New Approaches of 4-Aryl-2-Hydrazinothiazole Derivatives Synthesis, Molecular Docking, and Biological Evaluations

In the field of the preparation of chemotherapeutic agents with new mechanism distinct from currently approved drugs is important. Theimplication of different members of Histone Acetyl Transferase (HAT) in cancer disease is well documented in literature, however the clinicallyeffective approved small inhibitor molecule is still lacking. Previous reports indicated that 4-aryl-2-hydrazinothiazole derivatives provided auseful start point to develop HAT inhibitors. Consequently, preparation and biological evaluation of a focused library of 4-aryl-2- hydrazinothiazole based derivatives as useful as anti-cancer agents. Synthesis of 4-aryl-2-hydrazinothiazoles (1a-d), (2a-d), (3a-c), (4a-b), (5ab), (6a-b) studied by either conventional method and free solvent microwave one pot method, the activity against different cancer cell-lines and the antimicrobial activities against different organisms also studied. It was found that all of the prepared thaizoles derivatives were active toward many cell lines (breast, liver, and prostate) where the more active compounds were 4a, 4b, and 6a. Most of these compounds showed highly activity as antibacterial for gram positive and gram negative. However it showed also antifungal activity. Molecular docking studies guided and proved the biological activities of these novel 4-aryl-2-hydrazinothiazoles. Also Infrared Radiation (IR), Proton Nuclear Magnetic Resonance (1H-NMR), Carbon-13 Nuclear Magnetic Resonance (13C-NMR), Gas chromatography–Mass Spectrometry (GC-MS), and elemental analysis were studied.
Atom, Chemistry, Science, Model, Molecular, Physics

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