A series of isonicotinoylhydrazones 2 were prepared by addition of some ary
loxyacetonitriles with isonicotinoylhydrazine in basic medium. These compou
nds have been further reacted with pyridinecarboxaldehydes to give the corr
esponding pyridylmethyleneamino derivatives 3-5. The new synthesized hydraz
ones and their pyridylmethyleneamino derivatives were tested for their acti
vity against mycobacteria, Gram-positive and Gram-negative bacteria. The cy
totoxicity was also tested. Several compounds showed a good activity agains
t Mycobacterium tuberculosis H37Rv and some isonycotinoylhydrazones 2 showe
d a moderate activity against a clinically isolated M. tuberculosis which w
as isoniazid resistant. (C) 1999 Editions scientifiques et medicales Elsevi
er SAS.