Search results for "ACETAMIDE"

showing 10 items of 142 documents

MICELLAR CHROMATOGRAPHIC PROCEDURE WITH DIRECT INJECTION FOR THE DETERMINATION OF SULFONAMIDES IN MILK AND HONEY SAMPLES

2001

The capability of liquid chromatography with micellar mobile phases of sodium dodecyl sulfate (SDS), of allowing the direct injection of biological fluids into reversed-phase columns, was applied to the determination of sulfonamides in milk and honey samples. The chromatographic behavior of a group of 15 sulfonamides was studied at pH 3.0 where the drugs showed a greater separation space. Acetonitrile was added to the mobile phase to decrease the retention of the most hydrophobic drugs and increase the efficiencies, which yielded a higher resolution. The samples were diluted with 0.10 M SDS to facilitate the solubilization of the matrix compounds and release the protein-bound drugs. The pro…

SulfamerazineChromatographyChemistryClinical BiochemistryPharmaceutical ScienceSulfadimethoxineSulfacetamideReversed-phase chromatographySulfapyridineBiochemistryHigh-performance liquid chromatographyAnalytical ChemistryMatrix (chemical analysis)medicineSulfaguanidinemedicine.drugJournal of Liquid Chromatography & Related Technologies
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New Gold(I) Organometallic Compounds with Biological Activity in Cancer Cells

2014

N-Heterocyclic carbene gold(I) complexes bearing a fluorescent coumarin ligand were synthesized and characterized by various techniques. The compounds were examined for their antiproliferative effects in normal and tumor cells in vitro; they demonstrated moderate activity and a certain degree of selectivity. The compounds were also shown to efficiently inhibit the selenoenzyme thioredoxin reductase (TrxR), whereas they were poorly effective towards the glutathione reductase (GR) and glutathione peroxidase enzymes. Notably, {3-[(7-methoxy-2-oxo-2H-chromen-4-yl) methyl]-1-methylimidazol-2-ylidene}(tetra-O-acetyl-1-thio-beta-D-glucopyranosido) gold(I) (3) showed a pronounced inhibition of TrxR…

Thioredoxin reductaseGlutathione reductaseMECHANISMSInorganic Chemistrychemistry.chemical_compoundCoumarinsCHEMISTRYTARGETSN-HETEROCYCLIC CARBENESCancerchemistry.chemical_classificationSelenocysteineGlutathione peroxidaseGold; carbenes; coumarins; enzyme; CancerBiological activityLigand (biochemistry)EnzymesenzymechemistryBiochemistryCancer cellIodoacetamideCarbenesANTICANCER AGENTSCOMPLEXESGold
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Total Synthesis of the Glycopeptide Recognition Domain of the P-Selectin Glycoprotein Ligand 1

2008

ThreonineGlycosylationGlycosylationOligosaccharidesCatalysischemistry.chemical_compoundSolid-phase synthesisProtein structureAcetamidesHumansChloroacetatesTrichloroacetic AcidBinding siteThreonineAntigens Viral TumorSialyl Lewis X AntigenBinding SitesMembrane GlycoproteinsGlycopeptidesTotal synthesisGeneral ChemistryGlycopeptideProtein Structure TertiaryP-SelectinchemistryBiochemistryP-selectin glycoprotein ligand-1Angewandte Chemie International Edition
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Discovery and validation of small-molecule heat-shock protein 90 inhibitors through multimodality molecular imaging in living subjects.

