Compound useful for the treatment of neuropathic pain

Bibliographic Details
Title: Compound useful for the treatment of neuropathic pain
Patent Number: 7,220,775
Publication Date: May 22, 2007
Appl. No: 10/637299
Application Filed: August 07, 2003
Abstract: This invention is directed to pyrimidine and indolone derivatives which are selective antagonists for the GAL3 receptor and are useful for the treatment of neuropathic pain and other abnormalities. This invention also provides a method of treating a subject suffering from an abnormality which comprises administering to the subject an amount of a compound of the invention effective to treat the subject's abnormality. This invention also provides a method of treating an abnormality in a subject which comprises administering to the subject a composition comprising a pharmaceutically acceptable carrier and a therapeutically effective amount of a GAL3 receptor antagonist.
Inventors: Blackburn, Thomas P. (Hoboken, NJ, US)
Assignees: H. Lundbeck A/S (Copenhagen-Valby, DK)
Claim: 1. A method of treating a subject suffering from neuropathic pain, which comprises administering to the subject an amount of a compound effective to treat the subject's neuropathic pain, wherein the compound has the structure: [chemical expression included] or a pharmaceutically acceptable salt thereof [chemical expression included]
Current U.S. Class: 514/416
Patent References Cited: 5576296 November 1996 Bartfai et al.
6511827 January 2003 Howard et al.
7081470 July 2006 Konkel et al.
514361 November 1992
667340 August 1995
WO9212997 August 1992
WO9815570 April 1998
WO9931130 June 1999
WO0002865 January 2000
WO0260392 August 2002




























































Other References: U.S. Appl. No. 10/638,242, filed May 2004, Konkel et al. cited by examiner
U.S. Appl. No. 10/723,961, filed Jul. 2004, Blackburn et al. cited by examiner
U.S. Appl. No. 11/298,116, filed Dec. 2005, Blackburn et al. cited by examiner
U.S. Appl. No. 11/343,810, filed Jan. 2006, Konkel et al. cited by examiner
U.S. Appl. No. 11/343,989, filed Jan. 2006, Konkel et al. cited by examiner
Swanson, C. J. et al. “Anxiolytic- and antidepressant-like profiles of the galanin-3 receptor (Gal3) antagonists SNAP 37889 and SNAP 398299” (2005) PNAS vol. 102, No. 48, pp. 17489-17494. cited by examiner
Liu, H. X. et al. “Effect of intrathecal galanin and its putative antagonist M35 on pain begavior in a neuropathic pain model” (2000) Brain Research vol. 886, pp. 67-72. cited by examiner
Silverman, Richard B. The Organic Chemistry of Drug Design and Drug Action, (1992) Published by Academic Press, pp. 65-71. cited by examiner
Ahmad, A., et al., “Identification And Molecular Cloning Of ANovel Galanin Receptor (GALR-2) In Rat Sensory Neurons”, Soc.Neurosci. Abstr. (1996) 22(3): 1682, Abstract No. 661.10 (Exhibit 10). cited by other
Ahmad, S., et al., “Molecular Cloning Of A Novel Widely Distributed Galanin Receptor Subtype (GALR2),” International Association for the Study of Pain (IASP Press)(1996) Abstract No. 81: 134 (Exhibit 11). cited by other
Ahmad, S. Et al., Astra Pain Control (1996), poster (Exhibit 12). cited by other
Bartfai, T., et al, “Galanin Receptor Ligand M40 Peptide Distinguishes Between Putative Galanin- Receptor Subtypes,” PNAS (USA)(1993) 90: 11287-11291 (Exhibit 13). cited by other
Branchek, et al., “Galanin Receptor Subtypes,” Trends In Pharmacological Sciences. Elsevier Trends Journal. (Mar. 2000) 21(3): 109-116 (Exhibit 14). cited by other
Gustafson, E., et al., “Distribution of a Rat Galanin Receptor mRNA in Rat Brain,” Neuroreport (1996) 7: 953-957 (Exhibit 15). cited by other
Kahl, U., et al., “Galanin Receptors,” DN&P (1995) 8(7): 404-410 (Exhibit 16). cited by other
O'Donnell, D., et al., “Neuroanatomical Distribution Of A Novel Rat Galanin Receptor Subtype,” Soc. Neurosci. Abstr. (1996) 22(2):1304, Abstract No. 517.9 (Exhibit 17). cited by other
