Search results for "Moiety"

showing 10 items of 621 documents

A phosphonamidate containing aromatic N-terminal amino group as inhibitor of leucine aminopeptidase-design, synthesis and stability.

2006

Fully deprotected phosphonamidate dipeptides, predicted as effective inhibitors of cytosolic leucine aminopeptidase, showed unexpected instability in water solution at pH below 12. Their hydrolysis rate was strictly correlated with basicity of the N-terminal amino group. To improve this feature a phosphonamidate analogue containing less basic, aromatic 2-aminophenylphosphonate residue in P1 position of the inhibitor was designed. The target compound was synthesised starting from diethyl 2-nitrophosphonate in several step procedure. The decrease in basicity of the terminal amino moiety of the modified analogue in fact resulted in satisfactory improvement of hydrolytic stability of the P–N bo…

PharmacologyModels MolecularMagnetic Resonance SpectroscopyChemistryStereochemistryphosphonamidateLAP inhibitorsOrganic ChemistryGeneral MedicineAminopeptidaseChemical synthesisResidue (chemistry)HydrolysisLeucyl AminopeptidaseOrganophosphorus CompoundsDrug StabilityDrug DesignDrug Discoveryhydrolytic stabilityMoietyChemical stabilityProtease InhibitorsLeucineLeucyl aminopeptidaseEuropean journal of medicinal chemistry
researchProduct

H2-antihistaminics. 20. Structure-activity relationships in H2-receptor antagonists containing a 4-pyrimidone moiety.

1984

In a series of 5,6-substituted 4- pyrimidones 1 a-v the H2-antihistaminic activity was determined (guinea-pig atrium) and lipophilicity data are given in form of Rmo -values. The influence of different substituents at position 5 or 6 of a pyrimidone moiety has been studied. Quantitative structure-activity analyses showed the importance of lipophilicity for drug activity. Additionally other physicochemical substituent-properties may play a major role.

PharmacologyStereochemistryImmunologyPharmacology toxicologyGuinea PigsHeartPyrimidinonesToxicologyLipidschemistry.chemical_compoundStructure-Activity RelationshipDrug activitychemistryHistamine H2 receptorHistamine H2 AntagonistsSolubilityLipophilicityMoietyAnimalsPharmacology (medical)PyrimidoneAgents and actions
researchProduct

Research Letter: Structural Combination of Established 5-HT2A Receptor Ligands: New Aspects of the Binding Mode

2010

MH.MZ, MDL 100907, and altanserin are structurally similar 4-benzoyl-piperidine derivatives and are well accommodated to receptor interaction models. We combined structural elements of different high-affinity and selective 5-HT(2A) antagonists, as MH.MZ, altanserin, and SR 46349B, to improve the binding properties of new compounds. Three new derivatives were synthesized with a 4-benzoyl-piperidine moiety as the lead structure. The in vitro affinity of the novel compounds was determined by a [³H]MDL 100907 competition binding assay. The combination of MH.MZ and SR 46349B resulted in a compound (8) with a moderate affinity toward the 5-HT(2A) receptor (K(i) = 57 nm). The remarkably reduced af…

PharmacologySteric effectsChemistryStereochemistryChemical structureLigand binding assayOrganic ChemistryPlasma protein bindingBiochemistrychemistry.chemical_compoundDrug DiscoveryAltanserinMolecular MedicineMoietyReceptorG protein-coupled receptorChemical Biology & Drug Design
researchProduct

Enantioselective Hydrogenation Catalysis Aided by a σ-Bonded Calix[4]arene to a P-Chirogenic Aminophosphane Phosphinite Rhodium Complex

2010

The first P-chirogenic aminophosphane−phosphinite (AMP*P) ligand (4a) supported on the upper rim of a calix[4]arene moiety was synthesized in two steps using the ephedrine methodology. Ligand 4a wa...

