Inhibition of Ocular Aldose Reductase by a New Benzofuroxane Derivative Ameliorates Rat Endotoxic Uveitis

<div>Chemical structure of the 5(6)-(Benzo[<i>d</i>]thiazol-2-ylmethoxy)benzofuroxane derivative BF-5m. Aldose reductase IC<sub>50</sub> = 0.42 ± 0.01 <i>μ</i>M in vitro.</div>

Mediators of Inflammation

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Figure 1

Figure 1: Inhibition of Ocular Aldose Reductase by a New Benzofuroxane Derivative Ameliorates Rat Endotoxic Uveitis 