急尖绣线菊中一微量新二萜生物碱

从蔷薇科绣线菊属植物急尖绣线菊（Ｓｐｉｒａｅａ ｊａｐｏｎｉｃａ ｖａｒ．ａｃｕｔａ Ｙｕ）的根部分离得到６个二萜生物碱,经光谱分析,其中５个来ｓｐｉｒａｍｉｎｅｓ Ａ（１）,Ｂ（２）,Ｐ（３）和Ｕ（４）及ｓｐｉｒａｄｉｎｅ Ｆ（５）,另一微量成分被鉴定为一新的二萜生物碱,命名为ｓｐｉｒａｍｉｎｅ Ｗ（６）。     

绣线菊碱H,I及O的化学结构

绣线菊碱Ｈ,Ｉ,Ｏ为Ａｔｉｓｉｎｅ型的新二匝生物碱,从毛萼绣线菊根中分离得到。本文根据波谱解析及化学转换,分别测定了它们的化学结构。     

粉花绣线菊复合群的化学分类研究

以粉花绣线菊复合群中二萜及二萜生物碱的结构特征,仿生合成及化学的相关性为基础,结合地理分布以及细胞学和形态学方面的研究资料,讨论粉花经菊复合群的化学分类,（１）具缩醛和二萜可能是绣线菊二萜生物碱的生源合成前体,（２）粉花绣线菊复合群是绣线菊属中特殊的,相对独立的类群;（３）我国西南尤其是横断山区是该复合群近代分化中心,有要能是起源中心;（４）对某些变种进行归并。     

中国北部绣线菊属的花粉形态及分类学意义

本文用光学显微镜和扫描电镜观察了中国北部绣线菊属ＳｐｉｒａｅａＬ．２１种及６个变种的花粉形态,描述了外壁纹饰的形态特征,指出了外壁纹饰特征在分类上的意义。绣线菊属的花粉为球形至长球形,外壁纹饰为条网状至条纹状。外壁纹饰类型不具有属内分组意义,但对一些种类具有一定的分类价值。花粉形态支持将曲枣绣线菊Ｓ．ｆｌｅｘｕｏｓａＦｉｓｃｈ。并入石蚕叶绣线菊Ｓ．ｃｈａｍｏｅｄｒｙｆｏｌｉａＬ．的观点［Ｍａｘｉｍｏｗｉｃｚ,Ｃ．Ｊ．（１８７９）、Ｒｅｈｄｅｒ,Ａｉ．（１９４０）］,不同意将蒙古绣线菊毛枝变种Ｓ．ｍｏｎｇｏｌｉｃａＭａｘｉｍ．ｖａｒ．ｔｏｍｅｎｔｕｌｏｓａＹｕ提升为贺兰山绣线菊Ｓ．ｔｏｍｅｎｔｕｌｏｓａ（Ｙｕ）Ｙ．Ｚ．Ｚｈａｏ［赵一之（１９８７）］。     

关于蒙古绣线菊毛枝变种及回折绣线菊的学名订正

支持将蒙古绣线菊毛反变是升为种的等级且于宁夏绣线菊同种,但其合法学名应为Ｓｐｉｒａｅａ ｔｏｍｅｎｔｕｌｏｓａ（Ｙｕ）Ｙ．Ｚ．Ｚｈａｏ。与此同时,本发现了真正的蒙古绣线菊的毛枝变种－－Ｓ．ｍｏｎｇｏｌｉｃａ Ｍａｘｉｍ．ｖａｒ．ｐｕｂｅｓｃｅｎｓ Ｙ．Ｚ．Ｚｈａｏ ｅｔ Ｔ．Ｊ．Ｗａｎｇ．     

急尖绣线菊的二萜生物碱成分

从急尖绣线菊根中分离鉴定了８个生物碱成分,其中６个为已知的绣线菊碱Ａ,Ｂ,Ｃ,Ｄ,Ｐ和Ｑ,另２个为新成分绣菊碱Ｔ和Ｕ,经波谱解析和比较和化学比较方法测定了各自的化学结构。     

狭叶绣线菊中的新二萜生物碱(快报)

我们从民间草药狭叶绣菊Spiraea japonica var. acuminata 中分离到15个新二萜生物碱及一新二萜成分,曾报道了其中绣线菊新碱A,B,C,D(spiramine A,B,C,D)的化学结构,现报道绣线菊新碱E,F,G,H,I (spiramine E,F,G,H,I)的化学结构。     

华北绣线菊二萜生物碱抗血小板聚集活性研究

采用Born氏比浊法观察华北绣线菊小叶变种中分离得到的总碱和 9个hetisine型C2 0 二萜生物碱及其衍生物体外对血小板活化因子 (PAF)、花生四烯酸 (AA)和二磷酸腺苷 (ADP)三种诱导剂引起的血小板聚集活性的影响 ,并初步探讨了构效关系。结果表明 ,华北绣线菊小叶变种中总碱对PAF和ADP诱导的血小板聚集均有明显的抑制作用 ;9个hetisine型C2 0 二萜生物碱中 ,有 8个显著抑制PAF诱导的血小板聚集 ,其活性与分子结构明显相关 ;此外 ,hetisine型生物碱及其衍生物对ADP诱导的血小板聚集亦有一定的抑制作用 ,但总碱及生物碱对AA诱导的聚集影响不明显。提示hetisine型C2 0 二萜生物碱具有抗血小板聚集活性。     

