Search results for "amide"

showing 10 items of 3119 documents

The conformation cis of N-acetyl-N-methyl-α,β-dehydroalanine N′-methylamide and saturated analogues

2007

A series of three homologous amino acids derivatives: N-acetyl-N-methyl-α,β–dehydroalanine N′-methylamide (1), N-acetyl-N-methyl-L-alanine N′-methylamide (2), and N-acetyl-N-methyl-DL-alanine N′-methylamide have been synthesised. The racemic species undergoes spontaneous separation into L and D-enantiomers. From these two chiral forms, the structure of L-enantiomer (3) was analysed. The molecules of 1 – 3 adopt the cis arrangement of the N-terminal amide bond. The molecular conformations are similar for 1 (φ, ψ = 94.6(1)°, −1.7(1)°) and 3 (φ, ψ = 111.5(1)°, −23.8(1)°), and also 2 (φ, ψ = −114.8(2)°, 29.5(2)°), if inversion through the chiral C2 carbon is considered. They are stabilised by i…

chemistry.chemical_classificationDouble bondDehydroamino acidsHydrogen bondStereochemistryMethylamidetrans-cis IsomerisationN-methylationSingle crystal structure analysisCondensed Matter PhysicsX-ray diffractionInorganic Chemistrychemistry.chemical_compoundCrystallographychemistryAmideIntramolecular forceMoleculePeptide bondGeneral Materials ScienceIsomerizationZeitschrift Fur Kristallographie
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Conformational investigation of α,β-dehydropeptides. IX. N-Acetyl-(E)-α,β-dehydrobutyrine N′-methylamide: stereoelectronic properties from infrared a…

2009

The Fourier transform infrared spectra of Ac-(E)-deltaAbu-NHMe were analyzed to determine the predominant solution conformation(s) of this (E)-alpha,beta-dehydropeptide-related compound and the electron density perturbation in its amide groups. The measurements were performed in dichloromethane and acetonitrile in the region of mode vs (N-H), amide I, amide II and vs (C(alpha)=Cbeta). The equilibrium geometrical parameters, calculated by a method based on the density functional theory with the B3LYP functional and the 6-31G* basis set, were used to support spectroscopic interpretation and gain some deeper insight into the molecule. The experimental and theoretical data were compared with th…

chemistry.chemical_classificationDouble bondHydrogen bondStereochemistryMethylamideBiochemistrychemistry.chemical_compoundEndocrinologychemistryAmideMoleculeDensity functional theoryAcetonitrileConformational isomerismThe Journal of Peptide Research
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Chemical conjugation of dexamethasone to a polyaspartamide and in vitro evaluation studies

2004

Two macromolecular conjugates of dexamethasone containing different drug amounts were synthesized using PHEA as the polymeric carrier and a succinic group as spacer. The content of linked drug was equal to 25.3% w/w (conjugate A) and 12.7% w/w (conjugate B). Both polymeric conjugates, unlike the free drug, were water-soluble and the amount of unlinked drug was evaluated to be approximately about 0.01% w/w. Both conjugates were relatively stable in vitro at pH 7.4 whereas in the presence of esterase only the conjugate B was able to release drug under the used experimental conditions. This dissimilar behavior has been attributed to the distinct macromolecular conformations assumed in aqueous …

chemistry.chemical_classificationDrugStereochemistrymedia_common.quotation_subjectPharmaceutical ScienceProdrugEsteraseCombinatorial chemistryDexamethasoneIn vitroPolyaspartamideHydrolysisEnzymechemistrySettore CHIM/09 - Farmaceutico Tecnologico ApplicativoDrug-polymer conjugatesMacromoleculemedia_commonConjugateJournal of Drug Delivery Science and Technology
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Approaching an experimental electron density model of the biologically active trans ‐epoxysuccinyl amide group—Substituent effects vs. crystal packing

2017

The trans-epoxysuccinyl amide group as a biologically active moiety in cysteine protease inhibitors such as loxistatin acid E64c has been used as a benchmark system for theoretical studies of environmental effects on the electron density of small active ingredients in relation to their biological activity. Here, the synthesis and the electronic properties of the smallest possible active site model compound are reported to close the gap between the unknown experimental electron density of trans-epoxysuccinyl amides and the well-known function of related drugs. Intramolecular substituent effects are separated from intermolecular crystal packing effects on the electron density, which allows us…

chemistry.chemical_classificationElectron densitybiology010405 organic chemistryChemistryCarboxylic acidOrganic ChemistryIntermolecular forceSubstituentActive siteContext (language use)010402 general chemistry01 natural sciences0104 chemical sciencesCrystallographychemistry.chemical_compoundAmideIntramolecular forcebiology.proteinPhysical and Theoretical ChemistryJournal of Physical Organic Chemistry
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Protochlorophyllide Reduction: Mechanisms and Evolution¶

2007

Protochlorophyllide (Pchlide) reductases are key enzymes in the process of chlorophyll biosynthesis. In this review, current knowledge on the molecular organization, substrate specificity and assembly of the light-dependent reduced nicotinamide adenine dinucleotide phosphate:Pchlide oxidoreductases are discussed. Characteristics of light-independent enzymes are also described briefly, and the possible reasons for the selection of light-dependent enzymes during the course of evolution are discussed.

chemistry.chemical_classificationEnzymeReduced nicotinamide-adenine dinucleotideProtochlorophyllideBiochemistrychemistrySubstrate specificityGeneral MedicinePhysical and Theoretical ChemistryChlorophyll biosynthesisBiologyBiochemistryPhotochemistry and Photobiology
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The Catalytic Mechanism of Carboxylesterases: A Computational Study

