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Design, Synthesis and Biological Evaluation of the Novel Antitumor Agent 2-benzyl-3, 4-dihydroisoquinolin-1(2H)-one and Its Derivatives

机译:新型抗肿瘤药2-苄基-3、4-二氢异喹啉-1(2H)-及其衍生物的设计,合成及生物学评价

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Tetrahydroisoquinoline and its derivatives have a wide range of biological activities, such as antitumor, antimicrobial, and analgesic properties and so on. Some tetrahydroisoquinoline alkaloid derivatives have been studied as antitumor drug molecules, but 2-benzyl-7-substituted-ethoxy]-3, 4-dihydro-1(2H)-isoquinolinone series have not been reported yet. In this paper, we would like to report the design, synthesis, and biological evaluation of the novel tetrahydroisoquinoline derivatives. Among those compounds, four new tetrahydroisoquinoline derivatives have not been reported before. All the newly synthesized compounds were characterized by ~1H NMR and their antitumor activities were evaluated by using HT-29, K562 and HepG2 cell line. 2-Benzyl-7-[2-(tert-butyl-4-piperazinecarboxylate) ethoxy]-3, 4-dihydro-1(2H)-isoquinolinone demonstrated good antitumor activity against K562 cancer cell with an IC_(50) of 1.58 μM.
机译:四氢异喹啉及其衍生物具有广泛的生物学活性,例如抗肿瘤,抗菌和镇痛特性等。已经研究了一些四氢异喹啉生物碱衍生物作为抗肿瘤药物分子,但是尚未报道2-苄基-7-取代的乙氧基] -3、4-二氢-1(2H)-异喹啉酮系列。在本文中,我们想报告新型四氢异喹啉衍生物的设计,合成和生物学评估。在这些化合物中,以前从未报道过四种新的四氢异喹啉衍生物。所有新合成的化合物均通过〜1H NMR表征,并使用HT-29,K562和HepG2细胞系评估其抗肿瘤活性。 2-苄基-7- [2-(4-哌嗪羧酸叔丁酯)乙氧基] -3,4-二氢-1(2H)-异喹啉酮对K562癌细胞具有良好的抗肿瘤活性,IC_(50)为1.58μM 。

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