Structure−Activity Relationship of Quinoline Derivatives as Potent and Selective α2C-Adrenoceptor Antagonists

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

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.


2018 ◽  
Vol 10 (17) ◽  
pp. 2069-2085 ◽  
Author(s):  
Etyene JG Silva ◽  
Adriana Bezerra-Souza ◽  
Luiz FD Passero ◽  
Márcia D Laurenti ◽  
Gláucio M Ferreira ◽  
...  

Planta Medica ◽  
2008 ◽  
Vol 74 (09) ◽  
Author(s):  
MA Brenzan ◽  
CV Nakamura ◽  
BPD Filho ◽  
T Ueda-Nakamura ◽  
MCM Young ◽  
...  

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