Search results for "CONFIGURATION"

showing 10 items of 601 documents

Effect of the ΔPhe residue configuration on a didehydropeptides conformation: A combined CD and NMR study.

2010

Conformations of two pairs of dehydropeptides with the opposite configuration of the ΔPhe residue, Boc-Gly-Δ(Z)Phe-Gly-Phe-OMe (Z-OMe), Boc-Gly-Δ(E)Phe-Gly-Phe-OMe (E-OMe), Boc-Gly-Δ(Z)Phe-Gly-Phe-p-NA (Z-p-NA), and Boc-Gly-Δ(E)Phe-Gly-Phe-p-NA (E-p-NA) were compared on the basis of CD and NMR studies in MeOH, trifluoroethanol (TFE), MeCN, chloroform, and dimethylsulfoxide (DMSO). The CD results were used as the additional input data for the NMR-based determination of the detailed solution conformations of the peptides. It was found that E-OMe is unordered and Z-OMe, Z-p-NA, and E-p-NA adopt the β-turn conformation. There are two overlapping β-turns in each of those peptides: type II and ty…

Models MolecularCircular dichroismanimal structuresdehydropeptide conformationMagnetic Resonance SpectroscopyStereochemistryProtein ConformationPhenylalanineBiophysicsStereoisomerismBiochemistrydehydrophenylalanine configurationBiomaterialschemistry.chemical_compoundResidue (chemistry)Protein structureotorhinolaryngologic diseasesMoleculeAmino Acid SequencePeptide sequenceChloroformintegumentary systemMolecular StructureCircular DichroismOrganic ChemistryTemperatureStereoisomerismGeneral MedicineNuclear magnetic resonance spectroscopySolutionsnuclear magnetic resonancedehydropeptideschemistrySpectrophotometryOligopeptidesBiopolymers
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A surprising switch in absolute configuration of anti-inflammatory macrolactones.

2016

Oxacyclododecindione-type macrolactones exhibit highly potent anti-inflammatory activities even at nanomolar concentration. After the determination of the relative configuration of the stereocenters at C14 and C15 by total synthesis of 4-dechloro-14-deoxyoxacyclododecindione and 14-deoxyoxacyclododecindione, the absolute configuration has now been assigned by X-ray crystallography. Surprisingly, the absolute configuration is (14S,15R) which differs for C15 from that of the well-known derivatives of (S)-curvularin. The biological activities of both enantiomers of 14-deoxyoxacyclododecindione, obtained by racemic synthesis and optical resolution, were investigated and the ring conformation of…

Models MolecularMacrocyclic CompoundsStereochemistryAnti-Inflammatory AgentsMolecular ConformationStereoisomerism010402 general chemistryRing (chemistry)Crystallography X-Ray01 natural sciencesBiochemistryStereocenterchemistry.chemical_compoundHumansPhysical and Theoretical ChemistryNatural product010405 organic chemistryChemistryOrganic ChemistryAbsolute configurationTotal synthesisStereoisomerismCurvularinHep G2 Cells0104 chemical sciencesEnantiomerOrganicbiomolecular chemistry
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Synthesis of Pyrrolo[1,2-a]pyrimidine Enantiomers via Domino Ring-Closure followed by Retro Diels-Alder Protocol

2017

From 2-aminonorbornene hydroxamic acids, a simple and efficient method for the preparation of pyrrolo[1,2-a]pyrimidine enantiomers is reported. The synthesis is based on domino ring-closure followed by microwave-induced retro Diels-Alder (RDA) protocols, where the chirality of the desired products is transferred from norbornene derivatives. The stereochemistry of the synthesized compounds was proven by X-ray crystallography. The absolute configuration of the product is determined by the configuration of the starting amino hydroxamic acid. peerReviewed

Models MolecularMagnetic Resonance SpectroscopyPyrimidinehydroxamic acidStereochemistryPharmaceutical ScienceChemistry Techniques SyntheticCrystallography X-RayHydroxamic Acids010402 general chemistryRing (chemistry)01 natural sciencesArticleDominoAnalytical Chemistrymicrowave chemistrylcsh:QD241-441chemistry.chemical_compoundlcsh:Organic chemistryDrug DiscoveryPhysical and Theoretical ChemistryN-heterocyclesta116Norbornenedomino reactions; hydroxamic acid; microwave chemistry; <i>N</i>-heterocycles; retro Diels-Alder reactionHydroxamic acidMolecular Structure010405 organic chemistryretro Diels-Alder reactionOrganic Chemistrydomino reactionsAbsolute configurationStereoisomerism0104 chemical sciencesPyrimidineschemistryChemistry (miscellaneous)Molecular MedicineEnantiomerChirality (chemistry)Molecules; Volume 22; Issue 4; Pages: 613
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Polyketide Derivatives from Mangrove Derived Endophytic Fungus Pseudopestalotiopsis theae

