54 resultados para Arquitectura moderna - s.19-20
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八月瓜属植物五枫藤(Holboellia latifolia Wall.)和驳骨草属植物小驳骨(Gendarussa vulgaris Nees)均为药用植物, 前者化学成分研究不深入, 后者的化学成分未见报道。川西茶藨(Ribes takare D. Don)为茶藨子属植物, 没有化学成分的报道。本论文对三个植物的化学成分和活性成分进行了研究, 主要通过色谱方法分离得到了48 个化合物, 采用波谱分析或与已知标准品对照等手段鉴定了它们的结构, 其中有1 个新的原小檗碱类化合物和3 个新的联苯类化合物,发现了具有细胞毒活性和α-葡萄糖苷酶抑制活性的化合物。1、从五枫藤地上部分的95%乙醇提取物中分离得到了12 个化合物: 五加苷K (1)、hederagenin 3-O- α-L-rhamnopyranosyl-(1→2)- α-L-arabinopyranoside (2)、β-萘乙酸(3) 、3-O-α-L-rhamnopyranosyl-(1→2)-[β-D-glucopyranosyl-(1→3)]-α-L-arabinopyranosyl oleanolic acid 28-O-α-L-rhamnopyranosyl-(1→4)-β-D-glucopyranosyl-(1→6)-β-D-glucopyranosyl ester (4) 、3-O- α-L-rhamnopyranosyl-(1→2)-O- β- D-glucopyranosyl-(1→2)- α-L-arabinopyranosyl oleanolic acid (5) 、3-O-( β-D-glucopyranosiduronic acid)-oleanolic acid 28-O- β-D-glucopyranoside (6)、lup-20(29)-en-3-one (7)、lupeol (8)、β-谷甾醇(9)、齐墩果酸(10)、乌苏酸(11)、β-胡萝卜苷(12)。化合物1 对Lu-06、N-04 和Bre-04 癌细胞株的GI50 分别是0.77µg/mL、1.26 µg/mL 和1.55 µg/mL, 化合物2 对N-04 癌细胞株的GI50 为2.44 µg/mL。2、从小驳骨地上部分的95%乙醇提取物中分离得到了1 个原小檗碱类新化合物13-hydroxyl gusanlung A (25), β-谷甾醇(9)、齐敦果酸(10)、β-胡萝卜苷(12)、棕榈酸(1-)甘油酯(13)、棕榈酸(14)、阿苯哒唑(15)、阿苯哒唑砜(16)、阿苯哒唑亚砜(17)、aurantiamide acetate (18)、华良姜素(19)、芫花素(20)、(-)-丁香树酯醇(21)、gusanlung B (22) 、eupteleasaponinsⅤ acetate (23)、gusanlungA (24)、刺五加苷E (26)、岩白菜素(27)、咖啡酸(28)。化合物25 对肝癌细胞株(HepG2) 的GI50 为2.08 µg/mL。3、从川西茶藨地上部分的95%乙醇提取物中分离鉴定了22 个化合物: β-谷甾醇(9) 、β- 胡萝卜苷(12) 、O-acetyloleanolic aldehyde (29),4,7,8-trimethoxy-2,3-methylenedioxydibenzofuran (30) 、3', 5-dimethoxy-3, 4-methylenedioxybiphenyl (31) 、桦木醇(32) 、6,7-dimethoxy-1-methyl-3,4-dihydroquinolin-2-one (33)、3'-hydroxy-5-methoxy-3,4-methylenedioxybiphenyl (34) 、7-hydroxy-4,8-dimethoxy-2,3-methylenedioxydibenzofuran (35)、桦木醛(36)、没食子酸(37) 、6β- 羟基-4- 烯-3- 酮- 豆甾醇(38) 、5α, 8α-epidioxy-(22E,24R)-ergosta-6, 22-dien-3β-ol (39)、verrucofortine (40)、6-methoxycalpogoniumisoflavone A (41)、2-羟基二苯甲酮(42)、桦木酸(43), 3, 5-二甲氧基苯甲酸-4-O-β-D-吡喃葡萄糖苷(44)、洋芹素(45)、刺槐素(46)、水杨酸(47)、洋芹素-5-O- β-D-葡萄糖苷(48), 化合物30、31 和35 为新的联苯化合物。化合物30的α-葡萄糖苷酶抑制率为10.2% (1.00 mg/mL); 化合物35 的抑制率为17.2% (1.00mg/mL)。4、综述了1960 年以来原小檗碱类化合物药理活性研究进展。 Plants Holboellia latifolia Wall and Gendarussa vulgaris Nees, are used as folkmedicine. Ribes takare D. Don belongs to the genus Ribes. The three plants have notbeen chemically studied in detail. Chemical and bioactive study of three plants led tothe isolation of 48 compounds by chromatography. Their structures were elucidatedon the basis of spectroscopic evidence or comparison with authentic samples. Amongthe 48 componds isolated one protoberberine alkaloid and three biphenyls are newones. Cytotoxic and