Search results for "LDOS"

showing 10 items of 108 documents

Conflicto entre los cabildos catedralicios y las inquisiciones ibéricas en la Edad Moderna

2021

UNESCO::HISTORIA0210-9093 553 Estudis: Revista de historia moderna 590302 2021 47 8168288 Conflicto entre los cabildos catedralicios y las inquisiciones ibéricas en la Edad Moderna López-Salazar CodesAna Isabel 159 180:HISTORIA [UNESCO]Revista de historia moderna 590302 2021 47 8168288 Conflicto entre los cabildos catedralicios y las inquisiciones ibéricas en la Edad Moderna López-Salazar Codes [0210-9093 553 Estudis]
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Aldosterone e sindromi coronariche acute: ruolo nel follow-up a breve e medio termine

2014

aldosterone sindrome coronarica acuta outcomeSettore MED/11 - Malattie Dell'Apparato Cardiovascolare
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Ar angiotenzīna sistēmu saistīto antihipertensīvo medikamentu aprite "A Apotheka - 58" 2015.gadā

2016

Hipertensija ir galvenais riska faktors kardiovaskulārām slimībām un smadzeņu infarktam. Viens no veidiem, kā to novērst, ir ar angiotenzīna sistēmu saistīto antihipertensīvu zāļu lietošana. Pie šiem medikamentiem pieder angiotenzīna konvertējošā enzīma inhibitoru (AKEi) un angiotenzīna receptora blokatoru (ARB) saturoši monopreparāti. Bakalaura darba mērķis bija izpētīt dažādu ar angiotenzīna sistēmu saistīto antihipertensīvo medikamentu apriti „A APOTHEKA - 58” 2015. gadā. Par pētījuma metodi autore ir izvēlējusies ārstu izrakstīto recepšu datu apkopošanu par 2015. gadu. Iegūtie dati liecina, ka 2015. gadā pieprasītāki bija AKEi saturoši monopreparāti nekā ARB saturoši monopreparāti. Auto…

angiotenzīna receptora blokatorirenīna – angiotenzīna – aldosterona sistēmaFarmācijaHipertensijaangiotenzīna konvertējošā enzīma inhibitoriantihipertensīvie medikamenti
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The Structure and Metabolism of Carbohydrates

1994

Compared with the variety of carbohydrates in plants, relatively few sugars or sugar derivatives are regularly found in animals either free or as components of more complex compounds. However, it is possible that sugars originating from plants in the diet are transiently retained in animals and distort the normal sugar spectrum. Approximately a dozen sugars and sugar derivatives are regularly found in animals: the pentoses d-ribose and 2-deoxy-d-ribose; the hexoses d-glucose, d-galactose, d-mannose, d-fructose and l-fucose; the uronic acids d-glucuronic acid and l-iduronic acid; and the hexosamines d-glucosamine and d-galactosamine. In addition, d-erythrose, d-ribulose, d-xylulose and d-sed…

chemistry.chemical_classificationAldose reductasebiologyPhosphoric Acid EstersMetabolismPentose phosphate pathwayHexosaminesSialic acidchemistry.chemical_compoundchemistryBiochemistrybiology.proteinSugarAlcohol dehydrogenase
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Structural Characterization of Glycoconjugate Polystyrene in Aqueous Solution

1999

Maltopentaose-carrying polystyrene was synthesized by the homopolymerization of vinylbenzyl maltopentaose amide. Resulted amphiphilc polymacromonomer was dissolved in 0.1 M urea aqueous solution, and its structure was characterized by small-angle X-ray scattering and molecular modeling. Maltopentaose-carrying polystyrene polymacromonomer was found to be represented by a molecular bottlebrush, composed of a large helix of polystyrene backbone and maltopentaose brushes. The molecular bottlebrush seems to be distributed randomly or many even be broken once or twice in segments with no apparent intersegmental spatial correlation. A large helix of polystyrene backbone is formed by a random seque…

chemistry.chemical_classificationAqueous solutionPolymers and PlasticsMolecular modelGlycoconjugateOrganic ChemistryRadical polymerizationInorganic Chemistrychemistry.chemical_compoundAldosechemistryAmidePolymer chemistryMaterials ChemistryUreaPolystyreneMacromolecules
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Glycoside synthesis via electrophile-induced activation of N-allyl carbamates

1993

Abstract O-Benzyl-, O-acyl-, N-acyl- and isopropylidene-protected glycosyl N-allylcarbamates, obtained from anomerically unprotected monosaccharides and allyl isocyanate, are activated by an electrophile-induced cyclisation and react with hydroxyl compounds to form the corresponding glycosides.

