Search results for "hydrolysis"

showing 10 items of 632 documents

DNA damage photo-induced by chloroharmine isomers: hydrolysis versus oxidation of nucleobases

2018

Photodynamic therapy (PDT) is an emerging clinical treatment currently being used against a wide range of both cancerous and noncancerous diseases. The search for new active photosensitizers as well as the development of novel selective delivery systems are the major challenges faced in the application of PDT. We investigated herein three chloroharmine derivatives (6-, 8- and 6,8-dichloroharmines) with quite promising intrinsic photochemical tunable properties and their ability to photoinduce DNA damage in order to elucidate the underlying photochemical mechanisms. Data revealed that the three compounds are quite efficient photosensitizers. The overall extent of photo-oxidative DNA damage i…

DNA damagemedicine.medical_treatmentSubstituentPhotodynamic therapyAntineoplastic Agents010402 general chemistryRing (chemistry)01 natural sciencesBiochemistryNucleobase//purl.org/becyt/ford/1 [https]Hydrolysischemistry.chemical_compoundIsomerism//purl.org/becyt/ford/1.4 [https]medicineDNA Breaks Single-StrandedPhysical and Theoretical ChemistryPurine metabolismClinical treatmentPhotosensitizing Agents010405 organic chemistryHydrolysisOrganic ChemistryCiencias QuímicasCombinatorial chemistry0104 chemical sciencesHarmineQuímica OrgánicachemistryPhotochemotherapyβ-CarbolinesDNA damageChlorineOxidation-ReductionCIENCIAS NATURALES Y EXACTASDNA Damage
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Characterization of Different Deoxyribonucleases in Human Lymphocytes

1975

Abstract Deoxyribonucleases, Disc Electrophoresis, Lymphocytes Four groups of deoxyribonuclease activities from human lymphocytes have been characterized by deoxyribonuclease assay in DNA-containing polyacrylamide gels following their separation by disc-electrophoresis. All activities hydrolyse DNA endonucleolytically. One neutral deoxyribo­ nuclease found in the cytoplasmic fraction prefers native or UV-irradiated DNA over denatured DNA as substrate and is a 5′-monoester former. Two groups of acid deoxyribonuclease activities are detectable in the nuclear fraction. Both are 3′-monoester formers. One is as well active with denatured DNA as with native DNA, the other one shows the same activ…

DNA BacterialCytoplasmUltraviolet RaysPolyacrylamideNucleic Acid DenaturationGeneral Biochemistry Genetics and Molecular Biologychemistry.chemical_compoundHydrolysismedicineHumansLymphocytesCell NucleusDeoxyribonucleasesSubstrate (chemistry)DeoxyribonucleaseDNAHydrogen-Ion ConcentrationElectrophoresis DiscRadiation Effectsmedicine.anatomical_structurechemistryBiochemistryCytoplasmDeoxyribonucleasesNucleusDNAZeitschrift für Naturforschung C
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Small Nitrogenous Compounds

1994

Because of the constant turnover of proteins, protein-bound and free amino acids exist in a dynamic equilibrium. The intracellular pool of free amino acids, which is replenished by the hydrolysis of existing proteins, by uptake from the intercellular space and by de novo synthesis, is available for protein synthesis and for the many other metabolic processes dependent upon amino acids. The concentration of free amino acids is always lower than that of the protein-bound residues, one limiting factor being the strong osmotic effects of such low molecular weight compounds. Thus, there is no specific amino acid store in an organism; it is more the case that enzymes and structural proteins thems…

De novo synthesischemistry.chemical_classificationHydrolysisEnzymechemistryBiochemistryHemolymphProtein biosynthesisIntracellularOrganismAmino acid
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Design of a knowledge and management system for starch bioconversion

2011

Abstract In this paper a knowledge acquisition and management system (KAMS) which allows the collection, analysis, ordering and storage of informations generated at starch liquefaction was developed. KAMS was structured on three levels: PostgreSQL as a backend, D2RQ as middle tier and Seaside as frontend. The system was used to store knowledge about the liquefaction process with the goal to be used as a decision support system in chosing the condition for this operation. The tests had shown that the implemented KAMS provides support for: Distributed acquisition of the scientific data generated by the researchers; Structured data storage; Support for the generation and storage of knowledge o…

Decision support systemEngineeringDatabaseProcess (engineering)business.industryBioconversionstarchLiquefactionGeneral Medicinecomputer.software_genreKnowledge acquisitionKnowledge management systemsemantic WebhydrolysisManagement systemMiddle tierbusinessSemantic WebcomputerProcedia Food Science
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Enantiomer separation by chiral-phase liquid chromatography of urethane derivatives of natural diacylglycerols previously fractionated by reversed-ph…

1991

Abstract Enantiomers of diacylglycerols such as 3,5-dinitrophenyl isocyanate (urethane) derivatives previously fractionated by reversed-phase high-performance liquid chromatography (HPLC) were separated by HPLC on a chiral phase column [N-( R )-1-(α-naphthyl)ethylamino-carbonyl-( S )-valine chemically bound to γ-aminopropylsilanized silica]. In addition to the separation of commercial monoacid-diacylglycerol isomers, separation of diacid-diacylglycerol isomers obtained from peanut oil and cottonseed oil triacylglycerols by chemical hydrolysis is reported. Hexane-ethylene dichloride-ethanol mixtures were used for elution of the diacylglycerol derivative isomers, which were detected by their …

