Search results for "amina"

showing 10 items of 2711 documents

The amphipathic peptide mellitin as a tool to study the membrane-dependent activation of tissue transglutaminase

2001

The role of membrane phospholipids on the cross-linking activity of guinea pig liver (tissue) transglutaminase has been investigated using the amphipathic model peptide melittin as glutaminyl substrate and the primary amine monodansylcadaverine as extrinsic amine donor. A marked increase of transglutaminase catalytic activity was observedin vitro assays in the presence of neutral membrane phospholipids. In contrast, activation was abolished in the presence of membranes containing pure anionic lipids. Enzyme activation could be ascribed to a direct binding of the lipid to the protein as demonstrated in enzymatic assays using a non membrane-interacting peptide (Cbz-Gln-Gly). The data obtained…

chemistry.chemical_classificationbiologyTissue transglutaminaseBioengineeringPeptideBiochemistryMelittinIn vitroAnalytical ChemistryEnzyme activatorchemistry.chemical_compoundMembranechemistryBiochemistryDrug DiscoveryAmphiphilebiology.proteinMolecular Medicinelipids (amino acids peptides and proteins)Lipid bilayerLetters in Peptide Science
researchProduct

ChemInform Abstract: Exploiting the CNC Side Chain in Heterocyclic Rearrangements: Synthesis of 4(5)-Acylamino-imidazoles.

2010

A new variation on the Boulton-Katritzky reaction is reported, namely, involving use of a CNC side chain. A novel Montmorillonite-K10 catalyzed nonreductive transamination of a 3-benzoyl-1,2,4-oxadiazole afforded a 3-(alpha-aminobenzyl)-1,2,4-oxadiazole, which was condensed with benzaldehydes to afford the corresponding imines. In the presence of strong base, these imines underwent Boulton-Katritzky-type rearrangement to afford novel 4(5)-acylaminoimidazoles.

chemistry.chemical_classificationchemistryStereochemistryTransaminationSide chainGeneral MedicineCatalysisChemInform
researchProduct

Exploiting the CNC Side Chain in Heterocyclic Rearrangements: Synthesis of 4(5)-Acylamino-imidazoles

2010

A new variation on the Boulton-Katritzky reaction is reported, namely, involving use of a CNC side chain. A novel Montmorillonite-K10 catalyzed nonreductive transamination of a 3-benzoyl-1,2,4-oxadiazole afforded a 3-(alpha-aminobenzyl)-1,2,4-oxadiazole, which was condensed with benzaldehydes to afford the corresponding imines. In the presence of strong base, these imines underwent Boulton-Katritzky-type rearrangement to afford novel 4(5)-acylaminoimidazoles.

chemistry.chemical_classificationchemistryTransaminationStereochemistryOrganic ChemistrySide chainSettore CHIM/06 - Chimica OrganicaPhysical and Theoretical Chemistryoxadiazole imidazole heterocyclic rearrangement transamination heterogeneous catalysisBiochemistryCatalysisOrganic Letters
researchProduct

Mercury Speciation in Floodplain Soils and Sediments along a Contaminated River Transect

1998

A novel mercury-specific sequential extraction procedure (SEP) for the assessment of mercury (Hg) speciation in soils and sediments, with emphasis on studying the interaction between Hg and organic matter (OM), was developed and tested. It was applied to determine Hg speciation in floodplain topsoils and surface sediments along the Hg-contaminated part of the river Elbe, and to simultaneously derive some information on the (re)mobilization potentials for Hg from these matrices. The majority of the total Hg in the ecosystem today is bound in the floodplains, which also still geographically reflect the historic emission record. Most of the Hg in both matrices is bound strongly to OM, suggesti…

chemistry.chemical_classificationgeographyEnvironmental Engineeringgeography.geographical_feature_categoryFloodplainEcologychemistry.chemical_elementManagement Monitoring Policy and LawContaminationPollutionFloodplain soilsMercury (element)chemistryEnvironmental chemistrySoil waterEnvironmental scienceOrganic matterEcosystemTransectWaste Management and DisposalWater Science and TechnologyJournal of Environmental Quality
researchProduct

Co(II)-mediated synthesis of 2-carbamimidoylbenzoates and isoindole-1,3-diaminates

2015

Abstract Phthalonitrile, acetoxime and cobalt(II) nitrate hexahydrate are combined in acetone with formation of stable and easy to handle Co(II) complex [Co{C6H4C(NH2)NC(ONCMe2)2}2](NO3)2 (1). Interaction of 1 with excess alcohols ROH (also used as solvents) and 2 equiv of (NH4)2S leads, in one-step, to alkyl 2-carbamimidoylbenzoate nitrates [C6H4COOR{2-C(NH2)2}]NO3 [R=CH3, C2H5, C3H7, CH(CH3)2]. Similarly, N1,N3-dialkyl-1H-isoindole-1,3-diaminate nitrates [C6H4C(NR′)NC(NR′)]NO3 [R=C3H7, C4H9, C(CH3)3, CH2CH2OH, CH2CH2SC2H5) can be directly produced from 1 by its reaction with 4 equiv of amines and 2 equiv of (NH4)2S in alcoholic media.

