Search results for "SUBSTITUTION"

showing 10 items of 536 documents

Characterization of the first extended-spectrum beta-lactamase-producing nontyphoidal Salmonella strains isolated in Tehran, Iran.

2009

The infections caused by Salmonella remain a significant public health problem throughout the world. beta-Lactams and fluoroquinolones are generally used to treat invasive Salmonella infections, but emergence and spread of antibiotic-resistant strains are being increasingly notified in many countries. In particular, detection of extended-spectrum beta-lactamases (ESBLs) in Salmonella spp. is a newly emerging threat worldwide. This study was carried out to characterize beta-lactamase-producing Salmonella strains identified in Tehran, Iran. Over the 2-year period from 2007 to 2008, 6 of 136 Salmonella isolates recovered from pediatrics patients, including three Salmonella enterica serotypes E…

Serotypemedicine.medical_specialtySalmonellamedicine.medical_treatmentMolecular Sequence DataDrug resistanceMicrobial Sensitivity TestsBiologyIranmedicine.disease_causeApplied Microbiology and BiotechnologyMicrobiologyPolymerase Chain Reactionbeta-LactamasesMicrobiologylaw.inventionSpecies SpecificitylawSalmonellaMolecular geneticsDrug Resistance Multiple BacterialmedicineHumansS. enteritidisSerotypingChildPolymerase chain reactionInfantSequence Analysis DNAbiology.organism_classificationVirologyPhenotypeAmino Acid SubstitutionSalmonella enteritidisSalmonella entericaChild PreschoolConjugation GeneticSalmonella InfectionsBeta-lactamaseAnimal Science and ZoologyGenes MDRFood ScienceFoodborne pathogens and disease
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Miscela binaria liquido ionico/[bmim][N3]: un mezzo efficace per la sintesi di arilazidi mediante SNAr

Settore CHIM/06 - Chimica Organicaionic liquids aromatic azides nucleophilic aromatic substitution
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La prestación de maternidad en los supuestos de gestación subrogada

2018

Surrogate pregnancy, as a technique of assisted reproduction prohibited by Spanish law, raises a number of legal questions than, in certain cases, trascend of the Civil Law. Specifically, it has been discussed about de possibility that de person or persons consigner in the gestation contract substitution have access to the provision for maternity benefit. Recently, the Spanish Supreme Court has responded to this issue in the sense of recognizing the right to the provision for maternity benefit to the father or mother ?in fact?, efecttively, develop own parental powers.

Social security:CIENCIAS JURÍDICAS [UNESCO]familiafamilyprestación de maternidadthe Spanish Supreme Court has responded to this issue in the sense of recognizing the right to the provision for maternity benefit to the father or mother ?in fact?as a technique of assisted reproduction prohibited by Spanish lawtrascend of the Civil Law. Specificallyin certain casesgestación por sustituciónhumanitiesEduardo Enrique Surrogate pregnancyinterés superior del menorUNESCO::CIENCIAS JURÍDICASgestation by substitutionmaternity benefitefecttivelydevelop own parental powers. Seguridad socialbest interest of the child. 438 453raises a number of legal questions than2386-4567 22661 Actualidad jurídica iberoamericana 502169 2018 9 6653335 La prestación de maternidad en los supuestos de gestación subrogada Taléns Viscontiit has been discussed about de possibility that de person or persons consigner in the gestation contract substitution have access to the provision for maternity benefit. Recentlyhealth care economics and organizations
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Substitution systems and nonextensive statistics

2015

Abstract Substitution systems evolve in time by generating sequences of symbols from a finite alphabet: At a certain iteration step, the existing symbols are systematically replaced by blocks of N k symbols also within the alphabet (with N k , a natural number, being the length of the k th block of the substitution). The dynamics of these systems leads naturally to fractals and self-similarity. By using B -calculus (Garcia-Morales, 2012) universal maps for deterministic substitution systems both of constant and non-constant length, are formulated in 1D. It is then shown how these systems can be put in direct correspondence with Tsallis entropy. A ‘Second Law of Thermodynamics’ is also prove…

Statistics and ProbabilityDiscrete mathematicsTsallis entropymedia_common.quotation_subjectSymbolic dynamicsBlock (permutation group theory)Substitution (algebra)Natural numberSecond law of thermodynamicsCondensed Matter PhysicsLimit (mathematics)Constant (mathematics)Mathematicsmedia_commonPhysica A: Statistical Mechanics and its Applications
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A non-linear optimization procedure to estimate distances and instantaneous substitution rate matrices under the GTR model.