2020

Chemical investigation of secondary metabolites from the endophytic fungus Pseudopestalotiopsis theae led to the isolation of eighteen new polyketide derivatives, pestalotheols I&ndash

Models MolecularMagnetic Resonance SpectroscopyStereochemistryPharmaceutical Science010402 general chemistry01 natural sciencesArticlePolyketidepolyketideDrug DiscoverymedicineEndophytesCytotoxicityPharmacology Toxicology and Pharmaceutics (miscellaneous)IC50lcsh:QH301-705.5endophytic fungusbiologyMolecular Structure010405 organic chemistryChemistryAbsolute configurationFungibiology.organism_classification0104 chemical sciencesAcinetobacter baumanniiPseudopestalotiopsis theaelcsh:Biology (General)<i>Pseudopestalotiopsis theae</i>PolyketidesFermentationColistincytotoxicityRhizophoraceaeAntibacterial activityTwo-dimensional nuclear magnetic resonance spectroscopymedicine.drugMarine Drugs
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The unique structure of complete lipopolysaccharide isolated from semi-rough Plesiomonas shigelloides O37 (strain CNCTC 39/89) containing (2S)-O-(4-o…

2013

The complete structure of semi-rough lipopolysaccharide (SR-LPS) of Plesiomonas shigelloides CNCTC 39/89 (serotype O37) has been investigated by (1)H and (13)C NMR spectroscopy, matrix-assisted laser-desorption/ionization time-of-flight MS, and chemical methods. The following structure of the single unit of the O-antigen has been established: [formula see text] in which α-D-Lenp is (2S)-O-(4-oxopentanoic acid)-α-D-Glcp residue which has not been found in nature. The absolute configuration of oxopentanoic acid moiety in α-d-Lenose residue was determined by NOESY experiment combined with molecular modeling (MM2 force field). The decasaccharide core is substituted at C-4 of the β-D-Glcp residu…

Models MolecularMolecular modelStereochemistryMolecular Sequence DataAnalytical chemistryDisaccharideBiochemistryAnalytical Chemistrychemistry.chemical_compoundResidue (chemistry)GlucosidesCarbohydrate ConformationMoietybiologyOrganic ChemistryAbsolute configurationO AntigensGeneral MedicineCarbon-13 NMRbiology.organism_classificationLevulinic AcidsCarbohydrate SequencechemistryPlesiomonas shigelloidesPlesiomonasTwo-dimensional nuclear magnetic resonance spectroscopyCarbohydrate Research
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Theory of CaL2,3-edge XAS using a novel multichannel multiple-scattering method

2003

A new method for calculating X-ray absorption spectroscopy (XAS) at the L2,3 edges of Ca and transition metals is presented. It is based on the multichannel multiple-scattering theory by Natoli et al. [Phys. Rev. B, (1990), 42, 1944-1968] combined with the eigen-channel R-matrix formalism. Atomic multiplet-like effects, owing to the Coulomb interaction of photoelectrons and the 2p hole, are taken into account through a configuration interaction ansatz for the final-state wavefunction. The various multiplet states lead to a set of channels for the photoelectron wavefunction, which is calculated in multiple-scattering theory. The method is applied to Ca, an important element for biological ap…

Models MolecularNuclear and High Energy PhysicsX-ray absorption spectroscopyRadiationElectronic correlationScatteringChemistrySpectrum AnalysisX-RaysConfiguration interactionMetalloproteinsCalciumScattering theoryAtomic physicsWave functionInstrumentationMultipletAnsatzJournal of Synchrotron Radiation
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A linear Fe-O-Fe unit in bis(dibenzyldimethylammonium) mu-oxo-bis[tribromoferrate(III)].

2006

The title compound, (C 16 H 20 )N) 2 [Fe 2 Br 6 O], crystallizes with one dibenzyldimethylammonium cation and one half of a μ-oxo-bis[tribromoferrate(III)] anion in the asymmetric unit. The bridging oxo group is situated on an inversion centre, resulting in a linear conformation for the Fe-O-Fe unit. The iron(III) cations have tetrahedral geometry, with bond angles in the range 106.8 (1)-112.2 (1)°. The ion pairs are held together by Coulombic forces and C-H···Br hydrogen bonds. Each Br - anion forms one hydrogen bond. No C-H···O hydrogen bonds are found between the O atom in the Fe-O-Fe unit and surrounding counter-cations, consistent with the linear configuration of the Fe-O-Fe unit.

