Search results for "Benzene"

showing 10 items of 1701 documents

P-Glycoprotein Influence on the Brain Uptake of a 5-HT2A Ligand: [18F]MH.MZ

2010

<i>Background/Aims:</i> The serotonergic system, especially the 5-HT<sub>2A</sub> receptor, is involved in various diseases and conditions. We have recently developed a new [<sup>18</sup>F]-5-HT<sub>2A</sub> receptor ligand using an analogue, MDL 100907, as a basis for molecular imaging with positron emission tomography. This tracer, [<sup>18</sup>F]MH.MZ, has been shown to be an adequate tool to visualize the 5-HT<sub>2A</sub> receptors in vivo. However, [<sup>18</sup>F]altanserin, similar in chemical structure, is a substrate of efflux transporters, such as P-glycoprotein (P-gp), of the blood-brain barrier…

Fluorine RadioisotopesPharmacologyBiologySerotonergicBlood–brain barrierMicePiperidinesPharmacokineticsCerebellummedicineAnimalsReceptor Serotonin 5-HT2AATP Binding Cassette Transporter Subfamily B Member 1ReceptorBiological PsychiatryP-glycoproteinMice KnockoutBrain uptakeBiological TransportLigand (biochemistry)Frontal LobeFluorobenzenesPsychiatry and Mental healthNeuropsychology and Physiological Psychologymedicine.anatomical_structureBlood-Brain BarrierPositron-Emission Tomographybiology.proteinNeuroscienceNeuropsychobiology
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SYNTHESIS AND IN VITRO AFFINITIES OF VARIOUS MDL 100907 DERIVATIVES AS POTENTIAL 18F-RADIOLIGANDS FOR 5-HT2A RECEPTOR IMAGING WITH PET

2008

Radiolabelled piperidine derivatives such as [(11)C]MDL 100907 and [(18)F]altanserin have played an important role in diagnosing malfunction in the serotonergic neurotransmission. A variety of novel piperidine MDL 100907 derivatives, possible to label with (18)F-fluorine, were synthesized to improve molecular imaging properties of [(11)C]MDL 100907. Their in vitro affinities to a broad spectrum of neuroreceptors and their lipophilicities were determined and compared to the clinically used reference compounds MDL 100907 and altanserin. The novel compounds MA-1 (53) and (R)-MH.MZ (56) show K(i)-values in the nanomolar range towards the 5-HT(2A) receptor and insignificant binding to other 5-HT…

Fluorine RadioisotopesReceptor StatusStereochemistryClinical BiochemistryPharmaceutical ScienceLigandsBinding CompetitiveBiochemistryChemical synthesisMiceRadioligand AssayStructure-Activity Relationshipchemistry.chemical_compoundPiperidinesDrug DiscoveryRadioligandAnimalsHumansReceptor Serotonin 5-HT2AReceptorMolecular Biology5-HT receptorOrganic ChemistryLigand (biochemistry)AffinitiesRatsFluorobenzenesKineticschemistryPositron-Emission TomographyAltanserinNIH 3T3 CellsMolecular MedicineRadiopharmaceuticals
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Total synthesis and evaluation of [18F]MHMZ.

2007

Radiochemical labeling of MDL 105725 using the secondary labeling precursor 2-[(18)F]fluoroethyltosylate ([(18)F]FETos) was carried out in yields of approximately 90% synthesizing [(18)F]MHMZ in a specific activity of approximately 50MBq/nmol with a starting activity of approximately 3GBq. Overall radiochemical yield including [(18)F]FETos synthon synthesis, [(18)F]fluoroalkylation and preparing the injectable [(18)F]MHMZ solution was 42% within a synthesis time of approximately 100 min. The novel compound showed excellent specific binding to the 5-HT(2A) receptor (K(i)=9.0 nM) in vitro and promising in vivo characteristics.

