毛喉鞘蕊花的微量成分

从唇形科毛喉鞘蕊花全草的氯仿提取物分离到２个新的微量成分,鞘蕊花戊素和已素。基于光谱分析,鞘蕊花戊素和已 素的化学结构分别鉴定为１α,７β－二乙酰氧基－８,１３－环氧－６β羟基勒丹－１４烯－１１－酮（１）和７β－乙酰氧基－８,１３环氧－６β,α－二羟基勒丹－１４烯－１１－酮（２）。     

毛萼鞘蕊花甲素的结构

从毛萼鞘蕊花(Coleus esquirolii(L(?)vl. )Dunn.)的茎、叶中分离鉴定了一个新的二萜化合物,毛萼鞘蕊花甲素(对映-17-乙酰氧基-贝壳杉烷-16β-醇),和三个已知化合物,对映-贝壳杉烷-16p,17-二醇,齐墩果酸和β-谷甾醇。     

黄鞘蕊花中两个新的醌式二萜

从黄鞘蕊花中得到２个新的醌式二萜（二聚体）,黄鞘蕊花乙素,黄鞘蕊花丙素和２个已知化合物蒲公英萜醇,齐墩果酸。     

黄鞘蕊花的化学成分

从黄鞘蕊花(Coleus xanthanthus C. Y. Wuet Y. C. Huang)中分得8种成分。其中1个是新的醌式二萜,命名为黄鞘蕊花甲素,其结构为17-methyl(15→16)abieo-16-methoxy-2α-acetoxy-coleon U.7个已知化合物。coleon U(2),sugiol(3),β—谷甾醇,胡萝卜甙,三十三烷醇,三十三烷和二十八烷酸。     

毛喉鞘蕊花化学及生理活性研究进展

本文简要综述了唇形科鞘蕊花属植物毛喉鞘蕊花(Coleus forskohlii(wild．)Briq．)化学及药理研究进展,尤其是二萜成分的研究状况。     

我国毛喉鞘蕊花的发掘与研究进展

本文介绍了哮喘病新药毛喉鞘蕊花的发掘过程,栽培条件下的形态特征和化学成分与印度毛喉鞘蕊花的区别,结果显示,二者并非同种植物,特将云南种定名为小江鞘蕊花。     

狗小肠鞘氨醇糖脂中长链碱组成的研究

 利用气相色谱、气相色谱-质谱联用等方法测定了狗小肠鞘氨醇糖脂中的长链碱组成。其主要的长链碱为鞘氨醇(Sphingosine)、异鞘氨醇(isosphingosine)、二氢鞘氨醇(Sphinganine)和植物鞘氨酸(Phyto-sphingosine)。一共分离出十三个鞘氨醇糖脂。在唯一的五糖基神经酰胺中异鞘氨醇是主要成份。在一个一糖基神经酰胺中植物鞘氨醇是主要成份。植植物鞘氨酸也是两个二糖基神经酰胺和一个三糖基神酰胺的主要长链碱。说明它不仅存于植物体内。     

毛喉鞘蕊花的化学成分研究

本文报导了,从产于滇东北的毛喉鞘蕊花(Coleus forskohlii Brig)的根茎中分离到四个二萜化合物,经光谱分析鉴定,其结构分别为1α,6β,7α-triacetyl-coleonol—B(1),I-acetyl—forskolin(2),coleonol-B(3),和deacetyl-forskolin(4)。化合物(1)和(2)是首次从该植物中分离到。     

鞘脂与细胞凋亡

随着生物技术的不断发展,近年来对鞘脂类物质的研究不断深入。鞘脂质除了在细胞骨架的迁移、血管发生、胚胎发育和信号转导等方面起重要作用外,最近的研究发现鞘脂及其代谢物(神经酰胺、鞘氨醇、鞘氨醇-1-磷酸)能诱导多种肿瘤和恶性增殖细胞(如腺癌、结肠癌、肝肿瘤、肺癌、鼻咽癌等)的凋亡。本文着重对鞘脂与细胞凋亡相关的最新研究进展进行综述。     

鞘磷脂代谢与脑缺血

鞘磷脂特别是鞘脂是髓鞘的主要成分,高度集中在中枢神经系统。在生理和病理生理条件下,具有生物活性的鞘磷脂及其代谢产物以及信号传导过程的重要性正在逐步被人们所认识。鞘脂代谢产物鞘氨醇及其前体物质神经酰胺与细胞生长停滞和凋亡有关,而1-磷酸鞘氨醇与增强细胞增殖、分化和细胞生存以及调节细胞的生理和病理过程有关,具有细胞外第一信使和细胞内第二信使的双重功能。这三者之间的相互转换、鞘脂代谢物的相对水平以及细胞的命运,受到鞘氨醇激酶的活性的强烈影响。鞘氨醇激酶可催化磷酸鞘氨醇产生1-磷酸鞘氨醇。1-磷酸鞘氨醇在中枢神经系统中与G蛋白偶联受体家族结合对中枢神经系统发挥作用。本文对鞘磷脂代谢过程中的鞘氨醇激酶、1-磷酸鞘氨醇及其受体与脑缺血之间的关系进行概述。     

