Synthesis and biological evaluation of thiophenylbenzofuran derivatives as potential P-glycoprotein inhibitors

2020 ◽  
Vol 201 ◽  
pp. 112422
Author(s):  
Chin-Chuan Hung ◽  
Chien-Yu Chen ◽  
Yu-Chieh Wu ◽  
Chien-Fu Huang ◽  
Yu-Chun Huang ◽  
...  
2012 ◽  
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pp. 2540-2548 ◽  
Author(s):  
Xiaoke Gu ◽  
Zhiguang Ren ◽  
Xiaobo Tang ◽  
Hui Peng ◽  
Yuanfang Ma ◽  
...  

2008 ◽  
Vol 51 (5) ◽  
pp. 1415-1422 ◽  
Author(s):  
Nicola Antonio Colabufo ◽  
Francesco Berardi ◽  
Roberto Perrone ◽  
Simona Rapposelli ◽  
Maria Digiacomo ◽  
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Heterocycles ◽  
2015 ◽  
Vol 90 (1) ◽  
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Takayuki Doi ◽  
Naoko Yamaguchi ◽  
Kosuke Ohsawa ◽  
Kazuoki Nakai ◽  
Masahito Yoshida ◽  
...  

Author(s):  
Jessica R. Gutierrez-Cano ◽  
Pradip D. Nahide ◽  
Velayudham Ramadoss ◽  
Yuvraj Satkar ◽  
Rafael Ortiz-Alvarado ◽  
...  

<p>A series of new 3,4-diarylmaleimides were synthesized in an optimized and efficient lineal sequence of three steps, starting from commercial maleimide. The biological evaluation of these compounds as enhancers (activity modulators) in the co-administration with doxorubicin treatment in breast cancer cells directly obtained from a patient, were essayed. The cancerous tissue BT026-512N was provided by the National Institute of Cancerology (INCAN) of México. This tissue was obtained by biopsy from a patient diagnosed with stage IIB ductal breast cancer. The results obtained in the assays, show decreased cell viability on the cultured cells for all of the maleimides synthesized in combinatorial administration with doxorubicin. The highest mortality effect was determined for maleimides <strong>9</strong> and <strong>29</strong> increased in close to three times the effect compared with treatment using only doxorubicin. Based on previous functionalized maleimides core reports and Molinspiration chemoinformatic analysis, these results could possibly point out to the Pg-p glycoprotein as bio-molecular action target of maleimides by kinase phosphorylation-inhibition, although more experimental data is necessary.</p>


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