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Several of the commonly used inhaled anesthetics (Fig. 3–1A) exist as mixtures of two stereoisomers (nonsuperimposable compounds that are mirror images of each other, having identical physicochemical properties except for the direction in which they rotate polarized light). For isoflurane stereoisomers in rats, the (+)-isomer is 17 to 53 percent more potent than the (–)-isomer.