Search results for "Models"

showing 10 items of 8211 documents

Understanding the Mechanism of the Intramolecular Stetter Reaction. A DFT Study

2012

The mechanism of the N-heterocyclic carbene (NHC)-catalyzed intramolecular Stetter reaction of salicylaldehyde 1 to yield chromanone 3 has been theoretically studied at the B3LYP/6-31G** level. This NHC-catalyzed reaction takes place through six elementary steps, which involve: (i) formation of the Breslow intermediate IN2; (ii) an intramolecular Michael-Type addition in IN2 to form the new C-C s bond; and (iii) extrusion of the NHC catalyst from the Michael adduct to yield chromanone 3. Analysis of the relative free energies in toluene indicates that while formation of Breslow intermediate IN2 involves the rate-determining step of the catalytic process, the intramolecular Michael-type addi…

Models MolecularStereochemistryPharmaceutical Scienceintramolecular Stetter reactionDFT calculationsArticleCatalysisAnalytical ChemistryStereocenterCatalysislcsh:QD241-441chemistry.chemical_compoundlcsh:Organic chemistryComputational chemistryHeterocyclic CompoundsDrug Discoveryintramolecular Michael additionorganocatalysisN-heterocyclic carbenesPhysical and Theoretical ChemistrymechanismsChemistryOrganic ChemistryStetter reactionorganocatalysis; <em>N</em>-heterocyclic carbenes; <em>umpolung</em> reactivity; intramolecular Stetter reaction; intramolecular Michael addition; mechanisms; DFT calculationsSalicylaldehydeChemistry (miscellaneous)Yield (chemistry)OrganocatalysisIntramolecular forceumpolung reactivityMolecular MedicineCarbeneMethaneMolecules
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Conformational investigation of ?,?-dehydropeptides.N-acetyl-(E)-dehydrophenylalanineN?-methylamide: conformational properties from infrared and theo…

2005

N-Acetyl-(E)-dehydrophenylalanine N'-methylamide [Ac-(E)-DeltaPhe-NHMe], one of a few representative (E)-alpha,beta-dehydroamino acids, was studied by FTIR in dichloromethane and acetonitrile. To support spectroscopic interpretations and to gain some deeper insight into the Ac-(E)-DeltaPhe-NHMe molecule, the Ramachandran potential energy surface was calculated by the B3LYP/6-31G*//HF/3-21G method and the conformers localized were fully optimized at the B3LYP/6-31 + G** level. The spectra and calculations were compared with those of the related molecules Ac-DeltaAla-NHMe and Ac-(Z)-DeltaPhe-NHMe. The title compound assumes two conformational states in equilibrium in dichloromethane solution …

Models MolecularStereochemistryPhenylalanineMolecular ConformationRing (chemistry)Biochemistrychemistry.chemical_compoundStructural BiologySpectroscopy Fourier Transform InfraredDrug DiscoveryMoleculeAcetonitrileMolecular BiologyConformational isomerismPharmacologyMethylene ChlorideHydrogen bondOrganic ChemistryHydrogen BondingGeneral MedicineMethylamideSolutionschemistryPotential energy surfaceThermodynamicsMolecular MedicineRamachandran plotJournal of Peptide Science
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Pyrophosphate-mediated magnetic interactions in Cu(II) coordination complexes.

2010

The reaction in water of Cu(NO(3))(2)·2.5H(2)O with 2,2'-bipyridine (bipy), 1,10-phenanthroline (phen), or 1,10-phenanthroline-5-amine (phenam), and sodium pyrophosphate (Na(4)P(2)O(7)), at various pHs, afforded three new copper(II)-pyrophosphate complexes, namely, {[Cu(bipy)(cis-H(2)P(2)O(7))](2)}·3H(2)O (1a), {[Cu(phen)(H(2)O)](4)(HP(2)O(7))(2)}(ClO(4))(2)·4H(2)O (2), and {[Cu(2)(phenam)(2)(P(2)O(7))](2)·25H(2)O}(n) (3). A solvent free crystalline phase of 1a was also isolated with formula {[Cu(bipy)(trans-H(2)P(2)O(7))](2)} (1b), which can be regarded as a pseudo-polymorph of 1a. Single crystal X-ray analyses revealed these compounds to have uncommon molecular architectures, with 3 being…

Models MolecularStereochemistryPolymersSodiumchemistry.chemical_elementCrystallography X-RayPyrophosphateInorganic Chemistrychemistry.chemical_compoundMagneticsStructure-Activity Relationship22'-DipyridylCoordination ComplexesMoleculePhysical and Theoretical ChemistryMathematical ComputingSolvent freeMolecular StructureCationic polymerizationHydrogen-Ion ConcentrationCopperDiphosphatesCrystallographychemistryThermodynamicsSingle crystalDimerizationCopperPhenanthrolinesInorganic chemistry
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The Molecular and Crystal Structure of tert-Butyl N.ALPHA.-tert-Butoxycarbonyl-L-(S-trityl)cysteinate and the Conformation-Stabilizing Function of We…

