Structure−Activity Relationship of Newly Synthesized Quinoline Derivatives for Reversal of Multidrug Resistance in Cancer

1997 ◽  
Vol 40 (13) ◽  
pp. 2047-2052 ◽  
Author(s):  
Tsuneji Suzuki ◽  
Nobuyuki Fukazawa ◽  
Kunio San-nohe ◽  
Wakao Sato ◽  
Osamu Yano ◽  
...  
2006 ◽  
Vol 49 (21) ◽  
pp. 6351-6363 ◽  
Author(s):  
Iisa P. J. Höglund ◽  
Satu Silver ◽  
Mia T. Engström ◽  
Harri Salo ◽  
Andrei Tauber ◽  
...  

2008 ◽  
Vol 61 (7) ◽  
pp. 531 ◽  
Author(s):  
Qiang Zhou ◽  
Jing Hou ◽  
Huamin Li ◽  
Li Cui ◽  
Han Jia ◽  
...  

Designed as a new series of molecules that contain the quinoline substructure, several 11H-indolo[3.2-c]quinoline derivatives were synthesized and subjected to biological evaluation. Several compounds were found to exhibit cytotoxic activity against the growth of colon (HTC-8), liver (BEL-7402), gastric (BCG-823), pulmonary gland (A549), and ovary (A2780) cancer cell lines. The structure–activity relationship of these compounds is discussed.


1995 ◽  
Vol 50 (8) ◽  
pp. 1245-1255 ◽  
Author(s):  
G. Toffoli ◽  
F. Simone ◽  
G. Corona ◽  
M. Raschack ◽  
B. Cappelletto ◽  
...  

Sign in / Sign up

Export Citation Format

Share Document