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1.
仙茅苷丙——仙茅根茎的新酚苷成分   总被引:4,自引:0,他引:4  
从仙茅(CurculigoorchioidesGaertn.)根茎中分离得到4个化合物,分别为curculigoside(1)、curculigosideB(2)、curculigosideC(3)和2,6-dimethoxylbenzoicacid(4)。其中,化合物3为一个新的酚苷类成分,命名为仙毛苷丙,用现代波谱方法(1H-NMR、13C-NMR、2D-NMR和ESI-MS)鉴定其化学结构为5-羟基-2-O-b-D-吡喃葡萄糖基苄基-3'-羟基-2',6'-二甲氧基苯甲酸酯。  相似文献   

2.
仙茅的化学成分研究   总被引:7,自引:0,他引:7  
从仙茅(Curculigo orchioides Gaertn.)根茎的乙醇提取物中分离鉴定了7个己知化合物,它们是:eureuligoside I(1),oreinol glueoside(2),3,3′,5,5′-tetramethoxy-7,9′:7′,9-diepoxy-lignan-4,4′-di-O-β-D-glucopyranoside(3),3-hydroxy-5-methyl-phenol-1-O-[β-D-glucopyranosyl-(1→6)-β-D-glucopyranoside](4),2,3,4,7-tetramethoxyxanthone(5),1,3,7-trimethylxanthine(6),daueosterol(7)。其中化合物3~7均为首次从该植物中分离得到。  相似文献   

3.
采用硅胶柱色谱、凝胶柱色谱、制备HPLC等手段,从海洋生物罗氏海盘车(Asterias rollestoni Bell.)中分离得到两个化合物,利用理化和波谱分析方法鉴定为2-(2′R-羟基-十五碳酰胺)-3-羟基-(2S,3R)-二十二烷1-O-β-D-葡萄吡喃糖苷(1)和2-{2′-羟基-(2′R,14′Z)-二十三碳烯酰胺}-3-羟基-(2S,3R,6E)-十五碳烯1-O-β-D-葡萄吡喃糖苷(2),它们都是未见报道的新化合物,分别命名为罗氏脑苷B和罗氏脑苷C。  相似文献   

4.
大叶仙茅中一个新的木脂素苷   总被引:1,自引:0,他引:1  
从采自云南西双版纳的大叶仙茅(Curculigo capitulata)中分离得到一个新的木脂素苷和8个已知化合物,通过光谱方法、化学方法和与参考文献比较(质谱,氢谱和碳谱)的方法鉴定了它们的结构。其中化合物2—7为首次从该植物中分离得到。  相似文献   

5.
从欧橄榄(Olea europaeaL.)干燥叶的乙酸乙酯部位分离得到5个裂环烯醚萜类化合物。通过波谱分析和理化常数对照等方法,上述化合物分别鉴定为6′-O-甲基橄榄苦苷(6′-O-methyloleuropein,1)、橄榄苦苷(oleu-ropein,2)、(1S)-methylelenolate(3)、3,4-二羟基苯乙基-4-甲酰基-3-甲酰甲基-4-己烯酯(4)和oleoside(5)。其中化合物1为新化合物。  相似文献   

6.
细穗玄参的脂溶性化学成分   总被引:3,自引:2,他引:1  
沈光明  田瑄 《西北植物学报》2004,24(7):1295-1297
从细穗玄参(Scrofella chinensis Maxim.)全草中分离并鉴定了8个化合物。利用光谱(MS、NMR、UV)和化学方法分别鉴定为5,7,3′-三羟基-4′-甲氧基黄酮(1)、3,5-二羟基-7,4′-二甲氧基黄酮(2)、5,6,7-三羟基-4′-甲氧基黄酮(3)、β-谷甾醇(4)、胡萝卜苷(5)、对甲氧基苯甲酸(6)、对苯酚(7)及二十九碳脂肪酸(8)。8个化合物均为首次从该植物中发现。  相似文献   

