Search results for "SoMe"

showing 10 items of 5114 documents

The sex determining region of Chironomus thummi is associated with highly repetitive DNA and transposable elements.

1993

The dominant male sex determiner in chromosome III of the midge Chironomus thummi thummi is closely linked to a large cluster of tandem-repetitive DNA elements, the Cla elements, which are otherwise highly repetitive and distributed over more than 200 sites on all chromosomes. Chromosome III displays a hemizygous cluster of Cla elements in males but not in females. The chromosomal location of this hemizygous Cla element cluster is in the region of the male determiner M as localized by cytogenetic analysis. With Cla elements as hybridization probe, it was possible to clone a large part of the sex determining region. Molecular analysis of the DNA of males and females in this region displayed …

Transposable elementMaleSex Determination AnalysisMolecular Sequence DataMolecular cloningBiologyChironomidaechemistry.chemical_compoundGeneticsAnimalsCloning MolecularRepeated sequenceGenetics (clinical)Repetitive Sequences Nucleic AcidGeneticsBase SequenceHybridization probeChromosomeChromosome MappingDNABiological EvolutionChromosome 3chemistryDNA Transposable ElementsFemaleRecombinationDNAChromosoma
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The evolutionary genetics of the hobo transposable element in the Drosophila melanogaster complex.

1994

Hobo elements are a family of transposable elements found in Drosophila melanogaster and its three sibling species: D. simulans, D. mauritiana and D. sechellia. Studies in D. melanogaster have shown that hobo may be mobilized, and that the genetic effects of such mobilizations included the general features of hybrid dysgenesis: mutations, chromosomal rearrangements and gonadal dysgenis in F1 individuals. At the evolutionary level some hobo-hybridizing sequences have also been found in the other members of the melanogaster subgroup and in many members of the related montium subgroup. Surveys of older collected strains of D. melanogaster suggest that complete hobo elements were absent prior t…

Transposable elementMolecular Sequence DataPlant ScienceDNA sequencingChromosomesSpecies SpecificityGeneticsMelanogasterAnimalsAmino Acid SequenceMauritianaSequence DeletionGeneticsbiologyBase SequenceHuman evolutionary geneticsGeneral Medicinebiology.organism_classificationBiological EvolutionHuman geneticsDrosophila melanogasterEvolutionary biologyInsect ScienceHorizontal gene transferDNA Transposable ElementsAnimal Science and ZoologyDrosophilaDrosophila melanogasterGenetica
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Lipid phase transition in saccharide-coated cholate-containing liposomes: coupling to the surrounding matrix.

2005

We performed FTIR measurements on cholate-containing liposomes (CCL) embedded in saccharide (trehalose or sucrose) matrixes with different contents of residual water. We obtained information on the CCL phase transition following the thermal evolution (310-70 K) of the IR spectrum of the carbonyl moieties of phospholipids in the frequency range 4225-4550 cm(-1). Furthermore, we simultaneously followed the thermal evolution of the water association band, which gave information on the behavior of the surrounding water-saccharide matrix. The analysis revealed a small sub-band of the water association band present in CCL but not in cholate-free liposomes, the thermal evolution of which is tightl…

Trehalose Liposomes Thermal behaviourSucroseSucroseSurface PropertiesLipid BilayersPhospholipidInfrared spectroscopydigestive systemPermeabilityPhase Transitionchemistry.chemical_compoundDrug Delivery Systemsstomatognathic systemHydrophilySpectroscopy Fourier Transform InfraredElectrochemistryGeneral Materials ScienceLipid bilayer phase behaviorFourier transform infrared spectroscopySpectroscopyPhospholipidsLiposomeChromatographydigestive oral and skin physiologyTemperatureTrehaloseWaterSurfaces and InterfacesCondensed Matter PhysicsTrehaloseSettore FIS/07 - Fisica Applicata(Beni Culturali Ambientali Biol.e Medicin)chemistryLiposomesCholatesHydrophobic and Hydrophilic InteractionsLangmuir : the ACS journal of surfaces and colloids
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Understanding the stereoselectivity in Brønsted acid catalysed Povarov reactions generating cis/trans CF3-substituted tetrahydroquinolines: a DFT stu…

