Search results for "triazol"

showing 10 items of 598 documents

Preventive effect of risedronate on bone loss and frailty fractures in elderly women treated with anastrozole for early breast cancer.

2011

The aim of this study was to assess the effect of adjuvant anastrozole, alone or associated with risedronate, on BMD and bone fracture risk in women more than 70 years old with hormone receptor-positive early breast cancer (EBC). In a group of 51 elderly women (aged 76.4 ± 5.0 years) considered for adjuvant aromatase inhibitors for EBC, 24 patients with T-scores ≥ -2 and no prevalent fractures received anastrozole 1 mg/day (group A), and 27 patients with T-scores < -2, or with T-scores ≥ -2 and prevalent fractures (group B), received anastrozole (1 mg/day) plus risedronate (35 mg/week). Both groups received supplementation with 1 g calcium carbonate and 800 IU vitamin D per day. Differen…

Endocrinology Diabetes and MetabolismOsteoporosisSeverity of Illness IndexCohort StudiesEndocrinologyBone DensityOrthopedics and Sports MedicineVitamin DAromataseOsteoporosis PostmenopausalAged 80 and overBone Density Conservation AgentsbiologyAromatase InhibitorsEtidronic AcidGeneral MedicineCombined Modality Therapymedicine.anatomical_structureFemaleRisedronic Acidmedicine.drugmusculoskeletal diseasesmedicine.medical_specialtyAntineoplastic Agents HormonalUrologyAnastrozoleBreast NeoplasmsAnastrozoleCalcium CarbonateNitrilesmedicineVitamin D and neurologyHumansBone ResorptionAgedNeoplasm StagingFemoral neckTrochanterbusiness.industryBone fractureTriazolesmedicine.diseaseSurgeryEarly breast cancer Anastrozole Osteoporosis Vertebral fractures ElderlyDietary SupplementsOrthopedic surgerybiology.proteinbusinessOsteoporotic FracturesFollow-Up Studies
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Disturbances in energy metabolism of Daphnia magna after exposure to tebuconazole.

2008

Abstract This study was conducted to investigate the change of some biochemical parameters in the aquatic invertebrate Daphnia magna following exposure to the fungicide tebuconazole and to determine the most sensitive biomarker among the ones tested in this species. Four biochemical biomarkers (protein, glycogen, lipids and caloric content) were correlated with feeding behaviour studies of D. magna after fungicide exposure. Juveniles of D. magna were exposed to four sublethal concentrations of tebuconazole (0.41, 0.52, 0.71 and 1.14 mg L−1) for 5 d. Daphnid samples were taken from each test and control group at 24, 48, 72, 96 and 120 h after the start of the experiment. Tebuconazole EC50 va…

Environmental EngineeringTime FactorsHealth Toxicology and MutagenesisDaphnia magnaBiologyToxicologychemistry.chemical_compoundAnimal scienceToxicity Tests AcuteEnvironmental ChemistryAnimalsEC50TebuconazoleDose-Response Relationship DrugfungiPublic Health Environmental and Occupational HealthAquatic animalGeneral MedicineGeneral ChemistryFeeding BehaviorPesticideTriazolesbiology.organism_classificationPollutionFungicidechemistryCladoceraDaphniaToxicityEnergy MetabolismBiomarkersChemosphere
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Triazolopyridines. Part 30. Hydrogen transfer reactions; pyridylcarbene formation

2013

The transfer hydrogenation reaction of (1,2,3)triaz olo(1,5-a)pyridines with Pd/C/Zn or Pd(OH) 2/C/Zn in water, ethanol or water/ethanol mixture ha s been explored. 4,5,6,7-Tetrahydro- triazolopyridines were obtained in good to medium yields. In addition, under the same conditions 2-substituted pyridines were also formed as a resul t of intermediate pyridylcarbene formation, by triazole ring opening and loss of nitrogen.

