-
1
-
-
0025572709
-
-
Walz, G.; Aruffo, A.; Kolanus, W.; Bevilacqua, M.; Seed, B. Science 1990, 250, 1130. Lowe, J. B.; Stoolman, L. M.; Nair, R. P.; Larsen, R. D.; Berhend, T. L.; Marks, R. M. Cell 1990, 63, 475
-
Phillips, M. L.; Nudelman, E.; Gaeta, F. C. A.; Perez, M.; Singhal, A. K.; Hakomori, S.; Paulson, J. C. Science 1990, 250, 1132. Walz, G.; Aruffo, A.; Kolanus, W.; Bevilacqua, M.; Seed, B. Science 1990, 250, 1130. Lowe, J. B.; Stoolman, L. M.; Nair, R. P.; Larsen, R. D.; Berhend, T. L.; Marks, R. M. Cell 1990, 63, 475.
-
(1990)
Science
, vol.250
, pp. 1132
-
-
Phillips, M.L.1
Nudelman, E.2
Gaeta, F.C.A.3
Perez, M.4
Singhal, A.K.5
Hakomori, S.6
Paulson, J.C.7
-
2
-
-
0000097517
-
-
Ichikawa, Y.; Lin, Y.-C.; Dumas, D. P.; Shen, G.-J.; Garcia-Junceda, E.; Williams, M. A.; Bayer, R.; Ketcham, C.; Walker, L. E.; Paulson, J. C.; Wong, C.-H. J. Am. Chem. Soc. 1992, 114, 9283.
-
(1992)
J. Am. Chem. Soc.
, vol.114
, pp. 9283
-
-
Ichikawa, Y.1
Lin, Y.-C.2
Dumas, D.P.3
Shen, G.-J.4
Garcia-Junceda, E.5
Williams, M.A.6
Bayer, R.7
Ketcham, C.8
Walker, L.E.9
Paulson, J.C.10
Wong, C.-H.11
-
4
-
-
0028097126
-
-
(a mixture of four diastereomers with 40- to 50-fold less activity)
-
Ragan, J. A.; Cooper, K. Bioorg. Med. Chem. Lett. 1994, 4, 2563 (a mixture of four diastereomers with 40- to 50-fold less activity).
-
(1994)
Bioorg. Med. Chem. Lett.
, vol.4
, pp. 2563
-
-
Ragan, J.A.1
Cooper, K.2
-
5
-
-
84987176222
-
-
(inactive). For active natural products inhibiting E-selectin, see: Narasinga Rao, B. N.; Anderson, M. B.; Musser, J. H.; Gilbert, J. H.; Schaefer, M. E.; Foxall, C.; Brandley, B. K. J. Biol. Chem. 1994, 269, 19663 (a semisynthetic C-fucoside of glycyrrhetinic acid was shown to be a potent inhibitor of E-, P-, and L-selectins).
-
Hanessian, S.; Prabhanjan, H. Synlett 1994, 868 (inactive). For active natural products inhibiting E-selectin, see: Narasinga Rao, B. N.; Anderson, M. B.; Musser, J. H.; Gilbert, J. H.; Schaefer, M. E.; Foxall, C.; Brandley, B. K. J. Biol. Chem. 1994, 269, 19663 (a semisynthetic C-fucoside of glycyrrhetinic acid was shown to be a potent inhibitor of E-, P-, and L-selectins).
-
(1994)
Synlett
, pp. 868
-
-
Hanessian, S.1
Prabhanjan, H.2
-
6
-
-
0028015857
-
-
x was reported: Graves, B. J.; Crowther, R. L.; Chandran, C.; Rumberger, J. M.; Li, S.; Huang, K.-S.; Presky, D. H.; Familletti, P. C.; Wolitzky, B. A.; Burns, D. K. Nature 1994, 367, 532
-
x was reported: Graves, B. J.; Crowther, R. L.; Chandran, C.; Rumberger, J. M.; Li, S.; Huang, K.-S.; Presky, D. H.; Familletti, P. C.; Wolitzky, B. A.; Burns, D. K. Nature 1994, 367, 532.
