Lactams substituted by cyclic succinates as inhibitors of...

Organic compounds -- part of the class 532-570 series – Organic compounds – Unsubstituted hydrocarbyl chain between the ring and the -c-...

Reexamination Certificate

Rate now

  [ 0.00 ] – not rated yet Voters 0   Comments 0

Details

Reexamination Certificate

active

07456278

ABSTRACT:
This invention relates to novel lactams having the Formula (I):to their pharmaceutical compositions and to their methods of use. These novel compounds inhibit the processing of amyloid precursor protein and, more specifically, inhibit the production of Aβ-peptide, thereby acting to prevent the formation of neurological deposits of amyloid protein. More particularly, the present invention relates to the treatment of neurological disorders related to β-amyloid production such as Alzheimer's disease and Down's Syndrome.

REFERENCES:
patent: 3828025 (1974-08-01), Hamanaka
patent: 4666829 (1987-05-01), Glenner et al.
patent: 4988827 (1991-01-01), Bergstein et al.
patent: 5087440 (1992-02-01), Cacheris et al.
patent: 5155215 (1992-10-01), Ranney
patent: 5281704 (1994-01-01), Love et al.
patent: 5283241 (1994-02-01), Bochis et al.
patent: 5412148 (1995-05-01), Keana
patent: 5417959 (1995-05-01), Wallace
patent: 5520904 (1996-05-01), Nosco et al.
patent: 5532359 (1996-07-01), Marsters et al.
patent: 5550126 (1996-08-01), Horwell et al.
patent: 5567411 (1996-10-01), Keana et al.
patent: 5578629 (1996-11-01), Ciccarone et al.
patent: 5593846 (1997-01-01), Shenk et al.
patent: 5595990 (1997-01-01), Baldwin et al.
patent: 5602145 (1997-02-01), Samanen
patent: 5618812 (1997-04-01), Castro Pineiro et al.
patent: 5672596 (1997-09-01), Wyvratt et al.
patent: 5679810 (1997-10-01), Love et al.
patent: 5703129 (1997-12-01), Felsenstein et al.
patent: 5710153 (1998-01-01), Ohmoto et al.
patent: 5710171 (1998-01-01), Dinsmore et al.
patent: 5756528 (1998-05-01), Anthony et al.
patent: 5760191 (1998-06-01), Snow et al.
patent: 5763437 (1998-06-01), Sato et al.
patent: 5801228 (1998-09-01), Hollister et al.
patent: 5804161 (1998-09-01), Long et al.
patent: 5852010 (1998-12-01), Graham et al.
patent: 5856326 (1999-01-01), Anthony et al.
patent: 5859012 (1999-01-01), Dinsmore et al.
patent: 5869682 (1999-02-01), DeSolms
patent: 5872135 (1999-02-01), DeSolms
patent: 5885995 (1999-03-01), Dinsmore
patent: 5891889 (1999-04-01), Anthony et al.
patent: 5905077 (1999-05-01), Jungheim et al.
patent: 5919785 (1999-07-01), Dinsmore et al.
patent: 5936089 (1999-08-01), Carpino
patent: 5965578 (1999-10-01), Ciccarone et al.
patent: 6331408 (2001-12-01), Zaczek et al.
patent: 6509333 (2003-01-01), Olson
patent: 2003/0119815 (2003-06-01), Olson
patent: 0107734 (1984-05-01), None
patent: 0276436 (1987-12-01), None
patent: 0421802 (1991-04-01), None
patent: 0434360 (1991-06-01), None
patent: 0606046 (1993-12-01), None
patent: 0652009 (1995-05-01), None
patent: 0727225 (1996-08-01), None
patent: 0842944 (1998-05-01), None
patent: WO 91/14460 (1991-10-01), None
