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1.
圆果雪胆中的皂甙成分   总被引:4,自引:1,他引:3  
从圆果雪胆(Hemsleya amabilis)的块茎中分离到10个化合物,其中3个雪胆皂甙是首次从该种植物中得到,它们的结构通过光谱和化学的方法鉴定为齐墩果酸-3-O-α-吡喃阿拉伯糖(1→3)-β-葡萄糖醛酸甙,28-O-β-D-吡喃葡萄糖齐墩果酸3-O-α-吡喃阿拉伯糖(1→3)-β-D-葡萄糖醛酸,28-O-β-D-吡喃葡萄糖齐墩果酸3-O-「β-D-吡喃葡萄糖(1→2)」-「α-吡喃阿  相似文献   

2.
日本续断中新五糖皂甙的结构及其核磁共振光谱   总被引:1,自引:0,他引:1  
从日本续断(Dipsacus japonicus Miq.)根的乙醇提取物中分得一个新的三萜皂甙,其结构被鉴定为3.-O-〖β-D-吡喃葡萄糖(1→)〗〖α-吡喃鼠李糖(1→3)〗-β-D-吡喃葡萄39糖(1→3)-α-L吡喃鼠李糖(1→2)-α-吡喃阿拉伯糖-齐墩酸。采用一维SEMDY谱和转坐标NOE差谱核磁共振新技术相结合的方法,对糖体间和9糖体与甙元间的连接顺连接位置进行了研究。该方法的结果  相似文献   

3.
从单条草(LysimachiacandidaLindl)全草中分离出3个皂甙类化合物,经波谱分析并结合化学方法鉴定为:报春花素A3OβD吡喃木糖基(1→2)βD吡喃葡萄糖基(1→4)[βD吡喃葡萄糖基(1→2)]αL吡喃阿拉伯糖甙(1)、原报春花素A3OβD吡喃木糖基(1→2)βD吡喃葡萄糖基(1→4)[βD吡喃葡萄糖基(1→2)]αL吡喃阿拉伯糖甙(lysikoianoside,2)和α菠甾醇葡萄糖甙(3)。其中1是新化合物,命名为单条草甙(candidoside)。  相似文献   

4.
红木荷树皮的化学成分   总被引:6,自引:0,他引:6  
从红木茶树皮中分离出4个化学成分,经光谱解析和化学降解,分别被鉴定为α-菠甾醇,α-菠甾醇葡萄糖甙,表儿茶素和一新的三萜皂甙22-O-当归酰酯-3-O(α-L-鼠李吡喃糖基(1→2))-(β-D-葡萄吡喃糖基(1→2)-β-D-半乳吡喃糖基(1→4))-β-D-葡萄糖醛酸甙。  相似文献   

5.
滇重楼地上部分的配糖体   总被引:7,自引:0,他引:7  
从滇重楼ParispolyphyllaSm.var.yunnanensis(Fr.)H-M,地上部分,分离出4个微量的配糖体,经光谱分析和化学降解证明其化学结构分别为25S-异钮替皂甙元-3-O-α-L-鼠李吡喃糖基(1→2)[α-L-鼠李吡喃糖基(1→4)]-β-D-葡萄吡喃甙(A),26-β-D-葡萄吡喃糖基-纽替皂甙元-3-O-α-L-鼠李吡喃糖基(1→2)[α-L-鼠李吡喃糖基(1→4)-β-D-葡萄吡喃糖甙(B),山奈酚-3-O-β-D-葡萄吡喃糖基(1→6)-β-D-葡萄吡喃甙(C),7-O-α-L-鼠李吡喃糖基-山奈酚-3-O-β-D-葡萄吡喃糖基(1→6)-β-D-葡萄糖甙(D)。  相似文献   

6.
慈溪麦冬甙A和B的结构   总被引:6,自引:0,他引:6  
从浙江慈溪产中药麦冬(Ophiopogon japonicum)中分离得到2个新的C27甾体甙--慈溪麦冬甙A(2)和B(3)以及已知甙ophiogenin3-氧-α-L-鼠李糖吡喃基(1→2)「β-D-木糖吡喃基(1→3)」-β-D-葡萄糖吡喃甙(2)和ophiogenin 3-氧-α-L-鼠李糖吡喃基(1→2)「β-D-木糖吡喃基(1→3)」「β-D-葡萄糖吡喃基(1→4)」-β-D-葡萄糖吡  相似文献   

