Search results for "Dative"

showing 10 items of 2381 documents

The effect of cadmium on oxidative stress in Beta vulgaris

2018

As a heavy metal, cadmium has strongly toxic effects on plants and can induce oxidative stress. It is absorbed by the roots and transported to the stems and leaves. The aim of the study was to evaluate the effect of various concentrations of cadmium on the metabolic activity of Beta vulgaris and assess the dependence of these processes on the content of metal in the plants. To demonstrate the effect of cadmium on metabolism, protein and photosynthetic pigment content, lipid peroxidation, and the activity of enzymes specific for oxidative stress in roots and shoots were measured. Seeds of B. vulgaris were treated with different concentrations of Cd supplied via a CdCl2 solution: 0 (control),…

cadmiumoxidative stressBeta vulgarisEcological Chemistry and Engineering S-Chemia I Inzynieria Ekologiczna S
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Impact of Glucose-Lowering Medications on Cardiovascular and Metabolic Risk in Type 2 Diabetes

2020

Type 2 Diabetes Mellitus (T2DM) is associated with a high risk of atherosclerotic cardiovascular (CV) disease. Among the well-known pathophysiologic factors, crucial roles are played by endothelial dysfunction (caused by oxidative stress and inflammation hyperglycemia-linked), increased activity of nuclear factor kB, altered macrophage polarization, and reduced synthesis of resident endothelial progenitor cells. As consequence, a potentially rapid progression of the atherosclerotic disease with a higher propensity to unstable plaque is arguable, finally leading to significantly increased cardiovascular mortality. Main managements are focused on both prevention and early diagnosis, by target…

cardiovascular riskcardiovascular risk; dipeptidyl peptidase-4 inhibitors; glucagon like peptide-1 receptor agonists; sodium glucose cotransporter-2 inhibitors; type 2 diabetes mellitustype 2 diabetes mellitusglucagon like peptide-1 receptor agonistslcsh:Medicine030209 endocrinology & metabolismInflammationType 2 diabetesDiseaseReview030204 cardiovascular system & hematologyHypoglycemiaBioinformaticsmedicine.disease_cause03 medical and health sciences0302 clinical medicinemedicineEndothelial dysfunctionAdverse effectbusiness.industrylcsh:RType 2 Diabetes MellitusGeneral Medicinemedicine.diseasesodium glucose cotransporter-2 inhibitorsmedicine.symptombusinessdipeptidyl peptidase-4 inhibitorsOxidative stressJournal of Clinical Medicine
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Oxidative stress and small, dense low-density lipoproteins: current and future perspectives

2019

Small, dense low-density lipoproteins (LDLs) are more susceptible to oxidation than their larger, more buoyant counterparts and therefore the biological modification of these LDL particles may, in part, be responsible for their atherogenic properties. Kotani et al. found that at multiple regression analysis there was an independent and significant inverse correlation between the mean LDL particle size and the oxidative stress status; notably, the authors adjusted not only for the traditional cardiovascular risk factors, but also for drug treatments. Higher levels of small, dense LDL concentrations significantly contribute to atherosclerosis, and lipoprotein size and subfractions may refine …

cardiovascular riskoxidative stremedicine.medical_specialtySmall dense ldldense LDLEndocrinology Diabetes and Metabolismdyslipidemiasmallmedicine.diseasemedicine.disease_causechemistry.chemical_compoundEndocrinologylow-density lipoproteinchemistryInternal medicineLow-density lipoproteinmedicineLow densityDisease risklipids (amino acids peptides and proteins)Inverse correlationDyslipidemiaOxidative stressLipoproteinExpert Review of Endocrinology & Metabolism
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Parthenolide and Its Soluble Analogues: Multitasking Compounds with Antitumor Properties

2022

Due to its chemical properties and multiple molecular effects on different tumor cell types, the sesquiterpene lactone parthenolide (PN) can be considered an effective drug with significant potential in cancer therapy. PN has been shown to induce either classic apoptosis or alternative caspase-independent forms of cell death in many tumor models. The therapeutical potential of PN has been increased by chemical design and synthesis of more soluble analogues including dimethylaminoparthenolide (DMAPT). This review focuses on the molecular mechanisms of both PN and analogues action in tumor models, highlighting their effects on gene expression, signal transduction and execution of different ty…

cell deathDMAPTparthenolideSettore BIO/10 - BiochimicaMedicine (miscellaneous)cancer therapyoxidative stressapoptosiGeneral Biochemistry Genetics and Molecular BiologyNF-κB
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The Charcot Marie Tooth Disease Mutation R94Q in MFN2 Decreases ATP Production but Increases Mitochondrial Respiration under Conditions of Mild Oxida…

2019

Charcot-Marie tooth disease is a hereditary polyneuropathy caused by mutations in Mitofusin-2 (MFN2), a GTPase in the outer mitochondrial membrane involved in the regulation of mitochondrial fusion and bioenergetics. Autosomal-dominant inheritance of a R94Q mutation in MFN2 causes the axonal subtype 2A2A which is characterized by early onset and progressive atrophy of distal muscles caused by motoneuronal degeneration. Here, we studied mitochondrial shape, respiration, cytosolic, and mitochondrial ATP content as well as mitochondrial quality control in MFN2-deficient fibroblasts stably expressing wildtype or R94Q MFN2. Under normal culture conditions, R94Q cells had slightly more fragmented…

cell_developmental_biologyBioenergeticsmitochondrial fusionChemistryMitophagymedicineMFN2PINK1Mitochondrionmedicine.disease_causePyruvate kinaseOxidative stressCell biology
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ChemInform Abstract: Oxidative (Cross-)Coupling Reactions Mediated by C-H Activation of Thiophene Derivatives by Using Molybdenum(V) Reagents.