2016

The Bronsted acid (BA) catalysed Povarov reactions of (E)-1-phenyl-N-(4-(trifluoromethyl)phenyl) methanimine with 1-vinylpyrrolidin-2-one (VPO) and with allyltrimethylsilane (ATMS), affording CF3-substituted cis/trans tetrahydroquinoline (THQ) derivatives, have theoretically been studied using the M06-2X functional together with the standard 6-31G(d) basis set. These BA catalysed Povarov reactions are multistep processes initialised by the nucleophilic attack of the non-substituted carbon atom of the nucleophilic ethylene on the imine carbon atom of the super-electrophilic protonated imine, yielding the corresponding cationic intermediate along the endo/exo stereoisomeric approach mode. Upo…

Trifluoromethyl010405 organic chemistryStereochemistryGeneral Chemical EngineeringImineProtonationGeneral Chemistry010402 general chemistry01 natural sciences0104 chemical scienceschemistry.chemical_compoundchemistryNucleophileIntramolecular forceStereoselectivityBrønsted–Lowry acid–base theoryCis–trans isomerismRSC Advances
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Enantioselective Zirconium-Catalyzed Friedel−Crafts Alkylation of Pyrrole with Trifluoromethyl Ketones

2009

The first catalytic enantioselective Friedel-Crafts alkylation of pyrrole with 2,2,2-trifluoroacetophenones to give pyrroles with a trifluoromethyl-substituted tertiary alcohol moiety bearing a quaternary stereogenic center is described. The reaction is achieved in the presence of a 3,3'-dibromo-BINOL-Zr(IV) complex to give the expected products with high yields (up to 98%) and good enantioselectivities (up to 93% ee). The absolute stereochemistry of the products has been determined by chemical correlation.

TrifluoromethylAlkylationOrganic ChemistryEnantioselective synthesisStereoisomerismKetonesAlkylationBiochemistryMedicinal chemistryCatalysisSubstrate SpecificityCatalysisStereocenterchemistry.chemical_compoundchemistryMoietyPyrrolesZirconiumPhysical and Theoretical ChemistryFriedel–Crafts reactionPyrroleOrganic Letters
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Catalytic asymmetric conjugate addition of terminal alkynes to β-trifluoromethyl α,β-enones.

2014

The first enantioselective conjugate alkynylation of β-trifluoromethyl α,β-enones using terminal alkynes and a taniaphos–Cu(I) complex as catalyst is described. Ketones bearing a trifluoromethylated propargylic chiral centre in the β-position were obtained with good yields and high enantiomeric excesses (up to 99%).

TrifluoromethylHydrocarbons FluorinatedMolecular StructureStereochemistryChemistryMetals and AlloysEnantioselective synthesisStereoisomerismGeneral ChemistryKetonesCatalysisSurfaces Coatings and FilmsElectronic Optical and Magnetic MaterialsCatalysischemistry.chemical_compoundAlkynylationTerminal (electronics)AlkynesMaterials ChemistryCeramics and CompositesEnantiomerConjugateChemical communications (Cambridge, England)
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Rotational spectra of gauche perfluoro-n-butane, C4F10; perfluoro-iso-butane, (CF3)3CF; and tris(trifluoromethyl)methane, (CF3)3CH

2007

Abstract The microwave spectra of the gauche conformer of perfluoro- n -butane, n -C 4 F 10 , of perfluoro- iso -butane, (CF 3 ) 3 CF, and of tris(trifluoromethyl)methane, (CF 3 ) 3 CH, have been observed and assigned. The rotational and centrifugal distortion constants for gauche n -C 4 F 10 are: A  = 1058.11750(7) MHz, B  = 617.6832(1) MHz, C  = 552.18794(1) MHz, Δ J  = 0.0257(5) kHz, δ J  = 0.0052(3) kHz. A C–C–C–C dihedral angle, ω , of ∼55° has been determined. These values agree well with those obtained from a coupled cluster (CCSD/cc-PVTZ) calculation. The rotational and centrifugal distortion constants for iso -C 4 F 10 and iso -C 4 HF 9 are: B o  = 816.4519(4) MHz, D J  = 0.023(2) …

TrifluoromethylMaterials scienceAnalytical chemistryButaneDihedral angleAtomic and Molecular Physics and OpticsSpectral linechemistry.chemical_compoundDipoleCoupled clusterchemistryRotational spectroscopyPhysical and Theoretical ChemistryConformational isomerismSpectroscopyJournal of Molecular Spectroscopy
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Diastereoselective synthesis of 2-phenyl-3-(trifluoromethyl)piperazines as building blocks for drug discovery.