Fluorine RadioisotopesStereochemistryClinical BiochemistryPharmaceutical ScienceBiochemistryBinding CompetitiveRadioligand AssayPiperidinesIn vivoDrug DiscoveryAnimalsRadionuclide imagingReceptor Serotonin 5-HT2ARadionuclide ImagingMolecular BiologyChemistryOrganic ChemistrySynthonTotal synthesisBrainBiological activityRadioligand AssayRatsFluorobenzenesKineticsYield (chemistry)Isotope LabelingSerotonin 5-HT2 Receptor AntagonistsMolecular MedicineSpecific activityKetanserinSerotonin AntagonistsRadiopharmaceuticalsNuclear chemistryBioorganicmedicinal chemistry letters
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Coupled cluster calculations of interaction energies in benzene–fluorobenzene van der Waals complexes

2007

Benzene-fluorobenzene complexes are used as model systems to simulate the interactions of the SBB-HCAII protein-ligand complex. Using the second-order Moller-Plesset [MP2] and the coupled cluster singles and doubles including connected triple excitations models recently implemented with Cholesky decompositions we evaluate accurate interaction energies for several benzene-fluorobenzene van der Waals complexes. We consider edge-to-face interactions and compare the results to those from a recent MP2 study and to experimental findings. In contrast to experimental trends, we find that the interaction tends to decrease with increasing fluorination and conclude that benzene-fluorobenzene complexes…

FluorobenzeneVan der Waals surfaceGeneral Physics and AstronomyMolecular physicsPhysics and Astronomy (all)chemistry.chemical_compoundsymbols.namesakeCoupled clusterchemistrysymbolsPhysical and Theoretical ChemistryAtomic physicsvan der Waals forceBenzeneCholesky decompositionChemical Physics Letters
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A photoswitchable helical peptide with light-controllable interface / transmembrane topology in lipidic membranes

2021

AbstractAccording to the three-step model, the spontaneous insertion and folding of helical transmembrane (TM) polypeptides into lipid bilayers is driven by three sequential equilibria: solution-to-membrane interface (MI) partition, unstructured-to-helical folding, and MI-to-TM helix insertion. However, understanding these three steps with molecular detail has been challenged by the lack of suitable experimental approaches to rapidly and reversibly perturb membrane-bound hydrophobic polypeptides out of equilibrium. Here, we report on a 24-residues-long hydrophobic α-helical polypeptide, covalently coupled to an azobenzene photoswitch (KCALP-azo), which displays a light-controllable TM/MI eq…

Folding (chemistry)chemistry.chemical_compoundCrystallographyMembraneAzobenzenechemistryPhotoswitchPhotoisomerizationMembrane topologyHelixLipid bilayer
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Studies on pathways of ring opening of benzene in a Fenton system

1995

Ring-opened products of benzene metabolism have been postulated to play a role in hematotoxicity and leukemogenesis. The reaction of benzene in the Fenton system was reexamined to determine the presence of compounds which might serve as intermediates in the formation of trans, trans-muconaldehyde (MUC), a microsomal hematotoxic metabolite of benzene. Benzene dihydrodiol (DHD) was found in this system based on coelution with authentic standard, ultraviolet (UV) absorption characteristics, and molecular weight. Incubation of DHD in the Fenton system resulted in the formation of phenol (PH), catechol (CAT), and products which reacted with thiobarbituric acid to form chromogens absorbing at 495…

Free RadicalsStereochemistryMetaboliteStereoisomerismIn Vitro TechniquesBiochemistryAldehydechemistry.chemical_compoundPhysiology (medical)AnimalsHumansPhenolBenzeneChromatography High Pressure LiquidCarcinogenchemistry.chemical_classificationAldehydesCatecholMolecular StructureHydroquinoneBenzeneStereoisomerismchemistrySpectrophotometryCarcinogensMicrosomes LiverFree Radical Biology and Medicine
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3 He NMR: from free gas to its encapsulation in fullerene

2013

The (3)He nuclear magnetic shieldings were calculated for single helium atom, its dimer, simple models of fullerene cages (He@Cn), and single wall carbon nanotubes. The performances of several levels of theory (HF, MP2, DFT-VSXC, CCSD, CCSD(T), and CCSDT) were tested. Two sets of polarization-consistent basis sets were used (pcS-n and aug-pcS-n), and an estimate of (3)He nuclear magnetic shieldings in the complete basis set limit using a two-parameter fit was established. Theoretical (3)He results reproduced accurately previously reported theoretical values for helium gas, dimer, and helium probe inside several fullerene cages. Excellent agreement with experimental values was achieved. (3)H…

