Napthoquinone derivatives as inhibitors of tau aggregation...

Drug – bio-affecting and body treating compositions – Designated organic active ingredient containing – Radical -xh acid – or anhydride – acid halide or salt thereof...

Reexamination Certificate

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C514S675000

Reexamination Certificate

active

07605179

ABSTRACT:
Provided are napthoquinone-type compounds which can be used to modulate the aggregation of protein (e.g. tau) associated with neurodegenerative disease (e.g. Alzheimer's disease). Structure-function characteristics for oxidised and reduced napthoquinone-type compounds, such as menadione-related compounds, are disclosed. The invention further provides methods of treatment or prophylaxis of neurodegenerative diseases and/or clinical dementias based on the compounds.

REFERENCES:
patent: 4897388 (1990-01-01), Malluche
patent: 5763479 (1998-06-01), Chayen et al.
patent: 6953974 (2005-10-01), Wischik et al.
patent: 2002/0016372 (2002-02-01), Allison
patent: 2006/0014216 (2006-01-01), Wischik et al.
patent: 0 737 671 (1996-10-01), None
patent: 8193026 (1996-07-01), None
patent: WO 93/11231 (1993-06-01), None
patent: WO 96/04915 (1996-02-01), None
patent: WO 96/30766 (1996-10-01), None
patent: WO 01/91740 (2001-12-01), None
patent: WO 02/055720 (2002-07-01), None
patent: WO 02/059150 (2002-08-01), None
patent: WO 02/075318 (2002-09-01), None
patent: WO 2005/030676 (2005-04-01), None
patent: WO 2006/032879 (2006-03-01), None
Prophylaxis. (n.d.). Merriam-Webster's Medical Dictionary. Retrieved Dec. 21, 2007, from Dictionary.com website: http://dictionary.reference.com/browse/prophylaxis.
Abstract, Thal, Prevention of Alzheimer disease, Alzheimer Disease and Associated Disorder, Jul.-Sep.:20(3 suppl 2):S97-9, 2006.
Surmeir, Calcium, ageing, neuronal vulnerability in Parkinson's disease, Lancet Neurology, 6:933-38, 2007.
Kamagai, Yoshito et al., “Inhibition of Nitric Oxide Formation by Neuronal Nitric Oxide Synthase by Quinones: Nitric Oxide Synthase as a Quinone Reductase”, XP-002217439 abstract, Chemical Research in Toxicology (1998).
Danoun, Saida et al., “Synthesis and Protozoacidal Activity of New 1,4-Naphthoquinones”, XP-002217440 abstract, Heterocyclic Communications: (1999).
Oommen, Elsie et al., “Antitumor Efficacy of Cyclodextrin-Complexed and Niosome-Encapsulated Plumbagin in Mice Bearing Melanoma B16F1”, XP-002217441 abstract, Pharmacy and Pharmacology Communications (1999).
Bhosale, S.H., et al., “Pharmacological Studies of Isomeric [sic] Juglones on the Isolated Frog Heart”, XP-002217442, Indian Journal of Pharmacology (1999).
Nishizawa Yoshinori, “Hair Growing and Restoring Agent”, Patent Abstracts of Japan, 11335244, Dec. 7, 1999.
Allison, A.C., “The possible role of vitamin K deficiency in the pathogenesis of Alzheimer's disease and in augmenting brain damage associated with cardiovascular disease”, XP-001117580, Medical hypothesis, vol. 57, No. 2, Aug. 2001.
Gong, C.X. et al., “Dephosphorylation of Alzheimer's disease abnormally phosphorylated tau by protein phosphatase-2A”, XP-000578896, Neuroscience, vol. 61, No. 4, 1994.
Ko, Li-wen, et al., “Menadione-induced tau dephosphorylation in cultured human neuroblastoma cells”, XP-001118168, Brain Research, Netherlands, Jun. 20, 1997.
U.S. Appl. No. 11/391,675, filed Mar. 29, 2006, C. M. Wischik, et al.
M. von Bergen, et al. “Assembly of tau protein into Alzheimer's paired helical filaments depends on a local sequence motif forming beta structure”, Proceedings of the National Academy of Sciences of USA, National Academy of Science, May 9, 2000, vol. 97, No. 10, pp. 5129-5134.
M. Pickhardt, et al., “Anthraquinones inhibit tau aggregation and dissolve Alzheimer paired helical filaments in vitro and in cells”, Journal of Biological Chemistry, 2005, vol. 280, pp. 3628-3635.
H. Aizawa, et al., “Microtubule-binding domain of tau proteins”, Journal of Biological Chemistry, 1988, vol. 263, pp. 7703-7707.
