Search results for "Derivatives"

showing 10 items of 432 documents

A dose-ranging study of indacaterol in obstructive airways disease, with a tiotropium comparison.

2008

This dose-ranging study assessed the bronchodilator efficacy and tolerability of indacaterol, a novel once-daily inhaled beta2-agonist, in subjects clinically diagnosed with COPD. Comparative data with tiotropium were collected. In the double-blind, core period of the study, 635 subjects with COPD (prebronchodilator FEV(1)40% of predicted and > or =1.0L; FEV1/FVC <70%) were randomized to receive indacaterol 50, 100, 200 or 400microg or placebo via multi-dose dry powder inhaler, or indacaterol 400microg via single-dose dry powder inhaler, once daily for 7 days. After completing double-blind treatment and washout, a subset of subjects from each treatment group entered an open-label extension …

Pulmonary and Respiratory MedicineAdultMalemedicine.medical_specialtyEfficacymedicine.drug_classScopolamine DerivativesQuinolonesFEV1/FVC ratioPulmonary Disease Chronic ObstructiveDouble-Blind MethodBronchodilatorForced Expiratory VolumeAdministration InhalationCOPDMedicineHumansTiotropium BromideIndacaterolAgedCOPDDose-Response Relationship Drugbusiness.industryTiotropiumTiotropium bromideMiddle AgedDose-ranging studymedicine.diseaseDry-powder inhalerrespiratory tract diseasesSurgeryBronchodilator AgentsTreatment OutcomeTolerabilityDoseAnesthesiaIndansIndacaterolFemaleSafetybusinessmedicine.drugRespiratory medicine
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Efficacy and safety of indacaterol and tiotropium in COPD patients according to dyspnoea severity.

2013

Background Guidelines for chronic obstructive pulmonary disease (COPD) recommend that treatment choices be based partly on symptoms. Methods A post-hoc analysis of pooled data from clinical studies compared the efficacy and safety of once-daily inhaled bronchodilators indacaterol (150 and 300 μg) and open-label tiotropium (18 μg) according to baseline dyspnoea severity on the modified Medical Research Council (mMRC) scale in patients with COPD (mMRC scores <2 = ‘less dyspnoea’; scores ≥2 = ‘more dyspnoea’). Outcomes were assessed after 26 weeks. Results The analysis included 3177 patients. In patients with less dyspnoea: indacaterol (both doses) improved 24-h post-dose (‘trough’) forced exp…

Pulmonary and Respiratory MedicineCopd patientsScopolamine DerivativesPulmonary diseaseQuinolonesPlaceboPulmonary Disease Chronic ObstructiveForced Expiratory VolumeMedicineHumansPharmacology (medical)In patientPooled dataTiotropium BromideRandomized Controlled Trials as TopicCOPDDose-Response Relationship Drugbusiness.industryBiochemistry (medical)Patient AcuityTreatment optionsmedicine.diseaserespiratory tract diseasesBronchodilator AgentsDyspneaAnesthesiaDelayed-Action PreparationsIndansIndacaterolbusinessmedicine.drugPulmonary pharmacologytherapeutics
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Blinded 12-week comparison of once-daily indacaterol and tiotropium in COPD.

2011

Two, once daily (q.d.) inhaled bronchodilators are available for the treatment of chronic obstructive pulmonary disease (COPD): the β(2)-agonist indacaterol and the anticholinergic tiotropium. This blinded study compared the efficacy of these two agents and assessed their safety and tolerability. Patients with moderate-to-severe COPD were randomised to treatment with indacaterol 150 μg q.d. (n=797) or tiotropium 18 μg q.d. (n=801) for 12 weeks. After 12 weeks, the two treatments had similar overall effects on "trough" (24 h post-dose) forced expiratory volume in 1 s. Indacaterol-treated patients had greater improvements in transition dyspnoea index (TDI) total score (least squares means 2.0…

Pulmonary and Respiratory MedicineSpirometryMalemedicine.drug_classScopolamine DerivativesQuinolonesSeverity of Illness IndexCholinergic AntagonistsDrug Administration ScheduleMedical Recordslaw.inventionPulmonary Disease Chronic ObstructiveRandomized controlled trialDouble-Blind MethodlawAdrenergic beta-2 Receptor AntagonistsForced Expiratory VolumemedicineAnticholinergicHumansTiotropium BromideAdverse effectAgedCOPDmedicine.diagnostic_testbusiness.industryTiotropium bromideMiddle Agedmedicine.diseaserespiratory tract diseasesBronchodilator AgentsTreatment OutcomeTolerabilitySpirometryAnesthesiaIndansIndacaterolFemalebusinessmedicine.drugThe European respiratory journal
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Alternative mechanisms for tiotropium

