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0040601367
-
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note
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In glycosidases, cleavage of the glycosidic C(1)-O(1) bond begins before protonation of the leaving group oxygen atom O(1) by the catalyzing acid; therefore the protonated glycoside only appears with a strongly elongated C(1)-O(1) bond (see ref 1c).
-
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0040008058
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note
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+ - HCl), 220, 208, 202, 190, 162, 106.
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0000130537
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16
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0040008056
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note
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3 calcd 237.1365).
-
-
-
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17
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84984529975
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Other acyclic amino-alcohol glycosidase inhibitors are known, such as tris(hydroxymethyl) aminomethane: (a) Larner, J.; Gillespie, R. E. J Biol. Chem. 1956, 233, 709.
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Larner, J.1
Gillespie, R.E.2
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0021858525
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(b) Dale, M. P.; Ensley, H. E.; Sastry, K. A. R.; Byers, L. D. Biochemistry 1985, 24, 3530.
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Dale, M.P.1
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Byers, L.D.4
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19
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37049081948
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(c) Fowler, P. A.; Haines, A. H.; Taylor, R. J. K.; Chrystal, E. J. T.; Gravestock, M. B. J. Chem. Soc., Perkin Trans. 1 1994, 2229.
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Chrystal, E.J.T.4
Gravestock, M.B.5
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20
-
-
0041195350
-
-
note
-
There was no observable inhibition by 1, 8, or 9 for the following glycosidases (1 mM nitrophenyl glycoside, 0.1 mM inhibitor in 0.1 M HEPES pH 6.8, 25 °C): green coffee beans α-galactosidase, Escherichia coli β-galactosidase, yeast β-glucosidase, almond β-glucosidase, jack beans α-mannosidase, snail acetone powder β-mannosidase. 2 was not tested with these enzymes.
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-
-
-
21
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0033582974
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Recent papers on α-L-fucosidase inhibitors: (a) Nishimura, Y.; Shitara, E.; Takeuchi, T. Tetrahedron Lett. 1999, 40, 2351.
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Nishimura, Y.1
Shitara, E.2
Takeuchi, T.3
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22
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0032814101
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and references cited therein
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(b) Peer, A.; Vasella, A. Helv. Chim. Acta 1999, 82, 1044 and references cited therein.
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Peer, A.1
Vasella, A.2
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23
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0033997821
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(c) Shitara, E.; Nishimura, Y.; Kojima, F.; Takeuchi, T. Bioorg. Med. Chem. 2000, 8, 343.
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Shitara, E.1
Nishimura, Y.2
Kojima, F.3
Takeuchi, T.4
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