Search results for "acids"

showing 10 items of 3520 documents

Molecular/chemical ecology in sponges. Evidence for an adaptive antibacterial response in Suberites domuncola

2004

Sponges (Porifera) represent the evolutionary oldest metazoan phylum still extant today. They have developed a complex Bauplan, based on the existence of structural and regulatory molecules; many of these have been cloned and analyzed in the past years. The demosponge Suberites domuncula has been used as a suitable model to demonstrate that these animals not only possess an adaptive immune response on the level of cytokines, but also, as pointed out here, on the level of synthesis of bioactive alkyl-lipid derivatives. From specimens of S. domuncula the two lyso-PAF (platelet-activating factor) compounds, 1-O-hexadecyl-sn-glycero-3-phosphocholine and 1-O-octadecyl-sn-glycero-3-phosphocholine…

chemistry.chemical_classificationEcologyATP synthasebiologyAntibacterial ResponseAquatic Sciencebiology.organism_classificationAcquired immune systemMicrobiologySuberites domunculaSpongeEnzymeDemospongechemistryBiochemistrybiology.proteinlipids (amino acids peptides and proteins)Ecology Evolution Behavior and SystematicsFunction (biology)
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A Study of the Effects of the Lewis Acid Catalysts on Oxa‐Diels‐Alder Reactions through Molecular Electron Density Theory

2020

chemistry.chemical_classificationElectron densityChemistryPolymer chemistryDiels alderNon-covalent interactionsGeneral ChemistryLewis acids and basesElectron localization functionCatalysisLewis acid catalysisChemistrySelect
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ChemInform Abstract: Lithium Enediolates and Dienediolates of Carboxylic Acids in Synthesis: Alkylation with Secondary Halides.

2010

Abstract High yields in the alkylation of dianions of α,β-unsaturated carboxylic acids with secondary halides can be obtained despite elimination reactions occurring. α-Regioselectivity for the alkylation of but-2-enoic acids ( 1–4 ) is seldom obtained. Although double bond stereoselectivity is higher than 99% for γ-alkylated products, stereoselectivity is rather poor for most of the α-alkylated products.

chemistry.chemical_classificationElimination reactionchemistryDouble bondchemistry.chemical_elementHalidelipids (amino acids peptides and proteins)LithiumStereoselectivityRather poorGeneral MedicineAlkylationMedicinal chemistryChemInform
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Utilization of C14-glucose for amino acids and protein synthesis by the sea urchin embryo

1962

chemistry.chemical_classificationEmbryo NonmammalianChemistryProtein metabolismProteinsEmbryoGeneral MedicineSea urchin embryoCarbohydrate metabolismEmbryo MammalianAmino acidchemistry.chemical_compoundGlucoseBiochemistryProtein BiosynthesisSea UrchinsProtein biosynthesisAnimalsCarbohydrate MetabolismAmino AcidsJournal of Cellular and Comparative Physiology
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Computer-Aided Rational Design of Catalytic Antibodies: The 1F7 Case.

2007

chemistry.chemical_classificationEngineering drawingCyclohexanecarboxylic AcidsMolecular StructureRotationbiologyStereochemistryChemistryChorismic AcidRational designAntibodies CatalyticStereoisomerismCatalytic antibodyGeneral ChemistryGeneral MedicineCatalysisCatalysisStructure-Activity RelationshipEnzymeCyclohexenesbiology.proteinComputer-aidedComputer SimulationAntibodyChemInform
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Synthesis of 1,3,5-Trisubstituted Hydantoins by Regiospecific Domino Condensation/Aza-Michael/O→N Acyl Migration of Carbodiimides with Activated α,β-…

2005

[reaction: see text] Carbodiimides and suitably activated alpha,beta-unsaturated carboxylic acids react effectively to afford a vast array of 1,3,5-trisubstituted hydantoins by means of a regiospecific domino condensation/aza-Michael/N--O acyl migration. The reaction works well in very mild conditions (20 degrees C, dichloromethane) with fumaric acid derivatives bearing an electron-withdrawing group in the beta position. Good results have been obtained also with less activated substrates bearing only one electron-withdrawing group in the beta position, using more polar solvents (acetonitrile, DMF), and in the presence of a base (2,4,6-trimethylpyridine). Reactions with asymmetric carbodiimi…

chemistry.chemical_classificationFumaric acidKetoneMolecular StructureBase (chemistry)ChemistryHydantoinsCarboxylic acidArylOrganic ChemistryCarboxylic AcidsRegioselectivityHydantoinStereoisomerismGeneral MedicineCondensation reactionMedicinal chemistryCarbodiimideschemistry.chemical_compoundMichael reactionOrganic chemistryChemoselectivityAcetonitrileAlkylDichloromethaneChemInform
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Transport of amino acids through liquid membranes supported on novel poly(vinylidenefluoride) porous flat-sheet matrix