星花绣线菊的组织培养及快速繁殖

1　植物名称　星花绣线菊 (Ｓｐｉｒａｅａｊａｐｏｎｉｃａｖａｒ.ｓｔｅｌｌｅｒｉｓ)。2　材料类别　茎尖、茎段、叶片、叶柄。3　培养条件　 ( 1 )愈伤组织诱导培养基 :ＭＳ 2 ,4 Ｄ 2 .0ｍｇ·Ｌ- 1 (单位下同 ) ＫＴ 0 .3;( 2 )愈伤组织继代培养基 :6,7 Ｖ 2 ,4 Ｄ 2 .0 ＫＴ 0 .2 5 ＮＡＡ 1 .0 ＬＨ 2 0 0 0 ;( 3)芽诱导培养基 :ＭＳ 6 ＢＡ 2 .0 ＮＡＡ 0 .1 ;( 4 )芽增殖培养基 :ＭＳ 6 ＢＡ0 .2 5 ＮＡＡ 0 .1 ;( 5 )生根培养基 :1 /2ＭＳ 6 ＢＡ0 .2 5 ＮＡＡ 0 .5。上述培养基的蔗糖含量为 3% ,琼脂为 0 .7% ,…     

南川绣线菊和细枝绣线菊分子水平研究

对6个野外居群(南川绣线菊和细枝绣线各3个)36个个体进行叶绿体(chloroplast,cp)DNA trnL-trnF片断测序分析.在南川绣线菊中发现了3个单倍型(Ros1-Ros3),在细枝绣线菊中发现了2个单倍型(Myr1-Myr2).两个种的序列联合分析对位排列后得到850 bp,共有9个变异位点,其中一个为碱基插入或缺失,另外8个为碱基置换,变异位点的百分率为0.11.对单倍型的遗传多样性分析表明同一区域亲缘关系相近的单倍型发生于同一居群中,并且存在着明显的分子系统地理学关系.以蔷薇科另两个外属植物Rosa californica 和 Sorbaria sorbifolia为外类群构建这两个种的最大简约(MP)树、最大似然(ML)树及贝叶斯树,结果获得了分辨良好的种间关系树.这表明在分子水平上两个种之间存在明显的差异,这与形态学上的表现是相一致的.遗传多样性分析结果表明了cpDNA trnL-trnF 片段对于绣线菊属的分子地理学研究还是比较有效的,可以通过进一步的大面积采样和分析来揭示植物的遗传结构、冰期避难所等问题.     

The Diterpenoid Alkaloids of Aconitum nagarurn var. lasiandrurn W. T. Wang and Its Chemotaxonomic Significance

From the roots of Aconitum nagarum var. lasiandrum W. T. Wang, seven diterpe- noid alkaloids were isolated and determined as follows: denudatine of atisine-type (7), songorine and songoramine of veatchine-type (1 and 12), virescenine of lycoctonine-type (13), neoline, 14-acetylneoline and fiavaconitine of aconitine-type (2, 3 and 8). A. nagarum var. lasiandrum W. T. Wang is a typical species of Ser. Bullatifolia which contained four types diterpenoid alkaloids. On the basis of distribution of diterpenoid alkaloids, phytogenesis add morphological evolution of Chinese species of genus Aconitum, probably Chinese species of genus Aconitum modernly advanced and divided from this serics.     

A Study on the Alkaloidal Components from Delphinium gyalanura Marq. et Shaw

From the roots of Delphinium gyalanum Marq. et Shaw native to China, a pair of new regioisomeric diterpenoid alkaloids as a mixture, named gyalanine A and B, was isolated whose structures were shown to be 4 and 5, respectively, on the basis of spectral data. The known diterpenoid alkaloids, delsemine A(1) and B(2), methyllycaconitine (3) and lycoctonine, were also obtained.     

Diterpenoid production in hairy root culture of Salvia sclarea L

Growth and diterpenoid accumulation (salvipisone, ferruginol, aethiopinone and 1-oxoaethiopinone) during the growth cycle of a Salvia sclarea hairy root culture are described. The roots transformed by Agrobacterium rhizogenes (LBA 9402) were cultured in half-strength B5 liquid medium supplemented with 30 g L(-1) sucrose under light (16 h/8 h light/dark). A culture period of 30 days was optimal for both biomass and diterpenoid production. The total content of four diterpenoids in the hairy roots [(27.3 +/- 0.6) mg g(-1) dry weight] was higher than that of roots of field-grown S. sclarea plants [(3.15 +/- 0.15) mg g(-1) dry weight]. In transformed roots, aethiopinone was the main diterpenoid, whereas the principal diterpenoid of natural roots was salvipisone.     