α-glucosidase inhibitory compounds had been found.1. Twelve compounds were isolated from the 95% ethanol extract of the aerial partof H. latifolia Wall. They were characterized as fellow: eleutheroside K (1),hederagenin-3-O- α-L-rhamnopyranosyl-(1→2)- α-L-arabinopyranoside (2),2-naphthyl acetic acid (3),3-O-α-L-rhamnopyranosyl-(1→2)-[β-D-glucopyranosyl-(1→3)]-α-L-arabinopyranosyl oleanolic acid 28-O-α-L-rhamnopyranosyl-(1→4)-β-D-glucopyranosyl-(1→6)-β-D-glucopyranosyl ester (4), 3-O- α-L-rhamnopyranosyl-(1→2)-O- β- D-glucopyranosyl-(1→2)- α-L-arabinopyranosyl oleanolic acid (5),3-O-( β-D-glucopyranosiduronic acid)-oleanolic acid-28-O- β-D-glucopyranoside (6),lup-20(29)-en-3-one (7), lupeol (8), β-sitosterol (9), oleanolic acid (10), ursolicacid (11), and β-daucosterol (12). Compound 1 showed moderate cytotoxicity againstLu-06 (GI50, 0.77 µg/mL), N-04 (GI50, 1.26 µg/mL) and Bre0-4 (GI50=1.55 µg/mL)and compound 2 showed moderate cytotoxicity against N-04 (GI50=2.44 µg/mL).2. A new protoberberine alkaloid, 13-hydroxyl gusanlung A (25), was isolated fromthe aerial part of Gendarussa vulgaris Nees, together with β-sitosterol (9), oleanolicacid (10), β-daucosterol (12), glycerol monopalmitate (13), palmific acid (14),albendazole (15), albendazole sulphone (16), albendazole sufloxide (17), aurantiamideacetate (18), kumatakenin (19), genkwanin (20), (-)-syringaresinol (21), gusanlung B(22), eupteleasaponinsⅤ acetate (23), gusanlung A (24), eleutheroside E (26),bergenin (27) and caffeic acid (28). Compound 25 showed cytotoxicity against HepG2 cells (GI50, 2.08 µg/mL).3. Phytochemical study of the Ribes takare D. Don led to the isolation of three newbiphenyls, 4,7,8-trimethoxy-2,3-methylenedioxydibenzofuran (30), 3', 5-dimethoxy-3,4-methylenedioxybiphenyl (31) and 7-hydroxy-4,8-dimethoxy-2,3-methylenedioxydibenzofuran (35), along with nineteenknown compounds, β-sitosterol (9), β-daucosterol (12), O-acetyloleanolic aldehyde(29), betulin (32), 6,7-dimethoxy-1-methyl-3,4-dihydroquinolin-2-one (33),3'-hydroxy-5-methoxy-3, 4-methylenedioxybiphenyl (34), betulinic aldehyde (36),gallic acid (37), stigmast-4-en-6β-ol-3-one (38), 5α, 8α-epidioxy-(22E, 24R)-ergosta-6,22-dien-3β-ol (39), verrucofortine (40), 6-methoxycalpogonium isoflavone A (41),2-hydroxybenzophenone (42), betulinic acid (43), 3,5-dimethoxygallic acid-4-O- β-D-glucopryranoside (44), apigenin (45), acacetin (46), salicylic acid (47) andapigenin-5-O- β-D-glucopryranoside (48). α-Glucosidase inhibitory rates ofcompound 30 and 35 were respectively 10.2% and 17.2% at a concentration of 1.00 mg/mL).4. Pharmacological activities of protoberberines were summarized.
