Search results for "Solid-phase synthesis"

showing 10 items of 60 documents

Solid-phase synthesis of a glycopeptide from the homophilic recognition domain of epithelial cadherin 1 using a O-pentafluorophenyluronium salt

1998

Abstract The β-turn forming glycopeptide 6 from the homophilic recognition domain of mouse epithelial cadherin 1 carrying a T N -antigen side chain was synthesised on solid phase using an allylic anchor and the new coupling reagent N , N - N ′, N ′-bis(tetramethylene)- O -pentafluorophenyluronium hexafluorophosphate 3 .

Allylic rearrangementCadherinStereochemistryOrganic ChemistryBiochemistryGlycopeptidechemistry.chemical_compoundSolid-phase synthesischemistryAntigenPhase (matter)HexafluorophosphateDrug DiscoverySide chainTetrahedron Letters
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Solution versus Fluorous versus Solid-Phase Synthesis of 2,5-Disubstituted 1,3-Azoles. Preliminary Antibacterial Activity Studies

2009

A small library of compounds with an oxa(thia)zole scaffold and structural diversity in both positions 2 and 5 has been synthesized. Double acylation of a protected glycine affords intermediate α-amido-β-ketoesters, which in turn can be dehydrated to afford 1,3-oxazoles or reacted with Lawesson’s reagent to furnish 1,3-thiazoles. This procedure was designed with its adaptation to fluorous techniques in mind. Thus, when a protected glycine with a fluorous tag in the ester moiety is used as a starting material, the synthesis can be easily completed without column chromatography purification of intermediate compounds with good to excellent yields, thus affording a suitable entry to the prepara…

AzolesStaphylococcus aureusANTIBACTERIAL ACTIVITYDrug Evaluation PreclinicalMicrobial Sensitivity TestsChemical synthesisSmall Molecule LibrariesAcylationchemistry.chemical_compoundSolid-phase synthesisColumn chromatographyAZOLESOrganic chemistryMoietyAntibacterial agentChemistryOrganic ChemistryCiencias QuímicasFLUOROUSCombinatorial chemistryAnti-Bacterial AgentsSolutionsQuímica OrgánicaMolecular ProbesSOLID-PHASELawesson's reagentAntibacterial activityCIENCIAS NATURALES Y EXACTAS
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Study of Epitope Imprinting for Small Templates: Preparation of NanoMIPs for Ochratoxin A

2019

BiomaterialsOchratoxin Achemistry.chemical_compoundSolid-phase synthesisTemplateRenewable Energy Sustainability and the EnvironmentChemistryMaterials ChemistryEnergy Engineering and Power TechnologyImprinting (psychology)Surface plasmon resonanceCombinatorial chemistryEpitopeChemNanoMat
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Implantation of silicon dioxide-based nanocrystalline hydroxyapatite and pure phase beta-tricalciumphosphate bone substitute granules in caprine musc…

2012

Abstract Background Osteoinductive bone substitutes are defined by their ability to induce new bone formation even at heterotopic implantation sites. The present study was designed to analyze the potential osteoinductivity of two different bone substitute materials in caprine muscle tissue. Materials and methods One gram each of either a porous beta-tricalcium phosphate (β-TCP) or an hydroxyapatite/silicon dioxide (HA/SiO2)-based nanocrystalline bone substitute material was implanted in several muscle pouches of goats. The biomaterials were explanted at 29, 91 and 181 days after implantation. Conventional histology and special histochemical stains were performed to detect osteoblast precurs…

Calcium Phosphateslcsh:Specialties of internal medicineClinical Neurology610 MedizinBiocompatible MaterialsCerasorbHydroxyapatiteOsteogenesislcsh:RC581-951610 Medical sciencesAnimalsSolid-Phase Synthesis TechniquesDentistry(all)GoatsMusclesResearchNanocrystallineSilicon DioxideEctopic bone formationDrug CombinationsDurapatiteß-tricalciumphosphateOtorhinolaryngologyOsteoinductionBone SubstitutesModels AnimalNanoparticlesFemaleNanoBone
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Solid-Phase Synthesis and Biological Evaluation of a Teleocidin Library—Discovery of a Selective PKC Down Regulator

