scholarly journals Molecular <em>docking </em>study of iclaprim derivatives with potential antineoplastic activity

2021 ◽  
Author(s):  
Marina Mijajlović ◽  
Teodora Tanasković ◽  
Miloš Nikolić ◽  
Nikola Nedeljković ◽  
Ana Stanković ◽  
...  
2018 ◽  
Author(s):  
M Hlavac ◽  
A Dwucet ◽  
A Westhoff ◽  
RE Kast ◽  
J Engelke ◽  
...  

1983 ◽  
Vol 48 (1) ◽  
pp. 304-311 ◽  
Author(s):  
Jiří Křepelka ◽  
Jan Beneš ◽  
Vladimír Pouzar ◽  
Jaroslav Vachek ◽  
Jiří Holubek

Condensation of triethyl ester of 1,1,5-pentanetricarboxylic acid (XI) with substituted guanidines XXII - XXIX gave acids II - IX, which were converted into esters XI - XIX. The acid II and the ester XI were obtained as mixtures of positional isomers. Analogously, condensation of the triester XXI with dicyanodiamide gave rise to acid X, whose nitrile group, under conditions of esterification of a carboxyl group, produced iminoether XX. In pharmacological tests for antineoplastic activity the compounds prepared exhibited weaker efficacy than 5-(2-amino-6-hydroxy-4-oxo-3,4-dihydro-5-pyrimidinyl)pentanoic acid (I), employed as standard.


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