Search results for "combinatorial"

showing 10 items of 1208 documents

Small molecule inhibitors of Apaf-1-related caspase- 3/-9 activation that control mitochondrial-dependent apoptosis

2006

10 pages, 5 figures.-- PMID: 16341125 [PubMed].-- Available online Dec 9, 2005.

Multiprotein complexCytochromeProtein-protein interactionsApoptosisCaspase 3MitochondrionLigandsCell LineChemical librarychemistry.chemical_compoundPeptide LibraryApoptosomesPeptoidHumansCombinatorial libraries inhibitorApoptosomeProtein PrecursorsMolecular BiologybiologyCaspase 3Intrinsic apoptosisCytochromes cCell BiologyCaspase InhibitorsCaspase 9Recombinant ProteinsMitochondriaCell biologyEnzyme ActivationCaspasa-9Apoptotic Protease-Activating Factor 1chemistryBiochemistryN-substituted GlycinesApoptosisCaspasa-3biology.proteinApoptosomeApaf-1Molecular recognitionSmall moleculeProtein BindingCell Death & Differentiation
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A positional scanning combinatorial library of peptoids as a source of biological active molecules: identification of antimicrobials

2003

9 pages, 4 figures, 2 schemes, 3 tables.-- PMID: 12959560 [PubMed].-- Printed version published in issue Sep-Oct 2003.-- Supporting information available at: http://pubs.acs.org/doi/suppl/10.1021/cc020075u

N-alkylglycineStereochemistryChemistryPositional scanning libraryMicrobial Sensitivity TestsGeneral ChemistryAntimicrobial activityAntimicrobialCombinatorial chemistryAnti-Bacterial AgentsPeptoidsPeptide LibraryChemical diversityCombinatorial Chemistry TechniquesMoleculeIdentification (biology)
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A New Entry to the Substituted Pyrrolo[3,2-c]quinoline Derivatives of Biological Interest by Intramolecular Heteroannulation of Internal Imines.

2004

New 1,3,4-substituted pyrrolo[3,2-c]quinoline derivatives were synthesised in good yields by oxidative heteroannulation of internal imines starting from easily prepared substituted 5-(2-aminophenyl)pyrroles and commercially available aryl and heteroaryl aldehydes. The reaction occurs as a one-pot process involving an intramolecular acid catalysed reaction.

NMR chemical shiftsArylOrganic ChemistryQuinolineGeneral MedicineBiochemistryInternal iminesCombinatorial chemistry2-c]quinoline derivativeschemistry.chemical_compoundchemistryIntramolecular forceDrug DiscoveryOrganic chemistryPyrrolo[3Intramolecular heteroannulationChemInform
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Data handling in NMR facilities and assignment of NMR spectra in synthetic chemistry labs: Why electronic structure validation should become part of …

2017

NMR spectra database010405 organic chemistryComputational chemistryChemistryGroup method of data handlingGeneral Materials ScienceGeneral ChemistryElectronic structure010402 general chemistry01 natural sciencesCombinatorial chemistry0104 chemical sciencesMagnetic resonance in chemistry : MRC
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Easy access to heterobimetallic complexes for medical imaging applications via microwave-enhanced cycloaddition

2015

The Cu(I)-catalysed Huisgen cycloaddition, known as “click” reaction, has been applied to the synthesis of a range of triazole-linked porphyrin/corrole to DOTA/NOTA derivatives. Microwave irradiation significantly accelerates the reaction. The synthesis of heterobimetallic complexes was easily achieved in up to 60% isolated yield. Heterobimetallic complexes were easily prepared as potential MRI/PET (SPECT) bimodal contrast agents incorporating one metal (Mn, Gd) for the enhancement of contrast for MRI applications and one “cold” metal (Cu, Ga, In) for future radionuclear imaging applications. Preliminary relaxivity measurements showed that the reported complexes are promising contrast agent…

NOTAmicrowavePhotochemistryFull Research Paperlcsh:QD241-441Metalchemistry.chemical_compoundlcsh:Organic chemistrycorroleDOTACorrolelcsh:ScienceOrganic ChemistryPorphyrinCombinatorial chemistryCycloadditionChemistryDOTAchemistryYield (chemistry)visual_artclick chemistryClick chemistryvisual_art.visual_art_mediumlcsh:QporphyrinMicrowaveBeilstein Journal of Organic Chemistry
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Structure and biological evaluation of amino-functionalized PVP nanogels for fast cellular internalization

2013

Abstract Aminopropyl methacrylamide chloride-graft-poly(N-vinyl pyrrolidone) nanogels (NGs) were designed to exploit the favorable properties of poly(N-vinyl pyrrolidone) (PVP), such as its high affinity to water and complexation ability of ions, molecules and macromolecules, with the availability of primary amino groups for bioconjugation reactions. A thorough structural characterization of the nanoscalar networks was performed via 1 H NMR and solid state 13 C NMR spectroscopies, while solid state NMR relaxation time measurements completed the NGs description in terms of polymer network density. Information on the hydrodynamic size and surface charge densities were sought via dynamic light…

Nanogels Poly(N-vinyl pyrrolidone) Microemulsion polymerization Proton spin–lattice relaxation time Cellular internalizationPolymers and PlasticsGeneral Chemical EngineeringNanogelsBiochemistrychemistry.chemical_compoundproton spin- lattice relaxation timeDynamic light scatteringmicroemulsion polymerizationPolymer chemistryMaterials ChemistryEnvironmental ChemistryMethacrylamideBovine serum albuminBioconjugationbiologyChemistryGeneral ChemistryCarbon-13 NMRCombinatorial chemistrypoly(N-vinyl pyrrolidone)biology.proteinProton NMRcellular internalizationSettore CHIM/07 - Fondamenti Chimici Delle TecnologieNanocarriersMacromolecule
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Orthogonal functionalisation of upconverting NaYF4 nanocrystals.

