C. J. F. BICHARD

Potent inhibition of glycogen phosphorylase by a spirohydantoin of glucopyranose: First pyranose analogues of hydantocidin

C. J. F. BICHARD, Edward P. Mitchell, Mark R. Wormald et al. · Tetrahedron Letters · 1995 · 136 citations

Medicinal Chemistry, Biochemistry, Medicine +10

Design of Inhibitors of Glycogen Phosphorylase: A Study of .alpha.- and .beta.-C-Glucosides and 1-Thio-.beta.-D-glucose Compounds

Kimberly A. Watson, Edward P. Mitchell, L.N. Johnson et al. · Biochemistry · 1994 · 121 citations

Glucose analogue inhibitors of glycogen phosphorylase: from crystallographic analysis to drug prediction using GRID force-field and GOLPE variable selection

Kimberly A. Watson, Edward P. Mitchell, L.N. Johnson et al. · Acta Crystallographica Section D Biological Crystallography · 1995 · 70 citations

Drug Target, Aldo-keto Reductase, Glycobiology +18

N‐acetyl‐<i>β</i>‐D‐glucopyranosylamine: A potent T‐state inhibitor of glycogen phosphorylase. A comparison with <i>α</i>‐D‐glucose

Nikos G. Oikonomakos, Maria Kontou, S.E. Zographos et al. · Protein Science · 1995 · 60 citations · Full text

The ring contraction of δ-lactones with leaving group α-substituents: a strategy for the synthesis of 2,5-disubstituted highly functionalised homochiral tetrahydrofurans

Sik-man S. Choi, Paul M. Myerscough, Antony J. Fairbanks et al. · Journal of the Chemical Society Chemical Communications · 1992 · 37 citations

Group α-Substituents, Engineering, Biochemistry +12