Continuing our studies on ribonucleotide reductase (RNR) mechanism-based inhibitors, we have now prepd. the diphosphates (DP) of 2'-O-allyl-1-β-D-arabinofuranosyl-uracil and -cytosine and 2'-O-allyl-9-β-D-arabinofuranosyl-adenine and evaluated their inhibitory activity against recombinant murine RNR. 2'-O-Allyl-araUDP proved to be inhibitory to RNR at an IC50 of 100 μM, whereas 2'-O-allyl-araCDP was only marginally active (IC50 1 mM) and 2'-O-allyl-araADP was completely inactive. The susceptibility of the parent nucleosides to phosphorylation by thymidine kinase and 2'-deoxycytidine kinase was also investigated, and all nucleosides proved to be poor substrates for the above-cited kinases. Moreover, prodrugs of 2'-O-allyl-araU and -araC monophosphates, namely 2'-O-allyl-5'-(phenylethoxy-L-alanyl phosphate)-araU and -araC, were prepd. and tested against tumor cell proliferation but proved to be inactive. A mol. modeling study has been conducted in order to explain our results. The data confirm that for both the natural and analog nucleoside diphosphates, the principal determinant interaction with the active site of RNR is with the diphosphate group, which forms strong hydrogen bonds with Glu623, Thr624, Ser625, and Thr209. Our findings indicate that the poor phosphorylation may represent an explanation for the lack of marked in vitro cytostatic activity of the test compds.

5'-Phosphoramidates and 5'-diphosphates of 2'-O-allyl-β-D- arabinofuranosyl-uracil, -cytosine, and -adenine: Inhibition of ribonucleotide reductase

MANFREDINI, Stefano;BARALDI, Pier Giovanni;DURINI, Elisa;VERTUANI, Silvia;
1999

Abstract

Continuing our studies on ribonucleotide reductase (RNR) mechanism-based inhibitors, we have now prepd. the diphosphates (DP) of 2'-O-allyl-1-β-D-arabinofuranosyl-uracil and -cytosine and 2'-O-allyl-9-β-D-arabinofuranosyl-adenine and evaluated their inhibitory activity against recombinant murine RNR. 2'-O-Allyl-araUDP proved to be inhibitory to RNR at an IC50 of 100 μM, whereas 2'-O-allyl-araCDP was only marginally active (IC50 1 mM) and 2'-O-allyl-araADP was completely inactive. The susceptibility of the parent nucleosides to phosphorylation by thymidine kinase and 2'-deoxycytidine kinase was also investigated, and all nucleosides proved to be poor substrates for the above-cited kinases. Moreover, prodrugs of 2'-O-allyl-araU and -araC monophosphates, namely 2'-O-allyl-5'-(phenylethoxy-L-alanyl phosphate)-araU and -araC, were prepd. and tested against tumor cell proliferation but proved to be inactive. A mol. modeling study has been conducted in order to explain our results. The data confirm that for both the natural and analog nucleoside diphosphates, the principal determinant interaction with the active site of RNR is with the diphosphate group, which forms strong hydrogen bonds with Glu623, Thr624, Ser625, and Thr209. Our findings indicate that the poor phosphorylation may represent an explanation for the lack of marked in vitro cytostatic activity of the test compds.
Manfredini, Stefano; Baraldi, Pier Giovanni; Durini, Elisa; Vertuani, Silvia; Balzarini, Jan; DE CLERCQ, Erik; Karlsson, Anna; Buzzoni, Valentina; Thelander, Lars
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/11392/1197544
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