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排序方式: 共有159条查询结果,搜索用时 15 毫秒
61.
A new synthesis of 3H-pyrimidin-4-ones, characterized by four different sets of decorations, is presented. The strategy is based on the synthetic elaboration of readily available α-substituted β-ketoesters that, upon transformation into the corresponding acyl enamines, have been cyclized to give 6H-1,3-oxazin-6-ones. These reactive intermediates have been in turn cleanly converted into highly functionalized pyirimidinones, by treatment with an appropriate primary amine. The whole sequence does not need the use of any metal mediator or catalyst. 相似文献
62.
63.
Kroumova V Gobbato E Basso E Mucedola L Giani T Fortina G 《Rapid communications in mass spectrometry : RCM》2011,25(15):2247-2249
Matrix-assisted laser desorption/ionization time-of-flight mass spectrometry (MALDI-TOF MS) has recently been demonstrated to be a powerful tool for the rapid identification of bacteria from growing colonies. In order to speed up the identification of bacteria, several authors have evaluated the usefulness of this MALDI-TOF MS technology for the direct and quick identification bacteria from positive blood cultures. The results obtained so far have been encouraging but have also shown some limitations, mainly related to the bacterial growth and to the presence of interference substances belonging to the blood cultures. In this paper, we present a new methodological approach that we have developed to overcome these limitations, based mainly on an enrichment of the sample into a growing medium before the extraction process, prior to mass spectrometric analysis. The proposed method shows important advantages for the identification of bacterial strains, yielding an increased identification score, which gives higher confidence in the results. 相似文献
64.
Miriam Góngora‐Benítez Dr. Alessandra Basso Dr. Thomas Bruckdorfer Dr. Miriam Royo Dr. Judit Tulla‐Puche Prof. Fernando Albericio 《Chemistry (Weinheim an der Bergstrasse, Germany)》2012,18(50):16166-16176
Enzyme‐labile protecting groups have emerged as a green alternative to conventional protecting groups. These groups introduce a further orthogonal dimension and eco‐friendliness into protection schemes for the synthesis of complex polyfunctional organic molecules. S‐Phacm, a Cys‐protecting group, can be easily removed by the action of a covalently immobilized PGA enzyme under very mild conditions. Herein, the versatility and reliability of an eco‐friendly combination of the immobilized PGA enzyme and the S‐Phacm protecting group has been evaluated for the synthesis of diverse Cys‐containing peptides. 相似文献
65.
Ivan Veronese Anna Galli Marie Claire Cantone Marco Martini Fabrizio Vernizzi Gianpaolo Guzzi 《Radiation measurements》2010,45(1):35-41
Interest is increasing in the development of new methodologies for accidental dose assessment, exploiting the luminescence and dosimetric properties of objects and materials which can be usually found directly on exposed subjects and/or in the contaminated area.In this work, several types of ceramics employed for dental prosthetics restoration, including both innovative materials used as sub-frames for the construction of the inner part of dental crowns (core), and conventional porcelains used for the fabrication of the external layer (veneer), were investigated with regard to their thermally and optically stimulated luminescence (TSL and OSL respectively) properties, in view of their potential application in accidental dosimetry.The sensitivity to ionizing radiation proved to strongly depend on the type and brand of ceramic, with minimum detectable dose ranging from few mGy up to several tens of mGy. A linear dose–response was observed for most of the samples. However, the luminescence signals were characterised by a significant fading, which has to be taken into account for a reliable accidental dose assessment after a radiation exposure event. 相似文献
66.
