Identification of flavonoid from leaves of gedi (Abelmoschus manihot L.) and its antioxidant activity
Mercy Taroreh, Ari Widiyantoro, Agnes Murdiati, Pudji Hastuti, Sri Raharjo
Abstract
Mercy Taroreh, Ari Widiyantoro, Agnes Murdiati, Pudji Hastuti, Sri Raharjo
Abstract
A flavonoid compound had been isolated from Abelmoschus manihotL. leaves. The leaves extract was obtained by maceration in methanol to obtain n-hexane-acetone-methanol sequential extracts. Further separation was done by flash chromatography using silica gel G - 60 as a stationary phase. The column was eluted subsequently using several mixture solvents including ethyl acetate, ethyl acetate/methanol (3:1,v/v,), ethyl acetate/methanol (1:1, v/v), ethyl acetate/methanol (1:3) and methanol at 2 mL/min flow rate. At the end of this fractionation, 112 fractions of 10 mL each was collected. Using bioassay-guided fractionation, seven isolates from fraction four were obtained. The isolate five showed the highest antioxidant activity in the 2,2-diphenyl-1-picrylhydarzyl (DPPH) radical scavenging test and then it was chosen for structure elucidation. The structure of the compound was determined based on spectroscopic data of UV, IR, 1H-NMR, and 13C-NMR. The isolated compound was proposed as 3,3’,5’ trihydroxy-4’ methoxy flavone. It exhibited antioxidant activity, with IC50 of 727.53 µg/mL.
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A flavonoid compound had been isolated from Abelmoschus manihotL. leaves. The leaves extract was obtained by maceration in methanol to obtain n-hexane-acetone-methanol sequential extracts. Further separation was done by flash chromatography using silica gel G - 60 as a stationary phase. The column was eluted subsequently using several mixture solvents including ethyl acetate, ethyl acetate/methanol (3:1,v/v,), ethyl acetate/methanol (1:1, v/v), ethyl acetate/methanol (1:3) and methanol at 2 mL/min flow rate. At the end of this fractionation, 112 fractions of 10 mL each was collected. Using bioassay-guided fractionation, seven isolates from fraction four were obtained. The isolate five showed the highest antioxidant activity in the 2,2-diphenyl-1-picrylhydarzyl (DPPH) radical scavenging test and then it was chosen for structure elucidation. The structure of the compound was determined based on spectroscopic data of UV, IR, 1H-NMR, and 13C-NMR. The isolated compound was proposed as 3,3’,5’ trihydroxy-4’ methoxy flavone. It exhibited antioxidant activity, with IC50 of 727.53 µg/mL.
Key concepts: Ethyl acetate, DPPH, Chemistry, Flavonoid, Chromatography, Methanol, Fractionation, Silica gel