The invention relates to azetidinyl, pyrrolidinyl, piperidinyl, and
hexahydroazepinyl compounds of Formula I and pharmaceutically acceptable
salts, prodrugs, or solvates thereof, wherein R.sup.1-R.sup.3 and Z are
defined as set forth in the specification. The invention is also directed
to the use compounds of Formula I to treat, prevent or ameliorate a
disorder responsive to the blockade of calcium channels, and particularly
N-type calcium channels. Compounds of the present invention are
especially useful for treating pain.
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