Photophysical, G-quadruplex DNA binding and cytotoxic properties of terpyridine complexes with a naphthalimide ligand

RSC Advances ◽  
2016 ◽  
Vol 6 (43) ◽  
pp. 36923-36931 ◽  
Author(s):  
Zhize Ou ◽  
Yimeng Qian ◽  
Yunyan Gao ◽  
Yunqing Wang ◽  
Guoqiang Yang ◽  
...  

The complex3inhibits A549 cells selectively over non-cancerous NIH3T3 cells, which may correlate with its selective G-quadruplex binding and nuclear location.

2015 ◽  
Vol 13 (30) ◽  
pp. 8335-8348 ◽  
Author(s):  
Basudeb Maji ◽  
Krishan Kumar ◽  
K. Muniyappa ◽  
Santanu Bhattacharya

G-quadruplex DNA binding dimeric ligands and their telomerase inhibition activity are reported.


2019 ◽  
Vol 90 ◽  
pp. 103074
Author(s):  
Gang Li ◽  
Haodong Tang ◽  
Chuanfeng Liu ◽  
Xiaoyu Liao ◽  
Sicong Li ◽  
...  

2004 ◽  
Vol 14 (14) ◽  
pp. 3627-3630 ◽  
Author(s):  
Bernard Juskowiak ◽  
Elzbieta Galezowska ◽  
Natalia Koczorowska ◽  
Tadeusz W Hermann

2002 ◽  
Vol 12 (3) ◽  
pp. 447-450 ◽  
Author(s):  
Sean M. Kerwin ◽  
Grace Chen ◽  
Jonathan T. Kern ◽  
Pei Wang Thomas

2008 ◽  
Vol 27 (4) ◽  
pp. 289-296 ◽  
Author(s):  
Blazej Rubis ◽  
Mariusz Kaczmarek ◽  
Natalia Szymanowska ◽  
Elzbieta Galezowska ◽  
Andrzej Czyrski ◽  
...  

2017 ◽  
Vol 27 (2) ◽  
pp. 329-335 ◽  
Author(s):  
Md. Monirul Islam ◽  
Shinobu Sato ◽  
Shingo Shinozaki ◽  
Shigeori Takenaka

2021 ◽  
Vol 22 (12) ◽  
pp. 6476
Author(s):  
Sabrina Dallavalle ◽  
Luce M. Mattio ◽  
Roberto Artali ◽  
Loana Musso ◽  
Anna Aviñó ◽  
...  

Curaxins and especially the second-generation derivative curaxin CBL0137 have important antitumor activities in multiple cancers such as glioblastoma, melanoma and others. Although most of the authors suggest that their mechanism of action comes from the activation of p53 and inactivation of NF-kB by targeting FACT, there is evidence supporting the involvement of DNA binding in their antitumor activity. In this work, the DNA binding properties of curaxin CBL0137 with model quadruplex DNA oligomers were studied by 1H NMR, CD, fluorescence and molecular modeling. We provided molecular details of the interaction of curaxin with two G-quadruplex structures, the single repeat of human telomere d(TTAGGGT)4 and the c-myc promoter Pu22 sequence. We also performed 1H and 31P NMR experiments were also performed in order to investigate the interaction with duplex DNA models. Our data support the hypothesis that the interaction of curaxin with G-quadruplex may provide a novel insight into the DNA-binding properties of CBL0137, and it will be helpful for the design of novel selective DNA-targeting curaxin analogues.


Sign in / Sign up

Export Citation Format

Share Document