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作 者:常睿洁[1] 覃江江[1] 成向荣[1] 金慧子[1] 张卫东[1,2]
机构地区:[1]上海交通大学药学院,上海200240 [2]第二军医大学药学院,上海200433
出 处:《天然产物研究与开发》2012年第3期291-297,328,共8页Natural Product Research and Development
基 金:supported by program NCET Foundation,NSFC(81102778);the Scientific Foundation of Shanghai China(No.09dZ1972200)
摘 要:从水朝阳旋覆花(Inula helianthus-aquatica)地上部分分离得到24个化合物,经波谱数据分析分别鉴定为aromaticin(1),8-epi-helenalin(2),bigelovin(3),2,3-dihydroaromaticin(4),carpesiolin(5),ergolide(6),inuchinenolide C(7),6α-acetoxy-isoinuviscolide(8),8-epi-inuviscolide(9),inuchinenolide B(10),tomentosin(11),11α,13-dihydrotomentosin(12),inuchinenolide A(13),4H-tomentosin(14),11β,13-dihydro-4H-tomentosin(15),11-epi-sundiversifolide(16),sundiversifolide(17),8,9,10-三羟基百里香酚(18),10-羟基-8,9-双氧亚异丙基百里香酚(19),8,10-二羟基-9-异丁酰百里香酚(20),8-羟基-9,10-二异丁酰百里香酚(21),8-羟基-9-异丁酰-10-(2-甲基丁酰)百里香酚(22),8,9-环氧-9,10-二异丁酰百里香酚(23)和8,9-环氧-3-异丁酰-10-(2-甲基丁酰)百里香酚(24)。除了化合物1~6外,其他化合物均为首次从该植物中分离得到。Twenty-four compounds were isolated from the aerial parts of Inula helianthus-aquatica. On the basis of spec- tral data, their structures were identified as aromaticin ( 1 ), 8-epi-helenalin (2), bigelovin (3), 2,3-dihydroaromaticin (4) ,carpesiolin (5), ergolide ( 6 ), inuchinenolide C ( 7 ), 6ct-acetoxy-isoinuviscolide ( 8 ), 8-epi-inuviscolide ( 9 ), inuchinenolide B ( 10 ), tomentosin ( 11 ), 11 ct, 13-dihydrotomentosin ( 12 ), inuchinenolide A ( 13 ), 4H-tomentosin (14), 11β, 13-dihydre-4H-tomentosin ( 15), 11-epi-sundiversifolide ( 16), sundiversifolide ( 17), 8,9,10-trihydroxythy- tool ( 18 ), 10-hydroxy-8,9-dioxyisopropylidenethymol ( 19 ), 8,10-dihydroxy-9-isobutyryloxythymol ( 20 ), 8-hydroxy-9, 10-diisobutyryloxythymol ( 21 ), 8-hydroxy-9-isobutyryloxy-10-(2-methylbutanoyl) thymol ( 22 ), 8,9-epoxy-3, 10-di- isobutyryloxythymol (23), and 8,9-epoxy-3-isobutyryloxy-10- (2-methylbutanoyl) thymol ( 24 ). All the compounds ex- cept 1-6 were isolated from this plant for the first time.
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