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新型芳香酰亚胺-多胺共轭物的合成与生物学评价

Synthesis and Biological Evaluation of Novel Aromatic Imide-Polyamine Conjugates.

作者信息

Li Ming, Wang Yuxia, Zhang Jianying, Xie Songqiang, Wang Chaojie, Wu Yingliang

机构信息

Department of Pharmacology, Shenyang Pharmaceutical University, Shenyang 110016, China.

Pharmaceutical College, Henan University, Kaifeng 475001, China.

出版信息

Molecules. 2016 Nov 30;21(12):1637. doi: 10.3390/molecules21121637.

Abstract

Three types of conjugates in which aromatic imide scaffolds were coupled to diverse amine/polyamine motifs were synthesized, and their antitumor activities were evaluated in vitro and in vivo. Results showed that the conjugate of 1,8-naphthilimide with spermine had pronounced effects on inhibiting tumor cell proliferation and inducing tumor cell apoptosis via ROS-mediated mitochondrial pathway. The in vivo assays on three H22 tumor transplant models revealed that compound exerted potent ability in preventing lung cancer metastasis and extending lifespan. Furthermore, the efficacy of in inhibiting tumor growth and improving body weight index were better than that of positive control, amonafide. Our study demonstrates that compound is a valuable lead compound for further investigation.

摘要

合成了三种将芳香族酰亚胺支架与不同胺/多胺基序偶联的共轭物,并在体外和体内评估了它们的抗肿瘤活性。结果表明,1,8-萘二甲酰亚胺与精胺的共轭物通过活性氧介导的线粒体途径对抑制肿瘤细胞增殖和诱导肿瘤细胞凋亡有显著作用。对三种H22肿瘤移植模型的体内试验表明,该化合物在预防肺癌转移和延长寿命方面具有强大能力。此外,该化合物在抑制肿瘤生长和改善体重指数方面的疗效优于阳性对照氨萘非特。我们的研究表明,该化合物是一种有价值的先导化合物,值得进一步研究。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ed9c/6273765/757cf98f0d94/molecules-21-01637-g001.jpg

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