From the n-BuOH soluble fraction of the leaves of Salix hulteni, six compounds were isolated as aldose reductase inhibitors. On the basis of spectral data, these compounds were identified as diosmetin-7-O-$eta$-D-glucoside (1), isoquercitrin (2), diosmetin-7-O-$eta$-D-xylosyl-(1$ ightarrow$6)- $eta$-D-glucoside (3), aromadendrin-3-O-$eta$-D-glucoside (4), astragalin (5), andp-hydroxyacetophenone glucoside (6). All of the isolates were evaluated in vitro for inhibitory activity against the aldose reductase. Of these, compounds 1-5 exhibited inhibitory activity against aldose reductase with $IC_{50}$ values ranging 1.4 to $5.8;{mu}M$.