昌都锦鸡儿紫檀素类化学成分的研究
详细信息    本馆镜像全文|  推荐本文 |  |   获取CNKI官网全文
摘要
昌都锦鸡儿是豆科锦鸡儿属植物,灌木,主产于我国西藏、青海。昌都锦鸡儿长期以来作为藏药藏锦鸡儿的主要植物来源之一,藏文名为“佐木兴”,其根茎具有活血化瘀、降压、消炎散肿等功效,内用治疗高血压、多血症、月经不调,外用治疗跌打损伤等症。本课题开展了昌都锦鸡儿化学成分的研究,实验采用硅胶、凝胶、制备薄层等色谱方法对昌都锦鸡儿根茎的氯仿萃取部分进行了系统分离,得到18个单体化合物,通过紫外光谱、红外光谱、质谱、核磁共振、X-射线晶体衍射等手段鉴定了其中10个化合物的结构,分别为8个紫檀素:Homopterocarpin(Can-6), 3-Hydroxy-8,9-dimethoxypterocarpan(Can-10) 3-hydroxy-4,9-dimethoxypterocarpan(Can-11),4-methyoxy-maackiain(Can-12), Medicarpin(Can-13), Maackiain(Can-14), 3,4-dihydroxy-9-methoxypterocarpan(Can-15), 3,4-dih-ydroxy-8,9-methylenedioxypterocarpan(Can-16); 2个异黄酮:Olibergin A(Can-17),Cajanin(Can-18);其它化合物结构正在鉴定之中。其中Can-6, Can-10, Can-12,Can-15, Can-16, Can-17为锦鸡儿属植物中首次得到的化合物。首次发现了昌都锦鸡儿中紫檀素类成分成对存在的特殊现象,并从色谱和波谱性质对它们进行了初步的讨论。
Caragana changduensis is a shrub of genus Caragana Fabra.,Leguminosae,mainly distributed in Tibet and Qinghai province. C. Changduensis of which Tibetanname is zuomuxing, has a profound medicinal history in Tibetan traditional medicine.Its rhizome has the efficacy of promoting blood flow, reducing blood pressure andeliminating inflammation, which can be treated with plethora, hypertension,catamenia disorder for internal use while bruises and contused wound for external use.Systematic isolation of chloroform extract of C. changduensis was carried out.Eighteen compounds were obtained by preparative chromatography methods of silicagel, Toyopearl, PTLC, et al. Based on UV, IR, MS, NMR and X-ray crystaldiffraction, ten of them were identified as fallows, 8 pterocarpans:Homopterocarpin(Can-6), 3-Hydroxy-8,9-dimethoxypterocarpan(Can-10) ,3-Hydrox-y-4,9-dimethoxypterocarpan (Can-11), 4-methyoxy-maackiain(Can-12), Medicarpin(Can-13), Maackiain(Can-14), 3,4-dihydroxy-9-methoxypterocarpan(Can-15), 3,4-di-hydroxy-8,9-methylenedioxypterocarpan(Can-16); 2 isoflavones: Olibergin A (Can-17), Cajanin(Can-18). The structures of the others are being identified. CompoundsCan-6, Can-10, Can-12, Can-15, Can-16, Can-17 are isolated from genus Caraganafor the first time. A special phenomenon of pterocarpan constituents existing in C.Changduensis have been discovered for the fist time. The chromatography andspectroscopy property of them have been discussed.
