The present invention relates to bicyclic heterocycles of general formula
##STR1##
wherein
- Ra to Rd, A to G and X are defined as in claim
1, the tautomers, the steroisomers and the salts thereof, particularly the physiologically
acceptable salts thereof with inorganic or organic acids or bases which have valuable
pharmacological properties, particularly an inhibiting effect on signal transduction
mediated by tyrosine kinases, their use for treating diseases, particularly tumoral
diseases, diseases of the lungs and respiratory tract, and the preparation thereof.
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