A methanol extract of nagkesar (buds of Mammea longifolia ), which showed strong radical scavenging activity, yielded 13 compounds by separations using column chromatography and HPLC. Structure elucidation of these compounds was achieved by 1 H and 13 C NMR, including DQF−COSY, TOCSY, DEPT, HMQC, HSQC, and HMBC. They include two new compounds, quercetin 3- O -(2‘ ‘,4‘ ‘di- E-p -coumaroyl)-α- l -rhamno-pyranoside and quercetin 3- O -(3‘ ‘,4‘ ‘-di- E-p -coumaroyl)-α- l -rhamnopyranoside, along with known compounds kaempferol, quercetin, the isopropylidenedioxy derivative of shikimic acid, kaempferol 3- O -(2‘ ‘,4‘ ‘-di- E - p -coumaroyl)-α- l -rhamnopyranoside, kaempferol 3- O -(3‘ ‘,4‘ ‘-di- E - p -coumaroyl)-α- l -rhamnopyranoside, kaempferol 3- O -α- l -rhamnopyranoside, quercetin 3- O -α- l -rhamnopyranoside, shikimic acid, kaempferol 3- O -β- d -glucopyranoside, quercetin 3- O -β- d -glucopyranoside, and β-sitosterol 3- O -β- d -glucopyranoside.
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Rao et al. (2002) studied this question.
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