2015

The use of MoCl5 renders possible the preparation of various synthetically important polycyclic thienoacenes.

chemistryMolybdenumReagentchemistry.chemical_elementGeneral MedicineOxidative phosphorylationThiophene derivativesCombinatorial chemistryCoupling reactionChemInform
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MoVReagents in Organic Synthesis

2016

The use of MoV reagents, and in particular MoCl5, in organic synthesis is surveyed. The oxidative treatment of aromatic substrates is the most common application. The unique properties of these reagents are due to their high oxidative power combined with exquisite Lewis acid properties. In several examples MoV reagents outperform other common oxidative coupling reagents. C–C bond formation through inter- and intramolecular oxidative coupling can lead to selective formation of five- to eight-membered ring systems. Mechanistic investigations of the courses of reactions involving MoV reagents and aromatic substrates indicate that radical cations are initially formed, entering the oxidative cou…

chemistry.chemical_classification010405 organic chemistryChemistryOrganic ChemistryAlkyne010402 general chemistry01 natural sciences0104 chemical scienceschemistry.chemical_compoundIntramolecular forceReagentOrganic chemistryStereoselectivityOxidative coupling of methaneOrganic synthesisLewis acids and basesPhysical and Theoretical ChemistryIsomerizationEuropean Journal of Organic Chemistry
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Influence of the Ligand of Palladium(0) Complexes on the Rate of the Oxidative Addition of Aryl and Activated Alkyl Bromides: Csp2 −Br versus Csp3 −B…

2017

Kinetic data by means of electrochemical techniques are used to characterize the reactivity of aryl bromides and activated alkyl bromides in oxidative addition to palladium(0) complexes generated from three precursors: Pd0(PPh3)4, {Pd0(dba)2 + 2 PPh3} and {Pd0(dba)2 + 2 P(o Tol)3} in DMF at 25 °C. It is established that, for the investigated substrates 1-6 and 7-11, the oxidative addition at the Csp3 Br bond is much faster than that at the Csp2 Br bond when the palladium(0) is ligated by two PPh3. This explains why the regioselectivity in Suzuki-Miyaura reactions performed from substrates bearing both Csp2 Br and Csp3 Br groups is in favour of the substitution at the Csp3 Br bond. It is in …

chemistry.chemical_classification010405 organic chemistryConcerted reactionLigandArylOrganic ChemistryRegioselectivitychemistry.chemical_element010402 general chemistryPhotochemistry01 natural sciencesMedicinal chemistryOxidative additionCatalysis0104 chemical sciencesInorganic Chemistrychemistry.chemical_compoundchemistryReactivity (chemistry)Physical and Theoretical ChemistryAlkylPalladiumChemCatChem
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Synthesis of α-aminonitriles using aliphatic nitriles, α-amino acids, and hexacyanoferrate as universally applicable non-toxic cyanide sources

2018

In cyanation reactions, the cyanide source is often directly added to the reaction mixture, which restricts the choice of conditions. The spatial separation of cyanide release and consumption offers higher flexibility instead. Such a setting was used for the cyanation of iminium ions with a variety of different easy-to-handle HCN sources such as hexacyanoferrate, acetonitrile or α-amino acids. The latter substrates were first converted to their corresponding nitriles through oxidative decarboxylation. While glycine directly furnishes HCN in the oxidation step, the aliphatic nitriles derived from α-substituted amino acids can be further converted into the corresponding cyanohydrins in an oxi…

chemistry.chemical_classification010405 organic chemistryCyanideIminiumCyanation010402 general chemistry01 natural sciencesPollution0104 chemical sciencesAmino acidchemistry.chemical_compoundchemistryGlycineEnvironmental ChemistryOrganic chemistryAcetonitrileOxidative decarboxylationAcetone cyanohydrinGreen Chemistry
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Rh(I) Coordination Chemistry of Chiral α-Aminophosphine(η6-arene)chromium Tricarbonyl Ligands

2003

The diastereoselective addition of Ph(2)PH to the chiral ortho-substituted eta(6)-benzaldimine complexes (eta(6)-o-X-C(6)H(4)CH=NAr)Cr(CO)(3) (1, X = MeO, Ar = p-C(6)H(4)OMe; 2, X = Cl, Ar = Ph) leads to the formation of the corresponding chiral aminophosphines (alpha-P,N) Ph(2)P-CH(Ar(1))-NHAr(2) (3, Ar(1) = o-C(6)H(4)(OCH(3))[Cr(CO)(3)], Ar(2) = p-C(6)H(4)OCH(3); 4, Ar(1) = o-C(6)H(4)Cl[Cr(CO)(3)], Ar(2) = Ph) in equilibrium with the starting materials. The uncomplexed benzaldimine (o-ClC(6)H(4)CH=NPh), 2', analogously produces an equilibrium amount of the corresponding aminophosphine Ph(2)P-CH(Ar(1))-NHAr(2) (4', Ar(1) = o-C(6)H(4)Cl, Ar(2) = Ph). Depending on the equilibrium constant, t…

chemistry.chemical_classification010405 organic chemistryStereochemistrychemistry.chemical_elementLigands010402 general chemistry01 natural sciencesOxidative additionMedicinal chemistryStyrenes0104 chemical sciencesCoordination complexInorganic ChemistryChromiumchemistryMixturesRhodium[CHIM.COOR]Chemical Sciences/Coordination chemistryPhysical and Theoretical ChemistryMolecular structureEquilibrium constantInorganic Chemistry
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