Search results for "derivati"

showing 10 items of 1360 documents

A simple HPLC assay for polyamines and their monoacetylderivatives

1993

polyamineSpermidineSettore BIO/10 - BiochimicaPutrescineSpermineN-acetyl-derivatives
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Design of New Polyaspartamide Copolymers for siRNA Delivery in Antiasthmatic Therapy

2020

Here, a novel protonable copolymer was realized for the production of polyplexes with a siRNA (inhibitor of STAT6 expression in asthma), with the aim of a pulmonary administration. The polycation was synthesized by derivatization of &alpha

polyaspartamidelcsh:RS1-441Pharmaceutical Science02 engineering and technologyArticlelcsh:Pharmacy and materia medica03 medical and health scienceschemistry.chemical_compoundpolyaminePEG ratioCopolymerpegylationDerivatization030304 developmental biologySTAT6polyplexechemistry.chemical_classification0303 health sciencesintegumentary systemMucinpolyplexesBiological membranePolymerasthma021001 nanoscience & nanotechnologychemistrysiRNABiophysicsPEGylationAmine gas treating0210 nano-technology
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Embeddings of Danielewski hypersurfaces

2008

In this thesis, we study a class of hypersurfaces in $\mathbb{C}^3$, called \emph{Danielewski hypersurfaces}. This means hypersurfaces $X_{Q,n}$ defined by an equation of the form $x^ny=Q(x,z)$ with $n\in\mathbb{N}_{\geq1}$ and $\deg_z(Q(x,z))\geq2$. We give their complete classification, up to isomorphism, and up to equivalence via an automorphism of $\mathbb{C}^3$. In order to do that, we introduce the notion of standard form and show that every Danielewski hypersurface is isomorphic (by an algorithmic procedure) to a Danielewski hypersurface in standard form. This terminology is relevant since every isomorphism between two standard forms can be extended to an automorphism of the ambiant …

polynomial automorphisms.Danielewski surfacespolynômes équivalentsequivalent polynomialslocally nilpotent derivations[MATH] Mathematics [math]dérivations localement nilpotentesstable equivalence problemDanielewski hypersurfacessurfaces de Danielewskihypersurfaces de Danielewskiproblème de l'équivalence stableautomorphismes polynomiaux
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Preparation of tungstophosphoric acid/cerium-doped NH2-UiO-66 Z-scheme photocatalyst: a new candidate for green photo-oxidation of dibenzothiophene a…

2021

International audience; The goal of this study was to introduce an effective visible-light induced photocatalytic system with a good ability for photocatalytic oxidative desulfurization (PODS) and denitrogenation (PODN) using molecular oxygen (O2) as an oxidant. In this regard, tungestophosphoric acid (PW12) was supported onto cerium-doped NH2-UiO-66 (PW12/Ce-NUiO-66) and employed for the photo-oxidation of dibenzothiophene (DBT) and quinoline (Qu). Herein, using cerium (Ce) as a “mediator” facilitated the separation of charge carriers, while NH2-UiO-66 remarkably enhanced the surface area with plentiful adsorption sites and shifted the adsorption edge of PW12to the visible region. The sum …

pore volumeAdsorption edgesLight02 engineering and technology01 natural scienceschemistry.chemical_compound[SPI]Engineering Sciences [physics]quinolineVisible-light irradiationMaterials Chemistryoxidizing agentOxidative desulfurizationirradiationQuinolineCerium021001 nanoscience & nanotechnologyOxidantsFlue-gas desulfurizationCeriumDibenzothiophenePhotocatalysisCharge carrierCarrier mobility0210 nano-technologychemistry.chemical_element010402 general chemistryMaximum EfficiencyCatalysisArticleuraniumAdsorptionphosphotungstic acidpore size distributiondibenzothiophene derivativegreen chemistryphotooxidationDopingdesulfurizationGeneral Chemistrysurface areaPhotocatalytic systems0104 chemical sciencesVisible light inducedDibenzothiophenesTungstophosphoric acidMolecular oxygenPhotocatalytic activitychemistryadsorptiondesorptionoxygenphotocatalysisNuclear chemistrycatalyst
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New indole and 7-azaindole derivatives as protein kinase inhibitors

2023

protein kinase inhibitorantiproliferativebis-indoleindole derivative7-azaindole derivativeanticancerSettore CHIM/08 - Chimica Farmaceutica
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Apoptotic induction on HeLa tumor cell line. A comparison of activity between pyrazolo[1,2-a]benzo[1,2,3,4]tetrazinone derivatives and their syntheti…

2009

pyrazolo[12-a]benzo[1234]tetrazinone derivativeApoptotic inductionSettore CHIM/08 - Chimica Farmaceutica
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(2-Pyridyl)sulfonyl Groups for ortho -Directing Palladium- Catalyzed Carbon-Halogen Bond Formation at Functionalized Arenes

