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(b) M. Komiyama, K. Matsumura and Y. Matsumoto, J. Chem. Soc., Chem. Commun., 1992, 640;
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19
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0347197769
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Ref. 2
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Ref. 2.
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20
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84985444005
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Hydrolysis of ribonucleoside 2′- and 3′-monophosphates by lanthanide ions has been examined extensively: S. Kuusela and H. Lönnberg J. Phys. Org. Chem., 1993, 6, 347.
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J. Phys. Org. Chem.
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Kuusela, S.1
Lönnberg, H.2
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21
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33847086713
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Monophosphate hydrolysis by metal ions other than lanthanide ions has been studied: (a) J. M. Harrowfield, D. R. Jones, L. F. Lindoy and A. M. Sargeson, J. Am. Chem. Soc., 1980, 102, 7733;
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J. Am. Chem. Soc.
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Harrowfield, J.M.1
Jones, D.R.2
Lindoy, L.F.3
Sargeson, A.M.4
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23
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0001464758
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and references cited therein
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(c) J. S. Seo, N.-D. Sung, R. C. Hynes and J. Chin, Inorg. Chem., 1996, 35, 7472 and references cited therein.
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Inorg. Chem.
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Seo, J.S.1
Sung, N.-D.2
Hynes, R.C.3
Chin, J.4
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24
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0002557903
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Pioneering works on the catalysis of lanthanide ions for the hydrolysis of phosphomonoesters were carried out about 40 years ago (a) E. Bamann, H. Trapmann and F. Fischler, Biochem. Z., 1953, 32, 89;
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Biochem. Z.
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Bamann, E.1
Trapmann, H.2
Fischler, F.3
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25
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0346567584
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However, these studies were made only in alkaline solutions, and thus the hydrolyses reported were much less efficient than those presented in the present paper. The catalysis by lanthanide ions is notably suppressed at a higher pH than 8, probably due to formation of the precipitates of metal hydroxide
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(b) M. Shimomura and F. Egami, Bull. Chem. Soc. Jpn., 1953, 26, 263. However, these studies were made only in alkaline solutions, and thus the hydrolyses reported were much less efficient than those presented in the present paper. The catalysis by lanthanide ions is notably suppressed at a higher pH than 8, probably due to formation of the precipitates of metal hydroxide.
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(1953)
Bull. Chem. Soc. Jpn.
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Shimomura, M.1
Egami, F.2
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26
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0346567599
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note
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IV at almost the same rates, providing dAp and pdA in nearly 1 :1 ratio (ref. 3f). These monophosphates are promptly hydrolysed to dA.
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28
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0346567598
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note
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IV.
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29
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0347827837
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note
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2 combination, is unlikely (see also refs. 3e and 3f).
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30
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0003992430
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ed. by Chemical Society of Japan, Maruzen
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a values of adenosine 5′-phosphate are 3.80 and 6.19, whereas the values of the 3′-phosphate are 3.65 and 5.83: Kagaku Binran Kiso-Hen, ed. by Chemical Society of Japan, Maruzen, 1984.
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(1984)
Kagaku Binran Kiso-Hen
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31
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0028286315
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Special Publication 25 The Chemical Society, London
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The bind constant for the complex formation of lanthanide(m) ions with adenosine monophosphate are around 104-fold greater that the corresponding values with dinucleotide: the former values are from Stability Constant Supplement No. 1, Special Publication 25 The Chemical Society, London, 1971, whereas the latter value are from M. Komiyama, N. Takeda, Y. Takahashi, Y. Matsumoto and M. Yashiro, Nucleosides, Nucleotides, 1994, 13, 1297.
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(1971)
Stability Constant Supplement No. 1
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-
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32
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0028286315
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The bind constant for the complex formation of lanthanide(m) ions with adenosine monophosphate are around 104-fold greater that the corresponding values with dinucleotide: the former values are from Stability Constant Supplement No. 1, Special Publication 25 The Chemical Society, London, 1971, whereas the latter value are from M. Komiyama, N. Takeda, Y. Takahashi, Y. Matsumoto and M. Yashiro, Nucleosides, Nucleotides, 1994, 13, 1297.
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(1994)
Nucleosides, Nucleotides
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Komiyama, M.1
Takeda, N.2
Takahashi, Y.3
Matsumoto, Y.4
Yashiro, M.5
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33
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0347197767
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note
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IV ion.
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36
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0022246350
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(c) A. George, P. Draganac and W. R. Farkas, Inorg. Chem., 1985, 24, 3627;
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(1985)
Inorg. Chem.
, vol.24
, pp. 3627
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George, A.1
Draganac, P.2
Farkas, W.R.3
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39
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37049067915
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(f) S. Kuusela A. Azhayev. A. Guzaev and H. Lönnberg, J. Chem. Soc., Perkin Trans. 2, 1995, 1197;
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(1995)
J. Chem. Soc., Perkin Trans. 2
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Kuusela, S.1
Azhayev, A.2
Guzaev, A.3
Lönnberg, H.4
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40
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0000889769
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(g) S. Kuusela, A. Guzaev and H. Lönnberg, J. Chem. Soc., Perkin Trans. 2, 1996, 1895.
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(1996)
J. Chem. Soc., Perkin Trans. 2
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Kuusela, S.1
Guzaev, A.2
Lönnberg, H.3
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