Expression Pattern of MRP in Human Tissues and Adult Solid Tumor Cell Lines

1995 ◽  
Vol 87 (16) ◽  
pp. 1256-1260 ◽  
Author(s):  
G. D. Kruh ◽  
K. T. Gaughan ◽  
A. Godwin ◽  
A. Chan
2019 ◽  
Vol 18 (4) ◽  
pp. 1051-1100
Author(s):  
Lenka Molčanová ◽  
Dominika Janošíková ◽  
Stefano Dall´Acqua ◽  
Karel Šmejkal

2011 ◽  
Vol 2 (3) ◽  
pp. 419-422 ◽  
Author(s):  
VESNA BUCAN ◽  
CLAUDIA Y.U. CHOI ◽  
ANDREA LAZARIDIS ◽  
PETER M. VOGT ◽  
KERSTIN REIMERS

Leukemia ◽  
2009 ◽  
Vol 23 (7) ◽  
pp. 1270-1277 ◽  
Author(s):  
A Furuhata ◽  
M Murakami ◽  
H Ito ◽  
S Gao ◽  
K Yoshida ◽  
...  

Tumor Biology ◽  
2015 ◽  
Vol 37 (6) ◽  
pp. 7959-7966 ◽  
Author(s):  
Jochen Winter ◽  
Dominik Kraus ◽  
Jan Reckenbeil ◽  
Rainer Probstmeier

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.


2013 ◽  
Vol 14 (10) ◽  
pp. 5911-5913 ◽  
Author(s):  
Mustafa Yildiz ◽  
Hakan Bozcu ◽  
Onur Tokgun ◽  
Ege Riza Karagur ◽  
Oktay Akyurt ◽  
...  

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

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