7.
吊石苣苔中的化学成分   总被引:5,自引:0,他引:5  
新鲜吊石苣苔全草用70%丙酮水溶液组织破碎提取,然后经Diaion HP-20,Toyopearl HW-40,硅胶等柱色谱技术进行分离纯化得到8个化合物,经波谱分析鉴定为5,7-二羟基-6,8,4′-三甲氧基黄酮(1),丁香酸(2),邻苯二甲酸-双-(2-乙基己基)酯(3),5,7-二羟基-6,8,4′-三甲氧基黄酮醇(4),7-羟基-6,8,4′-三甲氧基-5-O--βD-葡萄糖黄酮苷(5),7-羟基-6,8,4′-三甲氧基-5-O-[-βD-葡萄糖-(1→6)]--βD-葡萄糖黄酮苷(6),4′,5-二羟基-7-甲氧基-6-C--βD-葡萄糖黄酮苷(7)和4′,5-二羟基-6,7-二甲氧基-8-C-β-D-葡萄糖黄酮苷(8)。除7-羟基-6,8,4′-三甲氧基-5-O--βD-葡萄糖黄酮苷和7-羟基-6,8,4′-三甲氧基-5-O-[β-D-葡萄糖-(1→6)]--βD-葡萄糖黄酮苷外,其余6个化合物均为首次从该植物中分离得到。  相似文献   

8.
芒果叶化学成分研究 II   总被引:1,自引:0,他引:1  
为探讨芒果(Mangifera indica L.)的化学成分,从芒果叶的70%乙醇提取物中分离鉴定了13个化合物,经波谱分析,分别鉴定为:(–)-secoisolariciresinol-9′-O-D-glucopyranoside(1)、7S,8R-erythro-4,7,9-trihydroxy-3,3′-dimethoxy-8-O-4′-neolignan-9′-O-β-D-glucopyranoside(2)、7R,8R-threo-4,7,9-trihydroxy-3,3′-dimethoxy-8-O-4′-neolignan-9′-O-β-D-glucopyranoside(3)、(7R/S,8R)-7,8-dihydro-9′-hydroxyl-3′-methoxyl-8-hydroxymethyl-7-(4-hydroxy-3-methoxyphenyl)-1′-benzofuranpropanol 9′-O-β-D-glucopyranoside(4)、citrusin D(5)、丁香苷(6)、2,6-二甲氧基-4-羟基苯基-1-O-β-D-葡萄糖苷(7)、原儿茶酸(8)、没食子酸(9)、没食子酸甲酯(10)、没食子酸乙酯(11)、4,5-二羟基-3-甲氧基苯甲酸(12)、β-胡萝卜苷(13)。其中化合物1~7和12为首次从芒果属植物中分离得到。  相似文献   

9.
艾纳香化学成分的研究   总被引:1,自引:0,他引:1  
从艾纳香(Blumea balsamifera DC.)中分离得到12个化合物,通过理化性质和波谱数据分析分别鉴定为;商路素(1),花椒油素(2),2,4-二羟基-6-甲氧基苯乙酮(3),5,7-二羟基色原酮(4),金丝桃苷(5),异槲皮苷(6),3′,4′,5,7-四羟基-3-甲氧基黄酮(7),槲皮素(8),槲皮素-3′-甲氧基-3-O-β-D-半乳吡喃糖苷(9),4′,5,7-三羟基-3,3′-二甲氧基黄酮(10),3,5,7-三羟基-3′,4′-二甲氧基黄酮(11),木犀草素(12).其中,化合物3-7和9- 11为首次从该属植物中分离得到.  相似文献   

10.
为研究柯拉斯那(Aquilaria crassna Pierre ex Lecomte)沉香的化学成分。实验采用多种柱色谱方法从该沉香中分离得到9个2-(2-苯乙基)色酮类化合物,通过现代波谱学技术分别鉴定为6-甲氧基-2-[2-(3′-羟基-4′-甲氧基苯基)乙基]色酮(1)、5-羟基-6-甲氧基-2-[2-(3′-羟基-4′-甲氧基苯基)乙基]色酮(2)、tetrahydrochromone F(3)、6-甲氧基-2-[2-(3′-甲氧基-4′-羟基苯基)乙基]色酮(4)、6-甲氧基-7-羟基-2-[2-(4′-甲氧基苯基)乙基]色酮(5)、6,7-二甲氧基-2-[2-(3′-羟基-4′-甲氧基苯基)乙基]色酮(6)、6,7-二甲氧基-2-[2-(4′-甲氧基苯基)乙基]色酮(7)、6-羟基-2-[2-(4′-羟基苯基)乙基]色酮(8)、5-羟基-2-[2-(2′-羟基苯基)乙基]色酮(9)。化合物2、3和5~9均为首次从柯拉斯那所得沉香中分离得到。采用MTT法对单体化合物的细胞毒活性进行测试,测试结果表明,化合物1,2和4具有微弱的细胞毒活性。  相似文献   

