排序方式: 共有38条查询结果,搜索用时 15 毫秒
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Bockhorst M. Burbach G. Burgwinkel R. Empt J. Guse B. Guse B. Haas K. -M. Hannappel J. Heinloth K. Hey T. Hoffmann-Rothe P. Honscheid K. Jahnen T. Jakob H. P. Jöpen N. Jüngst H. Kirch U. Klein F. -J. Kostrewa D. Lindemann L. Link J. Manns J. Menze D. Merkel H. Merkel R. Neuerburg W. Paul E. Plötzke R. Schenk U. Schmidt S. Scholmann J. Schütz P. Schultz-Coulon H. -C. Schweitzer M. Schwille W. J. Tran M. -Q. Umlauf G. Vogl W. Wedemeyer R. Wehnes F. Wißkirchen J. Wolf A. 《Zeitschrift fur Physik C Particles and Fields》1994,63(1):37-47
The reactions pK
+ and pK
+ 0 have been measured with the multiparticle detector system SAPHIR at ELSA in Bonn. Besides the differential cross sections the polarization and, for the first time, the 0 polarization have been determined in a photon induced reaction. All data are presented as functions of the photon energy (from threshold up to 1.47 GeV) and of the kaon production angle (0°–180°). The polarization of both and 0 is substantial at all energies and varies strongly with the production angle.This work is supported by the Bundesminister für Forschung und Technologie (BMFT), FK 06 BN 621 I 相似文献
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A new phenolic glucoside gallate, vanillic acid 4-O-beta-D-(6'-O-galloyl) glucopyranoside (1) was isolated from the bark of Terminalia macroptera Guill.et Perr., together with 3,3',4'-tri-O-methylellagic acid (2) and two triterpene glucopyranosyl esters, 24-deoxysericoside (3) and chebuloside II (4). Compounds 2-4, not described previously for this plant, showed antimicrobial activities against Bacillus subtilis, while 3 and 4 possessed haemolytic properties. In both assays 1 was found to be inactive. 相似文献
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Kudoh T Fukuoka M Ichikawa S Murayama T Ogawa Y Hashii M Higashida H Kunerth S Weber K Guse AH Potter BV Matsuda A Shuto S 《Journal of the American Chemical Society》2005,127(24):8846-8855
We previously developed cyclic ADP-carbocyclic ribose (cADPcR, 2) as a stable mimic of cyclic ADP-ribose (cADPR, 1), a Ca(2+)-mobilizing second messenger. A series of the N1-ribose modified cADPcR analogues, designed as novel stable mimics of cADPR, which were the 2"-deoxy analogue 3, the 3"-deoxy analogue 4, the 3"-deoxy-2"-O-(methoxymethyl) analogue 5, the 3"-O-methyl analogue 6, the 2",3"-dideoxy analogue 7, and the 2",3"-dideoxydidehydro analogue 8, were successfully synthesized using the key intramolecular condensation reaction with phenylthiophosphate-type substrates. We investigated the conformations of these analogues and of cADPR and found that steric repulsion between both the adenine and N9-ribose moieties and between the adenine and N1-ribose moieties was a determinant of the conformation. The Ca(2+)-mobilizing effects were evaluated systematically using three different biological systems, i.e., sea urchin eggs, NG108-15 neuronal cells, and Jurkat T-lymphocytes. The relative potency of Ca(2+)-mobilization by these cADPR analogues varies depending on the cell-type used: e.g., 3"-deoxy-cADPcR (4) > cADPcR (2) > cADPR (1) in sea urchin eggs; cADPR (1) > cADPcR (2) approximately 3"-deoxy-cADPcR (4) in T-cells; and cADPcR (2) > cADPR (1) > 3"-deoxy-cADPcR (4) in neuronal cells, respectively. These indicated that the target proteins and/or the mechanism of action of cADPR in sea urchin eggs, T-cells, and neuronal cells are different. Thus, this study represents an entry to cell-type selective cADPR analogues, which can be used as biological tools and/or novel drug leads. 相似文献
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Takayoshi Tsuzuki Natsumi Sakaguchi Dr. Takashi Kudoh Satoshi Takano Masato Uehara Dr. Takashi Murayama Prof. Dr. Takashi Sakurai Dr. Minako Hashii Prof. Dr. Haruhiro Higashida Karin Weber Prof. Dr. Andreas H. Guse Dr. Tomoshi Kameda Dr. Takatsugu Hirokawa Dr. Yasuhiro Kumaki Prof. Dr. Barry V. L. Potter Dr. Hayato Fukuda Dr. Mitsuhiro Arisawa Prof. Dr. Satoshi Shuto 《Angewandte Chemie (International ed. in English)》2013,52(26):6633-6637
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Wagner GK Black S Guse AH Potter BV 《Chemical communications (Cambridge, England)》2003,(15):1944-1945
Nicotinamide 8-Br-hypoxanthine dinucleotide (8-Br-NHD+) was cyclised at the N1 position by the ADP-ribosyl cyclase from Aplysia californica to give cyclic 8-Br-inosine diphosphoribose (8-Br-N1-cIDPR), a novel membrane-permeant agonist of Ca2+ release in human T cells. 相似文献