2013

A simple and straightforward method for the orthogonal functionalisation of upconverting NaYF4 nanocrystals (UCNCs)-doped withYb(3+) and Er(3+)-based on N-(3-dimethylaminopropyl)-N'-ethylcarbodiimide/N-hydroxysuccinimide (EDC/NHS) selective reactions between two dyes and two different reactive groups present at the periphery of the upconverting nanocrystals is reported. Organic-soluble UCNCs of 10 and 50 nm in size are encapsulated efficiently in a 1:1 mixture of two commercial 3000 Da poly(ethylene glycol) derivatives with two different reactive groups (amino and carboxylic groups). The water-dispersible UCNCs are non-cytotoxic, stable in the physiological environment, and present free ami…

NanoparticleSuccinimideslanthanides; nanocrystals; nanoparticles; polymersCatalysislaw.inventionPolyethylene Glycolschemistry.chemical_compoundFluoridesDynamic light scatteringnanocrystalsConfocal microscopylawOrganic chemistryReactivity (chemistry)lanthanidesYttriumpolymerschemistry.chemical_classificationMolecular StructureOrganic ChemistryGeneral ChemistryPolymerCombinatorial chemistrychemistryCovalent bondNanoparticlesAmine gas treatingEthylene glycolChemistry (Weinheim an der Bergstrasse, Germany)
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Nanoassemblies Based on Supramolecular Complexes of Nonionic Amphiphilic Cyclodextrin and Sorafenib as Effective Weapons to Kill Human HCC Cells

2015

Sorafenib (Sor), an effective chemiotherapeutic drug utilized against hepatocellular carcinoma (HOC), robustly interacts with nonionic amphiphilic cyclodextrin (aCD, SC6OH), forming, in aqueous solution, supramolecular complexes that behave as building blocks of highly water-dispersible colloidal nanoassemblies. SC6OH/Sor complex has been characterized by complementary spectroscopic techniques, such as UV-vis, steady-state fluorescence and anisotropy, resonance light scattering and H-1 NMR. The spectroscopic evidences and experiments carried out in the presence of an adamantane derivative, which competes with drug for CD cavity, agree with the entrapment of Sor in aCD, pointing out the role…

NiacinamideErythrocytesPolymers and PlasticsCell SurvivalAdamantaneDrug CompoundingSupramolecular chemistryBioengineeringNanotechnologyAdamantaneAntineoplastic AgentsBinding CompetitiveHemolysisAmphiphilic Cyclodextrins; Nanoparticles; Sorafenib; HCC cellsHCC cellsBiomaterialschemistry.chemical_compoundSurface-Active AgentsIn vivoCell Line TumorAmphiphileMaterials ChemistryHumanschemistry.chemical_classificationCyclodextrinsAqueous solutionCyclodextrinPhenylurea CompoundsSorafenibFluorescenceCombinatorial chemistrydigestive system diseasesNanostructuresBINDING INTERACTION THERAPY PHARMACOKINETICS BIOAVAILABILITY NANOPARTICLESDrug LiberationKineticsnanoassembliecyclodextrinchemistryDelayed-Action PreparationsProton NMRHepatocytes
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A novel approach for obtaining α,β-diaminophosphonates bearing structurally diverse side chains and their interactions with transition metal ions stu…

2020

Aminophosphonates are an important group of building blocks in medicinal and pharmaceutical chemistry. Novel representatives of this class of compounds containing nontypical side chains are still needed. The aza-Michael-type addition of amines to phosphonodehydroalanine derivatives provides a simple and effective approach for synthesizing N′-substituted α,β-diaminoethylphosphonates and thus affords general access to aminophosphonates bearing structurally diverse side chains. Thermodynamic analysis of the chosen aminophosphonates at physiological pH proves that they serve as potent chelators for copper(II) ions and moderate chelators for nickel(II) ions.

Nickelchemistry010405 organic chemistryGeneral Chemical EngineeringSide chainchemistry.chemical_elementGeneral Chemistry010402 general chemistry01 natural sciencesCombinatorial chemistryCopperTransition metal ions0104 chemical sciencesRSC Advances
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Non-toxic cyanide sources and cyanating agents

2018

The present review gives an overview over non-toxic cyanation agents and cyanide sources used in the synthesis of structurally diverse products containing the nitrile function. Nucleophilic as well as electrophilic agents/systems that transfer the entire CN-group were taken in consideration. Reactions in which a preexisting carbon functionality is transformed into a nitrile function by addition of nitrogen are however not covered here.

Nitrile010405 organic chemistryCyanideOrganic ChemistryCyanation010402 general chemistry01 natural sciencesBiochemistryCombinatorial chemistry0104 chemical scienceschemistry.chemical_compoundchemistryNucleophileElectrophilePhysical and Theoretical ChemistryOrganic & Biomolecular Chemistry
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