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

Author:

Song Feng1,Bian Yunqiang1,Liu Jing1,Li Zhenghua1,Zhao Li1,Fang Junman2,Lai Yonghong2,Zhou Meng2

Affiliation:

1. Shandong Key Laboratory of Biophysics, Institute of Biophysics, Dezhou University, Dezhou 253023, Shandong,China

2. School of Life Sciences, Dezhou University, Dezhou 253023, Shandong,China

Abstract

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.

Funder

Natural Science Foundation of Anhui Province

National Natural Science Foundation of China

Taishan Young Scholars Program of Shandong Province

Publisher

Bentham Science Publishers Ltd.

Subject

Drug Discovery,General Medicine

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