北京大学学报（医学版）
北京大學學報（醫學版）
북경대학학보（의학판）
JOURNAL OF BEIJING MEDICAL UNIVERSITY(HEALTH SCIENCES)
2009年
2期
221-225
,共5页
红树科%白骨壤%化学%分离和提纯%中药鉴定
紅樹科%白骨壤%化學%分離和提純%中藥鑒定
홍수과%백골양%화학%분리화제순%중약감정
目的:研究红树植物白骨壤(Avicennia marina)叶子部位次生代谢产物的结构多样性.方法:采用多种色谱方法进行分离纯化,通过波谱方法,并对照文献鉴定化合物结构.结果:分离并鉴定了21个苯丙素和萘醌类化合物,包括3个新化合物,分别是erythro-guaiacylglycerol-β-ferulic acid ether(1),marinnone A(16)和marinnone B(17);18个已知物,分别是threo-guaiacylglycerol-β-ferulic acid ether(2),eleutheroside E2(3),(+)-lirioresinol A(4),dihydroxymethyl-his(3,5-dimethoxy-4-hydroxyphenyl)tetrahydrofuran-9-O-β-glucopyranoside(5),(+)-lyonire-sinol 3α-O-β-D-glucopyranoside(6),(-)-lyoniresinol 3α-O-β-D-glucopyranoside(7),epi-pinoresinol(8),leucoseceptoside A(9),jionoside C(10),salsaside A(11),ilicifolioside A(12),acteoside(13),isoacteoside(14),ethyl ferulate(15),avicennone D(18),avicenone E(19),avicennol C(20),stenocarpoquinone B(21),其中化合物1和2互为差向异构体,16和17互为同分异构体.结论:化合物1,16,17为新化合物,13个已知化合物2～12,14,15为首次从该属植物中获得.
目的:研究紅樹植物白骨壤(Avicennia marina)葉子部位次生代謝產物的結構多樣性.方法:採用多種色譜方法進行分離純化,通過波譜方法,併對照文獻鑒定化閤物結構.結果:分離併鑒定瞭21箇苯丙素和萘醌類化閤物,包括3箇新化閤物,分彆是erythro-guaiacylglycerol-β-ferulic acid ether(1),marinnone A(16)和marinnone B(17);18箇已知物,分彆是threo-guaiacylglycerol-β-ferulic acid ether(2),eleutheroside E2(3),(+)-lirioresinol A(4),dihydroxymethyl-his(3,5-dimethoxy-4-hydroxyphenyl)tetrahydrofuran-9-O-β-glucopyranoside(5),(+)-lyonire-sinol 3α-O-β-D-glucopyranoside(6),(-)-lyoniresinol 3α-O-β-D-glucopyranoside(7),epi-pinoresinol(8),leucoseceptoside A(9),jionoside C(10),salsaside A(11),ilicifolioside A(12),acteoside(13),isoacteoside(14),ethyl ferulate(15),avicennone D(18),avicenone E(19),avicennol C(20),stenocarpoquinone B(21),其中化閤物1和2互為差嚮異構體,16和17互為同分異構體.結論:化閤物1,16,17為新化閤物,13箇已知化閤物2～12,14,15為首次從該屬植物中穫得.
목적:연구홍수식물백골양(Avicennia marina)협자부위차생대사산물적결구다양성.방법:채용다충색보방법진행분리순화,통과파보방법,병대조문헌감정화합물결구.결과:분리병감정료21개분병소화내곤류화합물,포괄3개신화합물,분별시erythro-guaiacylglycerol-β-ferulic acid ether(1),marinnone A(16)화marinnone B(17);18개이지물,분별시threo-guaiacylglycerol-β-ferulic acid ether(2),eleutheroside E2(3),(+)-lirioresinol A(4),dihydroxymethyl-his(3,5-dimethoxy-4-hydroxyphenyl)tetrahydrofuran-9-O-β-glucopyranoside(5),(+)-lyonire-sinol 3α-O-β-D-glucopyranoside(6),(-)-lyoniresinol 3α-O-β-D-glucopyranoside(7),epi-pinoresinol(8),leucoseceptoside A(9),jionoside C(10),salsaside A(11),ilicifolioside A(12),acteoside(13),isoacteoside(14),ethyl ferulate(15),avicennone D(18),avicenone E(19),avicennol C(20),stenocarpoquinone B(21),기중화합물1화2호위차향이구체,16화17호위동분이구체.결론:화합물1,16,17위신화합물,13개이지화합물2～12,14,15위수차종해속식물중획득.