7.
柴胡皂甙s的结构鉴定   总被引:4,自引:0,他引:4  
从南柴胡(BupleurumscorzonerifoliumWild.)根中分得5个三萜皂甙。根据理化性质和波谱数据,鉴定其中新皂甙为3β,16α,23,28四羟基齐墩果烷11,13(18)二烯3OβD吡喃葡萄糖基(1→6)[αL吡喃鼠李糖基(1→4)]βD吡喃葡萄糖甙,命名为柴胡皂甙s(saikosaponins)。另4个皂甙分别为柴胡皂甙a、c、b1、b2。  相似文献   

8.
自头序Song木70%EtOH提取物分得6个化合物,应用光谱技术(IR,MS,HNMR,^13CNMR,DEPT,2DNMR)及化学方法,确定了他们的结构,分别为β-谷甾醇(Ⅰ),胡萝卜甙(Ⅱ),齐墩果酸(Ⅲ),竹节参皂甙1(Ⅳ),竹节参皂甙Ⅳa(ChikusetsusapominⅣa)(Ⅴ),常春藤皂甙元-28-O-β-吡喃葡萄糖醛酸(1→4)-β-D-吡喃葡萄糖甙(Ⅵ),以上化合物均为首次从该  相似文献   

9.
仙茅根茎中的配糖体   总被引:5,自引:0,他引:5  
从仙茅( Curculigo orchioidesGaertn) 根茎中分离到7 个化合物, 经光谱分析推定其化学结构分别为: 2, 6 - 二甲氧基苯甲酸(A) ; 苔黑酚葡萄糖甙(B) ; 仙茅素A (C) ; 仙茅甙(D) ; 24s, 3β, 11α, 16β, 24 - 四羟基环阿尔廷醇- 3 - O- α- L- 鼠李吡喃糖基(1 →2) - β-D- 葡萄吡喃糖甙(E) ; 24s, 3β, 11α, 16β, 24 - 四羟基环阿尔廷醇- 3- O- β- D- 葡萄吡喃糖基(1 →2) - β- D- 葡萄吡喃糖甙(F) 和胡萝卜甙(G) 。F为一新甙。  相似文献   

10.
从川麦冬(Ophiopogon japonicus)根部乙醇提取物中分离得到四个已知化合物,经波谱分析确定其结构分别为:龙脑7-O-β-D-吡喃葡萄糖甙(1),龙脑7-O-〔β-D-呋喃芹糖(1→6)〕-β-D吡喃葡萄糖甙(2),4-烯丙基-1,2-苯本酚1-O-〔α-L-吡喃鼠李糖(1→6)〕-β-D-吡喃葡萄糖甙(3),5-烯-1β,3β,16β,22S-胆甾四醇1-O-α-L-吡喃鼠李糖16  相似文献   

11.
Five triterpene saponins never reported before, hederifoliosides A-E, and four known triterpene saponins were isolated from the tubers of Cyclamen hederifolium. The structures of hederifoliosides A-E were determined as 3β,16α-dihydroxy-13β,28-epoxyolean-30-oic acid 3-O-{[β-D-glucopyranosyl-(1 → 2)-O]-β-D-xylopyranosyl-(1 → 2)-O-β-D-glucopyranosyl-(1 → 4)-O-α-L-arabinopyranoside}, 3β,16α-dihydroxy-13β,28-epoxyolean-30-oic acid 3-O-{[β-D-glucopyranosyl-(1 → 2)-O]-β-D-xylopyranosyl-(1 → 2)-O-[β-D-glucopyranosyl-(1 → 3)]-O-β-D-glucopyranosyl-(1 → 4)-O-α-L-arabinopyranoside}, 3β,16α-dihydroxy-13β,28-epoxyolean-30-al 3-O-{[β-D-glucopyranosyl-(1 → 2)-O]-β-D-xylopyranosyl-(1 → 2)-O-[β-D-glucopyranosyl-(1 → 3)]-O-[β-D-glucopyranosyl-(1 → 6)]-O-β-D-glucopyranosyl-(1 → 4)-O-α-L-arabinopyranoside}, 30-O-β-D-glucopyranosyl-(1 → 2)-O-β-D-glucopyranosyl-3β,16α,30-trihydroxyolean-12-en-28-al 3-O-{[β-D-glucopyranosyl-(1 → 2)-O]-β-D-xylopyranosyl-(1 → 2)-O-β-D-glucopyranosyl-(1 → 4)-O-α-L-arabinopyranoside}, 30-O-β-D-glucopyranosyl-(1 → 2)-O-β-D-glucopyranosyl-3β,16α,28,30-tetrahydroxyolean-12-en 3-O-{[β-D-glucopyranosyl-(1 → 2)-O]-β-D-xylopyranosyl-(1 → 2)-O-[β-D-glucopyranosyl-(1 → 3)]-O-β-D-glucopyranosyl-(1 → 4)-O-α-L-arabinopyranoside}, by a combination of one- and two-dimensional NMR techniques, and mass spectrometry. The cytotoxic activity of the isolated compounds was evaluated against a small panel of cancer cell lines including Hela, H-446, HT-29, and U937. None of the tested compounds, in a range of concentrations between 1 and 50 μM, caused a significant reduction of the cell number.  相似文献   

