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Design, Synthesis and Biological Evaluation of Novel anticancer agent Sprio Indolone Compounds

机译:新型抗癌剂Sprio Indolone化合物的设计,合成和生物学评价

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摘要

Indolone is a kind of natural product which was widely existed in the animal bodies and plants, which possess varieties of biological activities, such as anti-bacterial, anti-tumor, anti-aging and anti-anxiety activities. As we all known that many sprio compounds which containing hetero atom such as O, N, S have good biological activities. In this paper, a series of spiro indolone derivatives was design with the combination of indolone and sprio scaffold, 6 novel target compounds were synthesized in 3 or 4 steps in 6%-17% overall yield, which were characterized by ~1H NMR and their biological activities on tumor cells growth inhibition on human hepatoma cell HePG2 and human leukemia cell K562 by MTT method were evaluated.
机译:吲哚菁是一种天然产品,其在动物体和植物中广泛存在,具有生物活性的品种,例如抗菌,抗肿瘤,抗衰老和抗焦虑活动。众所周知,许多含有杂原子如O,N,S的Sprio化合物具有良好的生物活性。在本文中,一系列螺吲哚胺衍生物具有吲哚和Sprio支架组合的设计,在6%-17%的总收率中合成了6个新的靶化合物,其特征在于〜1H NMR及其评估了MTT方法对人肝癌细胞Hepg2和人白血病细胞K562对人肝癌细胞生长抑制的生物活性。

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