Indole Alkaloids, Synthetic Dimers and Hybrids with Potential In Vivo Anticancer Activity

被引:22
|
作者
Song, Feng [1 ,2 ]
Bian, Yunqiang [1 ]
Liu, Jing [1 ,3 ]
Li, Zhenghua [1 ]
Zhao, Li [1 ]
Fang, Junman [2 ]
Lai, Yonghong [2 ]
Zhou, Meng [2 ]
机构
[1] Dezhou Univ, Shandong Key Lab Biophys, Inst Biophys, Dezhou 253023, Shandong, Peoples R China
[2] Dezhou Univ, Sch Life Sci, Dezhou 253023, Shandong, Peoples R China
[3] Hefei Univ, Sch Biol Food & Environm Engn, Hefei 230000, Anhui, Peoples R China
基金
中国国家自然科学基金;
关键词
Indole alkaloids; Dimers; Hybrids; In vivo; Cancer; Mechanisms of action; HISTONE DEACETYLASE INHIBITORS; N-SUBSTITUTED; 7-AZAINDOLES; BIOLOGICAL EVALUATION; ANTITUMOR-ACTIVITY; TUMOR-GROWTH; KINASE INHIBITORS; CANCER-CELLS; CHALCONE DERIVATIVES; COMBRETASTATIN A-4; UP-REGULATION;
D O I
10.2174/1568026620666200908162311
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
Indole, a heterocyclic organic compound, is one of the most promising heterocycles found in natural and synthetic sources since its derivatives possess fascinating structural diversity and various therapeutic properties. Indole alkaloids, synthetic dimers and hybrids could act on diverse targets in cancer cells, and consequently, possess potential antiproliferative effects on various cancers both in vitro and in vivo. Vinblastine, midostaurin, and anlotinib as the representative of indole alkaloids, synthetic dimers and hybrids respectively, have already been clinically applied to treat many types of cancers, demonstrating indole alkaloids, synthetic dimers and hybrids are useful scaffolds for the development of novel anticancer agents. Covering articles published between 2010 and 2020, this review emphasizes the recent development of indole alkaloids, synthetic dimers and hybrids with potential in vivo therapeutic application for cancers.
引用
收藏
页码:377 / 403
页数:27
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