18, 6370-6377.
J. Ko, S. Humbert, R.T. Bronson, S. Takahashi, A.B. Kulkarni et al. p35 and p39 are essential for cdk5 function during neurodevelopment. J. Neurosci. 2001, 21, 6758-6771.
C. Tarricone, R. Dhavan, J. Peeng. Mol. Cell. 2001, 8, 657.
M.D. Nguyen, J.P. Julien. Cyclin dependent kinase 5 in amyotrophic lateral sclerosis. Neurosignals. 2003, 12, 215-220.
L.F. Lau, M.K. Ahlijanian. Role of cdk5 in the pathogenesis of Alzheimer’s disease. Neurosignals. 2003, 12, 209-214.
P.D. Smith, S.J. Crocker, V. Jackson-Lewis, K.L. Jordan-Sciutto, S. Hayley et al. Cyclin dependent kinase 5 is a mediator of dopaminergic neuron loss in a mouse model of Parkinson’s disease. Proc. Natl. Acad. Sci. U.S.A. 2003, 100, 13650-13655.
B. Bu, J. Li, P. Davies, I. Vincent. Deregulation of CDK5, hyperphosphorylation, and cytoskeletal pathology in the Niemann-pick type C murine model. J. Neurosci. 2002, 22, 6515-6525.
J. Wang, S. Liu, Y. Fu, J.H. Wang, Y. Lu. CDK5 activation induces hippocampal CA1 cell death by directly phosphorylating NMDA receptors. Nat. Neuroscience. 2003, 6, 1039-1047.
A. Scalbert, G. Williamson. J. Nutr. 2000, 130, 2073S-2085S.
I. Erlund, L.M. Silaste, G. Alfthan, M. Rantala, Y. Kesanieni, A. Aro. Eur. J. Clin. Nutr. 2000, 56, 891-898.
L. Meijer, E. Bisagni, M. Legraverend. W019961129.Patent. 96-FR1905, 9720842, 1997, 52.
L. Meijer, E. Raymond. Acc. Chem. Res. 2003, 2, 584.
W.F. De-Azevedo, S. Leclerc, L. Meijer, L. Havlicek, M. Strand et al. Inhibition of cyclin dependent kinase by purine analogues: Crystal structure of human cdk2 complexed with Roscovitine. Eur. J. Biochem. 1997, 243, 518-526.
M. Mapelli, L. Massimiliano, C. Crovace, M.A. Seeliger, Li-Huei.Tsai, L. Meijer, A. Musacchio. Mechanism of CDK5/p25 Binding by CDK Inhibitors. J. Med. Chem. 2005, 48, 671-679.
Y. Metty, M. Gompel, V. Thomas, M. Garnier, M. Leost et al. Aloisine, a new family of CDK/GSK-3inhibitors. SAR study, crystal structure in complex with CDK2, enzyme selectivity and cellular effects. J. Med. Chem. 2003, 46, 222-236.
R. Hoessel, S. Leclerc, A.J. Endicott, E.M. Nobel, A. Lawrie et al. Indirubin, the active constituent of Chinese leukemia medicine, inhibit cyclin dependent kinase. Nat. Cell. Biol. 1999, 1, 60-67.
J.K. Laha, X. Zhang, L. Qiao, M. Liu, S. Chatterjee, S. Robinson, K.S. Kosik, G.D. Cuny. Structure-activity relationship study of 2,4-diaminothiazoles as cdk5/p25 kinase inhibitors. Bioorg. Med. Chem. Lett. 2011, 21, 2098-2101.
J. Malmstrom, J. Viklund, C. Slivo, A. Costa, M. Maudet, C. Sandelin, G. Hiller, L.L. Olsson, A. Aagaard, S. Geschwinder, Y. Xue, M. Vasange. Synthesis and structure-activity relationship of 4-(1,3-benzothiazol-2-yl)-thiophene-2-sulphonamide as cyclin dependent kinase 5 (cdk5)/p25 inhibitors. Bioorg. Med. Chem. Lett. 2012, 22, 5919-5923.
R.Singh, Geetanjali, N. Sharma. Monoamine Oxidase Inhibitors for Neurological Disorders: A review. Chem. Biol. Lett., 2014, 1(1), 33-39.
I. Aprahamian, F. Stella, & O.V. Forlenza. New treatment strategies for Alzheimer’s disease: is there a hope? Indian J. Med. Res., 2013, 138, 449-460.
P. Padmaja. Total Synthesis of Bioactive Lactones: Prelactone E, epi-Prelactones V, E, Nonenolides (Z-isomers) and Stagonolide E. Int. Arch. Sci. Technol., 2013, 13(1), 1-6.
K. Gogoi. Synthesis and biophysical studies of PNA and chimeric PNA-DNA antisense oligomers with five atom linkages. Int. Arch. Sci. Technol., 2013, 13(1), 7-13.