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41.
Amina Chnirheb Mourad Harir Basem Kanawati Agnes Fekete Mohammed El Azzouzi Norbert Hertkorn Philippe Schmitt-Kopplin 《Analytical and bioanalytical chemistry》2010,398(5):2325-2334
The hydrolysis of the herbicide safener mefenpyrdiethyl (1-(2, 4-dichlorophenyl)-4, 5-dihydro-5-methyl-1H-pyrazole-3,5-dicarboxylic acid diethyl ester) was investigated in aqueous solutions in the pH range from 2 to 9 and the temperature
range from 298 to 323 K. The kinetics of hydrolysis were pseudo first order and were found to be strongly pH and temperature
dependent. While near-constant in acidic medium, the hydrolysis rates strongly increased in alkaline pH, and total hydrolysis
was observed at pH 11. Two main hydrolysis products, mefenpyrethyl (monoester) and mefenpyr (dicarboxylic acid) were isolated
by ultrahigh-pressure liquid chromatography (UHPLC) and characterized using high-resolution Fourier transform ion cyclotron
resonance mass spectroscopy (ICR-FT/MS) as well as 1H, 13C and 2D NMR analyses. Additionally, a density functional theory (DFT) investigation explained the stability of the pesticide
at pH 7 and the high reactivity of the pesticide in alkaline medium. The key nucleophilic reaction partner is hydroxyl ions
instead of neutral water molecules. Furthermore, the calculated activation barrier for hydrolysis in alkaline medium is in
agreement with the extrapolated and experimentally determined activation barrier at pH 14. 相似文献
42.
Amina A. El-Taras Ibrahim M. EL-Mehasseb Abd El-Motaleb M. Ramadan 《Comptes Rendus Chimie》2012,15(4):298-310
The picolyl hydrazone ligands derived from picolonic acid hydrazide and α-pyridyle ketone (L1, L2 and L3), α-acetyl thiophene (L4), α-formyl or α-acetyl phenol (L5 and L6 respectively) and 2-hydroxy-1-naphthaldehyde (L7) react with equimolecular amount of vanadyl sulfate in refluxing methanol to yield oxidovanadium (IV) complexes. The structure of the obtained ligands and their oxidovanadium (IV) complexes were characterized by various physicochemical techniques, viz. elemental analysis, molar conductance, magnetic susceptibility measurements, thermal analysis (TGA & DTG), IR, electronic absorption and ESR spectral studies. Cyclic voltammeteric behavior of the complexes has also been discussed. Five-coordinate square-pyramidal structure was proposed for all complexes. A monomeric nature was reported for complexes (2), (3), (6), and (7), while dimeric structures were suggested for complexes (1), (4) and (5). The ability of the complexes to catalyze the aerobic oxidation of catechol to the light absorbing o-quinone has been investigated. The results obtained show that all complexes catalyze this oxidation reaction and large variations in the rate were observed. Electrochemical data for most complexes show that there is a linear relationship between their ability to oxidize catechole and their E1/2 potentials. The most effective catalysts were those complexes which exhibited E1/2 values approached to the E° value of the natural tyrosinase enzyme isolated from mushroom, while those that largely deviated from that potential exhibited lower oxidase catalytic activity. The probable mechanistic implications of the catalytic oxidation reactions are discussed. 相似文献
43.
A new simple extractive spectrophotometric method has been developed for the determination of levofloxacin (I), norfloxacin (II), and ciprofloxacin (III) in pure form and tablets. The method is based on the formation of blue‐colored ion‐pair associates between the drugs and the inorganic complex, cobalt (II) thiocyanate, at pH 2.5. Those ion‐pair associates are readily extracted into an n‐butanol‐dichloromethane solvent mixture (3.5:6.5) and determined spectrophotometrically at 623 nm. The concentration range is 20–240 μg mL?1 for the three studied drugs. The proposed method was successfully applied to determine these drugs in their tablet formulations, and the results are in good agreement with those obtained by the reference methods. 相似文献
44.
