Conformationally constrained nucleoside phosphonic acids - potent inhibitors of human mitochondrial and cytosolic 5′(3′)-nucleotidasesElectronic supplementary information (ESI) available: (1) Calculated geometry and NMR parameters for C3′-endo and C2′-endo conformations of [6′R] and [6′S]-epimers of compound 9i. (2) Backbone NMR chemical shift perturbations obtained for cdN complexes (compounds 12d, 13, 15, 31 and 32). (3) Calculated distances of the metal ion and coordinating atoms in 3 differe

• Main Authors: Šimák, Ond ej, Pachl, Petr, Fábry, Milan, Bud šínský, Miloš, Jandušík, Tomáš, Hnízda, Aleš, Skleni ková, Radka, Petrová, Magdalena, Veverka, Václav, ezá ová, Pavlína, Brynda, Ji í, Rosenberg, Ivan
• Format: Article
• Language: English
• ISSN: 1477-0520; 1477-0539
• DOI: 10.1039/c4ob01332h

This work describes novel in vitro inhibitors of human mitochondrial (mdN) and cytosolic (cdN) 5′(3′)-deoxynucleotidases. We designed a series of derivatives of the lead compound ( S )-1-[2-deoxy-3,5- O -(phosphonobenzylidene)-β- d - threo -pentofuranosyl]thymine bearing various substituents in the para position of the benzylidene moiety. Detailed kinetic study revealed that certain para substituents increase the inhibitory potency (iodo derivative; K mdN i = 2.71 μM) and some induce a shift in selectivity toward cdN (carboxy derivative, K cdN i = 11.60 μM; iodoxy derivative, K cdN i = 6.60 μM). Crystal structures of mdN in complex with three of these compounds revealed that various para substituents lead to two alternative inhibitor binding modes within the enzyme active site. Two binding modes were also identified for cdN complexes by heteronuclear NMR spectroscopy. Conformationally constrained nucleoside phosphonic acids - potent inhibitors of human mitochondrial and cytosolic 5′(3′)-deoxynucleotidases.