A review: Synthesis characterization and in vitro anti-mycobacterial activity of some novel benzothiazole

Heterocyclic compounds, analogs, and derivatives have received a lot of interest recently because of their advantageous biological and pharmacological properties. Flexible substrates include the heterocyclic compounds that benzothiazole and its analogs can be used to synthesize. The benzothiazole nucleus is utilized to create a wide variety of pharmaceuticals. The biological activity of benzothiazole derivatives has recently undergone some intriguing alterations. These compounds stand out in the world of medicinal chemistry due to their high pharmacological potential. According to the World Health Organisation, Mycobacterium tuberculosis is the most dangerous chronic disease that can spread. The spread of Mycobacterium tuberculosis resistance is a serious issue. The examined bacterial strains were only partially and ineffectively active. Mycobacterium tuberculosis (Mtb), the bacterium that causes human tuberculosis (TB), is more common in multidrug-resistant strains, which is one of the main factors driving the development of new drugs to treat this variety of diseases. They have also been subjected to a traditional method of testing for their antibacterial and antifungal qualities. According to the outcomes of the activities, compounds exhibited moderate to good antibacterial and antifungal activity.