The Chemotaxonomy of Chinese Species of the Genus Aconitum L. (Ranunculaceae)

On the basis of biosynthsis, distribution of diterpenoid alkaloids as well as morphological evolution of Chinese species L. (Ranunculaceae), chemotaxonomy of the genus Aconitum is discussed: 1, Subgen. Lycoctonum, containing lycoctonine-type alkaloids and Subgen. Aconitum containing aconitine-type alkaloids, were probably differetiated at the early stage of evolution of the genus Aconitum and evolved respectively in their own ways. 2, In Subgen. Aconitum: (1) Ser. Bullatifolia, containing mainly atisine-, veatchine-type alkaloids, and amino, alcohol and ester base of aconitine-type, and distributed in Hengduan Mountain and Jingsha River valley, where is the centre of modern differentiation of species of Aconitum, is probably a series from which Chinese species of the genus Aconitum were derived; (2) Ser. Inflata, containing mainly aconitine, mesaconitine and bypaconitine, is an advanced group; (3) Ser. Grsndituberosa, containing mainly aconitine and songorine, is related to Ser. Bulatifolia; (4) Ser. stylosa and Ser. volubilia, containing mainly yunaconitine and other anisyl ester alkaloids form another advanced branch. 3, Ser. Tangutica and A. naviculare of Ser. Rotaundifolia, containing atisine and lactone-type alkaloids may be a specialized group in high mountains and have occurred at early stage of evolution of the genus Aconitum. 4, Subgen. Gymnaconitum, containing atisine-type alkaloids and amino alcohol of aconitine type, may als be a specialized group in high mountains. 5, A. franchetii Finet. et Gagnep. mainly containing ester bases of aconitine-typeand closed to A. chasmanthum Stapf, is best placed into Ser. Ambigua.     

大理翠雀碱甲的化学结构

从大理翠雀Delphynium taliense Franch根中分得五个二萜生物碱,其中四个已有报告,分别鉴定为methyllycaconitine,delsemine、大理翠雀碱乙(talitine B)、大理翠雀碱丙(talitine C)。本文主要通过质谱、红外光谱、核磁共振氢谱及其碳谱对大理翠雀碱甲的化学结构所进行的推导。     

Five New C19‐Diterpenoid Alkaloids from Delphinium tianshanicum W.T.Wang

Five new diterpenoid alkaloids, tianshanitines A‐E ( 1  –  5 ), along with ten known compounds ( 6  –  15 ), were isolated from the EtOH extracts of the whole plant of Delphinium tianshanicum W.T.Wang . Their structures were determined based on extensive spectroscopic analyses, including 1D‐ and 2D‐NMR, HR‐ESI‐MS, and the structure of tianshanitine C ( 3 ) was confirmed by X‐ray diffraction analysis. Tianshanitine A ( 1 ) is the first example of natural diterpenoid alkaloid containing a benzoyl group at C(1) position. Tianshanitine B ( 2 ) is a rare natural diterpenoid alkaloid bearing a OH group at C(16) position. Compounds 1  –  5 , 6 , 8 , 10 , 12 and 14 were evaluated for cytotoxicity against HCT116, MCF‐7 and HepG2 human cancer cell lines.     

Spiramine derivatives induce apoptosis of Bax−/−/Bak−/− cell and cancer cells

Spiramine C–D, the atisine-type diterpenoid alkaloids isolated from the Chinese herbal medicine Spiraea japonica complex, are shown to have anti-inflammatory effects in vitro. In this study, we report that spiramine derivatives of spiramine C–D bearing α,β-unsaturated ketone induce apoptosis of Bax^−/−/Bak^−/− MEFs cell, which is positively corresponding their cytotoxicity of tumor cell lines including multidrug resistance MCF-7/ADR. The results indicated that oxazolidine ring is necessary, and derivatives bearing double ‘Michael reaction acceptor’ group would significantly increased activities both of inducing apoptosis of Bax^−/−/Bak^−/− cells and cytotoxicity of tumor cells. The result indicated that spiramine derivative with α,β-unsaturated ketone group is a new anti-cancer agent with a capability of inducing apoptosis of cancer cells in Bax/Bak-independent manner.     

Diterpenoids from Neoboutonia glabrescens (Euphorbiaceae)

Glabrescin, a daphnane diterpenoid, neoboutonin, a degraded diterpenoid with a novel skeleton, and neoglabrescins A and B, two rhamnofolane derivatives, have been isolated from the stem bark of Neoboutonia glabrescens Prain (Euphorbiaceae), together with the known tigliane derivative, baliospermin, and the known daphnane, montanin. Other constituents include squalene, 3-acetylaleuritolic acid, oleanolic acid and sitosterol, and the phenolic compounds 9-methoxy-1,7-dimethylphenanthrene and 2,3,8-tri-O-methylellagic acid. The structures were assigned on the basis of spectral studies and comparison with published literature data. The structures of neoglabrescins A and B were derived for their acetylated derivatives and, in the case of neoglabrescin A, confirmed by X-ray crystallographic analysis.