Search results for "chlorophenyl"

showing 10 items of 128 documents

CCDC 274237: Experimental Crystal Structure Determination

2006

Related Article: G.Stajer, A.E.Szabo, P.Sohar, A.Csampai, R.Sillanpaa|2006|J.Mol.Struct.|784|239|doi:10.1016/j.molstruc.2005.09.011

8a-(4-Chlorophenyl)-78-dihydro-1H-pyrrolo(12-a)pyrimidine-26-dioneSpace GroupCrystallographyCrystal SystemCrystal StructureCell ParametersExperimental 3D Coordinates
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Glycopyrronium bromide blocks differentially responses mediated by muscarinic receptor subtypes.

1993

To analyse the potency of glycopyrronium bromide in blocking responses mediated via subtypes of muscarinic receptors in vitro, we tried to determine its equilibrium dissociation constants at prejunctional muscarinic receptors inhibiting the twitch response of rabbit vas deferens (presumed M1 type), at M2 (paced at left atria), M3 (guinea pig ileum) muscarinic receptor subtypes and at the muscarinic receptor of the rabbit iris sphincter (not M1-M4, not m5). Glycopyrronium bromide shifted to the right the curve for inhibition of the twitch response induced by the agonist McN-A-343, and the methacholine-induced curves for inhibition of rat atrial contraction, and for tonic contraction of guine…

AgonistMalemedicine.medical_specialtymedicine.drug_classGuinea PigsIrisMuscarinic AntagonistsIn Vitro TechniquesModels BiologicalVas DeferensInternal medicineMuscarinic acetylcholine receptorMuscarinic acetylcholine receptor M4medicineAnimalsMethacholine CompoundsGlycopyrronium bromidePharmacologyChemistryVas deferens(4-(m-Chlorophenylcarbamoyloxy)-2-butynyl)trimethylammonium ChlorideMuscarinic acetylcholine receptor M3ParasympatholyticsMuscarinic acetylcholine receptor M2HeartMuscle SmoothGeneral MedicineMuscarinic acetylcholine receptor M1GlycopyrrolateRatsEndocrinologymedicine.anatomical_structureFemaleRabbitsmedicine.drugNaunyn-Schmiedeberg's archives of pharmacology
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Menaquinone-dependent succinate dehydrogenase of bacteria catalyzes reversed electron transport driven by the proton potential.

1998

Succinate dehydrogenases from bacteria and archaea using menaquinone (MK) as an electron acceptor (succinate/menaquinone oxidoreductases) contain, or are predicted to contain, two heme-B groups in the membrane-anchoring protein(s), located close to opposite sides of the membrane. All succinate/ubiquinone oxidoreductases, however, contain only one heme-B molecule. In Bacillus subtilis and other bacteria that use MK as the respiratory quinone, the succinate oxidase activity (succinate-->O2), and the succinate/menaquinone oxidoreductase activity were specifically inhibited by uncoupler (CCCP, carbonyl cyanide m-chlorophenylhydrazone) or by agents dissipating the membrane potential (valinomycin…

Carbonyl Cyanide m-Chlorophenyl HydrazoneVitamin KHemeBiochemistryCatalysisMembrane PotentialsElectron TransportValinomycinchemistry.chemical_compoundOxidoreductaseElectrochemistryEnzyme Inhibitorschemistry.chemical_classificationMembrane potentialBinding SitesbiologyBacteriaChemistryElectron Transport Complex IISuccinate dehydrogenaseElectron acceptorbiology.organism_classificationElectron transport chainSuccinate DehydrogenaseBiochemistrybiology.proteinProtonsBacteriaEuropean journal of biochemistry
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CCDC 255647: Experimental Crystal Structure Determination

2005

Related Article: T.S.B.Baul, W.Rynjah, E.Rivarola, C.Pettinari, A.Linden|2005|J.Organomet.Chem.|690|1413|doi:10.1016/j.jorganchem.2004.12.013

Di-n-butyl-(5-((E)-2-(4-chlorophenyl)-1-azenyl)-2-hydroxybenzoato)-(5-((E)-2-(4-methylphenyl)-1-azenyl)-2-hydroxybenzoato)-tin(iv)Space GroupCrystallographyCrystal SystemCrystal StructureCell ParametersExperimental 3D Coordinates
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CCDC 206077: Experimental Crystal Structure Determination

2006

Related Article: S.Azzouzi, M.El Messaoudi, M.Esseffar, R.Jalal, F.H.Cano, M.del Carmen Apreda-Rojas, L.R.Domingo|2005|J.Phys.Org.Chem.|18|522|doi:10.1002/poc.892

Diethyl 3-(p-chlorophenyl)-2-(N'-(p-chlorophenyl)-N'-(2'7'-dimethyl-5'-oxo-5'6'-dihydro-2H-(124)triazepin-3'-yl)hydrazino)-23-dihydro(134)thiadiazole-25-dicarboxylateSpace GroupCrystallographyCrystal SystemCrystal StructureCell ParametersExperimental 3D Coordinates
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CCDC 255649: Experimental Crystal Structure Determination

2005

Related Article: T.S.B.Baul, W.Rynjah, E.Rivarola, C.Pettinari, A.Linden|2005|J.Organomet.Chem.|690|1413|doi:10.1016/j.jorganchem.2004.12.013

Dimethyl-(5-((E)-2-(4-chlorophenyl)-1-azenyl)-2-hydroxybenzoato)-(5-((E)-2-(4-methylphenyl)-1-azenyl)-2-hydroxybenzoato)-tin(iv)Space GroupCrystallographyCrystal SystemCrystal StructureCell ParametersExperimental 3D Coordinates
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p-Chlorophenylalanine treatment depresses the number of synaptic ribbon profiles in the rat pineal gland, but does not abolish their day-night rhythm

