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Pyrazolo 3,4-g quinoxaline compounds that inhibit PDGF receptor protein tyrosine kinase

机译:抑制PDGF受体蛋白酪氨酸激酶的吡唑并[3,4-g]喹喔啉化合物

摘要

This invention relates to pyrazolo[3,4-g]quinoxaline compounds exhibiting protein tyrosine kinase inhibition activity of the formula: IMAGE where: ------ may be a double bond; R, R2, R3 and R4 are as described in claim 1; a pharmaceutically acceptable salt thereof. More specifically, compounds of this invention are novel as selective inhibitors of the PDGF-R protein tyrosine kinase and can be applied as potential therapeutic agents for various disease states which are characterized by uncontrolled cellular proliferation. Further, the present invention provides pharmaceutical compositions and a method for treating such disorders comprising the administration to a patient of a PDGF receptor inhibiting effective amount of a pyrazolo[3,4-g]quinoxaline compound exhibiting protein tyrosine kinase inhibition activity. Processes for the preparation of pyrazolo[3,4-g]quinoxaline compounds are also described.
机译:本发明涉及具有下式的蛋白酪氨酸激酶抑制活性的吡唑并[3,4-g]喹喔啉化合物:式中:------可以是双键; R,R2,R3和R4如权利要求1所述;其药学上可接受的盐。更具体地,本发明的化合物作为PDGF-R蛋白酪氨酸激酶的选择性抑制剂是新颖的,并且可以用作针对以不受控制的细胞增殖为特征的各种疾病状态的潜在治疗剂。此外,本发明提供了用于治疗此类疾病的药物组合物和方法,其包括向患者施用PDGF受体抑制有效量的表现出蛋白酪氨酸激酶抑制活性的吡唑并[3,4-g]喹喔啉化合物。还描述了吡唑并[3,4-g]喹喔啉化合物的制备方法。

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