Search results for "pyridazine"

showing 10 items of 69 documents

Sodium-glucose cotransporter type 2 inhibitors prevent ponatinib-induced endothelial senescence and disfunction: A potential rescue strategy

2021

Background: Ponatinib (PON), a third-generation tyrosine kinase inhibitor (TKI), has proven cardiovascular toxicity, with no known preventing agents usable to limit such side effect. Sodium-glucose cotransporter type 2 (SGLT2) inhibitors are a new class of glucose-lowering agents, featuring favorable cardiac and vascular effects. Aims: We assessed the effects of the SGLT2 inhibitors empagliflozin (EMPA) and dapagliflozin (DAPA) on human aortic endothelial cells (HAECs) and underlying vasculo-protective mechanisms in an in vitro model of PON-induced endothelial toxicity. Methods and results: We exposed HAECs to PON or vehicle (DMSO) in the presence or absence of EMPA (100 and 500 nmol/L) or …

Physiologymedicine.drug_classCellPharmacologyAutophagy; Ponatinib; Sodium-glucose cotransporter type 2 (SGLT2) inhibitors; Tyrosine kinase inhibitors; Vascular toxicityTyrosine-kinase inhibitorFlow cytometrychemistry.chemical_compoundmedicineAutophagyHumansViability assayDapagliflozinCellular SenescencePharmacologyTyrosine kinase inhibitorsMatrigelmedicine.diagnostic_testChemistrySodiumImidazolesEndothelial CellsEndothelial stem cellPyridazinesmedicine.anatomical_structureGlucoseDiabetes Mellitus Type 2Sodium-glucose cotransporter type 2 (SGLT2) inhibitorsToxicityPonatinibMolecular MedicineVascular toxicity
researchProduct

Control of Programmed Cell Death by Distinct Electrical Activity Patterns

2010

Electrical activity and sufficient supply with survival factors play a major role in the control of apoptosis in the developing cortex. Coherent high-frequency neuronal activity, which efficiently releases neurotrophins, is essential for the survival of immature neurons. We studied the influence of neuronal activity on apoptosis in the developing cortex. Dissociated cultures of the newborn mouse cerebral cortex were grown on multielectrode arrays to determine the activity patterns that promote neuronal survival. Cultures were transfected with a plasmid coding for a caspase-3-sensitive fluorescent protein allowing real-time analysis of caspase-3-dependent apoptosis in individual neurons. Ele…

Programmed cell deathCognitive NeuroscienceAction PotentialsApoptosisBiologySynaptic TransmissionMiceCellular and Molecular NeurosciencemedicineAnimalsPremovement neuronal activityCells CulturedCerebral CortexNeuronsKinaseCell biologyCortex (botany)Mice Inbred C57BLPyridazinesNerve growth factorAnimals NewbornApoptosisbiology.proteinGabazineNerve NetNeurotrophinmedicine.drugCerebral Cortex
researchProduct

A straightforward copper-free palladium methodology for the selective alkynylation of a wide variety of S-, O-, and N-based mono- and diheterocyclic …

2009

Abstract High-yield alkynylations are successfully achieved by a simple and widely accessible catalytic system for an unprecedented variety of heterocyclic bromides and chlorides in position -2, -3 or -5: pyridine, quinoline, thiophene, furan, thiazole, benzothiazole, pyrimidine, pyridazine, pyrazine, dioxepin halides are efficiently functionalized in short time reactions. This copper-free methodology employs 1 mol % palladium only, with inexpensive PPh3 and amine base. The ionic liquid solvent allows a straigtforward separation of products and recycling opportunity. Unsuitable substrates and secondary reactions are also reported in order to point out further progress in cross-coupling usin…

Pyrazine010405 organic chemistry[CHIM.ORGA]Chemical Sciences/Organic chemistryOrganic ChemistryQuinolinechemistry.chemical_element010402 general chemistry01 natural sciencesBiochemistryCombinatorial chemistry0104 chemical sciencesPyridazinechemistry.chemical_compoundchemistryBenzothiazoleHeck alkynylation reaction[ CHIM.ORGA ] Chemical Sciences/Organic chemistryDrug DiscoveryIonic liquidThiopheneThiazoleComputingMilieux_MISCELLANEOUSPalladium
researchProduct

From Mononuclear Compounds to [2 × 2] Metallogrids: Ferromagnetically Coupled Systems Built by Nickel(II) and 3,6-Bis(2′-pyridyl)pyridazine (dppn)

2020

Mono-, di-, tri-, and tetranuclear compounds of nickel(II) of formula [Ni(dppn)3](NCS)2·0.5dppn (1), [{Ni(dppn)(NCS)}2(μ-dppn)(μ-NCS)]NCS (2), [Ni3(dppn)2(N3)2(μ-dppn)2(μ-N3)2](ClO4)2·CH3CH2OH·2H2O...

