Indolinones substituted by heterocycles, the preparation...

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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C514S235200, C514S249000, C514S252060, C514S323000, C514S339000, C514S338000, C514S377000, C514S383000, C514S394000, C514S217080, C546S201000, C546S277700, C548S266400, C548S454000, C548S455000, C548S468000, C540S575000, C544S144000, C544S235000, C544S238000

Reexamination Certificate

active

07148249

ABSTRACT:
The present invention relates to heterocyclically substituted indolinones of general formulawhereinR1to R5and X are defined as in claim 1, the tautomers, the diastereomers, the enantiomers, the mixtures thereof, the prodrugs thereof and the salts thereof, particularly the physiologically acceptable salts thereof which have valuable pharmacological properties, in particular an inhibiting effect on various receptor tyrosine kinases and cyclin/CDK complexes and on the proliferation of endothelial cells and various tumour cells, pharmaceutical compositions containing these compounds, their use and processes for preparing them.

REFERENCES:
patent: 6762180 (2004-07-01), Roth et al.
patent: 6858641 (2005-02-01), Roth et al.
patent: WO 01/16130 (2001-03-01), None
patent: WO 01/27080 (2001-04-01), None
patent: WO 01/27081 (2001-04-01), None
Kandile, N. G. et al. Revue Roumaine de Chimie 1991, 36(1-3), 245.
Copy of International Search Report Reference #PCT/EP 03/09978.

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