A set of pyridine derivatives bearing a substituted alkylthio chain or a pi
peridyl ring in position 2 or 4 were synthesized, and their antimycobacteri
al and antifugal activities were evaluated. Chemical structures were confir
med by IR and NMR data, and by elemental analysis. Minimum inhibitory conce
ntrations (MIC) were used for the evaluation of microbiological activity in
vitro. The compounds were moderately active against both Mycobacterium tub
erculosis and nontuberculous mycobacteria. The most active compound was 2-c
yanomethylthiopyridine-4-carbonitrile (7) with MTC against Mycobacterium ka
nsasii in the range of 8-4 mu mol/l. The antifungal activities of the compo
unds were relatively low. (C) 1999 Elsevier Science S.A. All rights reserve
d.