Search results for "Polyamin"

showing 10 items of 160 documents

Hormonal regulation of S-adenosylmethionine synthase transcripts in pea ovaries

1996

Two cDNA clones coding for S-adenosyl-L-methionine synthase (SAMs, EC 2.5.1.6) have been isolated from a cDNA library of gibberellic acid-treated unpollinated pea ovaries. Both cDNAs were sequenced showing a high degree of identity but coding for different SAMs polypeptides. The presence of two SAMs genes in pea was further confirmed by Southern analysis. Expression of the SAMs genes in the pea plant was found at different levels in vegetative and reproductive tissues. We characterized the expression levels of SAMs genes during the development or senescence of pea ovaries. Northern analysis showed that transcription of SAMs genes in parthenocarpic fruits was upregulated by auxins in the sam…

AgingMolecular Sequence DataSequence HomologyPlant ScienceBiologyGenes PlantParthenocarpychemistry.chemical_compoundPlant Growth RegulatorsGene Expression Regulation PlantAuxinComplementary DNAPolyaminesGeneticsAmino Acid SequenceRNA MessengerGeneGibberellic acidchemistry.chemical_classificationMessenger RNAAniline CompoundsBase SequencecDNA libraryPeasfood and beveragesMethionine AdenosyltransferaseSequence Analysis DNAGeneral MedicineEthylenesIsoenzymesBiochemistrychemistryRNA PlantFruitGibberellinAgronomy and Crop Science
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RGD-mimic polyamidoamine-montmorillonite composites with tunable stiffness as scaffolds for bone tissue-engineering applications

2017

This paper reports on the development of montmorillonite (MMT)-reinforced hydrogels, based on a peptidomimetic polyamidoamine carrying guanidine pendants (AGMA1), as substrates for the osteo-induction of osteoblast precursor cells. AGMA1 hydrogels of various degrees of crosslinking responded favourably to MMT reinforcement, giving rise to composite hydrogels with shear storage modulus G', when fully swollen in water, up to 200 kPa, i.e. 20 times higher than the virgin hydrogels and of the same order or higher than other hydrogel-based composites proposed for orthopaedic applications. This significant improvement was ascribed to the effective interpenetration between the polymer matrix and t…

AgmatinepolyamidoaminesBiomedical EngineeringMedicine (miscellaneous)montmorilloniteBone and BonesCell LineBiomaterialsMicebone regenerationMaterials Testingmental disordersPolyaminesAnimalsBone regeneration; Composite; Montmorillonite; Osteo-inductive; Polyamidoamines; Biomedical Engineering; Medicine (miscellaneous); Biomaterialscompositeosteo-inductiveQMOsteoblastsTissue EngineeringTissue Scaffoldstechnology industry and agricultureHydrogelsBentoniteRBOligopeptides
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New Insight to the Chemistry of Polyaza[n]paracyclophanes. A 15N NMR Study

2001

AldehydesMagnetic Resonance SpectroscopyNitrogen IsotopesChemistryOrganic ChemistryTitrimetryHydrogen-Ion ConcentrationEthers CyclicMetalsCationsAlkanesPolyaminesOrganic chemistryChemistry (relationship)The Journal of Organic Chemistry
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Development and in vitro Evaluation of Antigen-Loaded Poly(amidoamine) Nanoparticles for Respiratory Epithelium Applications

2013

A poly(amidoamine) with disulfide linkages in the main chain and 4-hydroxybutyl and ω-carboxy-PEG groups (9:1 ratio) as side chains was prepared by Michael addition polymerization of cystamine bisacrylamide with 4-hydroxybutylamine and ω-carboxy-PEG-amine. To develop therapeutic protein formulations for improved delivery of antigen via the intranasal route, nanoparticles were prepared from this polymer by self-assembly with p24 or ovalbumin as the model proteins and CpG as the adjuvant. The nanoparticles incorporated the antigens and adjuvant from the feed solution with high efficiency (∼90 %) and have sizes of 112 and 169 nm, respectively, with low positive surface charge (∼+2 mV). Formula…

AmidoamineNanoparticleRespiratory MucosaBiochemistryModels Biologicalchemistry.chemical_compoundAntigenMETIS-302364CystamineIR-90175Drug DiscoveryPolymer chemistryPolyaminesHumansGeneral Pharmacology Toxicology and PharmaceuticsAntigensParticle SizeAdministration IntranasalCells CulturedPharmacologybiologyOrganic ChemistryPoly(amidoamine)OvalbuminchemistryPolymerizationbiology.proteinBiophysicsMolecular MedicineRespiratory epitheliumNanoparticles
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o-Phthalaldehyde–N-acetylcysteine polyamine derivatives: formation and stability in solution and in C18 supports

2001

A comparative study of different derivatization procedures has been performed in order to improve the stability of the reaction products o-phthalaldehyde-N-acetylcysteine (OPA-NAC) polyamines. Procedures such as solution derivatization, solution derivatization followed by retention on a packing support, derivatization on different packing supports and on-column derivatization, have been optimized and compared. The degradation rate constant (k) of the derivative was dependent on the procedure used and on the analyte. For the spermine (the most unstable isoindol tested) k was 8 +/- 2 x 10(-2) min(-1) in solution versus 7.7 +/- 1.1 x 10(-4) min(-1) on the (C18) solid support. The results obtai…

AnalyteChromatographyChemistryElutionGeneral ChemistryStandard solutionSensitivity and SpecificityAcetylcysteineMatrix (chemical analysis)O-Phthalaldehydechemistry.chemical_compoundDrug StabilityReagentPolyaminesSpectrophotometry UltravioletSolid phase extractionDerivatizationChromatography High Pressure Liquido-PhthalaldehydeJournal of Chromatography B: Biomedical Sciences and Applications
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Polyfunctional recognition of pyridinedicarboxylate anions with macrocyclic polyamine receptors containing heteroaromatic groups.

