Search results for "Nitrous Acid"

showing 10 items of 42 documents

The azide/tetrazole equilibrium: an investigation in the series of furo- and thieno[2,3-e]tetrazolo[3,2-d]pyrimidine derivatives

2016

Abstract Starting from 7(8)-chlorofuro(thieno)[3,2- d ]pyrimidines 1 , the corresponding 7(8)-hydrazinofuro(thieno)[3,2- d ]pyrimidines 2 were obtained by reaction with hydrazine. By treatment with nitrous acid, compounds 2 gave fused furo- and thieno[2,3- e ]tetrazolo[1,5- c ]pyrimidines 3 T and 4 T in excellent yields, which in solution exist in equilibrium with 7(8)-azidofuro(thieno)[3,2- d ]pyrimidines 3 A and 4 A . Compounds 3 T / 3 A and 4 T / 4 A represent useful substrates for investigating the azide/tetrazole equilibrium: it has been examined as a function of solvent, temperature, and their structure. We have observed that, in solution, in both 3 and 4 the equilibrium was strongly …

Nitrous acidPyrimidine010405 organic chemistryStereochemistryOrganic Chemistry010402 general chemistry01 natural sciencesBiochemistryMedicinal chemistryTautomer0104 chemical sciencesSolventchemistry.chemical_compoundchemistryDrug DiscoveryTetrazoleAzideSolvent effectsEquilibrium constantTetrahedron
researchProduct

ChemInform Abstract: Antimicrobial and Antineoplastic Activities of New 4-Diazopyrazole Derivatives.

2010

Abstract Several new 4-diazopyrazole derivatives were prepared by the reaction of 3-methyl-5(substituted-benzamido)pyrazoles with an excess of nitrous acid in acetic acid solution. The compounds were tested for antiretroviral activity in HIV-1 infected MT-4 cells and antiproliferative effects against a panel of human leukemia, lymphoma and solid tumor cell lines. They were also tested for activity against representative gram-negative ( Shigella, Salmonella ) and gram-positive ( S. aureus, D group Streptococcus ) bacteria as well as fungi ( C. albicans, C. paratropicalis, C. neoformans and A. fumigatus ). Compounds were devoid of anti HIV-1 and antimicotic activities, whereas they were activ…

Nitrous acidSalmonellabiologyStereochemistryGeneral MedicineGroup streptococcusAntimicrobialbiology.organism_classificationmedicine.disease_causeCorpus albicansMicrobiologychemistry.chemical_compoundchemistryCell culturemedicineShigellaBacteriaChemInform
researchProduct

Facile synthesis of 5-benzamido-4-diazopyrazole derivatives, a class of biologically active agents and key intermediates

1995

Abstract By reacting l-R1-3-R2-5-(R3-substituted)benzamidopyrazoles with a great ex-cess of nitrous acid in acetic acid media, the related 4-diazoderivatives in 65–80% yields were obtained.

Nitrous acidchemistry.chemical_compoundAcetic acidChemistryOrganic ChemistryOrganic chemistryBiological activity
researchProduct

ChemInform Abstract: Facile Synthesis of 5-Benzamido-4-diazopyrazole Derivatives, a Class of Biologically Active Agents and Key Intermediates.

2010

Abstract By reacting l-R1-3-R2-5-(R3-substituted)benzamidopyrazoles with a great ex-cess of nitrous acid in acetic acid media, the related 4-diazoderivatives in 65–80% yields were obtained.

Nitrous acidchemistry.chemical_compoundAcetic acidchemistryBiological activityGeneral MedicineCombinatorial chemistryChemInform
researchProduct

Synthesis and anti-staphylococcal activity of new 4-diazopyrazole derivatives.

2012

Abstract Several new 4-diazopyrazole derivatives 6a – g and 9a – c were obtained by the reaction of 1-(R-substituted-phenyl)-3-(1,3-dimethyl-1 H -pyrazol-5-yl)ureas 5a – g and N -(1,3-dimethyl-1 H -pyrazol-5-yl)-2-(R-substituted-phenyl)acetamides 8a – c respectively with a sevenfold excess of nitrous acid in acetic acid solution. The compounds were assayed for their activity against the Staphylococcus aureus reference strains ATCC 25923, ATCC 29213 and ATCC 6538, as well as six veterinary strains. The best anti-staphylococcal profile was showed by [(R-substituted-phenyl)acetyl](4-diazonio-1,3-dimethyl-1 H -pyrazol-5-yl)azanides 9a , c . Compound 9c was also able at 3.1 μg mL −1 to inhibit o…

