Search results for "SoMe"

showing 10 items of 5114 documents

Synthetic Approaches to Anti-Inflammatory Macrolactones of the Oxacyclododecindione Type

2015

Various synthetic approaches to the oxacyclododecindione-type macrolactones, known for their potent anti-inflammatory activity, are presented. These include an attempted carbonylative ring closure, a hydroacylation route, and an approach by ring-closing metathesis and double bond isomerization, as well as a strategy including ring-closing metathesis/unsaturation. The last route allowed the preparation of a bioactive analogue of the recently described 14-deoxyoxacyclododecindione.

chemistry.chemical_classificationDouble bondStereochemistrymedicine.drug_classOrganic ChemistryHydroacylationTotal synthesisMetathesisRing (chemistry)Anti-inflammatoryRing-closing metathesischemistrymedicinePhysical and Theoretical ChemistryIsomerizationEuropean Journal of Organic Chemistry
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ChemInform Abstract: Synthetic Approaches to Antiinflammatory Macrolactones of the Oxacyclododecindione Type.

2015

A variety of attempts to synthesize oxacyclododecindione macrolactones through carbonylative ring-closure, intramolecular alkyne hydroacyalation, and Ru-catalyzed double bond isomerization fails.

chemistry.chemical_classificationDouble bondchemistryStereochemistryIntramolecular forceSalt metathesis reactionOxacyclododecindioneAlkyneGeneral MedicineIsomerizationChemInform
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Tin compounds interaction with membranes of egg lecithin liposomes.

2007

This work is a continuation of earlier research concerning the influence of tin compounds on the dynamic properties of liposome membranes produced with lecithin hen egg yolks (EYL). The experiments were carried out at room temperature (about 25 ∞C). Four tin compounds were chosen, including three organic ones, (CH3)4Sn, (C2H5)4Sn and (C3H7)3SnCl, and one inorganic, SnCl2. The investigated compounds were admixed to water dispersions of liposomes. The content of the admixture changed within the range 0 mol-% to 11mol-% in proportion to EYL. Two spin probes were used in the experiment: 2,2,6,6-tetramethylpiperidine- 1-oxyl (TEMPO) and 2-ethyl-2-(15-methoxy-15-oxopentadecyl)-4,4-dimethyl-3-oxaz…

chemistry.chemical_classificationEgg lecithinLiposomefood.ingredientChromatographyIonic bondingchemistry.chemical_elementLecithinEgg YolkGeneral Biochemistry Genetics and Molecular BiologyCyclic N-Oxideschemistry.chemical_compoundfoodMembraneHydrocarbonchemistryLiposomesChlorinePhosphatidylcholinesAnimalsFemaleSpin LabelsTinChickensNuclear chemistryZeitschrift fur Naturforschung. C, Journal of biosciences
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Binding and isomerization energies for the Cu/CN and Cu(I)CN interactions

1993

Abstract Binding and isomerization energies of the CuCN, CuNC, CuCN+, and CuNC+ systems were investigated by means of a multireference CI perturbatively selected, MRCI-PS approach. The inclusion of the main dynamical correlation effects are evaluated. The binding energies for CuCN and CuNC are 4.37 and 4.03 eV, respectively, and those for CuCN+ and CuNC+ are 0.08 and 1.61 eV. Calculated isomerization energies are 7.86 and 35.98 kcal/mol for CuCN and Cu(I)CN isomerizations, respectively.

chemistry.chemical_classificationElectronic correlationBinding energyGaussian orbitalGeneral Physics and AstronomyConfiguration interactionBond-dissociation energyCrystallographychemistryComputational chemistryElectron affinityPhysical and Theoretical ChemistryInorganic compoundIsomerizationChemical Physics
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Hypusinated eIF5A is required for the translation of collagen.

