Search results for "acetamide"

showing 10 items of 142 documents

Heterogeneous response to differentiation induction with different polar compounds in a clonal rat rhabdomyosarcoma cell line (BA-HAN-1C)

1989

The clonal rat rhabdomyosarcoma cell line BA-HAN-1C was tested for its susceptibility to differentiation induction with different polar compounds. This cell line is composed of proliferating mononuclear tumour cells, some of which spontaneously fuse to form terminally differentiated postmitotic myotube-like giant cells. Exposure of BA-HAN-1C cells to dimethylsulphoxide (DMSO), hexamethylene bisacetamide (HMBA), sodium butyrate (NaBut) and N-monomethylformamide (NMF) resulted in a significant inhibition of proliferation (P less than 0.001) and in a simultaneous increase in differentiation. The response was most pronounced after exposure to NMF as evidenced by a marked increase in the creatin…

Cancer ResearchCellular differentiationAntineoplastic AgentsBiologyPeripheral blood mononuclear cellHexamethylene bisacetamideCell LineCell Fusionchemistry.chemical_compoundAcetamidesRhabdomyosarcomaTumor Cells CulturedAnimalsDimethyl SulfoxideCreatine KinaseCell fusionFormamidesDimethyl sulfoxideCell DifferentiationSodium butyrateMolecular biologyClone CellsRatsButyratesOncologychemistryBiochemistryCell cultureGiant cellButyric AcidResearch ArticleBritish Journal of Cancer
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Simultaneous analysis of lysine, Nɛ-carboxymethyllysine and lysinoalanine from proteins

2007

Protein quality was assayed by simultaneous measurement of lysine (Lys), carboxymethyllysine (CML) and lysinoalanine (LAL). GC-FID analysis of N-tert-butyl dimethylsilyl (tBDMSi) derivatives of these amino acids was undertaken. tBDMSi derivates were separated on a CP-SIL 5CB commercially fused silica capillary column (25 m × 0.25 mm i.d., 0.25 μm film thickness) employing a thermal gradient programmed from 200 to 300 °C. The identity of tBDMSi derivatives of Lys, CML and LAL was established by GC–MS while FID detection was employed for quantification. Analytical parameters such as linearity (lysine 350–4200 μM, LAL 3–81 μM, CML 16–172 μM), precision (1–13% variation coefficients), accuracy …

Chromatography GasG proteinEggsFluoroacetatesClinical BiochemistryLysineLysinoalanineBiochemistryAnalytical Chemistrysymbols.namesakeCaseinAcetamidesOrganosilicon CompoundsNɛ-CarboxymethyllysineLysinoalanineSoy proteinchemistry.chemical_classificationGas chromatographyChromatographyChemistryLysineProteinProteinsCell BiologyGeneral MedicineGlutenMaillard ReactionMaillard reactionsymbolsInfant FoodProtein qualityFood Analysis
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Self-assembled dendrimers with uniform structure

2008

Calix[4]arenes substituted at their wide rim by four aryl urea residues (1) form hydrogen-bonded dimers in apolar solvents. Replacement of one urea residue by an acetamido moiety leads to calix[4]arene derivatives (5) which form hydrogen-bonded tetramers under the same conditions. Both self-assembly processes occur independently. Therefore, molecules have been prepared in which a tetra-urea calix[4]arene and a tri-urea mono acetamide derivative are covalently connected between their narrow rims by a long, mainly aliphatic chain [-O-(CH(2))(n)-C(O)-NH-(CH(2))(m)-O-] (7). In the presence of an equimolar amount of tetra-tosyl urea calix[4]arene () they form dendritic assemblies since the well …

DendrimersMagnetic Resonance SpectroscopyStereochemistryHydrogen bondArylOrganic ChemistryHydrogen BondingNuclear magnetic resonance spectroscopyCrystallography X-RayBiochemistrychemistry.chemical_compoundCrystallographychemistryCovalent bondDendrimerProton NMRMoietylipids (amino acids peptides and proteins)Physical and Theoretical ChemistryDimerizationAcetamideOrganic & Biomolecular Chemistry
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Organometallic complexes with biological molecules. XI. Solid state and in vivo investigations of some diorganotin(IV)-chloramphenicol and cycloserin…

