Search results for "molecular conformation"

showing 10 items of 376 documents

Molecular Docking approach on the Topoisomerase I inhibitors series included in the NCI anti-cancer agents mechanism database

2006

Topoisomerase I (Top1) is an essential enzyme participating to all those processes associated with separation of DNA strands. It manages superhelical tensions through the transient breakage of one strand of duplex DNA, followed by the unwinding of supercoiled DNA. Camptothecins, a class of alkaloids extracted from the wood of a Chinese tree, were found to be potent inhibitors of Topoisomerase I. The National Cancer Institute (NCI) Anti-cancer Agents Mechanism Database contains several camptothecins derivatives, classified as selective Top1 inhibitors. In this work we performed molecular docking studies on 24 camptothecin-like inhibitors present in this database (using Autodock 3.0.5). In or…

Models MolecularDatabases FactualProtein ConformationStereochemistryMolecular ConformationAntineoplastic AgentsTopoisomerase I inhibitorsTopoisomerase-I Inhibitorcomputer.software_genreCatalysisInorganic Chemistrychemistry.chemical_compoundEnzyme InhibitorsPhysical and Theoretical ChemistryAutodockchemistry.chemical_classificationBinding SitesDatabasebiologyTopoisomeraseOrganic ChemistryActive siteDNAAutoDockUnited StatesComputer Science ApplicationsEnzymeDNA Topoisomerases Type INational Institutes of Health (U.S.)Computational Theory and MathematicschemistryDocking (molecular)Molecular dockingbiology.proteinDNA supercoilCamptothecincomputerDNA
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New concepts in multidentate ligand chemistry: effects of multidentarity on catalytic and spectroscopic properties of ferrocenyl polyphosphines.

2008

This tutorial review devoted to ligand chemistry deals with the design and properties of ferrocenyl polyphosphines, an original class of multidentate ligands. The development of a varied library of ferrocenyl tetra-, tri- and diphosphine ligands is reviewed. The multidentate nature of these species has led to unique spectroscopic and catalytic properties, in which the spatial proximity of phosphorus atoms is crucial. Regarding their catalytic applications, the key issues of catalyst longevity and ultralow catalyst loadings are discussed. Another part is concerned with fundamental advances gained in physical chemistry for structure elucidation by the study of the intriguing “through-space” N…

Models MolecularDenticityMagnetic Resonance SpectroscopyMetallocenesferrocenyl polyphosphinesSuzukiMolecular ConformationSonogashira coupling010402 general chemistryLigands01 natural sciencescatalystsCatalysisCatalysis[ CHIM.CATA ] Chemical Sciences/Catalysisthrough-space interactionOrganometallic CompoundsOrganic chemistryCombinatorial Chemistry Techniques[CHIM.COOR]Chemical Sciences/Coordination chemistryFerrous CompoundsAminationComputingMilieux_MISCELLANEOUSGroup 2 organometallic chemistryCombinatorial Chemistry Techniquesnuclear spin-spin coupling010405 organic chemistryChemistryLigand[ CHIM.COOR ] Chemical Sciences/Coordination chemistrySonogashiraaminationStereoisomerismGeneral ChemistryNuclear magnetic resonance spectroscopy[CHIM.CATA]Chemical Sciences/CatalysisReference StandardsCombinatorial chemistry0104 chemical sciencesmultidentarityHeckChemical Society reviews
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Piperazine bridged resorcinarene cages.

2010

The one-pot Mannich condensation of resorcinarenes with piperazine and an excess of formaldehyde under high dilution conditions results in a helical cage, namely, a covalently linked dimer of two resorcinarenes connected via four piperazine bridges in yields ranging from 20 to 40%. The compounds were analyzed by NMR spectroscopy, ESI mass spectrometry, and single crystal X-ray diffraction. The helical cages can encapsulate small guest molecules by adapting the cavity volume by changing the helical pitch according to the guest size.