Selve et al., “Galanin receptor antagonists attenuate spinal antinociceptive effects of DAMGO, tramadol and non-opioid drugs in rats,” Brain Res. (Oct. 7, 1996) 735(2): 177-187 (Exhibit 18). cited by other
Smith, et al., “Cloned Human and Rat Galanin GALR3 Receptors,” The Journal of Biological Chemistry. (Sep. 1998) 273(36): 23321-23326 (Exhibit 19). cited by other
Xu, X.J., et al., “New High Affinity Peptide Antagonists to the Spinal Galanin Receptor,” Br. J. Pharmacol. (1995) 116: 2076-2080 (Exhibit 20). cited by other
Bionet Research Ltd. Catalog #11L-312S (1-Phenyl-3-{[3-(trifluoromethyl)phenyl]imino}-1,3-dihydro-2H-indol-2-one) (Exhibit 21). cited by other
Chemical Abstracts Registry No. 61038-64-0 (Exhibit 22). cited by other
Chemical Abstracts Registry No. 41230-77-7 (Exhibit 23). cited by other
Chemical Abstracts Registry No. 130186-15-1 (Exhibit 24). cited by other
Chemical Abstracts Registry No. 130186-16-2 (Exhibit 25). cited by other
Chemical Abstracts Registry No. 130186-17-3 (Exhibit 26). cited by other
Chemical Abstracts Registry No. 130186-18-4 (Exhibit 27). cited by other
Chemical Abstracts Registry No. 130186-21-9 (Exhibit 28). cited by other
Chemical Abstracts Registry No. 130270-13-2 (Exhibit 29). cited by other
Chemical Abstracts Registry No. 133939-75-0 (Exhibit 30). cited by other
Chemical Abstracts Registry No. 56984-58-8 (Exhibit 31). cited by other
Chemical Abstracts Registry No. 77910-42-0 (Exhibit 32). cited by other
Chemical Abstracts Registry No. 70010-41-2 (Exhibit 33). cited by other
Chemical Abstracts Registry No. 189264-35-5 (Exhibit 34). cited by other
Chemical Abstracts Registry No. 88291-04-7 (Exhibit 35). cited by other
Chemical Abstracts Registry No. 88291-07-0 (Exhibit 36). cited by other
Chemical Abstracts Registry No. 154118-05-5 (Exhibit 37). cited by other
Chemical Abstracts Registry No. 155717-81-0 (Exhibit 38). cited by other
Chemical Abstracts Registry No. 155717-82-1 (Exhibit 39). cited by other
Chemical Abstracts Registry No. 159967-24-5 (Exhibit 40). cited by other
Chemical Abstracts Registry No. 138601-94-2 (Exhibit 41). cited by other
Chemical Abstracts Registry No. 136647-69-3 (Exhibit 42). cited by other
Chemical Abstracts Registry No. 136647-72-8 (Exhibit 43). cited by other
Chemical Abstracts Registry No. 77297-28-0 (Exhibit 44). cited by other
Chemical Abstracts Registry No. 43002-26-2 (Exhibit 45). cited by other
Chemical Abstracts Registry No. 303954-69-2 (Exhibit 46). cited by other
Chemical Abstracts Registry No. 122725-53-5 (Exhibit 47). cited by other
Chemical Abstracts Registry No. 122803-89-8 (Exhibit 48). cited by other
Chemical Abstracts Registry No. 303149-10-2 (Exhibit 49). cited by other
Chemical Abstracts Registry No. 303149-08-8 (Exhibit 50). cited by other
Chemical Abstracts Registry No. 303149-06-6 (Exhibit 51). cited by other
Chemical Abstracts Registry No. 303984-47-6 (Exhibit 52). cited by other
Chemical Abstracts Registry No. 303149-14-6 (Exhibit 53). cited by other
Chemical Abstracts Registry No. 303149-12-4 (Exhibit 54). cited by other
Chemical Abstracts Registry No. 303984-51-2 (Exhibit 55). cited by other
Chemical Abstracts Registry No. 303984-49-8 (Exhibit 56). cited by other
Chemical Abstracts Registry No. 303954-48-7 (Exhibit 57). cited by other
Chemical Abstracts Registry No. 303984-52-3 (Exhibit 58). cited by other
Chemical Abstracts Registry No. 303984-60-3 (Exhibit 59). cited by other
Chemical Abstracts Registry No. 303984-61-4 (Exhibit 60). cited by other
Chemical Abstracts Registry No. 303984-62-5 (Exhibit 61); and. cited by other
Chemical Abstracts Registry No. 303984-68-1 (Exhibit 62). cited by other
Assistant Examiner: Olson, Eric S.
Primary Examiner: Jiang, Shaojia Anna
Attorney, Agent or Firm: Kalinchak, Stephen G.
Accession Number: edspgr.07220775
Database: USPTO Patent Grants
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Language:English