Search results for "TYR"

showing 10 items of 2017 documents

Prognostic role of soluble PD-1 and BTN2A1 in overweight melanoma patients treated with nivolumab or pembrolizumab: finding the missing links in the …

2023

Individual response to immune checkpoint inhibitors (ICIs) is currently unpredictable in patients with melanoma. Recent findings highlight a striking improvement in the clinical outcomes of overweight/obese patients treated with ICIs, which seems driven, at least in part, by programmed cell death protein 1 (PD-1)-mediated T-cell dysfunction. A putative role of butyrophilins (BTNs) is under investigation as a novel mechanism of cancer immune evasion and obesity-associated inflammation. This study investigates the role of baseline plasma levels of soluble PD-1 (sPD-1), soluble programmed cell death ligand 1 (sPD-L1), BTN2A1 (sBTN2A1), BTN3A1 (sBTN3A1), along with body mass index (BMI), as pr…

butyrophilinsOncologyBTN2A1PD-1melanomacirculating immune checkpointssoluble immune checkpointspredictive biomarker
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Inside c-kit tyrosine kinase: molecular modeling and QSAR in the search of new inhibitors

2010

c-kit tyrosine kinasemolecular modelingQSAR
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Density Functional Theory Investigation on the Nucleation and Growth of Small Palladium Clusters on a Hyper-Cross-Linked Polystyrene Matrix

2014

Density functional theory calculations were employed to investigate the nucleation and growth of small palladium clusters, up to Pd9, into a microcavity of the porous hyper-cross-linked polystyrene (HPS). The geometries and the electronic structures of the palladium clusters inside the HPS cavity, following the one-by-one atom addition, are affected by a counterbalance between the Pd–phenyl (Pd−Φ) and Pd–Pd interactions. The analysis performed on energetics, cavity distortions, and cluster geometries indeed suggest that the cluster growth is dominated by the Pd−Φ interactions up to the formation of Pd4 aggregates, whereas the metal–metal interactions actually rule the growth of the larger c…

catalysispolymeric supportNucleationchemistry.chemical_elementSurfaces Coatings and FilmsElectronic Optical and Magnetic MaterialsMatrix (mathematics)chemistry.chemical_compoundGeneral EnergychemistryChemical physicsComputational chemistryAtomCluster (physics)Density functional theoryPolystyrenePhysical and Theoretical ChemistryElasticity (economics)Metal nanoparticlemetal-phenyl interactionPalladiumThe Journal of Physical Chemistry C
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Multi-layered, covalently supported ionic liquid phase (mlc-SILP) as highly cross-linked support for recyclable palladium catalysts for the suzuki re…

2011

The reaction between an excess of 1,4-bis(3-vinylimidazolium-1-yl) bromide and a mercaptopropyl-modified amorphous silica gel or ordered mesoporous silica SBA-15 in the presence of azobisisobutyronitrile (AIBN) afforded new materials, which have a high loading of imidazolium moieties. These materials, which contain a highly cross-linked polymeric network, have been denoted as multi-layered, covalently supported ionic liquid phase (mlc-SILP) and have been used as support for palladium catalysts containing a high loading of the metal (10 wt%). Such materials were characterized by several techniques (13C magic angle spinning nuclear magnetic resonance, the Brunauer–Emmett–Teller technique, sma…

catalyst recyclingInorganic chemistryAzobisisobutyronitrilechemistry.chemical_elementGeneral ChemistrySettore CHIM/06 - Chimica OrganicaMesoporous silicapalladiumCatalysisBiphenyl compoundchemistry.chemical_compoundSuzuki reactionchemistryIonic liquidMagic angle spinningPalladiumionic liquidAdvanced Synthesis and Catalysis
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Visible Light-Induced Sulfonylation/Arylation of Styrenes in a Double Radical Three-Component Photoredox Reaction

2019

Simultaneous sulfonylation/arylation of styrene derivatives is achieved in a photoredox-catalyzed three-component reaction using visible light. A broad variety of difunctionalized products is accessible in mostly excellent yields and high diastereoselectivity. The developed reaction is scalable and suitable for the modification of styrene-functionalized biomolecules. Mechanistic investigations suggest the transformation to be operating through a designed sequence of radical formation and radical combination.

chemistry.chemical_classification010405 organic chemistryChemistryBiomoleculeOrganic ChemistryPhotoredox catalysisGeneral Chemistry010402 general chemistryPhotochemistry01 natural sciencesCatalysis0104 chemical sciencesStyrenechemistry.chemical_compoundRadical formationVisible spectrum
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A pillar[5]arene-containing cross-linked polymer: synthesis, characterization and adsorption of dihaloalkanes and n-alkylene dinitriles

