Heterocyclic are provided which are sodium/proton exchange (NHE) inhibitors
which have the structure
##STR1##
wherein n is 1 to 5; X is N or CR5 wherein R5 is
H, halo, alkenyl, alkynyl, alkoxy, alkyl, aryl or heteroaryl; Z is a heteroaryl
gorup, R1, R2, R3 and R4 are as defined
herein, and where X is N. R1 is preferably aryl or heteroaryl, and are
useful as antianginal and cardioprotective agents. In addition, a method is provided
for preventing or treating angina pectoris, cardiac dysfunction, myocardial necrosis,
and arrhythmia employing the above heterocyclic derivatives.