Pyridylfurans and pyrroles as Raf kinase inhibitors

Drug – bio-affecting and body treating compositions – Designated organic active ingredient containing – Heterocyclic carbon compounds containing a hetero ring...

Reexamination Certificate

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C514S252180, C514S272000, C514S274000, C514S318000, C514S336000, C514S343000, C544S123000, C544S295000, C544S315000, C544S331000, C546S194000, C546S276400, C546S283400

Reexamination Certificate

active

10488576

ABSTRACT:
Compounds and their use as pharmaceuticals particularly as Raf kinase inhibitors for the treatment of neurotraumatic diseases, cancer, chronic neurodegeneration, pain, migraine and cardiac hypertrophy.

REFERENCES:
patent: 2 306 108 (1997-04-01), None
patent: WO 97/36587 (1997-10-01), None
patent: WO 00/64422 (2000-11-01), None
patent: WO 01/38324 (2001-05-01), None
patent: WO 01/66539 (2001-09-01), None
patent: WO 01/66540 (2001-09-01), None
patent: WO 02/24680 (2002-03-01), None
De Laszlo et al., “Pyrroles and other heterocycles as inhibitors of p38 kinase”, Bioorg. Med. Chem. Lett., vol. 8, 1998, pp. 2689-2694.
De Laszlo et al., “Potent, orally abosorbed glucagon receptor antagonists”, Bioorg. Med. Chem. Lettl, vol. 9, 1999, pp. 641-646.
Liveton et al., “Design and Synthesis of Potent, Selective and Orally Bioavailable Tetrasubstituted Imidazole Inhibitors of p38 Mitogen-Activated Protein Kinase”, J. Med. Chem., vol. 42, No. 12, 1999, pp. 2180-2190.
Kalmes et al., “Raf-1 is activated by the p38 mitogen-activated protein kinase inhibitor”, Febs Letters, vol. 444, No. 1, 1999. pp. 71-74.
Wermuth, C.G. (ed.), “Chapter 13: Molecular Variations Based on Isosteric Replacements”,The Practice of Medicinal Chemistry, pp. 204-237, Academic Press Ltd., Copyright (1996), XP-002190259.

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