Models MolecularOne halfMolecular StructureHydrogen bondChemistryIronTetrahedral molecular geometryHydrogen BondingGeneral MedicineCrystal structureIon pairsCrystallography X-RayGeneral Biochemistry Genetics and Molecular BiologyIonOxygenQuaternary Ammonium CompoundsCrystallographyMolecular geometryLinear configurationActa crystallographica. Section C, Crystal structure communications
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Three-Dimensional Classification of Lower Third Molars and Their Relationship to the Mandibular Canal.

2021

PURPOSE To develop a novel classification making full use of radiographic three-dimensional (3D) information to describe the position, geometric configuration of a mandibular third molar (M3M) and its spatial relation to neighboring structures such as the mandibular canal (MC). The classification presented in this study helps to establish a common language and serves as a framework for further studies, for example, on 3D parameters influencing prognosis of the M3M and level of difficulty associated with its removal. MATERIAL AND METHODS A total of 8 parameters were included in the classification including position, the cranio-caudal height, the number of roots of the M3M as well as its spat…

MolarRadiographyGeometric configurationMandibular NerveMandibular canalMandibleInferior alveolar nerveMandibular third molar03 medical and health sciences0302 clinical medicinePosition (vector)medicineHumans610 Medicine &amp; healthRetrospective StudiesOrthodonticsbusiness.industryTooth Impacted030206 dentistrySpatial relationmedicine.anatomical_structureOtorhinolaryngology030220 oncology & carcinogenesisTooth ExtractionSurgeryMolar ThirdOral SurgerybusinessJournal of oral and maxillofacial surgery : official journal of the American Association of Oral and Maxillofacial Surgeons
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Electromagnetic properties of low-lying states in neutron-deficient Hg isotopes: Coulomb excitation of Hg-182, Hg-184, Hg-186 and Hg-188

2019

The neutron-deficient mercury isotopes serve as a classical example of shape coexistence, whereby at low energy near-degenerate nuclear states characterized by different shapes appear. The electromagnetic structure of even-mass 182-188 Hg isotopes was studied using safe-energy Coulomb excitation of neutron-deficient mercury beams delivered by the REX-ISOLDE facility at CERN. The population of $ 0^{+}_{1,2}$01,2+, $ 2^{+}_{1,2}$21,2+and $ 4^{+}_{1}$41+states was observed in all nuclei under study. Reduced E2 matrix elements coupling populated yrast and non-yrast states were extracted, including their relative signs. These are a sensitive probe of shape coexistence and may be used to validate…

MomentsIntruder01 natural sciencesMOMENTSNuclear ExperimentPhysicseducation.field_of_studyYrastBohr modelLIFETIMESddc:Mean field theorysymbolsFísica nuclearAtomic physicsydinfysiikkaConfigurationNuclear and High Energy PhysicsELECTRIC-MONOPOLE TRANSITIONS3106PopulationElectric-monopole transitionsDEFORMED BANDSLifetimesCoulomb excitationNUCLEAR[PHYS.NEXP]Physics [physics]/Nuclear Experiment [nucl-ex]114 Physical sciencessymbols.namesakeIsomerismSHAPE COEXISTENCE0103 physical sciencesNuclear fusionNuclear Physics - ExperimentNeutronNuclear010306 general physicseducationCONFIGURATIONDeformed bands010308 nuclear & particles physicsINTRUDERShape coexistence2207 Física Atómica y NuclearDecayPhysics and Astronomy13. Climate actionISOMERISMInteracting boson modelDECAY
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Hydrolase–like catalysis and structural resolution of natural products by a metal–organic framework

2020

[EN] The exact chemical structure of non-crystallising natural products is still one of the main challenges in Natural Sciences. Despite tremendous advances in total synthesis, the absolute structural determination of a myriad of natural products with very sensitive chemical functionalities remains undone. Here, we show that a metal-organic framework (MOF) with alcohol-containing arms and adsorbed water, enables selective hydrolysis of glycosyl bonds, supramolecular order with the so-formed chiral fragments and absolute determination of the organic structure by single-crystal X-ray crystallography in a single operation. This combined strategy based on a biomimetic, cheap, robust and multigr…

Multidisciplinary010405 organic chemistryChemistryChemical structureScienceQSupramolecular chemistryAbsolute configurationGeneral Physics and AstronomyTotal synthesisGeneral ChemistryMetal-organic frameworks010402 general chemistry01 natural sciencesCombinatorial chemistryGeneral Biochemistry Genetics and Molecular BiologyArticle0104 chemical sciencesCatalysisHydrolysisHydrolaseBiocatalysisMoleculelcsh:Qlcsh:ScienceNature Communications
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