Degree of unsaturationChromatographyChemistryElutionOrganic ChemistryGeneral MedicineReversed-phase chromatographyBiochemistryIsocyanateHigh-performance liquid chromatographyAnalytical ChemistryHydrolysischemistry.chemical_compoundOrganic chemistryRacemic mixtureEnantiomerJournal of Chromatography A
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Analysis and fractionation of natural source diacylglycerols as urethane derivatives by reversed-phase high-performance liquid chromatography

1991

Abstract Reversed-phase high-performance liquid chromatography on a thermostatted octadecylsilyl column was used to separate and fractionate mixtures of diacylglycerols after derivatization with 3,5-dinitrophenyl isocyanate (urethane derivatives). In addition to the separation of commercial diacylglycerol species, the separation of diacylglycerols obtained from peanut oil and cottonseed oil triacylglycerols by chemical hydrolysis is reported. Acetonitrile-acetone mixtures were used for elution of the diacylglycerol urethane derivatives. Unsaturated and saturated derivatives were detected by their refractive indices. They were then collected and their fatty acids analysed as methyl esters by…

Degree of unsaturationChromatographyElutionGlycerideOrganic ChemistryGeneral MedicineFractionationBiochemistryHigh-performance liquid chromatographyAnalytical ChemistryHydrolysischemistry.chemical_compoundchemistryOrganic chemistrylipids (amino acids peptides and proteins)DerivatizationDiacylglycerol kinaseJournal of Chromatography A
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Specificity of deoxyribonuclease hydrolysis determined by high-performance liquid anion-exchange chromatography

1980

DeoxyribonucleasesChromatographyLymphomaIon exchangeChemistryOrganic ChemistryDeoxyribonucleaseDNANeoplasms ExperimentalGeneral MedicineChromatography Ion ExchangeBiochemistryCell LineAnalytical ChemistryDNA metabolismMiceHydrolysisBiochemistryAnimalsChromatography High Pressure LiquidJournal of Chromatography A
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An isocratic high-pressure liquid chromatographic purification method for radioactively labeled deoxyribonucleoside triphosphates.

1976

Abstract A method is described for the rapid purification of radioactively labeled deoxyribonucleoside tri­phosphates from their spontaneously emerging hydrolysis products deoxyribonucleoside diphosphate, deoxyribonucleoside monophosphate, and deoxyribonucleoside. The separations which are finished within 3 min or less are carried out on a 0.1X5 cm column filled with LiChrosorb-NH2 , using isocratic elution with 0.025 м potassium phosphate, pH 6 .8 , in a high-pressure liquid chromatograph at room temperature and a flow rate of 30 ml · h-1(flow velocity 63.7 cm·min-1).

Deoxyribonucleosidechemistry.chemical_compoundHydrolysisIsocratic elutionChromatographychemistryPotassium phosphateHigh pressureDeoxyribonucleotidesPurification methodsGeneral Biochemistry Genetics and Molecular BiologyChromatography High Pressure LiquidZeitschrift fur Naturforschung. Section C, Biosciences
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Identification of lipid binders in old oil paintings by separation of 4-bromomethyl-7-methoxycoumarin derivatives of fatty acids by liquid chromatogr…

2005

A HPLC-fluorescence method for identification of drying oils from binding media or protective film used in pictorial works of art prior to conservation or restoration is proposed. Fluorescence derivatization of fatty acids released by hydrolysis of structural drying oils is studied. The derivatization reagent was 4-(bromomethyl)-7-methoxycoumarin with 18-crown-6 as catalyst. Mobile phase was programmed from methanol-water (90:10 v/v) to methanol-water (100:0 v/v) in 25 min. The excitation and emission wavelengths were 325 and 395 nm, respectively. Under these chromatographic conditions, coumarin derivatives of myristic, palmitic, oleic and stearic acids were satisfactorily resolved. The met…

Detection limitChromatographyOrganic ChemistryDrying oilGeneral MedicineReference StandardsBiochemistryHigh-performance liquid chromatographyLipidsAnalytical ChemistryPalmitic acidchemistry.chemical_compoundHydrolysisVegetable oilSpectrometry FluorescencechemistryPaintingsStearic acidUmbelliferonesDerivatizationChromatography High Pressure LiquidJournal of chromatography. A
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Flow-injection spectrophometric determination of propoxur with p-aminophenol

1992

Abstract The spectrophotomeric determination of propoxur [2-(1-methyxlthoxy)phenyl methyl carbamate] was carried out with p -aminophenol (PAP) in a flow system. The method involves the on-line hydrolysis with NaOH of propoxur to 2-isopropoxyphenol and the oxidation of PAP to its relative quinone imine with KIO 4 and the reaction between the phenolate and the quinone imine. A four-channel flow manifold was employed to carry out all the different steps of the reaction considered, monitoring the indo dye formed at 600 nm. The developed procedure provides a typical calibration line of A = 0.000 7 + 1.8 × 10 3 C ( A = absorbance; C = concentration in M) with a regression coefficient of 0.9998 an…

Detection limitChromatographyP-AminophenolIminePropoxurBiochemistryAnalytical ChemistryMethyl carbamateQuinoneAbsorbanceHydrolysischemistry.chemical_compoundchemistryEnvironmental ChemistrySpectroscopyAnalytica Chimica Acta
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