Search results for "resorcinol"

showing 10 items of 32 documents

Resorcinol Functionalized Gold Nanoparticles for Formaldehyde Colorimetric Detection

2019

[EN] Gold nanoparticles functionalized with resorcinol moieties have been prepared and used for detecting formaldehyde both in solution and gas phases. The detection mechanism is based on the color change of the probe upon the aggregation of the nanoparticles induced by the polymerization of the resorcinol moieties in the presence of formaldehyde. A limit of detection of 0.5 ppm in solution has been determined. The probe can be deployed for the detection of formaldehyde emissions from composite wood boards.

Detection limitResorcinolGeneral Chemical EngineeringFormaldehydeNanoparticleResorcinolArticlelcsh:Chemistrychemistry.chemical_compoundchemistryPolymerizationlcsh:QD1-999Colloidal goldFormaldehydegold nanoparticlescolorimetric detectionGold nanoparticlesformaldehydeGeneral Materials ScienceresorcinolColorimetric detectionNuclear chemistryNanomaterials
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Alkylresorcinol Metabolites in Urine and Plasma as Potential Biomarkers of Rye and Wheat Fiber Consumption in Prostate Cancer Patients and Controls

2015

Alkylresorcinols (ARs) are phytochemicals mainly associated with rye/wheat bran. Plasma ARs and their plasma and urine metabolites are considered as biomarkers for whole-grain rye/wheat intake. However ARs metabolite day and night variations have not been studied in prostate cancer patients yet. We investigated ARs metabolites 3, 5-dihydroxy-benzoic acid (DHBA), and 3-(3, 5-dihydroxyphenyl)-1-propanoic acid (DHPPA) in urine and plasma in prostate cancer patients and in control group. DHPPA in 12-h overnight urine correlated with the intake of rye bread and bread fiber across short time periods (3 days). Plasma DHPPA concentration was significantly greater in the prostate cancer group than i…

Dietary FiberMaleCancer Researchmedicine.medical_specialty030309 nutrition & dieteticsMetaboliteMedicine (miscellaneous)030209 endocrinology & metabolismUrineExcretion03 medical and health scienceschemistry.chemical_compoundProstate cancer0302 clinical medicineAlkylresorcinolInternal medicineHydroxybenzoatesmedicineHumansTriticumAged0303 health sciencesNutrition and DieteticsPhenylpropionatesBranSecaledigestive oral and skin physiologyCase-control studyProstatic Neoplasmsfood and beveragesBreadResorcinolsMiddle Agedmedicine.disease6. Clean waterCircadian Rhythm3. Good healthEndocrinologyOncologychemistryBiochemistryCase-Control StudiesPotential biomarkersBiomarkersNutrition and Cancer
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Conformational properties of methylene bridged resorcarenes

1998

Abstract Conformations and conformational interconversions of resorcarene 1c have been studied by molecular mechanics calculations. As with calix[4]arenes the general stability of the four basic conformations is cone > partial cone > 1,2-alternate > 1,3-alternate. The lowest energy is calculated for a pinched cone conformer with C2v symmetry stabilised by intramolecular hydrogen bonds of the two “parallel” resorcinol units as donors. The topomerisation of the cone conformation proceeds via the partial cone and 1,2-alternate intermediates with a calculated barrier of 9.9 kcal mol−1 which is in excellent agreement with the experimental value.

Hydrogen bondChemistryOrganic ChemistryResorcinolResorcinareneBiochemistryCrystallographychemistry.chemical_compoundCone (topology)Computational chemistryIntramolecular forceDrug DiscoveryCalixareneMethyleneConformational isomerismTetrahedron
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Oxaaza cyclophanes in the recognition of nucleotides. The role of oxygen and electron-rich aromatic rings

2007

Dioxapolyaza cyclophanes derived from resorcinol and different polyamine chains have been studied in aqueous solution as abiotic receptors for nucleotides. The presence of the additional ethyleneoxy subunits is reflected in a higher basicity and in a significant increase in the log K values for the interaction with nucleotides relative to that of related polyazacyclophanes.