1997

Flat-sheet membranes from poly(vinylidenefluoride) (PVDF) were prepared by the phase inversion process. LiCl was used as a modifying agent. The porosity, maximum pore size and LEPW (liquid entry pressure of water) were determined. Three types of these membranes were tested as a support for n-decanol supported liquid membranes (SLM). Transport of eight amino acids, selected to cover a wide variety of side chains, and of phenylalanine methyl ester through n-decanol SLM were studied. The ability of amino acids to permeates through these membranes depends on the type of flat-sheet PVDF used as a support. An increase in porosity and pore size of the microporous matrix resulted in an increase of …

chemistry.chemical_classificationGeneral Chemical EngineeringGeneral ChemistryMicroporous materialPVDF flat-sheetAmino acidMatrix (chemical analysis)membrane stabilityMembraneFlux (metallurgy)chemistryChemical engineeringSide chainOrganic chemistrysupported liquid membranePhase inversion (chemistry)amino acids transportPorosity
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A DFT study of the role of the Lewis acid catalysts in the [3 + 2] cycloaddition reaction of the electrophilic nitrone isomer of methyl glyoxylate ox…

2015

The molecular mechanism and stereoselectivity of the BF3 Lewis acid catalyzed [3 + 2] cycloaddition (32CA) reaction between C-methoxycarbonyl nitrone and cyclopentene has been theoretically studied using DFT methods at the MPWB1K/6-31G(d) computational level. The BF3 catalyst accelerates the 32CA reaction by decreasing the activation energy leading to the formation of the trans cycloadduct as the kinetic product, in agreement with the experimental data. Inclusion of solvent effects slightly increases the activation energy and decreases the exothermic character of the 32CA reaction as a consequence of a better solvation of nitrone than the transition state and the cycloadduct. The use of the…

chemistry.chemical_classificationGeneral Chemical EngineeringGeneral ChemistryPhotochemistryMedicinal chemistryCycloadditionNitroneCatalysischemistry.chemical_compoundchemistryNucleophileCyclopenteneReactivity (chemistry)Lewis acids and basesSolvent effectsRSC Advances
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Time- and concentration-dependent metabolic and genomic responses to exposure to resin acids in brown trout (Salmo trutta m. lacustris)

2006

The presence of metabolically conjugated resin acids (RAs) in the bile is considered to be a sensitive indicator for exposure of fish to pulp and paper industry effluents; however, to our knowledge, no comprehensive kinetic study of this response has been made. Juvenile brown trout (Salmo trutta m. lacustris) were exposed to a waterborne mixture of seven RAs (wood rosin) in time (0.1-192.0 h; average concentration, 8 microg/L) and dose (average concentrations, 0, 0.6, 4, 14, and 78 microg/L; 10 d) series, and total RAs were analyzed in bile. In time-dependent exposure, total RAs in bile increased up to 24 h. In concentration-dependent exposure, RAs increased along with the concentration of …

chemistry.chemical_classificationGenomeTime FactorsbiologyTroutHealth Toxicology and MutagenesisColorMetabolismbiology.organism_classificationTranscriptomeTroutBrown troutEnzymeGene Expression RegulationLiverchemistryBiochemistryGene expressionProtein biosynthesisAnimalsBileEnvironmental ChemistrySalmoAcidsEnvironmental Toxicology and Chemistry
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C-Glycosyl amino acids through hydroboration-cross-coupling of exo-glycals and their application in automated solid-phase synthesis.

2013

O-Glycosylation is one of the most important post-translational modifications of proteins. The attachment of carbohydrates to the peptide backbone influences the conformation as well as the solubility of the conjugates and can even be essential for binding to specific ligands in cell-cell interactions or for active transport over membranes. This makes glycopeptides an interesting class of compounds for medical applications. To enhance the long-term availability of these molecules in vivo, the stabilization of the glycosidic bond between the amino acid residue and the carbohydrate is of interest. The described modular approach affords β-linked C-glycosyl amino acids by a sequence of Petasis …

chemistry.chemical_classificationGlycosylationStereochemistryOrganic ChemistryMucin-1CarbohydratesGlycopeptidesGlycosidic bondGeneral ChemistryCatalysisCoupling reactionGlycopeptideAmino acidHydroborationchemistry.chemical_compoundSolid-phase synthesischemistrySuzuki reactionHumansGlycosylAmino AcidsProtein Processing Post-TranslationalSolid-Phase Synthesis TechniquesChemistry (Weinheim an der Bergstrasse, Germany)
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