-
1
-
-
0000135606
-
Significance of Sialic Acids
-
Schauer R. Wien: Springer
-
Reutter R., Köttgen E.K., Bauer C., Gerok W., Biological J. Significance of Sialic Acids. Schauer R. Sialic Acids Chemistry, metabolsm and Function, Cell Biology monographs. Vol. 10:1982;263-305 Springer, Wien
-
(1982)
Sialic Acids Chemistry, Metabolsm and Function, Cell Biology Monographs
, vol.10
, pp. 263-305
-
-
Reutter, R.1
Köttgen, E.K.2
Bauer, C.3
Gerok, W.4
Biological, J.5
-
7
-
-
0002561512
-
Sialic Acids Regulate Cellular and Molecular Recognition
-
H. Ogura, A. Hasegawa, & T. Suami. Weinheim-New York: VCH
-
Schauer R. Sialic Acids Regulate Cellular and Molecular Recognition. Ogura H., Hasegawa A., Suami T. Carbohydrates. 1992;340-401 VCH, Weinheim-New York
-
(1992)
Carbohydrates
, pp. 340-401
-
-
Schauer, R.1
-
12
-
-
0026064998
-
-
Burmeister W.-P., Daniels R.S., Dayan S., Gagnon J., Cusack S., Ruigrok R.W.H. Virology. 180:1991;266-272
-
(1991)
Virology
, vol.180
, pp. 266-272
-
-
Burmeister, W.-P.1
Daniels, R.S.2
Dayan, S.3
Gagnon, J.4
Cusack, S.5
Ruigrok, R.W.H.6
-
13
-
-
0027287506
-
-
von Itzstein M., Wu W.-Y., Kok G.B., Pegg M.S., Dyason J.C., Jin B., Phan T.V., Smythe M.L., White H.F., Oliver S.W., Colman P.M., Varghese J.N., Ryan D.M., Woods J.M., Bethell R.C., Hotham V.J., Cameron J.M., Penn C.R. Nature. 363:1993;418-423
-
(1993)
Nature
, vol.363
, pp. 418-423
-
-
Von Itzstein, M.1
Wu, W.-Y.2
Kok, G.B.3
Pegg, M.S.4
Dyason, J.C.5
Jin, B.6
Phan, T.V.7
Smythe, M.L.8
White, H.F.9
Oliver, S.W.10
Colman, P.M.11
Varghese, J.N.12
Ryan, D.M.13
Woods, J.M.14
Bethell, R.C.15
Hotham, V.J.16
Cameron, J.M.17
Penn, C.R.18
-
14
-
-
0030865641
-
-
Wong C.-H., Moris-Varas F., Hung S.-C., Marron T.G., Lin C.-C., Gong K.W., Weitz-Schmidt G. J. Am. Chem. Soc. 119:1997;8152-8158
-
(1997)
J. Am. Chem. Soc.
, vol.119
, pp. 8152-8158
-
-
Wong, C.-H.1
Moris-Varas, F.2
Hung, S.-C.3
Marron, T.G.4
Lin, C.-C.5
Gong, K.W.6
Weitz-Schmidt, G.7
-
20
-
-
0042389552
-
-
Wang X., Niu Y., Cao X., Zhang L., Zhang L.-H., Ye X.-S. Bioorg. Med. Chem. 11:2003;4217-4224
-
(2003)
Bioorg. Med. Chem.
, vol.11
, pp. 4217-4224
-
-
Wang, X.1
Niu, Y.2
Cao, X.3
Zhang, L.4
Zhang, L.-H.5
Ye, X.-S.6
-
22
-
-
0030013606
-
-
Drug Future. 21:1996;375-382
-
(1996)
Drug Future
, vol.21
, pp. 375-382
-
-
-
23
-
-
0033584065
-
-
Florio P., Thomson R.J., Alafaci A., Abo S., von Itzstein M. Bioorg. Med. Chem. Lett. 9:1999;2065-2068
-
(1999)
Bioorg. Med. Chem. Lett.
, vol.9
, pp. 2065-2068
-
-
Florio, P.1
Thomson, R.J.2
Alafaci, A.3
Abo, S.4
Von Itzstein, M.5
-
24
-
-
15644379365
-
-
Smith P.W., Sollis S.L., Howes P.D., Cherry P.C., Starkey I.D., Cobley K.N., Weston H., Scicinski J., Merrit A., Whittington A., Wyatt P., Taylor N., Green D., Bethell R., Madar S., Fenton R.J., Morlay P.J., Pateman T., Beresford A. J. Med. Chem. 41:1998;787-797
-
(1998)