Models MolecularMagnetic Resonance Spectroscopychemistry.chemical_elementElectronsResorcinolElectronAbiotic ReceptorsHydrocarbons AromaticBiochemistryMedicinal chemistryOxygenchemistry.chemical_compoundCrown EthersOrganic chemistryComputer SimulationNucleotidePhysical and Theoretical Chemistrychemistry.chemical_classificationAqueous solutionNucleotidesChemistryOrganic ChemistryAromaticityOxygenPotentiometryPolyamineOrg. Biomol. Chem.
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An electrospray ionization Fourier transform ion cyclotron resonance mass spectrometric study of the gas-phase stabilities and fragmentation ofN-alky…

2006

Five N-alkylated ammonium resorcarene derivatives, differing either in the nitrogen atom or in the lower rim alkyl chain, were studied using electrospray ionization Fourier transform ion cyclotron resonance mass spectrometry. The main purpose was to clarify the fragmentation and the relative stabilities of the protonated molecules by collision-induced dissociation (CID) experiments. The results indicate that fragmentation of the upper rim alkyl amino substituents at the 2-position occurs readily. Variation in the gas-phase stabilities of these molecules was also observed. In addition, the proposed fragmentation pathways are depicted.

Spectrometry Mass Electrospray IonizationChemical ionizationAlkylationCollision-induced dissociationChemistryElectrospray ionizationOrganic ChemistryAnalytical chemistryResorcinolsCyclotronsMass spectrometryPhase TransitionIon sourceFourier transform ion cyclotron resonanceAnalytical ChemistryQuaternary Ammonium CompoundsFragmentation (mass spectrometry)OxazinesSpectroscopy Fourier Transform InfraredGasesSpectroscopyIon cyclotron resonanceRapid Communications in Mass Spectrometry
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Mass spectrometric studies of benzoxazine resorcarenes

2002

Eleven differently substituted 3,4-dihydro-2H-1,3-benzoxazine resorcarenes were studied by electrospray ionisation (ESI) and matrix-assisted laser desorption/ionisation (MALDI) mass spectrometry, using Fourier transform ion cyclotron resonance (FT-ICR) and time-of-flight (TOF) mass spectrometers, respectively. Under ESI conditions it was possible to transfer the intact resorcarenes from solution to the gas phase, yielding [M + H]+ and [M + 2H]+ ions as the main ions observed. Energy increase of the ions induced ready decomposition through successive eliminations of four CH2NR groups. Ion-molecule reactions showed that the ionising proton was situated somewhere inside the molecule and could …

Spectrometry Mass Electrospray IonizationElectrosprayChemistryOrganic ChemistryAnalytical chemistryResorcinolsMass spectrometryAlkali metalFourier transform ion cyclotron resonanceAnalytical ChemistryIonFragmentation (mass spectrometry)Spectrometry Mass Matrix-Assisted Laser Desorption-IonizationReagentOxazinesMoleculeSpectroscopyRapid Communications in Mass Spectrometry
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4,5,6,7-Tetrahydro-isoxazolo-[4,5-c]-pyridines as a new class of cytotoxic Hsp90 inhibitors.

2014

Hsp90 is considered an interesting therapeutic target for anticancer drug development. Here we describe a new class of 4,5,6,7-tetrahydro-isoxazolo-[4,5-c]-pyridine compounds. A small library of derivatives has been synthesized and investigated. Some reported compounds show interesting properties combining both notable binding to Hsp90 and potent cell growth inhibitory activity. N-5 substitution with a 2,4 resorcinol carboxamide appears crucial for activity. Moreover, a derivative bearing a hydroxamic acid residue bound to C-3 amide portion was found to inhibit both Hsp90 and HDAC6.

