Abstract
Abstract3,5‐Diphenylcyclohex‐2‐en‐1‐one (1) was used as a starting material for the synthesis of new derivatives of hydrazones 3, 4, organic compounds that involves thiazole ring 5–8 and azine moieties 10–17. The biological activity, minimum inhibitory concentration (MIC) and cytotoxicity values of the most active compounds of these derivatives were screened. Compounds 7 a, 7 b and 8 b revealed the best results against all screened biological activity. Derivatives 7 a, 7 b and 8 b revealed moderate to weak cytotoxicity.
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