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101.
反相键合相高效液相色谱法分离测定萘普生 总被引:1,自引:0,他引:1
建立了分离测定萘普生和溴代萘普生的反相键合相高效液相色谱法。采用ODS柱,以添加50mmol/L乳酸并用高氯酸调节pH为2.5的80%甲醇-水溶液作为流动相,以苯甲酸为内标物,测定了不对称合成工艺产物中萘普生和溴代萘普生的含量。方法的准确度分别为99.83%~102.07%(萘普生)和99.0%~100.83%(溴代萘普生),相对标准偏差分别小于2.58%(萘普生)和3.64%(溴代萘普生)。方法可用于工艺条件的选择和质量检测。 相似文献
102.
用单扫示波极谱法,在生理盐水底液中,25℃时邻硝基对甲基苯胺于-0.82±0.01伏(SC)处有一良好的二阶导数还原峰,浓度为2×10(-8)-1×10(-5)mol/L时,与峰电流呈良好的线性关系,可作分析测定,检测限为1×10-8mol/L。许多无机离子不干扰测定。此外,还证明其电极过程为吸附过程,n=4,提出了电极反应机理。 相似文献
103.
104.
[structure: see text] Total synthesis of a cyclic depsipeptide with proposed structure of palau'amide is achieved, which features a stereoselective elaboration of its 5,7-dihydroxy-2,6-dimethyldodec-2-en-11-ynoic acid unit. The synthetic compound has potent cytotoxicity against three tumor cell lines but different rotation and NMR data compared to those reported for palau'amide, which implies that its conformation is close to that of palau'amide but that some stereochemistry in palau'amide was misassigned. 相似文献
105.
Jingfei Luan Zhigang Zou Minghui Lu Guoyou Luan Yanfeng Chen 《Research on Chemical Intermediates》2006,32(1):31-42
In2BiTaO7 was synthesized using the solid-state reaction method and its photocatalytic properties were investigated. The results of
powder X-ray diffraction (XRD) indicated that the compound crystallizes in the pyrochlore-type structure, cubic system with
space group Fd-3m. The lattice parameter is 10.6972(1) ?. In addition, the compound shows strong optical absorption in the
visible region (λ > 420 nm) and the band gap of In2BiTaO7 was estimated to be about 2.47 eV. For the photocatalytic reaction, H2 or O2 evolution was observed from CH3OH/H2O or AgNO3 solution respectively with In2BiTaO7 as the photocatalyst under visible light irradiation, indicating that In2BiTaO7 is responsive to visible light for splitting water. Furthermore, the catalyst remained photoactive in the wavelength range
up to 510 nm. Photocatalytic degradation of methylene blue (MB) dye over the compound was further investigated under visible
light irradiation. The results showed that complete removal of aqueous MB could be achieved after irradiation for 135 min
over In2BiTaO7. Furthermore, under visible light irradiation In2BiTaO7 showed markedly higher catalytic activity compared to P-25 for MB photocatalytic degradation. 相似文献
106.
利用双缩脲试剂,在可见光区建立了N-磷酰化二肽、二肽以及磷酰化多肽的分光光度定量分析方法。在经典的双缩脲分光光度法的实验条件下,观察到N-磷酰化二肽、二肽与双缩脲试剂的复合物的最大吸收波长均为620nm及N-磷酰基对二肽有很强的增色作用。 相似文献
107.
Simultaneous determination of triterpene saponins in ginseng drugs by high-performance liquid chromatography 总被引:3,自引:0,他引:3
A HPLC method for the simultaneous determination of 11 triterpene saponins with four-type aglycones (protopanaxadiol, protopanaxatriol, ocotillol and oleanolic acid types) in Ginseng drugs was developed and validated. Using a gradient of acetonitrile and 10 mM K-phosphate buffer (pH 5.80) as the mobile phase and UV detection at 196 nm, more than 18 ginsenosides with different aglycones were separated satisfactorily within 60 min. The detection limits (signal/noise> or =3) were 0.1 microg for ginsenosides Rb1, Rc, Rd, Re and Rg1, chikusetsusaponin III, and notoginsenoside R2, 0.2 microg for gisenoside Ro and chikusetsusaponin IVa, 0.3 microg for chikusetsusaponin IV, and 3 microg for majonoside R2. The calibration curve of each saponin had a correlation coefficient close to 1. Intra- and interday precisions were less than 2.1% (n=5) and 3.3% (n=15), respectively. The recovery rates of extraction were in the range of 96.4-102.7% for all ginsenosides. By adopting this method, the determinations of 11 ginsenosides in three Ginseng drugs derived from Panax ginseng, Panax vietnamensis var. fuscidiscus and Panax japonicus (Japan) were achieved. 相似文献
108.
109.
光学活性甲苄菊酯的合成及其结构与活性关系的研究 总被引:4,自引:0,他引:4
本文改进了Goffinet方法,完成了(±)-trans菊酸的拆分;改进了Campbel?方法,只用一种拆分剂(奎宁)完成了对(±)-cis菊酸的拆分。用IR、~1HNMR、旋光度测定等方法确定了各甲苄菊酯光学异构体的结构。生物试验表明结构与活性有如下关系:1,各异构体中以1R-酯的杀虫活性为高,尤其(-)-(1R,3R)-trans甲苄菊酯对全部测试昆虫均显示较高的杀虫活性;2,昆虫不同,各异构体的活性次序也略有差异。 相似文献
110.
Hamza MS Zou X Banka R Brown KL van Eldik R 《Dalton transactions (Cambridge, England : 2003)》2005,(4):782-787
Ligand substitution reactions of the vitamin B12 analog cyanoimidazolylcobamide, CN(Im)Cbl, with cyanide were studied. Cyanide substitutes imidazole (Im) in the alpha-position more slowly than it substitutes dimethylbenzimidazole in cyanocobalamin (vitamin B12). The kinetics of the displacement of Im by CN- showed saturation behaviour at high cyanide concentration; the limiting rate constant was found to be 0.0264 s(-1) at 25 degrees C and is characterized by the activation parameters: DeltaH(not =) = 111 +/- 2 kJ mol(-1), DeltaS(not =) = +97 +/- 6 J K(-1) mol(-1), and DeltaV(not =) = +9.3 +/- 0.3 cm3 mol(-1). These parameters are interpreted in terms of an I(d) mechanism. The equilibrium constant for the reaction of CN(Im)Cbl with CN- was found to be 861 +/- 75 M(-1), which is significantly less than that obtained for the reaction of cyanocobalamin with CN- (viz. 10(4) M(-1)). pKbase-off for the base-on/base-off equilibrium was determined spectrophotometrically and found to be 0.99 +/- 0.05, which is about 0.9 pH units higher than that obtained previously in the case of cyanocobalamin. In addition, the kinetics of the base-on/base-off reaction was studied using a pH-jump technique and the data obtained revealed evidence for an acid catalyzed reaction path. The results obtained in this study are discussed in reference to those reported previously for cyanocobalamin. 相似文献