Models MolecularDimerPhenylalanineOrganic ChemistryFormaldehydeMolecular ConformationStereoisomerismNuclear magnetic resonance spectroscopyResorcinareneCrystallography X-RayBiochemistryPiperazineschemistry.chemical_compoundPiperazinechemistryCovalent bondPolymer chemistryMoleculeOrganic chemistryPhysical and Theoretical ChemistryCalixarenesSingle crystalPiperazineOrganic letters
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Molecular orbital studies on brominated diphenyl ethers. Part I—conformational properties

2005

Polybrominated diphenyl ethers (PBDEs) are widely used as additive flame retardants and quantities in the environment are on the rise. Because they are structurally related to polychlorinated biphenyls and also to thyroid hormones, there is serious concern that PBDEs may pose a danger to human health. Knowledge of their conformational properties is key to assessing their environmental fate and risk. The conformational properties of PBDEs were investigated by quantum chemical methods including semiempirical self-consistent field molecular orbital (SCF-MO), ab initio SCF-MO and density functional theory (DFT). Conformational analyses of model congeners 2,2',4,6'-tetrabromodiphenyl ether and 2…

Models MolecularEnvironmental EngineeringStereochemistryPhenyl EthersHealth Toxicology and MutagenesisPolybrominated BiphenylsMolecular ConformationPublic Health Environmental and Occupational HealthAb initioEtherGeneral MedicineGeneral ChemistryPollutionBrominated Diphenyl EthersChemistry Techniques Analyticalchemistry.chemical_compoundPolybrominated diphenyl etherschemistryComputational chemistryAb initio quantum chemistry methodsEnvironmental ChemistryMolecular orbitalDensity functional theoryConformational isomerismFlame RetardantsChemosphere
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A new family of "clicked" estradiol-based low-molecular-weight gelators having highly symmetry-dependent gelation ability.

2011

Reported herein is the discovery of a novel family of "clicked" estradiol-based LMWGs whose gelation ability highly depends on the gelator symmetry. These LMWGs that gel different organic solvents in the presence of H(2)O even at concentrations as low as 0.04 wt% are readily accessible using "click" chemistry.

Models MolecularEstradiolChemistryMetals and AlloysMolecular ConformationGeneral ChemistryCatalysisSurfaces Coatings and FilmsElectronic Optical and Magnetic MaterialsMolecular Weightotorhinolaryngologic diseasesMaterials ChemistryCeramics and CompositesOrganic chemistryClick ChemistrySymmetry (geometry)GelsChemical communications (Cambridge, England)
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Selective recognition of neutral guests in an aqueous medium by a biomimetic calix[6]cryptamide receptor

2015

The design of artificial receptors that can efficiently work in water is a challenging research area. A possible biomimetic approach for the elaboration of such receptors consists of associating a hydrophobic cavity with a polar polyfunctional binding site. On this basis, a hydrophilic calix[6]cryptamide decorated with oligo(ethylene glycol) units (i.e. 8) was synthesized through an efficient [1 + 1] macrocyclization reaction as the key-step. The complexation of neutral molecules was evaluated by NMR spectroscopy through competition experiments either in apolar or aqueous media. In both media, host 8 can bind neutral species that display H-bonding acceptor and donor groups such as amides or…

Models MolecularEthylene GlycolMagnetic Resonance SpectroscopyStereochemistryAllosteric regulationMolecular ConformationCrystallography X-Ray010402 general chemistry01 natural sciencesBiochemistrychemistry.chemical_compoundBiomimetic MaterialsCalixareneUreaMoleculeaqueous mediumartificial receptorsbiomimeticsPhysical and Theoretical ChemistryBinding siteta116010405 organic chemistryHydrogen bondOrganic ChemistryWaterHydrogen BondingNuclear magnetic resonance spectroscopyAmidesAcceptor0104 chemical scienceschemistryCyclizationCalixarenesHydrophobic and Hydrophilic InteractionsEthylene glycolOrganic & Biomolecular Chemistry
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Matrix Isolation and Ab Initio Study of Trans−Trans and Trans−Cis Dimers of Formic Acid

2010

Six trans-trans and five trans-cis dimeric structures of formic acid (HCOOH) are revealed by ab initio calculations. Four trans-trans and two trans-cis dimers are identified in the IR absorption spectra in argon matrices. The trans-cis dimers are obtained by narrow-band IR excitation of the vibrational transitions of the trans-trans dimers. Two trans-trans (tt3 and tt6) and one trans-cis (tc4) dimer are characterized experimentally for the first time. The tunneling decay rates of two trans-cis dimers (tc1 and tc4) are evaluated at different temperatures. A greater lifetime of the trans-cis dimers at elevated temperatures compared to the cis-monomer suggests that the high-energy conformers c…