EthanolOrganic ChemistryTriazolechemistry.chemical_elementHydrogen transferRing (chemistry)Transfer hydrogenationNitrogenlcsh:QD241-441chemistry.chemical_compoundchemistrylcsh:Organic chemistryPolymer chemistryOrganic chemistryARKIVOC
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CCDC 766325: Experimental Crystal Structure Determination

2010

Related Article: L.Kiss, E.Forro, R.Sillanpaa, F.Fulop|2010|Tetrahedron|66|3599|doi:10.1016/j.tet.2010.03.030

Ethyl 1-((1R*2R*3R*4R*)-3-((t-butoxycarbonyl)amino)-4-(ethoxycarbonyl)-2-hydroxycyclopentyl)-1H-123-triazole-4-carboxylateSpace GroupCrystallographyCrystal SystemCrystal StructureCell ParametersExperimental 3D Coordinates
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The influence study of the number of substituted heteroaryls at the non-K region of pyrene structure on the photophysical properties based on the exa…

2022

The study of the photophysical properties (thermal - thermogravimetric analysis and optical - absorption, emission in the solution and in powder, quantum efficiency of emission and efficient fluorescence lifetime in the solution) with the focus on the influence of the number of substituted 1-decyl-1H-1,2,3-triazole groups at the non-K region of pyrene structure. To the best of our knowledge, the investigation of the impact of the number of heteroaryl groups at the non-K region of pyrene is reported for the first time. The obtained results for monosubstituted derivative (1) were compared to di- (2, 3) and tetra- (4) analogues previously reported by us in the literature. In addition, theoreti…

Experimental studyPyrene derivativeTriazole motifSubstitution patternPhotophysical propertiesJournal of Molecular Structure
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Hydrogen bonding versus π-stacking in ferromagnetic interactions. Studies on a copper triazolopyridine complex

2013

Magnetic susceptibility measurements show weak ferromagnetic exchange between the copper(II) ions of a novel triazolopyridine derivative [Cu(TPT)(H2O)2(BF4)](BF4)·2H2O (TPT = 3-{6-([1,2,3]triazolo[1,5-a]pyrid-3-yl)-2-pyridyl}-[1,2,3]triazolo[1,5-a]pyridine). Mononuclear [Cu(TPT)(H2O)2(BF4)]+ entities are connected through O–H⋯F, C–H⋯F and π⋯π interactions to give a 3D framework. Ferromagnetic properties are discussed on the basis of the interactions network.

Ferromagnetic material propertiesStereochemistryHydrogen bondStackingchemistry.chemical_elementGeneral ChemistryCondensed Matter PhysicsCopperMagnetic susceptibilityCrystallographychemistry.chemical_compoundchemistryFerromagnetismPyridineGeneral Materials ScienceTriazolopyridineCrystEngComm
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An ANRORC approach to the synthesis of perfluoroalkylated 1,2,4-triazole-carboxamides

2009

A series of perfluoroalkyl-1,2,4-triazole-carboxamides has been obtained through an ANRORClike rearrangement (Addition of Nucleophile, Ring-Opening and Ring-Closure) of 5- perfluoroalkyl-1,2,4-oxadiazole-3-carboxamides with methylhydrazine or hydrazine. The initial addition of the bidentate nucleophile to the electrophilic C(5) of the 1,2,4-oxadiazole ring, followed by ring opening and ring closure, leads to the formation of triazoles in good yield under mild experimental conditions. In some cases, a competitive ANRORC-enlargement reaction to form 1,2,4-triazin-6-ones was also observed. Obtained carboxamidotriazoles have also been explored as precursors for the synthesis of 3(5)-perfluoroal…

Fluorinated heterocycles triazole oxadiazole ANRORC rearrangementschemistry.chemical_compoundchemistryOrganic ChemistryTriazole124-TriazoleOxadiazoleSettore CHIM/06 - Chimica OrganicaCombinatorial chemistry
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Carbon Nanotubes Conjugated with Triazole-Based Tetrathiafulvalene-Type Receptors for C60 Recognition