2001

The title compound, C31H37NO4S [systematic name: (R)-tert-butyl-2-[(tert-butoxycarbonyl)amino]-3-(tritylsulfanyl)propanoate] is an L-cysteine derivative with three functions: NH2, COOH and SH, blocked by protecting groups tert-butoxycarbonyl, tert-butyl and trityl, respectively. The main chain of the molecule adopts the extended, nearly all-trans C5 conformation with the intramolecular N-H...O=C hydrogen bond. The urethane group is not involved in any intermolecular hydrogen bonding. Only weak intermolecular hydrogen bonds and hydrophobic contacts are observed in the crystal structure. These are C-H...O hydrogen bonds and CH/pi interactions with donor...acceptor distances, C...O ca. 3.5 A a…

Models MolecularStereochemistryPopulationMolecular ConformationCrystallography X-RayRing (chemistry)chemistry.chemical_compoundSpectroscopy Fourier Transform InfraredDrug DiscoveryMoleculeCysteineC5 conformationWeak hydrogen bondseducationConformational isomerismeducation.field_of_studyS-tritylcysteineChemistryHydrogen bondCrystal structureIntermolecular forceHydrogen BondingGeneral ChemistryGeneral MedicineFTIR spectroscopyIntramolecular forceIndicators and ReagentsGasesAb initio calculationsMethyl groupChemical and Pharmaceutical Bulletin
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A thermodynamic insight into the recognition of hydrophilic and hydrophobic amino acids in pure water by aza-scorpiand type receptors.

2014

Interactions of different hydrophilic (His, Asp, Glu,) and hydrophobic (Ala, Phe, Tyr, Trp) amino acids in water with a scorpiand aza-macrocycle (L1) containing a pyridine group in the ring and its derivative (L2) bearing a naphthalene group in the tail have been analysed by potentiometric and calorimetric measurements. Theoretical calculations corroborate that major attractive forces that hold the adduct together are hydrogen bonds and salt-bridges, even though other interactions such as π-stacking or NH(+)⋯π may contribute in the case of hydrophobic amino acids and L2. Calorimetric measurements indicate that the interactions between L1 and the different amino acids are principally driven …

Models MolecularStereochemistryPotentiometric titrationCalorimetryBiochemistryAdductchemistry.chemical_compoundPyridineOrganic chemistryPhysical and Theoretical ChemistryAmino AcidsNaphthalenechemistry.chemical_classificationHydrogen bondOrganic ChemistrySolvationWaterHydrogen BondingReceptors ArtificialCrown CompoundsAmino acidSolutionsChaotropic agentchemistryPotentiometryThermodynamicsHydrophobic and Hydrophilic InteractionsOrganicbiomolecular chemistry
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Hydrogen and copper ion-induced molecular reorganizations in scorpionand-like ligands. A potentiometric, mechanistic, and solid-state study.

2007

Two aza scorpionand-like macrocycles (L2 and L3) have been prepared. L2 consists of a tren amine with two of its arms cyclizized with a 2,6-bis(bromomethyl)pyridine. In L3, the remaining pendant arm has been further functionalized with a fluorophoric naphthalene group. X-ray data on the compounds [H(L3)]ClO4.H2O (1) and [H3(L3)](H2PO4)3.H2O (2) as well as solution studies (pH-metry, UV-vis, and fluorescence data) show the movement of the pendant arm as a result of the protonation degree of the macrocycles and of the formation of intramolecular hydrogen bonds. X-ray data on the complexes [Cu(L2)](ClO4)2]2.H2O (3) and [Cu(L3)](ClO4)2 (4) and solution studies on Cu2+ coordination show the impl…

Models MolecularStereochemistryPotentiometric titrationProtonationLigandsInorganic ChemistryMetalchemistry.chemical_compoundX-Ray DiffractionPyridinePolymer chemistryMoleculePhysical and Theoretical ChemistryIonsMolecular StructureHydrogen bondWaterHydrogen-Ion ConcentrationPhosphorus AcidsKineticschemistryvisual_artIntramolecular forcevisual_art.visual_art_mediumPotentiometryAmine gas treatingCopperHydrogenInorganic chemistry
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Influence of the C-terminus of the glycophorin A transmembrane fragment on the dimerization process

2000

The monomer-dimer equilibrium of the glycophorin A (GpA) transmembrane (TM) fragment has been used as a model system to investigate the amino acid sequence requirements that permit an appropriate helix-helix packing in a membrane‐mimetic environment. In particular, we have focused on a region of the helix where no crucial residues for packing have been yet reported. Various deletion and replacement mutants in the C‐terminal region of the TM fragment showed that the distance between the dimerization motif and the flanking charged residues from the cytoplasmic side of the protein is important for helix packing. Furthermore, selected GpA mutants have been used to illustrate the rearrangement o…