2012

Up-regulation of the folding machinery of the heat-shock protein 90 (Hsp90) chaperone protein is crucial for cancer progression. The two Hsp90 isoforms (α and β) play different roles in response to chemotherapy. To identify isoform-selective inhibitors of Hsp90(α/β)/cochaperone p23 interactions, we developed a dual-luciferase (Renilla and Firefly) reporter system for high-throughput screening (HTS) and monitoring the efficacy of Hsp90 inhibitors in cell culture and live mice. HTS of a 30,176 small-molecule chemical library in cell culture identified a compound, N -(5-methylisoxazol-3-yl)-2-[4-(thiophen-2-yl)-6-(trifluoromethyl)pyrimidin-2-ylthio]acetamide (CP9), that binds to Hsp90(α/β) an…

Thymidine kinase activityProtein FoldingImmunoprecipitationLactams MacrocyclicBlotting WesternMice NudeThiophenesBiologyThioacetamideTritiumSmall Molecule LibrariesMiceco-chaperone p23Luciferases FireflyHeat shock proteinCell Line TumorNeoplasmsAcetamidesDrug DiscoveryBenzoquinonesAnimalsHumansImmunoprecipitationProtein IsoformsLuciferaseHSP90 Heat-Shock ProteinsLuciferases RenillaProstaglandin-E SynthasesMultidisciplinaryCell growthImidazolesbioluminescence imagingHsp90Small moleculeMolecular biologydrug developmentHigh-Throughput Screening Assayssmall-molecule inhibitorsIntramolecular OxidoreductasesLeadPNAS PlusCell culturePositron-Emission TomographyPyrazinesbiology.proteinPET/computed tomography imagingTomography X-Ray ComputedProceedings of the National Academy of Sciences of the United States of America
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Alachlor and Bentazone Losses from Subsurface Drainage of Two Soils

2004

International audience; Atrazine (6-chloro-N2-ethyl-N4-isopropyl-1,3,5-triazine-2,4-diamine) is frequently detected at high concentrations in ground water. Bentazone [3-isopropyl-1H-2,1,3-benzothiadiazin-4(3H)-one 2,2-dioxide] plus alachlor (2-chloro-2',6'-diethyl-N-methoxymethylacetanilide) is a potential herbicide combination used as a substitute for atrazine. Thus, the objective of this study was to assess the environmental risk of this blend. Drainage water contamination by bentazone and alachlor was assessed in silty clay (Vertic Eutrochrept) and silt loam (Aquic Hapludalf) soils under the same management and climatic conditions. Drainage volumes and concentrations of alachlor and bent…

[SDE] Environmental SciencesEnvironmental EngineeringInceptisolCEMAGREFRain[SDV]Life Sciences [q-bio]010501 environmental sciencesManagement Monitoring Policy and LawBenzothiadiazines01 natural scienceschemistry.chemical_compoundSoilAlfisolAcetamidesWater MovementsHumansAtrazineLeaching (agriculture)DrainageWaste Management and DisposalComputingMilieux_MISCELLANEOUS0105 earth and related environmental sciencesWater Science and TechnologyHydrologyHerbicidesAlachlorBELY04 agricultural and veterinary sciences15. Life on landECOPollution6. Clean water[SDV] Life Sciences [q-bio]AgronomychemistryLoamSoil water[SDE]Environmental Sciences040103 agronomy & agriculture0401 agriculture forestry and fisheriesEnvironmental scienceFranceSeasonsWater Pollutants Chemical
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Prodrugs of sulfacetamide: Synthesis, X-ray structure, Hirshfeld analysis, antibacterial assessment, and docking studies

2022

Abstract New prodrugs of sulfacetamide as azo compounds were synthesized and have been evidenced through elemental and spectral analyses. Their synthesis was carried out by coupling the diazonium salt of sulfacetamide with activated carbanion salt of ethyl acetoacetate at 0 ˚C to afford the hydrazono derivative 3. Other prodrugs as sulfacetamide-pyrazoles, 5a, 5b and 5c were furnished via cyclocondensation of 3 with aryl/heteroaryl hydrazines. X-ray diffraction for single crystal was used to confirm the molecular and supramolecular structures of 3. In addition, DFT studies were performed to analyze the geometric parameters and compute the electronic properties of 3 and 5a-c. Hirshfeld analy…

biologyArylOrganic ChemistrySupramolecular chemistryActive siteSulfacetamideProdrugCombinatorial chemistryAnalytical ChemistryInorganic Chemistrychemistry.chemical_compoundchemistryDocking (molecular)Ethyl acetoacetatebiology.proteinmedicineSpectroscopyCarbanionmedicine.drugJournal of Molecular Structure
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CCDC 1547609: Experimental Crystal Structure Determination

