(1S,5S)-3-(5,6-dichloropyridin-3-yl)-3,6-diazabicyclo[3.2.0]...

Organic compounds -- part of the class 532-570 series – Organic compounds – Heterocyclic carbon compounds containing a hetero ring...

Reexamination Certificate

Rate now

  [ 0.00 ] – not rated yet Voters 0   Comments 0

Details

Reexamination Certificate

active

07902371

ABSTRACT:
The present invention relates to the salt (1S,5S)-3-(5,6-dichloropyridin-3-yl)-3,6-diazabicyclo[3.2.0]heptane benzenesulfonate and to methods of preparing the salt.

REFERENCES:
patent: 2004/0242641 (2004-12-01), Buckley et al.
patent: 2004/0242644 (2004-12-01), Buckley et al.
patent: 2005/0261348 (2005-11-01), Buckley et al.
patent: 2006/0035936 (2006-02-01), Buckley et al.
patent: 01/81347 (2001-11-01), None
patent: 2004/106342 (2004-12-01), None
Arneric, et al., “Cholingeric channel modulators as a novel therapeutic strategy for Alzheimer's disease,” Exp. Opin. Invest. Drugs 5(1): 79-100 (1996).
Arneric, et al., “Neuronal nicotinic acetycholine receptors,” Psychopharmacology: The Fourth Generation of Progress 95-110 (1995).
Brittain, et al., “Polymorphism in Pharmaceutical Solids,” NY: Marcel Dekker, Inc, 185: 1-2 (1999).
Carty, et al., “Cox-2 inhibitors. Potential for reducing NSAID side-effects in treating inflammatory disease,” Emerging Drugs: The Prospect for Improved Medicines, Annual Executive Briefing, Chapter 19: 391-411 (1996).
Chaplan, et al., “Quantitative assessment of tactile allodynia in the rat paw,” Journal of Neuroscience Methods 53:55-63 (1994).
Cherny, et al. “Opioid Analgesics, Comparative features and prescribing guidelines,” Drugs 51(5): 713-737 (1996).
Decker, et al., “Effects of ABT-418, a novel cholinergic channel ligand, on place learning in septal-lesioned rats,” European Journal of Pharmacology 261:217-222 (1994).
Dray, et al., “New pharmacological strategies for pain relief,” Annu. Rev. Pharmacol. Toxicol. 36:253-280 (1996).
Dray, et al., “Pharmacology of chronic pain,” TiPS 15:190-197 (1994).
Kim, et al., “An experimental model for peripheral neuropathy produced by segmental spinal nerve ligation in the rat,” Pain 50:355-363 (1992).
Lindstrom, et al. “Nicotinic acetylcholine receptors in health and disease,” Molecular Neurobiology 15:193-222 (1997).
Lloyd, et al., “The potential of subtype-selective neuronal nicotinic acetylcholine receptor agonists as therapeutic agents,” Life Sciences 62(17/18): 1601-1606 (1998).
Lukas, et al. “Expression of ganglia-type nicotinic acetylcholine receptors and nicotinic ligand binding sites by cells of the IMR-32 human neuroblastoma clonal line,” Journal of Pharmacology and Experimental Therapeutics 265(1): 294-302 (1993).
Muzaffar, et al., “Polymorphism and Drug Availability,” J. of Pharmacy (Lahore) 1(1): 59-66 (1979).
Pabreza, et al, “[3H]cytosine binding to nicotinic cholinergic receptors in brain,” Molecular Pharmacology 39:9-12 (1990).
Prescott, et al., Methods in cell biology, vol. XIV, Academic Press, New York, NY, p. 33 et seq. (1976).
U S Pharmacopeia, 1843-1844 (1995).
Williams, et al., “Beyond the tobacco debate: dissecting out the therapeutic potential of nicotine,” Exp. Opin. Invest. Drugs 5(8): 1035-1045 (1996).
Williams, et al., “Emerging molecular approaches to pain therapy,” Journal of Medicinal Chemistry 42(9): 1481-1500 (1999).

LandOfFree

Say what you really think

Search LandOfFree.com for the USA inventors and patents. Rate them and share your experience with other people.

Rating

(1S,5S)-3-(5,6-dichloropyridin-3-yl)-3,6-diazabicyclo[3.2.0]... does not yet have a rating. At this time, there are no reviews or comments for this patent.

If you have personal experience with (1S,5S)-3-(5,6-dichloropyridin-3-yl)-3,6-diazabicyclo[3.2.0]..., we encourage you to share that experience with our LandOfFree.com community. Your opinion is very important and (1S,5S)-3-(5,6-dichloropyridin-3-yl)-3,6-diazabicyclo[3.2.0]... will most certainly appreciate the feedback.

Rate now

     

Profile ID: LFUS-PAI-O-2711035

  Search
All data on this website is collected from public sources. Our data reflects the most accurate information available at the time of publication.