2016

A pillar[5]arene-containing cross-linked polymer was synthesized via Williamson reaction involving monohydroxy pillar[5]arene with chloromethylated polystyrene. Its adsorption behavior towards guests was investigated. It was found that the pillar[5]arene-containing polymer exhibited good adsorption capacities towards dihaloalkanes and dinitriles by host-guest complexation.

chemistry.chemical_classification010405 organic chemistryGeneral Chemical EngineeringPillarGeneral ChemistryPolymer010402 general chemistry01 natural sciences0104 chemical sciencesCharacterization (materials science)chemistry.chemical_compoundAdsorptionchemistryPolymer chemistryPolystyreneRSC Advances
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Rh(I) Coordination Chemistry of Chiral α-Aminophosphine(η6-arene)chromium Tricarbonyl Ligands

2003

The diastereoselective addition of Ph(2)PH to the chiral ortho-substituted eta(6)-benzaldimine complexes (eta(6)-o-X-C(6)H(4)CH=NAr)Cr(CO)(3) (1, X = MeO, Ar = p-C(6)H(4)OMe; 2, X = Cl, Ar = Ph) leads to the formation of the corresponding chiral aminophosphines (alpha-P,N) Ph(2)P-CH(Ar(1))-NHAr(2) (3, Ar(1) = o-C(6)H(4)(OCH(3))[Cr(CO)(3)], Ar(2) = p-C(6)H(4)OCH(3); 4, Ar(1) = o-C(6)H(4)Cl[Cr(CO)(3)], Ar(2) = Ph) in equilibrium with the starting materials. The uncomplexed benzaldimine (o-ClC(6)H(4)CH=NPh), 2', analogously produces an equilibrium amount of the corresponding aminophosphine Ph(2)P-CH(Ar(1))-NHAr(2) (4', Ar(1) = o-C(6)H(4)Cl, Ar(2) = Ph). Depending on the equilibrium constant, t…

chemistry.chemical_classification010405 organic chemistryStereochemistrychemistry.chemical_elementLigands010402 general chemistry01 natural sciencesOxidative additionMedicinal chemistryStyrenes0104 chemical sciencesCoordination complexInorganic ChemistryChromiumchemistryMixturesRhodium[CHIM.COOR]Chemical Sciences/Coordination chemistryPhysical and Theoretical ChemistryMolecular structureEquilibrium constantInorganic Chemistry
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Tapered copolymers of styrene and 4‐vinylbenzocyclobutene via carbanionic polymerization for crosslinkable polymer films

2019

chemistry.chemical_classification540 Chemistry and allied sciencesMaterials sciencePolymers and PlasticsKineticsPolymerStyrenechemistry.chemical_compoundAnionic addition polymerizationchemistryPolymerization540 ChemiePolymer chemistryMaterials ChemistryCopolymerPhysical and Theoretical Chemistry
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Films from styrene–butyl acrylate lattices using maleic or succinic surfactants: mechanical properties, water rebound and grafting of the surfactants

2000

Abstract A series of anionic and zwitterionic maleic surfactants have been synthesized and engaged in styrene–butyl acrylate emulsion polymerization. Some non-reactive succinic analogs have been synthesized in order to perform their comparison with the maleic surfactants in polymerization experiments. Films from the obtained lattices were cast, and their mechanical properties and the water rebound were tested. The results of water rebound demonstrate significant difference between the films prepared with maleic or succinic surfactants. Water rebound of the films after 34 days in the case of succinic surfactants was found to be between 51 and 95%, while for maleic surfactants it is only 25–4…

chemistry.chemical_classificationAcrylateAbsorption of waterMaterials sciencePolymers and PlasticsButyl acrylateOrganic ChemistryEmulsion polymerizationPolymerStyrenechemistry.chemical_compoundchemistryPolymerizationChemical engineeringPolymer chemistryMaterials ChemistryIonomerPolymer
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Core-shell polyacrylate and polystyrene-block-polyacrylate stars

2005

The polymerization of p-(iodomethyl)styrene (PIMS) yields well-defined branched polymers with reactive iodomethyl groups. The branched poly[p-(iodomethyl)styrene] was used as the transfer agent in the iodine mediated radical polymerization of vinyl monomers. The polymerization proceeds in a controlled way and yields polystyrene and poly(t-butyl acrylate) star polymers with reactive groups at the end of their arms. Polymers so obtained were also used to prepare stars with block copolymer arms: polystyrene-block-poly(t-butyl acrylate). The characterization of star structures was performed by NMR and gel permeation chromatography with absolute molar mass detection (MALLS). Preliminary characte…

chemistry.chemical_classificationAcrylateMaterials sciencePolymers and PlasticsOrganic ChemistryRadical polymerizationChain transferPolymerStyrenechemistry.chemical_compoundPolymerizationchemistryPolymer chemistryMaterials ChemistryCopolymerPolystyrenePolymer
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