11.
Seven compounds have been isolaed from the roots of Curculigo orchioides. On the basis of spectral analysis,their structures were elucidated as 2,6-dimethoxy benzoic acid (A),orcinol glucopyranoside(B),curculigine A(C),curculigoside(D),24s,3β,11α,16,24-tetrahyaroxycycloartenol-3-O-α-L-rhamnopyranosyl(1→2)-β-D-glucopyranoside(E),24s,3β,11a,16β,24-tetrahydroxycycloartenol-3-O-β-d-glucopyranosyl(1→2)-β-D-glucopyranoside(F) and dancosterol(G). Saponin F is a new tritepenoid compound.  相似文献   

12.
Allium inutile Makino in Bot.Mag.Tokyo 12:104.1898.- Nothoscordum inutile(Makino)kitamura in Bot.Mag.Tokyo 59:35.1946.  相似文献   

13.
ObjectiveTo investigate the effect of curculigoside on mice with simulated perimenopausal depression.MethodGavage with high, medium, small dose of curculigoside once daily for 30 d consecutive days. Record the related behavior index. The wet weights and viscera indexes of the mouse uterus, thymus, and spleen were measured. Half of the brain was homogenized and tested for 5-HT and DA concentrations. The levels of serum E2, T, FSH, and LH were measured as well. Finally, histological changes in the uterus, thymus, spleen, and hypothalamus were observed under a light microscope.Resultcurculigoside can enhance the activity and latency time of the mice, increase mouse memory, and decrease electric shocks and immobility times in the TST and FST experiments. Mice treated with curculigoside showed significantly enhancement in viscera indexes of the thymus, spleen, and uterus; significantly elevated levels of serum E2 and T; significantly increased brain 5-HT and DA concentrations; significantly decreased levels of serum FSH and LH; and improvements in the histopathological lesions of the uterus, hypothalamus, thymus, and spleen. The high dose of curculigoside produced the best results.ConclusionAll doses of curculigoside are associated with reversing hormone (E2, T, FSH, and LH) disorders in perimenopausal syndrome and adjusting imbalanced 5-HT and DA levels, representing a therapeutic effect in perimenopausal depression.  相似文献   

14.
Six phenolic compounds isolated from Curculigo orchioides, including 2,6-dimethoxy benzoic acid (1), curculigoside A (2), curculigoside B (3), curculigine A (4), curculigine D (5) and 3,3′,5,5′-tetramethoxy-7,9′:7′,9-diepoxylignan-4,4′-di-O-β-d-glucopyranoside (6), together with the ethanol extract of Curculigo orchioides were evaluated for their activity on osteoblasts in neonatal rat calvaria cultures and multinucleated osteoclasts derived from rat marrow cells so as to characterize the antiosteoporotic components of this plant and explore the relationship of chemical structure with antiosteoporotic activity. The proliferation of osteoblast was assayed by MTT methods. The activity of ALP (alkaline phosphatase) and TRAP (tartrate-resistant acid phosphatase) was measured by p-nitrophenyl sodium phosphate assay. The TRAP stain was used to identify osteoclast in morphology. The resorption pit area on the bone slices formed by osteoclast was measured by computer image processing. The ethanol extract exhibited stimulatory effect on both the osteoblast proliferation and the ALP activity. Six compounds all increased the osteoblast proliferation, and compounds (1), (2) and (4) also slightly increased the osteoblastic ALP activity. Compounds (1), (2), (3), (6) and the ethanol extract decreased area of bone resorption pit, osteoclastic formation and TRAP activity. These results indicated that phenolic compounds are antiosteoporotic chemical constituents from Curculigo orchioides, and their activities are related with chemical structures.  相似文献   