引文
[1]赵一之,中国锦鸡儿属的分类学研究,内蒙古大学学报(自然科学版),1993,24(6):631~653
    [2]牛西午,中国锦鸡儿属的资源研究——分布及分种描述,西北植物学报,1999,15(9):107~133
    [3]卫生部药典委员会,卫生部药品标准,北京:人民卫生出版社
    [4]西藏自治区藏医院药物研究所,中华本草藏药卷,上海:上海科学技术出版社,2002,343~344
    [5]青海省药品检验所,青海省藏医药研究所,中国藏药,上海:上海科学技术出版社,1996,268~270
    [6]中国药品生物制品检定所,云南省药品检验所,中国民族药志,第二卷,北京:人民卫生出版社,1990,572~575
    [7]罗达尚,新修晶珠本草,成都:四川科学技术出版社,2004,400~402
    [8]杨永昌,藏药志,青海:青海人民出版社,1991,297~298
    [9]中国医学百科全书编辑委员会,中国医学百科全书,上海:上海科学技术出版社,1999,207
    [10]罗尚达,中华藏草本,北京:民族出版社,1997,134~135
    [11] Oldrich Lapcik, Isoflavonoids in non-leguminous taxa: A rarity or a rule,Phytochemistry, 2007, 68: 2909~2916
    [12] Leticia Jimenez-Gonzalez, Miriam Alvarez-Corral, Manuel Munoz-Dorado et al,Pterocarpans: interesting natural products with antifungal activity and otherbiological properties, Phytochem Rev, 2008, 7: 125~154
    [13] Ahmad VU, Iqbal S, Nawaz SA et al, Isolation of four new pterocarpans fromZygophyllum eurypterum with enzyme-inhibition properties, Chem Biodivers,2006, 3: 996~1003
    [14] Abdel-Kader MS, Phenolic constituents of Ononis vaginalis roots, Planta Med,2001, 67: 388~390
    [15] Breytenbach JC, Rall GJH, Structure and synthesis of isoflavonoid analogs fromNeorautanenia amboensis Schinz, J Chem Soc Perkin Trans 1, 1980, 1804~1809
    [16] Babu UV, Bhandari SPS, Garg HS Barbacarpan, A pterocarpan from Crotalariabarbata, Phytochemistry, 1998, 48: 1457~1459
    [17] Braz Filho R, De Moraes MPL, Gottlieb OR, The chemistry of BrazilianLeguminosae, Part LVII, Pterocarpans from Swartzia laevicarpa, Phytochemistry,1980, 19: 2003~2006
    [18] Bezuidenhoudt, Brandt EV, Ferreira D, Flavonoid analogs from Pterocarpusspecies, Phytochemistry, 1987, 26: 531~535
    [19] Brink AJ, Rall GJH, Breytenbach JC, Pterocarpans of Neorautanenia edulis andN. Amboensis, Phytochemistry, 1977, 16: 273~276
    [20] Belofsky G, Percivill D, Lewis K et al, Phenolic metabolites of Dalea versicolorthat enhance antibiotic activity against model pathogenic bacteria, J Nat Prod,2004, 67: 481~484
    [21] Brink M, Nel W, Rall GJH et al, Neorautanenia isoflavanoids II Neofolin andficinin, two new furoisoflavanoids from Neorautanenia ficifolia, J S Afr Chem I,1966, 19: 24~37
    [22] Brink Cvd, Engelbrecht JP, Graham DE, Neorautanenia isoflavanoids IVFicifolinol, folitenol, and folinin, three new pterocarpans from the root bark ofNeorautanenia ficifolia, J S Afr Chem I, 1970, 23: 24~33
    [23] Brink AJ, Rall GJH, Engelbre JP, Structures of some minor pterocarpans ofNeorautanenia edulis, Phytochemistry, 1974, 13: 1581~1585
    [24] Belofsky G, Carreno R, Lewis K et al, Metabolites of the ''smoke tree'', Daleaspinosa, potentiate antibiotic activity against multidrug-resistant Staphylococcusaureus, J Nat Prod, 2006, 69: 261~264
    [25] Costa dos Santos C, Lima MAS, Silveira ER, Micromolecular secondarymetabolites of Erythroxylum barbatum, Biochem Syst Ecol, 2003, 31: 661~664
    [26] Cook JT, Ollis WD, Sutherland IO et al, Pterocarpans from Dalbergia spruceana,Phytochemistry, 1978, 17: 1419~1422
    [27] Da Silva GL, de Abreu Matos FJ, Silveirat ER, 4'-Dehydroxycabenegrin A-Ifrom roots of Harpalyce brasiliana, Phytochemistry, 1997, 46: 1059~1062
    [28] Deshpande VH, Shastri RK, Phenolics of Albizzia lebbek, A. amara and A.Procera, Indian J Chem Sect B, 1977, 15: 201~204
