Synthesis of novel substituted indeno[1,2-b]indole derivatives of the type of 5,6,7,8-tetrahydroindeno[1,2-b]indole-9,10-diones and 5H-indeno[1,2-b]indole-6,9,10-triones, which show pronounced inhibition of the human protein kinase CK2, and the use thereof as active ingredients in medicaments and/or drug products in particular for the treatment of neoplastic diseases.
合成新型取代的indeno[1,2-b]indole衍
生物,包括5,6,7,8-四氢indeno[1,2-b]indole-9,10-二酮和5H-indeno[1,2-b]indole-6,9,10-三酮,这些衍
生物表现出明显的人类蛋白激酶CK2的抑制作用,并将其用作药物的活性成分,尤其用于治疗肿瘤疾病。