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本学位论文由5 章组成。第1 章报道了两头尖中三萜皂苷类化合物的全扫描电喷雾多级质谱分析及银莲花素A 的电喷雾质谱裂解规律;第2 和3 章报道了两种银莲花属药用植物化学成分的研究结果;第4 章报道了银莲花素A 的化学结构修饰及其对一种蛋白酪氨酸磷酸酯酶(PTP-1B)的抑制活性;第5 章综述了电喷雾质谱在皂苷类化合物结构鉴定中的应用进展。 第1 章报道了运用全扫描电喷雾多级质谱对两头尖中三萜皂苷类化合物的快速定性检测,共检测出18 个准分子离子峰,根据多级质谱数据并结合文献报道,对其中的15 个准分子离子峰进行了归属,并区分了一些同分异构体;更有意思的是,发现了3 个未见文献报道的三萜皂苷类化合物。根据它们的多级质谱数据,对其结构分别进行了初步解析。本章同时对银莲花素A 特殊的质谱裂解途径通过衍生物制备及其质谱分析进行了确认。 第2 和3 章,分别报道了两头尖和打破碗花花中水溶性多糖苷的分离纯化和结构鉴定。采用D101 大孔树脂和反复硅胶柱层析等分离手段,从两头尖水溶性部分分离得到8 个三萜皂苷类化合物,通过红外、电喷雾质谱和核磁共振等现代谱学方法,并结合传统的化学手段鉴定了它们的结构,其中4 个化合物为新化合物,分别命名为多被银莲花皂苷19、多被银莲花皂苷20、多被银莲花皂苷21和多被银莲花皂苷22。从打破碗花花水溶性部位分离得到6 个三萜皂苷类化合物,通过现代谱学手段,并结合传统的化学方法对它们进行了鉴定,其中1 个为新化合物,命名为打破碗花花苷H。 第4 章报道了以银莲花素A 及其同系物为先导化合物,进行化学结构修饰并对修饰产物进行广泛的生物活性筛选,发现在银莲花素A 及其同系物的结构中引入一些酸性基团后,其生物活性发生了变化,一些修饰产物显示出很强的PTP-1B 抑制作用,提示这些化合物有可能用于治疗II 型糖尿病。 第5 章综述了电喷雾多级质谱用于皂苷类化合物结构鉴定的研究进展。 This dissertation composes of five chapters. The first chapter elaborates the detection and qualification of the triterpenoidal saponins in Anemone raddeana by positive and negative full scan ESI-MSn. This part also reports the special fragmentation pathway of Raddeanin A by ESI-MS/MS. The second and third chapters present the phytochemical investigation of two medicinal plants from Anemone. The fourth part dwells on the structure modification of Raddeanin A and their inhibitory activity against PTP-1B. The last part is a review on the progress in the application of ESI-MSn in the structure identification of saponins. The first chapter reports the application of full scan ESI-MSn for fast analysis of triterpenoid saponins in Anemone raddeana. Eighteen quasi- molecular ion peaks were detected in the positive full scan ESI-MS and fifteen of them were identified by analysis of their tandem mass spectral data in the negative ion mode. Several isomers were differentiated. More interesting, three unreported triterpenoid saponins in this medicinal plant were detected and their structures were deduced according to the dissociation pathway of the known triterpenoidal saponins. This chapter also confirms the special fragmentation pathway of Raddeanin A by its derivative and the mass spectral analysis. The second and third chapters expatiate on the isolation and identification of the chemical constituents from A. raddeana and A. hupehensis. Eight compounds were isolated from the roots and stems of A. raddeana by methanol extraction and repeated column chromatography (including D101 and silica gel), and their structures were determined on the basis of IR, ESI-MS, NMR and chemical methods (including acid hydrolysis and alkaline saponification). Among them, four are new triterpenoid saponins and named as Raddeanoside R19, Raddeanoside R20, Raddeanoside R21 and Raddeanoside R22. Six compounds were isolated from the whole plants of A. hupehensis by the same methods as above, and their structures were also determined with the same way. One of them was confirmed to be new triterpenoid saponins and named as hupehensis saponin H. In the fourth chapter, in order to look for new active compounds, the structure of Raddeanin A and its analogs were modified. It was found that the modified products exhibited obvious inhibitory activity against PTP-1B when several acid groups were introduced. The fifth chapter summarizes the progress on the application of ESI-MSn in the structure identification of saponins.