patent: WO 92/00374 (1992-01-01), None
patent: WO 92/06966 (1992-04-01), None
patent: WO 92/16524 (1992-10-01), None
patent: WO 92/17215 (1992-10-01), None
patent: WO 92/17460 (1992-10-01), None
patent: WO 94/03437 (1994-02-01), None
patent: WO 94/05634 (1994-03-01), None
patent: WO 94/14776 (1994-07-01), None
patent: WO 94/22496 (1994-10-01), None
patent: WO 95/09633 (1995-04-01), None
patent: WO 95/09838 (1995-04-01), None
patent: WO 95/14471 (1995-06-01), None
patent: WO 95/22966 (1995-08-01), None
patent: WO 95/35308 (1995-12-01), None
patent: WO 96/17833 (1996-06-01), None
patent: WO 96/18602 (1996-06-01), None
patent: WO 96/20918 (1996-07-01), None
patent: WO 96/29313 (1996-09-01), None
patent: WO 96/31243 (1996-10-01), None
patent: WO 96/33166 (1996-10-01), None
patent: WO 96/39137 (1996-12-01), None
patent: WO 97/18207 (1997-05-01), None
patent: WO 97/19053 (1997-05-01), None
patent: WO 97/27852 (1997-08-01), None
patent: WO 97/36877 (1997-10-01), None
patent: WO 97/36879 (1997-10-01), None
patent: WO 97/36900 (1997-10-01), None
patent: WO 97/38664 (1997-10-01), None
patent: WO 97/45412 (1997-12-01), None
patent: WO 98/38177 (1998-03-01), None
patent: WO 98/15828 (1998-04-01), None
patent: WO 98/16523 (1998-04-01), None
patent: WO 98/22430 (1998-05-01), None
patent: WO 98/22433 (1998-05-01), None
patent: WO 98/22441 (1998-05-01), None
patent: WO 98/22493 (1998-05-01), None
patent: WO 98/22494 (1998-05-01), None
patent: WO 98/27053 (1998-06-01), None
patent: WO 98/28268 (1998-07-01), None
patent: WO 98/28980 (1998-07-01), None
patent: WO 98/35941 (1998-08-01), None
patent: WO 98/37079 (1998-08-01), None
patent: WO 98/41510 (1998-09-01), None
patent: WO 98/44797 (1998-10-01), None
patent: WO 98/51665 (1998-11-01), None
patent: WO 98/58915 (1998-12-01), None
patent: WO 99/00654 (1999-01-01), None
patent: WO 99/03826 (1999-01-01), None
patent: WO 99/07730 (1999-02-01), None
patent: WO 99/07731 (1999-02-01), None
patent: WO 99/17777 (1999-04-01), None
patent: WO 99/18951 (1999-04-01), None
patent: WO 99/19305 (1999-04-01), None
patent: WO 99/30815 (1999-06-01), None
patent: WO 99/32453 (1999-07-01), None
patent: WO 99/66934 (1999-12-01), None
patent: WO 99/67219 (1999-12-01), None
patent: WO 99/67220 (1999-12-01), None
patent: WO 99/67221 (1999-12-01), None
patent: WO 00/07995 (2000-02-01), None
patent: WO 00/24392 (2000-05-01), None
patent: WO 00/24967 (2000-05-01), None
patent: WO 00/27666 (2000-05-01), None
patent: WO 00/28331 (2000-05-01), None
patent: WO 00/38618 (2000-07-01), None
patent: WO 01/05236 (2001-01-01), None
patent: WO 01/09703 (2001-02-01), None
patent: WO 01/10297 (2001-02-01), None
patent: WO 01/10667 (2001-02-01), None
patent: WO 01/10773 (2001-02-01), None
patent: WO 01/11714 (2001-02-01), None
patent: WO 01/19797 (2001-03-01), None
patent: WO 01/60826 (2001-08-01), None
patent: WO 01/87354 (2001-11-01), None
Achour et al.,Synth. Commun. 1994, 24(20), pp. 2899-2905 (Scheme 3).
Ahmed et al.,FEBS Letters, (1984), vol. 174, pp. 76-79.
