Search results for "Decarboxylation"

showing 10 items of 56 documents

Ketorolac beats ketoprofen: lower photodecarboxylation, photohemolysis and phototoxicity

2013

Ketorolac shows reduced photohemolytic activity and low phototoxicity against human skin fibroblasts when compared to ketoprofen. The low decarboxylation quantum yield together with the efficient non-radiative deactivation of the triplet and singlet excited states of ketorolac are believed to be responsible for this behaviour.

PharmacologyKetoprofenDecarboxylationChemistryOrganic ChemistryPharmaceutical ScienceQuantum yieldHuman skinPharmacologyPhotochemistryBiochemistryKetorolacExcited stateDrug DiscoverymedicineMolecular MedicineSinglet statePhototoxicitymedicine.drugMedChemComm
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Zur Wirkung von Butazolidin im Intermedi�rstoffwechsel

1956

Butazolidin (Phenylbutazone) inhibits the oxidative decarboxylation of pyruvate and α-ketoglutarate in a final concentration of 10 mg-% (3,24 · 10−4 m). Data are presented suggesting that the β-ketothiolase is inhibited. The following enzymes or enzyme systems are not inhibited: The enzymes of the respiratory chain, the enzymes of the citric acid cycle with exception of α-ketoglutaric oxidase, the glycolysis of hexosediphosphate (slight inhibition), acetate thiokinase, sulfanilamid transacetylase, pyruvic decarboxylase from yeast, arginase, xanthine oxidase, and D-amino acid oxidase.

Pharmacologychemistry.chemical_classificationOxidase testRespiratory chainGeneral MedicineCitric acid cyclechemistry.chemical_compoundEnzymechemistryBiochemistryAcetate thiokinaseXanthine oxidaseOxidative decarboxylationPyruvate decarboxylaseNaunyn-Schmiedebergs Archiv f�r Experimentelle Pathologie und Pharmakologie
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Regional differences of substrate oxidation capacity in rat hearts: effects of extra load and endurance training.

1990

Male rats, aged 17 weeks at the end of experiments, were divided into four groups. Two groups lived in normal cage conditions with or without extra load (20% of the body weight) and two groups were trained by running with or without extra load for 8 weeks. Oxidation rates of succinate, glutamate + malate, palmitoylcarnitine, and pyruvate, and the activities of lactate dehydrogenase, citrate synthase, isocitrate dehydrogenase and cytochrome oxidase were measured in homogenates of the right ventricle and in those of the subendocardial and subepicardial layers of the left ventricle. Oxidation rates of succinate and palmitoylcarnitine tended to be higher in the subendocardium than in the subepi…

Pyruvate decarboxylationMalemedicine.medical_specialtyPhysiologyPhysical exerciseCitrate (si)-Synthasechemistry.chemical_compoundEndurance trainingPhysiology (medical)Lactate dehydrogenaseInternal medicinePhysical Conditioning AnimalmedicineCitrate synthaseCytochrome c oxidaseAnimalsPalmitoylcarnitinebiologyMusclesMyocardiumBody WeightRats Inbred StrainsRatsmedicine.anatomical_structureEndocrinologychemistryVentriclebiology.proteinPhysical EnduranceCardiology and Cardiovascular MedicineEnergy MetabolismOxidation-ReductionBasic research in cardiology
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Pyruvate kinase type M2: a crossroad in the tumor metabolome.

2002

Cell proliferation is a process that consumes large amounts of energy. A reduction in the nutrient supply can lead to cell death by ATP depletion, if cell proliferation is not limited. A key sensor for this regulation is the glycolytic enzyme pyruvate kinase, which determines whether glucose carbons are channelled to synthetic processes or used for glycolytic energy production. In unicellular organisms pyruvate kinase is regulated by ATP, ADP and AMP, by ribose 5-P, the precursor of the nucleic acid synthesis, and by the glycolytic intermediate fructose 1,6-P2 (FBP), thereby adapting cell proliferation to nutrient supply. The mammalian pyruvate kinase isoenzyme type M2 (M2-PK) displays the …

Pyruvate decarboxylationNutrition and DieteticsPyruvate dehydrogenase kinaseFatty AcidsPyruvate KinaseMedicine (miscellaneous)Glutamic AcidPyruvate dehydrogenase phosphataseBiologyPKM2Pyruvate dehydrogenase complexPyruvate carboxylaseNeoplasm ProteinsBiochemistryNeoplasmsAnimalsHumansGlycolysisPyruvate kinaseCell DivisionHydrogenThe British journal of nutrition
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Pyruvate fermentation by Oenococcus oeni and Leuconostoc mesenteroides and role of pyruvate dehydrogenase in anaerobic fermentation.

