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111.
Ammar S Mahjoub MA Charfi N Skandarani I Chekir-Ghedira L Mighri Z 《Chemical & pharmaceutical bulletin》2007,55(3):385-388
A new skeleton of an O-heteroside natural substance named zinolol, the first representative of a new class of aminated hydroxyhydroquinone, has been isolated from the whole plant Anagallis monelli. Its structure has been established by one and two dimensional NMR spectroscopic procedures. Antioxidant, mutagenic, antimutagenic activities were realised and positive results were recorded. 相似文献
112.
Meryem Saidi Phuoc Hoang Ho Pankaj Yadav Fabrice Salles Clarence Charnay Luc Girard Leila Boukli-Hacene Philippe Trens 《Molecules (Basel, Switzerland)》2021,26(24)
This paper reports on the comparison of three zirconium-based metal organic frameworks (MOFs) for the capture of carbon dioxide and ethanol vapour at ambient conditions. In terms of efficiency, two parameters were evaluated by experimental and modeling means, namely the nature of the ligands and the size of the cavities. We demonstrated that amongst three Zr-based MOFs, MIP-202 has the highest affinity for CO2 (−50 kJ·mol−1 at low coverage against around −20 kJ·mol−1 for MOF-801 and Muc Zr MOF), which could be related to the presence of amino functions borne by its aspartic acid ligands as well as the presence of extra-framework anions. On the other side, regardless of the ligand size, these three materials were able to adsorb similar amounts of carbon dioxide at 1 atm (between 2 and 2.5 µmol·m−2 at 298 K). These experimental findings were consistent with modeling studies, despite chemisorption effects, which could not be taken into consideration by classical Monte Carlo simulations. Ethanol adsorption confirmed these results, higher enthalpies being found at low coverage for the three materials because of stronger van der Waals interactions. Two distinct sorption processes were proposed in the case of MIP-202 to explain the shape of the enthalpic profiles. 相似文献
113.
114.
Hoseini L Roozbeh J Sagheb M Karbalay-Doust S Noorafshan A 《Micron (Oxford, England : 1993)》2009,40(2):226-230
Anabolic androgenic steroids are widely used by athletes for increasing their muscle mass. These drugs are also used by some patients with chronic renal disease. But the effect of these drugs on the renal structure has received less attention. To investigate which parts of the kidney are affected by these drugs, mice kidneys were studied stereologically after injection of nandrolone decanoate (ND), an anabolic androgenic steroid. The treated group received nandrolone decanoate intraperitoneally (solved in olive oil) in doses of 3mg/kg of body weight and administered in one, two and three doses, respectively, in the first, second and third week of treatment. The mice in the control group received an olive oil solution. One week after the last injection, the mice were anaesthetized and their kidney removed. The analysis of data revealed that the weight of kidney was increased approximately 30% (p < or = 0.006) and its volume increased approximately 25% (p < or = 0.02) in ND treated mice in comparison with the control group. The volume of the cortex increased in ND treated animals approximately 44% (p < or = 0.006). Proximal convoluted tubules (PCT) and distal convoluted tubules (DCT) volume increased approximately 25% (p < or = 0.02) and approximately 68% (p < or = 0.02) in ND treated mice. The volume of glomeruli, other ducts, connective tissues, vessels and the length of PCT, DCT, collecting and Henle's ducts and vessels did not show significant differences. CONCLUSION: ND can increase the volume of the renal cortex and its two main parts, i.e. PCT and DCT in mice. 相似文献
115.
Samia Mahouche Nejib Mekni Leila Abbassi Philippe Lang Christian Perruchot Mohamed Jouini Fayna Mammeri Mireille Turmine Hatem Ben Romdhane Mohamed M. Chehimi 《Surface science》2009,603(21):3205-3211
Bis-alkynylated oligoethyleneglycol (OEG) and a monopropargyl-functionalized perfluorinated ethylene glycol (FEG) were clicked to azide-functionalized gold surface (Au–N3) at room temperature via the well known 1,3 cycloaddition click chemical reaction. The Au–N3 substrate was obtained by nucleophilic attack of NaN3 on gold substrates modified by the electrochemical reduction of the , +N2–C6H4–CH2Br diazonium salt. This electrochemical process yields aryl layer-modified gold of the type Au–C6H4–CH2Br (hereafter Au–Br). The untreated and modified gold plates were examined by XPS, PMIRRAS and contact angle measurements. XPS brought evidence for electrografting aryl layers by the detection of Br3d; azide functionalization by the increase of the N/Br atomic ratio; and click reaction of OEG with Au–N3 by the increase of O/N ratio. In addition, the perfluorinated plate (Au-FEG) exhibited F1s and characteristic C1s peaks from -(CF2)7- chain and terminal CF3. Infra red spectroscopy (PMIRRAS) evidenced (i) grafting N3 to Au–Br; (ii) characteristic stretching bands, from ethylene glycol units, C–O–C (1100–1300 cm−1); CF2 (1000–1100 cm−1) and CF3 (1100–1350 cm−1) from FEG grafts; and (iii) suppression of alkynyl bands from OEG and FEG after surface click chemistry. More importantly, PMIRRAS results support an important bridging of the bispropargyl oligoethylene glycol at the gold surface. Water drop contact angles were found to be 48.7° and 83.0° for Au-OEG and Au-FEG, respectively, therefore highlighting the control over the hydrophilic/hydrophobic character of the clicked substrate.This work shows that clicking macromolecules to grafted, diazonium salt-derived aryl layers is a novel, simple and valuable approach for designing robust, functional surface organic coatings. 相似文献
116.
