Search results for "lactone"

showing 10 items of 335 documents

Synthesis and degradation of poly (2-hydroxyethyl methacrylate)-graft-poly (ε-caprolactone) copolymers

2004

Abstract Poly (e-caprolactone) macromonomers carrying a methacryloyl end groups were synthesized using different lanthanide derivatives as catalysts, and characterized by SEC and 1 H NMR. Hydrophilic–hydrophobic copolymers from macromonomers and 2-hydroxyethyl methacrylate (HEMA) were obtained by solution free radical polymerization. Depending on the feed ratio of the two components, different copolymer structures were obtained. The expected graft structure of the copolymers was confirmed by 1 H NMR. Thermal properties of the copolymers were determined by DSC and TGA. Hydrolytic and enzymatic degradations of the materials were performed. Poly (2-hydroxyethyl methacrylate)- graft -poly (e-ca…

Materials sciencePolymers and PlasticsRadical polymerizationtechnology industry and agricultureCationic polymerizationCondensed Matter PhysicsMethacrylateMacromonomerRing-opening polymerizationchemistry.chemical_compoundchemistryMechanics of MaterialsPolycaprolactonePolymer chemistryMaterials ChemistryCopolymerCaprolactonePolymer Degradation and Stability
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Smart polymeric coatings for damage visualization in substrate materials

2012

For damage indication needs in polymer composites, three smart acrylic coatings based on microencapsulated crystal violet lactone leuco dye with embedded developer silica gel and methyl 4-hydroxybenzoate were elaborated. Damage visualization ability upon duralumin substrates was tested. Indentation tests were conducted in the interval of 0.0005–0.55 J of mechanical work. Digital image analysis was used for evaluation of the visual response in the form of “bruise” spots. The measure of response intensity was relative excess of blue color above achromatic gray in the scanned images of the “bruise” spots. This technique allowed detecting influence of the coating formulations onto the substrat…

Materials scienceSilica gelMechanical EngineeringSubstrate (printing)engineering.materialVisualizationchemistry.chemical_compoundCrystal violet lactonechemistryCoatingIndentationengineeringGeneral Materials ScienceComposite materialDuraluminLeuco dyeJournal of Intelligent Material Systems and Structures
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Polycaprolactone/gelatin-based scaffolds with tailored performance: in vitro and in vivo validation

2019

Abstract Nanofibrous scaffolds composed of polycaprolactone (PCL) and gelatin (Ge) were obtained through a hydrolytic assisted electrospinning process. The PCL-to-Ge proportion (100/0 to 20/80), as well as the dissolution time (24, 48, 72, 96, 120 h) into a 1:1 formic/acetic acid solvent before electrospinning were modified to obtain the different samples. A strong influence of these factors on the physicochemical properties of the scaffolds was observed. Higher Ge percentage reduced crystallinity, allowed a uniform morphology and increased water contact angle. The increase in the dissolution time considerably reduced the molar mass and, subsequently, fibre diameter and crystallinity were a…

Materials sciencefood.ingredientBiocompatibilityPolyestersMyocardial InfarctionNanofibersBioengineering02 engineering and technology010402 general chemistry01 natural sciencesGelatinCell LineScaffoldBiomaterialsContact angleMiceCrystallinitychemistry.chemical_compoundfoodMaterials TestingCell AdhesionAnimalsHumansTailoredRats WistarMaterialsDissolutionCells CulturedCell ProliferationMolar massTissue EngineeringTissue ScaffoldsMyocardiumin vitro021001 nanoscience & nanotechnologyElectrospinningRats0104 chemical sciencesMice Inbred C57BLDisease Models Animalin vivochemistryChemical engineeringMechanics of MaterialsPolycaprolactoneLeukocytes MononuclearGelatinBiocompatibility0210 nano-technologyMaterials Science and Engineering: C
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Mitochondrial dynamics in type 2 diabetes: Pathophysiological implications

2017

Mitochondria play a key role in maintaining cellular metabolic homeostasis. These organelles have a high plasticity and are involved in dynamic processes such as mitochondrial fusion and fission, mitophagy and mitochondrial biogenesis. Type 2 diabetes is characterised by mitochondrial dysfunction, high production of reactive oxygen species (ROS) and low levels of ATP. Mitochondrial fusion is modulated by different proteins, including mitofusin-1 (MFN1), mitofusin-2 (MFN2) and optic atrophy (OPA-1), while fission is controlled by mitochondrial fission 1 (FIS1), dynamin-related protein 1 (DRP1) and mitochondrial fission factor (MFF). PARKIN and (PTEN)-induced putative kinase 1 (PINK1) partici…

