野生荆条籽中挥发油成分的研究

用水蒸气蒸馏法从荆条中提取挥发油,用气相色谱-质谱联用技术对挥发油成分进行分离和结构鉴定。从荆条籽的挥发油中鉴定出了51个组分,用气相色谱面积归一法确定了各个组分的相对百分含量,其挥发油的主要组成是β-榄香烯(27.98%),芳樟醇(12.39%),贝壳杉烯(12.00%),δ-榄香烯(10.54%),乙酯异冰片脂(8.98%)等。     

抱茎蓼挥发油成分及其抗菌活性的研究

水蒸气蒸馏法从抱茎蓼全草中提取挥发油,用气相色谱-质谱联用技术对其挥发油组分进行分离和鉴定,运用气相色谱面积归一化法确定各组分的相对含量,并利用正构烷烃系列物质对各组分进行定性确定,从抱茎蓼全草的挥发油中检出41个组分,占全油的99.21%,鉴定出38个组分,其主要组分是石竹烯(16.98%)、3-己烯-1-醇(14.69%)、3-辛烯-3醇(8.89%)、a-里哪醇(7.13%)、β-环柠檬醛(6.36%)等。对抱茎蓼全草的挥发油做了抗菌试验,其挥发油对大肠埃希菌(ATCC25922株)、肠炎沙门菌(50040株)、金黄色葡萄球菌(ATCC25925株)有显著地抑制和灭活作用。     

球花毛麝香挥发油的成分研究

本文用气相色谱和毛细管色谱-质谱-计算机法,分离了球花毛麝香[Adenosma indi-anum(Lour.)Merr]挥发油组分54个,鉴定了35个成分,并测定了含量。主要成分有α-蒎烯、β-蒎烯、柠檬烯、对伞花烃、桉树脑、芳樟醇、小茴香酮、甲基茴香醚和δ-愈疮木烯。     

GC-MS法分析曼陀罗挥发油的化学成分

用水蒸气蒸馏法从曼陀罗中提取挥发油,并用气相色谱/质谱联用技术(GC-MS)对挥发油的化学成分进行分离鉴定,用气相色谱峰面积归一化法确定各组分的相对含量.结果从曼陀罗挥发油中鉴定出58种化合物,占总挥发油量的92.37%.其中主要成分为5,6-二氢-6-戊基-2H-吡喃-2-酮(44.29%)、二苯胺(12.50%)、四十四烷(10.41%)、二十烷(4.19%)、(E)-3-己烯-1-醇(2.38%)、3,7,11,15-四甲基-2-十六碳烯-1-醇(2.28%)等.     

黄花补血草挥发性化学成分研究

为了研究黄花补血草挥发油的化学成分,本文采用了水蒸气蒸馏法从黄花补血草中提取挥发油,并用GC-MS法采用最佳分析条件对化学成分进行鉴定,用峰面积归一化法测定各化合物在挥发油中的相对百分含量;通过研究,鉴定出70种化合物,其峰面积相对含量约占挥发油总量82.12%。黄花补血草挥发油的主要组分为2-硝基乙醇(59.63%)、正二十四烷(3.71%)、二苯胺(2.31%)、6,10,14-三甲基-2-十五烷酮(1.79%)、正二十一烷(1.57%)、丙二醇(1.40%)等。     

假烟叶树叶挥发油化学成分分析

采用水蒸汽蒸馏法、两相溶剂萃取法提取,运用毛细管气相色谱-质谱联用法结合计算机检索对茄科植物假烟叶树(Solanum verbascifoliumL.)叶挥发油的化学成分进行分析和鉴定。其新鲜叶片提取10 h的挥发油得率为0.0611%。经毛细管色谱分离出18个峰,共鉴定出17种化合物,占挥发油总量的99.73%;用气相色谱面积归一化法计算各组分的相对含量,其主要化学成分为:大牻牛儿烯D(37.07%),咕巴烯(26.29%),1β-(1-甲基乙基)-4,7-二甲基-1α,2,4a()β,5,8,8a()α-六氢萘(13.63%),石竹烯(8.03%),1-β乙烯基-1-α甲基-2,β4-β双(1-甲基乙烯基)-环己烷(5.81%),-γ榄香烯(2.16%),α-筚澄茄油烯(2.06%),异喇叭烯(0.98%)。以上8种化合物占总挥发油含量的90.22%。     

桂产罗勒挥发油化学成分的分析

采用GC-MS法建立桂产罗勒挥发油的化学成分分析方法。采用水蒸汽蒸馏法提取罗勒挥发油,用GC-MS联用技术分离并鉴定其成分,并用面积归一化法测定成分的相对含量。共鉴定出54个化合物,占挥发油总量的90.21%。桂产罗勒挥发油的主要成分是对烯丙基茴香醚、(+)表-双环倍半水芹烯、3,7,11-三甲基-(Z,E)-1,3,6,10-十二碳四烯,与文献报道的其他产地的罗勒油的化学成分存在显著差异。     