    [29] Da Silva AJM, Coelho AL, Simas ABC et al, Synthesis and pharmacologicalevaluation of prenylated and benzylated pterocarpans against snake venom,BioorgMed Chem Lett, 2004, 14: 431~435
    [30] Dornbos DL Jr, Spencer GF, Miller RW, Medicarpin delays alfalfa seedgermination and seedling growth, Crop Sci, 1990, 30: 162~166
    [31] Fukai T, Nishizawa J, Yokoyama et al, 5 New isoprenoid-substituted flavonoids,kanzonols F-J, from Glycyrrhiza uralensis, Heterocycles, 1993, 36: 2565~2576
    [32] Fukai T, Cai BS, Maruno K et al, An isoprenylated flavanone from Glycyrrhizaglabra and rec-assay of licorice phenols, Phytochemistry, 1998, 49: 2005~2013
    [33] Fraishtat PD, Popravko SA, Wulfson NS, Isolation and identification ofpterocarpans from the roots of cultured species of clover, Bioorg Khim, 1981, 7:927~936
    [34] Goda Y, Katayama M, Ichikawa K et al, Inhibitors of prostaglandin biosynthesisfrom Dalbergia odorifera, Chem Pharm Bull, 1985, 33: 5606~5609
    [35] Ingham JL, Mulheirn LJ, Isoflavonoid phytoalexins from fungus-inoculatedleaves of Apios tuberosa, Phytochemistry, 1982, 21: 1409~1413
    [36] Ingham JL, Keen NT, Markham et al, Dolichins A and B, two pterocarpans frombacteriatreated leaves of Dolichos biflorus, Phytochemistry, 1981, 20: 807~809
    [37] Ingham JL, Markham KR, New dextrorotatory pterocarpan phytoalexins fromleaflets of Nissolia fruticosa, Z Naturforsch C, 1984, 39: 13~17
    [38] Ingham JL, Phytoalexin production by species of the genus Caragana, ZNaturforsch C, 1979, 34: 293~295
    [39] Ingham JL, Dewick PM, A new isoflavan phytoalexin from leaflets of Lotushispidus, Phytochemistry, 1979, 18: 1711~1714
    [40] Ingham JL, Tahara S, Isoneorautenol and other pterocarpan phytoalexins fromCalopogonium mucunoides, Z Naturforsch C, 1985, 40: 482~489
    [41] Iinuma M, Ohyama M, Tanaka T, Flavonoids in roots of Sophora prostrata,Phytochemistry, 1995, 38: 539~543
    [42] Ingham JL, Dewick PM, Sparticarpin: a pterocarpan phytoalexin from Spartiumjunceum, Z Naturforsch C, 1980, 35: 197~200
    [43] Ingham JL, Dewick, The structure of desmocarpin, a pterocarpan phytoalexinfrom Desmodium gangeticum, Z Naturforsch C, 1984, 39: 531~534
    [44] Jain AK, A new pterocarpan glycoside from Trifolium pratense, J Indian ChemSoc, 1988, 65: 69
    [45] Juck DBF, De Rezende LC, David JP et al, Two new isoflavonoids fromBowdichia virgilioides, Nat Prod Res, 2006, 20: 27~30
    [46] Khaomek P, Ruangrungsi N, Saifah E et al, A new pterocarpan from Erythrinafusca, Heterocycles, 2004, 63: 879~884
    [47] Kiuchi F, Chen X, Tsuda Y, Four new phenolic constituents from licorice (rootof Glycyrrhiza sp), Heterocycles, 1990, 31: 629~636
    [48] Kitagawa I, Chen WZ, Hori K et al, Five new flavonoid constituents from theroots of Glycyrrhiza aspera PALL, Chem Pharm Bull, 1998, 46: 1511~1517
    [49] Kurosawa K, Ollis WD, Sutherland IO et al, Mucronulatol, mucroquinone andmucronucarpan, isoflavonoids from Machaerium mucronulatum and M. VillosumPhytochemistry, 1978, 17: 1405~1411
    [50] Kinoshita T, Ichinose K, Takahashi C et al, The isolation of a new class ofisoflavonoid metabolites from Sophora tomentosa L, Chem Pharm Bull, 1986,34: 3067~3070
    [51] Lin YL, Kuo YH, 6a,12a-Dehydro-b-toxicarol and derricarpin, two newisoflavonoids from the roots of Derris oblonga Benth, Chem Pharm Bull, 1993,41: 1456~1458
    [52] Liu Y, Ma Xx, Chen HB et al, Chemical constituents of Hedysarum gmelinii, JChi Pha Sci, 2005, 14: 75~78