Adriano F. Lima Fernanda G. Basso Ana P. D. Ribeiro Vanderlei S. Bagnato Josimeri Hebling Giselle M. Marchi Carlos A. de Souza Costa 《Photochemistry and photobiology》2014,90(1):201-206
The aim of this study was to evaluate the effect of low‐level laser therapy (LLLT) on odontoblast‐like cells exposed to a bleaching agent. Mouse dental papilla cell‐23 cells were seeded in wells of 24‐well plates. Eight groups were established according to the exposure to the bleaching agent and LLLT (0, 4, 10 and 15 J cm?2). Enamel–dentin disks were adapted to artificial pulp chambers, which were individually placed in wells containing Dulbecco's modified Eagle's medium (DMEM). A bleaching agent (35% hydrogen peroxide [BA35%HP]) was applied on enamel (15 min) to obtain the extracts (DMEM + BA35%HP components diffused through enamel/dentin disks). The extracts were applied (1 h) to the cells, and then subjected to LLLT. Cell viability (Methyl tetrazolium assay), alkaline phosphatase (ALP) activity, as well as gene expression of ALP, fibronectin (FN) and type I collagen, were evaluated. The bleaching procedures reduced the cell viability, ALP activity and gene expression of dentin proteins. Laser irradiation did not modulate the cell response; except for FN, as LLLT decreased the gene expression of this protein by the cells exposed to the BA35%HP. It can be concluded that BA35%HP decreased the activities of odontoblasts that were not recovered by the irradiation of the damaged cells with low‐level laser parameters tested. 相似文献
67.
Cleverson C. Bocca Rodrigo M. Pontes Ernani A. Basso 《Journal of Molecular Structure》2004,710(1-3):105-110
The influence of hyperconjugative interactions on bond lengths of some allylic compounds (H2CCH–CH2–M(CH3)3; M=C, Si, Ge) has been investigated through NBO calculations using ab initio and density functional methods. The optimized structural parameters, at the B3LYP/6-31+G(d,p) and HF/6-31+G(d,p) levels, showed a good agreement with the resonance theory. Partial geometry optimization with orbital interactions removed confirmed the observations and revealed that σ→σ* interactions, together with the more common σ→π* ones, play an important role in determining the variations in bond lengths on going from C to Ge. 相似文献
68.
Dietrich SA Banfi L Basso A Damonte G Guanti G Riva R 《Organic & biomolecular chemistry》2005,3(1):97-106
A conformationally restricted cyclic pentapeptide, containing an unsaturated 9-membered lactam as a semi-rigid scaffold, was prepared in a very convergent manner, through tandem Ugi reaction/ring closing metathesis. 相似文献
69.
Oreste Livi Giuliana Biagi Pier Luigi Ferrarini Gianpaolo Primofiore Claudio Mori 《Journal of heterocyclic chemistry》1983,20(6):1729-1733
This paper describes the preparation of three series of 1-phenyl-1,2,3-triazol derivatives with an ester, amide or ether group on the phenyl ring. These derivatives were obtained from 4-hydroxyphenyl- and 4-aminophenyltriazoles, previously synthesized by us, by means of a nucleophilic substitution reaction with acetic anhydride, acyl and alkyl halides. The largest part of compounds were tested in an agricultural chemicals, nutrition and animal health screening programme. 相似文献
70.
Targeting wide-range oncogenic transformation via PU24FCl, a specific inhibitor of tumor Hsp90 总被引:4,自引:0,他引:4
Vilenchik M Solit D Basso A Huezo H Lucas B He H Rosen N Spampinato C Modrich P Chiosis G 《Chemistry & biology》2004,11(6):787-797
Agents that inhibit Hsp90 function hold significant promise in cancer therapy. Here we present PU24FCl, a representative of the first class of designed Hsp90 inhibitors. By specifically and potently inhibiting tumor Hsp90, PU24FCl exhibits wide-ranging anti-cancer activities that occur at similar doses in all tested tumor types. Normal cells are 10- to 50-fold more resistant to these effects. Its Hsp90 inhibition results in multiple anti-tumor-specific effects, such as degradation of Hsp90-client proteins involved in cell growth, survival, and specific transformation, inhibition of cancer cell growth, delay of cell cycle progression, induction of morphological and functional changes, and apoptosis. In concordance with its higher affinity for tumor Hsp90, in vivo PU24FCl accumulates in tumors while being rapidly cleared from normal tissue. Concentrations achieved in vivo in tumors lead to single-agent anti-tumor activity at non-toxic doses. 相似文献