chemistry.chemical_classificationphthalonitrilesChemistryStereochemistrymetal assisted (mediated) synthesisOrganic Chemistrychemistry.chemical_elementN1oximesBiochemistryMedicinal chemistryPhthalonitrilechemistry.chemical_compoundNitrateDrug DiscoveryAcetone3-diaminatesIsoindoleCobaltta116alkyl 2-carbamimidoylbenzoatesN3-dialkyl-isoindole-1AlkylTetrahedron
researchProduct

Diphosphines of dppf-Type Incorporating Electron-Withdrawing Furyl Moieties Substantially Improve the Palladium-Catalysed Amination of Allyl Acetates

2005

Highly active Pd/diphosphine catalytic systems incorporating new, air-stable ferrocenyl-furylphosphines allow nucleophilic allylic amination at room temperature with unprecedented turnover frequencies. For instance, in the presence of 0.01 mol % catalyst the coupling of aniline to allyl acetate occurs at a TOF of more than 10,000 h - 1 ; even the addition of the less nucleophile morpholine to allyl acetate is observed with a TOF of 4250 h - 1 . The amination of the sterically demanding geranyl acetate, a monoterpene derivative of interest in the flavour industry, at low catalyst loadings demonstrates the scope of this methodology, which provides in addition noticeable advantages in terms of…

chemistry.chemical_compoundAllylic rearrangementchemistryNucleophileAllyl acetateMorpholineDiphosphinesOrganic chemistrychemistry.chemical_elementGeneral ChemistryAminationPalladiumCatalysisAdvanced Synthesis & Catalysis
researchProduct

Preparation of N,O-Aminals as Synthetic Equivalents of H2C=NAr and (H2C=NHAr)+ Ions: Neutral and Acid-promoted Transformations

1988

A general method for the synthesis of N,O-aminals derived from primary aromatic amines is described. The reactivity of these compounds under neutral and acidic conditions has been studied and the title compounds can be envisaged as general purpose H2C=NAr or (H2C=NHAr)+ equivalents. N,O-Aminals have been converted into perhydrotriazines by moderate heating and into bis(4-aminoaryl) methane derivatives or N-benzylarylamines, respectively when heated in acidic media with pH control. Reduction of N, O-acetals with sodium cyanoborohydride has revealed that the C-O bond is broken exclusively in acidic media.

chemistry.chemical_compoundAnilineChemistrySodium cyanoborohydrideFormaldehydeHemiaminalOrganic chemistryAmine gas treatingReactivity (chemistry)Medicinal chemistryMethaneIon
researchProduct

Efficient Synthesis of 1,4,7-Triazacyclononane and 1,4,7-Triazacyclononane-Based Bifunctional Chelators for Bioconjugation

2014

The reaction of diethylenetriamine with chloroacetaldehyde yielded a bicyclic aminal intermediate for the synthesis of 1,4,7-triazacyclononane (TACN), a macrocyclic polyamine the derivatives of which find applications as catalysts, bleaching agents, and chelators for medical imaging. This new synthetic protocol outperforms the synthetic methods described so far because it does not involve any cyclization step. Moreover, this aminal intermediate allowed access to a new family of TACN derivatives functionalized on the carbon skeleton, for example, C-aminomethyl-TACN. This novel compound is a precursor of valuable bifunctional chelating agents for nuclear medicine, in particular, for the prepa…

chemistry.chemical_compoundBioconjugationchemistryBicyclic moleculeOrganic ChemistryDiethylenetriamineAminalOrganic chemistryChloroacetaldehydeChelationPhysical and Theoretical ChemistryBifunctionalCatalysisEuropean Journal of Organic Chemistry
researchProduct

Detecting residues of urea and carbamate pesticides

2004

chemistry.chemical_compoundCarbamate pesticidesChromatographyPesticide residuechemistryEnvironmental chemistryUreaGas chromatographyPesticideContaminationFood contaminant
researchProduct

ChemInform Abstract: Chemical Compounds and Toxicological Assessments of Drinking Water Stored in Polyethylene Terephthalate (PET) Bottles: A Source …

2012

A declaration of conformity according to European regulation No. 10/2011 is required to ensure the safety of plastic materials in contact with foodstuffs. This regulation established a positive list of substances that are authorized for use in plastic materials. Some compounds are subject to restrictions and/or specifications according to their toxicological data. Despite this, the analysis of PET reveals some non-intentionally added substances (NIAS) produced by authorized initial reactants and additives. Genotoxic and estrogenic activities in PET-bottled water have been reported. Chemical mixtures in bottled water have been suggested as the source of these toxicological effects. Furthermo…

chemistry.chemical_compoundChemical mixturesChemistryEnvironmental chemistryExtraction (chemistry)Plastic materialsPolyethylene terephthalateExtraction methodsSample preparationGeneral MedicineContaminationBottled waterChemInform
researchProduct