On the formation of 4-[N,N-bis(2-chloroethyl)amino]phenyl acetic acid esters of hecogenin and aza-homo-hecogenin and their antileukemic activity

Charalambos Camoutsis , Dimitrios Trafalis , George Pairas , Athanasios Papageorgiou
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引用次数: 10

Abstract

The p-[N,N-bis(2-chloroethyl)amino]phenylacetic acid esters of hecogenin and aza-homo-hecogenin have been prepared and their antineoplastic activity was evaluated against two basic drug screening systems in rodents, P388 lymphocytic and L1210 lymphoid murine leukemias. Among the compounds tested, the p-[N,N-bis(2-chloroethyl)amino]phenylacetic acid ester of aza-homo-hecogenin was appeared to possess a significant higher antileukemic effect. These results support that the alkylating esters of hecogenin produce important antitumor activity as well as, indicate that the aza-homo-hecogenin ester exhibits significantly higher activity due to lactam group (–NHCO–) modification.

异型豆豆素和异型豆豆素的4-[N,N-双(2-氯乙基)氨基]苯基乙酸酯的形成及其抗白血病活性
制备了异源原素和异源原素的p-[N,N-双(2-氯乙基)氨基]苯乙酸酯,并在小鼠P388淋巴细胞白血病和L1210淋巴细胞白血病两种基本药物筛选系统中对其抗肿瘤活性进行了评价。在所测试的化合物中,aza-homo- heocgenin的p-[N,N-双(2-氯乙基)氨基]苯乙酸酯似乎具有显著较高的抗白血病作用。这些结果表明,异构体素的烷基化酯具有重要的抗肿瘤活性,同时,由于内酰胺基团(- nhco -)修饰,异构体素的异构体素酯具有明显更高的活性。
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