Effect of abietane diterpenes from Plectranthus grandidentatus on T- and B-lymphocyte proliferation

Five known abietane diterpenes of the royleanone and coleon type, namely, fatty acid esters of 7alpha-acyloxy-6beta-hydroxyroyleanone (1), grandidone A (2), 7alpha-acetoxy-6beta-hydroxyroyleanone (3), 6beta,7alpha-dihydroxyroyleanone (4) and coleon U (5), isolated from Plectranthus grandidentatus, were evaluated for their effect on the proliferation of human lymphocytes induced by the mitogen PHA. All except 4, showed a dose-dependent suppressor effect, with 3 yielding the most potent antiproliferative activity, followed by 5. These two compounds, that represent diterpenes of the royleanone and coleon type respectively, were also shown to be potent inhibitors of mouse splenocyte proliferation induced by ConA or LPS mitogens. However, the sensitivity of ConA-stimulated splenocytes to their suppressive effect was higher, suggesting a preferential inhibition of T-lymphocyte proliferation. The antiproliferative activity of 3 seemed to be exerted without affecting the expression of the lymphocyte activation marker CD69. On the contrary, 5 was shown to reduce the expression of CD69 of TCD8(+) and B-cells, suggesting a relationship between its antiproliferative effect and the expression of this early marker of activation on these cell populations. The capacity of 5 to induce apoptosis on ConA-stimulated splenocytes could also be related with its antiproliferative activity.     

Insect-antifeedant and antibacterial activity of diterpenoids from species of Plectranthus

Bio-assay guided fractionation of an acetone extract of leaf material from Plectranthus saccatus Benth. resulted in the isolation of a beyerane diterpenoid. This compound, characterised by spectroscopic methods as ent-3beta-(3-methyl-2-butenoyl)oxy-15-beyeren-19-oic acid, showed insect antifeedant activity against Spodoptera littoralis. Known quinonoid abietane diterpenoids obtained from new sources included a mixture of the (4R,19R) and (4R,19S) diastereoisomers of coleon A from P. aff. puberulentus J.K. Morton, coleon A lactone from P. puberulentus J.K. Morton, and coleon U and coleon U quinone from P. forsteri 'Marginatus' Benth. These compounds, and the crude acetone extracts from the leaf surfaces of 11 species of Plectranthus, were tested for antifeedant activity against S. littoralis, antibacterial activity against Bacillus subtilis and Pseudomonas syringae and antifungal activity against Cladosporium herbarum. The coleon A mixture showed potent antifeedant activity against S. littoralis, whereas coleon U showed the greatest antimicrobial activity.     

New Isoflavonoid Glycosides from the Rhizomes of Iris leptophylla Lingelsh.

Two new isoflavonoid glucosides, 5-hydroxy-6,7-methylenedioxy-isoflavone-4＇-O-D-glucopyranosyl （2→〉l）-L-rhamnoside （irilone-bioside） （compound 1） and 5,4＇-methoxy-6,7-methylenedioxyisoflavone-3＇-O-β-D-glucoside （irisleptophyllidin） （compound 2）, together with five known compounds, nigricanin- 4＇-O-β-D-glucoside （compound 3）, irifloside （compound 4）, irigenin （compound 5）, 5, 3＇, 4＇-trimethoxy-6,7-methylenedioxyisoflavone （compound 6）, and nigricanin （compound 7） were isolated from the alcoholic extract of rhizomes of Iris leptophylla Lingelsh. Their structures were elucidated by spectroscopic methods.     

二色补血草地上部分的化学成分

二色补血草﹝Limonium bicolor ( Bunge) Kuntze﹞为补血草属( Limonium Mill.)越年生草本植物,耐盐碱和抗逆性强,全草均可入药,具有补血止血、调经益气、抗菌消炎和温中健脾的作用[1],含有黄酮、多糖、挥发油和甾体等成分[2-7],其中,黄酮类成分具有较强的抗氧化能力,多糖对Hela细胞有明显抑制作用[8-11]。前人对二色补血草化学成分和药理活性已有一定研究,但对其地上部分的化学成分尚缺乏系统分析。为此,作者对二色补血草地上部分乙醇提取物进行了分离和鉴定,为该种的进一步开发利用和药理药效研究提供基础实验数据。     