PyridazineNickelchemistry.chemical_compoundchemistrychemistry.chemical_elementGeneral Materials ScienceGeneral ChemistryCondensed Matter PhysicsMedicinal chemistryCrystal Growth & Design
researchProduct

ChemInform Abstract: A Straightforward Copper-Free Palladium Methodology for the Selective Alkynylation of a Wide Variety of S-, O-, and N-Based Mono…

2009

Abstract High-yield alkynylations are successfully achieved by a simple and widely accessible catalytic system for an unprecedented variety of heterocyclic bromides and chlorides in position -2, -3 or -5: pyridine, quinoline, thiophene, furan, thiazole, benzothiazole, pyrimidine, pyridazine, pyrazine, dioxepin halides are efficiently functionalized in short time reactions. This copper-free methodology employs 1 mol % palladium only, with inexpensive PPh3 and amine base. The ionic liquid solvent allows a straigtforward separation of products and recycling opportunity. Unsuitable substrates and secondary reactions are also reported in order to point out further progress in cross-coupling usin…

Pyridazinechemistry.chemical_compoundchemistryBenzothiazolePyrazineIonic liquidQuinolineThiophenechemistry.chemical_elementOrganic chemistryGeneral MedicineThiazolePalladiumChemInform
researchProduct

Synthesis of a bridgehead nitrogen system. Imidazo[1,5-b]pyridazine derivatives

1979

3,4-Dibenzoyl-2-oxobutyrate 4-semicarbazone (6a), ethyl 2,4-dioxo-3-phenacylvalerate 3-semicarbazone (6b) and diethyl phenacyloxalectate 3-semicarbazone (6c) via acid catalysed intramolecular cyclization afforded 2-phenyl-4-R-3H-imidazo[1,5-d]pyridazine-5,7-(6H)diones (8d,e,f). Elemental analyses and spectroscopic data (ir, nmr, ms) were in good agreement with the assigned structures.

Pyridazinechemistry.chemical_compoundchemistryOrganic ChemistryIntramolecular cyclizationOrganic chemistrychemistry.chemical_elementMedicinal chemistryNitrogenJournal of Heterocyclic Chemistry
researchProduct

CCDC 1977985: Experimental Crystal Structure Determination

2020

Related Article: Mouad Filali, El Mestafa El Hadrami, Rosaria Bruno, Giovanni De Munno, Abdeslem Bentama, Miguel Julve, Salah-Eddine Stiriba|2020|J.Mol.Struct.|1217|128420|doi:10.1016/j.molstruc.2020.128420

Space GroupCrystallography4-{[(prop-2-yn-1-yl)oxy]methyl}-36-bis(pyridin-2-yl)pyridazineCrystal SystemCrystal StructureCell ParametersExperimental 3D Coordinates
researchProduct

CCDC 1561792: Experimental Crystal Structure Determination

2017

Related Article: Tile Gieshoff, Anton Kehl, Dieter Schollmeyer, Kevin D. Moeller, Siegfried R. Waldvogel|2017|J.Am.Chem.Soc.|139|12317|doi:10.1021/jacs.7b07488

Space GroupCrystallographyCrystal System12-bis(4-chlorophenyl)-44-dimethyltetrahydropyridazine-36-dioneCrystal StructureCell ParametersExperimental 3D Coordinates
researchProduct

CCDC 902867: Experimental Crystal Structure Determination

2013

Related Article: T.F.Mastropietro,N.Marino,D.Armentano,G.De Munno,C.Yuste,F.Lloret,M.Julve|2013|Cryst.Growth Des.|13|270|doi:10.1021/cg301415p

Space GroupCrystallographyCrystal SystemCrystal StructureCell Parameters(mu2-3-(pyridin-2-yl)-6-(pyridin-2-yl)pyridazine)-(mu2-hydroxo)-tris(perchlorato)-triaqua-di-copper(ii) monohydrateExperimental 3D Coordinates
researchProduct

CCDC 1964202: Experimental Crystal Structure Determination

2020

Related Article: Rosaria Bruno, Nadia Marino, Joan Cano, Alejandro Pascual Alvarez, Abdeslem Ben Tama, Francesc Lloret, Miguel Julve, Giovanni De Munno|2020|Cryst.Growth Des.|20|6478|doi:10.1021/acs.cgd.0c00650

Space GroupCrystallographyCrystal SystemCrystal StructureCell ParametersExperimental 3D Coordinatesbis(mu-36-bis(pyridin-2-yl)pyridazine)-bis(mu-azido)-bis(36-bis(pyridin-2-yl)pyridazine)-diazido-tri-nickel(ii) bis(perchlorate) ethanol solvate dihydrate
researchProduct