Design, Synthesis, and in Vitro Activity of Catamphiphilic Reverters of Multidrug Resistance:  Discovery of a Selective, Highly Efficacious Chemosensitizer with Potency in the Nanomolar Range

1999 ◽  
Vol 42 (10) ◽  
pp. 1687-1697 ◽  
Author(s):  
Elisabetta Teodori ◽  
Silvia Dei ◽  
Patricia Quidu ◽  
Roberta Budriesi ◽  
Alberto Chiarini ◽  
...  
2002 ◽  
Vol 46 (6) ◽  
pp. 2038-2040 ◽  
Author(s):  
Joseph Nkemgu-Njinkeng ◽  
Vera Rosenkranz ◽  
Michael Wink ◽  
Dietmar Steverding

ABSTRACT Seven peptidyl proteasome inhibitors were tested for in vitro activity against Trypanosoma brucei bloodstream forms. Two compounds showed activity in the low nanomolar range. In general, trypanosomes were more susceptible to the compounds than were human HL-60 cells. The data support the potential of proteasome inhibitors for rational antitrypanosomal drug development.


2005 ◽  
Vol 15 (4) ◽  
pp. 1161-1164 ◽  
Author(s):  
Dominique Potin ◽  
Michele Launay ◽  
Eric Nicolai ◽  
Maud Fabreguette ◽  
Patrice Malabre ◽  
...  

PLoS ONE ◽  
2015 ◽  
Vol 10 (11) ◽  
pp. e0142678 ◽  
Author(s):  
Anna Mrozek-Wilczkiewicz ◽  
Ewelina Spaczynska ◽  
Katarzyna Malarz ◽  
Wioleta Cieslik ◽  
Marzena Rams-Baron ◽  
...  

1994 ◽  
Vol 37 (3) ◽  
pp. 348-355 ◽  
Author(s):  
John C. Cheronis ◽  
Eric T. Whalley ◽  
Lisa G. Allen ◽  
Sharon D. Loy ◽  
Megan W. Elder ◽  
...  

2012 ◽  
Vol 55 (7) ◽  
pp. 3216-3227 ◽  
Author(s):  
Dijana Pešić ◽  
Kristina Starčević ◽  
Ana Toplak ◽  
Esperanza Herreros ◽  
Jaume Vidal ◽  
...  

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