Abietanes from Plectranthus grandidentatus and P. hereroensis against methicillin- and vancomycin-resistant bacteria

The antimicrobial activity of 10 natural abietanes isolated from Plectranthus grandidentatus and P. hereroensis acetonic extract was evaluated against methicillin-resistant Staphylococcus aureus (MRSA) and vancomycin-resistant Enterococcus faecalis (VRE). The results revealed that the most active diterpenes were coleon U (1), 7alpha-acetoxy-6beta-hydroxyroyleanone (2) and horminone (3). Minimum inhibitory concentration (MIC) values ranging 0.98-15.63 microg/ml were obtained for MRSA clinical strains, and MIC values of 15.63 and 31.25 microg/ml were obtained for VRE clinical strains. Some structure-activity relationships are emphasized.     

华麻花头根中的蜕皮甾酮类成分

从华麻花头(Serratula chinensis S．Moore)根中分得7种蜕皮甾酮类化合物,经光谱分析和化学方法,分别鉴定为：20-羟基蜕皮松(1),podecdysone C(2),3-氧-乙酰基-20-羟基蜕皮松(3),20-羟基蜕皮松-20,22．-缩丁醛(4),shidasterone(5),atrotosterone C(6)和carthamosterone(7),其中20-羟基蜕皮松-20,22．缩丁醛为一新的化合物。     

Studies on the Chemical Constituents of the Leaves of WTBX]Pseudotaxus chienii (Cheng) Cheng

Fourteen compounds were isolated from the leaves of Pseudotaxus chienii (Cheng) Cheng which is uniquely indigenous to China, and their structures were identified mainly by spectrum analyses. Among them, 13 known compounds were determined as: 2-guaiacylpropane-1, 3-diol (1), vanillic acid (2), 3-methoxy-4-hydroxy cinnamic acid (3). 3. 5-dimethoxy-phenol (4), taxicatin (5), 5-oxymaltol (6), quercetin-3-rhamnoside (7), (±)-catechin (8), ecdysterone (9), β-sitosterol (10), D-glucose (11), (±)-10-nonacosanol (12) and octacosanoic acid (13). All these compounds butβ-sitosterol were isolated from this plant for the first time. Compounds 1 and 6 have never been reported in plant kingdom. Another compound was tentatively established as a new compound, named pseudotaxlactone (14).     

Chemical Constituents from Roots of Jatropha curcas

Thirteen compounds were isolated from the roots of datropha curcas L. Combining the determination of physico-chemical constants and spectral analyses (IR, 1H-NMR, 13C-NMR, EIMS, FABMS), the structures of the compounds were identified as 5α-stigmastane-3, 6-dione (1), nobiletin (2), β-sitosterol (3), taraxerol (4), 2S-tetracosanoic acid glyceride-1(5),5-hydroxy-6,7-dimethoxycoumarin (6), jatropholone A (7), jatropholone B (8), 6-methoxy-7-hydroxycoumarin (9), caniojane (10), 3-hydroxy-4-methoxybenzaldehyde (11), 3-methoxy-4-hydroxybenzoic acid (12) and daucosterol (13). Among them, compound 5 is a new compound which has never been reported in China and abroad, compound 1, 2, 9, 10, 11, 12 were first time isolated from the plant, 7 and 8 are a pair of stereoisomers which can be inverted in dilute basic solution. 10 is a diterpenoid containing peroxide bridge.     

鞭打绣球中的一个新单萜苷

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.     

一株地衣内生真菌Daldinia childiae的化学成分

本研究对分离自星点梅衣属地衣Punctelia sp.的一株内生真菌蔡氏轮层炭壳菌Daldinia childiae进行大米固体发酵培养,乙酸乙酯萃取发酵产物,采用硅胶柱色谱法、重结晶等方法分离纯化次生代谢产物,结合核磁共振波谱与质谱技术对单体化合物进行结构解析,运用DPPH法测定化合物的自由基清除能力。结果分离得到8个化合物,分别鉴定为4-hydroxy-benzeneethanol（1）、4-methoxy-5-car- bomethoxy-6-pentyl-2H-pyran-2-one（2）、1-(2,6-dihydroxyphenyl)butan-1-one（3）、8-methoxy-1-naphthol（4）、1,8-dimethoxynaphthalene（5）、methyl 2-undecenoate-3-undecanoate-cyclohexyl-1,4-dienyl ester（6）、uracil（7）和acetic acid（8）,化合物1、6和8均首次从轮层炭壳菌属Daldinia中分离得到;化合物4在浓度为3mg/mL时具有较强的自由基清除活性,化合物3和5具有轻微的自由基清除能力。本研究为进一步挖掘轮层炭壳菌属的代谢产物奠定基础。