Fused cyclic systems useful as inhibitors of TEC family...

Drug – bio-affecting and body treating compositions – Designated organic active ingredient containing – Having -c- – wherein x is chalcogen – bonded directly to...

Reexamination Certificate

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Details

C544S247000, C544S250000, C514S267000

Reexamination Certificate

active

07855214

ABSTRACT:
The present invention relates to compounds useful as inhibitors of Tec family protein kinases. These compounds have the general formula I:or a pharmaceutically acceptable salt thereof, wherein R1, R2, R3, R4, R5, G, Cy1, and X are as defined herein. The invention also provides pharmaceutically acceptable compositions comprising said compounds and methods of using the compositions in the treatment of various disease, conditions, or disorders.

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patent: 03077921 (2003-09-01), None
International Search Report for corresponding PCT Application No. PCT/US2005/002725, Jun. 28, 2005.
Database Registry, American Chemical Society; Feb. 28, 2003, XP002331999.
Database Registry, American Chemical Society; Jan. 21, 2003, XP002332000.
Database Chemical Abstracts, STN Database Accession No. XP002332001, 1963.
Orfi et al. “Heterocondensed Quinazolones: Synthesis and protein-tyrosine kinase inhibitory activity of 3,4-dihydro-1H, 6H-[1,4] oxazino-[3,4-b]quinazolin-6-one derivatives”, Bioorganic and Medicinal Chemistry, 4(4), 547-551, (1996).
Parfitt et al, “Cyclic amidines. XVI. Tetraazanaphtho[1,2,3-fg]naphthacenes” J. Chem. Soc. (1963) pp. 3062-3066.

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