Ardnt,H.C.Synthesis 1979, pp. 202-204.
Arora et al.,J. Med. Chem., 30: p. 918 (1987).
Ballestri et al.,J. Org. Chem 56, p. 678 (1991).
Barnett et al.,Tetrahedron Lett. 1997, 38 (5), p. 735.
Barton and McCarobie,J. Chem. Soc. Perkin Trans. 1, p. 1574 (1975).
Barton and Motherwell,Pure&Appl. Chem. 53, p. 15 (1981).
Becket, PM. J. Crimmin, M. H. Davis, and Z. Spavold,Synlett(1993), pp. 137-138.
Belletire et al.,Tet. Lett.1984, 25, pp. 5969-5972.
Bettembourg et al.,Bull. Soc. Chim. Fr. 1963, pp. 2449-2451.
Bioorg. Med. Chem. Lett. (1998), 8 (12), pp. 1443-1448.
Bioorg. Med. Chem. Lett., vol. 8, No. 16, pp. 2077-2080 (1998).
Bock et al.,J. Med. Chem. 1993, 36, pp. 4276-4292.
Bock et al.,J. Med. Chem., 1989, 32, pp. 13-16.
Bock et al.,J. Org. Chem 1987, 52, pp. 3232-3239.
Bodine et al.,Synth. Commun. 1982, 12, p. 787.
Borenstein et al.,Heterocycles, 22, 1984, pp. 2433-2438.
Braun,MSynthesis 1989, p. 856.
Brechbeil ,M and O. Gansow,Bioconjugate Chem.1991, 2, p. 187.
Brechbiel,M and O. Gansow,J. Chem. Soc. Perkin Trans.1992, 1, p. 1175.
Brinkley,MBioconjugate Chemistry 1992, 3 (1).
Brown et al.,Tetrahedron Letters, 1971, 8, pp. 667-670.
Buege et al.,Arch. Pharm. 1994, 327 (2), pp. 99-103.
Bull. Soc. Chim. Fr. (1971), (6), pp. 2290-2295.
Carey F. A.and R. J. Sundberg, “Advanced Organic Chemistry, Part A,”New York: Plenum Press, 1990, pp. 304-305, 342-347, 475-479, 695-698.
Chamberlin, A. R.Chem. Rev. 1997, 97, pp. 2243-2266.
Chumpradit et al., J. Med. Chem., 32: p. 1431 (1989).
Chumpradit et al., J. Med. Chem., 34: p. 877 (1991).
Cohen et al.,J. Org. Chem. 1995, 60, p. 2022.
“Comprehensive Organic Functional Group Transformations,” ed. A. R. Katritsky, O. Meth-Cohn, and C. W. Rees, vol. 5, pp. 274-281 (1995).
Davis S.G. et al.,Synlett 1995, p. 700.
Deshpande S.et al.,J. Nucl. Med. 1990, 31, p. 473.
Donetti, A.J. Med. Chem 1972, 15, (6), pp. 590-592.
Duhammel et al., Tetrahedron Asymmetry 1991, 2 (3), pp. 203-206.
Eckardt et al., Helv. Chim. Acta, 55, 1972, pp. 2432-2434, 2438.
Eckelman et al.,J. Nucl. Med., vol. 20(4), pp. 350-357 (1979).
Ellis et al.,Aust. J. Chem., 26,: p. 907 (1973).
Evans B. E et al., “Method for Drug Discovery: Development of Potent, Selective, Orally Effective Cholecystokinin Antagonists,” Journal of Medicinal Chemistry, vol. 31, No. 12, 1988, pp. 2235-2246.
Crimmins M. T. et al., J. Am. Chem Soc. 1997, 119, pp. 7883-7884.
D. A. Evans, A

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

Lactams substituted by cyclic succinates as inhibitors of... does not yet have a rating. At this time, there are no reviews or comments for this patent.

If you have personal experience with Lactams substituted by cyclic succinates as inhibitors of..., we encourage you to share that experience with our LandOfFree.com community. Your opinion is very important and Lactams substituted by cyclic succinates as inhibitors of... will most certainly appreciate the feedback.

Rate now

     

Profile ID: LFUS-PAI-O-4034619

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