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61.
Tetsuo Suami Hiroaki Sasai Kazuhiro Matsuno Nobuo Suzuki Yoshimasa Fukuda Osamu Sakanaka 《Tetrahedron letters》1984,25(40):4533-4536
Tunicamycins and their eight analogs have been synthesized by condensation of a N-acetyl-D-glucosamine derivative and an anomeric chloride of tunicaminyl uracil, followed by deprotections and N-acylation. 相似文献
62.
Two new phenolic compounds, glicoricone (3) and licofuranone (4), were isolated from a species of licorice brought from the northwestern region of China, and their structures were assigned. Among the twelve licorice constituents examined for the inhibition of monoamine oxidase (MAO), six compounds, 3, 4, genistein (6), licopyranocoumarin (7), licocoumarone (14) and glycyrrhisoflavone (15), inhibited the enzyme with the IC50 (concentration required for 50% inhibition of the enzyme activity) values of 6.0 x 10(-5)-1.4 x 10(-4) M. Glycyrrhizin (1) also inhibited MAO with the IC50 value of 1.6 x 10(-4) M. 相似文献
63.
Norio Miyoshi Kiyoaki Hara Issei Yokoyama Giiti Tomita Masaru Fukuda 《Photochemistry and photobiology》1988,47(5):685-688
Abstract— The absorption and fluorescence spectra, and the fluorescence lifetime of acridine orange (AO) were measured in a wide range of the sodium dodecyl sulfate (SDS) concentration below and above the critical micelle concentration (cmc). The fluorescence consisted of two components with different lifetimes; short (<3 ns) and long (>3 ns). The short and long lifetime components are attributed to the AO monomer and dimer associated with detergent, respectively. The lifetime of the dimer increased with increasing the SDS concentration just below the cmc. It decreased suddenly to a constant value just above the cmc. The lifetime of the monomer showed only a slight increase in the concentration range of SDS employed. 相似文献
64.
Copper mediated alkyl-transfer reaction of trialkylaluminum (R3Al) with (E)-4,4-difluoro-5-hydroxyallylic alcohol derivative smoothly proceeded to give the corresponding 2-alkylated 4-fluoro-5-hydroxyhomoallylic alcohol derivative with completely Z and 2,5-syn selective manner. Regio- and stereoselective conversion of the C5-hydroxyl group of the fluoroolefin thus obtained to amino group could be achieved through one-pot mesylation and azidation reaction. 相似文献
65.
The stability constants of the ternary complexes containing UTP, 2,2′-bipyridyl (bipy), and Co2+, Ni2+, Cu2+, or Zn2+ (M2+) have been determined by potentiometric titrations (Table 1). Changes in stability are quantified by Δlog KM = log K–log K. For the Co2+, Ni2+, Cu2+, and Zn2+ systems Δlog KM is 0.10, ?0.13, 0.36, and 0.15, respectively. All these ternary complexes are considerably more stable than would be expected on statistical grounds; indeed, for Co2+, Cu2+, and Zn2+, UTP4? binds more tightly to M (bipy)2+ than to M2+. An UV. difference spectroscopic study suggests that stacked adducts between bipyridyl and the pyrimidine moiety of uridine are formed. 1H-NMR. studies of the bipy/uridine, bipy/UTP, and bipy/UTP/Zn2+ systems (Figs. 1 and 2) confirm the presence of stacking in the binary adducts and in the ternary complex. There is also evidence for the existence of the stacked protonated complex, Zn(bipy) (HUTP)?, with the proton at the γ-phosphate group. The acidity constant of this ternary complex has been measured (Fig. 3). The observed stability enhancement of stacked adducts by the formation of a metal ion bridge is discussed (Fig. 4) and biological implications are indicated. 相似文献
66.
Oku T 《Chemical communications (Cambridge, England)》2002,(4):302-303
The three-dimensional potential map of YB56 was obtained by inverse Fourier transformation of three-dimensional phases and amplitudes in three high-resolution images taken along the [100], [110] and [111] directions of YB56 crystals; the size of the imaging region was 14 nm x 14 nm x approximately 4 nm, and the image directly showed the three-dimensional potential map of the crystal, a useful method for three-dimensional structure analysis in nanoscale regions. 相似文献
67.
