-
4
-
-
0343655960
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-
note
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+; 100).
-
-
-
-
5
-
-
0343655959
-
-
note
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+; 100).
-
-
-
-
6
-
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0343655958
-
-
7 All the double reciprocal substrate-initial velocity plots were linear. Enzyme (0.14 μg for adenosine and 2′-deoxy-adenosine; 1.4 μg for compounds 4-7; 5.6 μg for 1 and until 22.4 μg for 2 and 3) was added to initiate the enzymatic reaction
-
7 All the double reciprocal substrate-initial velocity plots were linear. Enzyme (0.14 μg for adenosine and 2′-deoxy-adenosine; 1.4 μg for compounds 4-7; 5.6 μg for 1 and until 22.4 μg for 2 and 3) was added to initiate the enzymatic reaction.
-
-
-
-
8
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-
0343655956
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-
Inhibition of 16 and 23% were observed when adenosine (39 μM) was incubated with 3′-C-vinyl-(ribo)-adenosine (60 μM) and 3′-C-ethyl-(ribo)-adenosine (60 μM) respectively.
-
Inhibition of 16 and 23% were observed when adenosine (39 μM) was incubated with 3′-C-vinyl-(ribo)-adenosine (60 μM) and 3′-C-ethyl-(ribo)-adenosine (60 μM) respectively.
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-
-
-
9
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0003518480
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John Wiley and Sons/Wiley-Interscience: New York
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Segel, I. H. In Enzyme Kinetics; John Wiley and Sons/Wiley-Interscience: New York, 1975; pp 41-43.
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Segel, I.H.1
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10
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77956483651
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Boyer, P. D., Ed.; Academic Press: New York
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Zielke, C. L.; Suelter, C. H. In The Enzymes, 3rd Ed.; Boyer, P. D., Ed.; Academic Press: New York, 1971; Vol. 4, pp 47-78.
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The Enzymes, 3rd Ed.
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Zielke, C.L.1
Suelter, C.H.2
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14
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0032499630
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and references cited therein
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Wang, Z.; Quiocho, F. A. Biochemistry 1998, 37, 8314-8324, and references cited therein.
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Wang, Z.1
Quiocho, F.A.2
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16
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0000556785
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Iimori T., Murai Y., Ohuchi S., Kodama Y., Ohtsuka Y., Oishi T. Tetrahedron Lett. 32:1991;7273-7276.
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Iimori, T.1
Murai, Y.2
Ohuchi, S.3
Kodama, Y.4
Ohtsuka, Y.5
Oishi, T.6
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19
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0025188174
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Rosemeyer H., Toth G., Golankiewicz B., Kazimierczuk Z., Bourgeois W., Kretschmer U., Muth H.-P., Seela F. J. Org. Chem. 55:1990;5784-5790.
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Toth, G.2
Golankiewicz, B.3
Kazimierczuk, Z.4
Bourgeois, W.5
Kretschmer, U.6
Muth, H.-P.7
Seela, F.8
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20
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-
0342350881
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19
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19
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21
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58149210438
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Desvaux H., Berthault P., Birlirakis N., Goldman M., Piotto M. J. Magn. Reson. 113:1995;47-52.
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Birlirakis, N.3
Goldman, M.4
Piotto, M.5
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22
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0003942864
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For a discussion relative to the conformational energy difference between axial and equatorial monosubstituted cyclohexanes by an ethynyl, a vinyl, an ethyl or a methyl group, see; John Wiley and Sons/Wiley-Interscience: New York
-
For a discussion relative to the conformational energy difference between axial and equatorial monosubstituted cyclohexanes by an ethynyl, a vinyl, an ethyl or a methyl group, see Eliel, E. L.; Wilen, H. S.; Mander, L. N. in Stereochemistry of Organic Compounds; John Wiley and Sons/Wiley-Interscience: New York, 1994, pp 690-700.
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(1994)
Stereochemistry of Organic Compounds
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Eliel, E.L.1
Wilen, H.S.2
Mander, L.N.3
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23
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15644379995
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and references cited therein
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Hattori, H.; Nozawa, E.; Iino, T.; Yoshimura, Y.; Shuto, S.; Shimamoto, Y.; Nomura, M.; Fukushima, M.; Tanaka, M.; Sasaki, T.; Matsuda, A. J. Med. Chem. 1998, 41, 2892-2902 and references cited therein.
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Hattori, H.1
Nozawa, E.2
Iino, T.3
Yoshimura, Y.4
Shuto, S.5
Shimamoto, Y.6
Nomura, M.7
Fukushima, M.8
Tanaka, M.9
Sasaki, T.10
Matsuda, A.11
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24
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0342350880
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Weltin, D.; Jung, P. M. J.; Holl, V.; Dauvergne, J.; Burger, A.; Dufour, P.; Aubertin, A. M.; Bischoff, P.; Biellmann, J.-F. unpublished results
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Weltin, D.; Jung, P. M. J.; Holl, V.; Dauvergne, J.; Burger, A.; Dufour, P.; Aubertin, A. M.; Bischoff, P.; Biellmann, J.-F. unpublished results.
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