Synthesis And Biological Evaluation Of Benzimidazole Derivatives As An Antitubercular And Antimicrobial Agents
Heterocyclic Compounds especially with Benzimidazole, Thiophene & Piperazine moieties were synthesized and investigated for their biological activities.
The Increasing global tuberculosis burden due to the curse of HIV, MDR and XRD TB has led to the search of newer therapeutic agents to tackle the menance.
The benzimidazole, Thiophene, Piperazine are an heterocyclic compounds. It is an important pharmacophore and privileged structure in medicinal chemistry. It plays a very important role with useful therapeutic activitiy such as antitubercular activity. literature shows that the benzimidazole, Thiophene, Piperazine derivatives are outstandingly effective compounds and a large number of reviews available for biochemical and pharmacological studies conformed that their molecules are useful against a wide variety of micro-organisms. Because of their importance, the methods for their synthesis have become a focus of synthetic organic chemists. Therefore in the present work study of chemistry of different derivative of substituted benzimidazole, Thiophene, Piperazine as well as various Antifungal, Antibacterial, Antitubercular activities).1
The structures of these compounds were established by means of IR, 1H-NMR,C13NMR and elemental analysis. All compounds were evaluated for antibacterial, antifungal and antitubercular activities. Most of the compounds have shown significant antibacterial, antifungal and antitubercular activity when compared with the standard drug. QSAR study were done by using Schrodinger software.
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