SYNTHESIS, ANTICANCER EVALUATION OF NEW CHALCONES, TRIAZOLES & INDOLES. Synthesis and Anticancer Evaluation of some novel substituted Triazole, Chalcone and Indole Analogues

      Аннотация: 1,2,3-Triazoles are an important group of heterocyclic compounds that are biologically active pharmacophore such as antimicrobial, antiviral, anti-diabetic, antiulcer and anticancer activity. This medication is a combination of two antibiotics: sulfamethoxazole and trimethoprim. It is used to treat a wide variety of bacterial infections (such as middle ear, urine, respiratory, and intestinal). It is also used to prevent and treat a certain type of pneumonia (pneumocystis-type) etc.Chalcone is an aromatic ketone and an enone that forms the central core for a variety of important biological compounds, which are known collectively as chalcones/ chalconoids. These scaffolds found in many naturally occurring sources and used as lead compounds for the synthesis of numerous heterocyclics which possess diverse biological activities and play pivotal role. Indole chemistry began to develop with the study of the dye indigo. Indigo can be converted to isatin and then to oxindole could converted to indole using zinc dust. These reported as biologically active, with a wide range of therapeutic properties such as antibacterial, antifungal, antiviral, antimalarial, anti-HIV, anticancer etc.

Ключевые слова: Synthesis, anticancer, Chalcones, Triazoles, Indoles