C.M. Wischik, F. Theuring and C.R. Harrington, “The molecular basis of tau protein pathology in Alzheimer's disease and related neurodegenerative dementias”, In Neurobiology of Alzheimer's Disease (Eds. D. Dawbarn & S.J. Allen) Oxford University Press, Oxford, pp. 103-206.
C. Wischik, “Molecular neuropathology of Alzheimer's disease”, John Libbey & Co., 1991, pp. 239-250.
R. Lai, “The Role of Abnormal Phosphorylation of Tau Protein in the Development of Neurofibrillary Pathology in Alzheimer's Disease”, pp. 1-243.
C. Wischik, “Molecular Neuropathology of Alzheimer's Disease” (1989), pp. 44-70.
Garcini et al.,Biochemical and Biophysical Research Communications, Self Assembly of Microtubule Associated Protein TAU into Filaments Resembling those found in Alzheimer Disease (1986), pp. 790-797.
Garcini et al.J. Biocehm. 102, No. 6, “In Vitro Conditions for the Self-Polymerization of the Microtubule-Associated Protein, Tau Factor” (1987), pp. 1415-1421.
Garcini et al.,Elsevier Science Publishers B.V., “Tau Factor Polymers are Similar to Paired Helical Filaments of Alzheimer's Disease” (1988), pp. 150-154.
Ksiezak-Reding and Yen,Neuron, vol. 6, pp. 717-728, Structural Stability of Paired Helical Filaments Requires Microtubule-Binding Domains of Tau: A Model for Self-Association (1991).
M. Goedert et al., “Tau Proteins of Alzheimer Paired Helical Filaments: Abnormal Phosphorylation of All Six Brain isoforms”,Neuron, vol. 8, pp. 159-168, Jan. 1992.
R. Jakes et al., “Identification of 3- and 4-repeat Tau Isoforms Within The PHF in Alzheimer's Disease”,The EMBO Journal, vol. 10, No. 10, pp. 2725-2729, 1991.
M. Novak et al., “Molecular Characterization of the Minimal Protease Resistant Tau Unit of the Alzheimer's Disease Paired Helical Filament”,The EMBO Journal, vol. 12, No. 1, pp. 365-370, 1993.
S.-H. Yen et al., “Alzheimer's Neurofibrillary Tangles Contain Unique Epitopes and Epitopes in Common With the Heat-Stable Microtubule Associated Proteins Tau and MAP2”,AJP, Jan. 1987, vol. 126, pp. 81-91.
J.P. Brion et al., “Characterization of a Partial cDNA Specific for the High Molecular Weight Microtubule-Associated Protein MAP2 That Encodes Epitopes Shared with Paired Helical Filaments of Alzheimer's Disease”,Dementia, 1990:1 pp. 304-315.
M.W. Klymkowsky, “Weaving a Tangled Web: the Interconnected Cytoskeleton”,Nature Cell Biology, vol. 1, No. 5, p. E121 (1999).
Fasulo et al., “Overexpression of Alzheimer's PHF core tau fragments: implications for the tau truncation hypothesis”, Rapid Science Publishers, Alzheimer's Research, vol. 2, No. 5, pp. 195-200, Oct. 1996.
Wille et al.,J. Cell Biol., 118 (1992) 573-584, Alzheimer-like paired helical filaments and antiparallel dimers formed from microtubule-associated protein tau in vitro.
Ksiezak-Reding and Wall,Neurobiology of Aging, vol. 15, No. 1, pp. 11-18. “Mass and Physical Dimensions of Two Distinct Populations of Paired Helical Filaments” (1993).
Wischik et al.,Proc. Natl. Acad. Sci. USA, vol. 85, pp. 4506-4510 (1988) “Isolation of a fragment of tau derived from the core of the paired helical filament of Alzheimer disease”.
Wischik et al.,Proc. Natl. Acad. Sci. USA, vol. 85, pp. 4884-4888, “Structural characterization of the core of the paired helical filament of Alzheimer disease” (1988).
Ksiezak-Reding, Assembled tau filaments differ from native paired helical filaments as determiend by scanning transmission electron microscopy (STEM) (1998), pp. 86-98.
Mena et al.,Journal of Neuropathology and Experimetnal Neurology, “A Progressive Depsotion of Paired Helical Filaments (PHF) in the Brain Characterizes the Evolution of Dementia in Alzheimer's Disease” (1991), pp. 474-490.
Mena et al.,Acta Neuropathol., Monitoring Pathological Assembly of tau and β-Amyloid Proteins in Alzheimer's Disease (1994), pp. 50-56.
Mena et al.,Acta Neuropathol, “Staging the Pathological Assembly of Truncated tau Protein into Paired Helical Filaments in Alzheimer's Disease” (1995), pp. 633-641.
C.M. Wischik et al. “Quantitative Analysis of Tau Protein in Paired Helical Filament Preparations: Implicati

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