Models MolecularFormatesSpectrophotometry InfraredFormic acidDimerMolecular ConformationAb initio010402 general chemistryPhotochemistry01 natural scienceschemistry.chemical_compoundAb initio quantum chemistry methods0103 physical sciencesPhysical and Theoretical ChemistryConformational isomerism010304 chemical physicsHydrogen bondMatrix isolationStereoisomerism0104 chemical sciences3. Good healthCrystallographychemistryQuantum TheoryThermodynamicsDimerizationCis–trans isomerismThe Journal of Physical Chemistry A
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EPR, ENDOR and TRIPLE Resonance and MO Studies on Ubiquinones (Q-n): Comparison of Radical Anions and Cations of Coenzymes Q-10 and Q-6 with the Mode…

1997

Radical anions and cations of the biologically important coenzymes Q-6 and Q-10, which have 6 and 10 unsaturated isoprene units in their side chains, respectively, have been generated in various solvents, and the results compared with those obtained for Q-0, a ubiquinone with no isoprene units, and for decylubiquinone Q-2 which has a saturated side chain. Hyperfine splitting constants (hfsc) of methyl and methoxy protons of the substituents in the quinone ring, and beta and gamma protons of the side chain were measured by EPR and ENDOR spectroscopy for both the radical anions and cations of Q-0, Q-6 and Q-10, and for the radical anion of Q-2. The relative signs of the hfsc were determined b…

Models MolecularFree RadicalsMolecular StructureUbiquinoneChemistryGeneral Chemical EngineeringRadicalElectron Spin Resonance SpectroscopyMolecular ConformationPhotochemistryResonance (chemistry)law.inventionQuinoneCrystallographyHemiterpeneslawPentanesButadienesSide chainMoleculeMolecular orbitalElectron paramagnetic resonanceHyperfine structureActa Chemica Scandinavica
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Ferrocene compounds: methyl 1′-aminoferrocene-1-carboxylate

2010

The title compund, [Fe(C(5)H(6)N)(C(7)H(7)O(2))], features one strong intermolecular hydrogen bond of the type N-H...O=C [N...O = 3.028 (2) A] between the amine group and the carbonyl group of a neighbouring molecule, and vice versa, to form a centrosymmetric dimer. Furthermore, the carbonyl group acts as a double H-atom acceptor in the formation of a second, weaker, hydrogen bond of the type C-H...O=C [C...O = 3.283 (2) A] with the methyl group of the ester group of a second neighbouring molecule at (x, -y - 1/2, z - 1/2). The methyl group also acts as a weak hydrogen-bond donor, symmetry-related to the latter described C-H...O=C interaction, to a third molecule at (x, -y - 1/2, z + 1/2) t…

Models MolecularHydrogen bondStereochemistryDimerCarboxylic AcidsMolecular ConformationHydrogen BondingGeneral MedicineAcceptorGeneral Biochemistry Genetics and Molecular BiologyCrystallographychemistry.chemical_compoundchemistryFerroceneCyclopentadienyl complexMoleculeFerrous CompoundsDimerizationMethyl groupCoordination geometryActa Crystallographica Section C Crystal Structure Communications
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Computational and experimental studies of size and shape related physical properties of hydroxyapatite nanoparticles

2011

In this work, the properties of hydroxyapatite (HAP) nanoparticles (NPs) have been studied both theoretically and experimentally focusing on computational analysis. HAP is widely used to fabricate implants, for drug delivery, etc. The physical properties of the nanosized HAP particles play an important role in the interaction with cells in the human body and are of great interest. Computer simulation was employed to understand the properties of HAP clusters (Ca(5)(PO(4))(3)OH) including formation energies, dipole moments and polarization (surface charges) by molecular mechanics (MM + , OPLS) and mostly by quantum semi-empirical Hartree-Fock (PM3) methods. The size of the simulated cluster i…

Models MolecularHydrogenMolecular Conformationchemistry.chemical_elementNanoparticleElectrons02 engineering and technologyElectron010402 general chemistry01 natural sciencesMolecular physicsPhysical PhenomenaCluster (physics)Computer SimulationGeneral Materials ScienceWork functionSurface chargeParticle SizeChemistryHydrogen bond021001 nanoscience & nanotechnologyCondensed Matter Physics0104 chemical sciencesCrystallographyDipoleDurapatiteNanoparticlesQuantum Theory0210 nano-technologyJournal of Physics: Condensed Matter
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