2009

Tiotropium is commonly used in the treatment of chronic obstructive pulmonary disease. Although largely considered to be a long-acting bronchodilator, its demonstrated efficacy in reducing the frequency of exacerbations and preliminary evidence from early studies indicating that it might slow the rate of decline in lung function suggested mechanisms of action in addition to simple bronchodilation. This hypothesis was examined in the recently published UPLIFT study and, although spirometric and other clinical benefits of tiotropium treatment extended to four years, the rate of decline in lung function did not appear to be reduced by the addition of tiotropium in this study. This article summ…

Pulmonary and Respiratory Medicinemedicine.medical_specialtyANTICHOLINERGIC BRONCHODILATORmedicine.drug_classRespiratory SystemScopolamine DerivativesPulmonary diseaseIPRATROPIUM BROMIDEIpratropium bromideOBSTRUCTIVE PULMONARY-DISEASEMUCOCILIARY CLEARANCECholinergic AntagonistsRECEPTORS MEDIATE STIMULATIONParasympathetic Nervous SystemAIRWAY SMOOTH-MUSCLEBronchodilatorBronchodilationMechanismsBRONCHIAL EPITHELIAL-CELLSAnimalsHumansMedicineCOPDPharmacology (medical)Tiotropium BromideIntensive care medicineLungLung functionInflammationCOPDbusiness.industryTiotropiumBiochemistry (medical)RemodellingTiotropium bromidemedicine.diseaseAcetylcholineBronchodilator Agentsrespiratory tract diseasesMucusClinical researchNONNEURONAL CHOLINERGIC SYSTEMCoughPOLYSPECIFIC CATION TRANSPORTERSAnesthesiaLUNG FIBROBLAST PROLIFERATIONbusinesshuman activitiesmedicine.drugPulmonary Pharmacology & Therapeutics
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FOURIER TRANSFORMS, FRACTIONAL DERIVATIVES, AND A LITTLE BIT OF QUANTUM MECHANICS

2020

We discuss some of the mathematical properties of the fractional derivative defined by means of Fourier transforms. We first consider its action on the set of test functions $\Sc(\mathbb R)$, and then we extend it to its dual set, $\Sc'(\mathbb R)$, the set of tempered distributions, provided they satisfy some mild conditions. We discuss some examples, and we show how our definition can be used in a quantum mechanical context.

Pure mathematicsfractional derivativesGeneral MathematicsMathematical propertiesFOS: Physical sciencesContext (language use)Mathematical Physics (math-ph)Action (physics)Fractional calculusFourier transformsSet (abstract data type)symbols.namesakeFourier transformfractional momentum operatorDual basissymbols46N50QuantumMathematical PhysicsMathematics
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On the Cauchy problem for microlocally symmetrizable hyperbolic systems with log-Lipschitz coefficients

2017

International audience; The present paper concerns the well-posedness of the Cauchy problem for microlocally symmetrizable hyperbolic systems whose coefficients and symmetrizer are log-Lipschitz continuous, uniformly in time and space variables. For the global in space problem we establish energy estimates with finite loss of derivatives, which is linearly increasing in time. This implies well-posedness in H ∞ , if the coefficients enjoy enough smoothness in x. From this result, by standard arguments (i.e. extension and convexification) we deduce also local existence and uniqueness. A huge part of the analysis is devoted to give an appropriate sense to the Cauchy problem, which is not evide…

Pure mathematicsloss of derivativeshyperbolic equationGeneral MathematicsMathematics::Analysis of PDEsmicrolocal symmetrizabilityhyperbolic equations; hyperbolic systems; log-lipschitz coefficientsSpace (mathematics)01 natural sciencesMathematics - Analysis of PDEslog-Lipschitz regularity; loss of derivatives; global and local Cauchy problem; well-posedness; non-characteristic Cauchy problemwell-posednessFOS: MathematicsInitial value problem[MATH.MATH-AP]Mathematics [math]/Analysis of PDEs [math.AP]Uniqueness0101 mathematics[MATH.MATH-AP] Mathematics [math]/Analysis of PDEs [math.AP]MathematicsSmoothness (probability theory)Spacetimelog-lipschitz coefficients010102 general mathematicsglobal and local Cauchy problemExtension (predicate logic)Lipschitz continuitynon-characteristic Cauchy problemhyperbolic equationshyperbolic systemMathematics Subject Classificationlog-Lipschitz regularityhyperbolic systemsAnalysis of PDEs (math.AP)
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Dimethylpyridin-4-ylamine-Catalysed Alcoholysis of 2-Amino-N,N,N-Trimethyl-9H-purine-6-ylammonium Chloride: An Effective Route to O6-Substituted Guan…