2000

Protein kinaseC (PKC) is linked to the signal-induced modulation of a wide variety of cellular processes, such as growth, differentiation, secretion, apoptosis, and tumor development. The design and synthesis of small molecules that regulate these different cellular signaling systems is at the forefront of modern drug design. Herein we report a) an efficient method for the synthesis of indolactamV (6), a PKC activator, and its N13-des(methyl) analogues (19) using a regioselective organometallic transformation, a convenient aminomalonate derivative (10) to introduce the appropriate functionality and an enantiospecific enzymic hydrolysis as key steps; b) the use of this method in the first so…

Cell signalingSolid-phase synthesisBiochemistryActivator (genetics)ChemistryOrganic ChemistryRegulatorGeneral ChemistryMARCKSSignal transductionSmall moleculeCatalysisProtein kinase CChemistry
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Solution-, solid-phase, and fluorous synthesis of beta,beta-difluorinated cyclic quaternary alpha-amino acid derivatives: a comparative study.

2008

The diastereoselective synthesis of cyclic beta,beta-difluorinated alpha-amino acid derivatives bearing a quaternary stereocenter is described. The process relies on the chemo- and diastereoselective addition of allylic organometallic reagents to fluorinated alpha-imino esters and a subsequent ring-closing metathesis reaction (RCM). Complete selectivity in the nucleophilic addition was achieved with (R)-phenylglycinol methyl ether as a chiral auxiliary. The resulting amino acids were introduced into peptide chains, which could facilitate the preparation of potentially bioactive dipeptide derivatives. In addition, the solution synthesis of these cyclic fluorinated alpha-amino acids was succe…

Chiral auxiliaryAllylic rearrangementNucleophilic additionDipeptideMolecular StructureChemistryOrganic ChemistryFluorine CompoundsAmino Acids CyclicEtherEstersStereoisomerismGeneral ChemistryCatalysisStereocenterSolutionschemistry.chemical_compoundSolid-phase synthesisSalt metathesis reactionOrganic chemistryIminesProtonsAminationChemistry (Weinheim an der Bergstrasse, Germany)
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A Classical Synthesis of the Collagen-like Peptides with the Sequence Z(GlyProPro)nOBut and their characterization with circular dichroism and ultrac…

1975

Oligopeptides with the sequence Z(GlyProPro)nOBut (n = 3–7) were synthesized along a clasical pathway. Generally long fragments were condensed in order to allow an easy separation of the products from the reactants. It is established by molecular weight determination and measurements of circular dichroism that the peptides form the collagen-like triple helix in methanol and that they assume the random coil conformation in dilute acetic acid. The circular dichroism spectra agree reasonably well with the corresponding spectra for (ProProGly)10 which was obtained by solid phase synthesis in another laboratory.

Circular dichroismCircular DichroismOrganic ChemistrySequence (biology)BiochemistryCatalysisRandom coilSpectral lineInorganic ChemistryAcetic acidchemistry.chemical_compoundCrystallographySolid-phase synthesischemistryDrug DiscoveryAmino Acid SequenceCollagenUltracentrifugePhysical and Theoretical ChemistryOligopeptidesUltracentrifugationTriple helixHelvetica Chimica Acta
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Of Thiols and Disulfides: Methods for Chemoselective Formation of Asymmetric Disulfides in Synthetic Peptides and Polymers.