Spectrometry Mass Electrospray IonizationMagnetic Resonance Spectroscopymedicine.drug_classStereochemistryPyridinesCarboxamideApoptosisResorcinolAnti-cancer drugschemistry.chemical_compoundResidue (chemistry)AmideDrug DiscoveryHeat shock protein 90 Anti-cancer drugs 4567-Tetrahydro-isoxazolo-[45-c]- pyridinesmedicineCytotoxic T cellHumansHeat shock protein 90HSP90 Heat-Shock ProteinsPharmacologyHydroxamic acidChemistryCell growthOrganic ChemistryGeneral MedicineNuclear magnetic resonance spectroscopy4 5 6 7-Tetrahydro-isoxazolo-[4 5-c]-pyridinesFlow CytometrySettore CHIM/08 - Chimica Farmaceuticahsp90Settore BIO/14 - Farmacologia4 5 6 7-Tetrahydro-isoxazolo-[4 5-c]-pyridines; Anti-cancer drugs; Heat shock protein 90;K562 CellsCell DivisionEuropean journal of medicinal chemistry
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Hydroxylation and conjugation of phenol by the frog Rana temporaria.

1985

1. Frogs injected with phenol excrete 67–95% of dose in 15h; 32–87% of dose are metabolites.2. Metabolites identified were phenyl sulphate (15–44% of dose), phenyl glucuronide (10–25% of dose), catechol sulphate (up to 7% of dose), quinol sulphate (1–25% of dose), resorcinol and catechol (traces).

StereochemistryHealth Toxicology and MutagenesisRana temporariaCatecholsGlucuronatesResorcinolSulfuric Acid EstersToxicologyHydroxylationBiochemistryHydroxylationchemistry.chemical_compoundPhenolsSalientiaPhenolAnimalsCarbon RadioisotopesChromatography High Pressure LiquidPharmacologyCatecholChromatographybiologyPhenolGeneral MedicineMetabolismResorcinolsbiology.organism_classificationHydroquinoneschemistryGRENOUILLEGlucuronideXenobiotica; the fate of foreign compounds in biological systems
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Selective Derivatization of Resorcarenes. 3. C2-Symmetrical and Transcavity Bridged Bis-Benzoxazines Derived from C2v-Symmetrical Tetratosylates

1998

The regioselective condensation of resorcarene tetratosylates 3/4 with formaldehyde and various primary amines readily gives bis-benzoxazines 5/6 in 65−86% yield. The chiral, C2-symmetrical structure of these compounds has been proved by NMR-spectroscopy and single-crystal X-ray analysis. Bis-benzoxazines 5f and 5i assume in the crystalline state a boat conformation in which the two resorcinol rings bearing the oxazine fragments are nearly parallel. The tosylated resorcinol units are horizontally arranged in a propeller-like fashion, and two intramolecular hydrogen bonds are formed between the phenolic hydroxy groups and the oxygens of the neighboring sulfonyl fragments. Molecular mechanics…

Sulfonylchemistry.chemical_classificationHydrogen bondCyclohexane conformationRegioselectivityGeneral ChemistryResorcinolResorcinarenePhotochemistryBiochemistryCatalysischemistry.chemical_compoundColloid and Surface ChemistrychemistryUnpaired electronIntramolecular forcePolymer chemistryJournal of the American Chemical Society
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A gas chromatography-mass spectrometric method to determine skin-whitening agents in cosmetic products.

2010

An analytical method is proposed here to determine three allowed (kojic acid, azelaic acid and arbutin) and two forbidden (resorcinol and hydroquinone) skin-whitening agents in cosmetics. The method is based on gas chromatography coupled with mass spectrometric detection, which allows the two prohibited target compounds to be identified unequivocally by means of their mass spectra acquired in full-scan mode at the retention time of these compounds. Owing to their low volatility, target analytes are derivatized using N,O-bis-(trimethylsilyl)trifluoroacetamide (BSTFA) (containing 1% trimethylchlorosylane) prior to injection into the chromatographic system. The accuracy and precision of the pr…

Trimethylsilyl CompoundsAzelaic acidChromatographyTime FactorsPigmentationmedia_common.quotation_subjectArbutinTemperatureResorcinolCosmeticsResorcinolsBSTFAMass spectrometryCosmeticsGas Chromatography-Mass SpectrometryAnalytical Chemistrychemistry.chemical_compoundchemistrymedicineGas chromatographyDermatologic AgentsGas chromatography–mass spectrometrymedia_commonmedicine.drugSkinTalanta
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