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10
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85030209794
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note
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2O (compounds 2 and 6, respectively).
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11
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85030208563
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note
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2-of THF).
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13
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85030210609
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note
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2-2′).
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14
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85030200651
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note
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28
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16
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37049099910
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Howarth, O.1
Jones, A.S.2
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Wyatt, P.G.4
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17
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85030203119
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note
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2O) δ 8.37-8.16 (m, 2 H; H-2 and H-8); 6.14-5.99 (m, 1 H; H-1′); 5.17-4.70 (m, 5 H; 2 H-2′, H-4′ and 2 H-5′).
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21
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0242651290
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Usdin, E.; Borchardt, R. T.; Creveling, C. R., Eds.; Elsevier: New York
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Hoffman, J.L.1
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23
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85030201586
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note
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14C] adenosine, 54.3 mCi/mmol (New England Nuclear); and inhibitor in a final volume of 0.2 mL. The reaction was started by addition of enzyme followed by incubation at 37 °C for 2.5 min. The reaction was terminated by heating in boiling water for 2 min., followed by centrifugation. After addition of 5 μ1 each of 5 mM solutions of adenosine, inosine, and product AdoHcy as markers, aliquots (5 × 5 μ1 each) were spotted on aluminum-supported silica gel 60 F254 TLC sheets (E. Merck). Chromatograms were developed in 1-butanol : acetic acid : water (12:3:5) for 100 min. Spots containing radioactive product were visualized under UV light, cut out, and counted after addition of Scintisol fluor. Each reaction was run in duplicate. Kinetic parameters were determined by Lineweaver-Burk plots.
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24
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85030200194
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note
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Antiviral data on compounds 1, 2, 5 and 6 were obtained from the U. S. Army Medical Research Institute of Infectious Diseases, Frederick, MD, USA.
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25
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0000359889
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0016683564
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Bunt, A.H.3
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