2018

In protein or peptide chemistry, thiols are frequently chosen as a chemical entity for chemoselective modification reactions. Although it is a well-established methodology to address cysteines and homocysteines in aqueous media to form S-C bonds, possibilities for the chemoselective formation of asymmetric disulfides have been less approached. Focusing on bioreversibility in conjugation chemistry, the formation of disulfide bonds is highly desirable for the attachment of thiol-containing bioactive agents to proteins or in cross-linking reactions, because disulfide bonds can combine stability in blood with degradability inside cells. In this Concept article, recent approaches in the field of…

Free RadicalsPolymersPeptide02 engineering and technologyConjugated system010402 general chemistryMicroscopy Atomic Force01 natural sciencesCatalysisPolymerizationReactivity (chemistry)DisulfidesSulfhydryl CompoundsProtecting groupSolid-Phase Synthesis Techniqueschemistry.chemical_classificationAqueous mediumOrganic ChemistryGeneral ChemistryPolymer021001 nanoscience & nanotechnologyCombinatorial chemistry0104 chemical scienceschemistryThiolQuantum TheorySelf-assembly0210 nano-technologyPeptidesChemistry (Weinheim an der Bergstrasse, Germany)
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Active Site Mapping of Xylan-Deconstructing Enzymes with Arabinoxylan Oligosaccharides Produced by Automated Glycan Assembly

2017

Xylan-degrading enzymes are crucial for the deconstruction of hemicellulosic biomass, making the hydrolysis products available for various industrial applications such as the production of biofuel. To determine the substrate specificities of these enzymes, we prepared a collection of complex xylan oligosaccharides by automated glycan assembly. Seven differentially protected building blocks provided the basis for the modular assembly of 2-substituted, 3-substituted, and 2-/3-substituted arabino- and glucuronoxylan oligosaccharides. Elongation of the xylan backbone relied on iterative additions of C4-fluorenylmethoxylcarbonyl (Fmoc) protected xylose building blocks to a linker-functionalized …

GlycanGlycoside HydrolasesStereochemistryOligosaccharidesSOLID-PHASE SYNTHESISXylose010402 general chemistryARABINOXYLANPLANT CELL WALL01 natural sciencesCatalysisSubstrate Specificity//purl.org/becyt/ford/1 [https]chemistry.chemical_compoundHydrolysisCellvibrioGlucuronoxylanCatalytic DomainArabinoxylan//purl.org/becyt/ford/1.4 [https]Organic chemistryBacteroidesGlycoside hydrolaseSolid-Phase Synthesis Techniqueschemistry.chemical_classificationbiology010405 organic chemistryHydrolysisCARBOHYDRATESOtras Ciencias QuímicasOrganic ChemistryCiencias QuímicasActive siteGeneral ChemistryXylan0104 chemical sciencescarbohydrates (lipids)Xylosidaseschemistrybiology.proteinXylansENZYMESCIENCIAS NATURALES Y EXACTAS
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Synthetic MUC1 Antitumor Vaccine Candidates with Varied Glycosylation Pattern Bearing R/S-configured Pam3 CysSerLys4.

2016

The Toll-like receptor 2 ligand Pam3 CysSer is of particular interest for the construction synthetic vaccines because of its ability to stimulate of the innate immune system. Such vaccines usually comprise Pam3 CysSer with the natural R-configuration at the glycerol 2-position. Pam3 CysSer peptide vaccines with natural configuration have been shown to be more efficient than the corresponding R/S diastereomers. In order to clarify whether the effect of the configuration of Pam3 Cys on the immune response also applies to glycopeptide vaccines, MUC1 glycopeptide-lipopeptide vaccines bearing either R- or R/S-configured Pam3 CysSerLys4 were compared for their immunological effects. In order to f…

GlycosylationGlycosylationLipoproteins010402 general chemistry01 natural sciencesBiochemistryCancer VaccinesEpitopechemistry.chemical_compoundMiceImmune systemAnimalsHumansMolecular BiologyMUC1Solid-Phase Synthesis TechniquesMice Inbred BALB CVaccines SyntheticInnate immune systembiology010405 organic chemistryOrganic ChemistryMucin-1GlycopeptidesImmunityLipopeptideStereoisomerismVirologyGlycopeptide0104 chemical scienceschemistrybiology.proteinMCF-7 CellsMolecular MedicineAntibodyChembiochem : a European journal of chemical biology
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