    [53] Li W, Koike K, Asada Y et al, Flavonoids from Glycyrrhiza pallidiflora hairyroot cultures, Phytochemistry, 2002, 60: 351~355
    [54] Li G, Wang J, Li X et al, Isolation and identification of pterocarpans andisoflavones from the pericarp of Sphaerophysa salsula DC, Zhongguo YaowuHuaxueZazhi, 2003, 13: 215~218
    [55] Lin LZ, He XG, Lindenmaier M et al, Liquid chromatography-electrosprayionization mass spectrometry study of the flavonoids of the roots of Astragalusmongholicus and A. Membranaceus, J Chromatogr A, 2000, 876: 87~95
    [56] Mitscher LA, Okwute SK, Gollapudi SR et al, Antimicrobial pterocarpans ofNigerian Erythrina mildbraedii, Phytochemistry, 1988, 27: 3449~3452
    [57] Mitscher LA, Gollapudi SR, Gerlach DC et al, Erycristin, a new antimicrobialpterocarpan from Erythrina crista-galli, Phytochemistry, 1988, 27: 381~385
    [58] Mitscher LA, Okwute SK, Gollapudi SR et al, The isolation and structuralcharacterization of two additional pterocarpan antimicrobial agents fromNigerian Erythrina mildbraedii, Heterocycles, 1988, 27: 2517~2522
    [59] Morimoto M, Insect antifeedants, pterocarpans and pterocarpol, in heartwood ofPterocarpus macrocarpus, Kruz. Biosci Biotech Biochem, 2006, 70: 1864~1868
    [60] Meragelman TL, Tucker KD, McCloud TG et al, Antifungal flavonoids fromHildegardia barteri, J Nat Prod, 2005, 68: 1790~1792
    [61] Matsuura N, Nakai R, Iinuma M et al, A prenylated flavanone from roots ofMaackia amurensis subsp. Buergeri, Phytochemistry, 1994, 36: 255~256
    [62] Miyase T, Ohtsubo A, Ueno A et al, Studies on the pterocarpans from Melilotusalba Desr, Chem Pharm Bull, 1982, 30: 1986~1991
    [63] Maximo P, Lourenco A, Feio SS et al, Flavonoids from Ulex airensis and Ulexeuropaeus ssp.europaeus, J Nat Prod, 2002, 65: 175~178
    [64] Matsuda H, Morikawa T, Xu FM et al, New isoflavones and pterocarpane withhepatoprotective activity from the stems of Erycibe expansa, Planta Med, 2004,70: 1201~1209
    [65] Manjary F, Petitjean, Conan JY et al, A prenylated pterocarpan from Munduleastriata, Phytochemistry, 1993, 33: 515~517
    [66] Maximo P, Lourenco A, A pterocarpan from Ulex parviflorus, Phytochemistry,1998, 48: 359~362
    [67] Militao GCG, Jimenez, Wilke DV et al, Antimitotic properties of pterocarpansisolated from Platymiscium floribundum on sea urchin eggs, Planta Med, 2005,71: 683~685
    [68] Militao GCG, Dantas INF, Pessoa C et al, Induction of apoptosis by pterocarpansfrom Platymiscium floribundum in HL-60 human leukemia cells, Life Sci, 2006,78: 2409~2417
    [69] Miyase T, Sano M, Yoshino K et al, Antioxidants from Lespedeza homoloba (II),Phytochemistry, 1999, 52: 311~319
    [70] Nakagawa M, Nakanishi K, Darko LL et al, Structures of cabenegrins A-I and A-II, potent antisnake venoms, Tetrahedron Lett, 1982, 23: 3855~3858
    [71] Nkengfack AE, Vouffo TW, Vardamides JC et al, Phenolic metabolites fromErythrina species, Phytochemistry, 1997, 46: 573~578
    [72] Nkengfack AE, Vardamides JC, Fomum ZT et al, Prenylated isoflavanone fromErythrina eriotricha, Phytochemistry, 1995, 40: 1803~1808
    [73] Pistelli L, Noccioli C, Appendino et al, Pterocarpans from Bituminaria morisianaand Bituminaria bituminosa, Phytochemistry, 2003, 64: 595~598
    [74] Purushothaman, Chandrasekharan, Balakrishna et al, Gangetinin and desmodin,two minor pterocarpanoids of Desmodium gangeticum, Phytochemistry, 1975, 14:1129~1130