2014

The catalytic mechanism of carboxylesterases (CEs, EC 3.1.1.1) is explored by computational means. CEs hydrolyze ester, amide, and carbamate bonds found in xenobiotics and endobiotics. They can also perform transesterification, a reaction important, for instance, in cholesterol homeostasis. The catalytic mechanisms with three different substrates (ester, thioester, and amide) have been established at the M06-2X/6-311++G**//B3LYP/6-31G* level of theory. It was found that the reactions proceed through a mechanism involving four steps instead of two as is generally proposed: (i) nucleophilic attack of serine to the substrate, forming the first tetrahedral intermediate, (ii) formation of the ac…

chemistry.chemical_classificationEsterificationStereochemistrycomputational studiesHydrolysisSubstrate (chemistry)AlcoholTransesterificationcatalytic mechanismCrystallography X-RayThioesterBiochemistryCatalysischemistry.chemical_compoundcarboxylesterasesNucleophilechemistryhydrolysisTetrahedral carbonyl addition compoundAmideBiocatalysisCarboxylic Ester Hydrolases
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Effect of compatibilization on the photo-oxidation behaviour of polyethylene/polyamide 6 blends and their nanocomposites

2015

Abstract Polymer based nanocomposites are increasingly attracting interest from academia and industry, and the use of polymer blends as matrices greatly increase their potential field of application. In order to improve their characteristics, the use of compatibilizers acting on the blend components is mandatory. However, this also leads to rising concerns regarding the behaviour of polymer blend based nanocomposites upon being subjected to photo-oxidative degradation. It is known that morphology can deeply influence the photo-oxidative behaviour, and this can be therefore deeply influenced by the blend components and by the use of compatibilizers. In this work, polymer blend nanocomposites…

chemistry.chemical_classificationFiller (packaging)NanocompositeMaterials scienceNanocompositePolymers and PlasticsPolymerCompatibilizationPolymer blendPolyethyleneCondensed Matter PhysicsLow-density polyethylenechemistry.chemical_compoundchemistryMechanics of MaterialsPolyamideMaterials ChemistryPhoto-oxidationPolymer blendComposite materialCompatibilization
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Restricted and complete-active-space multiconfiguration linear response calculations of the polarizability of formamide and urea

1991

Abstract Using the polarized basis sets of Sadlej, we have carried out multiconfiguration linear response (MCLR) calculations of static and dynamic polarizabilities of water, carbon dioxide, formamide and urea. It is found that the polarized basis sets give a good description of the polarizabilities. The uncorrelates (self-consistent field) polarizabilities are in general 10% or more lower than the experimental values. The correlation as introduced in the complete-active-space (CAS) and restricted-active-space (RAS) MCLR calculations recovers the major part of this deviation.

chemistry.chemical_classificationFormamideField (physics)Basis (linear algebra)Triatomic moleculeGeneral Physics and AstronomyMolecular physicschemistry.chemical_compoundchemistryComputational chemistryPolarizabilityUreaPhysics::Atomic PhysicsComplete active spacePhysics::Chemical PhysicsPhysical and Theoretical ChemistryInorganic compoundChemical Physics Letters
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Fast proton conduction in hydrogen bonded microheterogeneous systems: Bis(2-ethylhexyl)phosphoric acid/N-methyl formamide liquid mixtures

2009

Structural and dynamical properties of bis(2-ethylhexyl)phosphoric acid (HDEHP)/N-methyl formamide (NMF) liquid mixtures in the whole composition range have been investigated by Fourier Transform Infrared spectroscopy (FT-IR), X-rays Diffraction (XRD), and AC complex impedance spectroscopy. Driven by hydrogen bond interactions among HDEHP PO(4)H group and NMF CO and NH groups, and also by steric effects among the HDEHP alkyl chains, the system microstructure is mainly characterized by the coexistence of spatially separated hydrophilic and hydrophobic nanodomains showing local organization and short-range order. The evolution of this structural feature with system composition has been highli…

chemistry.chemical_classificationFormamideHydrogen bondAnalytical chemistryInfrared spectroscopyFast proton conduction systems Microheterogeneous liquid mixtures Bis(2-ethylhexyl)phosphoric acid N-methyl formamidePercolation thresholdSurfaces Coatings and FilmsElectronic Optical and Magnetic MaterialsBiomaterialschemistry.chemical_compoundColloid and Surface ChemistrychemistryX-ray crystallographyFourier transform infrared spectroscopyPhosphoric acidAlkylSettore CHIM/02 - Chimica FisicaJournal of Colloid and Interface Science
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Determination of molecular weights and Stokes' radii of non-denatured proteins by polyacrylamide gradient gel electrophoresis. 1. An equation relatin…

1982

Untreated and processed gel plates of polyacrylamide (PAA) gradient gels were cut into strips perpendicularly to their length, and the wet and dry matter of the sections was determined. In untreated gels the apparent dry matter, as well as the relative dry matter, are a linear function of the gel length. In processed gels, however, only the apparent gel concentration increases linearly with the gel length, whereas the relative dry matter increases linearly with the square root of the gel length. The %T (content in polyacrylamide) was calculated from the apparent dry matter. The gel gradients used were found to be linear with respect to %T. Six different calibration proteins were run and the…

chemistry.chemical_classificationGel electrophoresisLinear function (calculus)ChromatographyMolecular massChemistryClinical BiochemistryPolyacrylamideAnalytical chemistryPolymerBiochemistryAnalytical ChemistryElectrophoresischemistry.chemical_compoundLinear regressionDry matterElectrophoresis
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