2014

The synthesis of enantiomerically pure cis- and trans-2-phenyl-3-(trifluoromethyl)piperazines is described. It involved, as the key step, a diastereoselective nucleophilic addition of the Ruppert-Prakash reagent (TMSCF3) to alpha-amino sulfinylimines bearing Ellman's auxiliary. This methodology allows an entry into hitherto unknown trifluoromethylated and stereochemically defined piperazines, key scaffold components in medicinal chemistry.

TrifluoromethylNucleophilic additionHydrocarbons FluorinatedMolecular StructureChemistryDrug discoveryOrganic ChemistryStereoisomerismSilanesCombinatorial chemistryCatalysisPiperazineschemistry.chemical_compoundReagentDrug DiscoveryOrganic chemistryIndicators and ReagentsThe Journal of organic chemistry
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Effect of tin and lead chlorotriphenyl analogues on fruit fly Drosophila hydei and liposomes membrane

2011

This article presents the results of a study investigating the biological activity of triphenyltin chloride (TPhT) and two metalloorganic compounds, triphenyllead chloride (TPhL) and triphenylmethane chloride (TPhC), in their interaction with model membranes and the living organisms of fruit flies Drosophila hydei. The study of model membranes (sonicated liposomes) was conducted using the electron spin resonance (ESR) spin probe technique, whereas the experiment on fruit flies involved investigating their viability on media containing the studied compounds. The test results clearly demonstrate that TPhT affects fruit flies more actively than TPhL (complete lethality after 7 days of culture …

Triphenyltin chlorideHealth Toxicology and MutagenesisToxicologyBiochemistryChloridechemistry.chemical_compoundOrganometallic CompoundsOrganotin CompoundsmedicineAnimalsLipid bilayerMolecular BiologyDrosophilaLiposomeTriphenylmethanebiologyCell MembranefungiElectron Spin Resonance SpectroscopyTrityl CompoundsGeneral Medicinebiology.organism_classificationMembraneLeadBiochemistrychemistryTinLiposomesModels AnimalDrosophila hydeiMolecular MedicineDrosophilamedicine.drugJournal of Biochemical and Molecular Toxicology
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Effect of Chlorotriphenyl Derivatives of Sn and Pb upon Biophysical Properties of Membranes

2009

Biophysical activity of two twin organometallic compounds Triphenyltin chloride (TPhT) and Triphenyllead chloride (TPhL) in their interreaction with model membranes, as well as with yeast cellsSaccharomyces cerevisiae, was investigated. Four measurement methods were used in the experiments: two physical methods (spin probes method and the electric method); two biological methods (minimal inhibitory concentration /MIC/ and yeast survival test). It has been found that the activity of TPhT in interaction with model membranes and yeast cells is distinctly greater than that of TPhL. The activity manifests itself by considerable increase in the fluidity of the middle part of liposome bilayer, cha…

Triphenyltin chlorideTime FactorsArticle SubjectCell SurvivalHealth Toxicology and Mutagenesislcsh:BiotechnologySaccharomyces cerevisiaelcsh:MedicineSaccharomyces cerevisiaelcsh:Chemical technologylcsh:TechnologyBiophysical PhenomenaMembrane PotentialsCell membranechemistry.chemical_compoundlcsh:TP248.13-248.65GeneticsmedicineOrganometallic CompoundsOrganotin Compoundslcsh:TP1-1185Molecular BiologyLiposomebiologyChemistrylcsh:TBilayerCell Membranelcsh:RElectron Spin Resonance SpectroscopyLauric AcidsGeneral Medicinebiology.organism_classificationLauric acidYeastMembranemedicine.anatomical_structureBiochemistryLiposomesBiophysicsMolecular MedicineBiotechnologyResearch ArticleJournal of Biomedicine and Biotechnology
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