The present invention relates to spiro (tetracarbon) substituted compound of Formula I, processes for their preparation, pharmaceutical compositions containing them as active ingredient, methods for the treatment of disease states associated with angiogenesis, such as cancers associated with protein tyrosine kinases, to their use as medicaments for use in the production of inhibition of tyrosine kinases reducing effects in warm-blooded animals such as humans.
本发明涉及公式I的螺环(四碳)取代化合物,其制备方法,含有其作为活性成分的药物组合物,用于治疗与血管生成有关的疾病状态的方法,例如与
蛋白酪氨酸激酶相关的癌症,以及它们作为药物用于制造抑制
酪氨酸激酶减少作用在温血动物(如人类)中的用途。