Search results for "TRIP"

showing 10 items of 2134 documents

From the covalent linkage of drugs to novel inhibitors of ribonucleotide reductase: synthesis and biological evaluation of valproic esters of 3'-C-me…

2014

We synthesized a series of serum-stable covalently linked drugs derived from 3'-C-methyladenosine (3'-Me-Ado) and valproic acid (VPA), which are ribonucleotide reductase (RR) and histone deacetylase (HDAC) inhibitors, respectively. While the combination of free VPA and 3'-Me-Ado resulted in a clear synergistic apoptotic effect, the conjugates had lost their HDAC inhibitory effect as well as the corresponding apoptotic activity. Two of the analogs, 2',5'-bis-O-valproyl-3'-C-methyladenosine (A160) and 5'-O-valproyl-3'-C-methyladenosine (A167), showed promising cytotoxic activities against human hematological and solid cancer cell lines. A167 was less potent than A160 but had interesting featu…

Deoxyribonucleoside triphosphateAdenosineCell SurvivalClinical BiochemistryAllosteric regulationPharmaceutical ScienceAntineoplastic AgentsPharmacologyBiochemistryHistone deacetylase (HDAC) inhibitorHistone DeacetylasesAdenosine TriphosphateAllosteric RegulationCell Line TumorDrug DiscoveryRibonucleotide ReductasesmedicineValproic acidHumansRibonucleotide reductase (RR) inhibitorEnzyme InhibitorsMolecular Biology3′-C-methyladenosineNucleoside analogueKinaseChemistryOrganic ChemistryApoptosiEstersSettore CHIM/08 - Chimica FarmaceuticaHematological and solid tumorHistone Deacetylase InhibitorsKineticsRibonucleotide reductaseBiochemistrySettore BIO/14 - FarmacologiaMolecular MedicineHistone deacetylaseNucleosideIntracellularmedicine.drug
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Insights into how nucleotide supplements enhance the peroxidase-mimicking DNAzyme activity of the G-quadruplex/hemin system

2012

Since the initial discovery of the catalytic capability of short DNA fragments, this peculiar enzyme-like property (termed DNAzyme) has continued to garner much interest in the scientific community because of the virtually unlimited applications in developing new molecular devices. Alongside the exponential rise in the number of DNAzyme applications in the last past years, the search for convenient ways to improve its overall efficiency has only started to emerge. Credence has been lent to this strategy by the recent demonstration that the quadruplex-based DNAzyme proficiency can be enhanced by ATP supplements. Herein, we have made a further leap along this path, trying first of all to deci…

DeoxyribozymeNanotechnologyBiology010402 general chemistryG-quadruplex01 natural sciencesCatalysischemistry.chemical_compoundAdenosine TriphosphateGeneticsNucleotideCatalytic efficiencyComputingMilieux_MISCELLANEOUSchemistry.chemical_classificationSupplementary data010405 organic chemistryNucleotides[CHIM.CATA]Chemical Sciences/CatalysisDNADNA Catalytic0104 chemical sciences[SDV.BBM.BP]Life Sciences [q-bio]/Biochemistry Molecular Biology/BiophysicsG-QuadruplexesCatalytic cyclechemistryBiochemistryPeroxidasesSynthetic Biology and ChemistryHeminOverall efficiencyHeminNucleic Acids Research
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Quantification of nortriptyline in plasma by HPLC and fluorescence detection

2009

Abstract A simple, sensitive and specific high-performance liquid chromatography method has been developed for the determination of nortriptyline (NT) in plasma samples. The assay involved derivatization with 9H-fluoren-9-ylmethyl chloroformate (Fmoc-Cl) and isocratic reversed-phase (C 18 ) chromatography with fluorescence detection. The developed method required only 100 μl of plasma sample, deproteinized and derivatized in one step. Calibration curves were lineal over the concentration range of 5–5000 ng/ml. The derivatization reaction was performed at room temperature in 20 min and the obtained NT derivative was stable for at least 48 h at room temperature. The within-day and between-day…

Detection limitChromatographyCalibration curveClinical BiochemistryNortriptylineCell BiologyGeneral MedicineDerivativeChloroformateBiochemistryHigh-performance liquid chromatographyFluorescenceAntidepressive AgentsRatsAnalytical Chemistrychemistry.chemical_compoundchemistryLimit of DetectionmedicineAnimalsHumansNortriptylineDerivatizationChromatography High Pressure Liquidmedicine.drugJournal of Chromatography B
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High-performance liquid chromatographic determination of sumatriptan after in vitro transdermal diffusion studies.