12.
金铁锁的新三萜皂甙   总被引:10,自引:0,他引:10  
从金铁锁(Psammosilene tunicoides W.C.Wu et C.Y.Wu)根部分离得到5个齐墩果烷型五环三萜皂苷,它们的结构通过波谱和化学方法分别鉴定为:3-O-β-D-galactopyranosyl-(1→2)-β-D-glucuronopyranosyl-gypsogenin(1),3-O-β-D-galactopyranosyl-(1→2)-[β-D-galactopyranosyl-(1→3)-β-D-glucuronopyranosyl-gypsogenin(2),3-O-β-D-galactopyranosyl-(1→2)-β-D-glucuronopyra-nosyl-gypsogenin-28-O-β-D-xylopyranosyl-(1→4)-[β-D-glucopyranosyl-(1→3)]-α-L-rhamnopyranosyl(1→2)-β-D-fucopyranoside(LobatosideI,3),3-O-β-D-galactopyranosyl-(1→2)-[β-D-xylopyranosyl-(1→3)-β-D-glucuronopyranosylgypsogenin-28-O-β-D-xylopyranosyl-(1→4)-[β-D-glucopyranosyl-(1→3)]-α-L-rhamnopyranosyl(1→2)-β-D-fucopyranoside(4),3-O-β-D-galactopyranosyl-(1→)-β-D-glucuro-nopyranosyl-grpsogenin-28-O-β-D-xylopyranosyl-(1→4)-[β-D-6-O-acetylglucopyranosyl-(1→3)-β-D-glucuro-nopyranosyl-gypsogenin-28-O-β-D-xylopyranosyl-(1→4)-[β-D-6-O-acetylglucopyranosyl-(1→3)]-α-L-rh-amnopyranosyl(1→2)-β-D-fucopyranoside(5),其中5为新化合物,1和2为首次从自然界中分离得到。  相似文献   

13.
New Cytotoxic Saponins from Lysimachia davurica Ledeb.   总被引:2,自引:0,他引:2  
To investigate the saponins from whole plants of Lysimachia davurica Ledeb., two new saponins named davuricoside I (compound 1) and E (compound 2) were isolated. Their chemical structures were elucidated as 3β, 16α, 28, 29-tetrihydroxy-olean-12-en-3-O-β-D-glucopyranosyl-(1→2)-β-D-glucuronopyranoside (compound 1) and 3β, 16α, 29-trihydroxy-13, 28-epoxy-oleanane-3-O-β-D-glucopyranosyl-(1→2)-β-D-glucuronopyranoside (compound 2) on the basis of their one- and two-dimensional nuclear magnetic resonance and mass spectrometry data, and chemical methods. Compound 1 showed significant cytotoxic activity against human A2780 cells.  相似文献   