Smrithi Krishnan R. Neethu Puthumadathil Amina H. Shaji K. Santhosh Kumar Gayathri Mohan Kozhinjampara R. Mahendran 《Chemical science》2021,12(2):639
Synthetic alpha-helix based pores for selective sensing of peptides have not been characterized previously. Here, we report large transmembrane pores, pPorA formed from short synthetic alpha-helical peptides of tunable conductance and selectivity for single-molecule sensing of peptides. We quantified the selective translocation kinetics of differently charged cationic and anionic peptides through these synthetic pores at single-molecule resolution. The charged peptides are electrophoretically pulled into the pores resulting in an increase in the dissociation rate with the voltage indicating successful translocation of peptides. More specifically, we elucidated the charge pattern lining the pore lumen and the orientation of the pores in the membrane based on the asymmetry in the peptide-binding kinetics. The salt and pH-dependent measurements confirm the electrostatic dominance and charge selectivity in controlling target peptide interaction with the pores. Remarkably, we tuned the selectivity of the pores to charged peptides by modifying the charge composition of the pores, thus establishing the molecular and electrostatic basis of peptide translocation. We suggest that these synthetic pores that selectively conduct specific ions and biomolecules are advantageous for nanopore proteomics analysis and synthetic nanobiotechnology applications.Synthetic alpha-helix based pores for selective sensing of peptides have not been characterized previously. 相似文献
45.
Khadija El Ouahdani Imane Es-safi Hamza Mechchate Mohammed Al-zahrani Ashraf Ahmed Qurtam Mohammed Aleissa Amina Bari Dalila Bousta 《Molecules (Basel, Switzerland)》2021,26(22)
The study of bioactive molecules of natural origin is a focus of current research. Thymus algeriensis and Artemisia herba-alba are two medicinal plants widely used by the Moroccan population in the traditional treatment of several pathologies linked to inflammation. This study aimed to evaluate the single and combined antioxidant, anti-inflammatory and analgesic effects of the essential oils extracted from these two medicinal plants, and also their potential toxicity. Essential oils were extracted using hydro-distillation in a Clevenger-type apparatus. The antioxidant activity was evaluated by two methods: the scavenging of the free radical DPPH, and the reduction in iron. Anti-inflammatory activity was evaluated by evaluating the edema development induced by carrageenan injecting, while the analgesic power was evaluated according to the number of abdominal contortions induced by the intraperitoneal injection of acetic acid (0.7%). The acute oral toxicity was performed to assess the potential toxicity of the studied EOs, followed by an analysis of the blood biochemical parameters. The results of the two antioxidant tests indicated that our extract mixture exhibits good iron reduction capacity and very interesting DPPH free radical scavenging power, with an IC50 of around 4.38 ± 0.98 μg/mL higher than that of the benchmark antioxidant, BHT. The anti-inflammatory test demonstrated that the mixture administered orally at a dose of 150 mg/kg has a better activity, exceeding that of 1% Diclofenac, with a percentage of maximum inhibition of the edema of 89.99 ± 4.08. The number of cramps in the mice treated with the mixture at a dose of 150 mg/kg is significantly lower (29.80 ± 1.92) than those of the group treated with Tramadol (42.00 ± 2.70), respectively. The toxicity results show no signs of toxicity with an LD50 greater than 150 mg/Kg. These interesting results show that the two plants’ EOs had an important anti-inflammatory, analgesic, and antioxidant activity, and also a powerful synergistic effect, which encourages further in-depth investigations on their pharmacological proprieties. 相似文献
46.
Igor A. Kaltashov Robert J. Cotter W. Harry Feinstone Gary W. Ketner Amina S. Woods 《Journal of the American Society for Mass Spectrometry》1997,8(10):1070-1077
Ferrichrome, a fungal siderophore that is also utilized by some bacterial species, was studied with liquid secondary ion mass spectrometry (LSIMS) and matrix-assisted laser desorption ionixation (MALDI) mass spectrometry. A strong ionic signal corresponding to a FeIII complex was observed with LSIMS in the positive ion mode. Switching the polarity of the mass spectrometer did not necessarily result in reduction of ferric ion, although certain conditions led to appearance of a FeII complex signal as well. The results of the structural studies of the metal ion-cyclic peptide complex with collisionally induced dissociation allowed unambiguous identification of the chelation sites. The action of the siderophore on FeIII was studied by in vitro chelation of ferric ion (from ferric citrate) by the iron-free ferrichrome. Effective chelation of ferric ion was compared to actions of the iron-free ferrichrome on other metal ions. Unlike LSIMS, desorption with MALDI did not form selectively molecular ions of intact ferrichrome: the spectra contained abundant peaks corresponding to the cyclic peptide itself and its nonspecific association with alkali metal ions. 相似文献
47.
