The preparation is described of hydrazides I, thiosemicarbazides II, I
II, IV and hydrazinothiazoles VIII, which can be considered as ''precu
rsors'' or ''open models'' for the synthesized benzoyl-, benzilidene-
and benzyl-hydrazinothiazoles V, VI and VII, analogous to 4-methyl and
4-phenyl substituted derivatives A, B and C, described and tested for
their MAOI activity in a previous paper. Biochemical assay on the new
prepared compounds allowed us to better clarify the structure-activit
y relationship also of compounds A, B and C of the precedent note. Mor
eover, on a group of derivatives, which showed a higher activity, a fu
rther test was performed to observe the possible correlation between M
AOI activity and both their lipophilicity and ability in interacting w
ith liposome bilayers, taken as a model of cell membrane.