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61.
Synthesis of 8-dipropylamino-7,8,9,10-tetrahydrophenanthridines as potential serotoninergic agonists
A number of 8-dipropylamino-7,8,9,10-tetrahydrophenanthridines have been prepared as analogs of the known serotoninergic agonist 8-hydroxy-2-(dipropylamino)tetralin (8-OH-DPAT) and their affinity for the 5-HT1A receptor subtype evaluated by radioligand binding assay. 相似文献
62.
Changes in the magnetic field-temperature phase diagram of CeSb with pressure have been determined up to 6kbar by magnetization measurements on a single crystal. High magnetic fields up to 70 kOe have been applied along a four fold axis of the rock-salt type structure. The features of the phase diagram are not changed by pressure except for a shift towards high temperature. The saturated magnetic moment and the hysteresis of the transition fields are independent of pressure. Variation of exchange energy with volume is deduced from the experimental results. It is shown that the effect of pressure and the magnetic volume anomaly at 0 K are essentially due to the variation of the exchange energy in the ferromagnetic (001) planes. 相似文献
63.
We compute the 2-rank of the wild kernel WK2(F) of a number field by constructing a 2-class group ad hoc. The main result generalizes in the more intricate case the canonical isomorphism established for odd primes under the assumption in a previous article (cf. (Acta. Arith. 67 (1994) 335; Math. Z. 238 (2001) 335)). It involves a criterium of triviality for the 2-part of the wild kernel of Galois number fields and, in the particular case of quadratic fields, it leads to a logarithmic interpretation of the diophantine conditions obtained by other authors. 相似文献
64.
In the present paper we classify the conformally flat contact metric
manifolds of dimension
satisfying
.
We prove that these manifolds are Sasakian of constant curvature 1. 相似文献
65.
A method is proposed to find the digital input signals to enter in nonlinear acoustical systems (power amplifiers, transducers, etc.) in order to obtain desired arbitrary response signals. The searched input signals are found by performing a Monte Carlo search guided by a simulated annealing process applied to a hidden model with a small number of parameters. The physical system is actually used in the optimization procedure, in a real-time manner, so that no theoretical model of the system response is required. The main aspects of the algorithm are described and illustrated with several examples. 相似文献
66.
67.
Mathieu Florence 《Inventiones Mathematicae》2008,171(1):175-189
Let p be a prime number, let K be a field of characteristic not p, containing the p-th roots of unity, and let r≥1 be an integer. We compute the essential dimension of ℤ/p
r
ℤ over K (Theorem 4.1). In particular,
i) We have edℚ(ℤ/8ℤ)=4, a result which was conjectured by Buhler and Reichstein in 1995 (unpublished).
ii) We have edℚ(ℤ/p
r
ℤ)≥p
r-1. 相似文献
68.
Caroline Mauve Jean Bleton Camille Bathellier Caroline Lelarge‐Trouverie Florence Guérard Jaleh Ghashghaie Alain Tchapla Guillaume Tcherkez 《Rapid communications in mass spectrometry : RCM》2009,23(16):2499-2506
The natural 13C/12C isotope composition (δ13C) of plants and organic compounds within plant organs is a powerful tool to understand carbon allocation patterns and the regulation of photosynthetic or respiratory metabolism. However, many enzymatic fractionations are currently unknown, thus impeding our understanding of carbon trafficking pathways within plant cells. One of them is the 12C/13C isotope effect associated with invertases (EC 3.2.1.26) that are cornerstone enzymes for Suc metabolism and translocation in plants. Another conundrum of isotopic plant biology is the need to measure accurately the specific δ13C of individual carbohydrates. Here, we examined two complementary methods for measuring the δ13C value of sucrose, glucose and fructose, that is, off‐line high‐performance liquid chromatography (HPLC) purification followed by elemental analysis and isotope ratio mass spectrometry (EA‐IRMS) analysis, and gas chromatography‐combustion (GC‐C)‐IRMS. We also used these methods to determine the in vitro 12C/13C isotope effect associated with the yeast invertase. Our results show that, although providing more variable values than HPLC~EA‐IRMS, and being sensitive to derivatization conditions, the GC‐C‐IRMS method gives reliable results. When applied to the invertase reaction, both methods indicate that the 12C/13C isotope effect is rather small and it is not affected by the use of heavy water (D2O). Copyright © 2009 John Wiley & Sons, Ltd. 相似文献
69.
Soriano Del Amo D Wang W Jiang H Besanceney C Yan AC Levy M Liu Y Marlow FL Wu P 《Journal of the American Chemical Society》2010,132(47):16893-16899
The Cu(I)-catalyzed azide-alkyne cycloaddition (CuAAC) is the standard method for bioorthogonal conjugation. However, current Cu(I) catalyst formulations are toxic, hindering their use in living systems. Here we report that BTTES, a tris(triazolylmethyl)amine-based ligand for Cu(I), promotes the cycloaddition reaction rapidly in living systems without apparent toxicity. This catalyst allows, for the first time, noninvasive imaging of fucosylated glycans during zebrafish early embryogenesis. We microinjected embryos with alkyne-bearing GDP-fucose at the one-cell stage and detected the metabolically incorporated unnatural sugars using the biocompatible click chemistry. Labeled glycans could be imaged in the enveloping layer of zebrafish embryos between blastula and early larval stages. This new method paves the way for rapid, noninvasive imaging of biomolecules in living organisms. 相似文献
70.
Dr. Nguyet Trang Thanh Chau Maxime Meyer Dr. Shinsuke Komagawa Dr. Floris Chevallier Prof. Yves Fort Prof. Masanobu Uchiyama Prof. Florence Mongin Dr. Philippe C. Gros 《Chemistry (Weinheim an der Bergstrasse, Germany)》2010,16(41):12425-12433
Homoleptic lithium tri‐ and tetraalkyl zincates were reacted with a set of bromopyridines. Efficient and chemoselective bromine–metal exchanges were realized at room temperature with a substoichiometric amount of nBu4ZnLi2?TMEDA reagent (1/3 equiv; TMEDA=N,N,N′,N′‐tetramethylethylenediamine). This reactivity contrasted with that of tBu4ZnLi2?TMEDA, which was inefficient below one equivalent. DFT calculations allowed us to rationalize the formation of N???Li stabilized polypyridyl zincates in the reaction. The one‐pot difunctionalization of dibromopyridines was also realized using the reagent stoichiometrically. The direct creation of C? Zn bonds in bromopyridines enabled us to perform efficient Negishi‐type cross‐couplings. 相似文献