    [75] Piccinelli AL, Fernandez MC, Cuesta-RubioO et al, Isoflavonoids isolated fromCuban propolis, J Agric Food Chem, 2005, 53: 9010~9016
    [76] Pueppke SG, VanEtten, Accumulation of pisatin and three additional antifungalpterocarpans in Fusarium solani infected epicotyls of Pisum sativum, PhysiolPlant Pathol, 1976, 8: 51~61
    [77] Palazzino G, Rasoanaivo P, Federici E et al, Prenylated isoflavonoids fromMillettia pervilleana, Phytochemistry, 2003, 63: 471~474
    [78] Park JA, Kim HJ, Jin C et al, A new pterocarpan, (-)-maackiain sulfate, from theroots of Sophora subprostrata, Arch Pharmacal Res, 2003, 26: 1009~1013
    [79] Pelter A, Amenechi PI, Isoflavonoid and pterocarpinoid extractives ofLonchocarpus laxiflorus, J Chem Soc C, 1969, 887~896
    [80] Rall GJH, Engelbrecht JP, Brink, Isolation, structure, and absolute configurationof (-)-2-hydroxypterocarpin, a new pterocarpan from Neorautanenia edulis,Tetrahedron, 1970, 26: 5007~5012
    [81] Robeson DJ, Ingham JL, New pterocarpan phytoalexins from Lathyrus nissolia,Phytochemistry, 1979, 18: 1715~1717
    [82] Rall GJH, Brink AJ, Engelbre JP, Isolation and structure of edulenol, A newpterocarpan from Neorautanenia edulis Casm, J S Afr Chem I, 1972, 25: 131
    [83] Ryu SY, Choi SU, Kim SK et al, In vitro antitumor activity of flavonoids fromSophora flavescens, Phytother Res, 1997, 11: 51~53
    [84] Song C, Zheng Z, Liu D et al, Pterocarpans and isoflavans from Astragalusmembranaceus bunge, Zhiwu Xuebao, 1997, 39: 1169~1171
    [85] Shaker KH, Dockendorff K, Bernhardt M et al, A new triterpenoid saponin fromOnonis spinosa and two new flavonoid glycosides from Ononis vaginalis, ZNaturforsch B, Chem Sci, 2004, 59: 124~128
    [86] Subarnas A, Oshima Y, Hikino H, Isoflavans and a pterocarpan from Astragalusmongholicus, Phytochemistry, 1991, 30: 2777~2780
    [87] Selvam C, Jachak SM, Oli RG et al, A new cyclooxygenase (COX) inhibitorypterocarpan from Indigofera aspalathoides, structure elucidation and determinati-on of binding orientations in the active sites of the enzyme by moleculardocking, Tetrahedron Lett, 2004, 45: 4311~4314
    [88] Silva VNT, Mara de Oliveira F, Conserva Lu, Phenolic derivatives and terpenesfrom Acosmium bijugum, Biochem Syst Ecol, 2001, 29: 1189~1192
    [89] Sakurai Y, Sakurai N, Taniguchi M et al, Rautandiols A and B, pterocarpans andcytotoxic constituents from Neorautanenia mitis, J Nat Prod, 2006, 69: 397~399
    [90] Tarus PK, Machocho AK, Chhabra SC, Flavonoids from Tephrosia aequilata,Phytochemistry, 2002, 60: 375~379
    [91] Tanaka H, Tanaka T, Etoh H, Three pterocarpans from Erythrina crista-galli,Phytochemistry, 1997, 45: 835~838
    [92] Tanaka H, Etoh H, Watanabe N et al, Erysubins C-F, four isoflavonoids fromErythrina suberosa var, Glabrescences. Phytochemistry, 2001, 56: 769~773
    [93] Tanaka H, Tanaka T, Etoh H, Two pterocarpans from Erythrina orientalis,Phytochemistry, 1997, 47: 475~477
    [94] Tanaka H, Tanaka T, Hosoya A et al, An isoflavan from Erythrina x bidwillii,Phytochemistry, 1998, 47: 1397~1400
    [95] Tanaka T, Ohyama M, Kawasaka Y, Tetrapterols A and B: novel flavonoidcompounds from Sophora tetraptera, Tetrahedron Lett, 1994, 35: 9043~9044
    [96] Ueno A, Ichikawa M, Fukushima S et al, Constituents of Lespedeza homoloba,Structures of lespein and lespedezin, Chem Pharm Bull, 1973, 21: 2715~2721