1995

It is largely unknown as to how the day/night rhythm of pineal synaptic ribbon number is regulated. Transcriptional events related to the nocturnal formation of new synaptic ribbons occur early in the morning, when pineal serotonin levels begin to increase. The present study was carried out in order to elucidate as to how altered serotonin levels affect the day/night changes in the number of synaptic ribbon profiles. To this end, male Sprague-Dawley rats received a single dose of p-chlorophenylalanine (pCPA, 300 mg/kg body weight, 72 hours before sacrifice), which depresses tryptophan hydroxylase activity and hence pineal serotonin levels. Control animals received saline injections. Experim…

MaleSerotoninendocrine systemmedicine.medical_specialtyTranscription GeneticArylamine N-AcetyltransferaseTryptophan HydroxylaseBiologyPineal GlandRats Sprague-DawleyMelatoninPineal glandReference ValuesInternal medicinemedicineFenclonineAnimalsCircadian rhythmSynaptic ribbonP chlorophenylalanineFenclonineGeneral MedicineTryptophan hydroxylaseCircadian RhythmRatsMicroscopy Electronmedicine.anatomical_structureEndocrinologynervous systemSynapsessense organsSerotoninAnatomyhormones hormone substitutes and hormone antagonistsDevelopmental Biologymedicine.drugAnnals of Anatomy - Anatomischer Anzeiger
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Characterization of the muscarine receptors involved in the modulation of serotonin release from the vascularly perfused small intestine of guinea pi…

1989

Isolated small intestinal segments of the guinea pig were arterially perfused and the release of 5-hydroxytryptamine (5-HT) and its metabolite 5-hydroxyindoleacetic acid (5-HIAA) into the portal venous effluent measured by HPLC with electrochemical detection. Test substances were applied via the arterial perfusion medium. McN-A-343, pilocarpine and oxotremorine inhibited concentration-dependently the outflow of 5-HT and 5-HIAA. Pirenzepine (0.03-0.1 mumol/l) which can discriminate between M1 and M2-receptor subtypes antagonized completely this inhibitory effect. In the presence of 1 mumol/l tetrodotoxin (TTx), all three muscarine receptor agonists increased the outflow of 5-HT and 5-HIAA. O…

Malemedicine.medical_specialtySerotoninPopulationGuinea PigsIndomethacinTetrodotoxinIn Vitro Techniqueschemistry.chemical_compoundInternal medicineMuscarinic acetylcholine receptorIntestine SmallmedicineOxotremorineAnimalsReceptoreducationNeurotransmitterPharmacologyeducation.field_of_studyMuscarineOxotremorine(4-(m-Chlorophenylcarbamoyloxy)-2-butynyl)trimethylammonium ChlorideGeneral MedicinePirenzepineHydroxyindoleacetic AcidPirenzepineReceptors MuscarinicPerfusionEndocrinologychemistryFemaleSerotoninmedicine.drugNaunyn-Schmiedeberg's archives of pharmacology
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Fluorescent styrylpyrylium probes for the imaging of mitochondria in live cells

2021

Eight styrylpyrylium tetrafluoroborate salts have been synthesized and fully optically characterized by UV-vis absorption and fluorescence steady-state/time-resolved spectroscopies. The new dyes exhibit strong emission bands with yellow–orange colours, depending on the substituents present in the structure. Notably, the Stokes shift recorded for some of them exceeds 100 nm, a very valuable feature for biological imaging. Four of them have been assayed as biological imaging agents by confocal laser scanning microscopy (CLSM) in the human hepatoma cell line Hep3B. It has been found that all the compounds efficiently stain intracellular structures which have been identified as mitochondria thr…

Membrane potentialCarbonyl Cyanide m-Chlorophenyl HydrazoneChemistryOrganic ChemistryColocalizationMitochondrionBiochemistryFluorescenceImaging agentsymbols.namesakeStokes shiftsymbolsBiophysicsPhysical and Theoretical ChemistryBiological imagingIntracellular
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Reactive oxygen species derived from the mitochondrial respiratory chain are not responsible for the basal levels of oxidative base modifications obs…

2004

The mitochondrial electron transport chain (ETC) is the most important source of reactive oxygen species (ROS) in mammalian cells. To assess its relevance to the endogenous generation of oxidative DNA damage in the nucleus, we have compared the background (steady-state) levels of oxidative DNA base modifications sensitive to the repair glycosylase Fpg (mostly 7,8-dihydro-8-oxoguanine) in wild-type HeLa cells and HeLa rho0 cells. The latter are depleted of mitochondrial DNA and therefore are unable to produce ROS in the ETC. Although the levels of ROS measured by flow cytometry and redox-sensitive probes in rho0 cells were only 10-15% those of wild-type cells, steady-state levels of oxidativ…

Mitochondrial ROSCarbonyl Cyanide m-Chlorophenyl HydrazoneMitochondrial DNADNA damageCells[SDV]Life Sciences [q-bio]Oxidative phosphorylationMitochondrionBiologyBiochemistryElectron Transport03 medical and health sciences0302 clinical medicinePhysiology (medical)AnimalsHumansComputingMilieux_MISCELLANEOUS030304 developmental biologyCell Nucleus0303 health sciencesGuanosineNucleotidesEscherichia coli ProteinsDNAFlow CytometryMitochondriaNuclear DNAMitochondrial respiratory chainDNA-Formamidopyrimidine GlycosylaseBiochemistryDNA glycosylaseMacrolidesReactive Oxygen SpeciesOxidation-Reduction030217 neurology & neurosurgeryDNA DamageHeLa Cells
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