2002

Dimethylpyridin-4-ylamine (DMAP)-catalysed reactions of 2-amino-N,N,N-trimethyl-9H-purine-6-ylammonium chloride with fluoropyridine methoxides and various other alkoxides in DMSO at 60 °C gave the corresponding coupling products in moderate to good yields between 20-87%. Under these reaction conditions, fluorinated O 6 -substituted Guanine derivatives have been synthesized which could not be obtained via known analogous literature procedures. The respective yields of known O 6 -substituted guanine derivatives could be significantly improved by using this method. The efficient use of DMAP as an excellent nucleophilic catalyst in the syntheses of O 6 -substituted Guanine derivatives has thus …

PurineReaction conditionsOrganic ChemistryGuanine derivativeschemistry.chemical_elementMedicinal chemistryChlorideCatalysisCatalysischemistry.chemical_compoundchemistryNucleophileNucleophilic aromatic substitutionFluorinemedicinemedicine.drugSynthesis
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Synthesis and electronic aspects of tetrahydrobenzothienopyrimidine derivatives

2015

Abstract The chemistry of thiophenes, pyrimidines, triazolopyrimidines and benzothiophenes has drawn much attention because of their biological activities. Their interesting properties are connected with their complex π-electron delocalisation effects. Herein the synthesis, crystal and molecular structures at 100 K and DFT calculated structures of three tetrahydrobenzothienopyrimidine derivatives are reported i.e. 4-hydrazino-5,6,7,8-tetrahydro[1]benzothieno[2,3-d]pyrimidine which was a substrate for 2-phenyl-8,9,10,11-tetrahydro[1]benzothieno[3,2-e][1,2,4]triazolo[1,5-c]pyrimidine and 3-methyl-9,10,11,12-tetrahydro-2H-[1]benzothieno[2′,3′:4,5]pyrimido[1,6-b][1,2,4]triazin-2-one. Moreover t…

Pyrimidinetetrahydrobenzothienopyrimidine derivativesHirshfeld surfaceOrganic ChemistryIntermolecular forceAromaticityCrystal structureRing (chemistry)DFT calculationsAnalytical ChemistryInorganic ChemistryCrystalchemistry.chemical_compoundcrystal structuresHOMA indexchemistryComputational chemistryThiopheneMoleculeSpectroscopyJournal of Molecular Structure
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A novel approach to predict aquatic toxicity from molecular structure

2008

The main aim of the study was to develop quantitative structure-activity relationship (QSAR) models for the prediction of aquatic toxicity using atom-based non-stochastic and stochastic linear indices. The used dataset consist of 392 benzene derivatives, separated into training and test sets, for which toxicity data to the ciliate Tetrahymena pyriformis were available. Using multiple linear regression, two statistically significant QSAR models were obtained with non-stochastic (R2=0.791 and s=0.344) and stochastic (R2=0.799 and s=0.343) linear indices. A leave-one-out (LOO) cross-validation procedure was carried out achieving values of q2=0.781 (scv=0.348) and q2=0.786 (scv=0.350), respecti…

Quantitative structure–activity relationshipEnvironmental EngineeringToxicity dataMolecular StructureLooHealth Toxicology and MutagenesisPublic Health Environmental and Occupational HealthGeneral MedicineGeneral ChemistryPollutionAquatic toxicologyToxicologyStructure-Activity RelationshipToxicity TestsBenzene derivativesTetrahymena pyriformisLinear regressionEnvironmental ChemistryBiological systemMathematicsChemosphere
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Palladium-catalysed direct cross-coupling of secondary alkyllithium reagents

2014

Palladium-catalysed cross-coupling of secondary C(sp(3)) organometallic reagents has been a long-standing challenge in organic synthesis, due to the problems associated with undesired isomerisation or the formation of reduction products. Based on our recently developed catalytic C-C bond formation with organolithium reagents, herein we present a Pd-catalysed cross-coupling of secondary alkyllithium reagents with aryl and alkenyl bromides. The reaction proceeds at room temperature and on short timescales with high selectivity and yields. This methodology is also applicable to hindered aryl bromides, which are a major challenge in the field of metal catalysed cross-coupling reactions.

Química organometàl·licachemistry.chemical_element010402 general chemistry01 natural sciencesORGANOLITHIUM COMPOUNDSALKYLZINC REAGENTSCatalysisMetalchemistry.chemical_compoundCompostos orgànics SíntesiOrganic chemistryINVERSIONARYL CHLORIDESCONFIGURATION010405 organic chemistryDERIVATIVESArylESTERSGeneral ChemistryCombinatorial chemistry0104 chemical scienceschemistryORGANIC HALIDESSELECTIVITYReagentvisual_artvisual_art.visual_art_mediumALKENYLATIONOrganic synthesisSelectivityIsomerizationPalladium
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