All ,6-adrenoceptor blocking drugs that have been described share the common property of being competitive inhibitors. They differ in their associated properties, the presence or absence of cardioselectivity, membrane stabilizing activity, and partial agonist activity. Recently some ,8-adrenoceptor blocking drugs have been reported which also possess a-adrenoceptor blocking activity. The associated properties have been used as a basis for classifying P-adrenoceptor blocking drugs (Fitzgerald, 1969(Fitzgerald, , 1972.The presence or absence of cardioselectivity is most useful for dividing P-adrenoceptor blocking drugs. The non-selective drugs (Division I) can be further divided according to the presence or absence of intrinsic sympathomimetic activity (ISA) and membrane stabilizing activity (Fitzgerald's groups I-IV). Group I possess both membrane activity and ISA, e.g. alprenolol, oxprenolol, group II just membrane action, e.g. propanolol, group III ISA but no membrane action, e.g. pindolol. Fitzgerald placed pindolol in group I but it should be placed in group III as it possesses a high degree of 0-adrenoceptor blocking potency in relation to its membrane activity (Prichard, 1974). Finally drugs in group IV have neither ISA nor membrane action, e.g. sotalol, timolol.The cardioselective drugs (Division II) can be similarly sub-divided into groups I-IV according to the presence or absence of ISA or membrane action (Fitzgerald grouped all these together as group V).Lastly there are new P-adrenergic receptor blocking drugs which in addition have a-adrenergic receptor blocking properties (Division III).