다릅나무 수피를 채취하여 건조시킨 후 분말로 제조하여 95% 에탄올로 추출하고 석유에테르, 디클로로메탄 및 에틸아세테이트로 분획하여 동결건조시켰다. 디클로로메탄 가용부 및 에틸아세테이트 가용부를 Sephadex LH-20과 silica gel 60으로 충진한 칼럼에서 다양한 용매를 사용하여 칼럼크로마토그래피를 실시하였다. 단리된 화합물들은 TLC로 확인한 후 $^1H-$, $^{13}C-NMR$, COSY, NOESY, HMQC, HMBC 등의 스펙트럼을 사용하여 정확한 구조를 구명하였고, FAB 및 EI-MS로써 분자량을 측정하였다. 기기분석 결과, 7-O-$\beta$-D-glucopyranosyl-4'-methoxyisoflavone, 7-O-$\beta$-glucopyranosyl(1'''->6'')-$\beta$-D-glucopyranosyl-4'-methoxyisoflavone, 7-O-$\beta$-D-glucopyranosyl(1''''->6''')-$\beta$-D-glucopyranosyl(1'''->6'')-$\beta$-D-glucopyransoyl-4'-methoxyisoflavone, 7-O-$\beta$-D-glucopyranosyl-4', 6-dimethoxyisoflavone으로 각각 동정하였다. 단리 물질의 항산화 활성은 DPPH법에 의한 라디칼 소거능을 측정하였으며, 항산화 활성은 $\alpha$-tocopherol보다 낮게 나타났지만 BHT와 비슷한 활성을 나타내었다.
Abstract
The dried barks of Maackia amurensis were ground, extracted with 95% EtOH, concentrated, and fractionated with a series of light petroleum ether, dichloromethane, ethyl acetate and water on a separatory funnel. Each fraction was concentrated, then a portion of dichloromethane and ethyl acetate soluble was chromatographed on a Sephadex LH-20 and silica gel 60 column using a various solvent system as eluents. The isolated compounds were identified by cellulose TLC, $^1H-$, $^{13}C-NMR$, COSY, NOESY, HMQC, HMBC, FAB and EI-MS. The structures were determined as: 7-O-$\beta$-D-glucopyranosyl-4'-methoxyisoflavone, 7-O-$\beta$-glucopyranosyl(1'''->6'')-$\beta$-D-glucopyranosyl-4'-methoxyisoflavone, 7-O-$\beta$-D-glucopyranosyl(1''''->6''')-$\beta$-D-glucopyranosyl(1'''->6'')-$\beta$-D-glucopyransoyl-4'-methoxyisoflavone, 7-O-$\beta$-D-glucopyranosyl-4', 6-dimethoxyisoflavone. The Free radical scavenging activity using DPPH of the isolated compounds were similar with that of BHT but lower than of $\alpha$-tocopherol.
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