Search results for "reaction mechanisms"

showing 10 items of 21 documents

A Dehydrogenase Dual Hydrogen Abstraction Mechanism Promotes Estrogen Biosynthesis: Can We Expand the Functional Annotation of the Aromatase Enzyme?

2018

Cytochrome P450 (CYP450) enzymes are involved in the metabolism of exogenous compounds and in the synthesis of signaling molecules. Among the latter, human aromatase (HA) promotes estrogen biosynthesis, which is a key pharmacological target against breast cancers. After decades of debate, interest in gaining a comprehensive picture of HA catalysis has been renewed by the recent discovery that compound I (Cpd I) is the reactive species of the peculiar aromatization step. Herein, for the first time, a complete atomic-level picture of all controversial steps of estrogen biosynthesis is presented. By performing cumulative quantum-classical molecular dynamics and metadynamics simulations of abou…

0301 basic medicineCell signalingDehydrogenase-Molecular Dynamics Simulation010402 general chemistryHydroxylation01 natural sciencesenzyme catalysisCatalysisEnzyme catalysisHydroxylation03 medical and health scienceschemistry.chemical_compoundAromataseCytochrome P-450 Enzyme SystemHumansAromatasechemistry.chemical_classificationhydrogen abstractionbiologyOrganic ChemistryAromatizationAndrostenedioneCytochrome P450EstrogensGeneral Chemistrymolecular dynamics0104 chemical sciencesreaction mechanisms030104 developmental biologyEnzymechemistryBiochemistrySettore CHIM/03 - Chimica Generale E Inorganicadensity functional calculationsbiology.proteinProtonsOxidoreductasesOxidation-ReductionHydrogen
researchProduct

Experimental and Theoretical Studies of Nonclassical d 0 Cyclopentadienyl Polyhydride Complexes of Molybdenum and Tungsten

1998

Low-temperature protonation of compounds Cp{sup *}MH{sub 5}(PMe{sub 3}) (M = Mo, 1; W, 2) by HBF{sub 4}{center_dot}Et{sub 2}O in CD{sub 2}Cl{sub 2} or CDFCl{sub 2} affords the thermally unstable hexahydride derivatives [Cp{sup *}MH{sub 6}(PMe{sub 3})]{sup +} (M = Mo, 3; W, 4). The corresponding protonation of 1- and 2-d{sup 5} affords 3- and 4-d{sup 5}, respectively. The {Delta}{delta} on going from H{sub 6} to HD{sub 5} is small for both compounds, but positive for 3 and negative for 4, and no isotopic perturbation of resonance (IPR) is observed. The T{sub 1min} at 400 MHz for [Cp{sup *}MH{sub 6}(PMe{sub 3})]{sup +} apparently doubles on going from Mo to W (52 ms for 3 and approximately 10…

AnionsReaction mechanismschemistry.chemical_elementProtonation010402 general chemistryLigands01 natural sciencesInorganic ChemistryCyclopentadienyl complexChemical structureMathematical methodsComputational chemistryMolecule[CHIM.COOR]Chemical Sciences/Coordination chemistryPhysical and Theoretical Chemistry010405 organic chemistryHydrideOrganic Chemistry3. Good health0104 chemical sciencesCrystallographychemistryChemical bondMolybdenumPotential energy surfaceDihydrogen complex
researchProduct

Molecular Basis of the Chemiluminescence Mechanism of Luminol

2019

Light emission from luminol is probably one of the most popular chemiluminescence reactions due to its use in forensic science, and has recently displayed promising applications for the treatment of cancer in deep tissues. The mechanism is, however, very complex and distinct possibilities have been proposed. By efficiently combining DFT and CASPT2 methodologies, the chemiluminescence mechanism has been studied in three steps: 1)luminol oxygenation to generate the chemiluminophore, 2)a chemiexcitation step, and 3)generation of the light emitter. The findings demonstrate that the luminol double-deprotonated dianion activates molecular oxygen, diazaquinone is not formed, and the chemiluminopho…

CASPT2010405 organic chemistryChemistryOrganic ChemistryGeneral Chemistryelectron transfer010402 general chemistryPhotochemistry01 natural scienceschemiluminescenceCatalysis0104 chemical sciencesLuminollaw.inventionreaction mechanismschemistry.chemical_compoundlawdensity functional calculationsTeoretisk kemicancerLight emissionTheoretical ChemistryChemiluminescenceChemistry – A European Journal
researchProduct

