首页> 外国专利> Camptothecin tetracyclic derivatives useful for inhibiting topoisomerase I and/or II pyridine intermediates thereof

Camptothecin tetracyclic derivatives useful for inhibiting topoisomerase I and/or II pyridine intermediates thereof

机译:喜树碱四环衍生物可用于抑制拓扑异构酶I和/或II吡啶中间体

摘要

Tetracyclic analogues of camptothecin of formula (I), their preparation processes, their use as medicaments and the pharmaceutical compositions containing them, where: R1, R2, R3, R4, R5 and R10 are as described in the specification. These Tetracyclic analogues of camptothecin, 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:式(I)的喜树碱的四环类似物,它们的制备方法,它们作为药物的用途以及包含它们的药物组合物,其中:R1,R2,R3,R4,R5和R10如说明书中所述。这些喜树碱的四环类似物,特别是包括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的生物学活性。和/或拓扑异构酶II。

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