0000000001311149

AUTHOR

Alberto Tárraga

showing 8 related works from this author

Combined study of anion recognition by a carbazole-based neutral tripodal receptor in a competitive environment

2012

Anion recognition studies have been carried out on a series of neutral synthetic receptors in which carbazole-2-carboxamide has been used as building block. Different ligands which include one to three carbazole units in their structure have been prepared. Binding experiments have been performed under competitive conditions in DMSO and DMSO-water solutions. The tripodal receptor offered a better host-guest association due to the synergistic effect of a well arranged set of hydrogen bonds. A selective response towards the biologically important pyrophosphate anion has been achieved. This selectivity is enhanced when studies are carried out with an increasing water content, which gets as high…

Hydrogen bondCarbazoleStereochemistryOrganic ChemistryMass spectrometryBiochemistryCombinatorial chemistryPyrophosphateIonchemistry.chemical_compoundchemistryProton NMRPhysical and Theoretical ChemistryAbsorption (chemistry)SelectivityOrganic & Biomolecular Chemistry
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A pyrroloquinazoline derivative with anti-inflammatory and analgesic activity by dual inhibition of cyclo-oxygenase-2 and 5-lipoxygenase

2002

Abstract In a previous study, we reported a new pyrroloquinazoline derivative, 3-(4′-acetoxy-3′,5′-dimethoxy)benzylidene-1,2-dihydropyrrolo[2,1- b ]quinazoline-9-one (PQ), which inhibited human purified 5-lipoxygenase activity and prostaglandin E 2 release in lipopolysaccharide-stimulated RAW 264.7 cells. In the present work, we show that PQ inhibits cyclo-oxygenase-2 activity in intact cell assays (human monocytes) and purified enzyme preparations (ovine isoenzymes) without affecting cyclo-oxygenase-1 activity. This behaviour was confirmed in vivo by using the zymosan-injected mouse air pouch model, where PQ caused a marked reduction in cell migration and leukotriene B 4 levels at 4 h, as …

medicine.medical_treatmentPharmacologyMonocytesMicechemistry.chemical_compoundIn vivomedicineAnimalsEdemaHumansCyclooxygenase InhibitorsPyrrolesLipoxygenase InhibitorsEnzyme InhibitorsProstaglandin E2Pain MeasurementPharmacologyAnalgesicsArachidonate 5-LipoxygenaseSheepCyclooxygenase 2 InhibitorsDose-Response Relationship DrugbiologyChemistryAnti-Inflammatory Agents Non-SteroidalZymosanMembrane ProteinsBiological activityIsoenzymesBiochemistryMechanism of actionCyclooxygenase 2Prostaglandin-Endoperoxide SynthasesEnzyme inhibitorArachidonate 5-lipoxygenaseQuinazolinesQuinolinesbiology.proteinFemalemedicine.symptomProstaglandin Emedicine.drug
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Ion pair recognition receptor based on an unsymmetrically 1,1'-disubstituted ferrocene-triazole derivative.

2012

The ferrocene-triazole derivative 4, available from 1,1'-bis(diazido)ferrocene by sequential functionalization through click-type chemistry and the Staudinger reaction, is elaborated as a lab-on-a-molecule for the selective sensing of HP(2)O(7)(3-) and Hg(2+). Receptor 4 behaves as a ratiometric fluorescent probe for HP(2)O(7)(3-) with a good selectivity over other anions, whereas in the presence of Hg(2+) it modifies the fluorescent emission of the pyrene unit, acting as a selective on-off fluorescent sensor for Hg(2+) with a low detection limit. The most salient feature of compound 4 is its behavior as an excellent electrooptical ion pair recognition receptor able to simultaneously recogn…

IonsMagnetic Resonance SpectroscopyMetallocenesOrganic ChemistryTriazolesPhotochemistryFluorescenceRedoxIonchemistry.chemical_compoundchemistryFerroceneElectrochemistryPyreneSpectrophotometry UltravioletStaudinger reactionFerrous CompoundsSelectivityDerivative (chemistry)Fluorescent DyesThe Journal of organic chemistry
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Single Heteroatom Fine-Tuning of the Emissive Properties in Organoboron Complexes with 7-(Azaheteroaryl)indole Systems