-
(1994)
Biochemistry
, vol.33
, pp. 10591
-
-
Cooke, R.M.1
Hale, R.S.2
Lister, S.G.3
Shah, G.4
Weir, M.P.5
-
7
-
-
0027742959
-
-
Ramphal, J. Y.; Zheng, Z.-L.; Perez, C.; Walker, L. E.; DeFrees, S. A.; Gaeta, F. C. A. J. Med. Chem. 1994, 37, 3459; DeFrees, S. A.; Gaeta, F. C. A.; Lin, Y.-C.; Ichikawa, Y.; Wong, C.-H. J. Am. Chem. Soc. 1993, 115, 7549. Yuen, C.- T.; Lawson, A. M.; Chai, W.; Larking, M.; Stoll, M. S.; Stuart, A.C.; Sullivan, F. X.; Ahern, T. J.; Feizi, T. Biochemistry 1992, 31, 9126
-
Brandley, B. K.; Kiso, M.; Abbas, S.; Nikrad, P.; Srivastava, O.; Foxall, C.; Oda, Y.; Hasegawa, A. Glycobiology 1993, 3, 633. Ramphal, J. Y.; Zheng, Z.-L.; Perez, C.; Walker, L. E.; DeFrees, S. A.; Gaeta, F. C. A. J. Med. Chem. 1994, 37, 3459; DeFrees, S. A.; Gaeta, F. C. A.; Lin, Y.-C.; Ichikawa, Y.; Wong, C.-H. J. Am. Chem. Soc. 1993, 115, 7549. Yuen, C.- T.; Lawson, A. M.; Chai, W.; Larking, M.; Stoll, M. S.; Stuart, A.C.; Sullivan, F. X.; Ahern, T. J.; Feizi, T. Biochemistry 1992, 31, 9126.
-
(1993)
Glycobiology
, vol.3
, pp. 633
-
-
Brandley, B.K.1
Kiso, M.2
Abbas, S.3
Nikrad, P.4
Srivastava, O.5
Foxall, C.6
Oda, Y.7
Hasegawa, A.8
-
8
-
-
0027109447
-
-
For previous work utilizing ethylene glycol spacer, see
-
For previous work utilizing ethylene glycol spacer, see: Ats, C.-S.; Lehmann, J.; Petry, S. Carbohydr. Res. 1992, 233, 125.
-
(1992)
Carbohydr. Res.
, vol.233
, pp. 125
-
-
Ats, C.-S.1
Lehmann, J.2
Petry, S.3
-
12
-
-
85022557603
-
-
The amino acid was prepared by L-threonine aldolase-catalyzed reaction of glycine (5 equiv) with O-benzylglycoaldehyde, pH 6.3 (78% yield) in press
-
The amino acid was prepared by L-threonine aldolase-catalyzed reaction of glycine (5 equiv) with O-benzylglycoaldehyde, pH 6.3 (78% yield). Vassilev, V. P.; Uchiyama, T.; Kajimoto, T.; Wong, C.-H. Tetrahedron Lett., in press.
-
Tetrahedron Lett.
-
-
Vassilev, V.P.1
Uchiyama, T.2
Kajimoto, T.3
Wong, C.-H.4
-
13
-
-
0028895061
-
-
The assay is similar to that previously reported Detailed inhibition analysis will be published separately
-
The assay is similar to that previously reported: DeFrees, S. A.; Kosch, W.; Way, W.; Paulson, J. C.; Sabesan, S.; Halcomb, R.; Huang, D.-H.; Ichikawa, Y.; Wong, C.-H. J. Am. Chem. Soc. 1995, 117, 66. Detailed inhibition analysis will be published separately.
-
(1995)
J. Am. Chem. Soc.
, vol.117
, pp. 66
-
-
DeFrees, S.A.1
Kosch, W.2
Way, W.3
Paulson, J.C.4
Sabesan, S.5
Halcomb, R.6
Huang, D.-H.7
Ichikawa, Y.8
Wong, C.-H.9
|