14.
Phytochemical investigation of the under-ground parts of Hydrocotyle bonariensis led to the isolation of five oleanane-type triterpenoid saponins, 3-O-{β-D-glucopyranosyl-(1 → 2)-[α-L-arabinopyranosyl-(1 → 3)]-β-D-glucuronopyranosyl}-21-O-(2-methylbutyroyl)-22-O-acetyl-R(1)-barrigenol, 3-O-{β-D-glucopyranosyl-(1 → 2)-[α-L-arabinopyranosyl-(1 → 3)]-β-D-glucuronopyranosyl}-21-O-(2-methylbutyroyl)-28-O-acetyl-R(1)-barrigenol, 3-O-{β-D-glucopyranosyl-(1 → 2)-[α-L-arabinopyranosyl-(1 → 3)]-β-D-glucuronopyranosyl}-21-O-acetyl-R(1)-barrigenol, 3-O-{β-D-glucopyranosyl-(1 → 2)-[α-L-arabinopyranosyl-(1 → 3)]-β-D-glucuronopyranosyl}-R(1)-barrigenol, and 3-O-{β-D-glucopyranosyl-(1 → 2)-[α-L-arabinopyranosyl-(1 → 3)]-β-D-glucuronopyranosyl}-22-O-(2-methylbutyroyl)-A(1)-barrigenol, together with the known saniculoside-R1. Their structures were established by 2D NMR techniques and mass spectrometry. Six compounds were evaluated against two human colon cancer cell lines, HCT 116 and HT-29. Two compounds showed weak cytotoxicity with IC(50) 24.1 and 24.0, 83.0 and 83.6 μM against HT-29 and HCT 116, respectively.  相似文献   

15.
从百合科植物大叶吊兰(Chlomphytum malayense)根茎中分离得到1个新的呋甾烷型甾体皂甙,命名为大叶吊兰甙E(chloromaloside E)。经波谱和化学方法证明明其结构为:26-0-β-D-glucopyranosyl-22-hydroxy-25(S)-5a-furostan-12-oxo-3β,26-diol-3-β-D-xylopyranosyl(1→3)〖α-L-ara  相似文献   

16.
古蔺雪胆中的新三萜皂苷   总被引:5,自引:1,他引:4  
从采自四川汉源县的古蔺雪胆(Hemsleya penxianensis var.gulinensiks)中分到9个三萜皂苷化合物,通过化学反应和光谱方法鉴定了它们的结构。其中7个为已知化合物,分别为齐墩果酸-28-O-β-D-比喃葡萄糖苷(1),3-O-β-D-吡喃葡萄糖醛基齐墩果酸苷(3),3-O-β-D-吡喃葡萄糖醛基—齐墩果酸—28-O-α-L-吡喃阿拉伯糖苷(4),3-O-β-D-吡喃葡萄糖醛基—齐墩果酸—28-O-β-D-吡喃葡萄糖苷(5),3-O-α-L-阿拉伯糖基—(1→3)—β—D-吡喃葡萄糖醛基—齐墩果酸—28—O—β—D—吡喃葡萄糖苷(6),3—O—(6′—丁酯)—β-D-吡喃葡萄糖醛基—齐墩果酸—28-O-α-L-阿拉伯糖苷(7),3-O-(6′-丁酯)—β—D吡喃葡萄糖醛基—齐墩果酸—28-O-β-D-吡喃葡萄糖苷(8)。两个新化合物,即雪胆皂苷A(2)和雪胆皂苷B(9)。  相似文献   

17.
金铁锁的两个新三萜皂苷   总被引:17,自引:0,他引:17  
从石竹科植物金铁锁(Psammosilene tunicoides W.C.Wu et C.Y.Wu)根部分离得到4个齐墩果酸型五环三萜皂苷。它们的结构通过波谱和化学方法分别鉴定为:3-O-β-D-galac-topyranosyl-(1→2 )-β-D-6-O-methylgtucuronopymnosyl-quillaic acid (1),3-O-β-D-galactopymnosyl-(1→2)-[β-D-xylopyranosyl-(1→3)]-β-D-gtucuronopyranosyl-quillaic acid (2),3-O-β-D-galactopyrano-syl-(1→2)-[β-D-xylopyranosyl-(1→3)]-β-D-6-O-methylgtucuronopyranosyl-quillaic acid(3),3-O-β-D-galactopymnosyl-(1→2)-[β-D-xylopyranosyl-(1→3)]-β-D-6-O-ethylgtucuronopyranosyl-quillaic acid(4)。其中1为木鳖子中发现的次甙,3和4为新化合物。  相似文献   

