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Background A new class of nicotinamide derivatives viz., N-((1H-pyrrol-2-yl)methylene)nicotinamide, N-((methyl-(phenyl)amino)methylene)nicotinamide, N-nicotinoylbenzimidothioic acid and N-(4-(methylthio)benzylidene)nicotinamide have been synthesized and their corrosion inhibition effect on mild steel in 0.5 M HCl was investigated by mass loss, Tafel polarization technique and AC impedance measurements. Results The inhibition efficiency of the inhibitors on mild steel in 0.5 M HCl has been studied based on concentration, time interval and temperature. Potentiodynamic polarization studies showed that all the examined inhibitors suppress both anodic and cathodic process and behave as mixed type of corrosion inhibitors. Conclusions The adsorption of all the inhibitors was found to obey Langmuir isotherm model. Electrochemical impedance data revealed that polarization resistance (R P ) increases and double layer capacitance (C dl ) decreases as the concentration of the inhibitors increases. FTIR, EDX and SEM analyses were performed to study the film persistency of the inhibitors.

A series of new 5-(2-amino-5-methylthiazol-4-yl)-1,3,4-oxadiazole-2-thiol derivatives 6(a–j) were designed and synthesized with various substituted aldehydes. The chemical structures were confirmed by elemental analyses, FT-IR, 1H NMR, and mass spectral studies. The antioxidant activity of the synthesized compounds was evaluated by 2,2-diphenyl-1-picrylhydrazyl (DPPH), hydroxyl, nitric oxide, and superoxide radical scavenging assay methods. Compounds 6a, 6e, and 6c showed significant radical scavenging potential due to the presence of electron donating substituent on substituted aldehydes.

We herein report a design and synthesis of new 1,3,5-triazine based pyrazole derivatives (5a-i) for anticancer activity targeting epidermal growth factor (EGFR) tyrosine kinase. The newly synthesized compounds were characterized...