Theoretical Studies of the Self Cleavage Pistol Ribozyme Mechanism

2021

AbstractRibozymes are huge complex biological catalysts composed of a combination of RNA and proteins. Nevertheless, there is a reduced number of small ribozymes, the self-cleavage ribozymes, that are formed just by RNA and, apparently, they existed in cells of primitive biological systems. Unveiling the details of these “fossils” enzymes can contribute not only to the understanding of the origins of life but also to the development of new simplified artificial enzymes. A computational study of the reactivity of the pistol ribozyme carried out by means of classical MD simulations and QM/MM hybrid calculations is herein presented to clarify its catalytic mechanism. Analysis of the geometries…

Coordination spherebiologyChemistryReaction mechanismsRibozymeActive siteRNAProtonationGeneral ChemistryMolecular dynamicsCleavage (embryo)QM/MMCatalysisPistol ribozymeQM/MMMolecular dynamicsSelf-cleavage ribozymesComputational chemistrybiology.proteinRNARibosomes
researchProduct

Multiple Roles of Isocyanides in Palladium-Catalyzed Imidoylative Couplings: A Mechanistic Study

2016

International audience; Kinetic, spectroscopic and computational studies examining a palladium-catalyzed imidoylative coupling highlight the dual role of isocyanides as both substrates and ligands for this class of transformations. The synthesis of secondary amides from aryl halides and water is presented as a case study. The kinetics of the oxidative addition of ArI with RNC-ligated Pd-0 species have been studied and the resulting imidoyl complex [(ArC=NR)Pd(CNR)(2)I] (Ar=4-F-C6H4, R = tBu) has been isolated and characterized by X-ray diffraction. The unprecedented ability of this RNC-ligated imidoyl-Pd complex to undergo reductive elimination at room temperature to give the amide in the p…

Denticityisocyanidepd-c bondStereochemistryeffective core potentialsIsocyanidechemistry.chemical_element010402 general chemistry01 natural sciencesMedicinal chemistry[ CHIM ] Chemical SciencesCatalysisReductive eliminationinsertionchemistry.chemical_compoundAmide[CHIM]Chemical Sciencescouplingsingle-carbonylation reactions010405 organic chemistryArylOrganic Chemistrycarbon-monoxidezerovalent palladiumGeneral Chemistrycyclopalladated complexespalladiumOxidative addition0104 chemical sciencesaryl halidesreaction mechanismsCatalytic cyclechemistryn-heterocyclessequential insertionPalladiumpalladated phenol derivatives
researchProduct

Scalable Constant pH Molecular Dynamics in GROMACS

2022

Molecular dynamics (MD) computer simulations are used routinely to compute atomistic trajectories of complex systems. Systems are simulated in various ensembles, depending on the experimental conditions one aims to mimic. While constant energy, temperature, volume, and pressure are rather straightforward to model, pH, which is an equally important parameter in experiments, is more difficult to account for in simulations. Although a constant pH algorithm based on the λ-dynamics approach by Brooks and co-workers [Kong, X.; Brooks III, C. L. J. Chem. Phys.1996, 105, 2414–2423] was implemented in a fork of the GROMACS molecular dynamics program, uptake has been rather limited, presumably due to…

ImidazolesmolekyylitpotentiaalienergiaHydrogen-Ion ConcentrationMolecular Dynamics Simulationmonomerspeptides and proteinsreaktiomekanismitmolecular mechanicspotential energyComputer Science Applicationsreaction mechanismspeptiditHumansmolekyylidynamiikkaproteiinitPhysical and Theoretical ChemistryAlgorithms
researchProduct

Copper‐Promoted Formation of Vinylsiloxanes

2020

The metathesis reactions of chlorovinylsilanes with copper(I) oxide are reported. The process is catalyzed by HCl which can be in situ generated via hydrolysis of chlorosilanes by traces of water present in the system. An appearance of olefin/CuCl π‐intermediates can provide a stereoselectivity of the process and alter the pathway of siloxanes formation employing Cu2O as the source of oxygen. It was also shown that acetonitrile may be available as a solvent for construction of the systems with large preparative capabilities, including those based on the use atmospheric oxygen in siloxane synthesis.