18.
丁愉  刘丹  赵璠  汤海峰  赵美 《生物磁学》2011,(8):1569-1572
目的:研究银莲花属植物小花草玉梅的化学成分。方法:采用硅胶柱色谱,凝胶柱色谱,反相柱色谱并结合制备高效液相色谱等技术分离纯化单体化合物,并根据理化性质及光谱数据鉴定结构。结果:分离并鉴定了4个化合物,分别是常春藤皂苷元-28-O-β-D-吡喃葡萄糖酯苷(1)、3-O-β-D-吡喃葡萄糖-(1→2)-α-L-吡喃阿拉伯糖-齐墩果酸皂苷元-28-O-α-L-吡喃鼠李糖-(1→4)-β-D-吡喃葡萄糖-(1→6)-β-D-吡喃葡萄糖酯苷(2)、3-O-β-D-吡喃葡萄糖-(1→2)-α-L-吡喃阿拉伯糖-常春藤皂苷元-28-O-α-L-吡喃鼠李糖-(1→4)-β-D-吡喃葡萄糖-(1→6)-β-D-吡喃葡萄糖酯苷(3)和3-O-β-D-吡喃核糖-(1→3)-α-L-吡喃鼠李糖-(1→2)-α-L-吡喃阿拉伯糖-常春藤皂苷元-28-O-α-L-吡喃鼠李糖-(1→4)-β-D-吡喃葡萄糖-(1→6)-β-D-吡喃葡萄糖酯苷(4)。结论:化合物1为首次从银莲花属植物中分离得到,2-4为首次从小花草玉梅中分离得到。  相似文献   

19.
Six new protopanaxadiol-type ginsenosides, named ginsenosides Ra(4) -Ra(9) (1-6, resp.), along with 14 known dammarane-type triterpene saponins, were isolated from the root of Panax ginseng, one of the most important Chinese medicinal herbs. The structures of the new compounds were determined by spectroscopic methods, including 1D- and 2D-NMR, HR-MS, and chemical transformation as (20S)- 3-O-{β-D-6-O-[(E)-but-2-enoyl]glucopyranosyl-(1→2)-β-D-glucopyranosyl}-20-O-[β-D-xylopyranosyl-(1→4)-α-L-arabinopyranosyl-(1→6)-β-D-glucopyranosyl]protopanaxadiol (1), (20S)-3-O-[β-D-6-O-acetylglucopyranosyl-(1→2)-β-D-glucopyranosyl]-20-O-[β-D-xylopyranosyl-(1→4)-α-L-arabinopyranosyl-(1→6)-β-D-glucopyranosyl]protopanaxadiol (2), (20S)-3-O-{β-D-6-O-[(E)-but-2-enoyl]glucopyranosyl-(1→2)-β-D-glucopyranosyl}-20-O-[β-D-glucopyranosyl-(1→6)-β-D-glucopyranosyl]protopanaxadiol (3), (20S)-3-O-{β-D-6-O-[(E)-but-2-enoyl]glucopyranosyl-(1→2)-β-D-glucopyranosyl}-20-O-[α-L-arabinopyranosyl-(1→6)-β-D-glucopyranosyl]protopanaxadiol (4), (20S)-3-O-{β-D-4-O-[(E)-but-2-enoyl]glucopyranosyl-(1→2)-β-D-glucopyranosyl}-20-O-[α-L-arabinofuranosyl-(1→6)-β-D-glucopyranosyl]protopanaxadiol (5), (20S)-3-O-{β-D-6-O-[(E)-but-2-enoyl]glucopyranosyl-(1→2)-β-D-glucopyranosyl}-20-O-[α-L-arabinofuranosyl-(1→6)-β-D-glucopyranosyl]protopanaxadiol (6). The sugar moiety at C(3) of the aglycone of each new ginsenoside is butenoylated or acetylated.  相似文献   

20.
从龙舌兰(Agave americana)的发酵叶汁中分离到一个新甾体皂苷。结合波谱和化学方法,新化合物的结构鉴定为替告皂苷元3-O-α-L-鼠李吡喃糖基-(1→3)-β-D-葡萄吡喃糖基-(1→2)-[β-D-葡萄吡喃糖基-(1→3)-β-D-葡萄吡喃糖基-(1→4)-β-D-半乳吡喃糖苷。  相似文献   

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