MiD51 mitochondrial dynamics proteins of 51 kDaΔΨm mitochondrial membrane potential0301 basic medicineMitochondrial fission factorClinical BiochemistryMitochondrial DegradationMFN2Review ArticleTXNIP thioredoxin interacting proteinMitochondrial DynamicsBiochemistryAdenosine TriphosphateGRP78 78 kDa glucose-regulated proteinMFF mitochondrial fission factorMFN2 mitofusin 2TRX2 thioredoxin 2Redox biologylcsh:QH301-705.5NF-κB nuclear factor kappa Blcsh:R5-920MitophagyType 2 diabetesDRP1 dynamin-related protein 1FIS1 fission protein 1BNIP3 BCL2/adenovirus E1B 19 kDa interacting protein 3MitochondriaOPA1 optic atrophy 1SIRT1/3 sirtuin 1/3Biochemistrymitochondrial fusionTGF-β1 transforming growth factor-β1Mitochondrial fissionOMM outer mitochondrial membranelcsh:Medicine (General)MiD49 mitochondrial dynamics proteins of 49Nox 4 NADPH oxidase-4IMM inner mitochondrial membraneFIS1ATF6 activating transcription factor 6PINK1mTOR mammalian target of rapamycinCHOP C/EBP homologous proteinBiologymdivi-1 mitochondrial division inhibitor-1Mitochondrial Proteins03 medical and health sciencesROS reactive oxygen speciessXBP1 spliced X-box binding protein 1UCP-1 uncoupling protein-1MFN1 mitofusin 1SOD superoxide dismutaseLC3 1 A/1B-light chain 3HumansPINK1 (PTEN)-induced putative kinase 1S3 15-OxospiramilactoneOrganic ChemistrymtDNA mitochondrial DNAAMPK AMP-activated protein kinase030104 developmental biologyDiabetes Mellitus Type 2Mitochondrial biogenesislcsh:Biology (General)Oxidative stressp38 MAPK p38 mitogen-activated protein kinasep62/SQSTM1 ubiquitin and sequestosome-1Reactive Oxygen SpeciesRedox Biology
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QSAR of Natural Sesquiterpene Lactones as Inhibitors of Myb-dependent Gene Expression

2017

Background Protein c-Myb is a therapeutic target. Some sesquiterpene lactones suppress Myb-dependent gene expression, which results in their potential anti-cancer activity. Material & methods Database ChEMBL is a representative of lactones for physicochemical and physiochemical properties. Data presented for 31 natural lactones are discussed in terms of quantitative structureactivity relationships with the objective to predict inhibitors of Myb-induced gene expression. Several constitutional descriptors are related to structure-activity. α-Methylene-γ-lactone groups enhance while OH functions worsen potency. The latter feature is in agreement with the fact that the more lipophilic the lacto…

Models Molecular0301 basic medicine030103 biophysicsQuantitative structure–activity relationshipStereochemistryQuantitative Structure-Activity RelationshipSesquiterpene lactoneSesquiterpeneLactonesProto-Oncogene Proteins c-myb03 medical and health scienceschemistry.chemical_compoundDrug DiscoveryGene expressionHumansStructure–activity relationshipMYBCytotoxicitychemistry.chemical_classificationBiological ProductsDose-Response Relationship DrugMolecular StructureCationic polymerizationGeneral MedicinechEMBLGene Expression RegulationchemistrySesquiterpenesLactoneCurrent Topics in Medicinal Chemistry
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N‐Terminal Modification of Gly‐His‐Tagged Proteins with Azidogluconolactone

2021

Site-specific protein modifications are vital for biopharmaceutical drug development. Gluconoylation is a non-enzymatic, post-translational modification of N-terminal HisTags. We report high-yield, site-selective in vitro α-aminoacylation of peptides, glycoproteins, antibodies, and virus-like particles (VLPs) with azidogluconolactone at pH 7.5 in 1 h. Conjugates slowly hydrolyse, but diol-masking with borate esters inhibits reversibility. In an example, we multimerise azidogluconoylated SARS-CoV-2 receptor-binding domain (RBD) onto VLPs via click-chemistry, to give a COVID-19 vaccine. Compared to yeast antigen, HEK-derived RBD was immunologically superior, likely due to observed diffe…

Models MolecularAzidesCOVID-19 VaccinesGlycosylationvirusesGlycineGluconatesBiochemistryLactoneschemistry.chemical_compoundAntigenHumansHistidineVaccines Virus-Like ParticleSeroconversionMolecular Biologychemistry.chemical_classificationMolecular StructurebiologyChemistryOrganic ChemistryAntibodies NeutralizingBiopharmaceuticalBiochemistrybiology.proteinClick chemistryMolecular MedicineAntibodyGlycoproteinConjugateChemBioChem
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Inhibitors of inducible NO synthase expression: total synthesis of (S)-curvularin and its ring homologues.

