Author/Authors :
Saghir, Farhat Punjab University College of Pharmacy - University of the Punjab - Lahore, Pakistan , Hussain, Khalid Punjab University College of Pharmacy - University of the Punjab - Lahore, Pakistan , Tahir, Muhammad Nawaz Department of Physics - University of Sargodha - Sargodha, Pakistan , Raza, Atif Punjab University College of Pharmacy - University of the Punjab - Lahore, Pakistan , Shehzadi, Naureen Punjab University College of Pharmacy - University of the Punjab - Lahore, Pakistan , Iftikhar, Sadaf Punjab University College of Pharmacy - University of the Punjab - Lahore, Pakistan , Shaukat, Ayisha Punjab University College of Pharmacy - University of the Punjab - Lahore, Pakistan , Naheed, Surriya Punjab University College of Pharmacy - University of the Punjab - Lahore, Pakistan , Siddique, Sidra Punjab University College of Pharmacy - University of the Punjab - Lahore, Pakistan
Abstract :
Pongamia pinnata (L.) Pierre (Family: Fabaceae) is a famous traditional medicinal plant, the flowers of which are used for
treating diabetes, however, the active constituent(s) is yet unidentified. Therefore, the present study aimed to carry out
antidiabetic activity-guided isolation of extracts of flowers. Hexane extract being the most active (EC50, 900 μg/mL) was
fractionated by partitioning and the most active hexane fraction (EC50, 570 μg/mL) was subjected to column
chromatography which gave three isomers of compound 1 (4-Methoxy-7-phenyl-5H-furo [3,2-g][1] benzopyran-5-one), a
furanoflavonoid. All the isomeric forms have equal antidiabetic activity (83.24%) with EC50 at 300 μg/mL. The activity of
the isolated compound was found to be higher as compared to standard drug acarbose (43.46%). Molecular docking
studies of the compound indicated higher binding energy scores with antidiabetic targets as compared to the standard drug
acarbose. The results of the present study indicate that the isolated compound may be developed into an antidiabetic drug.
Keywords :
Pongamia pinnata (L.) Pierre , diabetes , Column chromatography , Single-crystal X-ray diffraction (XRD) , Molecular docking studies