A set of N,N'-diarylalkanediamides was synthesized. The compounds were test
ed for their antimycobacterial and antialgal activity. The antimycobacteria
l activity of N,N'-diarylalkanediamides depends on the lipophilicity of the
respective acid. Antimycobacterially active substances were found only in
the series of N,N'-diarylethanediamides and N,N'-diarylbutanediamides. Othe
r compounds (derivatives of pentane-, hexane-, octane- and nonanediamide) w
ere inactive against various strains of mycobacteria. The compounds inhibit
ed growth and chlorophyll production in Chlorella vulgaris. Their relativel
y low antialgal activity is probably connected with their lowered aqueous s
olubility, and hence by a restricted passage of the inhibitor through the h
ydrophilic regions of thylakoid membranes.