amp;ohgr;-2-(tetrazolylalkyl)cyclohexyl-2-aminoalkanoic acids as antagonists of excitatory amino acid receptors

摘要

The present invention pertains to antagonists of excitatory amino acid receptors, their method or preparation as well as compositions pertaining to them, which have the general formula: ##STR1## wherein R1 and R2 are selected from the group of hydrogen and C1 to C6 lower alkyl; the stereoisomers being in their resolved or racemic form; n and m are independently 0, 1, 2, or 3; and pharmaceutically acceptable salts thereof.