PhosphiniteLigandOrganic ChemistryEnantioselective synthesischemistry.chemical_elementMedicinal chemistryRhodiumInorganic Chemistrychemistry.chemical_compoundHydrogenation catalysischemistryMoietyOrganic chemistryPhysical and Theoretical ChemistryOrganometallics
researchProduct

DNA-binding and in vitro cytotoxic activity of platinum(II) complexes of curcumin and caffeine

2019

Abstract Three Pt(II) complexes containing the natural ligands curcumin and caffeine, namely [Pt(curc)(PPh3)2]Cl (1), [PtCl(curc)(DMSO)] (2) (curc = deprotonated curcumin) and trans-[Pt(caffeine)Cl2(DMSO)] (3), were synthesized and fully characterized. The data obtained suggest that, for both 1 and 2, the anion of curcumin is coordinated to the platinum ion via the oxygen atoms of the β-diketonate moiety. Spectroscopic features reveal that in 2 and 3, a DMSO molecule is S-bonded to the metal centre. For 3, all data indicate a square-planar geometry formed by a 9-N bonded caffeine, two trans chloride anions and a DMSO. The three complexes undergo changes in solution upon incubation for 24 h;…

PhotoactivationCurcuminCytotoxicityIntercalation (chemistry)chemistry.chemical_elementCaffeine; Curcumin; Cytotoxicity; DNA interaction; Natural ligands; Photoactivation; Platinum(II) complexAntineoplastic Agents010402 general chemistryLigands01 natural sciencesBiochemistryMedicinal chemistryNucleobaseInorganic Chemistrychemistry.chemical_compoundDrug StabilityCoordination ComplexesCaffeineCell Line TumorMoietyMoleculeAnimalsHumansPlatinumMolecular Structure010405 organic chemistryDNA0104 chemical sciencesDNA interactionchemistryCurcuminPlatinum(II) complexCattleCaffeine Curcumin Cytotoxicity DNA interaction Natural ligands Photoactivation Platinum(II) complexCisplatinDrug Screening Assays AntitumorSelectivityPlatinumNatural ligandsCis–trans isomerism
researchProduct

Conjugating pillararene dye in dye-sensitized solar cells

2021

Summary The improvement of open-circuit voltage (VOC) is a crucial goal to develop efficient dye-sensitized solar cells (DSSCs). Here, conjugating pillar[5]arene dyes (PPI and PPII) are designed, synthesized, and applied in DSSCs. The presence of pillar[5]arene moiety in the dyes inhibits the dye aggregation and charge recombination in the DSSCs, leading to the enhancement of VOC. PPI with a single D-π-A backbone and a pillar[5]arene moiety achieves a VOC of 715 mV, which is much higher than the reference dye (VOC of 674 mV) with the same D-π-A backbone but no pillar[5]arene moiety. PPII with 2 D-π-A backbones also achieves a VOC of 746 mV and a much higher short-circuit photocurrent (JSC) …

PhotocurrentMaterials scienceGeneral EngineeringPillarGeneral Physics and AstronomyGeneral ChemistryElectrolytePillararenePhotochemistrychemistry.chemical_compoundDye-sensitized solar cellGeneral EnergychemistryPhenothiazineMoietyGeneral Materials ScienceCell Reports Physical Science
researchProduct

Computational modeling of single-versus double-anchoring modes in di-branched organic sensitizers on TiO2 surfaces: structural and electronic propert…

2014

We present a first-principles DFT investigation of the adsorption geometry on the anatase (101) surface of a prototypical di-branched organic dye based on the extended tetrathiafulvalene moiety, incorporating two anchoring cyanoacrylic acid units. Reduced model systems with one and two anchoring groups have been initially studied to investigate the vibrational frequencies related to TiO2 dye adsorption. Our calculations confirm that the reduced systems can be used as reliable models to study the anchoring modes and that the conclusions extracted from the reduced systems can be extrapolated to the entire molecule. A series of molecular structures have been investigated to simulate the anchor…

