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101.
Ryckebusch A Gilleron P Millet R Houssin R Lemoine A Pommery N Grellier P Sergheraert C Hénichart JP 《Chemical & pharmaceutical bulletin》2005,53(10):1324-1326
Protein farnesyltransferase of Plasmodium falciparum is a potential target in the treatment of malaria for which increased drug resistance is observed. The design, synthesis and evaluation of a series of N-(4-piperidinyl)benzamides is reported. The most potent compounds showed in vitro activity against the parasite at submicromolar concentrations. 相似文献
102.
A new transient regime in the relaxation towards absolute equilibrium of the conservative and time-reversible 3D Euler equation with a high-wave-number spectral truncation is characterized. Large-scale dissipative effects, caused by the thermalized modes that spontaneously appear between a transition wave number and the maximum wave number, are calculated using fluctuation dissipation relations. The large-scale dynamics is found to be similar to that of high-Reynolds number Navier-Stokes equations and thus obeys (at least approximately) Kolmogorov scaling. 相似文献
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[reaction: see text] A series of experiments are described that suggest that the Rh-catalyzed reductive aldol reaction proceeds by addition of a Rh(I) hydride, generated in situ, to the reacting acrylate followed by a stereochemistry-controlling aldol addition reaction. On the basis of this hypothesis, reaction conditions are engineered that allow for increased substrate scope. 相似文献
105.
Ngoc Hoa Tran Huy Pauline Chaigne Ingrid Dchamps Louis Ricard Franois Mathey 《Heteroatom Chemistry》2005,16(1):44-48
The 1,2‐dihydro‐1,2‐diphosphinine decacarbonylditungsten complex 1 has been used as a synthetic equivalent of the corresponding 1,2‐dianion 2 . These two 1,2‐positions can be linked by a (CH2)4 bridge to yield a [4.4.0] bicyclic structure 6 whose identity has been confirmed by X‐ray crystal structure analysis. Alternatively, two ω‐iodohexyl chains can be grafted onto these positions and the resulting diiodo derivative 9 transformed into a long‐chain bis‐phosphine 10 by reaction with lithium diphenylphosphide. This bis‐phosphine gives a chelate complex with PdCl2 whose trans‐stereochemistry was established by X‐ray crystal structure analysis. © 2005 Wiley Periodicals, Inc. Heteroatom Chem 16:44–48, 2005; Published online in Wiley InterScience (www.interscience.wiley.com). DOI 10.1002/hc.20073 相似文献
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A rapid glycomic profiling method is described wherein N-glycans from plasma samples individually labelled with aniline, 2-aminobenzamide and 2-aminoacridone are mixed, co-injected and separated in the same HILIC-fluorescence run. Transfer of the multiplexed method to UPLC-fluorescence permits an increase in sample throughput from 24 to 864 plasma samples per day. 相似文献
110.
Aurélie Roland Pauline Bros Anaïs Bouisseau Florine Cavelier Rémi Schneider 《Analytica chimica acta》2014
Ochratoxin A (OTA) exhibits potent nephrotoxic, carcinogenic and teratogenic effects and its maximum level in wines has been set to 2 μg L−1 by regulation. Consequently, the analytical procedures for OTA determination in wines have to be both very sensitive and reliable. In this paper, we compared two quantification methods: the stable isotope dilution assay (SIDA) and the diastereomeric dilution assay (DIDA). For this purpose, non-natural analogues of OTA were synthesized: the labeled OTA (OTA-d4) as a diastereomeric mixture for the SIDA and one non-natural OTA’s diastereomer (OTA-dia) for the DIDA. To quantify OTA in red grapes, musts or wines, the sample preparation was optimized using immunoaffinity column extraction and the analysis was performed by LC–MS/MS in Multiple Reaction Monitoring mode. A validation procedure in agreement with the International Organization of Vine and Wine recommendations was conducted. It appeared that SIDA quantification exhibited excellent sensitivity (LOD < 1 ng L−1), accuracy (recovery = 98%), repeatability (RSD < 3%) and intermediate reproducibility (RSD < 4%) compared to quantification by DIDA. Indeed, DIDA method did not provide satisfactory results demonstrating that immunoaffinity extraction is exclusively selective for the natural OTA and not for its diastereomer, which therefore cannot be considered as a good internal standard for this particular method. 相似文献