Models MolecularStereochemistryProtein ConformationMutantMolecular Sequence DataBiochemistryProtein structureGlycophorinAmino Acid SequenceGlycophorinsMolecular BiologyProtein secondary structurePeptide sequencebiologyChemistryC-terminusProteïnes de membranaMembrane ProteinsTransmembrane proteinPeptide FragmentsBiochemistryMembrane proteinbiology.proteinDimerizationResearch Article
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β-turn tendency in N-methylated peptides with dehydrophenylalanine residue: DFT study.

2010

The tendency to adopt β-turn conformation by model dipeptides with α,β-dehydrophenylalanine (ΔPhe) residue in the gas phase and in solution is investigated by theoretical methods. We pay special attention to a dependence of conformational properties on the side-chain configuration of dehydro residue and the influence of N-methylation on β-turn stability. An extensive computational study of the conformational preferences of Z and E isomers of dipeptides Ac-Gly-(E/Z)-ΔPhe-NHMe (1a / 1b) and Ac-Gly-(E/Z)-ΔPhe-NMe(2) (2a/2b) by B3LYP/6-311++G(d,p) and MP2/6-311++G(d,p) methods is reported. It is shown that, in agreement with experimental data, Ac-Gly-(Z)-ΔPhe-NHMe has a great tendency to adopt …

Models MolecularStereochemistryProtein ConformationPhenylalanineBiophysicsdehydrophenylalaninesolvent effectsBiochemistryMethylationBiomaterialschemistry.chemical_compoundResidue (chemistry)Protein structureβ‐turn tendencyAmideE isomersDFT methodsHydrogen bondOrganic ChemistryGeneral Medicinechemistrytheoretical conformational analysisIntramolecular forceTheoretical methodsPolarSolvent effectsPeptidesZBiopolymers
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Structure-Activity Relationships and X-ray Structures Describing the Selectivity of Aminopyrazole Inhibitors for c-Jun N-terminal Kinase 3 (JNK3) ove…

2009

c-Jun N-terminal kinase 3alpha1 (JNK3alpha1) is a mitogen-activated protein kinase family member expressed primarily in the brain that phosphorylates protein transcription factors, including c-Jun and activating transcription factor-2 (ATF-2) upon activation by a variety of stress-based stimuli. In this study, we set out to design JNK3-selective inhibitors that had >1000-fold selectivity over p38, another closely related mitogen-activated protein kinase family member. To do this we employed traditional medicinal chemistry principles coupled with structure-based drug design. Inhibitors from the aminopyrazole class, such as SR-3576, were found to be very potent JNK3 inhibitors (IC(50) = 7 nm)…

Models MolecularStereochemistryProtein ConformationPyrazoleCrystallography X-RayBiochemistryp38 Mitogen-Activated Protein Kinaseschemistry.chemical_compoundStructure-Activity RelationshipProtein structureMitogen-Activated Protein Kinase 10Insulin-Secreting CellsStructure–activity relationshipAnimalsHumansEnzyme InhibitorsPhosphorylationProtein kinase AMolecular BiologyCells CulturedIndazolebiologyActivating Transcription Factor 2Active siteCell BiologyActivating transcription factor 2RatschemistryProtein Structure and Foldingbiology.proteinPyrazolesSelectivityJournal of Biological Chemistry
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Controlling quaternary structure assembly: subunit interface engineering and crystal structure of dual chain avidin.

2006

Dual chain avidin (dcAvd) is an engineered avidin form, in which two circularly permuted chicken avidin monomers are fused into one polypeptide chain. DcAvd can theoretically form two different pseudotetrameric quaternary assemblies because of symmetry at the monomer-monomer interfaces. Here, our aim was to control the assembly of the quaternary structure of dcAvd. We introduced the mutation I117C into one of the circularly permuted domains of dcAvd and scanned residues along the 1-3 subunit interface of the other domain. Interestingly, V115H resulted in a single, disulfide locked quaternary assembly of dcAvd, whereas I117H could not guide the oligomerisation process even though it stabilis…

Models MolecularStereochemistryProtein subunitBiotinGene ExpressionCrystal structureCrystallography X-RayLigandsProtein EngineeringProtein–protein interactionchemistry.chemical_compoundBiotinStructural BiologyAnimalsDisulfidesProtein Structure QuaternaryMolecular BiologyChromatography High Pressure LiquidbiologyProtein engineeringHydrogen-Ion ConcentrationAvidinCrystallographyProtein SubunitsMonomerchemistryMutationbiology.proteinChromatography GelThermodynamicsProtein quaternary structureChickensAvidinJournal of molecular biology
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