REFERENCES
- Mikhailopulo , I. A. 2007 . Biotechnology of nucleic acid constituents—state of the art and perspectives . Current Org. Chem. , 11 : 317 – 335 .
- Esipov , R. S. , Gurevich , A. I. , Chuvikovsky , D. V. , Chupova , L. A. , Muravyova , T. I. and Miroshnikov , A. I. 2002 . Overexpression of Eherichia coli genes encoding nucleoside phosphorylases in the pET/B121 (DE3) system yields active recombinant enzymes . Protein Expes. Purif. , 24 : 56 – 60 .
- Zaitseva , G. W. , Kvasyuk , E. I. , Vaaks , E. V. , Barai , V. N. , Bokut , S. B. , Zinchenko , A. I. and Mikhailopulo , I. A. 1994 . Chemical-enzymatic synthesis of 3′-amino-2′,3′-dideoxy-β -D-ribofuranosides of natural heterocyclic bases and their 5′-monophosphates . Nucleosides & Nucleotides , 13 : 819 – 834 .
- Dolezal , K. , Popa , I. , Krystof , V. , Spichal , L. , Fojtikova , M. , Holub , J. , Lenobel , R. , Schmülling , T. and Strand , M. 2006 . Preparation and biological activity of 6-benzyaminopurine derivatives in plants and human cancer cells . Bioorg. Med. Chem. , 14 : 875 – 884 . and references therein
- Ishii , Y. , Kasukabe , T. and Honma , Y. 2005 . Immediate up-regulation of the calcium-binding protein S100P and its involvement in the cytokinin-induced differentiation of human myeloid leukemia cells . Biochim. Biophys. Acta , 1745 : 156 – 165 .
- Gao , Z.-G. and Jacobson , K. A. 2004 . Partial agonists for A3 adenosine receptors . Current Topics Med. Chem. , 4 : 855 – 862 .
- Zinchenko , A. I. , Barai , V. N. , Lyakhovets , V. I. , Kulak , T. I. , Kvasyuk , E. I. and Mikhailopulo , I. A. 1988 . Synthesis of 9-(β -D-ribofuranosyl)-6-benzylpurine and an affinity sorbent based on it . Bioorg. Chem. (Moow) , 14 : 1401 – 1404 .
- Mikhailopulo , I. A. , Kvasyuk , E. I. , Lyakhovets , V. I. , Popov , I. L. , Eroshevskaya , L. A. , Barai , V. N. and Zintchenko , A. I. 1984 . Synthesis of kinetin riboside and its 5′-monophosphae by immobilized bacterial cells . Nucl. Acid Res. Symp. Series , 14 : 291
- Standard reaction conditions: the donor-acceptor ratio was 1.5–3:1 (mol); 5 mM K-phosphate buffer (pH 7.0); heterogeneous reaction mixture was gentle stirred at 50 °C monitoring the progress of reaction by TLC and HPLC; after the reaction reached constant equilibrium, SiO2 was added and the mixture was evaporated to dryness, residue co-evaporated twice with abs EtOH, and SiO2 with products was placed on the top of a column packed with SiO2 in a mixture of CH2Cl2-MeOH (95:5, vol). Elution with a linear gradient of MeOH in CH2Cl2-MeOH (95:5, vol) gave the desired nucleosides