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利用重离子和紫外线辐照诱变相结合的方法对兽疫链球菌CVCC1917进行了诱变处理,获得1株高产透明质酸菌株H-7。结果表明,该突变株产透明质酸(HA)能力提高了3倍多,产率稳定为1.8g/L~2.3g/L。
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随着新技术的发展,嵌入式系统已经越来越多地应用于工业现场控制、数字图像处理、网络设备和信息家电等复杂的控制系统中,然而缺乏操作系统支持的嵌入式设备已经不能满足日益提高的性能需求。本文介绍了韩国ADC公司推出的不同于ARM系列体系结构的CPU—SE 3208以及如何在基于SE 3208的Jupiter开发板的硬件基础上,建立μCLinux操作系统的开发平台,并在开发板上移植μCLinux操作系统和应用程序以及在μCLinux操作系统下开发多进程的应用程序。
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基于现代气象资料所建立的西安、汉中地区冬季降雪天数与年冬季平均气温之间的相关关系,根据清代档案所记载的西安与汉中地区冬季降雪日数,恢复了西安与汉中地区1736~1910年的年冬季平均气温,重建了1736~1999年西安与汉中地区年冬季平均气温序列。序列分析表明,这两个地区年冬季平均气温变化趋势一致:18世纪和20世纪为暖期,19世纪为冷期,且20世纪的增暖趋势明显。与利用树轮重建的镇安初春(3~4月)温度序列对比分析表明:西安、汉中地区冬季平均气温与镇安初春温度的低频变化趋势基本一致,但镇安较西安与汉中有
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New carbazole-based polymers, which contain various content of electro-active fragments in the main chain connected via alkylene spacers, have been synthesized by Ni(0)-catalyzed Yamamoto-type aryl-aryl coupling reactions. These compounds represent amorphous materials of high thermal stability with glass-transition temperatures of 139-151 degrees C and thermal decomposition starting at temperatures above 400 degrees C. UV-vis absorption and photoluminescence emission spectra of the materials confirmed that the conjugated segments in the macromolecules are rather short.
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beta-NaYF4 microcrystals with a variety of morphologies, such as microrod, hexagonal microprism, and octadecahedron, have been synthesized via a facile hydrothermal route. X-ray diffraction (XRD), scanning electron microscopy (SEM), transmission electron microscopy (TEM), high-resolution transmission electron microscopy (HRTEM), and photoluminescence (PL) spectra were used to characterize the samples. The intrinsic structural feature of beta-NaYF4 seeds and two important external factors, namely, the pH values in the initial reaction solution and fluoride sources, are responsible for shape determination of beta-NaYF4 microcrystals. It is found that the organic additive trisodium citrate (Cit(3-)) as a shape modifier has the dynamic effect by adjusting the growth rate of different facets under different experimental conditions, resulting in the formation of the anisotropic geometries of various beta-NaYF4 microcrystals. The possible formation mechanisms for products with various architectures have been presented. A systematic study on the photoluminescence of Tb3+-doped beta-NaYF4 samples with rod, prism, and octadecahedral shapes has shown that the optical properties of these phosphors are strongly dependent on their morphologies and sizes.
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The microwave (MW)-based thermal process was applied to the preparation of hexagon-shaped gold nanoplates. The fort-nation of gold nanoplates occurs rapidly in a single step, carried out by directly heating a reaction mixture of HAuCl4 with sodium citrate in an MW reactor. And the gold nanoplates were characterized by UV-visible spectroscopy, X-ray diffraction (XRD) and transmission electron microscopy (TEM). The experimental results indicated that the sizes and morphologies of the gold nanomaterials strongly depend both on the heating methods and molar ratio of HAuCl4 to sodium citrate in the initial reaction mixture. At the molar ratio 5 : 4 (HAuCl4 to sodium citrate), hexagonal nanoplates with large Au (111) crystallographic facet were preferentially synthesized by the MW assistant method.
