scholarly journals Identification of Michael Acceptor-Centric Pharmacophores with Substituents That Yield Strong Thioredoxin Reductase Inhibitory Character Correlated to Antiproliferative Activity

2013 ◽  
Vol 19 (11) ◽  
pp. 1149-1165 ◽  
Author(s):  
Fei-Fei Gan ◽  
Kamila K. Kaminska ◽  
Hong Yang ◽  
Chin-Yee Liew ◽  
Pay-Chin Leow ◽  
...  
2008 ◽  
Vol 22 (6) ◽  
pp. 2072-2083 ◽  
Author(s):  
Eng‐Hui Chew ◽  
Jun Lu ◽  
Tracey D. Bradshaw ◽  
Arne Holmgren

2021 ◽  
Author(s):  
Jovica Branković ◽  
◽  
Vesna Milovanović ◽  
Zorica D. Petrović ◽  
Vladimir P. Petrović

Gallic hydrazones, as gallic acid derivatives, are known as pharmacophores of numerous multipotent agents. Among them, antiproliferative activity is one of the most important. On the other hand, thioredoxin reductase (TrxR1) is a part of the thioredoxin system, one of the most important systems responsible for maintaining the redox equilibrium inside the cell. It is overexpressed in different forms of tumors. Bearing this in mind, TrxR1 is a valid target for the development of compounds with potential antiproliferative activity. For this purpose, eight gallic acid-based hydrazones are selected and examined in silico for their potential inhibitory activity towards TrxR1.


2020 ◽  
Vol 44 (15) ◽  
pp. 5762-5773 ◽  
Author(s):  
Tatiyana V. Serebryanskaya ◽  
Mikhail A. Kinzhalov ◽  
Vladimir Bakulev ◽  
Georgii Alekseev ◽  
Anastasiya Andreeva ◽  
...  

Water soluble Pd(ii) and Pt(ii)–ADC species synthesized via the metal-mediated coupling of isocyanides and 1,2-diaminobenzene have demonstrated antitumor potential.


Planta Medica ◽  
2010 ◽  
Vol 76 (12) ◽  
Author(s):  
G Marchetti ◽  
K Silva ◽  
A Ruiz ◽  
I Sousa ◽  
S Tinti ◽  
...  

Planta Medica ◽  
2012 ◽  
Vol 78 (11) ◽  
Author(s):  
R Tundis ◽  
B Deguin ◽  
MR Loizzo ◽  
M Bonesi ◽  
S Michel ◽  
...  

2017 ◽  
Author(s):  
A Vasas ◽  
I Lajter ◽  
P Forgó ◽  
N Kúsz ◽  
N Bózsity ◽  
...  

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