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. 2005 Apr;14(4):873–888. doi: 10.1110/ps.041216105

Table 1.

Chemical structures of the C-(β-D-glucopyranosyl) azoles 2-4, showing the numbering system used and inhibition constants

graphic file with name PS0412161t1.jpg

For the chemical names used consult Hadady et al. (2004).

a

Taken from Martin et al. (1991).

b

Calculated from double-reciprocal plots with varied Glc-1-P concentrations (3–20 mM), constant concentrations of glycogen (1% w/v) and AMP (1 mM) and 0.2–1.0 mM inhibitor as described in Materials and Methods.

c

Calculated from double-reciprocal plots with 0.1–0.4 mM of inhibitor.

d

Calculated from double-reciprocal plots with 20–50 μM of inhibitor.