1998

Abstract Diorganotin(IV) derivatives of chloramphenicol, {=D-(-)threo-2,2-dichloro-N-[ β -hydroxy- α -(hydroxymethyl)- β -(4-nitrophenyl)ethyl]acetamide (=Hchloramph)}, and D-cycloserine, {=(R)-4-amino-3-isoxazolidone [=Hcyclos]} have been prepared. The stoichiometries of the obtained compounds were R 2 SnClantib and R 2 Snantib 2 (antib −1 =chloramph −1 , R=methyl and phenyl; antib −1 =cyclos −1 , R=methyl). The solid state configuration of the complexes was investigated by I.R. and Mossbauer spectroscopy, from which structural hypotheses were inferred. In particular, the experimental data suggested monomer structures both for R 2 Sn(IV)Clchloramph and R 2 Sn(IV)chloramph 2 , in which chlo…

DenticityChemistryStereochemistrychemistry.chemical_elementBiochemistryInorganic ChemistryCrystallographychemistry.chemical_compoundTrigonal bipyramidal molecular geometryDeprotonationOctahedronMössbauer spectroscopyHydroxymethylTinAcetamide
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A Co(III) complex of carbonic anhydrase inhibitor methazolamide and the amino-imino ‘aib’ ligand formed by reaction of acetone and ammonia

1993

Abstract Reaction of Co(NO 3 ) 2 ·6H 2 O with methazolamide {[ N -(3-methyl-5-sulfamoyl-1,3,4-thiadiazol-2(3 H )-ylidene)acetamide] (Hmacm)} and ammonia in acetone to produce [Co(methazolamidate)(2-methyl-2-amino-4-iminopentane) 2 (NH 3 )](NO 3 ) 2 ·2H 2 O is described. The ligand 2-methyl-2-amino-4-iminopentane (aib) is the product obtained from the condensation of two ammonia and two acetone molecules. The complex crystallizes in the monoclinic space group P 2 1 / c with a =16.713(5), b =9.180(1), c =20.273(1) A, β=97.44(4)° for Z =4. The R value is 0.081 for 2150 significant reflections. The Co(III) ion exhibits a nearly regular octahedral arrangement with the CoN bond distances in the …

DenticitybiologyLigandStereochemistrymedicine.drug_classImineMedicinal chemistryInorganic Chemistrychemistry.chemical_compoundDeprotonationchemistryCarbonic anhydraseMaterials Chemistrymedicinebiology.proteinCarbonic anhydrase inhibitorPhysical and Theoretical ChemistryMethazolamideAcetamidemedicine.drugInorganica Chimica Acta
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Contributions to the analysis of organic xenobiotics in fish

1995

For the residue-analysis of fish samples, a method has been developed to separate the medium polar triazines and acetamides together with lipophilic xenobiotics (organochlorine pesticides, PCBs and octachlorostyrene) from fish tissue. The detection limits of the analytes are mostly within the ppt-range (ng/kg fillet) and vary between 40 and 1050 ng/kg fillet of fish. Their recoveries range from 75 to 108%, spiked at 1.5 μg/kg. The substances are extracted with a mixture of petroleum ether/ethylacetate (2:1) using a soxhlet apparatus. Subsequently, the lipids in the sample extracts are reduced to 0.4% by gel chromatography. A 5 g silica gel clean-up separates the analytes according to their …

Detection limitGel permeation chromatographychemistry.chemical_compoundChlorophenoxy herbicideChromatographyChemistryElutionSilica gelPetroleum etherGas chromatography–mass spectrometryBiochemistryAcetamideAnalytical ChemistryFresenius' Journal of Analytical Chemistry
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Response to Agomelatine Treatment is Independent of Smoking Status and Dosage: Results From the AGOPSYCH Study.

2018

Abstract Introduction Cigarette smoking influences response to antidepressant treatment. It accelerates the metabolism of several cytochrome P450 (CYP) subtypes, including CYP1A2, and therefore bears the risk of pharmacokinetic interactions with psychotropic drugs using that pathway. Agomelatine is a substrate of CYP1A2; the association between nicotine use and agomelatine dosage, however, has never been studied before. Methods Smoking habits were correlated with agomelatine doses and treatment outcomes in a sample of 27 patients with lifetime diagnoses within the schizophrenia spectrum who received agomelatine treatment in addition to their stable antipsychotic treatment regimen because of…