野生蜂窝草籽中挥发油的研究

采用水蒸气蒸馏法从野生蜂窝草籽中提取挥发油,利用气相色谱-质谱联用技术对其挥发油中的化学组分进行分离和结构鉴定,运用气相色谱面积归一化法确定各个组分的相对百分含量。从蜂窝草籽挥发油中鉴出56种成分,主要组分是油酸(12.57%),棕榈酸(10.36%),1-辛烯-3-醇(7.96%),石竹烯(5.98%),2,4,6-三甲基-1,3,6-庚三烯(5.63%)等。对蜂窝草籽挥发油进行了抗氧化实验和抗菌实验,结果表明蜂窝草籽挥发油对.OH有明显的清除作用,蜂窝草籽挥发油对实验菌株均有明显的抑制和灭活作用特别是对大肠杆菌ATCC25922株和肠炎沙门菌50040株的抗菌活性表现得更为显著。     

前胡挥发油胆碱酯酶抑制作用及化学成分研究

运用微孔高通量筛选方法研究前胡挥发油胆碱酯酶抑制活性,并用气相色谱-质谱联用技术辅以Kovats指数鉴定挥发油的主要化学成分。结果显示前胡挥发油对乙酰胆碱酯酶和丁酰胆碱酯酶均具有明显的抑制作用,当前胡挥发油浓度为1μL/mL时,其抑制率分别为(63.76±1.99)%和(51.53±1.70)%;其挥发油共鉴定出32种化学成分,主要有α-蒎烯、左旋-β-蒎烯、月桂烯、1-甲基-3-(1-甲基乙基)苯、(R)-1-甲基-4-(1-甲基乙烯基)环己烯、萜品醇、2-羟基-5-甲基苯乙酮等。本研究结果提示前胡有可能对老年痴呆等神经退行性疾病有一定的治疗作用。     

新鲜罗汉果风味成分的GC-MS分析

利用气相色谱-质谱联用仪对新鲜罗汉果的乙醚萃取物的风味成分进行分析,并结合计算机检索对其化学成分进行分析和鉴定,结果显示:从新鲜罗汉果风味物质中分离出42个组分,并鉴定出其中的26个化合物,占风味挥发油色谱峰面积的83.69％.用气相色谱峰面积归一化法测定了各组分的相对质量分数,新鲜罗汉果风味挥发油中相对质量分数较高的...     

小黄皮叶挥发油的化学成分

利用水蒸气蒸馏法提取小黄皮叶挥发油,运用毛细管气相色谱-质谱联用法对挥发油进行了分析,分离出40个峰,鉴定了其中的37种成分,所鉴定成分占挥发油总量的99.87%,其主要化学成分为单萜及倍半萜类化合物。     

OH-induced free radicals in 3'-UMP and poly(U): spin-trapping and radical chromatography

Characterization of OH-induced free radicals using 3'-UMP and poly(U) was performed by a method combining spin-trapping and radical chromatography. A N2O-saturated aqueous solution containing 3'-UMP and 2-methyl-2-nitrosopropane as a spin-trap was X-irradiated. The spin adducts generated by the reactions of OH radicals with 3'-UMP were separated by paired-ion HPLC and the separated spin adducts were identified by ESR spectroscopy. In the case of poly(U), the spin adducts were digested to oligonucleotides with RNase A and then separated and identified in the same manner as 3'-UMP. The free radicals observed for poly(U) were identical to those for 3'-UMP. The 5-yl radical and the 6-yl radical were identified as precursors of various oxidized products of the base moiety, and the 4'-yl radical and 5'-yl radical, formed by H-abstraction at the C-4' and C-5' positions of the sugar moieties, respectively, were identified as precursors of strand breaks. The 1'-yl radical, produced by H-abstraction at the C-1' position of the sugar moiety, was also identified. From the similarity of the free radicals of 3'-UMP and poly(U), it is suggested that the reactivities of OH radicals with nucleotides are identical to those in polynucleotides.     

陕西南部地区茶叶挥发性成分的研究

用水蒸气蒸馏法分别从陕西南部不同产地的茶叶中提取挥发油,利用气相色谱-质谱联用技术对挥发油中的化学成分进行分离和结构鉴定,运用气相色谱面积归一化法确定各个成分的相对百分含量。从南郑县茶叶挥发油中鉴出51种成分,从宁强县茶叶挥发油中鉴出47种成分,从西乡县茶叶挥发油中鉴出46种成分,各挥发油成分存在着一定的差异。对陕南不同产地茶叶的挥发油做了抗氧化试验,结果表明各挥发油对.OH均有明显的清除作用。     