Amina Amassad Meir Shillor Mircea Sofonea 《Mathematical Methods in the Applied Sciences》1999,22(3):267-284
We consider a mathematical model which describes the bilateral quasistatic contact of a viscoelastic body with a rigid obstacle. The contact is modelled with a modified version of Coulomb's law of dry friction and, moreover, the coefficient of friction is assumed to depend either on the total slip or on the current slip. In the first case, the problem depends upon contact history. We present the classical formulations of the problems, the variational formulations and establish the existence and uniqueness of a weak solution to each of them, when the coefficient of friction is sufficiently small. The proofs are based on classical results for elliptic variational inequalities and fixed point arguments. We also study the dependence of the solutions on the perturbations of the friction coefficient and obtain a uniform convergence result. Copyright © 1999 John Wiley & Sons, Ltd. 相似文献
48.
Pankaj Bandhoria Vivek K. Gupta Musarat Amina Naresh K. Satti Prabhu Dutt Krishan A. Suri 《Journal of chemical crystallography》2006,36(2):153-159
6α,7α-epoxy-5α,17α,dihydroxy-1-oxo-22R-witha-2,24-dienolide (C28H38O6) was isolated from Withania somnifera leaves. The structure of the withanolide was established by spectral analysis and X-ray diffraction studies as withanone. The compound crystallizes in the orthorhombic space group P212121 with unit cell parameters: a = 9.191(10) Å, b = 12.858(6) Å, c = 21.400(16) Å, Z = 4. The crystal structure was solved by direct methods and refined to R = 0.0603 for 1742 observed reflections. There is positional disorder of the H atom in a hydroxy group (O5), resulting in two possible hydrogen-bond linkages. All the rings of the steroid skeleton are trans connected. Ring A exists in a half-chair conformation, ring B is intermediate between a half-chair and a sofa, ring C a distorted chair, and five-membered ring D is intermediate between a half-chair and an envelope. The δ-lactone ring E adopts a sofa conformation. The twist along the length of the steroid nucleus is negligible [C19–C10…C13–C18=1.8°]. Both the hydroxy groups are involved in hydrogen bonding. 相似文献
49.
Jackson SN Wang HY Woods AS Ugarov M Egan T Schultz JA 《Journal of the American Society for Mass Spectrometry》2005,16(2):133-138
After water, lipids are the most common biomolecules found in the brain (12%). A brief perusal of the physiology, anatomy,
and pathophysiology of the brain illustrates the importance of lipids. Recent advances in mass spectrometry have allowed the
direct probing of tissues. However, most studies have focused on proteins. In the present work, matrix-assisted laser desorption/ionization
time-of-flight mass spectrometry (MALDI-TOFMS) and MALDI-ion mobility (IM)-TOFMS were employed for direct analysis of phospholipids
in rat brain tissue. Molecular ions (MH+) corresponding to phosphatidylcholines, phosphatidylethanolamines, and sphingomyelin, were recorded. When studying pharmacology,
we learn that many therapeutic compounds are stored in the body’s adipose tissue. MALDI-TOFMS and MALDI- IM-TOFMS were thus
used to analyze rat brain tissue with chlorisondamine added directly onto the tissue slice. With both techniques, noncovalent
complexes between the tissue phospholipids and chlorisondamine were detected. In addition, MALDI-IM-TOFMS of noncovalent complexes
between phospholipids and chlorisondamine displayed a mobility between that of an isobaric lipid and peptide. 相似文献
50.