scholarly journals Cytotoxic Bioactivity of Some Phenylpropanoic Acid Derivatives

2012 ◽  
Vol 7 (10) ◽  
pp. 1934578X1200701 ◽  
Author(s):  
Guillermo F. Reta ◽  
Carlos E. Tonn ◽  
Carla Ríos-Luci ◽  
Leticia G. León ◽  
Eduardo Pérez-Roth ◽  
...  

In this study, we synthesized a series of phenylpropanoic acid derivatives based on modifications at four selected points of the molecular scaffold. The in vitro antiproliferative activities of the compounds were examined in representative human solid tumor cell lines. A SAR was established pointing out the relevance of the substituents. The best activity profiles were obtained for the derivatives bearing more lipophilic esters (GI50 3.1-21 μM).

2010 ◽  
Vol 20 (5) ◽  
pp. 1504-1506 ◽  
Author(s):  
Simonas Rudys ◽  
Carla Ríos-Luci ◽  
Eduardo Pérez-Roth ◽  
Inga Cikotiene ◽  
José M. Padrón

2021 ◽  
Author(s):  
Exequiel O. J. Porta ◽  
María Sol Ballari ◽  
José M. Padrón ◽  
Guillermo R. Labadie

Aim: We proposed to determine the antiproliferative activity of a series of synthetic salirasib analogs, presenting or not a 1,2,3-triazole linker, against five different cancer cell lines. Results: Bioassay, cheminformatic, and in silico ADME-Tox allowed the identification of new potent analogs. SAR analysis allowed the identification of structural and physicochemical features that benefit the antiproliferative activity. Conclusion: Isoprenyl R chains with three or more isoprene units, or long aliphatic R chains are the preferred ones within the active compounds. Likewise, we have identified three compounds with better activity profiles than salirasib against all the cell lines tested.


1996 ◽  
Vol 224 (2) ◽  
pp. 189-197 ◽  
Author(s):  
Masafumi Wasa ◽  
Barrie P. Bode ◽  
Steven F. Abcouwer ◽  
Cynthia L. Collins ◽  
Kenneth K. Tanabe ◽  
...  

Sign in / Sign up

Export Citation Format

Share Document