J. Med. Chem.
, vol.41
, pp. 787-797
-
-
Smith, P.W.1
Sollis, S.L.2
Howes, P.D.3
Cherry, P.C.4
Starkey, I.D.5
Cobley, K.N.6
Weston, H.7
Scicinski, J.8
Merrit, A.9
Whittington, A.10
Wyatt, P.11
Taylor, N.12
Green, D.13
Bethell, R.14
Madar, S.15
Fenton, R.J.16
Morlay, P.J.17
Pateman, T.18
Beresford, A.19
-
28
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2342549853
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note
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13C NMR, and/or mass spectral data, in full agreement with their assigned structures and stereochemistries
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29
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0004133516
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Gaussian, Inc., Pittsburgh PA
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a were obtained via quantum calculations calibrated with known carboxylic acids; Gaussian 92/DFT, Revision F.3: Frisch, M. J.; Trucks, G. W.; Schlegel H. B.; Gill, P. M. W.; Johnson, B. G.; Wong, M. W.; Foresman, J. B.; Robb, M. A.; Head-Gordon, M.; Replogle, E. S.; Gomperts, R.; Andres, J. L.; Raghavachari, K.; Binkley, J. S.; Gonzalez, C.; Martin, R.L.; Fox, D. J.; Defrees, D. J.; Baker, J.; Stewart, J. J. P.; Pople, J. A., Gaussian, Inc., Pittsburgh PA, 1993
-
(1993)
Gaussian 92/DFT, Revision F.3
-
-
Frisch, M.J.1
Trucks, G.W.2
Schlegel, H.B.3
Gill, P.M.W.4
Johnson, B.G.5
Wong, M.W.6
Foresman, J.B.7
Robb, M.A.8
Head-Gordon, M.9
Replogle, E.S.10
Gomperts, R.11
Andres, J.L.12
Raghavachari, K.13
Binkley, J.S.14
Gonzalez, C.15
Martin, R.L.16
Fox, D.J.17
Defrees, D.J.18
Baker, J.19
Stewart, J.J.P.20
Pople, J.A.21
more..
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37
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0000445956
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2O, at a temperature of 37°C and using a mixing time of 1 s. Integration of NOE signals was performed after an exponential multiplication (lb=0.3 Hz) and a baseline correction
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2O, at a temperature of 37°C and using a mixing time of 1 s. Integration of NOE signals was performed after an exponential multiplication (lb=0.3 Hz) and a baseline correction, Stott K., Stonehouse J., Keeler J., Hwang T.-L., Shaka A.J. J. Am. Chem. Soc. 112:1995;4199-4200
-
(1995)
J. Am. Chem. Soc.
, vol.112
, pp. 4199-4200
-
-
Stott, K.1
Stonehouse, J.2
Keeler, J.3
Hwang, T.-L.4
Shaka, A.J.5
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38
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2342549408
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note
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2O)
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39
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0025390935
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MOPAC a Semiempirical Molecular Orbital Program (Special Issue)
-
Stewart James J.P. MOPAC a Semiempirical Molecular Orbital Program (Special Issue). J. Comput. Aided Mol. Des. 4(1):1990;1-105
-
(1990)
J. Comput. Aided Mol. Des.
, vol.4
, Issue.1
, pp. 1-105
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Stewart James, J.P.1
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40
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0031570392
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b Inhibitors were added to a reaction mixture containing 2 mg/mL asialofetuin as acceptor, 0.5 mU/mL purified rat liver α-2,6-sialyltransferase (Boehringer M. 981 583) and 1 μM CMP-9-fluoresceinyl-Neu5Ac. After 1 h incubation at 37°C, fluorescence of the reaction product was read at 530 nm.
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b Inhibitors were added to a reaction mixture containing 2 mg/mL asialofetuin as acceptor, 0.5 mU/mL purified rat liver α-2, 6-sialyltransferase (Boehringer M. 981 583) and 1 μM CMP-9-fluoresceinyl-Neu5Ac. After 1 h incubation at 37°C, fluorescence of the reaction product was read at 530 nm. Laroy W., Maras M., Fiers W., Contreras R. Anal. Biochem. 249:1997;108-111
-
(1997)
Anal. Biochem.
, vol.249
, pp. 108-111
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Laroy, W.1
Maras, M.2
Fiers, W.3
Contreras, R.4
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42
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2342547948
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note
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The ratio of compounds 5 and 6 was determined on the amount of each compound isolated by flash chromatography (silica gel)
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43
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2342550778
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note
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13CNMR signal areas, a 1/9 ratio of compounds 5/6 in favor of the axial conformation
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47
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2342550333
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note
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A solution of the amine (1 equiv) ethyl glycoxylate (1.2 equiv) and paradisulfonic acid (0.01 equiv) was refluxed in toluene until complexion of the reaction
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