2004

A simple, accurate, precise and rapid HPLC method with UV detection has been validated in order to determine the in vitro transdermal absorption of sumatriptan succinate. The HPLC method is a modification of that described by Nozal et al. [M.J. Nozal, J.L. Bernal, L. Toribio, M.T. Martin, F.J. Diez, J. Pharm. Biomed. Anal. 30 (2002) 285-291]. Separation was carried out on a 250 mm Kromasil C18 column at room temperature. The detector response, at 282.7 nm, was found to be linear in a concentration range between 0.145 and 145 microM. The limit of detection (LOD) was 0.019 microM and the limit of quantification (LOQ) was 0.145 microM.

Detection limitChromatographyChemistrySumatriptanSwineDiffusionSkin AbsorptionClinical BiochemistryAnalytical chemistryPharmaceutical ScienceAbsorption (skin)Reversed-phase chromatographyIn Vitro TechniquesAdministration CutaneousHigh-performance liquid chromatographyAnalytical ChemistrySumatriptan SuccinateDrug DiscoveryAnimalsDiffusion Chambers CultureQuantitative analysis (chemistry)SpectroscopyChromatography High Pressure LiquidTransdermalSkinJournal of pharmaceutical and biomedical analysis
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Determination of amitraz and its transformation products in pears by ethyl acetate extraction and liquid chromatography-tandem mass spectrometry.

2008

A method has been developed for identification and quantification of the acaricide amitraz and its transformation products, 2,4-dimethylaniline (DMA), 2,4-dimethylformamidine (DMF) and N-2,4-dimethylphenyl-N-methylformamidine (DMPF) in pears. The analytes were extracted using ethyl acetate and anhydrous sodium sulphate. Analysis was performed by liquid chromatography-electrospray tandem mass spectrometry (LC-ESI-MS/MS) in the positive ion mode using a triple quadrupole (QqQ) instrument. Two precursor-product ion transitions were monitored for each compound in the selected reaction monitoring (SRM) mode. The method was validated with pears taken from the orchard before the amitraz treatment …

Detection limitChromatographyMaximum Residue LimitAniline CompoundsToluidinesSulfatesOrganic ChemistrySelected reaction monitoringEthyl acetatePesticide ResiduesReproducibility of ResultsGeneral MedicineAcetatesBiochemistryHigh-performance liquid chromatographySensitivity and SpecificityAnalytical ChemistryTriple quadrupole mass spectrometerPyruschemistry.chemical_compoundchemistryLiquid chromatography–mass spectrometryTandem Mass SpectrometryAmitrazChromatography LiquidJournal of chromatography. A
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Optimization of LC–MS/MS using triple quadrupole mass analyzer for the simultaneous analysis of carbosulfan and its main metabolites in oranges

2006

This paper describes an analytical method involving a simple solvent extraction for the simultaneous liquid chromatography coupled to quadrupole tandem mass spectrometry (LC-MS/MS) determination of carbosulfan, its most toxic metabolite--carbofuran--, and its other main metabolites--3-hydroxycarbofuran, 3-ketocarbofuran, 3-hydroxy-7-phenolcarbofuran, 3-keto-7-phenolcarbofuran, 7-phenolcarbofuran and dibutylamine--in oranges. Chromatography was performed on a Zorbax Bonus-RP (150 mm x 2.1 mm, 5 microm). The mobile phase was a ternary gradient water-methanol-acetonitrile with 1.0 mM ammonium acetate at flow rate of 0.2 ml min(-1). The LC separation and MS/MS optimization were studied to selec…

Detection limitChromatographyMetaboliteAnalytical chemistryTandem mass spectrometryBiochemistryAnalytical ChemistryTriple quadrupole mass spectrometerStandard curvechemistry.chemical_compoundchemistryLiquid chromatography–mass spectrometryEnvironmental ChemistrySample preparationCarbosulfanSpectroscopyAnalytica Chimica Acta
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Ultra-high performance liquid chromatography-quadrupole time-of-flight mass spectrometry to identify contaminants in water: an insight on environment…

