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New tetracyclic camptothecin analog topoisomerase inhibitors, used as antitumor, antiviral and antiparasitic agents

机译:新型四环喜树碱类似物拓扑异构酶抑制剂,用作抗肿瘤药,抗病毒药和抗寄生虫药

摘要

The invention relates to new tetracyclic analogues of camptothecin, their preparation processes, their use as medicaments and the pharmaceutical compositions containing them. Said analogues, which include in particular 3-hydroxy-3-(4-oxo-4,6-dihydroindolizino [1,2-b] quinoline-2-yl)pentanoic acid, have a powerful biological activity inhibiting topoisomerase I and/or topoisomerase II.
机译:本发明涉及喜树碱的新的四环类似物,其制备方法,其作为药物的用途以及含有它们的药物组合物。所述类似物,尤其包括3-羟基-3-(4-氧代-4,6-二氢吲哚并[1,2-b]喹啉-2-基)戊酸,具有强大的抑制拓扑异构酶I和/或生物学活性。拓扑异构酶II。

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