2008

The interaction of the biologically relevant anions deriving from the six pyridinedicarboxylic acids (H2PDC) with two macrocyclic receptors containing a pentamine chain and a bipyridine (1) or a phenanthroline (2) moiety, as well as with the aliphatic analogue [21]aneN7 (3), was studied by means of spectroscopic methods (UV-vis, NMR) and potentiometric titrations affording the stability constants of the adducts formed. All three receptors form stable complexes with the substrates thanks to the formation of several salt bridges and hydrogen bond contacts, as observed in the crystal structure of the H8[3(2,6-PDC)4] x H2O x 0.5 EtOH solid compound. Additional pi-stacking interactions between t…

AnionsModels MolecularMacrocyclic CompoundsStereochemistryPyridinesPhenanthrolineStatic ElectricityCarboxylic AcidsHydrocarbons Aromaticchemistry.chemical_compoundBipyridineMolecular recognitionPolymer chemistryPolyaminesMoietychemistry.chemical_classificationBinding SitesHydrogen bondSpectrum AnalysisOrganic ChemistryHydrogen BondingDicarboxylic acidchemistryStability constants of complexesPotentiometryAliphatic compoundThe Journal of organic chemistry
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Toward a Rational Design of Polyamine-Based Zinc-Chelating Agents for Cancer Therapies.

2020

In vitro viability assays against a representative panel of human cancer cell lines revealed that polyamines L1a and L5a displayed remarkable activity with IC50 values in the micromolar range. Preliminary research indicated that both compounds promoted G1 cell cycle arrest followed by cellular senescence and apoptosis. The induction of apoptotic cell death involved loss of mitochondrial outer membrane permeability and activation of caspases 3/7. Interestingly, L1a and L5a failed to activate cellular DNA damage response. The high intracellular zinc-chelating capacity of both compounds, deduced from the metal-specific Zinquin assay and ZnL2+ stability constant values in solution, strongly sup…

Antineoplastic AgentsApoptosis01 natural sciences03 medical and health scienceschemistry.chemical_compoundStructure-Activity RelationshipCell Line TumorDrug DiscoveryPolyaminesHumansCytotoxicityCaspase030304 developmental biologyChelating Agents0303 health sciencesbiologyMolecular StructureChemistryRational designG1 Phase Cell Cycle Checkpoints0104 chemical sciencesCell biology010404 medicinal & biomolecular chemistryZincModels ChemicalApoptosisCell cultureDrug Designbiology.proteinMolecular MedicineQuantum TheoryDrug Screening Assays AntitumorPolyamineG1 phaseIntracellularJournal of medicinal chemistry
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Thermodynamics and fluorescence emission studies on potential molecular chemosensors for ATP recognition in aqueous solution †

1999

The interaction of the open-chain polyamine N-(3-aminopropyl)-N′-[3-(anthrylmethyl)aminopropyl]ethane-1,2-diamine (L) with the relevant anionic forms of adenosine 5′-triphosphate (ATP), adenosine 5′-diphosphate (ADP) and adenosine 5′-monophosphate (AMP) is described. Unambiguous criteria for defining thermodynamic selectivity based on the use of effective stability constants are presented. The interaction of L and several other topologically similar polyammonium receptors with ATP has been shown to occur through electrostatic and π-stacking intermolecular forces. The π-stacking binding mode is modulated by the protonation degree of ATP as indicated by fluorescence emission titrations. Evide…

Aqueous solutionInorganic chemistryIntermolecular forceProtonationFluorescenceCombinatorial chemistryAdenosinechemistry.chemical_compoundchemistrymedicineTitrationSelectivityPolyaminemedicine.drugJournal of the Chemical Society, Perkin Transactions 2
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Electrochemistry of copper complexes with macrocyclic polyamines containing pyrazole units.

2006

The voltammetric behaviour of bi- and mono-nuclear complexes formed in solution by Cu(2+) with three polyazacyclophanes containing pyrazole units in aqueous solution is described. Cyclic and square wave voltammetric responses at glassy carbon electrodes indicate that the reduction of copper-macrocycle complexes in solution takes place in two successive one-electron per Cu transfer processes coupled with preorganization and protonation reactions that mimic the behaviour of superoxide dismutase. The electrochemistry of ternary Cu(2+)-receptor-dopamine complexes exhibits significant differences with respect to the protection of the neurotransmitter from post-electron transfer cyclization react…

Aqueous solutionMacrocyclic CompoundsSuperoxide DismutaseDopamineInorganic chemistryMolecular Mimicrychemistry.chemical_elementProtonationSquare wavePyrazoleGlassy carbonElectrochemistryCopperInorganic Chemistrychemistry.chemical_compoundchemistryPolymer chemistryElectrochemistryOrganometallic CompoundsPolyaminesPyrazolesTernary operationCopperDalton transactions (Cambridge, England : 2003)
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Proton coordination by polyamine compounds in aqueous solution

1999

Abstract The present article is concerned with proton transfer reactions in aqueous solution of open-chain, macrocyclic and macropolycyclic or cage compounds having nitrogen atoms as protonation sites in the molecular framework, although several compounds with additional different donors will be considered. The main purpose of this review is to collect some significant examples of proton transfer processes in order to show how the electronic properties and molecular topology of polyamines affect the thermodynamic parameters of their protonation equilibria.

Aqueous solutionProtonChemistryInorganic chemistryProtonationInorganic Chemistrychemistry.chemical_compoundComputational chemistryMaterials ChemistryPhysical and Theoretical ChemistryMolecular topologyNuclear ExperimentPolyamineElectronic propertiesCoordination Chemistry Reviews
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