2019

Fullerene receptors prepared by a twofold CuI -catalyzed azide-alkyne cycloaddition (CuAAC) reaction with -extended tetrathiafulvalene (exTTF) have been covalently linked to singlewalled carbon nanotubes (SWCNTs) and multi-walled carbon nanotubes (MWCNTs). The nanoconjugates obtained were characterized by several analytical, spectroscopic and microscopic techniques (TEM, FTIR, Raman, TGA and XPS), and evaluated as C60 receptors by UV-Vis spectroscopy. The complexation between the exTTF-triazole receptor in the free state and C60 was also studied by UV-Vis and 1 H NMR titrations, and compared with analogous triazole-based tweezer-type receptors containing the electron-acceptor 11,11,12,12-t…

FullereneFULLERENEShost-guest interactionsTriazoleCarbon nanotubeCOMMUNICATIONConjugated systemHOSTS010402 general chemistry01 natural scienceslaw.inventionchemistry.chemical_compoundsymbols.namesakeTCAQAZIDESlawCHEMISTRYAROMATICITYPHOTOINDUCED ELECTRON-TRANSFERcarbon nanotubes010405 organic chemistryCOMPLEXATIONQuímica orgánicaAromaticityEXTTFGeneral Chemistrypi-extended tetrathiafulvalenes0104 chemical sciencesCrystallographychemistrydensity functional calculationssymbolsDensity functional theoryRaman spectroscopyTetrathiafulvalene
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X-ray Single Crystal Structure, Tautomerism Aspect, DFT, NBO, and Hirshfeld Surface Analysis of a New Schiff Bases Based on 4-Amino-5-Indol-2-yl-1,2,…

2021

Four different new Schiff basses tethered indolyl-triazole-3-thione hybrid were designed and synthesized. X-ray single crystal structure, tautomerism, DFT, NBO and Hirshfeld analysis were explored. X-ray crystallographic investigations with the aid of Hirshfeld calculations were used to analyze the molecular packing of the studied systems. The H···H, H···C, S···H, Br···C, O···H, C···C and N···H interactions are the most important in the molecular packing of 3. In case of 4, the S···H, N···H, S···C and C···C contacts are the most significant. The results obtained from the DFT calculations indicated that the thione tautomer is energetically lower than the thiol one by 13.9545 and 13.7464 kcal…

General Chemical Engineeringtautomerism aspectInorganic Chemistrysymbols.namesakeGeneral Materials SciencetyppiyhdisteetDebyechemistry.chemical_classificationkemiallinen synteesiCrystallographyX-rayCondensed Matter Physicsindolyl-triazole-3-thioneTautomerSchiff bases; indolyl-triazole-3-thione; tautomerism aspect; Hirshfeld Surface AnalysisCrystallographyDipolechemistryQD901-999Thiolsymbols1 2 4 triazole 3 thioneSchiff basesHirshfeld Surface AnalysisSingle crystaltautomeriaNatural bond orbitalCrystals; Volume 11; Issue 9; Pages: 1041
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1,2,3-Oligotriazoles modified halloysite nanotubes as potential active biological species: synthesis and characterization

2022

In the last years, the development of nano-formulations for cancer treatment represents one of the major challenges of the scientific research. The prodrug strategy, that combines chemotherapeutic agents with nanocarriers such as halloysite nanotubes (HNTs), is a promising strategy both to improve the biological activity of the drug molecules and to reduce the side effects of drugs. Herein we report the synthesis and characterization of a HNTs prodrug based on 1,2,3-triazole units covalently linked to HNTs external surface, bearing different positively charged moieties, which could present interesting pharmacological activities.

Halloysite nanotubes123-oligotriazolecovalent modificationOrganic ChemistryHuisgen reactionSettore CHIM/06 - Chimica OrganicaHNTs-prodrugSettore CHIM/02 - Chimica FisicaArkivoc
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