GC-MS法测定阳荷花挥发油的成分

为分析阳荷Zingiber striolatum Diels.花挥发油中的成分,采用水蒸气蒸馏的方法提取阳荷花中的挥发性成分,应用气相色谱-质谱联用法对化学成分进行鉴定,用峰面积归一化法测定各个化合物在挥发油中的相对百分含量。检测出59个化学成分,鉴定了其中55个化学成分总提物的95.54%。其中烯烃类占49.08%,醇类化合物占22.39%,醛类化合物占6.07%,酯类占4.72%,氧化物占4.25%,酮类化合物占2.26%,,还含有少量的烷烃占2.19%,苯的衍生物占1.81%。     

链霉菌AC-57及其产生的阿克拉霉素A的研究

During the course of screening for new antitumor antibiotics, a new anthracycline antibiotic--aclacinomycin A was separated from the broth and mycelium of Streptomyces AC-57. The strain AC-57 was isolated from the soil collected in the Shanghai suburbs. According to its culture and physiological characteristics the producer was identified as Str. galilaeus AC-57. The broth and mycelium were extracted and treated with solvents as usual way. The aclacinomycin A was separated by silica-gel column chromatography eluted with chrolo-form-methanol. Aclacinomycin A, its aglycone and sugar components were identified by comparison of their physico-chemical and spectral data (MS, UV, IR, 1H-NMR, and 13C-NMR) with authentic compound, purified from the market sample.     

Triacylbenzenes and long-chain volatile ketones from Cochlospermum tinctorium rhizome

The composition of the volatile fraction from Cochlospermum tinctorium rhizome was investigated by GC and GC-MS; among 11 constituents detected, eight were identified as straight chain ketonic compounds. In addition, five triacylbenzenes were isolated from a petrol extract of the rhizome, separated by HPLC and identified by their spectral data.     

Identification of some plasma metabolites of 6, 7-3-H-estrone glucosiduronate in male dogs.

Following the constant infusion of 6, 7-3-H-estrone glucosiduronate in male dogs for a period of 120 minutes, the radioactive metabolites present in the plasma were separated by solvent partition, DEAE-Sephapadex, Celite partition and thin layer chromatography. The identities of the individual estrogens and estrogen conjugates were confirmed by specific activity determinations after chromatography in several different solvent systems, enzyme hydrolysis and steroids and their derivatives. Most of the radioactivity in the plasma was identified as estrone glucosiduronate. The major metabolite present was estradiol-17-beta-3-glucosiduronate. Small amounts of estradiol-17-alpha-3-glucosiduronate and free estrone were also identified. Three other minor conjugates were separated, but positive identification could not be made.     

人尿中一种抗菌物质三甲氧苄二氨基嘧啶的分离、纯化和鉴定

三甲氧苄二氨基嘧啶 (trimethoprim)作为一种二氢叶酸还原酶的抑制剂[1,2 ] ,它对E .coli二氢叶酸还原酶的抑制率是对人的 10 0 0 0倍[3 ,4] ,是一种常见的用于治疗细菌感染的化学药物 .它抑制细菌的主要机理是通过阻止四氢叶酸的合成从而达到抑菌作用 ,如果与磺胺类药物 (sulf     

Identification of UDP-galactose: lactose (lactosylceramide) alpha-4 and beta-3 galactosyltransferases in human kidney

Two galactosyltransferases were identified in human kidney microsomes which both transfer galactose from UDP Gal to lactose as well as to lactosylceramide. Using a solubilized and a partially purified enzyme preparation sufficient product could be obtained for detailed structural analysis. The trisaccharide products were isolated by gel permeation chromatography and separated by preparative high performance thin layer chromatography. The anomeric configuration of the transferred galactose was determined by specific glycosidase digestion and the linkage was identified by methylation and gas-liquid-chromatography. The glycolipid products were not separated but analyzed directly, before and after alpha or beta galactosidase digestion, by methylation, hydrolysis and thin layer chromatography. Into both acceptor substrates galactose was incorporated in alpha 1-4 (30%) and beta 1-3 (70%) linkages. The alpha 1-4 galactosyltransferase is responsible for the synthesis of the Pk antigen Gal alpha 1-4 Gal beta 1-4 Glc-ceramide in human kidney. The beta 1-3 galactosyltransferase has not previously been identified.     

Identification of tissue proteins by amino acid analysis after purification by two-dimensional electrophoresis

Mouse brain proteins were separated by two-dimensional electrophoresis (2-DE). The proteins of a section of the 2-DE pattern were blotted onto hydrophobic membranes and 43 of them were excised and hydrolyzed by liquid-phase hydrolysis. The amino acid composition of these proteins was determined by orthophthaldialdehyde precolumn derivatization and compared with the compositions of known proteins stored in the NBRF sequence database. An identification program named ASA was developed for this purpose. The ASA program includes correction and weighting factors, data reduction by molecular weight windows, and exclusion or inclusion of certain organisms as desired. As a control, eight test proteins and five well-known proteins from mouse brain, all separated by 2-DE, were correctly identified by the program. Out of the 43 brain proteins selected, 19 were identified with high confidence.