FullereneHelium atomDimerAb initiochemistry.chemical_elementGeneral ChemistryCarbon nanotubeMolecular physicslaw.inventionchemistry.chemical_compoundchemistryComputational chemistrylawPhysics::Atomic and Molecular ClustersGeneral Materials ScienceBenzeneBasis setHeliumMagnetic Resonance in Chemistry
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Local aromaticity mapping in the vicinity of planar and nonplanar molecules

2019

We report on nucleus-independent magnetic shielding (NICS) scans over the centers of six- and five-membered rings in selected metal phthalocyanines (MPc) and fullerene C60 for more accurate characterization of local aromaticity in these compounds. Detailed tests were conducted on model aromatic molecules including benzene, pyrrole, indole, isoindole, and carbazole and subsequently applied to H2 Pc, ZnPc, Al(OH)Pc, and CuPc. Similar behavior of three selected magnetic probes, Bq, 3 He, and 7 Li+ , approaching perpendicularly the ring centers, was observed. For better visualization of shielding zone over the centers of aromatic rings, we introduced a simple mathematical procedure: the first a…

FullereneNICS010304 chemical physicsCarbazoleChemical shiftAromaticityGeneral Chemistryaromaticity010402 general chemistryRing (chemistry)curve derivatives01 natural sciencesMolecular physics0104 chemical sciencesIonchemistry.chemical_compoundbenzenemetal phthalocyanineschemistrypyrrole0103 physical sciencesMoleculeGeneral Materials ScienceIsoindoleMagnetic Resonance in Chemistry
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Transesterification of rapeseed oil over acid resins promoted by supercritical carbon dioxide

2011

The methanolysis of rapeseed oil catalyzed by commercial styrene-divinylbenzene macroporous acid resins was performed in a batch reactor at 100-140 °C and 10-46 MPa to study the effect of supercritical carbon dioxide (scCO2) on the performances of the process. Reaction temperatures of 120-140 °C were necessary to obtain high enough yields of fatty acid methyl esters. Upon addition of scCO2 faster transesterification kinetics was obtained also at the lowest investigated operating pressure (10-11 MPa), working in two fluid phase systems. Experiments performed changing the reaction time indicated that most of the esters were formed during the first 3 h. When the pressure was increased at 38-46…

General Chemical EngineeringMethanolysiKineticsBatch reactorOperating pressurePolymeric acidHeterogeneous catalysisCatalysiCatalysisHeterogeneous catalysiIon exchange resinSupercritical carbon dioxideOrganic chemistryFatty acid methyl esterRapeseed oilEsterPhysical and Theoretical ChemistryVegetable oils Supercritical fluid extractionIon-exchange resinStyreneReaction systemReaction timeBiodieselFluid phasiTwo-fluid Batch reactorSupercritical carbon dioxideEsterificationChemistryReaction kineticTransesterificationSettore ING-IND/27 - Chimica Industriale E TecnologicaFatty acidCondensed Matter PhysicsPhase behaviourTransesterificationCarbon dioxideReaction temperatureMacroporouStyrene-divinylbenzeneBiodieselEnhancement effectIon exchangeThe Journal of Supercritical Fluids
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Orientation of the acidity probes benzene, acetonitrile and pyridine in SAPO-5 and GaAPO-5 molecular sieves: an FTIR microscopy study

1997

The adsorption and desorption behaviour of benzene, acetonitrile (CD3CN) and pyridine for large crystals of SAPO-5 and GaAPO-5 is studied using FTIR microscopy with polarised IR radiation. From the analysis of the polarised adsorption bands it is concluded that the adsorbates are ordered in the molecular sieves at 373 K. The orientation of molecules interacting with Bronsted or Lewis acid sites and of physisorbed molecules are discussed. Benzene adsorbed at Bronsted sites is oriented with the aromatic ring parallel to the crystallographic c-axis of the molecular sieve, whereas physisorbed benzene is oriented with the aromatic ring parallel to the crystallographic a,bplane. Acetonitrile can …

General EngineeringAromaticityGeneral ChemistryPhotochemistryMolecular sievechemistry.chemical_compoundAdsorptionchemistryPyridineGeneral Materials ScienceLewis acids and basesPyridiniumBenzeneAcetonitrileMicroporous Materials
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