2006

Abstract Motivation: The general-time-reversible (GTR) model is one of the most popular models of nucleotide substitution because it constitutes a good trade-off between mathematical tractability and biological reality. However, when it is applied for inferring evolutionary distances and/or instantaneous rate matrices, the GTR model seems more prone to inapplicability than more restrictive time-reversible models. Although it has been previously noted that the causes for intractability are caused by the impossibility of computing the logarithm of a matrix characterised by negative eigenvalues, the issue has not been investigated further. Results: Here, we formally characterize the mathematic…

Statistics and ProbabilityOptimization problemBase Pair MismatchBiochemistryLinkage DisequilibriumNonlinear programmingInterpretation (model theory)Evolution MolecularApplied mathematicsComputer SimulationDivergence (statistics)Molecular BiologyEigenvalues and eigenvectorsPhylogenyMathematicsSequenceModels GeneticSubstitution (logic)Chromosome MappingGenetic VariationSequence Analysis DNAComputer Science ApplicationsComputational MathematicsComputational Theory and MathematicsNonlinear DynamicsLogarithm of a matrixAlgorithmAlgorithmsBioinformatics (Oxford, England)
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2020

Electrophilic (het)arenes can undergo reactions with nucleophiles yielding π- or Meisenheimer (σ-) complexes or the products of the SNAr addition/elimination reactions. Such building blocks have only rarely been employed for the design of enzyme inhibitors. Herein, we demonstrate the combination of a peptidic recognition sequence with such electrophilic (het)arenes to generate highly active inhibitors of disease-relevant proteases. We further elucidate an unexpected mode of action for the trypanosomal protease rhodesain using NMR spectroscopy and mass spectrometry, enzyme kinetics and various types of simulations. After hydrolysis of an ester function in the recognition sequence of a weakly…

StereochemistryCarboxylic acidmedicine.medical_treatmentPharmaceutical Science010402 general chemistry01 natural sciencesAnalytical ChemistryNucleophileNucleophilic aromatic substitutionDrug DiscoverymedicineEnzyme kineticsPhysical and Theoretical Chemistrychemistry.chemical_classificationProteasebiology010405 organic chemistryOrganic ChemistryActive siteCysteine proteaseMeisenheimer complex0104 chemical scienceschemistryChemistry (miscellaneous)biology.proteinMolecular MedicineMolecules
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Regioselective substitution of 6,7-dichloroquinoline-5,8-dione: synthesis and X-ray crystal structure of 4a,10,11-triazabenzo[3,2-a]fluorene-5,6-dion…

2003

6,7-Dichloroquinoline-5,8-dione (1) was reacted with a number of 2-aminopyridine derivatives. Of the several possible products of this reaction, 4a,10,11-triazabenzo[3,2-a]fluorene-5,6-dione (6), produced by condensation and rearrangement, was obtained as the major product, and its structure was subsequently unambigously determined by X-ray crystallographic study. Ortho-quinones were produced via nucleophilic substitution at position C7, which was unexpected, considering that para-quinones were produced via C6 substitution in the reaction between compound 1 and ethyl acetoacetate in our previous work. Such unexpected nucleophilic substitution at C7 provides an effective, yet simple route, t…

StereochemistryClinical BiochemistryPharmaceutical ScienceAntineoplastic AgentsCrystallography X-RayBiochemistryMedicinal chemistryChemical synthesisInhibitory Concentration 50chemistry.chemical_compoundNucleophilic aromatic substitutionDrug DiscoveryTumor Cells CulturedNucleophilic substitutionHumansMolecular BiologySubstitution reactionFluorenesMolecular StructureOrganic ChemistryQuinonesRegioselectivityStereoisomerismQuinonechemistryDoxorubicinEthyl acetoacetateQuinolinesMolecular MedicineAcid hydrolysisDrug Screening Assays AntitumorBioorganic & Medicinal Chemistry
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Synthesis and cytotoxicity of 6,11-Dihydro-pyrido- and 6,11-Dihydro-benzo[2,3-b]phenazine-6,11-dione derivatives

