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VOL. 11, ISSUE 2 (2026)
Phytochemical Profiling and alpha-amylase inhibitory potential of Bauhinia monandra extractives
Authors
Yusuf Olalekan Barnabas
Abstract
Diabetes mellitus continues to be a major non-communicable disease burden, particularly in sub-Saharan Africa, driving interest in plant-derived inhibitors of carbohydrate-metabolising enzymes. Bauhinia monandra Kurz (Fabaceae) is used across West Africa, India and tropical America in the traditional management of diabetes mellitus, yet the molecular basis of its activity against pancreatic alpha-amylase remains unresolved, and its flowers are essentially unstudied. This study profiled the phytochemistry of B. monandra leaf and flower and evaluated their alpha-amylase inhibitory potential. Air-dried leaf and flower material were separately extracted with ethanol and partitioned successively into n-hexane, dichloromethane, ethyl acetate, and aqueous fractions. Alpha-amylase inhibition was measured by the 3,5-dinitrosalicylic acid (DNSA) method with acarbose as the reference standard; total phenolic content (TPC) and total flavonoid content (TFC) were quantified; constituents were characterised by LC-MS and GC-MS; and identified compounds were docked against pancreatic alpha-amylase (PDB: 1HNY) using AutoDock Vina. The ethyl acetate fractions of both organs displayed the strongest, concentration-dependent inhibition, consistent with their highest phenolic and flavonoid contents. LC-MS identified quercetin, quercetin-3-O-rutinoside (rutin), quercetin-3-O-rhamnoside, and kaempferol derivatives, while GC-MS revealed beta-sitosterol, stigmasterol, and lupeol alongside fatty acid derivatives. Molecular docking positioned the identified flavonoids within the catalytic triad (Asp197, Glu233, Asp300) of alpha-amylase, with rutin and kaempferol achieving binding energies superior to acarbose. The results furnish the first integrated phytochemical and mechanistic rationale for the antidiabetic use of B. monandra, identify ethyl acetate-soluble flavonoids as the principal bioactive agents, and establish the flower as a credible source of alpha-amylase inhibitors.
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Pages:97-106
How to cite this article:
Yusuf Olalekan Barnabas "Phytochemical Profiling and alpha-amylase inhibitory potential of <i>Bauhinia monandra</i> extractives". International Journal of Academic Research and Development, Vol 11, Issue 2, 2026, Pages 97-106
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