Advances on Synthesis, Derivatization and Bioactivity of Isatin: A Review.

BACKGROUND Isatin (IST) is a crucial pharmacologically active compound, chemically known as indole-1H-2,3- dione. Development of different IST based analogues acquired significant awareness because of its pronounced therapeutic importance such as analgesic, anticancer, anti-inflammatory, antitubercular, antimicrobial, antifungal, antiviral (effective against SARS coronavirus 3C protease) and many other activities, and represent an important class of heterocyclic compounds that can be used as a precursor for the synthesis of many useful drugs. OBJECTIVE Previously many articles were reported on IST synthesis and their different pharmacological activities but herein, we mentioned 59 different synthesis schemes of several IST derivatives/hybrids derived from the substitution of the nitrogen, aromatic ring, the second and third position of IST along with most potent molecule among each of synthesized libraries with their structural activity relationship (SAR). Using these standardized approaches several biological important compounds were developed like sunitinib, nintedanib, indirubin, etc and several studies have been carried out in nowadays to develop newer compounds having fewer side effects and also overcome the problem of resistance. CONCLUSION This report critically reviews the different strategies for the designs and synthesis of several IST based compounds having different biological activities with SAR which can favour further investigation and modification for the development of new and more potent entities.