2003

6,11-Dihydro-pyrido[2,3-b]phenazine-6,11-diones and 6,11-dihydro-benzo[2,3-b]phenazine-6,11-diones were synthesized from 6,7-dichloro-5,8-quinolinedione and 2,3-dichloro-1,4-naphthoquinone. The study on the cytotoxicity on these products revealed that the pyridophenazinediones, tetracyclic heteroquinone analogues with three nitrogen atoms exhibited a high cytotoxicity on several human tumor cell lines. Compound 9c and 9e showed in vitro antitumor activity comparable or superior to doxorubicin against the human ovarian tumor cells (SK-OV-3) and the human CNS cells (XF 498). The IC(50) value for compound 9e was 0.06 microM against the human CNS cells (XF 498), which was 2.6 times higher than …

StereochemistryClinical BiochemistryPhenazinePharmaceutical ScienceAntineoplastic AgentsCrystallography X-RayBiochemistryChemical synthesisInhibitory Concentration 50Structure-Activity Relationshipchemistry.chemical_compoundDrug DiscoveryTumor Cells CulturedNucleophilic substitutionHumansStructure–activity relationshipCytotoxicityMolecular BiologyMolecular StructureOrganic ChemistryIn vitroQuinonechemistryDoxorubicinCell cultureQuinolinesPhenazinesMolecular MedicineDrug Screening Assays AntitumorNaphthoquinonesBioorganic & Medicinal Chemistry
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Electrochemical and DFT studies of the oxidative decomposition of the trihydride complexes Cp*M(dppe)H3 (M = Mo, W) in acetonitrile

2006

International audience; A detailed electrochemical study of the oxidative decomposition of the trihydride complexes Cp*M(dppe)H3 (M = Mo, W) in acetonitrile is presented. For the Mo complex, the decomposition occurs by four different pathways involving classical and non-classical tautomers, whereas only the classical form is accessible for the W derivative. Each of the decomposition pathways has been quantitatively assessed by analyses of the linear sweep voltammograms. In addition to the previously established (B. Pleune, D. Morales, R. Meunier-Prest, P. Richard, E. Collange, J. C. Fettinger and R. Poli, J. Am. Chem. Soc., 1999, 121, 2209–2225) deprotonation, disproportionation, and H2 red…

StereochemistryDisproportionation010402 general chemistryElectrochemistry01 natural sciencesMedicinal chemistryDFTCatalysisReductive eliminationTungstenchemistry.chemical_compoundDeprotonationComplexMaterials Chemistrypentamethylcyclopentadienyl[CHIM.COOR]Chemical Sciences/Coordination chemistryAcetonitrileComputingMilieux_MISCELLANEOUSMolybdenumPhenylphosphinoethane010405 organic chemistryChemistry[ CHIM.COOR ] Chemical Sciences/Coordination chemistryGeneral ChemistryAssociative substitutionRate-determining stepTautomer0104 chemical sciences[CHIM.THEO]Chemical Sciences/Theoretical and/or physical chemistryTrihydridoPentamethylcyclopentadienyl ligand
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Unique regioselectivity in the C(sp3)-H α-alkylation of amines: the benzoxazole moiety as a removable directing group.

2014

The benzoxazol-2-yl- substituent was found to act as a removable activating and directing group in the Ir-catalyzed alkylation of C(sp(3))-H bonds adjacent to nitrogen in secondary amines. It can be easily introduced by oxidative coupling or by an SNAr reaction, and it can be removed by hydroxide or by hydride reduction. For 1,2,3,4-tetrahydroisoquinolines, activation exclusively takes place in the 3-position. A variety of activated as well as unactivated terminal olefins are suitable reaction partners.

StereochemistryHydrideOrganic ChemistrySubstituentRegioselectivityAlkylationBenzoxazoleBiochemistryMedicinal chemistrychemistry.chemical_compoundchemistryNucleophilic aromatic substitutionMoietyOxidative coupling of methanePhysical and Theoretical ChemistryOrganic letters
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