2013

Ultra-high pressure liquid chromatography-quadrupole time-of-flight mass spectrometry (UHPLC-QqTOF-MS) acquiring full scan MS data for quantification, and automatic data dependent information product ion spectra (IDA-MS/MS) without any predefinition of the ions by the user was checked for identifying organic contaminants in water samples. The use of a database with more than 2000 compounds achieved high confidence results for a wide number of contaminants based upon retention time, accurate mass, isotopic pattern and MS/MS library searching. More than 20 contaminants, mostly pharmaceuticals, but also mycotoxins and polyphenols were unambiguously identified. Furthermore, the combination of s…

Detection limitChromatographyTime FactorsChemistryOrganic ChemistryAnalytical chemistryWaterGeneral MedicineContaminationMass spectrometryBiochemistryLibrary searchingAnalytical ChemistryTriple quadrupole mass spectrometerMolecular WeightRiversTandem Mass SpectrometryPrincipal component analysisQuadrupole time of flightUltra high performancePesticidesChromatography High Pressure LiquidWater Pollutants ChemicalJournal of chromatography. A
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Identification of unknown pesticides in fruits using ultra-performance liquid chromatography–quadrupole time-of-flight mass spectrometry

2007

Abstract Ultra-high-performance liquid chromatography–quadrupole time-of-flight mass spectrometry (UPLC-QqTOF-MS) is an emerging technique offering more rapid and efficient separation, as well as the possibility to obtain accurate mass measurement and tandem mass spectrometry (MS/MS). This paper deals with the use of UPLC-QqTOF-MS to identify the pesticide residues present in complex pear extracts. Carbendazim, imazalil, and ethoxyquin were successfully identified because of the accurate mass determination of their protonated molecule and their major fragments in the product ion mass spectra. A few plastic and latex additives were also found, most of them probably coming from the packaging …

Detection limitElectrosprayChromatographyCalibration curveChemistryOrganic ChemistryAnalytical chemistryGeneral MedicineTandem mass spectrometryMass spectrometryBiochemistryAnalytical ChemistryTriple quadrupole mass spectrometerLiquid chromatography–mass spectrometryMass spectrumJournal of Chromatography A
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Vanadium and molybdenum concentrations in particulate from Palermo (Italy): analytical methods using voltammetry

2014

The main purpose of this work was to develop a reliable method for the determination of vanadium (V) and molybdenum (Mo) in atmosphere particles or aerosols because they can not be readily measured using conventional techniques. For this research, 30 particulate samples were collected from five different stations located at Palermo, Italy. We used the catalytic adsorptive stripping voltammetry and differential pulsed voltammetry to measure Vand Mo in atmospheric particulate, respectively. The represented method includes advantages of high sensitivity, high selectivity, simplicity, reproducibility, speed and low costs. The quantification limits for V and Mo are, respectively, 0.57 and 0.80 n…

Detection limitReproducibilityRelative standard deviationAnalytical chemistrychemistry.chemical_elementVanadiumParticulatesSettore CHIM/12 - Chimica Dell'Ambiente E Dei Beni CulturalichemistryMolybdenumEnvironmental chemistryvanadium molybdenum particulate voltammetry PalermoAdsorptive stripping voltammetrySettore CHIM/01 - Chimica AnaliticaVoltammetryGeneral Environmental Science
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Determination of type A and type B trichothecenes in paprika and chili pepper using LC-triple quadrupole-MS and GC-ECD.

2011

There is a need to develop sensitive and accurate analytical methods for determining deoxynivalenol (DON), HT-2 toxin and T-2 toxin in paprika to properly assess the relevant risk of human exposure. An optimized analytical method for determination of HT-2 toxin and T-2 toxin using capillary gas chromatography with electron capture detection and another method for determination of DON by liquid chromatography-mass spectrometry in paprika was developed. The method for determination of HT-2 toxin and T-2 toxin that gave the best recoveries involved extraction of the sample with acetonitrile-water (84:16, v/v), clean-up by solid-phase extraction on a cartridge made of different sorbent material…

Detection limitResidue (complex analysis)ChromatographyChromatography GasElutionChemistryExtraction (chemistry)Mass SpectrometryAnalytical ChemistryTriple quadrupole mass spectrometerT-2 ToxinHumansSample preparationGas chromatographySolid phase extractionCapsicumTrichothecenesChromatography LiquidTalanta
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