Počet záznamů: 1  

Conformationally constrained nucleoside phosphonic acids - potent inhibitors of human mitochondrial and cytosolic 5'(3')-nucleotidases

  1. 1.
    0435239 - ÚOCHB 2015 RIV GB eng J - Článek v odborném periodiku
    Šimák, Ondřej - Pachl, Petr - Fábry, Milan - Buděšínský, Miloš - Jandušík, T. - Hnízda, Aleš - Skleničková, Radka - Petrová, Magdalena - Veverka, Václav - Řezáčová, Pavlína - Brynda, Jiří - Rosenberg, Ivan
    Conformationally constrained nucleoside phosphonic acids - potent inhibitors of human mitochondrial and cytosolic 5'(3')-nucleotidases.
    Organic & Biomolecular Chemistry. Roč. 12, č. 40 (2014), s. 7971-7982. ISSN 1477-0520. E-ISSN 1477-0539
    Grant CEP: GA ČR GA203/09/0820; GA ČR GA13-24880S; GA ČR GA13-26526S; GA MŠMT(CZ) LK11205; GA AV ČR KAN200520801
    Institucionální podpora: RVO:61388963 ; RVO:68378050
    Klíčová slova: 5'(3')-nucleotidase * structure * inhibition * cdN * mdN * nucleoside * SAR * phosphonic acid
    Kód oboru RIV: CC - Organická chemie
    Impakt faktor: 3.562, rok: 2014

    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)-beta-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-i(mdN) = 2.71 mu M) and some induce a shift in selectivity toward cdN (carboxy derivative, K-i(cdN) = 11.60 mu M; iodoxy derivative, K-i(cdN) = 6.60 mu M). 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.
    Trvalý link: http://hdl.handle.net/11104/0239546

     
     
Počet záznamů: 1  

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