H. Sakurai M. Fukuda Y. Hayashibe Y. Sayama K. Masumoto T. Ohtsuki 《Journal of Radioanalytical and Nuclear Chemistry》1997,217(2):267-271
A highly sensitive determination of fluorine in standard rocks by photon activation using the19F(,n)18F reaction combined with pyrohydrolysis for the separation of18F has been reported. The irradiation energy was operated at 20 MeV to avoid the interference from Na, because Na is one of the major element in rocks and18F is also produced from Na via23Na(,n)18F reaction above its threshold energy, 20.9 MeV. After irradiation, fluorine was extracted by pyrohydrolysis and separated as LaF3 precipitate. It was ascertained that the average recovery of fluorine in standard rocks was about 90% and the precipitate was of high radiochemical purity. This method was applied to the analysis of ten GSJ rock reference samples and two USGS standard rocks issued by the Geological Survey of Japan and the United States Geological Survey, respectively. The detection limit of this method was 0.02 g/g, and the results obtained by this method were in good agreement with the recommended values. This method was easily applied to the determination of a few ppm level of fluorine in rock samples, such as ultrabasic rock and feldspar. 相似文献
68.
Ryuichi Iemura Tsuneo Kawashima Toshikazu Fukuda Keizo Ito Goro Tsukamoto 《Journal of heterocyclic chemistry》1987,24(1):31-37
Several types of benzimidazole derivatives were prepared and were screened for H 1-antihistaminic activity. Most of the compounds showed potent antihistaminic activity in vitro. Among them 2-[(1-piperazinyl)methyl]-benzimidazoles 14 and 2-[(1-homopiperazinyi)methyl]benzimidazoles 15 exhibited potent activity also in vivo. 相似文献
69.
Tsuda M Izui N Shimbo K Sato M Fukushi E Kawabata J Katsumata K Horiguchi T Kobayashi J 《The Journal of organic chemistry》2003,68(13):5339-5345
A novel cytotoxic 16-membered macrodiolide, amphidinolide X (1), has been isolated from a marine dinoflagellate Amphidinium sp. (strain Y-42). The gross structure of 1 was elucidated on the basis of spectroscopic data including one-bond and long-range (13)C-(13)C correlations. The relative and absolute stereochemistries were determined by combined analyses of NOESY data and (1)H-(1)H and (1)H-(13)C coupling constants of 1 and NMR data of the degradation products. Amphidinolide X (1) is the first macrodiolide consisting of polyketide-derived diacid and diol units from natural sources. The biosynthetic origins of 1 were investigated by means of feeding experiments with (13)C-labeled acetates. 相似文献
70.
Takeo Iida Motoharu Nakanishi Kunio Got
《Journal of polymer science. Part A, Polymer chemistry》1974,12(4):737-749
Poly(vinyl chloride) (PVC) alone or mixed with 10 wt-% and 50 wt-% TiO2, SnO2, ZnO, and Al2O3 were pyrolyzed by using a pyrolysis gas chromatograph. Benzene, toluene, ethylbenzene, o-xylene, styrene, naphthalene, and various chlorobenzenes were identified. No hydrocarbons could be detected in pyrolysis products of any samples at 200°C. More aromatic hydrocarbons than aliphatic hydrocarbons are released from the PVC–TiO2 system and in preheated PVC. The contrary result is observed in the PVC–ZnO and PVC–SnO2 systems. Aromatics having methyl endgroups are easily released from the PVC–ZnO and PVC–SnO2 systems and at elevated pyrolysis temperature, because methylene groups are easily isolated along the chain by ZnO, SnO2 and the heating. The release of ethylbenzene o-xylene, and chlorobenzenes suggests a repeated dehydrochlorination and recombination of HCl and Cl2 to double bonds along the chain. Possible decomposition mechanisms of PVC are discussed. 相似文献