2008

(S)-Curvularin and its 13-, 14-, and 16-membered lactone homologues were synthesized through a uniform strategy in which a Kochi oxidative decarboxylation and ring-closing metathesis reactions constitute the key processes. In the evaluation of the anti-inflammatory effects of the synthesized compounds in assays using cells stably transfected with a human iNOS promoter-luciferase reporter gene construct, the 14- and 16-membered homologues showed a slightly higher inhibitory effect towards iNOS promoter activity than curvularin itself. However, the larger ring homologues also exhibited higher cytotoxicity, manifest in downregulated eNOS promoter activity. In contrast, the di-O-acetyl and 4-ch…

Models MolecularDrug Evaluation PreclinicalNitric Oxide Synthase Type IICrystallography X-RayBiochemistryGene Expression Regulation EnzymologicCell LineLactonesEnosDrug DiscoveryHumansGeneral Pharmacology Toxicology and PharmaceuticsEnzyme InhibitorsCytotoxicityPromoter Regions GeneticOxidative decarboxylationPharmacologychemistry.chemical_classificationReporter genebiologyMolecular StructureChemistryOrganic ChemistryTotal synthesisStereoisomerismCurvularinTransfectionbiology.organism_classificationBiochemistryCyclizationMolecular MedicineZearalenoneLactoneHeLa CellsChemMedChem
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Nuclear magnetic resonance spectroscopic study of beta-lactoglobulin interactions with two flavor compounds, gamma-decalactone and beta-ionone.

2002

Interactions between a well-characterized protein, beta-lactoglobulin, and two flavor compounds, beta-ionone and gamma-decalactone, were studied by 2D NMR spectroscopy. NMR spectra were recorded in aqueous solution (pH 2.0, 12 mM NaCl, 10% D(2)O) under conditions such that beta-lactoglobulin is present in a monomeric state. TOCSY and NOESY spectra were recorded on the protein and the complexes between protein and ligands. The spectra of the NH-CH(alpha) region showed the cross-signals due to the coupling between N- and C-bonded protons in the polypeptide backbone. The observed chemical shift variations in the presence of ligands can be assigned to changes in the protein conformation. It app…

Models MolecularKetoneMagnetic Resonance SpectroscopyStereochemistryProtein ConformationLactoglobulinsIononechemistry.chemical_compoundLactonesSpectroscopyBeta-lactoglobulinFlavorchemistry.chemical_classificationBinding SitesbiologyMolecular StructureTerpenesGeneral ChemistryNuclear magnetic resonance spectroscopyNMR spectra databasechemistryOdorantsbiology.proteinPhysical chemistryGeneral Agricultural and Biological SciencesNorisoprenoidsTwo-dimensional nuclear magnetic resonance spectroscopyJournal of agricultural and food chemistry
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New antitumoral acetogenin ‘Guanacone type’ derivatives: Isolation and bioactivity. Molecular dynamics simulation of diacetyl-guanacone

2007

We describe herein the isolation and semisynthesis of four acetogenin derivatives (1-4) as well as their ability to inhibit the mitochondrial respiratory chain and several tumor cell lines. In addition, four nanoseconds (ns) of MD simulation of compound 4, in a fully hydrated POPC bilayer, is reported.

Models MolecularMagnetic Resonance SpectroscopyAcetogeninsStereochemistryLipid BilayersClinical BiochemistryMolecular ConformationRespiratory chainPharmaceutical ScienceBiochemistryChemical synthesisAnnonaElectron TransportLactoneschemistry.chemical_compoundPolyketideCell Line TumorDrug DiscoveryHumansComputer SimulationFuransMolecular BiologyPOPCBilayerOrganic ChemistryHydrogen BondingAntineoplastic Agents PhytogenicSemisynthesisMitochondrial respiratory chainchemistrySeedsAcetogeninPhosphatidylcholinesMolecular MedicineIndicators and ReagentsFatty AlcoholsBioorganic & Medicinal Chemistry
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Stereoselective synthesis of the published structure of feigrisolide A. Structural revision of feigrisolides A and B.

2006

The total synthesis of the proposed structure of feigrisolide A is reported. Ethyl (S)-3-hydroxybutyrate was the chiral starting material. A Brown asymmetric allylation and an Evans aldol reaction were key steps of the synthesis. The NMR data of the synthetic product are different from those of the natural product. The published structure of feigrisolide A is therefore erroneous. A subsequent comparison of spectral data strongly suggests that feigrisolides A and B are identical with (-)-nonactic acid and (+)-homononactic acid, respectively.

Models MolecularMagnetic Resonance SpectroscopyStereochemistryMolecular ConformationStereoisomerismChemical synthesischemistry.chemical_compoundLactonesStructure-Activity RelationshipAldol reactionSpectral dataNatural productMolecular StructureChemistryorganic chemicalsOrganic ChemistryEnantioselective synthesisTotal synthesisStereoisomerismGeneral MedicineNuclear magnetic resonance spectroscopyNmr dataAnti-Bacterial AgentsProduct (mathematics)Aldol condensationStereoselectivityThe Journal of organic chemistry
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