ABSTRACT1,3-Thiazolylidenehydrazinylidene ethylpyridinium bromide monohydrate, 1,3 -thiazolylidenehydrazinium bromide and 1,3-thiazolylidenehydrazine derivatives were synthesized by heterocyclization of 2-(1-substituted ethylidene)hydrazinecarbothioamides, characterized and screened for their anti-bacterial activities. 3h showed the highest inhibitory effect against all types of bacterial compared to Moxiflo xacin. The structures of synthesized compounds were established by spectroscopic (IR, 1 H,13 C-N MR, Mass) and X-ray analyses.