DrugOncologyAdultMalemedicine.medical_specialtymedia_common.quotation_subject030226 pharmacology & pharmacyNicotine03 medical and health sciencesYoung Adult0302 clinical medicinePharmacokineticsInternal medicineAcetamidesmedicineAgomelatineHumansPharmacology (medical)Young adultmedia_commonPsychiatric Status Rating ScalesDose-Response Relationship Drugbusiness.industryDepressionSmokingGeneral MedicineMiddle Agedmedicine.diseaseAntidepressive Agents030227 psychiatry3. Good healthPsychiatry and Mental healthRegimenTreatment OutcomeSchizophreniaAntidepressantFemalebusinessmedicine.drugPharmacopsychiatry
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Binding of [3H][D-Ala2, MePhe4, Gly-ol5] Enkephalin, [3H][D-Pen2, D-Pen5]Enkephalin, and [3H]U-69,593 to Airway and Pulmonary Tissues of Normal and S…

1997

Abstract Bhargava, H. N., V. M. Villar, J. Cortijo and E. J. Morcillo. Binding of [3H][D-Ala2, MePhe4, Gly-ol5]enkephalin, [3H][D-Pen2, D-Pen5]enkephalin, and [3H]U-69,593 to airway and pulmonary tissues of normal and sensitized rats. Peptides 18(10) 1603–1608, 1997.—The role of endogenous opioid peptides in the regulation of bronchomotor tone, as well as in the pathophysiology of asthma is uncertain. We have studied the binding of highly selective [3H]labeled ligands of μ-([D-Ala2, MePhe4, Gly-ol5]enkephalin; DAMGO), δ ([D-Pen2, D-Pen5]enkephalin; DPDPE), and κ-(U-69,593) opioid receptors to membranes of trachea, main bronchus, lung parenchyma and pulmonary artery obtained from normal (uns…

Hypersensitivity ImmediateMalemedicine.medical_specialtyPyrrolidinesEnkephalinPhysiologymedicine.drug_classRespiratory SystemBenzeneacetamidesPulmonary ArteryBiochemistryRats Sprague-DawleyCellular and Molecular Neurosciencechemistry.chemical_compoundEndocrinologyOpioid receptorU-69593Internal medicineParenchymamedicineAnimalsReceptorOpioid peptideLungChemistryCell MembraneEnkephalinsEnkephalin Ala(2)-MePhe(4)-Gly(5)-respiratory systemAsthmaRatsDAMGOEndocrinologyOpioidReceptors OpioidEnkephalin D-Penicillamine (25)-Protein Bindingmedicine.drugPeptides
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Cytokines with Possible Clinical Utility

1987

Biological response modifiers (BRM) are agents aimed at reducing tumor growth, not primarily by exerting direct cytotoxic effects but by modulation of tumor gene expression (e.g., induction of differentiation) or by enhancing host defense mechanisms directed against cancer cells. BRM as primary therapy or as adjuncts to cytotoxic agents in the treatment of cancers have attracted increasing interest in view of stagnating clinical results in many areas [1], and there is increasing evidence of in vitro and in vivo efficacy of these agents. Furthermore, advances in molecular biology suggesting that oncogenes and their products play a crucial role in oncogenesis support approaches to modulation …

In vivoCancer cellCancer researchmedicineCytotoxic T cellBiological response modifiersBiologyCytotoxicityCarcinogenesismedicine.disease_causeHexamethylene bisacetamideIn vitro
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Gas-phase ion chemistry of protonated melatonin

2009

The gas-phase ion chemistry of protonated melatonin has been investigated by mass spectrometric (MS) techniques involving chemical ionisation, fast atom bombardment and electrospray ionisation. Either naturally-occurring or collision-induced decomposition experiments have been carried out using side chain tetra-deuterium-labelled derivatives, as well as the corresponding N–D derivatives obtained by exchange with D2O. The analysis of experimental results allows definite pathways for the formation of the ion at m/z 174 to be assigned and sheds some more light on the overall fragmentation pathways. Experiments on labelled derivatives evidenced H–D scrambling processes during fragmentation.

IonsElectrospraySpectrometry Mass Electrospray IonizationChemistryElectrospray ionizationInorganic chemistryDeuterium Exchange MeasurementProtonationmelatonin ESI/MS ESI/MS/MSion chemistryGeneral MedicineFast atom bombardmentPhotochemistryAtomic and Molecular Physics and OpticsIonFragmentation (mass spectrometry)AmmoniaTandem Mass SpectrometryAcetamidesProton affinityQuantum TheoryGasesProtonsSpectroscopyGas-phase ion chemistryMelatonin
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