Inorganic ChemistryReaction mechanismVinylsiloxanesChemistryReaction mechanismsPolymer chemistrychemistry.chemical_elementMetathesisChlorovinylsilanesMetathesisCopperCopperEuropean Journal of Inorganic Chemistry
researchProduct

High Turnover Catalase Activity of a Mixed‐Valence Mn II Mn III Complex with Terminal Carboxylate Donors

2015

The neutral dimanganese(II,III) complex [Mn-2(BCPMP)-(OAc)(2)] [1; BCPMP3- = 2,6-bis({(carboxymethyl)[(1-pyridyl)-methyl] amino} methyl)-4-methylphenolato] has been synthesized and characterized. The complex contains two terminal carboxylate donors. Complex 1 was found to be an effective catalyst for the disproportionation of H2O2 with high catalytic rate and a turnover number of 7500, the highest turnover reported to date for a catalase mimic. The rates and TON were significantly higher than recorded for a dicationic dimanganese( II,III) counterpart ([Mn-2(BPBP)(OAc)(2)]center dot(ClO4)(2), 2; BPBP- = 2,6-bis{[bis(2-pyridylmethyl)amino]methyl}-4-butylphen-olato), which lacks the terminal c…

ManganeseReaction mechanismbiologyChemistryEnzyme modelsReaction mechanismschemistry.chemical_elementDisproportionationManganeseCatalaseHydrogen peroxidePhotochemistryMedicinal chemistryCatalysisTurnover numberInorganic Chemistrychemistry.chemical_compoundDinucleating ligandsCatalytic cycleCatalasebiology.proteinCarboxylateta116European Journal of Inorganic Chemistry
researchProduct

Unraveling the Reaction Mechanism of Enzymatic C5-Cytosine Methylation of DNA. A Combined Molecular Dynamics and QM/MM Study of Wild Type and Gln119 …

2016

M.HhaI is a DNA methyltransferase from Haemophilus hemolyticus that catalyzes the transfer of a methyl group from S-adenosyl-l-methionine (SAM) to the C5 position of a cytosine. This enzyme is a paradigmatic model for C5 DNA methyltransferases due to its major homology to mammalian enzymes and to the availability of high-resolution structures of the DNA–enzyme complex. In spite of the number of experimental and theoretical analyses carried out for this system, many mechanistic details remain unraveled. We have used full atomistic classical molecular dynamics simulations to explore the protein–SAM–DNA ternary complex, where the target cytosine base is flipped out into the active site for bot…

MethyltransferaseStereochemistry010402 general chemistry01 natural sciencesMolecular mechanicsenzyme catalysisCatalysisQM/MMchemistry.chemical_compound0103 physical sciencesA-DNATernary complex010304 chemical physicsbiologyChemistryActive siteGeneral Chemistryfree energy profiles0104 chemical sciencesreaction mechanismsBiochemistrybiology.proteinQM/MM methodsstring methodDNA-methylationCytosineDNA
researchProduct

Synthesis of Densely Functionalised 5-Halogen-1,3-oxazin-2-ones byHalogen-Mediated Regioselective Cyclisation of N-Cbz-ProtectedPropargylic Amines: A…

2013

A very efficient synthesis of 5-halogen-1,3-oxazin-2-ones has been accomplished by the halocyclisation reaction of chiral nonracemic N-carbobenzyloxy (N-Cbz)-protected propargylic amines by using I-2, Br-2 and Cl-2 as electrophile sources. The nature of the halogen influences the reaction time and yield. However, in all cases the reaction is totally regioselective taking place through a 6-endo-dig process regardless of the nature of the halogen and of the substituents in the starting material. To rationalise the experimental results, theoretical studies at the B3LYP/6-311G* level have been performed.

Propargylic aminesReaction mechanismChemistryReaction mechanismsOrganic ChemistryRegioselectivityGeneral ChemistryCatalysisOxazinonesDensity functional calculationsRegioselectivityHalocyclisationYield (chemistry)FISICA APLICADAHalogenElectrophileOrganic chemistry
researchProduct