scholarly journals Some inhibitors of purine nucleoside phosphorylase

2011 ◽  
Vol 57 (5) ◽  
pp. 526-534 ◽  
Author(s):  
L.H. Pogosian ◽  
L.S. Nersesova ◽  
M.G. Gazariants ◽  
Z.S. Mkrtchian ◽  
J.I. Akopian

Purine nucleoside phosphorylase (PNP) catalyzes reversible phosphorolysis of purine deoxy- and ribonucleosides with formation (d)Rib-1-P and corresponding bases. PNP plays a leading role in the cell metabolism of nucleosides and nucleotides, as well as in maintaining the immune status of an organism. The major aim of the majority of studies on the PNP is the detection of highly effective inhibitors of this enzyme, derivatives of purine nucleosides used in medicine as immunosuppressors, which are essential for creating selective T-cell immunodeficiency in a human body for organ and tissue transplantation.The present work is devoted to the study of the effects of some synthetic derivatives of purine nucleosides on activity of highly purified PNP from rabbit spleen and also from human healthy and tumor tissues of lung and kidneys. Purine nucleoside analogues modified at various positions of both the heterocyclic base and carbohydrate residues have been investigated. Several compounds, including 8-mercapto-acyclovir, 8-bromo-9-(3,4-hydroxy-butyl)guanine, which demonstrated potent PNP inhibition, could be offered for subsequent study as immunosuppressors during organ and tissue transplantation.

1993 ◽  
Vol 36 (13) ◽  
pp. 1847-1854 ◽  
Author(s):  
John A. Secrist ◽  
Shri Niwas ◽  
Jerry D. Rose ◽  
Y. Sudhakar Babu ◽  
Charles E. Bugg ◽  
...  

1993 ◽  
Vol 36 (1) ◽  
pp. 55-69 ◽  
Author(s):  
John A. Montgomery ◽  
Shri Niwas ◽  
Jerry D. Rose ◽  
John A. Secrist ◽  
Y. Sudhakar Babu ◽  
...  

1993 ◽  
Vol 36 (24) ◽  
pp. 3771-3783 ◽  
Author(s):  
Mark D. Erion ◽  
Shri Niwas ◽  
Jerry D. Rose ◽  
Subramaniam Ananthan ◽  
Mark Allen ◽  
...  

2010 ◽  
Vol 75 (12) ◽  
pp. 1249-1257 ◽  
Author(s):  
Ivan Votruba ◽  
Jana Trýznová ◽  
Petra Břehová ◽  
Eva Tloušťová ◽  
Květoslava Horská ◽  
...  

The structure-activity study on the phosphates of phosphonomethoxypropyl derivatives of purine bases interacting with human purine nucleoside phosphorylase has shown that the most efficient inhibitors of the enzyme are (R)- and (S)-PMPGp with Ki ~ 1.9 × 10–8 and/or 2.2 × 10–8 mol/l. The kinetic experiments have proven, with the exception of both enantiomers of PMP-8-BrDAPp, strictly competitive character of inhibition for all ANP monophosphates tested. Bromine derivatives exhibited uncompetitive and mixed type of inhibition as well. These results were confirmed by docking studies. The substitution of purine moiety with the bromine at the position 8 lead to an allosteric binding of these compounds toward the enzyme.


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