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Cholinesterase, α-glucosidase, tyrosinase and urease inhibitory activities of compounds from fruits of <i>Rinorea oblongifolia</i> C.H. Wright (Violaceae)

Aristide Mfifen Munvera, Alfred Ngenge Tamfu, Blandine Marlyse Wache Ouahouo, Selçuk Küçükaydın, Jean Noël Nyemb, Marcelle Aude Fokam Mafo, Emar Carlain Djappa Tchapo, Pierre Mkounga, Augustin Ephrem Nkengfack

2023Natural Product Research13 citationsDOIOpen Access PDF

Abstract

From Rinorea oblongifolia fruits, 3-Nor-4β-friedelan-24-ol (1) and 3-decyl-6,7,8-trimethoxy-2H,5H-furo[4,3,2-de]isochromene-2,5-dione (4), new derivatives alongside, 28-hydroxyfriedelan-3-one (2), friedelin (3), 3,3’,4,4’,5’-pentamethylcoruleoellagic acid (5), hexamethylcoruleoellagic acid (6), 3’,4,4’,5,5’-pentamethylcoruleoellagic acid (7), and fatty compounds 8-11 were isolated and characterized using HRESIMS, EIMS, 1D and 2D NMR. In vitro enzyme inhibition of compounds 1, 2, 4, 5, 6 and 7 were evaluated on acetylcholinesterase (AChE), butyrylcholinesterase (BChE), α-glucosidase, urease and tyrosinase. Against AChE and BChE, the phenolic compounds 4, 5, 6, and 7 had good activity probably due to the phenolic nature and methoxy substituents. Compounds 4, 5, 6 and 7 exhibited good α-glucosidase inhibition especially compound 4 whose IC50 = 42.45 ± 0.46 µg/mL was close that of acarbose (IC50 = 20.52 ± 0.84 µg/mL) standard drug. Urease and tyrosinase were appreciably inhibited by the compounds. Overall results of enzyme inhibitory assays indicate Rinorea oblongifolia, fruits and its constituents as potential remedy for enzymatic disorders.

Topics & Concepts

TyrosinaseChemistryButyrylcholinesteraseUreaseStereochemistryIC50EnzymeAcarboseAcetylcholinesteraseTraditional medicineBiochemistryAchéIn vitroMedicinePhytochemistry and Bioactivity StudiesChemical synthesis and alkaloidsPhytochemistry and Biological Activities