2021

Related Article: Walter Can��o��n-Mancisidor, Patricio Hermosilla-Iba��n��ez, Evgenia Spodine, Vero��nica Paredes-Garci��a, Carlos J. Go��mez-Garci��a, Guillermo Mi��nguez Espallargas, Diego Venegas-Yazigi|2021|Cryst.Growth Des.|21|6213|doi:10.1021/acs.cgd.1c00640

bis(hexakis(mu-acetato)-(mu-oxo)-tris(acetamide)-tri-iron(iii)) acetamide bis(tetrafluoroborate) monohydrateSpace GroupCrystallographyCrystal SystemCrystal StructureCell ParametersExperimental 3D Coordinates
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Low-generation dendrimers with a calixarene core and based on a chiral C2-symmetric pyrrolidine as iminosugar mimics

2012

The preparation of low-generation dendrimers based on a simple calix[4]arene scaffold by insertion of the iminosugar-analogue C2-symmetric 3,4-dihydroxypyrrolidine is described. This methodology allows a rapid incorporation of a considerable number of iminosugar-like moieties in a reduced volume and in a well-defined geometry. The inclusion of alkali-metal ions (sodium and potassium) in the polar cavity defined by the acetamide moieties at the lower rim of the calixarene was demonstrated, which allows also the rigidification of the dendrimer structure and the iminosugar presentation in the clusters. The combination of the supramolecular properties of calixarenes with the advantage of a dend…

calixarenesLetterOrganic ChemistrySupramolecular chemistryIminosugarmultivalencyCombinatorial chemistryPyrrolidinedendrimerslcsh:QD241-441Chemistrychemistry.chemical_compoundlcsh:Organic chemistrychemistryDendrimerCalixareneiminosugarslcsh:Qlcsh:ScienceAcetamidecation-responsive systemBeilstein Journal of Organic Chemistry
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CCDC 1896308: Experimental Crystal Structure Determination

2019

Related Article: Arun Pal, Santanu Chand, Joan Cano Boquera, Francesc Lloret, Jian-Bin Lin, Shyam Chand Pal, Madhab C. Das|2019|Inorg.Chem.|58|6246|doi:10.1021/acs.inorgchem.9b00471

catena-[bis(mu-33'-[hydrazine-12-diylidenebis(eth-1-yl-1-ylidene)]dipyridine)-bis(mu-44'-oxydibenzoato)-di-cobalt(ii) NN-dimethylacetamide unknown solvate]Space GroupCrystallographyCrystal SystemCrystal StructureCell ParametersExperimental 3D Coordinates
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Recognition of N-Alkyl- and N-Aryl-Acetamides by N-Alkyl Ammonium Resorcinarene Chlorides

2014

N-alkyl ammonium resorcinarene chlorides are stabilized by an intricate array of intra- and intermolecular hydrogen bonds that leads to cavitand-like structures. Depending on the upper-rim substituents, self-inclusion was observed in solution and in the solid state. The self-inclusion can be disrupted at higher temperatures, whereas in the presence of small guests the self-included dimers spontaneously reorganize to 1:1 host-guest complexes. These host compounds show an interesting ability to bind a series of N-alkyl acetamide guests through intermolecular hydrogen bonds involving the carbonyl oxygen (C=O) atoms and the amide (NH) groups of the guests, the chloride anions (Cl(-)) and ammoni…

chemistry.chemical_classificationHydrogen bondStereochemistryArylOrganic ChemistryIntermolecular forceGeneral Chemistrymacromolecular substancesResorcinareneMedicinal chemistryCatalysischemistry.chemical_compoundchemistryAmideAmmoniumresorcinarenes; NMR titration; amides; host-guest complexes; X-ray crystallographyta116AlkylAcetamide
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