    [97] Van Heerden FR, Brandt EV, Roux DG, Structure and synthesis of somecomplex pyranoisoflavonoids from the bark of Dalbergia nitidula Welw. ex Bak,J Chem Soc Perkin Trans 1, 1978, 137~145
    [98] Wanjala CCW, Juma BF, Bojase et al, Erythrinaline alkaloids and antimicrobialflavonoids from Erythrina latissima, Planta Med, 2002, 68: 640~642
    [99] Yahara S, Emura S, Feng H et al, Studies on the constituents of the bark ofDalbergia hupeana, Chem Pharm Bull, 1989, 37: 2136~2138
    [100] Yenesew A, Midiwo JO, Guchu SM et al, Three isoflav-3-enes and a 2-arylbenzofuran from the root bark of Erythrina burttii, Phytochemistry, 2002, 59:337~341
    [101] Yamamoto H, Ichimura M, Tanaka T et al, A trifolirhizin malonate fromSophora flavescens var. angustifolia and its stability, Phytochemistry, 1991, 30:1732~1733
    [102] Kessmann H, Edwards R, Geno PW, Stress responses in alfalfa (Medicagosativa L.).V. Constitutive and elicitor-induced accumulation of isoflavonoidconjugates in cell suspension cultures, Plant Physiol, 1990, 94: 227~232
    [103] Maria JC F,Yvone BM, Pouliquem et al, Cytotoxic Flavonoids fromPlatymiscium floribundum, J Nat Prod, 2005, 68: 423~426
    [104]李伟东,阚毓铭,洪敏等,后莫紫檀素、美迪紫檀素对人肝癌细胞抑制作用的研究,沈阳药科大学学报,2001,18(3):211~212
    [105]阚毓铭,朱荃,陈龙等,从刺果甘草中分离出的后莫紫檀素对Hep-2细胞的作用,中国药学杂志,1994,29(10):608~609
    [106] Nashira CV, Laila SE, Jaime MS et al, Trypanocidal activity of a newpterocarpan and other secondary metabolites of plants from Northeastern Brazilflora, Bioorganic Medicinal Chemistry, 2008, 16: 1676~1682
    [107] Morimoto M, Fukumto H, Hiratani M et al, Insect antifeedants, pterocarpansand pterocarpol, in heartwood of Pterocarpus macrocarpus Kruz, Biosci BiotechBiochem, 2006, 70: 1864~1868
    [108] Gardenia CGM, Daniel PB, Claudia P et al, Comparative cytotoxicity of 2,3,9-trimethoxypterocarpan in leukemia cell lines (HL-60, Jurkat, Molt-4, and K562)and human peripheral blood mononuclear cells, J Nat Med, 2007, 61: 196~199
    [109] Thitima Rukachaisirikul, Phongsak Innok, Nuntana A et al, AntibacterialPterocarpans from Erythrina subumbrans, Journal of Ethnopharmacology, 2007,110: 171~175
    [110] Tamara L. Meragelman, Kenneth D, Thomas G et al, Antifungal Flavonoidsfrom Hildegardia barteri, J Nat Prod, 2005, 68: 1790~1792
    [111] Chaudhuri SK et al, Isolation and structure identification of an active DNAstrand scission agent, 3,4-dihydroxy-8,9-methylenedioxypterocarpan, J Nat Prod,1995, 58: 1966~1969
    [112]王玉兰,陈未名,李广义,藏药鬼箭锦鸡儿的化学成分,中草药,1986,17(8):8~10
    [113]郑敏燕,鬼箭锦鸡儿化学成分的研究:[硕士学位论文],西北师范大学,2001
    [114]杨敬芝,李建北,张万隆等,鬼箭锦鸡儿化学成分的研究,中草药,2003,34(5):405~406
    [115]郝英魁,藏药鬼箭锦鸡儿化学成分的研究:[硕士学位论文],天津大学,2007
    [116]房士明,藏药昌都锦鸡儿化学成分的研究: [硕士学位论文],天津大学,2007
    [117]邓雁如,江艳烽,席婵娟等,( 6aR,11aR)-3-羟基-4 ,9-二甲氧基紫檀烷分子的晶体结构,化学物理学报,2004,17(4):454~458
    [118]赵玉英,王斌,郭敏杰等,苦参黄酮类成分的研究,植物学报,1993,35(4):304~306
    [119]李丹,左海军,高慧媛等,苦参的化学成分,沈阳药科大学学报,2004,21(5):346~348
    [120] Chihiro Ito, Masataka Itoigawa, Tetsufumi Kanematsu et al, Isoflavonoids fromDalbergia olivari, Phytochemistry, 2003, 64: 1265~1268
    [121] Alain K, Waffo, Guy AA et al, Indicanines B and C, two isoflavonoidderivatives from the root bark of Erythrina indica, Phytochemistry, 2000, 53:981~985

© 2004-2018 中国地质图书馆版权所有 京ICP备05064691号 京公网安备11010802017129号

地址:北京市海淀区学院路29号 邮编:100083

电话:办公室:(+86 10)66554848;文献借阅、咨询服务、科技查新:66554700