2017

International audience; We describe an efficient palladium-catalyzed selective C-H ortho-monohalogenation (X=I, Br, Cl, F) of various functionalized (2-pyridyl) aryl-sulfones. ortho-, meta-and para-functionalization is tolerated at the arene group which undergoes C-H halogenation. Some modifications are also possible on the 2-(arylsulfonyl) heteroaryl directing groups. A comparison of the halogenation efficiency suggests that bromination is the practical method of choice, while chlorination and fluorination are possible but more challenging. Under forcing conditions ortho-dihalogenation can also be achieved.

pyridyl sulfonechemistry.chemical_elementelectrophilic fluorinationolefinationphenols010402 general chemistry01 natural sciencesMedicinal chemistryCatalysis[ CHIM.ORGA ] Chemical Sciences/Organic chemistryarene C-H functionalizationhalogenationn-(2-pyridyl)sulfonyl groupOrganic chemistryacidsSulfonylchemistry.chemical_classificationortho-arylationHalogen bond010405 organic chemistryChemistry[CHIM.ORGA]Chemical Sciences/Organic chemistryHalogenationGeneral Chemistryindolespalladiumfluorination0104 chemical sciencesderivativesactivationCarbonprotecting groupPalladium
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Synthesis, Electrochemistry, and Photophysics of Aza-BODIPY Porphyrin Dyes

2016

International audience; The synthesis of dyad and triad aza-BODIPY-porphyrin systems in two steps starting from an aryl-substituted aza-BODIPY chromophore is described. The properties of the resulting aza-BODIPY-porphyrin conjugates have been extensively investigated by means of electrochemistry, spectroelectrochemistry, and absorption/emission spectroscopy. Fluorescence measurements have revealed a dramatic loss of luminescence intensity, mainly due to competitive energy transfer and photoinduced electron transfer involving charge separation followed by recombination.

resonance energy-transferporphyrinoidstetraarylazadipyrromethenes010402 general chemistryPhotochemistryElectrochemistry01 natural sciences7. Clean energy[ CHIM ] Chemical SciencesCatalysisFluorescence spectroscopyPhotoinduced electron transfersinglet oxygentransfersphotoinduced electron-transferphotoinduced electron transferchemistry.chemical_compoundgeneration[CHIM]Chemical Scienceselectrogenerated chemiluminescencespectroscopic propertiespolyadsAbsorption (electromagnetic radiation)aza-BODIPYs010405 organic chemistryfullereneOrganic ChemistryGeneral ChemistryChromophorefluorescence spectroscopyPorphyrinFluorescence0104 chemical sciences3. Good healthchemistryelectrochemistryderivativesLuminescence
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The Missing Member of the Partially O-Alkylated Resorcinarene Family: Synthesis and Conformation of Methyl Tetramethoxy Resorcinarene

2013

An improved Lewis acid catalyzed synthesis method for methyl tetramethoxy resorcinarene is described, which produced the missing lower rim methyl derivative of this partially O-alkylated resorcinarene family. Structural characterization by means of variable temperature NMR experiments and single crystal X-ray diffraction studies furthermore revealed that the resorcinarene core adopts different conformations in the solid state and in solution. peerReviewed

resorcinareneChemistryStereochemistryOrganic ChemistryMethyl derivativeSolid-stateResorcinareneAlkylationtetramethoxy resorcinareneBiochemistryCatalysissupramolekyylikemiasupramolekulaarinen kemiaLewis acids and basesPhysical and Theoretical Chemistryta116Single crystalresorsinareenitetrametoksiresorsinareeni
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Phytochemical investigation of the needles of Abies nebrodensis (Lojac.) Mattei

2019

Abies nebrodensis (Lojac.) Mattei (Pinaceae) is a species living in a very small population only in a confined area of Sicily. In this study, the dichloromethane extract of the leaves was analyzed. Apart from three already known metabolites namely dehydroabietic acid; maltol; and rheosmin, previously detected in other species of Abies, a lanostane derivative was isolated. Its chemical structure was elucidated by means of extensive spectroscopic methods.

rheosminAbies nebrodensiChemical structurePopulationMaltolPlant Science01 natural sciencesBiochemistryLanostaneAnalytical ChemistrySettore BIO/01 - Botanica Generalechemistry.chemical_compoundOrganic chemistrySettore BIO/15 - Biologia FarmaceuticaAbies nebrodensiseducationeducation.field_of_studymaltolbiology010405 organic chemistrySettore BIO/02 - Botanica SistematicaOrganic ChemistrySettore CHIM/06 - Chimica Organicabiology.organism_classification0104 chemical sciences010404 medicinal & biomolecular chemistrychemistryPhytochemicalPinaceaedehydroabietic acidlanostaneDerivative (chemistry)
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