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今天,重视知识创新是为了发展知识经济。知识经济与传统经济不同,是以不断创新的知识为主要基础而发展的。有效的创新体系若无经济的密切配合,只能是无源之水、无的之矢。
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In this paper, we introduce a very convenient method to produce water soluble C-60 derivatives- fullerols by the reaction of C-60 with potassium in toluene solution, FT-IR, H-1 NMR and FABMS proved the multi-hydroxyl and C-60 cage structures of the products, The properties of unstability to light, heat, basicity of aqueous solution and the solubility in some common polar solvents were also described.
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C_(60)(OH)_x的简便合成及性质孙大勇,刘子阳,郭兴华,佘益民,周雨,刘淑莹(中国科学院长春应用化学研究所应用谱学开放实验室,长春,130022)关键词C_(60),水溶性富勒醇,钾,不稳定性,溶解度水溶性C60化合物的合成及性质研究作为C60?..
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为了进一步完善裙带菜单倍体克隆(简称单克隆,以下同)育苗技术,实现该技术的产业化,本文对单克隆的快速扩增以及育苗条件进行了优化研究。获得如下结果:一、光对裙带菜排卵的干扰现象:一般附苗后4-5天雌雄配子即已形成。接近成熟的卵囊细胞翘起,长度达到50-55μm,直径为19-20μm,一到两天后即可排卵。精子囊略透明,颜色微绿。在11:13(L:D)的光周期下,排卵一般在黑暗开始后5分钟即已开始,5-15分钟后达到高峰。排卵的过程只有几秒钟。卵排出后停留在卵囊开口处,仍与卵囊牢固相连。虽然排卵过程只有几秒钟,一旦这个过程受到光的干扰,就会诱导卵脱离卵囊。实验证实,5-6μmol m~(-2)s~(-1)的微弱光强(显微镜下镜检的光强)即能引起95%的卵从卵囊脱落。根据我们的观察,一旦卵已排出并与卵囊相连,将不再受光的干扰而脱落。脱落的卵很快死亡分解。将配子已经形成但尚未释放的培养转移至连续光下以后,卵仍能排放,但排出的卵大部分脱落(75%),进一步说明了光对排卵的干扰作用。在育苗实践中,为了方便工作,育苗车间内在天黑后的2-3小时内仍有照明,而在第二天早晨取样观察,就会发现许多空的卵囊。我们的实验证实了这是由于排卵过程受到光的干扰引起的。因此,在育苗实践中,为了提高出苗率,在出苗期间,天黑后2-3小时内育苗车间内应避免照明,以降低光导卵的脱落。二、单克隆快速扩增以及育苗条件的优化:(一)、单克隆快速扩增的优化。实验结果表明:1、单克隆快速生长的适宜光照强度为80-120μmol m~(-2)s~(-1)。单克隆的培养密度宜控制在1-10g/L。接种密度以1g/L为宜。2、单克隆藻体内能贮藏氮,因此在单克隆快速扩增过程中,可采用间歇施肥法补充氮源。实验证明,培养液中氨态氮的适宜浓度为20μmol/L,可维持单克隆6天的生长之用(单克隆培养密度1-10g/L)。3、实验证明,在65天内,“老水”对单克隆的生长没有明显的抑制作用。而且,PES培养基除氮的其它成分也可满足单克隆65天的生长需求。4、单克隆快速生长的适宜温度为22 ℃。另外,单克隆密度与消光值之间存在着线形关系,可以通过测量消光值来计算单克隆的培养密度和鲜重,以代替称量法测鲜重。综上,可提出如下单克隆快速扩增的模式:温度为22 ℃;初始光强控制在80-120 μmol m~(-2)s~(-1);单克隆的接种密度为1g/L;PES培养基(除去氮的成分)可供单克隆65天的培养之用,在这65天内,每隔六天左右将初始氨态氮补充至20 μmol/L;单克隆的培养密度控制在1-10g/L;单克隆培养密度和鲜重可通过测量消光值计算得到。