2021

ABSTRACT Translation of mRNAs that encode peptide sequences with consecutive prolines (polyproline) requires the conserved and essential elongation factor eIF5A to facilitate the formation of peptide bonds. It has been shown that, upon eIF5A depletion, yeast ribosomes stall in polyproline motifs, but also in tripeptide sequences that combine proline with glycine and charged amino acids. Mammalian collagens are enriched in putative eIF5A-dependent Pro-Gly-containing tripeptides. Here, we show that depletion of active eIF5A in mouse fibroblasts reduced collagen type I α1 chain (Col1a1) content, which concentrated around the nuclei. Moreover, it provoked the upregulation of endoplasmic reticul…

chemistry.chemical_classificationEndoplasmic reticulumRNA-Binding ProteinsTranslation (biology)Cell BiologyTripeptideSaccharomyces cerevisiaeBiologyCell biologyAmino acidElongation factorCollagen type I alpha 1MicechemistryPeptide Initiation FactorsUnfolded protein responseAnimalsCollagenRibosomesPolyproline helixJournal of cell science
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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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Studies on Regulation of the Peroxisomal β-Oxidation at the 3-Ketothiolase Step

2002

The peroxisomal 3-oxoacyl-CoA thiolase (thiolase) is the last enzyme involved in the β-oxidation of fatty acids. The enzyme cleaves long chain fatty acyl-CoA to generate acetyl-CoA and shortened acyl-CoA. The enzyme is nuclear encoded, synthesized in the cytoplasm and transported into peroxisomes. The thiolase B gene is inducible by the peroxisome proliferator compounds, like other genes involved in β-oxidation of fatty acids in peroxisomes.

chemistry.chemical_classificationEnzymeBiochemistryPeroxisome proliferatorChemistryThiolaseCytoplasmPeroxisomeLong chainGene3-ketoacyl-CoA thiolase
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Purification of rat liver epoxide hydratase to apparent homogeneity.

1975

Epoxide hydratase (EC 4.2.1.63) is a microsomal enzyme which catalyses the conversion of epoxides to trans-dihydrodiols. Epoxides, produced by the action of microsomal monooxygenases (EC 1.14.1.1) from aromatic and olefinic compounds, are thought to be responsible for many of the harinful effects of polycyclic hydrocarbons and related compounds. Thus epoxide hydratase, together with glutathione 9transferases, (EC 2.5.1.18) may play an important role in the removal of carcinogenic and cytotoxic metabolites (for reviews see [l-3]). It has been reported [4,5] that dihydrodiols formed from some polycyclic hydrocarbons (benz(a)anthracene and benzo(a)pyrene) are reactivated by the microsomal mono…

chemistry.chemical_classificationEpoxide HydrolasesMaleAnthraceneBiophysicsCell BiologyGlutathioneMonooxygenaseBiochemistryRatsMolecular Weightchemistry.chemical_compoundEnzymechemistryBiochemistryStructural BiologyGeneticsMicrosomeMicrosomes LiverPyreneAnimalsPolycyclic HydrocarbonsMolecular BiologyCarcinogenHydro-LyasesFEBS letters
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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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Biochemical characterization of two functional human liver acyl-CoA oxidase isoforms 1a and 1b encoded by a single gene

2007

Abstract Human acyl-CoA oxidase 1 (ACOX1) is a rate-limiting enzyme in peroxisomal fatty acids β-oxidation and its deficiency is associated with a lethal, autosomal recessive disease, called pseudoneonatal-adrenoleukodystrophy. Two mRNA variants, transcribed from a single gene encode ACOX1a or ACOX1b isoforms, respectively. Recently, a mutation in a splice site has been reported [H. Rosewich, H.R. Waterham, R.J. Wanders, S. Ferdinandusse, M. Henneke, D. Hunneman, J. Gartner, Pitfall in metabolic screening in a patient with fatal peroxisomal β-oxidation defect, Neuropediatrics 37 (2006) 95–98.], which results in the defective peroxisomal fatty acids β-oxidation. Here, we show that these mRNA…

chemistry.chemical_classificationGene isoformOxidase testBiophysicsCell BiologyBiologyPeroxisomeBiochemistryIsozymeMolecular biologyArticleEnzyme ActivationIsoenzymesMolecular WeightEnzymechemistryBiochemistryLiverEnzyme StabilityAcyl-CoA oxidaseACOX1HumansHeterologous expressionAcyl-CoA OxidaseMolecular Biology
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