PharmacologyNitrous acidStaphylococcus aureusDose-Response Relationship DrugMolecular StructureStereochemistryOrganic ChemistryBiofilmGeneral MedicineMicrobial Sensitivity Testsmedicine.disease_causeSettore BIO/19 - Microbiologia GeneraleSettore CHIM/08 - Chimica FarmaceuticaAnti-Bacterial Agentschemistry.chemical_compoundStructure-Activity RelationshipchemistryStaphylococcus aureusBiofilmsDrug DiscoverymedicinePyrazolesAcetic acid solution4-diazopyrazoles anti-staphylococcal activity anti-biofilm activityAzo CompoundsEuropean journal of medicinal chemistry
researchProduct

Explaining the phenomenon of nitrate tolerance.

2005

During the last century, nitroglycerin has been the most commonly used antiischemic and antianginal agent. Unfortunately, after continuous application, its therapeutic efficacy rapidly vanishes. Neurohormonal activation of vasoconstrictor signals and intravascular volume expansion constitute early counter-regulatory responses (pseudotolerance), whereas long-term treatment induces intrinsic vascular changes, eg, a loss of nitrovasodilator-responsiveness (vascular tolerance). This is caused by increased vascular superoxide production and a supersensitivity to vasoconstrictors secondary to a tonic activation of protein kinase C. NADPH oxidase(s) and uncoupled endothelial nitric oxide synthase …

PhysiologyVasodilator AgentsPharmacologymedicine.disease_causeNitric OxideProstacyclin synthaseNitric oxidechemistry.chemical_compoundNitroglycerinSuperoxidesPeroxynitrous AcidmedicineCyclic GMP-Dependent Protein KinasesAnimalsHumansBiotransformationchemistry.chemical_classificationReactive oxygen speciesNADPH oxidasebiologyChemistrySuperoxidePhosphoric Diester HydrolasesAldehyde Dehydrogenase MitochondrialDrug ToleranceAldehyde DehydrogenaseCyclic Nucleotide Phosphodiesterases Type 1VasodilationOxidative StressBiochemistryVasoconstrictioncardiovascular systembiology.proteinEndothelium VascularCardiology and Cardiovascular MedicineSoluble guanylyl cyclaseReactive Oxygen SpeciesPeroxynitriteOxidative stressSignal TransductionCirculation research
researchProduct

Hypoxia-induced dysfunction of rat diaphragm

2004

Contains fulltext : 47331.pdf (Publisher’s version ) (Closed access) Oxidants may play a role in hypoxia-induced respiratory muscle dysfunction. In the present study we hypothesized that hypoxia-induced impairment in diaphragm contractility is associated with elevated peroxynitrite generation. In addition, we hypothesized that strenuous contractility of the diaphragm increases peroxynitrite formation. In vitro force-frequency relationship, isotonic fatigability, and nitrotyrosine levels were assessed under hypoxic (Po(2) approximately 6.5 kPa) and hyperoxic (Po(2) approximately 88.2 kPa) control conditions and also in the presence of authentic peroxynitrite (60 min), ebselen (60 min), and t…

Pulmonary and Respiratory MedicineAzolesMalemedicine.medical_specialtyPhysiologyDiaphragmAetiology screening and detection [ONCOL 5]In Vitro TechniquesIsoindolesNitric oxideContractilitychemistry.chemical_compoundTranslational research [ONCOL 3]Physiology (medical)Internal medicineOrganoselenium CompoundsPeroxynitrous AcidmedicineRespiratory muscleAnimalsRespiratory systemEnzyme InhibitorsRats WistarHypoxiaHeart lung and circulation [UMCN 2.1]Renal disorder [IGMD 9]omega-N-MethylarginineNitrotyrosineCell BiologyHypoxia (medical)Tissue engineering and pathology [NCMLS 3]musculoskeletal systemRatsPathogenesis and modulation of inflammation [N4i 1]EndocrinologychemistryBiochemistryMuscle FatigueTyrosineRat DiaphragmLipid Peroxidationmedicine.symptomPeroxynitriteMuscle ContractionAmerican Journal of Physiology - Lung Cellular and Molecular Physiology
researchProduct

Chemical model systems for cellular nitros(yl)ation reactions.