依以上模式,并及时进行扩养,单克隆的鲜重平均日增长率可达25%,以此增长率计算,10g单克隆经一个月培养后鲜重可达8070克,可培育苗帘2000多个,实现海面养殖1000多亩,达到了生产性育苗的要求。(二)、单克隆育苗条件的优化 根据实验结果,可采取如下的育苗优化措施:1、光对排卵有干扰作用。因此,在出苗期间,在天黑后2-3小时内,育苗车间内应避免照明,以降低光导的卵子脱落。2、1μmol/L磷(PO_4~(3-) -P)和70 μmolm/L氮(NH_4~+-N)有利于加速出苗。3、铁对配子体的发育有明显的促进作用。2.5μmolm/L的Fe(III)能使出苗时间提前1-2天,出苗率增加15%左右。4、单克隆育苗较适宜的温度为17 ℃。依以上条件,4-5天左右即可出苗,比一般出苗时间提前1-2天。出苗率也有所增加,例如在实验室条件下,出苗率由原来的50-60%增至80-90%,增加了30%左右。本项研究进一步完善了裙带菜单克隆育苗技术,将大大有利于该技术的进一步推广。
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海洋微生物拥有丰富多样的次生代谢途径,其中海洋生物内生真菌次生代谢产物研究日益受到天然产物化学界的重视。本论文以菌丝体生物量、发酵产物重量、抗菌与细胞毒活性、薄层色谱分析结果以及高效液相色谱分析结果等为评价依据对采自青岛沿海的13株海藻内生真菌在四种液体培养基上的静置发酵产物进行了综合评价,并从中选择了黑曲霉Aspergillus niger EN-13(分离自褐藻囊藻Colpomenia sinuosa)和杂色曲霉A. versicolor EN-7(分离自褐藻鼠尾藻Sargassum thunbergii)两株真菌进行了30升规模发酵(分别采用GPYM培养基和PDB培养)和化学成分的研究,对分离得到的大部分化合物进行了初步的生物活性筛选。 发酵提取物采用常规的硅胶柱层析、反相硅胶柱层析,凝胶Sephadex LH-20柱层析、制备薄层层析、半制备高效液相色谱以及重结晶等分离手段,得到单体化合物。利用各种现代波谱技术(IR、UV、EI-MS、FAB-MS、HR-ESI-MS、1H-NMR、13C-NMR、DEPT、1H-1H COSY、HSQC、HMBC等)并结合化学方法从两种菌株发酵提取物中鉴定了55个化合物的结构。其中从菌株A. niger EN-13分离鉴定了31个化合物,发现9个新化合物,包括2个鞘酯类化合物(AN-1~2)、3个萘并-γ-吡喃酮类化合物(AN-3~5)、3个苯乙基取代的α-吡喃酮类化合物(AN-17, AN-19~20)和1个甾体Diels-Alder加成产物(AN-21),另有1个新的天然环二肽(AN-27)被分离鉴定;从菌株A. versicolor EN-7分离鉴定了24个化合物,发现2个新化合物,为蒽醌AV-12与AV-17,另外,从前一菌株(A. niger EN-13)中鉴定的2个新鞘酯类化合物(AN-1~2)在A. versicolor EN-7中也被再次分离到。 对大部分单体化合物进行了抗菌活性、DPPH自由基清除活性和细胞毒活性测试。结果显示新化合物AN-1、AN-5和AN-20具有弱或中等强度的抑制白色念珠菌生长的活性,AN-4、AN-5、AN-21显示了弱或中等强度的抑制黑曲霉生长的活性,AV-12、AV-17显示了弱的抑制大肠杆菌生长的活性。在DPPH自由基清除活性筛选中,AN-5显示了中等强度的活性,其EC50为109.3 mM,与阳性对照BHT相近(EC50为81.8 mM)。其它部分已知化合物在抗菌和DPPH自由基清除活性的筛选中也显示了弱或中等强度的活性。在针对人肝癌细胞株SMMC-7721和人肺腺癌细胞株A549的体外细胞毒活性筛选中,所测样品均未显示显著活性。
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对1个六倍体栽培燕麦(A.sativa)健壮燕麦和3个六倍体野燕麦(A.fatua)通北燕麦、五台燕麦和日本燕麦进行了C-带核型比较,结果表明,栽培燕麦与野燕麦C-带带型基本相似,但同时在多个染色体上不同材料间又有C-带多态性存在,多态性C-带显现在1C,4C,5C,8,10,13,15,19,20号染色体上.此研究结果可为这些种质资源在燕麦遗传育种中的研究和利用提供细胞学依据.