chemistry.chemical_classificationDipeptideorganic chemicalsOrganic ChemistryDisaccharideGlycosideBiochemistryMedicinal chemistrychemistry.chemical_compoundchemistryAldoseDrug DiscoveryElectrophileMonosaccharidelipids (amino acids peptides and proteins)GlycosylStereoselectivityTetrahedron Letters
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Noncovalent Saccharide Recognition by Means of a Tetrakis(bile acid)-Porphyrin Conjugate: Selectivity, Cooperation, and Stability

2010

Molecular recognition of Glu, Glc 2 -Glc 6 and Mal 3 by a tetrakis(bile acid)―porphyrin conjugate has been studied by using ESI-FTICR mass spectrometry. The bile acid conjugate was observed to form 1:1 noncovalent complexes with saccharides. The conjugate was found to have size-selectivity towards saccharides with three or more glucose residues. The Glc 3 and Glc 4 also formed kinetically the most stable complexes. The electron capture dissociation (ECD) experiments revealed that in complexation of an oligosaccharide three glucose residues interact with the bile acid conjugate, whereas additional glucose residues are susceptible to fragmentation. The ECD results also showed the significance…

chemistry.chemical_classificationElectron-capture dissociationBile acidmedicine.drug_classStereochemistryOrganic ChemistryOligosaccharidePorphyrinchemistry.chemical_compoundMolecular recognitionchemistryAldosemedicineNon-covalent interactionsPhysical and Theoretical ChemistryConjugateEuropean Journal of Organic Chemistry
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Synthesis of β-d-mannosides from β-d-glucosides via an intramolecular Sn2 reaction at C-2

1992

Abstract The selective synthesis of β- d -mannosides was achieved by first synthesizing β- d -glucosides that carry a N -phenylcarbamoyl protecting group at O-3. These derivatives were transformed into the corresponding β- d -mannosides by intramolecular nucleophilic substitution with inversion of configuration at C-2, the O -triflyl group being the leaving group. Subsequent intramolecular attack of the neighboring carbamoyl group resulted in the formation of the 2,3-carbonate of the desired β d -mannoside.

chemistry.chemical_classificationMannosidesIntramolecular reactionStereochemistryMolecular Sequence DataOrganic ChemistryLeaving groupGeneral MedicineBiochemistryAnalytical ChemistryCarbohydrate SequenceGlucosidesIsomerismAldosechemistryMannosidesIntramolecular forceNucleophilic substitutionSN2 reactionProtecting groupGlycoproteinsCarbohydrate Research
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Stereoselective Synthesis of β-1-O-Acyl Derivatives of Carbohydrates: An Application of the Cesium Effect.

1992

Abstract The stereoselective formation of anomerically pure 1-O-acyl derivatives of protected carbohydrates is achieved by reaction of the α-glycosyl halogenoses with cesium caboxylates.

chemistry.chemical_classificationStereochemistryOrganic Chemistrychemistry.chemical_elementBiochemistryAcylationchemistry.chemical_compoundAldosechemistryCaesiumDrug DiscoverySN2 reactionOrganic chemistrylipids (amino acids peptides and proteins)StereoselectivityCarboxylateTetrahedron Letters
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Qualitative and quantitative evaluation of mono- and disaccharides in d-fructose, d-glucose and sucrose caramels by gas–liquid chromatography–mass sp…

1999

The monosaccharide (D-fructose, D-glucose, anhydrosugars), disaccharide (glucobioses) and pseudodisaccharide (di-D-fructose dianhydrides) content of D-fructose, D-glucose and sucrose caramels has been determined by gas-liquid chromatography-mass spectrometry (GLC-MS) of their trimethylsilyl (TMS) or TMS-oxime derivatives. The chromatographic profiles revealed significant differences in the disaccharide/pseudodisaccharide distribution depending on the caramel source: a D-fructose caramel contains prominent proportions of di-D-fructose dianhydrides, a D-glucose caramel mainly D-glucobioses, and a sucrose caramel similar proportions of both disaccharide/pseudodisaccharide series. It is notewor…

chemistry.chemical_classificationSucroseChromatographySilylationOrganic ChemistryDisaccharideKetoseGeneral MedicineBiochemistryAnalytical Chemistrychemistry.chemical_compoundchemistryAldoseD-GlucoseMonosaccharideOrganic chemistryGas chromatographyJournal of Chromatography A
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