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11.
Maj-Britt Schmidt Andersen Mette Kristensen Claudine Manach Estelle Pujos-Guillot Sanne Kellebjerg Poulsen Thomas Meinert Larsen Arne Astrup Lars Dragsted 《Analytical and bioanalytical chemistry》2014,406(7):1829-1844
While metabolomics is increasingly used to investigate the food metabolome and identify new markers of food exposure, limited attention has been given to the validation of such markers. The main objectives of the present study were to (1) discover potential food exposure markers (PEMs) for a range of plant foods in a study setting with a mixed dietary background and (2) validate PEMs found in a previous meal study. Three-day weighed dietary records and 24-h urine samples were collected three times during a 6-month parallel intervention study from 107 subjects randomized to two distinct dietary patterns. An untargeted UPLC-qTOF-MS metabolomics analysis was performed on the urine samples, and all features detected underwent strict data analyses, including an iterative paired t test and sensitivity and specificity analyses for foods. A total of 22 unique PEMs were identified that covered 7 out of 40 investigated food groups (strawberry, cabbages, beetroot, walnut, citrus, green beans and chocolate). The PEMs reflected foods with a distinct composition rather than foods eaten more frequently or in larger amounts. We found that 23 % of the PEMs found in a previous meal study were also valid in the present intervention study. The study demonstrates that it is possible to discover and validate PEMs for several foods and food classes in an intervention study with a mixed dietary background, despite the large variability in such a dataset. Final validation of PEMs for intake of foods should be performed by quantitative analysis. Figure
Examples of two urinary exposure markers for cabbage (left) and beetroot (right) found in the study from an untargeted LC‐MS metabolomics analysis of urine samples and self‐reported food intake data 相似文献
12.
13.
Thomas G. Kristensen 《Journal of mathematical chemistry》2010,48(2):287-289
The Tanimoto coefficient has previously been proven to be a metric, but only in the case of binary valued vectors. Moreover,
it has been proven that the Tanimoto coefficient for real valued vectors is not a metric. This means that it is not immediately
possible to use metric based data structures for accelerating Tanimoto queries. This note presents a method for transforming
Tanimoto queries into range queries in Euclidian space, making it possible to use metric data structures, as well as data
structures designed for Euclidian space. 相似文献
14.
Bromine-lithium exchange using tert-butyllithium at -78 degrees C initiates a cascade process whereby either xanthone derivatives or pentacyclic 13-azadibenzo[a,de]anthracenes are produced in high yields. The reaction proceeds via a sequential intramolecular trapping of organolithium intermediates. 相似文献
15.
The propagation of ultrasound through an austenitic weld is investigated experimentally as well as in a numerical simulation. The weld is insonified at normal incidence to the fusion line with a longitudinal contact transducer. In order to experimentally trace the ultrasound through the weld, slices of different thicknesses from the original weld have been fabricated. Through-transmission A-scans have then been produced for each weld slice and compared with the corresponding numerical simulation. A comparison of the direction of ultrasound propagation through the weld for the two approaches shows quite good agreement. However, attenuation due to scattering at grain boundaries in the weld is poorly modelled in the simulation. In order to improve this, a better model of the weld is needed. 相似文献
16.
A non-linear Diophantine condition involving perfect squares and arising from an inhomogeneous wave equation on the torus guarantees the existence of a smooth solution. The exceptional set associated with the failure of the Diophantine condition and hence of the existence of a smooth solution is studied. Both the Lebesgue and Hausdorff measures of this set are obtained. 相似文献
17.
Overtone spectrum of o, m and p-nitrobenzaldehydes and p-chlorobenzaldehyde has been studied in 2000–12000 cm−1 region. Vibrational frequencies and anharmonicity constants for aryl as well as alkyl CH stretch vibrations have been determined.
We have also determined the internuclear distances for the aryl CH bond in the different molecules. The small variation observed
in these distances is an indication of the substitution effect.
It is observed that in the case of p-disubstituted benzens, the shift in aryl CH bond is proportional to sum of the Hammet σ of the substituents. However in the
case of o-disubstituted benzenes it is only 80% of the para-substituted shift. 相似文献
18.
Jan Bornholdt Dr. Jakob Felding Dr. Rasmus P. Clausen Dr. Jesper L. Kristensen 《Chemistry (Weinheim an der Bergstrasse, Germany)》2010,16(41):12474-12480
The pyrimidine‐2‐sulfonyl (pymisyl) group is introduced as a new protecting group that can be used to activate aziridines towards ring opening. It is readily introduced and removed under mild conditions. Regioselective ring opening of pymisyl‐protected 2‐methyl‐aziridine with organocuprates gives the corresponding sulfonamides in high yields, and the pymisyl group can subsequently be removed upon treatment with a thiolate. The versatility of this new nitrogen protecting group is illustrated with a new synthesis of Selegiline, a monoamine oxidase‐B inhibitor marketed for the treatment of Parkinson’s disease. 相似文献
19.
We announce new structural properties of 1-homogeneous rank-1 convex integrands, and discuss some of their consequences. 相似文献
20.
Simon D. NielsenGarrick P. Smith Mikael BegtrupJesper L. Kristensen 《Tetrahedron》2011,67(29):5261-5267
The development of a new fluorous-tagged ammonia-equivalent for the synthesis of N-alkylated amino acids is described. The required building blocks were readily accessed in high yield and purity using F-SPE purification technique. Coupling of the fluorous-tagged hydroxylamines with a selection of boronic acids and glyoxalic acid gave the desired N-alkylated amino acids. Subsequent removal of the fluorous tag via catalytic hydrogenation was investigated using a number of different catalysts and solvents. A more robust de-tagging procedure involves the transformation of the amino acid to the corresponding methyl ester followed by a Mo(CH3CN)3(CO)3 mediated N-O bond cleavage. 相似文献