2016

The application of organoboron compounds as light-absorbing or light-emitting species in areas as relevant as organic electronics or biomedicine has motivated the search for new materials which contribute to the progress of those applications. This article reports the synthesis of four-coordinate boron complexes based on the unexplored 7-(azaheteroaryl)indole ligands. An easy synthetic approach has enabled the fine-tuning of the electronic structure of the organoboron species by modifying a heteroaromatic component in the conjugated system. Furthermore, a comprehensive characterization by X-ray diffraction, absorption and emission spectroscopy, both in solution and in the solid state, cycli…

Organic electronicsIndole test010405 organic chemistryOrganic ChemistryHeteroatomchemistry.chemical_elementElectronic structureFour-coordinate boron complexFluorophoreConjugated system010402 general chemistryBioimaging01 natural sciencesCombinatorial chemistry0104 chemical scienceschemistryOrganic chemistryEmission spectrumCyclic voltammetryBoronThe Journal of Organic Chemistry
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[3.3]Ferrocenophanes with guanidine bridging units as multisignalling receptor molecules for selective recognition of anions, cations, and amino acid…

2007

The synthesis, electrochemical, and optical properties of a new [3.3]ferrocenophane framework in which two ferrocene subunits, with similar electronic environments, are linked through two substituted guanidine moieties, are reported. The receptors 4-7 have been prepared in good yields by the reaction of bis(carbodiimide) 3 with primary amines. This architecture is exceptionally "tunable" because a variety of "legs" may be appended to the basic [3.3]ferrocenophane scaffold to give a wide range of signaling units. These receptors show remarkable ion-sensing properties, due to the presence of a redox active unit (ferrocene), and an amphoteric binding site (guanidine). In this nitrogen-rich str…

AnionsModels MolecularMetallocenesInorganic chemistryCrystallography X-RayRedoxCatalysisMetalchemistry.chemical_compoundMolecular recognitionCationsElectrochemistryMoleculeFerrous CompoundsAmino AcidsGuanidineGuanidineCarbodiimideFluorescent Dyeschemistry.chemical_classificationSpectrum AnalysisOrganic ChemistryGeneral ChemistryAmino acidCrystallographyFerrocenechemistryvisual_artvisual_art.visual_art_mediumChemistry (Weinheim an der Bergstrasse, Germany)
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CCDC 1449799: Experimental Crystal Structure Determination

2016

Related Article: Miriam Más-Montoya, Laura Usea, Arturo Espinosa Ferao, María F. Montenegro, Carmen Ramírez de Arellano, Alberto Tárraga, José N. Rodríguez-López, and David Curiel|2016|J.Org.Chem.|81|3296|doi:10.1021/acs.joc.6b00265

Space GroupCrystallography13-octyl-77-diphenyl-7H13H-8lambda57lambda5-indolo[1'7':345][132]diazaborinino[16-a][31]benzimidazoleCrystal SystemCrystal StructureCell ParametersExperimental 3D Coordinates
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CCDC 893127: Experimental Crystal Structure Determination

2013

Related Article: Francisco Otón , María del Carmen González , Arturo Espinosa , Carmen Ramírez de Arellano , Alberto Tárraga , and Pedro Molina|2012|J.Org.Chem.|77|10083|doi:10.1021/jo301570u

Space GroupCrystallography1-[4-(1-Pyrenyl)-123-triazol-1-yl]-1'-(quinaldoylamino)ferroceneCrystal SystemCrystal StructureCell ParametersExperimental 3D Coordinates
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CCDC 1449800: Experimental Crystal Structure Determination

2016

Related Article: Miriam Más-Montoya, Laura Usea, Arturo Espinosa Ferao, María F. Montenegro, Carmen Ramírez de Arellano, Alberto Tárraga, José N. Rodríguez-López, and David Curiel|2016|J.Org.Chem.|81|3296|doi:10.1021/acs.joc.6b00265

Space GroupCrystallographyCrystal SystemCrystal StructureCell Parameters77-diphenyl-7H-8lambda57lambda5-indolo[1'7':345][132]diazaborinino[61-b][13]benzoxazoleExperimental 3D Coordinates
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