The present investigation aimed to identify the bioactive compounds inOpuntia ficus cladode and their pharmaceutical importance, which was evaluated through phytochemical and in-silico screening. The cladode’s phytochemical screening revealed alkaloids, tannins, flavonoids, phenols, proteins, terpenoids,glycosides, steroids, saponins etc. A total of 25 compounds were identified in the gas chromatography and mass spectrometry (GC-MS) analysis, and an active metabolite 2-Thophene carboxylic acid-5methyl was selected for in-silico docking study againstfour human protein targets namely, Human Estrogen receptor (PDB ID: 3ERT) (anti-cancer), HIV-1 envelope glycoprotein (PDB ID: 4CC8) (anti-HIV), Human C-reactive protein (PDB ID: 1GNH) (anti-inflammation) and Human 11beta-hydroxysteroid dehydrogenase type I (11beta-HSD1) (PDB ID: 1XU7) (anti-diabetes) respectively via Schrodinger version 9.3. Among the four target proteins, the potent inhibition observed against Human 11beta-hydroxysteroid dehydrogenase type I (11beta-HSD1) (PDB ID: 1XU7) is involved in type 2 diabetes. Therefore, Opuntia ficuscladodes can be explored in managing type 2 diabetes.
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