Physics and Astronomy (all); Physical and Theoretical ChemistryAnataseDenticityGeneral Physics and AstronomyAnchoring02 engineering and technology010402 general chemistry021001 nanoscience & nanotechnology01 natural sciences7. Clean energyPlanarity testing0104 chemical sciences[CHIM.THEO]Chemical Sciences/Theoretical and/or physical chemistryPhysics and Astronomy (all)chemistry.chemical_compoundAdsorptionchemistryComputational chemistryChemical physicsMoleculeMoietyPhysical and Theoretical Chemistry0210 nano-technologyComputingMilieux_MISCELLANEOUSTetrathiafulvalene
researchProduct

Electrochemical study of intramolecular charge transfer complexes derived from 1,4-naphthoquinone Part 1. Electroreduction

1995

Abstract Electrochemical investigations (polarography, cyclic voltammetry, rotating ring-disk electrode voltammetry) of intramolecular charge transfer complexes (AC) derived from 1,4-naphthoquinone were performed in acetonitrile. It is concluded that in the first one-electron stage of its electrochemical reduction the AC is in a complexed form. At the same time the amino moiety, which shows a marked inductive (−I) effect, acts as an electron donor in the donor-acceptor (D-A) interaction. Facilitation of the reduction of the quinone part by the aryl amine residue is compensated by the D-A interaction, which makes the electroreduction more difficult. By using ultramicroelectrodes it was shown…

PolarographyChemistryGeneral Chemical EngineeringInorganic chemistryElectron donorUltramicroelectrodeAnalytical Chemistrychemistry.chemical_compoundIntramolecular forceElectrochemistryMoietyCyclic voltammetryAcetonitrileVoltammetryJournal of Electroanalytical Chemistry
researchProduct

Bioinspired catechol-terminated self-assembled monolayers with enhanced adhesion properties

2013

The role of the catechol moiety in the adhesive properties of mussel proteins and related synthetic materials has been extensively studied in the last years but still remains elusive. Here, a simplified model approach is presented based on a self-assembled monolayer (SAM) of upward-facing catechols thiol-bound to epitaxial gold substrates. The orientation of the catechol moieties is confirmed by spectroscopy, which also showed lack of significant amounts of interfering o-quinones. Local force-distance curves on the SAM measured by atomic force microscopy (AFM) shows an average adhesion force of 45 nN, stronger than that of a reference polydopamine coating, along with higher reproducibility …

PolydopamineIndolesPolymersCatecholsBiocompatible MaterialsNanotechnologyMolecular Dynamics Simulationengineering.materialBiomimèticaMicroscopy Atomic ForceBiomaterialsMolecular dynamicschemistry.chemical_compound:Enginyeria química [Àrees temàtiques de la UPC]Coated Materials BiocompatibleCoatingMonolayerMoietyGeneral Materials ScienceMagnetite NanoparticlesAdhesive surfaceCatecholChemistrySAMsAdhesivenessSelf-assembled monolayerGeneral ChemistryAdhesionBiomimetic polymersChemical engineeringCatecholengineeringPrintingMagnetic nanoparticlesBiomimeticGoldBiotechnology
researchProduct

18F-Radiolabeling, Preliminary Evaluation of Folate-pHPMA Conjugates via PET

2014

The synthesis of a 10.5 kDa and a 52.5 kDa polymer, based on pHPMA functionalized with tyramine for (18) F-labeling and a folate derivative as targeting moiety, is reported. FCS studies are conducted using Oregon Green-labeled conjugates. No aggregation is observed for the 10.5 kDa conjugate, but strong aggregation for the 52.5 kDa conjugate. In vivo studies are conducted using Walker-256 mammary carcinoma model to determine body distribution as function of size and especially targeting unit. These in vivo studies show a higher short time (2 h) accumulation for both conjugates in the tumor than for untargeted pHPMA, confirmed by blockade studies. The 10.5 kDa polymer accumulates with 0.46% …

Polymers and PlasticsBioengineeringTyramineWalker 256 carcinomaBiomaterialsMammary carcinomachemistry.chemical_compoundchemistryBiochemistryIn vivoMaterials ChemistryDistribution (pharmacology)MoietyBiotechnologyConjugateMacromolecular Bioscience
researchProduct