15.
Bioassay-directed fractionation of the cytotoxicity active fraction of the whole plant from Solanum lyratum led to the isolation of a new steroidal saponin, diosgenin 3-O-beta-D-glucopyranosiduronic acid methyl ester (2), as well as four known compounds, diosgenin (1), diosgenin 3-O-beta-D-glucopyranosiduronic acid (3), diosgenin 3-O-alpha-L-rhamnopyranosyl-(1-->2)-beta-D-glucopyranosiduronic acid (4), diosgenin 3-O-alpha-L-rhamnopyranosyl-(1-->2)-beta-D-glucuroniduronic acid methyl ester (5). The structures of the isolated compounds were elucidated on the basis of their spectral data and chemical evidences. Compound 1 was isolated for the first time from this plant, and compound 3 was isolated as a new natural product. Cytotoxic activities of the isolated compounds were evaluated and the cytotoxicities of compounds 2-5 reported for the first time.  相似文献   

16.
从地衣绿槽枝衣( Sulcaria virens) 中分离得到一个新的亚油酸异丙叉衍生物, 通过波谱学方法包括2D-NMR 确定其化学结构为: 9, 10-O-异丙叉基- (12 Z)-十八碳烯酸(1) 。同时还得到其它12 个已知化合物:( 9 Z, 12 Z )-十八碳二烯酸(2), 扁枝衣二酸(3), ( R ) -松萝酸(4), 枕酸甲酯( 5), 黑茶渍素(6) , virensic acid ( 7), abieslactone (8), 3α-羟基羊毛甾-7, 24-二烯-26, 23 R-内酯(9), 蒲公英赛醇(10 ), 蒲公英赛酮 ( 11 ), (22 E , 24 R )-5α, 8α-过氧麦角甾-6, 22-二烯-3β-醇(12) 和2, 2′-四氢角鲨烯(13)。  相似文献   

17.
Liu L  Li AL  Zhao MB  Tu PF 《化学与生物多样性》2007,4(12):2932-2937
Two new tetralones, pyrolones A (1) and B (2), and a new flavonol glycoside, 2'-O-(4-hydroxybenzoyl)hyperin (3), were isolated from Pyrola calliantha (whole plant), together with six structurally related compounds, including 2'-O-galloylhyperin (4), hyperin (5), formononetin (6), quercetin 3-O-alpha-L-arabinopyranoside (7), quercetin 3-O-alpha-L-arabinofuranoside (8), and kaempferol 3-O-beta-D-galactopyranoside (9). The structures and absolute configurations of the new compounds were elucidated on the basis of spectroscopic (UV, ORD, CD, NMR) and mass-spectrometric (HR-ESI-MS) analyses.  相似文献   

18.
Four new xanthone glucosides, 3-hydroxy-2-methoxyxanthone-4-O-β-D-glucopyranoside ( 1 ), 4,8-dihydroxy-2-methoxyxanthone-3-O-β-D-glucopyranoside ( 2 ), 2-methoxyxanthone-5-O-β-D-glucopyranoside ( 3 ), 4-hydroxy-2-methoxyxanthone-3-O-β-D-glucopyranoside ( 4 ), a new phenolic acid, 4,4-dihydroxy-3,3-imino-di-benzoic acid monomethyl ester ( 5 ), and a new isoquinoline, methyl 6-hydroxy-1-oxo-1,2,3,4-tetrahydroisoquinoline-4-carboxylate ( 6 ) were isolated from the fruit of Hypericum patulum. The structural elucidation of the isolated compounds was primarily based on HR-ESI-MS, UV, IR, 1D and 2D NMR. All compounds were evaluated for their inhibitory effect against LPS-induced NO production in RAW 264.7 cells. Compound 2 , 3 exhibited moderate inhibitory activity against NO production.  相似文献   

19.
从鞭打绣球(Hemiphragma heterophyllum Wall.)全草中分离到1个新单萜苷和7个已知化合物.通过波谱数据分析,新单萜苷的结构鉴定为(4S)-α-萜烯醇-8-O-β-D-比喃木糖-(1→6)-β-D-比喃葡萄糖苷,已知化合物分别鉴定为globularin(2)、(2S 3S,4R,9E)-1,3,4-trihydroxy-2-[(2'R)-hydroxy-tetracosanoylamino]-9-octadecene(3)、β-香树素(4)、齐墩果酸(5)、肉桂酸(6)、β-谷甾醇(7)和胡萝卜甙(8).除化合物2外,其余化合物均为首次从鞭打绣球中分离得到.  相似文献   

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