2005

ABSTRACT The heterofermentative lactic acid bacteria Oenococcus oeni and Leuconostoc mesenteroides are able to grow by fermentation of pyruvate as the carbon source (2 pyruvate → 1 lactate + 1 acetate + 1 CO 2 ). The growth yields amount to 4.0 and 5.3 g (dry weight)/mol of pyruvate, respectively, suggesting formation of 0.5 mol ATP/mol pyruvate. Pyruvate is oxidatively decarboxylated by pyruvate dehydrogenase to acetyl coenzyme A, which is then converted to acetate, yielding 1 mol of ATP. For NADH reoxidation, one further pyruvate molecule is reduced to lactate. The enzymes of the pathway were present after growth on pyruvate, and genome analysis showed the presence of the corresponding st…

Pyruvate decarboxylationPyruvate dehydrogenase kinaseEcologyPyruvate Dehydrogenase ComplexPyruvate dehydrogenase phosphataseBiologyPyruvate dehydrogenase complexPhysiology and BiotechnologyApplied Microbiology and BiotechnologyPyruvate carboxylaseCulture MediaGram-Positive CocciBiochemistryPyruvate oxidase activityFermentationPyruvic AcidFermentationAnaerobiosisDihydrolipoyl transacetylaseLeuconostocFood ScienceBiotechnologyApplied and environmental microbiology
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Analysis of the Decarboxylation Step in Mammalian Histidine Decarboxylase

2008

We report a hybrid quantum mechanics/molecular mechanics theoretical study on the reaction mechanism of mammalian histidine decarboxylase that allows us to obtain valuable insights on the structure of the cofactor-substrate adduct (external aldimine) in the active site of rat histidine decarboxylase. By means of molecular dynamics simulations, we traced the potential of mean force corresponding to the decarboxylation reaction of the adduct both in the active site of the enzyme and in aqueous solution. By comparing this process in both media, we have identified the key electrostatic interactions that explain the lowering of the free energy barrier in the enzyme. Our analysis also offers a va…

Reaction mechanismbiologyChemistryStereochemistryDecarboxylationActive siteCell BiologyBiochemistryHistidine decarboxylaseMolecular mechanicsAdductMolecular dynamicsbiology.proteinBinding siteMolecular BiologyJournal of Biological Chemistry
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Durch sterische effekte stabilisierte ß-ketocarbonsäuren

1989

Abstract Increasing steric hindrance in β-keto carboxylic acids leads to an increasing kinetic stability towards decarboxylation, till systems are reached which are completely stable at room temperature. Simultaneously the tautomeric equilibrium is changed in favour of the (Z)-enol, and finally in favour of the (E)-configurated enol.

Steric effectschemistry.chemical_compoundChemistryDecarboxylationOrganic ChemistryDrug DiscoveryOrganic chemistryKeto–enol tautomerismAliphatic compoundBiochemistryMedicinal chemistryTautomerEnolTetrahedron Letters
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ChemInform Abstract: Photoinduced Functionalization of the C-20 Methyl Group of the Nor-diterpene Atractyligenin.

2010

Abstract Irradiation of the nor-diterpene atractyligenin at λ =254 nm in methanol gave, on one hand, the decarboxylation product, and provided, on the other hand, the transformation of the C-20 angular methyl into a methylene-carbomethoxy group. A photochemical pathway involving formation of C-19/C-20 bond is suggested.

Terpenechemistry.chemical_compoundDecarboxylationChemistryStereochemistrySurface modificationGeneral MedicineMethanolDiterpeneAtractyligeninMethyl groupChemInform
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Catalytic aerobic oxidative decarboxylation of α-trifluoromethyl-α-hydroxy acids to trifluoromethyl ketones

2003

Abstract The oxidative decarboxylation of α-trifluoromethyl-α-hydroxy acids to trifluoromethyl ketones is carried out under mild catalytic aerobic conditions using a cobalt(III) complex in the presence of pivalaldehyde.

TrifluoromethylChemistryDecarboxylationOrganic Chemistrychemistry.chemical_elementGeneral MedicineMedicinal chemistryBiochemistryCatalysischemistry.chemical_compoundDrug DiscoveryOrganic chemistryCobaltOxidative decarboxylationTetrahedron
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The potential of positively-charged cellulose sponge for malolactic fermentation of wine, using Oenococcus oeni

2001

Malolactic fermentation (MLF) is a secondary bioconversion developed in some wines involving malic acid decarboxylation. The induction of MLF in wine by cultures of free and immobilized Oenococcus oeni cells was investigated. This work reports on the effect of surface charges in the immobilization material, a recently described fibrous sponge, as well as the pH and the composition of the media where cells are suspended. A chemical treatment provided positive charge to the sponges (DE or DEAE) and gave the highest cell loadings and subsequent resistance to removal. Preculture media to grow the malolactic bacteria before the immobilization procedure were also evaluated. We have established fa…

WineChromatographybiologyBioconversionDecarboxylationfood and beveragesBioengineeringbiology.organism_classificationApplied Microbiology and BiotechnologyBiochemistrychemistry.chemical_compoundchemistryBiochemistryMalolactic fermentationMalic acidCelluloseBacteriaBiotechnologyOenococcus oeniEnzyme and Microbial Technology
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