A novel Brönsted acidic room temperature ionic liquid (1‐H‐3‐methyl‐imidazolium bisulfate) is found to catalyze efficiently the acetylation of a wide rang of alcohols as well as phenols with acetic anhydride in good to excellent yields at 50°C under solvent‐free conditions. Products are easily isolated by extraction with ether and the protocol is mild and green, compared to the existing method based on toxic solvents. 相似文献
117.
Gabriella Leo Laura Cartechini Piero Pucci Antonio Sgamellotti Gennaro Marino Leila Birolo 《Analytical and bioanalytical chemistry》2009,395(7):2269-2280
The identification of proteinaceous components in paintings remains a challenging task for several reasons. In addition to
the minute amount of sample available, complex and variable chemical composition of the paints themselves, possible simultaneous
presence of several binders and contaminants, and degradation of the original materials due to aging and pollution are complicating
factors. We proposed proteomic strategies for the identification of proteins in binders of paintings that can be adapted to
overcome the requirements and difficulties presented by specific samples. In particular, we worked on (1) the development
of a minimally invasive method based on the direct tryptic cleavage of the sample without protein extraction; (2) the use
of microwave to enhance the enzymatic digestion yield, followed by the analysis of the peptide mixtures by nanoLC-MS/MS with
electrospray ionization (ESI). Moreover, as an additional tool to tackle the problem of contaminating proteins, we exploited
the possibility of generating an exclusion list of the mass signals that in a first run had been fragmented and that the mass
spectrometer had to ignore for fragmentation in a subsequent run. The methods, tested on model samples, allowed the identification
of milk proteins in a sample from paintings attributed to Cimabue and Giotto, thirteenth-century Italian masters, decorating
the vaults of the upper church in the Basilica of St. Francis in Assisi, Italy. 相似文献
118.
Davarani SS Najafi NM Ramyar S Masoumi L Shamsipur M 《Chemical & pharmaceutical bulletin》2006,54(7):959-962
Electrochemical oxidation of catechol and some 3-substituted catechols (1a--c) has been studied in the presence of 2-chloro-5,5-dimethyl-1,3-cyclohexanedione (3) in aqueous solution using cyclic voltammetry and controlled-potential coulometry. The results indicate that the quinones derived from catechols (1a--c) participate in a Michael addition reaction with 2-chloro-5,5-dimethyl-1,3-cyclohexanedione (3) with consumption of only two electrons per molecule of (1a--c) to from the corresponding benzoforans (10a--c). The electrochemical synthesis of benzofurans has been successfully performed at a carbon rod electrode and in an undivided cell with high yields and purity. 相似文献
119.
We investigate the QCD ghost model of dark energy in the framework of RS II braneworld. We assume there is an energy flow between the brane and bulk, and hence the continuity equation for the ghost dark energy is violated, while it is still preserved for the dark matter on the brane. We find that with the brane-bulk interaction, the equation of state parameter of ghost dark energy on the brane, can cross the phantom line w D =?1 at the present time, which confirms by some cosmological evidences. This result is in contrast to the standard cosmology where w D of ghost dark energy never cross the phantom line and the universe enters a de Sitter phase at the late time. 相似文献
120.
In this study, an extraction and preconcentration technique using solid-phase extraction (SPE) along with hollow fiber (HF) has been developed as an ultra-preconcentration technique for some triazole pesticides in aqueous samples. Triazole pesticides were employed as model compounds to assess the method and were monitored by gas chromatography-flame ionization detection (GC-FID). Initially, an aqueous solution of target analytes was passed through an RP-8 SPE cartridge and then the adsorbed analytes were eluted with μL amounts of toluene. The collected elute was slowly introduced into an HF that had one end blocked. This allowed precipitation inside the lumen and pores of the HF. Finally, the obtained HF was mounted on a home-made solid-phase microextraction syringe and entered into the GC injection port for thermal desorption-GC analysis. The effect of various experimental parameters including injection port temperature, desorption time, state of HF, washing solvent, elution solvent and its volume, sample volume, etc. were investigated for finding the optimum conditions. The calibration graphs were linear in the ranges of 2-1000 ng/mL (penconazole and hexaconazole), 5-1000 ng/mL (tebuconazole), 15-1000 ng/mL (triticonazole) and the detection limits (LODs) ranged from 0.6 to 4.5 ng/mL. The enhancement factors were in the range of 870-950. The relative standard deviations (RSD%) for five repeated experiments (C=250 ng/mL of each pesticide) varied from 4.5 to 8.7%. The relative recoveries obtained for analytes in grape juice samples, spiked with different levels of each pesticide, were in the range of 87-119%. 相似文献