Cytotoxicity and Structure-Activity Relationship Studies of Aqua-Triphenyltin(IV) Carboxylates on Human Cancer Cell Lines

2007 ◽  
Vol 30 (2-3) ◽  
Author(s):  
Chee Chin Fei ◽  
Lo Kong Mun
2018 ◽  
Vol 47 ◽  
pp. 26-37 ◽  
Author(s):  
Romeu A. Videira ◽  
Paula B. Andrade ◽  
Luís S. Monteiro ◽  
Patrícia Valentão ◽  
Paula M.T. Ferreira ◽  
...  

2005 ◽  
Vol 277-279 ◽  
pp. 23-27 ◽  
Author(s):  
Min Jin Kwon ◽  
Hwan Mook Kim ◽  
Dae Duk Kim ◽  
Jung Sun Kim

A series of 5-substituted 2-(p-methoxyphenyl)-1H-benzimidazoles was synthesized and evaluated for cytotoxicity against 4 human cancer cell lines, HCT 15, PC-3, A549, and ACHN. Except for the 5-chloro analogue, most of the 5-substituted compounds showed significant cytotoxicities in these cell lines. However, the structure activity relationship study revealed that neither the electronic nor the lipophilic parameters of the 5-substituents were related to cytotoxicity. Moreover, none of the analogues showed significant NF к-β inhibition activity implying that cytotoxicity was not related to this mechanism. The 5-methyl analogue was the most potent compound in this series with a GI50 of 0.9 µM in the A549 cell line.


Planta Medica ◽  
2007 ◽  
Vol 73 (09) ◽  
Author(s):  
IO Mondranondra ◽  
A Suedee ◽  
A Kijjoa ◽  
M Pinto ◽  
N Nazareth ◽  
...  

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