首页> 外国专利> Indazole compounds, pharmaceutically acceptable prodrug, pharmaceutically active metabolite, or pharmaceutically acceptable salt, pharmaceutical compositions, method for treating a mammalian disease condition mediated by protein kinase activity and method for modulating the activity of a protein receptor protein kinase

Indazole compounds, pharmaceutically acceptable prodrug, pharmaceutically active metabolite, or pharmaceutically acceptable salt, pharmaceutical compositions, method for treating a mammalian disease condition mediated by protein kinase activity and method for modulating the activity of a protein receptor protein kinase

机译:吲唑化合物,药学上可接受的前药,药学上有活性的代谢产物或药学上可接受的盐,药物组合物,用于治疗蛋白激酶活性介导的哺乳动物疾病的方法以及调节蛋白受体蛋白激酶活性的方法

摘要

"INDAZOL COMPOUNDS, PHARMACEUTICALLY ACCEPTABLE PRO-DRUG, PHARMACEUTICALLY ACTIVE METABOLITE, OR PHARMACEUTICALLY ACCEPTABLE SALT, PHARMACEUTICAL COMPOSITIONS, METHOD OF TREATING AN ACTIVE HARMFUL MEDICINE HARMFUL TREATMENT PROTEIN KINASE ". Indazole compounds have been described that modulate and / or inhibit the activity of certain protein kinases. These compounds and the pharmaceutical compositions containing them are capable of mediating tyrosine kinase signal transduction, and thereby modulate and / or inhibit unwanted cell proliferation. The invention also relates to the therapeutic or prophylactic use of pharmaceutical compositions containing these compounds and to methods of treating cancer and other disease states associated with unwanted angiogenesis and / or cell proliferation, such as diabetic retinopathy, neurovascular glaucoma , rheumatoid arthritis, and psoriasis, by administering effective amounts of these compounds.
机译:“吲哚化合物,药学上可接受的前药,药学上有效的代谢物或药学上可接受的盐,药品组合物,治疗活性有害药物有害治疗蛋白激酶的方法”。已经描述了吲唑化合物,其调节和/或抑制某些蛋白激酶的活性。这些化合物和包含它们的药物组合物能够介导酪氨酸激酶信号转导,从而调节和/或抑制有害的细胞增殖。本发明还涉及含有这些化合物的药物组合物的治疗或预防用途,以及涉及与不希望的血管生成和/或细胞增殖有关的癌症和其他疾病状态的方法,例如糖尿病性视网膜病,神经血管性青光眼,类风湿性关节炎和牛皮癣,通过施用有效量的这些化合物。

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