2009

S-nitros(yl)ation belongs to the redox-based posttranslational modifications of proteins but the underlying chemistry is controversial. In contrast to current concepts involving the autoxidation of nitric oxide ( • NO, nitrogen monoxide), we and others have proposed the formation of peroxynitrite (oxoperoxonitrate (1-)) as an essential intermediate. This requires low cellular fluxes of 'NO and superoxide ( • O 2 - ), for which model systems have been introduced. We here propose two new systems for nitros(yl)ation that avoid the shortcomings of previous models. Based on the thermal decomposition of 3-morpholinosydnonimine, equal fluxes of • NO and • O 2 - were generated and modulated by the …

StereochemistrySwineNitrosationIn Vitro TechniquesPhotochemistryNitric OxideBiochemistryRedoxArticlechemistry.chemical_compoundElectrophilic substitutionPhysiology (medical)Peroxynitrous AcidAnimalsAutoxidationPhenolNitrosoniumSuperoxideSuperoxide DismutaseGlutathioneIsocitrate DehydrogenasePeroxynitrous acidchemistryModels ChemicalMolsidomineNitrosationCattlePeroxynitriteFree radical biologymedicine
researchProduct

Effect of pH and nitrite concentration on nitrite oxidation rate

2011

The effect of pH and nitrite concentration on the activity of the nitrite oxidizing bacteria (NOB) in an activated sludge reactor has been determined by means of laboratory batch experiments based on respirometric techniques. The bacterial activity was measured at different pH and at different total nitrite concentrations (TNO 2). The experimental results showed that the nitrite oxidation rate (NOR) depends on the TNO 2 concentration independently of the free nitrous acid (FNA) concentration, so FNA cannot be considered as the real substrate for NOB. NOB were strongly affected by low pH values (no activity was detected at pH 6.5) but no inhibition was observed at high pH values (activity wa…

Waste component removalPH rangeUnclassified drugRespirometric techniqueLaboratory methodPHOxidation ratesPH valueNitriteSaturation constantBatch reactorPH effectOxidation kineticsDissociation constantNitrobacterKinetic expressionWaste Disposal FluidInhibition constantschemistry.chemical_compoundBacteriumBioreactorsNitrous acidNitriteBacterial activityReaction kineticsBacteria (microorganisms)Waste Management and DisposalIn Situ Hybridization FluorescenceInhibitionPriority journalFree nitrous acidMicroscopyNitrous acidSewagebiologyFluorescence in situ hybridizationPH effectsGeneral MedicineSaturationRespirometryHydrogen-Ion ConcentrationInorganic acidsNitrite oxidizing bacteriaCalibrationOxidation-ReductionEnvironmental EngineeringInorganic chemistryBioreactorParameterizationBioengineeringActivated sludge reactorsArticleNumerical modelNitrous acid derivativeReaction rateParameter calibrationBatch experimentsNitrite-oxidizing bacteriaOxidationDietary NitrateNitritesTECNOLOGIA DEL MEDIO AMBIENTEExperimental studyBacteriaConcentration (process)Renewable Energy Sustainability and the EnvironmentBacteriologyNitrobacterOxidation reductionNitrogen removalConcentration (composition)biology.organism_classificationInorganic acidsMicrobial activityKineticschemistryActivated sludgeNitrite oxidationHigh pH valueSwitch functionConcentration (parameters)Oxidation processEffect of pHProtein expressionSubstrateControlled studyWaste disposalBioresource Technology
researchProduct

Involvement of Peroxynitrite on the Early Loss of P450 in Short-Term Hepatocyte Cultures

2001

The biological chemistry of nitric oxide (NO) in the oxygenated cellular environment is extremely complex. It involves the direct interaction of NO with specific biomolecules and the so-called indirect effects, due to secondary more potent oxidant species derived from NO which are also able to react with DNA, lipids, thiols and transition metals (Wink et al. 1996; Nathan, 1992). In addition to its regulatory role as a signalling molecule (Nathan, 1992; Moncada and Palmer, 1991) it has become evident that NO (or NO-derived species) is a critical factor involved in various toxicological mechanisms (Wink et al. 1996; Wang et al. 1998; Estevez et al. 1999; Wink et al. 1999). Some controversy ex…

chemistry.chemical_compoundPeroxynitrous acidmedicine.anatomical_structureChemistryHepatocyteCellmedicineCarbohydrate metabolismPhenotypeFunction (biology)PeroxynitriteNitric oxideCell biology
researchProduct