Design, synthesis and biological evaluation of hybrids of β-carboline and salicylic acid as potential anticancer and apoptosis inducing agents-Reference-Cited by-同舟云学术

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Design, synthesis and biological evaluation of hybrids of β-carboline and salicylic acid as potential anticancer and apoptosis inducing agents

Published:2016-11-08 Issue:1 Volume:6 Page:
ISSN:2045-2322
Container-title:Scientific Reports
language:en
Short-container-title:Sci Rep

Author:

Xu Qi-Bing,Chen Xiang-Fan,Feng Jiao,Miao Jie-Fei,Liu Ji,Liu Feng-Tao,Niu Bi-Xi,Cai Jin-Yang,Huang Chao,Zhang Yanan,Ling Yong

Publisher

Springer Science and Business Media LLC

Subject

Multidisciplinary

Link

http://www.nature.com/articles/srep36238.pdf

Reference26 articles.

1. Cao, R., Peng, W., Wang, Z. & Xu, A. β-Carboline alkaloids: biochemical and pharmacological functions. Curr. Med. Chem. 14, 479−500 (2007).

2. Kamal, A. et al. Design and synthesis of C3-pyrazole/chalcone-linked beta-carboline hybrids: antitopoisomerase-I, DNA-interactive, and apoptosis-inducing anticancer agents. Chem. Med. Chem. 9(9), 2084–2098 (2014).

3. He, L. et al. Ruthenium-Arene-beta-Carboline Complexes as Potent Inhibitors of Cyclin-Dependent Kinase 1: Synthesis, Characterization and Anticancer Mechanism Studies. Chemistry 19, 12152–12160 (2013).

4. Han, X. et al. A series of beta-carboline derivatives inhibit the kinase activity of PLKs. PLoS One 7, e46546 (2012).

5. Herraiz, T., Gonzalez, D., Ancin-Azpilicueta, C., Aran, V. J. & Guillen, H. beta-Carboline alkaloids in Peganum harmala and inhibition of human monoamine oxidase (MAO). Food Chem. Toxicol. 48, 839–845 (2010).

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