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Abstract
The indole and azaindole classes of heterocyclic compounds are among the most active and powerful classes of chemicals due to the great variety of biological and pharmacological effects they exhibit. As part of this research, we synthesized oxyindole hydrazine carboxymide, which inhibits ACHE and tyrosine kinase, and cyclized azaindole sulphonamide, which acts on PhosphotidylIonositide 3-kinase and Acetylchlorine Esterase. All of these chemicals were created synthetically and then analyzed using spectroscopic methods. The chemicals that were synthesized were tested for several purposes, including anti-cancer activity using the MTT assay in HeLa and MCF cell lines, anti-bacterial activity using the cup plate agar diffusion method, in vivo behavioral pharmacological activity, and Alzheimer's activity using the Ellmans method and in vitro brain ACHES. Research into docking has revealed promising interactions with a variety of receptors. Excellent anti-cancer, anti-Alzheimer's, and antibacterial action was exhibited by all of the compounds. Oxindole hydrazine carboxymide, acetylchlorine esterase inhibitors, aza indole sulphonamide, cancer, bacteria, cup plate agar diffusion method, Ellman's method